[
  {
    "phenotype_id": "PH1701",
    "phenotype_version_id": 3627,
    "name": "Chronic paediatric conditions: Other neurological (excluding epilepsy and headaches)",
    "definition": "This code list is part of a set of harmonised code lists to identify chronic paediatric\nconditions across primary and secondary care datasets across the UK.\n\n- ICD-10 neurological conditions as per Hardelid 2014 (epilepsy and headaches excluded) and mapped to SNOMED and Read v2 using CALIBER.\n- Includes other neurological disorders (e.g., cerebral palsy, paralysis, degenerative neurological disease, myopathies, dystonia, disease of myelination, neuropathy, hydrocephalus and  intracranial vascular events).\n- Includes congenital abnormalities of the brain / spinal cord and associated syndromes, neurological conditions of the perinatal period and presence of cerebrospinal fluid drainage devices.\n- Further separated into four subgroups i) cerebral palsy and paralysis, ii) congenital neurological condition, iii) other neurological condition (not epilepsy, headaches, cerebral palsy, paralysis or congenital neurological disorder) and iv) neurological devices.\n\n### Methods\n\nChronic paediatric conditions were defined as health problems requiring medical follow-up\nfor more than 12 months in 50% or more of cases. Code lists were produced by mapping\nexisting ICD-10 codes for chronic paediatric conditions to SNOMED and Read v2 codes\nusing the CALIBER R package, with review by paediatric sub-specialists.\n\nAn established ICD-10 code list of chronic paediatric conditions (Hardelid 2014)\nwas used as the basis for the new lists.1  Chronic paediatric conditions were defined\nas any health problem requiring medical follow-up (hospital admission, outpatient\nfollow up or use of support services such as physiotherapy) for more than 12 months\nin 50% or more of cases.[1]  A Chronic Paediatric Conditions Committee of paediatric\nsub-specialists was established. The original ICD-10 list was screened by two paediatricians\nand acute conditions removed, with disagreements resolved by a third paediatrician.\nConditions which were likely acute and would not fulfil our chronic disease definition\nwere excluded, including skeletal injuries and self-harm. Drug-induced conditions\nwere excluded as chronicity was not known. Infections other than human immunodeficiency\nvirus (HIV), hepatitis B or C, or congenital infections (syphilis / toxoplasmosis\n/ rubella / herpes simplex virus / cytomegalovirus) were excluded. Chronic sequelae\nof infections were retained.\n\nPublished code lists were then identified for Read v2 and SNOMED codes for well-characterised\nconditions including asthma, diabetes, cystic fibrosis and cancer. The remaining\nICD-10 codes were mapped to SNOMED and Read v2 codes using the CALIBER R package\nand Technology Reference Update Distribution NHS Data Migration tables [2] to produce\nnew code lists suitable for primary care data. These resulting code lists were screened\nby two sub-specialists to ensure conditions were chronic and in the correct subgroup\nwith disagreements resolved by a third clinician.\n\n### References:\n\n1. Hardelid P, Dattani N, Gilbert R. Estimating the prevalence of chronic conditions in children who die in England, Scotland and Wales: a data linkage cohort study. BMJ Open 2014; 4: e005331.\n2. CALIBER codelists-package: Generate ICD, Read and OPCS codelists in CALIBER codelists: Generate ICD10, Read and OPCS codelists, [https://rdrr.io/rforge/CALIBERcodelists/man/CALIBERcodelists-package.html](https://rdrr.io/rforge/CALIBERcodelists/man/CALIBERcodelists-package.html) (accessed 19 October 2022).\n\n",
    "implementation": "We have considered conditions to be active if they had been coded for in the preceding\nfive years. In addition, conditions from the following subgroups were considered\nto be permanent, therefore active if coded for at any time: metabolic, diabetes,\ncystic fibrosis, transplant, receiving palliative care, other congenital multisystem\nsyndromes and chromosomal abnormalities, immunological and cerebral palsy / paralysis\n(a subgroup of \"Other neurology\" code list).\n",
    "publications": [],
    "validation": "",
    "citation_requirements": "To our knowledge, these are the first set of harmonised code lists for chronic paediatric\nconditions that span commonly used primary and secondary care coding systems in the\nUK. We hope they will prove a valuable resource for the paediatric research community\nand welcome suggestions for further development ([Olivia.Swann@ed.ac.uk](mailto:Olivia.Swann@ed.ac.uk)).\n",
    "created": "2025-01-18T19:59:30.786898Z",
    "author": "Swann OV, Williams TC, Fraser LK, Farrell J, Parker M, Kennedy J, Seabourne M, Brophy S, Harrison EM, Docherty AB, Pollock L",
    "collections": [
      {
        "name": "Phenotype Library",
        "value": 18
      }
    ],
    "tags": null,
    "organisation": null,
    "world_access": 2,
    "updated": "2025-01-19T16:01:42.681977Z",
    "sex": [
      {
        "name": "Both",
        "value": "3"
      }
    ],
    "type": [
      {
        "name": "Disease or syndrome",
        "value": "2"
      }
    ],
    "ontology": [
      {
        "name": "Paediatrics",
        "value": 842203
      },
      {
        "name": "Paediatric and Perinatal Pathology",
        "value": 842275
      }
    ],
    "phenoflowid": "",
    "data_sources": [
      {
        "name": "Hospital Episode Statistics Admitted Patient Care",
        "value": 2,
        "uid": "6599230a-df54-4615-937c-d724d239491f",
        "url": "https://healthdatagateway.org/en/dataset/875",
        "datasource_id": 875
      },
      {
        "name": "OpenSAFELY SNOMED CT",
        "value": 36,
        "datasource_id": 36
      },
      {
        "name": "Patient Episode Dataset for Wales (PEDW)",
        "value": 40,
        "uid": "4c33a5d2-164c-41d7-9797-dc2b008cc852",
        "url": "https://healthdatagateway.org/en/dataset/318",
        "datasource_id": 318
      },
      {
        "name": "Welsh Longitudinal General Practice Dataset (WLGP) - Welsh Primary Care",
        "value": 502,
        "uid": "33fc3ffd-aa4c-4a16-a32f-0c900aaea3d2",
        "url": "https://healthdatagateway.org/en/dataset/355",
        "datasource_id": 355
      }
    ],
    "coding_system": [
      {
        "name": "SNOMED  CT codes",
        "value": 9
      },
      {
        "name": "ICD10 codes",
        "value": 4
      },
      {
        "name": "Read codes v2",
        "value": 5
      }
    ],
    "event_date_range": "2021/01/01 - 2021/01/01",
    "concept_information": [
      {
        "concept_id": 4116,
        "concept_version_id": 11471,
        "concept_name": "Other neurological - cerebral palsy and paralysis (ICD-10)",
        "coding_system": {
          "id": 4,
          "name": "ICD10 codes",
          "description": "ICD10 Codes"
        },
        "phenotype_id": "PH1701",
        "phenotype_version_id": 3627,
        "phenotype_name": "Chronic paediatric conditions: Other neurological (excluding epilepsy and headaches)",
        "code_attribute_header": null,
        "codes": [
          {
            "code": "G80",
            "description": "Cerebral palsy",
            "attributes": null
          },
          {
            "code": "G800",
            "description": "Spastic quadriplegic cerebral palsy",
            "attributes": null
          },
          {
            "code": "G801",
            "description": "Spastic diplegic cerebral palsy",
            "attributes": null
          },
          {
            "code": "G802",
            "description": "Spastic hemiplegic cerebral palsy",
            "attributes": null
          },
          {
            "code": "G803",
            "description": "Dyskinetic cerebral palsy",
            "attributes": null
          },
          {
            "code": "G804",
            "description": "Ataxic cerebral palsy",
            "attributes": null
          },
          {
            "code": "G808",
            "description": "Other cerebral palsy",
            "attributes": null
          },
          {
            "code": "G809",
            "description": "Cerebral palsy, unspecified",
            "attributes": null
          },
          {
            "code": "G81",
            "description": "Hemiplegia",
            "attributes": null
          },
          {
            "code": "G810",
            "description": "Flaccid hemiplegia",
            "attributes": null
          },
          {
            "code": "G811",
            "description": "Spastic hemiplegia",
            "attributes": null
          },
          {
            "code": "G819",
            "description": "Hemiplegia, unspecified",
            "attributes": null
          },
          {
            "code": "G82",
            "description": "Paraplegia and tetraplegia",
            "attributes": null
          },
          {
            "code": "G820",
            "description": "Flaccid paraplegia",
            "attributes": null
          },
          {
            "code": "G821",
            "description": "Spastic paraplegia",
            "attributes": null
          },
          {
            "code": "G822",
            "description": "Paraplegia, unspecified",
            "attributes": null
          },
          {
            "code": "G823",
            "description": "Flaccid tetraplegia",
            "attributes": null
          },
          {
            "code": "G824",
            "description": "Spastic tetraplegia",
            "attributes": null
          },
          {
            "code": "G825",
            "description": "Tetraplegia, unspecified",
            "attributes": null
          },
          {
            "code": "G83",
            "description": "Other paralytic syndromes",
            "attributes": null
          },
          {
            "code": "G830",
            "description": "Diplegia of upper limbs",
            "attributes": null
          },
          {
            "code": "G831",
            "description": "Monoplegia of lower limb",
            "attributes": null
          },
          {
            "code": "G832",
            "description": "Monoplegia of upper limb",
            "attributes": null
          },
          {
            "code": "G833",
            "description": "Monoplegia, unspecified",
            "attributes": null
          },
          {
            "code": "G834",
            "description": "Cauda equina syndrome",
            "attributes": null
          },
          {
            "code": "G835",
            "description": "Locked-in syndrome",
            "attributes": null
          },
          {
            "code": "G836",
            "description": "Upper motor neuron facial paralysis",
            "attributes": null
          },
          {
            "code": "G838",
            "description": "Other specified paralytic syndromes",
            "attributes": null
          },
          {
            "code": "G839",
            "description": "Paralytic syndrome, unspecified",
            "attributes": null
          }
        ]
      },
      {
        "concept_id": 4117,
        "concept_version_id": 11477,
        "concept_name": "Other neurological - cerebral palsy and paralysis (Reda v2)",
        "coding_system": {
          "id": 5,
          "name": "Read codes v2",
          "description": "Read codes v2"
        },
        "phenotype_id": "PH1701",
        "phenotype_version_id": 3627,
        "phenotype_name": "Chronic paediatric conditions: Other neurological (excluding epilepsy and headaches)",
        "code_attribute_header": null,
        "codes": [
          {
            "code": "F137000",
            "description": "Athetoid cerebral palsy",
            "attributes": null
          },
          {
            "code": "F137100",
            "description": "Double athetosis",
            "attributes": null
          },
          {
            "code": "F137.11",
            "description": "Athetoid cerebral palsy",
            "attributes": null
          },
          {
            "code": "F137111",
            "description": "Congenital athetosis",
            "attributes": null
          },
          {
            "code": "F137.12",
            "description": "Athetosis - congenital",
            "attributes": null
          },
          {
            "code": "F164.00",
            "description": "Brown-Sequard syndrome",
            "attributes": null
          },
          {
            "code": "F22..00",
            "description": "Hemiplegia",
            "attributes": null
          },
          {
            "code": "F220.00",
            "description": "Flaccid hemiplegia",
            "attributes": null
          },
          {
            "code": "F221.00",
            "description": "Spastic hemiplegia",
            "attributes": null
          },
          {
            "code": "F22..11",
            "description": "Hemiparesis",
            "attributes": null
          },
          {
            "code": "F222.00",
            "description": "Left hemiplegia",
            "attributes": null
          },
          {
            "code": "F222.11",
            "description": "Left sided weakness",
            "attributes": null
          },
          {
            "code": "F223.00",
            "description": "Right hemiplegia",
            "attributes": null
          },
          {
            "code": "F223.11",
            "description": "Right sided weakness",
            "attributes": null
          },
          {
            "code": "F22z.00",
            "description": "Hemiplegia NOS",
            "attributes": null
          },
          {
            "code": "F23..00",
            "description": "Congenital cerebral palsy",
            "attributes": null
          },
          {
            "code": "F230.00",
            "description": "Congenital diplegia",
            "attributes": null
          },
          {
            "code": "F230000",
            "description": "Congenital paraplegia",
            "attributes": null
          },
          {
            "code": "F230100",
            "description": "Cerebral palsy with spastic diplegia",
            "attributes": null
          },
          {
            "code": "F230.11",
            "description": "Paraplegia - congenital",
            "attributes": null
          },
          {
            "code": "F230111",
            "description": "Spastic diplegic cerebral palsy",
            "attributes": null
          },
          {
            "code": "F230z00",
            "description": "Congenital diplegia NOS",
            "attributes": null
          },
          {
            "code": "F231.00",
            "description": "Congenital hemiplegia",
            "attributes": null
          },
          {
            "code": "F23..11",
            "description": "Congenital spastic cerebral palsy",
            "attributes": null
          },
          {
            "code": "F23..12",
            "description": "Infantile cerebral palsy",
            "attributes": null
          },
          {
            "code": "F23..13",
            "description": "Littles disease",
            "attributes": null
          },
          {
            "code": "F23..14",
            "description": "Cerebral atonia",
            "attributes": null
          },
          {
            "code": "F232.00",
            "description": "Congenital quadriplegia",
            "attributes": null
          },
          {
            "code": "F232.11",
            "description": "Tetraplegia - congenital",
            "attributes": null
          },
          {
            "code": "F233.00",
            "description": "Congenital monoplegia",
            "attributes": null
          },
          {
            "code": "F234.00",
            "description": "Infantile hemiplegia NOS",
            "attributes": null
          },
          {
            "code": "F23y.00",
            "description": "Other congenital cerebral palsy",
            "attributes": null
          },
          {
            "code": "F23y000",
            "description": "Ataxic infantile cerebral palsy",
            "attributes": null
          },
          {
            "code": "F23y100",
            "description": "Flaccid infantile cerebral palsy",
            "attributes": null
          },
          {
            "code": "F23y200",
            "description": "Spastic cerebral palsy",
            "attributes": null
          },
          {
            "code": "F23y300",
            "description": "Dyskinetic cerebral palsy",
            "attributes": null
          },
          {
            "code": "F23y400",
            "description": "Ataxic diplegic cerebral palsy",
            "attributes": null
          },
          {
            "code": "F23y500",
            "description": "Worster-Drought syndrome",
            "attributes": null
          },
          {
            "code": "F23y511",
            "description": "Congenital suprabulbar paresis",
            "attributes": null
          },
          {
            "code": "F23yz00",
            "description": "Other infantile cerebral palsy NOS",
            "attributes": null
          },
          {
            "code": "F23z.00",
            "description": "Congenital cerebral palsy NOS",
            "attributes": null
          },
          {
            "code": "F24..00",
            "description": "Other paralytic syndromes",
            "attributes": null
          },
          {
            "code": "F240.00",
            "description": "Quadriplegia",
            "attributes": null
          },
          {
            "code": "F240000",
            "description": "Flaccid tetraplegia",
            "attributes": null
          },
          {
            "code": "F240100",
            "description": "Spastic tetraplegia",
            "attributes": null
          },
          {
            "code": "F240.11",
            "description": "Tetraplegia",
            "attributes": null
          },
          {
            "code": "F241.00",
            "description": "Paraplegia",
            "attributes": null
          },
          {
            "code": "F241000",
            "description": "Flaccid paraplegia",
            "attributes": null
          },
          {
            "code": "F241100",
            "description": "Spastic paraplegia",
            "attributes": null
          },
          {
            "code": "F242.00",
            "description": "Diplegia of upper limbs",
            "attributes": null
          },
          {
            "code": "F243.00",
            "description": "Monoplegia of lower limb",
            "attributes": null
          },
          {
            "code": "F244.00",
            "description": "Monoplegia of upper limb",
            "attributes": null
          },
          {
            "code": "F245.00",
            "description": "Monoplegia unspecified",
            "attributes": null
          },
          {
            "code": "F24y.00",
            "description": "Other specified paralytic syndromes",
            "attributes": null
          },
          {
            "code": "F24yz00",
            "description": "Other paralytic syndromes NOS",
            "attributes": null
          },
          {
            "code": "F24yz11",
            "description": "Specified palsy NEC",
            "attributes": null
          },
          {
            "code": "F24z.00",
            "description": "Paralysis NOS",
            "attributes": null
          },
          {
            "code": "F2A..00",
            "description": "Hemiparesis",
            "attributes": null
          },
          {
            "code": "F2Az.00",
            "description": "Hemiparesis NOS",
            "attributes": null
          },
          {
            "code": "F2B..00",
            "description": "Cerebral palsy",
            "attributes": null
          },
          {
            "code": "F2B0.00",
            "description": "Spastic quadriplegic cerebral palsy",
            "attributes": null
          },
          {
            "code": "F2By.00",
            "description": "Other cerebral palsy",
            "attributes": null
          },
          {
            "code": "F2Bz.00",
            "description": "Cerebral palsy NOS",
            "attributes": null
          },
          {
            "code": "Fyu9000",
            "description": "[X]Other infantile cerebral palsy",
            "attributes": null
          }
        ]
      },
      {
        "concept_id": 4118,
        "concept_version_id": 11478,
        "concept_name": "Other neurological - cerebral palsy and paralysis (SNOMED-CT)",
        "coding_system": {
          "id": 9,
          "name": "SNOMED  CT codes",
          "description": "SNOMED CT codes"
        },
        "phenotype_id": "PH1701",
        "phenotype_version_id": 3627,
        "phenotype_name": "Chronic paediatric conditions: Other neurological (excluding epilepsy and headaches)",
        "code_attribute_header": null,
        "codes": [
          {
            "code": "102831000119104",
            "description": "Paralytic syndrome of both lower limbs as sequela of stroke (disorder)",
            "attributes": null
          },
          {
            "code": "103761000119107",
            "description": "Paralytic syndrome of all four limbs as sequela of stroke (disorder)",
            "attributes": null
          },
          {
            "code": "11538006",
            "description": "Quadriplegia (disorder)",
            "attributes": null
          },
          {
            "code": "12367511000119101",
            "description": "Paraplegia due to and following cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "128188000",
            "description": "Cerebral palsy (disorder)",
            "attributes": null
          },
          {
            "code": "140281000119108",
            "description": "Hemiparesis as late effect of cerebrovascular disease (disorder)",
            "attributes": null
          },
          {
            "code": "1593000",
            "description": "Infantile hemiplegia (disorder)",
            "attributes": null
          },
          {
            "code": "16171003",
            "description": "Double athetosis (disorder)",
            "attributes": null
          },
          {
            "code": "1670004",
            "description": "Cerebral hemiparesis (disorder)",
            "attributes": null
          },
          {
            "code": "1845001",
            "description": "Paraparesis (disorder)",
            "attributes": null
          },
          {
            "code": "18751000119106",
            "description": "Monoplegia of leg dominant side as sequela of cerebrovascular disease (disorder)",
            "attributes": null
          },
          {
            "code": "18761000119108",
            "description": "Monoplegia of arm dominant side as sequela of cerebrovascular disease (disorder)",
            "attributes": null
          },
          {
            "code": "192949002",
            "description": "Congenital paraplegia (disorder)",
            "attributes": null
          },
          {
            "code": "192958009",
            "description": "Hypotonic cerebral palsy (disorder)",
            "attributes": null
          },
          {
            "code": "192964002",
            "description": "Flaccid tetraplegia (disorder)",
            "attributes": null
          },
          {
            "code": "192965001",
            "description": "Spastic tetraplegia (disorder)",
            "attributes": null
          },
          {
            "code": "192966000",
            "description": "Flaccid paraplegia (disorder)",
            "attributes": null
          },
          {
            "code": "192967009",
            "description": "Spastic paraplegia (disorder)",
            "attributes": null
          },
          {
            "code": "20022000",
            "description": "Hemiparesis (disorder)",
            "attributes": null
          },
          {
            "code": "22881000119100",
            "description": "Quadriplegia with quadriparesis (disorder)",
            "attributes": null
          },
          {
            "code": "230773005",
            "description": "Spastic cerebral palsy (disorder)",
            "attributes": null
          },
          {
            "code": "230777006",
            "description": "Monoplegic cerebral palsy affecting upper limb (disorder)",
            "attributes": null
          },
          {
            "code": "230778001",
            "description": "Monoplegic cerebral palsy affecting lower limb (disorder)",
            "attributes": null
          },
          {
            "code": "230780007",
            "description": "Dyskinetic cerebral palsy (disorder)",
            "attributes": null
          },
          {
            "code": "230781006",
            "description": "Dystonic/rigid cerebral palsy (disorder)",
            "attributes": null
          },
          {
            "code": "23728006",
            "description": "Partial bilateral paralysis (disorder)",
            "attributes": null
          },
          {
            "code": "249944006",
            "description": "Monoparesis - arm (disorder)",
            "attributes": null
          },
          {
            "code": "249945007",
            "description": "Monoparesis - leg (disorder)",
            "attributes": null
          },
          {
            "code": "275468009",
            "description": "Congenital quadriplegia (disorder)",
            "attributes": null
          },
          {
            "code": "278284007",
            "description": "Right hemiplegia (disorder)",
            "attributes": null
          },
          {
            "code": "278285008",
            "description": "Left hemiplegia (disorder)",
            "attributes": null
          },
          {
            "code": "278286009",
            "description": "Right hemiparesis (disorder)",
            "attributes": null
          },
          {
            "code": "278287000",
            "description": "Left hemiparesis (disorder)",
            "attributes": null
          },
          {
            "code": "278512001",
            "description": "Ataxic cerebral palsy (disorder)",
            "attributes": null
          },
          {
            "code": "27982003",
            "description": "Brown-SÃ©quard syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "281411007",
            "description": "Spastic diplegia (disorder)",
            "attributes": null
          },
          {
            "code": "290311000119102",
            "description": "Monoplegia of left dominant lower limb (disorder)",
            "attributes": null
          },
          {
            "code": "290321000119109",
            "description": "Monoplegia of left nondominant lower limb (disorder)",
            "attributes": null
          },
          {
            "code": "290331000119107",
            "description": "Monoplegia of right dominant lower limb (disorder)",
            "attributes": null
          },
          {
            "code": "290341000119103",
            "description": "Monoplegia of right nondominant lower limb (disorder)",
            "attributes": null
          },
          {
            "code": "290401000119108",
            "description": "Complete paraplegia (disorder)",
            "attributes": null
          },
          {
            "code": "290411000119106",
            "description": "Incomplete paraplegia (disorder)",
            "attributes": null
          },
          {
            "code": "290461000119109",
            "description": "Spastic hemiplegia of left dominant side (disorder)",
            "attributes": null
          },
          {
            "code": "290471000119103",
            "description": "Spastic hemiplegia of left nondominant side (disorder)",
            "attributes": null
          },
          {
            "code": "290481000119100",
            "description": "Spastic hemiplegia of right dominant side (disorder)",
            "attributes": null
          },
          {
            "code": "290491000119102",
            "description": "Spastic hemiplegia of right nondominant side (disorder)",
            "attributes": null
          },
          {
            "code": "29093005",
            "description": "Crossed hemiparesis (disorder)",
            "attributes": null
          },
          {
            "code": "290931000119108",
            "description": "Monoplegia of lower limb due to and following cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "291091000119102",
            "description": "Monoplegia of left nondominant upper limb due to and following cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "291111000119105",
            "description": "Monoplegia of right nondominant upper limb due to and following cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "291121000119103",
            "description": "Monoplegia of upper limb due to and following cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "29188005",
            "description": "Complete bilateral paralysis (disorder)",
            "attributes": null
          },
          {
            "code": "292851000119109",
            "description": "Lacunar ataxic hemiparesis of right dominant side (disorder)",
            "attributes": null
          },
          {
            "code": "292861000119106",
            "description": "Lacunar ataxic hemiparesis of left dominant side (disorder)",
            "attributes": null
          },
          {
            "code": "294041000119107",
            "description": "Flaccid hemiplegia of left dominant side (disorder)",
            "attributes": null
          },
          {
            "code": "294051000119109",
            "description": "Flaccid hemiplegia of left nondominant side (disorder)",
            "attributes": null
          },
          {
            "code": "294061000119106",
            "description": "Flaccid hemiplegia of right dominant side (disorder)",
            "attributes": null
          },
          {
            "code": "294071000119100",
            "description": "Flaccid hemiplegia of right nondominant side (disorder)",
            "attributes": null
          },
          {
            "code": "294101000119109",
            "description": "Hemiplegia of left dominant side (disorder)",
            "attributes": null
          },
          {
            "code": "294111000119107",
            "description": "Hemiplegia of left nondominant side (disorder)",
            "attributes": null
          },
          {
            "code": "294121000119100",
            "description": "Hemiplegia of right dominant side (disorder)",
            "attributes": null
          },
          {
            "code": "294131000119102",
            "description": "Hemiplegia of right nondominant side (disorder)",
            "attributes": null
          },
          {
            "code": "29426003",
            "description": "Paralytic syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "298282001",
            "description": "Spastic quadriparesis (disorder)",
            "attributes": null
          },
          {
            "code": "29951000119107",
            "description": "Ataxic hemiparesis (disorder)",
            "attributes": null
          },
          {
            "code": "307355007",
            "description": "Congenital athetosis (disorder)",
            "attributes": null
          },
          {
            "code": "313434001",
            "description": "Residual hemiplegia (disorder)",
            "attributes": null
          },
          {
            "code": "330311000119100",
            "description": "Monoplegia of right upper limb (disorder)",
            "attributes": null
          },
          {
            "code": "330321000119107",
            "description": "Monoplegia of left upper limb (disorder)",
            "attributes": null
          },
          {
            "code": "330411000119109",
            "description": "Lacunar ataxic hemiparesis of left nondominant side (disorder)",
            "attributes": null
          },
          {
            "code": "330421000119102",
            "description": "Lacunar ataxic hemiparesis of right nondominant side (disorder)",
            "attributes": null
          },
          {
            "code": "330471000119101",
            "description": "Neuromuscular scoliosis co-occurrent and due to cerebral palsy (disorder)",
            "attributes": null
          },
          {
            "code": "34209003",
            "description": "Cerebral hemiplegia (disorder)",
            "attributes": null
          },
          {
            "code": "361000119103",
            "description": "Paralytic syndrome on one side of the body as late effect of cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "371079004",
            "description": "Paraplegic cerebral palsy (disorder)",
            "attributes": null
          },
          {
            "code": "371120001",
            "description": "Quadriplegic spinal paralysis (disorder)",
            "attributes": null
          },
          {
            "code": "372310001",
            "description": "Paralysis due to lesion of spinal cord (disorder)",
            "attributes": null
          },
          {
            "code": "404689008",
            "description": "Alternating hemiplegia (disorder)",
            "attributes": null
          },
          {
            "code": "41764006",
            "description": "Monoplegia of upper limb (disorder)",
            "attributes": null
          },
          {
            "code": "425491009",
            "description": "Contracture of gastrocnemius muscle due to paralysis (disorder)",
            "attributes": null
          },
          {
            "code": "425642008",
            "description": "Monoplegia of dominant lower limb as a late effect of cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "425882004",
            "description": "Paralytic syndrome as late effect of stroke (disorder)",
            "attributes": null
          },
          {
            "code": "426167003",
            "description": "Monoplegia of lower limb affecting dominant side (disorder)",
            "attributes": null
          },
          {
            "code": "426536006",
            "description": "Monoplegia of upper limb affecting non-dominant side (disorder)",
            "attributes": null
          },
          {
            "code": "426934001",
            "description": "Monoplegia of lower limb affecting non-dominant side (disorder)",
            "attributes": null
          },
          {
            "code": "427065003",
            "description": "Monoplegia of dominant upper limb as a late effect of cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "427432001",
            "description": "Paralytic syndrome as late effect of thalamic stroke (disorder)",
            "attributes": null
          },
          {
            "code": "430947007",
            "description": "Paralytic syndrome of nondominant side as late effect of stroke (disorder)",
            "attributes": null
          },
          {
            "code": "430959006",
            "description": "Paralytic syndrome of dominant side as late effect of stroke (disorder)",
            "attributes": null
          },
          {
            "code": "432991000",
            "description": "Organophosphate induced paralysis Type II (disorder)",
            "attributes": null
          },
          {
            "code": "43486001",
            "description": "Hemiplegic cerebral palsy (disorder)",
            "attributes": null
          },
          {
            "code": "441688003",
            "description": "Incomplete quadriplegia due to spinal cord lesion between first and fourth cervical vertebra (disorder)",
            "attributes": null
          },
          {
            "code": "441705005",
            "description": "Complete quadriplegia due to spinal cord lesion between first and fourth cervical vertebra (disorder)",
            "attributes": null
          },
          {
            "code": "441717007",
            "description": "Hemiplegia of nondominant side (disorder)",
            "attributes": null
          },
          {
            "code": "441722007",
            "description": "Spastic hemiplegia of nondominant side (disorder)",
            "attributes": null
          },
          {
            "code": "441794001",
            "description": "Incomplete quadriplegia due to spinal cord lesion between fifth and seventh cervical vertebra (disorder)",
            "attributes": null
          },
          {
            "code": "441887006",
            "description": "Monoplegia of lower limb as late effect of cerebrovascular disease (disorder)",
            "attributes": null
          },
          {
            "code": "441892008",
            "description": "Spastic hemiplegia of dominant side (disorder)",
            "attributes": null
          },
          {
            "code": "441894009",
            "description": "Monoplegia of nondominant lower limb as a late effect of cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "441951003",
            "description": "Monoplegia of upper limb of dominant side (disorder)",
            "attributes": null
          },
          {
            "code": "441980007",
            "description": "Complete quadriplegia due to spinal cord lesion between fifth and seventh cervical vertebra (disorder)",
            "attributes": null
          },
          {
            "code": "441991000",
            "description": "Hemiparesis as late effect of cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "442020005",
            "description": "Flaccid hemiplegia of dominant side (disorder)",
            "attributes": null
          },
          {
            "code": "442024001",
            "description": "Hemiplegia as late effect of cerebrovascular disease (disorder)",
            "attributes": null
          },
          {
            "code": "442077006",
            "description": "Flaccid hemiplegia of nondominant side (disorder)",
            "attributes": null
          },
          {
            "code": "442097001",
            "description": "Monoplegia of upper limb as late effect of cerebrovascular disease (disorder)",
            "attributes": null
          },
          {
            "code": "442155009",
            "description": "Hemiplegia of dominant side (disorder)",
            "attributes": null
          },
          {
            "code": "442181008",
            "description": "Monoplegia of nondominant upper limb as a late effect of cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "442668000",
            "description": "Hemiplegia of nondominant side as late effect of cerebrovascular disease (disorder)",
            "attributes": null
          },
          {
            "code": "442676003",
            "description": "Hemiplegia of dominant side as late effect of cerebrovascular disease (disorder)",
            "attributes": null
          },
          {
            "code": "442733008",
            "description": "Hemiplegia as late effect of cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "44395000",
            "description": "Spastic tetraplegia with rigidity syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "4523006",
            "description": "Babinski-Nageotte syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "48163001",
            "description": "Triparesis (disorder)",
            "attributes": null
          },
          {
            "code": "48601000119107",
            "description": "Paralytic syndrome on one side of the body as effect of cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "48662007",
            "description": "Cerebral paraplegia (disorder)",
            "attributes": null
          },
          {
            "code": "48721008",
            "description": "Quadriplegic cerebral palsy (disorder)",
            "attributes": null
          },
          {
            "code": "49275006",
            "description": "Athetoid paralysis (finding)",
            "attributes": null
          },
          {
            "code": "50582007",
            "description": "Hemiplegia (disorder)",
            "attributes": null
          },
          {
            "code": "54099005",
            "description": "Diplegia of upper limbs (disorder)",
            "attributes": null
          },
          {
            "code": "54314008",
            "description": "Putti-Chavany syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "54364001",
            "description": "Lethal neonatal spasticity (disorder)",
            "attributes": null
          },
          {
            "code": "56409008",
            "description": "Monoplegic cerebral palsy (disorder)",
            "attributes": null
          },
          {
            "code": "58193001",
            "description": "Diplegic cerebral palsy (disorder)",
            "attributes": null
          },
          {
            "code": "5822000",
            "description": "Athetosis with spastic paraplegia (disorder)",
            "attributes": null
          },
          {
            "code": "59103002",
            "description": "Cerebral paralysis with homolateral ataxia (disorder)",
            "attributes": null
          },
          {
            "code": "60389000",
            "description": "Paraplegia (disorder)",
            "attributes": null
          },
          {
            "code": "609553000",
            "description": "Paralytic syndrome of both lower limbs (disorder)",
            "attributes": null
          },
          {
            "code": "609554006",
            "description": "Paralytic syndrome of all four limbs (disorder)",
            "attributes": null
          },
          {
            "code": "609557004",
            "description": "Paralytic syndrome on one side of the body (disorder)",
            "attributes": null
          },
          {
            "code": "609609004",
            "description": "Paralytic syndrome of one limb (disorder)",
            "attributes": null
          },
          {
            "code": "6481005",
            "description": "Diplegia (disorder)",
            "attributes": null
          },
          {
            "code": "672441000119103",
            "description": "Hemiplegia of nondominant side due to and following ischemic cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "672461000119104",
            "description": "Hemiplegia of dominant side due to and following ischemic cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "674161000119102",
            "description": "Monoplegia of upper limb due to and following ischemic cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "68107009",
            "description": "Cerebral paresis with homolateral ataxia (disorder)",
            "attributes": null
          },
          {
            "code": "690271000119104",
            "description": "Hemiplegia of nondominant side due to and following embolic cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "698291007",
            "description": "Acute paraplegia (disorder)",
            "attributes": null
          },
          {
            "code": "698292000",
            "description": "Chronic paraplegia (disorder)",
            "attributes": null
          },
          {
            "code": "698741009",
            "description": "Acute complete quadriplegia due to spinal cord lesion between first and fourth cervical vertebra (disorder)",
            "attributes": null
          },
          {
            "code": "698742002",
            "description": "Chronic incomplete quadriplegia due to spinal cord lesion between first and fourth cervical vertebra (disorder)",
            "attributes": null
          },
          {
            "code": "698743007",
            "description": "Acute complete quadriplegia due to spinal cord lesion between fifth and seventh cervical vertebra (disorder)",
            "attributes": null
          },
          {
            "code": "698744001",
            "description": "Chronic incomplete quadriplegia due to spinal cord lesion between fifth and seventh cervical vertebra (disorder)",
            "attributes": null
          },
          {
            "code": "698754002",
            "description": "Chronic paralysis due to lesion of spinal cord (disorder)",
            "attributes": null
          },
          {
            "code": "698755001",
            "description": "Acute paralysis due to lesion of spinal cord (disorder)",
            "attributes": null
          },
          {
            "code": "702314005",
            "description": "Non-spastic cerebral palsy (disorder)",
            "attributes": null
          },
          {
            "code": "702315006",
            "description": "Dystonic cerebral palsy (disorder)",
            "attributes": null
          },
          {
            "code": "702316007",
            "description": "Choreic cerebral palsy (disorder)",
            "attributes": null
          },
          {
            "code": "702317003",
            "description": "Chorea-athetoid cerebral palsy (disorder)",
            "attributes": null
          },
          {
            "code": "702318008",
            "description": "Mixed cerebral palsy (disorder)",
            "attributes": null
          },
          {
            "code": "702319000",
            "description": "Bilateral cerebral palsy (disorder)",
            "attributes": null
          },
          {
            "code": "702320006",
            "description": "Triplegic cerebral palsy (disorder)",
            "attributes": null
          },
          {
            "code": "702321005",
            "description": "Pentaplegic cerebral palsy (disorder)",
            "attributes": null
          },
          {
            "code": "702463005",
            "description": "Paralytic syndrome of two limbs (disorder)",
            "attributes": null
          },
          {
            "code": "702464004",
            "description": "Paralytic syndrome of three limbs (disorder)",
            "attributes": null
          },
          {
            "code": "702465003",
            "description": "Paralytic syndrome on both sides of the body (disorder)",
            "attributes": null
          },
          {
            "code": "716335003",
            "description": "Congenital suprabulbar paresis (disorder)",
            "attributes": null
          },
          {
            "code": "721398001",
            "description": "Brown-Sequard syndrome of cervical spinal cord (disorder)",
            "attributes": null
          },
          {
            "code": "721399009",
            "description": "Brown-Sequard syndrome at first cervical level (disorder)",
            "attributes": null
          },
          {
            "code": "721400002",
            "description": "Brown-Sequard syndrome at second cervical level (disorder)",
            "attributes": null
          },
          {
            "code": "721401003",
            "description": "Brown-Sequard syndrome at third cervical level (disorder)",
            "attributes": null
          },
          {
            "code": "721402005",
            "description": "Brown-Sequard syndrome at fourth cervical level (disorder)",
            "attributes": null
          },
          {
            "code": "721403000",
            "description": "Brown-Sequard syndrome at fifth cervical level (disorder)",
            "attributes": null
          },
          {
            "code": "721404006",
            "description": "Brown-Sequard syndrome at sixth cervical level (disorder)",
            "attributes": null
          },
          {
            "code": "721405007",
            "description": "Brown-Sequard syndrome at seventh cervical level (disorder)",
            "attributes": null
          },
          {
            "code": "721406008",
            "description": "Brown-Sequard syndrome at eighth cervical level (disorder)",
            "attributes": null
          },
          {
            "code": "721481000",
            "description": "Brown-SÃ©quard syndrome of thoracic spinal cord (disorder)",
            "attributes": null
          },
          {
            "code": "721482007",
            "description": "Brown-SÃ©quard syndrome at first thoracic level (disorder)",
            "attributes": null
          },
          {
            "code": "721483002",
            "description": "Brown-SÃ©quard syndrome at second thoracic level (disorder)",
            "attributes": null
          },
          {
            "code": "721484008",
            "description": "Brown-SÃ©quard syndrome at third thoracic level (disorder)",
            "attributes": null
          },
          {
            "code": "721485009",
            "description": "Brown-SÃ©quard syndrome at fourth thoracic level (disorder)",
            "attributes": null
          },
          {
            "code": "721486005",
            "description": "Brown-SÃ©quard syndrome at fifth thoracic level (disorder)",
            "attributes": null
          },
          {
            "code": "721487001",
            "description": "Brown-SÃ©quard syndrome at sixth thoracic level (disorder)",
            "attributes": null
          },
          {
            "code": "721488006",
            "description": "Brown-SÃ©quard syndrome at seventh thoracic level (disorder)",
            "attributes": null
          },
          {
            "code": "721489003",
            "description": "Brown-SÃ©quard syndrome at eighth thoracic level (disorder)",
            "attributes": null
          },
          {
            "code": "721490007",
            "description": "Brown-SÃ©quard syndrome at ninth thoracic level (disorder)",
            "attributes": null
          },
          {
            "code": "721491006",
            "description": "Brown-SÃ©quard syndrome at tenth thoracic level (disorder)",
            "attributes": null
          },
          {
            "code": "721492004",
            "description": "Brown-SÃ©quard syndrome at eleventh thoracic level (disorder)",
            "attributes": null
          },
          {
            "code": "721493009",
            "description": "Brown-SÃ©quard syndrome at twelfth thoracic level (disorder)",
            "attributes": null
          },
          {
            "code": "721523001",
            "description": "Brown-SÃ©quard syndrome of lumbar spinal cord (disorder)",
            "attributes": null
          },
          {
            "code": "721524007",
            "description": "Brown-SÃ©quard syndrome at first lumbar level (disorder)",
            "attributes": null
          },
          {
            "code": "721525008",
            "description": "Brown-SÃ©quard syndrome at second lumbar level (disorder)",
            "attributes": null
          },
          {
            "code": "721526009",
            "description": "Brown-SÃ©quard syndrome at third lumbar level (disorder)",
            "attributes": null
          },
          {
            "code": "721527000",
            "description": "Brown-SÃ©quard syndrome at fourth lumbar level (disorder)",
            "attributes": null
          },
          {
            "code": "721528005",
            "description": "Brown-SÃ©quard syndrome at fifth lumbar level (disorder)",
            "attributes": null
          },
          {
            "code": "722033000",
            "description": "Macrocephaly, short stature, paraplegia syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "722209002",
            "description": "Spastic paraplegia, intellectual disability, palmoplantar hyperkeratosis syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "723156000",
            "description": "Flaccid diplegia of upper limbs (disorder)",
            "attributes": null
          },
          {
            "code": "723157009",
            "description": "Spastic diplegia of upper limbs (disorder)",
            "attributes": null
          },
          {
            "code": "723158004",
            "description": "Diplegia of lower limbs (disorder)",
            "attributes": null
          },
          {
            "code": "723159007",
            "description": "Flaccid monoplegia of upper limb (disorder)",
            "attributes": null
          },
          {
            "code": "723160002",
            "description": "Spastic monoplegia of upper limb (disorder)",
            "attributes": null
          },
          {
            "code": "723161003",
            "description": "Flaccid monoplegia of lower limb (disorder)",
            "attributes": null
          },
          {
            "code": "723162005",
            "description": "Spastic monoplegia of lower limb (disorder)",
            "attributes": null
          },
          {
            "code": "723621000",
            "description": "Spastic tetraplegia, retinitis pigmentosa, intellectual disability syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "733650000",
            "description": "Adult familial nephronophthisis with spastic quadriparesia syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "75019001",
            "description": "Athetoid cerebral palsy (disorder)",
            "attributes": null
          },
          {
            "code": "763402002",
            "description": "Spastic paraplegia, neuropathy, poikiloderma syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "763403007",
            "description": "Spastic paraplegia, facial cutaneous lesion syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "77015008",
            "description": "Crossed hemiplegia (disorder)",
            "attributes": null
          },
          {
            "code": "785809005",
            "description": "Mills syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "79520009",
            "description": "Monoparesis (disorder)",
            "attributes": null
          },
          {
            "code": "79633009",
            "description": "Spastic hemiplegia (disorder)",
            "attributes": null
          },
          {
            "code": "80420005",
            "description": "Monoplegia of lower limb (disorder)",
            "attributes": null
          },
          {
            "code": "80935004",
            "description": "Flaccid hemiplegia (disorder)",
            "attributes": null
          },
          {
            "code": "84455002",
            "description": "Spinal paraplegia (disorder)",
            "attributes": null
          },
          {
            "code": "86022000",
            "description": "Monoplegia (disorder)",
            "attributes": null
          },
          {
            "code": "860881004",
            "description": "Flaccid diplegia of lower extremities (disorder)",
            "attributes": null
          },
          {
            "code": "89437009",
            "description": "Cerebral paraparesis (disorder)",
            "attributes": null
          },
          {
            "code": "91327001",
            "description": "Quadriparesis (disorder)",
            "attributes": null
          },
          {
            "code": "95651005",
            "description": "Chronic progressive paraparesis (disorder)",
            "attributes": null
          },
          {
            "code": "95652003",
            "description": "Congenital flaccid paralysis (disorder)",
            "attributes": null
          },
          {
            "code": "97381000119100",
            "description": "Neurogenic bladder due to quadriplegia (disorder)",
            "attributes": null
          },
          {
            "code": "97391000119102",
            "description": "Paraplegia with neurogenic bladder (disorder)",
            "attributes": null
          },
          {
            "code": "9753004",
            "description": "Triplegia (disorder)",
            "attributes": null
          }
        ]
      },
      {
        "concept_id": 4119,
        "concept_version_id": 11479,
        "concept_name": "Other neurological - congenital neurological condition (ICD-10)",
        "coding_system": {
          "id": 4,
          "name": "ICD10 codes",
          "description": "ICD10 Codes"
        },
        "phenotype_id": "PH1701",
        "phenotype_version_id": 3627,
        "phenotype_name": "Chronic paediatric conditions: Other neurological (excluding epilepsy and headaches)",
        "code_attribute_header": null,
        "codes": [
          {
            "code": "P10",
            "description": "Intracranial laceration and haemorrhage due to birth injury",
            "attributes": null
          },
          {
            "code": "P100",
            "description": "Subdural haemorrhage due to birth injury",
            "attributes": null
          },
          {
            "code": "P101",
            "description": "Cerebral haemorrhage due to birth injury",
            "attributes": null
          },
          {
            "code": "P102",
            "description": "Intraventricular haemorrhage due to birth injury",
            "attributes": null
          },
          {
            "code": "P103",
            "description": "Subarachnoid haemorrhage due to birth injury",
            "attributes": null
          },
          {
            "code": "P104",
            "description": "Tentorial tear due to birth injury",
            "attributes": null
          },
          {
            "code": "P108",
            "description": "Other intracranial lacerations and haemorrhages due to birth injury",
            "attributes": null
          },
          {
            "code": "P109",
            "description": "Unspecified intracranial laceration and haemorrhage due to birth injury",
            "attributes": null
          },
          {
            "code": "P112",
            "description": "Unspecified brain damage due to birth injury",
            "attributes": null
          },
          {
            "code": "P210",
            "description": "Severe birth asphyxia",
            "attributes": null
          },
          {
            "code": "P522",
            "description": "Intraventricular (nontraumatic) haemorrhage, grade 3, of fetus and newborn",
            "attributes": null
          },
          {
            "code": "P523",
            "description": "Unspecified intraventricular (nontraumatic) haemorrhage of fetus and newborn",
            "attributes": null
          },
          {
            "code": "P525",
            "description": "Subarachnoid (nontraumatic) haemorrhage of fetus and newborn",
            "attributes": null
          },
          {
            "code": "P526",
            "description": "Cerebellar (nontraumatic) and posterior fossa haemorrhage of fetus and newborn",
            "attributes": null
          },
          {
            "code": "P528",
            "description": "Other intracranial (nontraumatic) haemorrhages of fetus and newborn",
            "attributes": null
          },
          {
            "code": "P529",
            "description": "Intracranial (nontraumatic) haemorrhage of fetus and newborn, unspecified",
            "attributes": null
          },
          {
            "code": "P57",
            "description": "Kernicterus",
            "attributes": null
          },
          {
            "code": "P570",
            "description": "Kernicterus due to isoimmunization",
            "attributes": null
          },
          {
            "code": "P578",
            "description": "Other specified kernicterus",
            "attributes": null
          },
          {
            "code": "P579",
            "description": "Kernicterus, unspecified",
            "attributes": null
          },
          {
            "code": "Q00",
            "description": "Anencephaly and similar malformations",
            "attributes": null
          },
          {
            "code": "Q000",
            "description": "Anencephaly",
            "attributes": null
          },
          {
            "code": "Q001",
            "description": "Craniorachischisis",
            "attributes": null
          },
          {
            "code": "Q01",
            "description": "Encephalocele",
            "attributes": null
          },
          {
            "code": "Q010",
            "description": "Frontal encephalocele",
            "attributes": null
          },
          {
            "code": "Q011",
            "description": "Nasofrontal encephalocele",
            "attributes": null
          },
          {
            "code": "Q012",
            "description": "Occipital encephalocele",
            "attributes": null
          },
          {
            "code": "Q018",
            "description": "Encephalocele of other sites",
            "attributes": null
          },
          {
            "code": "Q019",
            "description": "Encephalocele, unspecified",
            "attributes": null
          },
          {
            "code": "Q02",
            "description": "Microcephaly",
            "attributes": null
          },
          {
            "code": "Q03",
            "description": "Congenital hydrocephalus",
            "attributes": null
          },
          {
            "code": "Q030",
            "description": "Malformations of aqueduct of Sylvius",
            "attributes": null
          },
          {
            "code": "Q031",
            "description": "Atresia of foramina of Magendie and Luschka",
            "attributes": null
          },
          {
            "code": "Q038",
            "description": "Other congenital hydrocephalus",
            "attributes": null
          },
          {
            "code": "Q039",
            "description": "Congenital hydrocephalus, unspecified",
            "attributes": null
          },
          {
            "code": "Q04",
            "description": "Other congenital malformations of brain",
            "attributes": null
          },
          {
            "code": "Q040",
            "description": "Congenital malformations of corpus callosum",
            "attributes": null
          },
          {
            "code": "Q041",
            "description": "Arhinencephaly",
            "attributes": null
          },
          {
            "code": "Q042",
            "description": "Holoprosencephaly",
            "attributes": null
          },
          {
            "code": "Q043",
            "description": "Other reduction deformities of brain",
            "attributes": null
          },
          {
            "code": "Q044",
            "description": "Septo-optic dysplasia",
            "attributes": null
          },
          {
            "code": "Q045",
            "description": "Megalencephaly",
            "attributes": null
          },
          {
            "code": "Q046",
            "description": "Congenital cerebral cysts",
            "attributes": null
          },
          {
            "code": "Q048",
            "description": "Other specified congenital malformations of brain",
            "attributes": null
          },
          {
            "code": "Q049",
            "description": "Congenital malformation of brain, unspecified",
            "attributes": null
          },
          {
            "code": "Q05",
            "description": "Spina bifida",
            "attributes": null
          },
          {
            "code": "Q050",
            "description": "Cervical spina bifida with hydrocephalus",
            "attributes": null
          },
          {
            "code": "Q051",
            "description": "Thoracic spina bifida with hydrocephalus",
            "attributes": null
          },
          {
            "code": "Q052",
            "description": "Lumbar spina bifida with hydrocephalus",
            "attributes": null
          },
          {
            "code": "Q053",
            "description": "Sacral spina bifida with hydrocephalus",
            "attributes": null
          },
          {
            "code": "Q054",
            "description": "Unspecified spina bifida with hydrocephalus",
            "attributes": null
          },
          {
            "code": "Q055",
            "description": "Cervical spina bifida without hydrocephalus",
            "attributes": null
          },
          {
            "code": "Q056",
            "description": "Thoracic spina bifida without hydrocephalus",
            "attributes": null
          },
          {
            "code": "Q057",
            "description": "Lumbar spina bifida without hydrocephalus",
            "attributes": null
          },
          {
            "code": "Q058",
            "description": "Sacral spina bifida without hydrocephalus",
            "attributes": null
          },
          {
            "code": "Q059",
            "description": "Spina bifida, unspecified",
            "attributes": null
          },
          {
            "code": "Q06",
            "description": "Other congenital malformations of spinal cord",
            "attributes": null
          },
          {
            "code": "Q060",
            "description": "Amyelia",
            "attributes": null
          },
          {
            "code": "Q061",
            "description": "Hypoplasia and dysplasia of spinal cord",
            "attributes": null
          },
          {
            "code": "Q062",
            "description": "Diastematomyelia",
            "attributes": null
          },
          {
            "code": "Q063",
            "description": "Other congenital cauda equina malformations",
            "attributes": null
          },
          {
            "code": "Q064",
            "description": "Hydromyelia",
            "attributes": null
          },
          {
            "code": "Q068",
            "description": "Other specified congenital malformations of spinal cord",
            "attributes": null
          },
          {
            "code": "Q069",
            "description": "Congenital malformation of spinal cord, unspecified",
            "attributes": null
          },
          {
            "code": "Q07",
            "description": "Other congenital malformations of nervous system",
            "attributes": null
          },
          {
            "code": "Q070",
            "description": "Arnold-Chiari syndrome",
            "attributes": null
          },
          {
            "code": "Q078",
            "description": "Other specified congenital malformations of nervous system",
            "attributes": null
          },
          {
            "code": "Q079",
            "description": "Congenital malformation of nervous system, unspecified",
            "attributes": null
          },
          {
            "code": "Q750",
            "description": "Craniosynostosis",
            "attributes": null
          },
          {
            "code": "Q751",
            "description": "Craniofacial dysostosis",
            "attributes": null
          },
          {
            "code": "Q754",
            "description": "Mandibulofacial dysostosis",
            "attributes": null
          },
          {
            "code": "Q85",
            "description": "Phakomatoses, not elsewhere classified",
            "attributes": null
          },
          {
            "code": "Q850",
            "description": "Neurofibromatosis (nonmalignant)",
            "attributes": null
          },
          {
            "code": "Q851",
            "description": "Tuberous sclerosis",
            "attributes": null
          },
          {
            "code": "Q86",
            "description": "Congenital malformation syndromes due to known exogenous causes, not elsewhere classified",
            "attributes": null
          },
          {
            "code": "Q860",
            "description": "Fetal alcohol syndrome (dysmorphic)",
            "attributes": null
          },
          {
            "code": "Q861",
            "description": "Fetal hydantoin syndrome",
            "attributes": null
          },
          {
            "code": "Q862",
            "description": "Dysmorphism due to warfarin",
            "attributes": null
          },
          {
            "code": "Q868",
            "description": "Other congenital malformation syndromes due to known exogenous causes",
            "attributes": null
          }
        ]
      },
      {
        "concept_id": 4120,
        "concept_version_id": 11480,
        "concept_name": "Other neurological - congenital neurological condition (Read v2)",
        "coding_system": {
          "id": 5,
          "name": "Read codes v2",
          "description": "Read codes v2"
        },
        "phenotype_id": "PH1701",
        "phenotype_version_id": 3627,
        "phenotype_name": "Chronic paediatric conditions: Other neurological (excluding epilepsy and headaches)",
        "code_attribute_header": null,
        "codes": [
          {
            "code": "1Bc0.00",
            "description": "Congenital dysarthria",
            "attributes": null
          },
          {
            "code": "1Bc0.11",
            "description": "Developmental dysarthria",
            "attributes": null
          },
          {
            "code": "B927.00",
            "description": "Neurofibromatosis - Von Recklinghausen's disease",
            "attributes": null
          },
          {
            "code": "B927.11",
            "description": "Von Recklinghausen's disease",
            "attributes": null
          },
          {
            "code": "B927.12",
            "description": "Neurofibromatosis type 1",
            "attributes": null
          },
          {
            "code": "B929.00",
            "description": "Neurofibromatosis type 2",
            "attributes": null
          },
          {
            "code": "F11x300",
            "description": "Cerebral degeneration due to congenital hydrocephalus",
            "attributes": null
          },
          {
            "code": "F233.11",
            "description": "Congenital spastic foot",
            "attributes": null
          },
          {
            "code": "F28y200",
            "description": "Enlarged brain",
            "attributes": null
          },
          {
            "code": "F28y300",
            "description": "Ventriculomegaly",
            "attributes": null
          },
          {
            "code": "F4Gy011",
            "description": "Encephalocoele of orbit",
            "attributes": null
          },
          {
            "code": "N374C00",
            "description": "Scoliosis in neurofibromatosis",
            "attributes": null
          },
          {
            "code": "P00..00",
            "description": "Anencephalus",
            "attributes": null
          },
          {
            "code": "P000.00",
            "description": "Acrania",
            "attributes": null
          },
          {
            "code": "P001.00",
            "description": "Amyelencephalus",
            "attributes": null
          },
          {
            "code": "P00..11",
            "description": "Congenital absence of brain",
            "attributes": null
          },
          {
            "code": "P002.00",
            "description": "Hemicephaly",
            "attributes": null
          },
          {
            "code": "P002.11",
            "description": "Hemianencephaly",
            "attributes": null
          },
          {
            "code": "P00y.00",
            "description": "Other specified anencephalus",
            "attributes": null
          },
          {
            "code": "P00z.00",
            "description": "Anencephalus NOS",
            "attributes": null
          },
          {
            "code": "P01..00",
            "description": "Craniorachischisis",
            "attributes": null
          },
          {
            "code": "P0z..00",
            "description": "Anencephalus and similar anomalies NOS",
            "attributes": null
          },
          {
            "code": "P1...00",
            "description": "Spina bifida",
            "attributes": null
          },
          {
            "code": "P10..00",
            "description": "Spina bifida with hydrocephalus",
            "attributes": null
          },
          {
            "code": "P100.00",
            "description": "Unspecified spina bifida with hydrocephalus",
            "attributes": null
          },
          {
            "code": "P100000",
            "description": "Spina bifida with hydrocephalus, unspecified",
            "attributes": null
          },
          {
            "code": "P100100",
            "description": "Cervical spina bifida with hydrocephalus",
            "attributes": null
          },
          {
            "code": "P100200",
            "description": "Thoracic spina bifida with hydrocephalus",
            "attributes": null
          },
          {
            "code": "P100300",
            "description": "Lumbar spina bifida with hydrocephalus",
            "attributes": null
          },
          {
            "code": "P100z00",
            "description": "Spina bifida with hydrocephalus NOS",
            "attributes": null
          },
          {
            "code": "P101.00",
            "description": "Arnold - Chiari syndrome",
            "attributes": null
          },
          {
            "code": "P101000",
            "description": "Chiari malformation type I",
            "attributes": null
          },
          {
            "code": "P10..11",
            "description": "Arnold - Chiari syndrome",
            "attributes": null
          },
          {
            "code": "P101100",
            "description": "Chiari malformation type II",
            "attributes": null
          },
          {
            "code": "P101.11",
            "description": "Closed spina bifida with Arnold-Chiari malformation",
            "attributes": null
          },
          {
            "code": "P101200",
            "description": "Chiari malformation type III",
            "attributes": null
          },
          {
            "code": "P101300",
            "description": "Chiari malformation type IV",
            "attributes": null
          },
          {
            "code": "P102.00",
            "description": "Spina bifida with hydrocephalus - open",
            "attributes": null
          },
          {
            "code": "P102000",
            "description": "Unspecified spina bifida with hydrocephalus - open",
            "attributes": null
          },
          {
            "code": "P102100",
            "description": "Cervical spina bifida with hydrocephalus - open",
            "attributes": null
          },
          {
            "code": "P102.12",
            "description": "Hydromyelocele with hydrocephalus",
            "attributes": null
          },
          {
            "code": "P102.13",
            "description": "Myelocele with hydrocephalus",
            "attributes": null
          },
          {
            "code": "P102.14",
            "description": "Rachischisis with hydrocephalus",
            "attributes": null
          },
          {
            "code": "P102200",
            "description": "Thoracic spina bifida with hydrocephalus - open",
            "attributes": null
          },
          {
            "code": "P102300",
            "description": "Lumbar spina bifida with hydrocephalus - open",
            "attributes": null
          },
          {
            "code": "P102400",
            "description": "Sacral spina bifida with hydrocephalus - open",
            "attributes": null
          },
          {
            "code": "P102z00",
            "description": "Spina bifida with hydrocephalus - open NOS",
            "attributes": null
          },
          {
            "code": "P103.00",
            "description": "Spina bifida with hydrocephalus - closed",
            "attributes": null
          },
          {
            "code": "P103000",
            "description": "Unspecified spina bifida with hydrocephalus - closed",
            "attributes": null
          },
          {
            "code": "P103100",
            "description": "Cervical spina bifida with hydrocephalus - closed",
            "attributes": null
          },
          {
            "code": "P103200",
            "description": "Thoracic spina bifida with hydrocephalus - closed",
            "attributes": null
          },
          {
            "code": "P103300",
            "description": "Lumbar spina bifida with hydrocephalus - closed",
            "attributes": null
          },
          {
            "code": "P103400",
            "description": "Sacral spina bifida with hydrocephalus - closed",
            "attributes": null
          },
          {
            "code": "P103z00",
            "description": "Spina bifida with hydrocephalus - closed NOS",
            "attributes": null
          },
          {
            "code": "P103z11",
            "description": "Thoracolumbar spina bifida with hydrocephalus - closed",
            "attributes": null
          },
          {
            "code": "P104.00",
            "description": "Spina bifida with hydrocephalus of late onset",
            "attributes": null
          },
          {
            "code": "P105.00",
            "description": "Spina bifida with stenosis of aqueduct of Sylvius",
            "attributes": null
          },
          {
            "code": "P10y.00",
            "description": "Other specified spina bifida with hydrocephalus",
            "attributes": null
          },
          {
            "code": "P10y000",
            "description": "Dandy - Walker syndrome with spina bifida",
            "attributes": null
          },
          {
            "code": "P10yz00",
            "description": "Other spina bifida with hydrocephalus NOS",
            "attributes": null
          },
          {
            "code": "P10z.00",
            "description": "Spina bifida with hydrocephalus NOS",
            "attributes": null
          },
          {
            "code": "P11..00",
            "description": "Spina bifida without mention of hydrocephalus",
            "attributes": null
          },
          {
            "code": "P110.00",
            "description": "Spina bifida without mention of hydrocephalus, unspecified",
            "attributes": null
          },
          {
            "code": "P110000",
            "description": "Spina bifida without mention of hydrocephalus, site unspecified",
            "attributes": null
          },
          {
            "code": "P110100",
            "description": "Cervical spina bifida without mention of hydrocephalus",
            "attributes": null
          },
          {
            "code": "P110.11",
            "description": "Split notochord syndrome",
            "attributes": null
          },
          {
            "code": "P110z00",
            "description": "Unspecified spina bifida without mention of hydrocephalus NOS",
            "attributes": null
          },
          {
            "code": "P111.00",
            "description": "Spinal hydromeningocele",
            "attributes": null
          },
          {
            "code": "P111000",
            "description": "Spinal hydromeningocele, unspecified",
            "attributes": null
          },
          {
            "code": "P111100",
            "description": "Cervical spinal hydromeningocele",
            "attributes": null
          },
          {
            "code": "P111200",
            "description": "Thoracic spinal hydromeningocele",
            "attributes": null
          },
          {
            "code": "P111z00",
            "description": "Spinal hydromeningocele NOS",
            "attributes": null
          },
          {
            "code": "P112.00",
            "description": "Hydromyelocele",
            "attributes": null
          },
          {
            "code": "P112000",
            "description": "Hydromyelocele of unspecified site",
            "attributes": null
          },
          {
            "code": "P112100",
            "description": "Hydromyelocele-cervical",
            "attributes": null
          },
          {
            "code": "P112200",
            "description": "Thoracic hydromyelocele",
            "attributes": null
          },
          {
            "code": "P112300",
            "description": "Lumbar hydromyelocele",
            "attributes": null
          },
          {
            "code": "P112z00",
            "description": "Hydromyelocele NOS",
            "attributes": null
          },
          {
            "code": "P113.00",
            "description": "Spinal meningocele",
            "attributes": null
          },
          {
            "code": "P113000",
            "description": "Spinal meningocele of unspecified site",
            "attributes": null
          },
          {
            "code": "P113100",
            "description": "Spinal meningocele-cervical",
            "attributes": null
          },
          {
            "code": "P113200",
            "description": "Thoracic spinal meningocele",
            "attributes": null
          },
          {
            "code": "P113300",
            "description": "Spinal meningocele-lumbar",
            "attributes": null
          },
          {
            "code": "P113z00",
            "description": "Spinal meningocele NOS",
            "attributes": null
          },
          {
            "code": "P114.00",
            "description": "Meningomyelocele",
            "attributes": null
          },
          {
            "code": "P114000",
            "description": "Meningomyelocele of unspecified site",
            "attributes": null
          },
          {
            "code": "P114100",
            "description": "Meningomyelocele-cervical",
            "attributes": null
          },
          {
            "code": "P114200",
            "description": "Thoracic meningomyelocele",
            "attributes": null
          },
          {
            "code": "P114300",
            "description": "Meningomyelocele-lumbar",
            "attributes": null
          },
          {
            "code": "P114z00",
            "description": "Meningomyelocele NOS",
            "attributes": null
          },
          {
            "code": "P115.00",
            "description": "Myelocele",
            "attributes": null
          },
          {
            "code": "P115000",
            "description": "Myelocele of unspecified site",
            "attributes": null
          },
          {
            "code": "P115100",
            "description": "Myelocele-cervical",
            "attributes": null
          },
          {
            "code": "P115200",
            "description": "Thoracic myelocele",
            "attributes": null
          },
          {
            "code": "P115300",
            "description": "Myelocele-lumbar",
            "attributes": null
          },
          {
            "code": "P115z00",
            "description": "Myelocele NOS",
            "attributes": null
          },
          {
            "code": "P116.00",
            "description": "Myelocystocele",
            "attributes": null
          },
          {
            "code": "P116000",
            "description": "Myelocystocele of unspecified site",
            "attributes": null
          },
          {
            "code": "P116100",
            "description": "Myelocystocele-cervical",
            "attributes": null
          },
          {
            "code": "P116200",
            "description": "Thoracic myelocystocele",
            "attributes": null
          },
          {
            "code": "P116300",
            "description": "Myelocystocele-lumbar",
            "attributes": null
          },
          {
            "code": "P116z00",
            "description": "Myelocystocele NOS",
            "attributes": null
          },
          {
            "code": "P117.00",
            "description": "Spina bifida without hydrocephalus - open",
            "attributes": null
          },
          {
            "code": "P117000",
            "description": "Unspecified spina bifida without hydrocephalus - open",
            "attributes": null
          },
          {
            "code": "P117100",
            "description": "Cervical spina bifida without hydrocephalus - open",
            "attributes": null
          },
          {
            "code": "P117.12",
            "description": "Rachischisis",
            "attributes": null
          },
          {
            "code": "P117200",
            "description": "Thoracic spina bifida without hydrocephalus - open",
            "attributes": null
          },
          {
            "code": "P117300",
            "description": "Lumbar spina bifida without hydrocephalus - open",
            "attributes": null
          },
          {
            "code": "P117400",
            "description": "Sacral spina bifida without hydrocephalus - open",
            "attributes": null
          },
          {
            "code": "P117z00",
            "description": "Spina bifida without hydrocephalus - open NOS",
            "attributes": null
          },
          {
            "code": "P118.00",
            "description": "Spina bifida without hydrocephalus - closed",
            "attributes": null
          },
          {
            "code": "P118000",
            "description": "Unspecified spina bifida without hydrocephalus - closed",
            "attributes": null
          },
          {
            "code": "P118100",
            "description": "Cervical spina bifida without hydrocephalus - closed",
            "attributes": null
          },
          {
            "code": "P118200",
            "description": "Thoracic spina bifida without hydrocephalus - closed",
            "attributes": null
          },
          {
            "code": "P118300",
            "description": "Lumbar spina bifida without hydrocephalus - closed",
            "attributes": null
          },
          {
            "code": "P118400",
            "description": "Sacral spina bifida without hydrocephalus - closed",
            "attributes": null
          },
          {
            "code": "P118z00",
            "description": "Spina bifida without hydrocephalus - closed NOS",
            "attributes": null
          },
          {
            "code": "P118z11",
            "description": "Thoracolumbar spina bifida without hydrocephalus - closed",
            "attributes": null
          },
          {
            "code": "P11y.00",
            "description": "Other specified spina bifida without hydrocephalus",
            "attributes": null
          },
          {
            "code": "P11y.11",
            "description": "Syringomyelocele",
            "attributes": null
          },
          {
            "code": "P11z.00",
            "description": "Spina bifida without mention of hydrocephalus NOS",
            "attributes": null
          },
          {
            "code": "P11z.11",
            "description": "Rachischisis",
            "attributes": null
          },
          {
            "code": "P11z.12",
            "description": "Syringomyelocele",
            "attributes": null
          },
          {
            "code": "P11z.13",
            "description": "Billroth's disease",
            "attributes": null
          },
          {
            "code": "P11z.14",
            "description": "Congenital hernia of dura mater",
            "attributes": null
          },
          {
            "code": "P1z..00",
            "description": "Spina bifida NOS",
            "attributes": null
          },
          {
            "code": "P2...00",
            "description": "Other nervous system congenital anomalies",
            "attributes": null
          },
          {
            "code": "P20..00",
            "description": "Encephalocele",
            "attributes": null
          },
          {
            "code": "P200.00",
            "description": "Encephalocystocele",
            "attributes": null
          },
          {
            "code": "P201.00",
            "description": "Encephalomyelocele",
            "attributes": null
          },
          {
            "code": "P20..11",
            "description": "Hydroencephalocele",
            "attributes": null
          },
          {
            "code": "P20..12",
            "description": "Cephalocele",
            "attributes": null
          },
          {
            "code": "P20..13",
            "description": "Congenital cerebral hernia",
            "attributes": null
          },
          {
            "code": "P20..15",
            "description": "Sinus pericranii",
            "attributes": null
          },
          {
            "code": "P20..16",
            "description": "Congenitalcerebral hernia",
            "attributes": null
          },
          {
            "code": "P202.00",
            "description": "Hydromeningocele - cranial",
            "attributes": null
          },
          {
            "code": "P204.00",
            "description": "Meningoencephalocele",
            "attributes": null
          },
          {
            "code": "P205.00",
            "description": "Frontal encephalocele",
            "attributes": null
          },
          {
            "code": "P206.00",
            "description": "Nasofrontal encephalocele",
            "attributes": null
          },
          {
            "code": "P20z.00",
            "description": "Encephalocele NOS",
            "attributes": null
          },
          {
            "code": "P20z000",
            "description": "Occipital encephalocele",
            "attributes": null
          },
          {
            "code": "P20z100",
            "description": "Encephalocele of other specified site",
            "attributes": null
          },
          {
            "code": "P21..00",
            "description": "Microcephalus",
            "attributes": null
          },
          {
            "code": "P210.00",
            "description": "Hydromicrocephaly",
            "attributes": null
          },
          {
            "code": "P211.00",
            "description": "Micrencephaly",
            "attributes": null
          },
          {
            "code": "P21z.00",
            "description": "Microcephalus NOS",
            "attributes": null
          },
          {
            "code": "P223.00",
            "description": "Agyria",
            "attributes": null
          },
          {
            "code": "P223.11",
            "description": "Lissencephaly",
            "attributes": null
          },
          {
            "code": "P224.00",
            "description": "Arhinencephaly",
            "attributes": null
          },
          {
            "code": "P225.00",
            "description": "Holoprosencephaly",
            "attributes": null
          },
          {
            "code": "P226.00",
            "description": "Microgyria",
            "attributes": null
          },
          {
            "code": "P226000",
            "description": "Congenital bilateral perisylvian syndrome",
            "attributes": null
          },
          {
            "code": "P226.11",
            "description": "Hypoplasia of brain gyri",
            "attributes": null
          },
          {
            "code": "P227000",
            "description": "Agenesis of cerebrum",
            "attributes": null
          },
          {
            "code": "P227100",
            "description": "Congenital hypoplasia of cerebrum",
            "attributes": null
          },
          {
            "code": "P228.00",
            "description": "Anomalies of corpus callosum",
            "attributes": null
          },
          {
            "code": "P228000",
            "description": "Congenital absence of corpus callosum",
            "attributes": null
          },
          {
            "code": "P228011",
            "description": "Agenesis of corpus callosum",
            "attributes": null
          },
          {
            "code": "P228100",
            "description": "Hypoplasia of corpus callosum",
            "attributes": null
          },
          {
            "code": "P228200",
            "description": "Aplasia of corpus callosum",
            "attributes": null
          },
          {
            "code": "P228300",
            "description": "Aicardi syndrome",
            "attributes": null
          },
          {
            "code": "P228z00",
            "description": "Anomaly of corpus callosum NOS",
            "attributes": null
          },
          {
            "code": "P229.00",
            "description": "Anomalies of hypothalamus",
            "attributes": null
          },
          {
            "code": "P22A.00",
            "description": "Anomalies of cerebellum",
            "attributes": null
          },
          {
            "code": "P22A000",
            "description": "Congenital absence of cerebellum",
            "attributes": null
          },
          {
            "code": "P22A011",
            "description": "Agenesis of cerebellum",
            "attributes": null
          },
          {
            "code": "P22A100",
            "description": "Hypoplasia of cerebellum",
            "attributes": null
          },
          {
            "code": "P22A200",
            "description": "Aplasia of cerebellum",
            "attributes": null
          },
          {
            "code": "P22Az00",
            "description": "Anomaly of cerebellum NOS",
            "attributes": null
          },
          {
            "code": "P22y000",
            "description": "Cebocephaly",
            "attributes": null
          },
          {
            "code": "P22y100",
            "description": "Familial aplasia of the vermis",
            "attributes": null
          },
          {
            "code": "P22y111",
            "description": "Joubert syndrome",
            "attributes": null
          },
          {
            "code": "P22y200",
            "description": "Gillespie syndrome",
            "attributes": null
          },
          {
            "code": "P22y300",
            "description": "Partial absence of septum pellucidum",
            "attributes": null
          },
          {
            "code": "P22z.11",
            "description": "Cerebellar hypoplasia",
            "attributes": null
          },
          {
            "code": "P23..00",
            "description": "Congenital hydrocephalus",
            "attributes": null
          },
          {
            "code": "P230.00",
            "description": "Aqueduct of Sylvius anomaly",
            "attributes": null
          },
          {
            "code": "P230000",
            "description": "Aqueduct of Sylvius obstruction",
            "attributes": null
          },
          {
            "code": "P230011",
            "description": "Aqueduct of Sylvius septum NEC",
            "attributes": null
          },
          {
            "code": "P230100",
            "description": "Aqueduct of Sylvius stenosis",
            "attributes": null
          },
          {
            "code": "P230.11",
            "description": "Hydrocephauls with anomaly of aqueduct of Sylvius",
            "attributes": null
          },
          {
            "code": "P230.12",
            "description": "Stenosis of aqueduct of Sylvius",
            "attributes": null
          },
          {
            "code": "P230200",
            "description": "Atresia of aqueduct of Sylvius NEC",
            "attributes": null
          },
          {
            "code": "P230z00",
            "description": "Aqueduct of Sylvius anomaly NOS",
            "attributes": null
          },
          {
            "code": "P231.00",
            "description": "Foramen of Magendie atresia",
            "attributes": null
          },
          {
            "code": "P232.00",
            "description": "Foramen of Luschka atresia",
            "attributes": null
          },
          {
            "code": "P233.00",
            "description": "Atresia of foramina of Magendie and Luschka",
            "attributes": null
          },
          {
            "code": "P233.11",
            "description": "Dandy - Walker syndrome",
            "attributes": null
          },
          {
            "code": "P233.12",
            "description": "Hydrocephalus with atresia of foramina of Magendie and Luschka",
            "attributes": null
          },
          {
            "code": "P234.00",
            "description": "Hydranencephaly",
            "attributes": null
          },
          {
            "code": "P235.00",
            "description": "X-linked hydrocephalus",
            "attributes": null
          },
          {
            "code": "P23y.00",
            "description": "Other specified congenital hydrocephalus",
            "attributes": null
          },
          {
            "code": "P23z.00",
            "description": "Congenital hydrocephalus NOS",
            "attributes": null
          },
          {
            "code": "P24..00",
            "description": "Other specified brain anomalies",
            "attributes": null
          },
          {
            "code": "P240.00",
            "description": "Congenital cerebral cyst",
            "attributes": null
          },
          {
            "code": "P240000",
            "description": "Single congenital cerebral cyst",
            "attributes": null
          },
          {
            "code": "P240100",
            "description": "Multiple congenital cerebral cysts",
            "attributes": null
          },
          {
            "code": "P240.11",
            "description": "Congenital intracerebral cyst",
            "attributes": null
          },
          {
            "code": "P240200",
            "description": "Schizencephaly",
            "attributes": null
          },
          {
            "code": "P240z00",
            "description": "Congenital cerebral cyst NOS",
            "attributes": null
          },
          {
            "code": "P241.00",
            "description": "Macroencephaly",
            "attributes": null
          },
          {
            "code": "P241.11",
            "description": "Megalencephaly",
            "attributes": null
          },
          {
            "code": "P241.12",
            "description": "Enlarged brain",
            "attributes": null
          },
          {
            "code": "P242.00",
            "description": "Macrogyria",
            "attributes": null
          },
          {
            "code": "P244.00",
            "description": "Ulegyria",
            "attributes": null
          },
          {
            "code": "P245.00",
            "description": "Congenital adhesions of cerebral meninges",
            "attributes": null
          },
          {
            "code": "P246.00",
            "description": "Septo-optic dysplasia",
            "attributes": null
          },
          {
            "code": "P247.00",
            "description": "Dysplasia of cerebral cortex",
            "attributes": null
          },
          {
            "code": "P249.00",
            "description": "Megalencephaly",
            "attributes": null
          },
          {
            "code": "P24x.00",
            "description": "Multiple brain anomalies",
            "attributes": null
          },
          {
            "code": "P24z.00",
            "description": "Other specified brain anomalies NOS",
            "attributes": null
          },
          {
            "code": "P25..00",
            "description": "Other specified spinal cord anomalies",
            "attributes": null
          },
          {
            "code": "P251.00",
            "description": "Hydromyelia",
            "attributes": null
          },
          {
            "code": "P251.11",
            "description": "Hydrorachis",
            "attributes": null
          },
          {
            "code": "P252.00",
            "description": "Congenital tethering of spinal cord",
            "attributes": null
          },
          {
            "code": "P25y.00",
            "description": "Other specified anomalies of spinal cord",
            "attributes": null
          },
          {
            "code": "P25y000",
            "description": "Amyelia",
            "attributes": null
          },
          {
            "code": "P25y100",
            "description": "Atelomyelia",
            "attributes": null
          },
          {
            "code": "P25y111",
            "description": "Myelatelia",
            "attributes": null
          },
          {
            "code": "P25y112",
            "description": "Myelodysplasia of spinal cord",
            "attributes": null
          },
          {
            "code": "P25y200",
            "description": "Congenital anomaly of spinal meninges",
            "attributes": null
          },
          {
            "code": "P25y400",
            "description": "Spinal cord hypoplasia",
            "attributes": null
          },
          {
            "code": "P25yz00",
            "description": "Other specified spinal cord anomalies NOS",
            "attributes": null
          },
          {
            "code": "P25z.00",
            "description": "Spinal cord anomalies NOS",
            "attributes": null
          },
          {
            "code": "P26..00",
            "description": "Disorder of neuronal migration and differentiation",
            "attributes": null
          },
          {
            "code": "P2x..00",
            "description": "Other specified nervous system anomalies",
            "attributes": null
          },
          {
            "code": "P2x0.00",
            "description": "Agenesis of nerve, unspecified",
            "attributes": null
          },
          {
            "code": "P2x1.00",
            "description": "Brachial plexus displacement",
            "attributes": null
          },
          {
            "code": "P2x6.00",
            "description": "Chiari malformation type I",
            "attributes": null
          },
          {
            "code": "P2xz.00",
            "description": "Other specified nervous system anomalies NOS",
            "attributes": null
          },
          {
            "code": "P2xz000",
            "description": "Agenesis of nerve NEC",
            "attributes": null
          },
          {
            "code": "P2y..00",
            "description": "Unspecified nervous system anomaly of brain, cord and nervous system",
            "attributes": null
          },
          {
            "code": "P2y0.00",
            "description": "Congenital brain anomaly",
            "attributes": null
          },
          {
            "code": "P2y1.00",
            "description": "Congenital spinal cord anomaly",
            "attributes": null
          },
          {
            "code": "P2yz.00",
            "description": "Unspecified nervous system anomaly NOS",
            "attributes": null
          },
          {
            "code": "P2z..00",
            "description": "Nervous system anomalies NOS",
            "attributes": null
          },
          {
            "code": "P6z..11",
            "description": "Chiari's malformation",
            "attributes": null
          },
          {
            "code": "PG04.00",
            "description": "Craniofacial dysostosis",
            "attributes": null
          },
          {
            "code": "PG04.11",
            "description": "Crouzon's disease",
            "attributes": null
          },
          {
            "code": "PG04.12",
            "description": "Trigorhinophalangeal dysplasia",
            "attributes": null
          },
          {
            "code": "PG0D.00",
            "description": "Mandibulofacial dysostosis",
            "attributes": null
          },
          {
            "code": "PG0D.12",
            "description": "Treacher - Collins syndrome",
            "attributes": null
          },
          {
            "code": "PK5..00",
            "description": "Tuberous sclerosis",
            "attributes": null
          },
          {
            "code": "PK5..11",
            "description": "Bourneville's disease",
            "attributes": null
          },
          {
            "code": "PK5..12",
            "description": "Epiloia",
            "attributes": null
          },
          {
            "code": "PK80.00",
            "description": "Fetal alcohol syndrome",
            "attributes": null
          },
          {
            "code": "PK81.00",
            "description": "Fetal hydantoin syndrome",
            "attributes": null
          },
          {
            "code": "PK84.00",
            "description": "Fetal valproate syndrome",
            "attributes": null
          },
          {
            "code": "PKy5C00",
            "description": "Treacher Collins syndrome",
            "attributes": null
          },
          {
            "code": "Pyu0.00",
            "description": "[X]Congenital malformations of the nervous system",
            "attributes": null
          },
          {
            "code": "Pyu0000",
            "description": "[X]Encephalocele of other sites",
            "attributes": null
          },
          {
            "code": "Pyu0100",
            "description": "[X]Other congenital hydrocephalus",
            "attributes": null
          },
          {
            "code": "Pyu0300",
            "description": "[X]Other specified congenital malformations of brain",
            "attributes": null
          },
          {
            "code": "Pyu0400",
            "description": "[X]Unspecified spina bifida with hydrocephalus",
            "attributes": null
          },
          {
            "code": "Pyu0600",
            "description": "[X]Other specified congenital malformations of spinal cord",
            "attributes": null
          },
          {
            "code": "Pyu0700",
            "description": "[X]Other specified congenital malformations of nervous system",
            "attributes": null
          },
          {
            "code": "Q007111",
            "description": "Fetal alcohol syndrome",
            "attributes": null
          },
          {
            "code": "Q200.00",
            "description": "Subdural and cerebral haemorrhage due to birth trauma",
            "attributes": null
          },
          {
            "code": "Q200000",
            "description": "Cerebral haemorrhage unspecified, due to birth trauma",
            "attributes": null
          },
          {
            "code": "Q200100",
            "description": "Subdural haemorrhage unspecified, due to birth trauma",
            "attributes": null
          },
          {
            "code": "Q200200",
            "description": "Local subdural haematoma due to birth trauma",
            "attributes": null
          },
          {
            "code": "Q200300",
            "description": "Tentorial tear due to birth trauma",
            "attributes": null
          },
          {
            "code": "Q200400",
            "description": "Brain injury due to birth trauma NOS",
            "attributes": null
          },
          {
            "code": "Q200411",
            "description": "Cerebral injury due to birth trauma",
            "attributes": null
          },
          {
            "code": "Q200600",
            "description": "Extradural haemorrhage in fetus or newborn",
            "attributes": null
          },
          {
            "code": "Q200700",
            "description": "Cerebral haemorrhage due to birth injury",
            "attributes": null
          },
          {
            "code": "Q200y00",
            "description": "Other specified subdural or cerebral haemorrhage due to birth trauma",
            "attributes": null
          },
          {
            "code": "Q200z00",
            "description": "Subdural or cerebral haemorrhage due to birth trauma NOS",
            "attributes": null
          },
          {
            "code": "Q200z11",
            "description": "Birth brain damage NOS",
            "attributes": null
          },
          {
            "code": "Q411.00",
            "description": "Perinatal intraventricular haemorrhage",
            "attributes": null
          },
          {
            "code": "Q411200",
            "description": "Intraventricular (nontraumatic) haemorrhage, grade 3, of fetus and newborn",
            "attributes": null
          },
          {
            "code": "Q411300",
            "description": "Intraventricular haemorrhage due to birth injury",
            "attributes": null
          },
          {
            "code": "Q412.00",
            "description": "Perinatal subarachnoid haemorrhage",
            "attributes": null
          },
          {
            "code": "Q412000",
            "description": "Subarachnoid haemorrhage due to birth injury",
            "attributes": null
          },
          {
            "code": "Q417.00",
            "description": "Intracranial nontraumatic haemorrhage of fetus and newborn",
            "attributes": null
          },
          {
            "code": "Q417000",
            "description": "Intracerebral (nontraumatic) haemorrhage of fetus and newborn",
            "attributes": null
          },
          {
            "code": "Q417100",
            "description": "Cerebellar (nontraumatic) and posterior fossa haemorrhage of fetus and newborn",
            "attributes": null
          },
          {
            "code": "Q424.00",
            "description": "Kernicterus due to isoimmunisation",
            "attributes": null
          },
          {
            "code": "Q437000",
            "description": "Bilirubin encephalopathy",
            "attributes": null
          },
          {
            "code": "Q437z00",
            "description": "Kernicterus of newborn NOS",
            "attributes": null
          },
          {
            "code": "Q48y500",
            "description": "Megalencephaly",
            "attributes": null
          },
          {
            "code": "Qyu2000",
            "description": "[X]Other intracranial lacerations and haemorrhages due to birth injury",
            "attributes": null
          },
          {
            "code": "Qyu5200",
            "description": "[X]Other intracranial (nontraumatic) haemorrhages of fetus and newborn",
            "attributes": null
          },
          {
            "code": "Qyu5700",
            "description": "[X]Other specified kernicterus",
            "attributes": null
          },
          {
            "code": "Qyu5F00",
            "description": "[X]Intracranial nontraumatic haemorrhage fetus newborn unspecified",
            "attributes": null
          }
        ]
      },
      {
        "concept_id": 4121,
        "concept_version_id": 11481,
        "concept_name": "Other neurological - congenital neurological condition (SNOMED-CT)",
        "coding_system": {
          "id": 9,
          "name": "SNOMED  CT codes",
          "description": "SNOMED CT codes"
        },
        "phenotype_id": "PH1701",
        "phenotype_version_id": 3627,
        "phenotype_name": "Chronic paediatric conditions: Other neurological (excluding epilepsy and headaches)",
        "code_attribute_header": null,
        "codes": [
          {
            "code": "109411007",
            "description": "Fronto-naso-ethmoidal dysostosis (disorder)",
            "attributes": null
          },
          {
            "code": "109415003",
            "description": "Spheno-frontal dysostosis (disorder)",
            "attributes": null
          },
          {
            "code": "109561000",
            "description": "Cerebrofacial dysplasia (disorder)",
            "attributes": null
          },
          {
            "code": "109905002",
            "description": "Acquired myelocele (disorder)",
            "attributes": null
          },
          {
            "code": "111338006",
            "description": "Agenesis of nerve (disorder)",
            "attributes": null
          },
          {
            "code": "111505001",
            "description": "Muscle-eye-brain disease, congenital muscular dystrophy (disorder)",
            "attributes": null
          },
          {
            "code": "111641000119102",
            "description": "Congenital choroid plexus cyst (disorder)",
            "attributes": null
          },
          {
            "code": "11197005",
            "description": "Hydromyelia (disorder)",
            "attributes": null
          },
          {
            "code": "11701009",
            "description": "Hemicephaly (disorder)",
            "attributes": null
          },
          {
            "code": "12275031000119106",
            "description": "Congenital cerebral ventriculomegaly (disorder)",
            "attributes": null
          },
          {
            "code": "126941005",
            "description": "Subdural intracranial hemorrhage due to birth trauma (disorder)",
            "attributes": null
          },
          {
            "code": "127329003",
            "description": "Congenital anomaly of visual system (disorder)",
            "attributes": null
          },
          {
            "code": "127551000119100",
            "description": "Congenital hypoplasia of brain (disorder)",
            "attributes": null
          },
          {
            "code": "128124001",
            "description": "Congenital anomaly of central nervous system (disorder)",
            "attributes": null
          },
          {
            "code": "14061004",
            "description": "Derencephalus (disorder)",
            "attributes": null
          },
          {
            "code": "14447001",
            "description": "Dandy-Walker syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "15552004",
            "description": "Osteogenesis imperfecta, recessive perinatal lethal, with microcephaly AND cataracts (disorder)",
            "attributes": null
          },
          {
            "code": "15671007",
            "description": "Encephalocele of orbit (disorder)",
            "attributes": null
          },
          {
            "code": "15985031000119102",
            "description": "Neonatal non-traumatic intraventricular hemorrhage (disorder)",
            "attributes": null
          },
          {
            "code": "16026008",
            "description": "Congenital cerebellar hypoplasia (disorder)",
            "attributes": null
          },
          {
            "code": "16054391000119102",
            "description": "Congenital hypoplasia of right optic nerve (disorder)",
            "attributes": null
          },
          {
            "code": "16054431000119107",
            "description": "Congenital hypoplasia of left optic nerve (disorder)",
            "attributes": null
          },
          {
            "code": "16054471000119105",
            "description": "Congenital hypoplasia of bilateral optic nerves (disorder)",
            "attributes": null
          },
          {
            "code": "171131006",
            "description": "Meningocele (disorder)",
            "attributes": null
          },
          {
            "code": "172069000",
            "description": "Congenital meningocele (disorder)",
            "attributes": null
          },
          {
            "code": "17231009",
            "description": "Fetal valproate syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "17761000119109",
            "description": "High lumbar myelomeningocele (disorder)",
            "attributes": null
          },
          {
            "code": "17771000119103",
            "description": "Low lumbar myelomeningocele (disorder)",
            "attributes": null
          },
          {
            "code": "1829003",
            "description": "Microcephalus (disorder)",
            "attributes": null
          },
          {
            "code": "19133005",
            "description": "Neurofibromatosis syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "19276002",
            "description": "Congenital cerebral cyst (disorder)",
            "attributes": null
          },
          {
            "code": "192814005",
            "description": "Cerebral degeneration due to congenital hydrocephalus (disorder)",
            "attributes": null
          },
          {
            "code": "203663000",
            "description": "Scoliosis in neurofibromatosis (disorder)",
            "attributes": null
          },
          {
            "code": "203923004",
            "description": "Acrania (disorder)",
            "attributes": null
          },
          {
            "code": "203934001",
            "description": "Cervical spina bifida with hydrocephalus (disorder)",
            "attributes": null
          },
          {
            "code": "203935000",
            "description": "Thoracic spina bifida with hydrocephalus (disorder)",
            "attributes": null
          },
          {
            "code": "203936004",
            "description": "Lumbar spina bifida with hydrocephalus (disorder)",
            "attributes": null
          },
          {
            "code": "203941007",
            "description": "Cervical spina bifida with hydrocephalus - open (disorder)",
            "attributes": null
          },
          {
            "code": "203942000",
            "description": "Thoracic spina bifida with hydrocephalus - open (disorder)",
            "attributes": null
          },
          {
            "code": "203943005",
            "description": "Lumbar spina bifida with hydrocephalus - open (disorder)",
            "attributes": null
          },
          {
            "code": "203944004",
            "description": "Sacral spina bifida with hydrocephalus - open (disorder)",
            "attributes": null
          },
          {
            "code": "203946002",
            "description": "Spina bifida with hydrocephalus - closed (disorder)",
            "attributes": null
          },
          {
            "code": "203948001",
            "description": "Cervical spina bifida with hydrocephalus - closed (disorder)",
            "attributes": null
          },
          {
            "code": "203949009",
            "description": "Thoracic spina bifida with hydrocephalus - closed (disorder)",
            "attributes": null
          },
          {
            "code": "203950009",
            "description": "Lumbar spina bifida with hydrocephalus - closed (disorder)",
            "attributes": null
          },
          {
            "code": "203951008",
            "description": "Sacral spina bifida with hydrocephalus - closed (disorder)",
            "attributes": null
          },
          {
            "code": "203954000",
            "description": "Spina bifida with hydrocephalus of late onset (disorder)",
            "attributes": null
          },
          {
            "code": "203955004",
            "description": "Spina bifida with stenosis of aqueduct of Sylvius (disorder)",
            "attributes": null
          },
          {
            "code": "203957007",
            "description": "Dandy-Walker syndrome with spina bifida (disorder)",
            "attributes": null
          },
          {
            "code": "203967002",
            "description": "Spinal hydromeningocele (disorder)",
            "attributes": null
          },
          {
            "code": "203969004",
            "description": "Cervical spinal hydromeningocele (disorder)",
            "attributes": null
          },
          {
            "code": "203974007",
            "description": "Cervical hydromyelocele (disorder)",
            "attributes": null
          },
          {
            "code": "203975008",
            "description": "Thoracic hydromyelocele (disorder)",
            "attributes": null
          },
          {
            "code": "203976009",
            "description": "Lumbar hydromyelocele (disorder)",
            "attributes": null
          },
          {
            "code": "203980004",
            "description": "Cervical spinal meningocele (disorder)",
            "attributes": null
          },
          {
            "code": "203981000",
            "description": "Thoracic spinal meningocele (disorder)",
            "attributes": null
          },
          {
            "code": "203982007",
            "description": "Lumbar spinal meningocele (disorder)",
            "attributes": null
          },
          {
            "code": "203985009",
            "description": "Cervical meningomyelocele (disorder)",
            "attributes": null
          },
          {
            "code": "203986005",
            "description": "Thoracic meningomyelocele (disorder)",
            "attributes": null
          },
          {
            "code": "203987001",
            "description": "Lumbar meningomyelocele (disorder)",
            "attributes": null
          },
          {
            "code": "203990007",
            "description": "Cervical myelocele (disorder)",
            "attributes": null
          },
          {
            "code": "203991006",
            "description": "Thoracic myelocele (disorder)",
            "attributes": null
          },
          {
            "code": "203992004",
            "description": "Lumbar myelocele (disorder)",
            "attributes": null
          },
          {
            "code": "203994003",
            "description": "Myelocystocele (disorder)",
            "attributes": null
          },
          {
            "code": "203996001",
            "description": "Cervical myelocystocele (disorder)",
            "attributes": null
          },
          {
            "code": "203997005",
            "description": "Thoracic myelocystocele (disorder)",
            "attributes": null
          },
          {
            "code": "203998000",
            "description": "Lumbar myelocystocele (disorder)",
            "attributes": null
          },
          {
            "code": "204003007",
            "description": "Cervical spina bifida without hydrocephalus - open (disorder)",
            "attributes": null
          },
          {
            "code": "204004001",
            "description": "Thoracic spina bifida without hydrocephalus - open (disorder)",
            "attributes": null
          },
          {
            "code": "204005000",
            "description": "Lumbar spina bifida without hydrocephalus - open (disorder)",
            "attributes": null
          },
          {
            "code": "204006004",
            "description": "Sacral spina bifida without hydrocephalus - open (disorder)",
            "attributes": null
          },
          {
            "code": "204008003",
            "description": "Spina bifida without hydrocephalus - closed (disorder)",
            "attributes": null
          },
          {
            "code": "204010001",
            "description": "Cervical spina bifida without hydrocephalus - closed (disorder)",
            "attributes": null
          },
          {
            "code": "204011002",
            "description": "Thoracic spina bifida without hydrocephalus - closed (disorder)",
            "attributes": null
          },
          {
            "code": "204012009",
            "description": "Lumbar spina bifida without hydrocephalus - closed (disorder)",
            "attributes": null
          },
          {
            "code": "204013004",
            "description": "Sacral spina bifida without hydrocephalus - closed (disorder)",
            "attributes": null
          },
          {
            "code": "204021005",
            "description": "Encephalomyelocele (disorder)",
            "attributes": null
          },
          {
            "code": "204022003",
            "description": "Hydromeningocele - cranial (disorder)",
            "attributes": null
          },
          {
            "code": "204036008",
            "description": "Lissencephaly (disorder)",
            "attributes": null
          },
          {
            "code": "204040004",
            "description": "Agenesis of cerebrum (disorder)",
            "attributes": null
          },
          {
            "code": "204042007",
            "description": "Congenital malformation of corpus callosum (disorder)",
            "attributes": null
          },
          {
            "code": "204043002",
            "description": "Hypoplasia of corpus callosum (disorder)",
            "attributes": null
          },
          {
            "code": "204044008",
            "description": "Aplasia of corpus callosum (disorder)",
            "attributes": null
          },
          {
            "code": "204046005",
            "description": "Anomalies of hypothalamus (disorder)",
            "attributes": null
          },
          {
            "code": "204047001",
            "description": "Anomalies of cerebellum (disorder)",
            "attributes": null
          },
          {
            "code": "204049003",
            "description": "Aplasia of cerebellum (disorder)",
            "attributes": null
          },
          {
            "code": "204052006",
            "description": "Cebocephaly (disorder)",
            "attributes": null
          },
          {
            "code": "204061006",
            "description": "Foramen of Magendie atresia (disorder)",
            "attributes": null
          },
          {
            "code": "204062004",
            "description": "Foramen of Luschka atresia (disorder)",
            "attributes": null
          },
          {
            "code": "204067005",
            "description": "Single congenital cerebral cyst (disorder)",
            "attributes": null
          },
          {
            "code": "204068000",
            "description": "Multiple congenital cerebral cysts (disorder)",
            "attributes": null
          },
          {
            "code": "204072001",
            "description": "Congenital adhesions of cerebral meninges (disorder)",
            "attributes": null
          },
          {
            "code": "204074000",
            "description": "Multiple brain anomalies (disorder)",
            "attributes": null
          },
          {
            "code": "204081007",
            "description": "Spinal cord hypoplasia (disorder)",
            "attributes": null
          },
          {
            "code": "204086002",
            "description": "Brachial plexus displacement (disorder)",
            "attributes": null
          },
          {
            "code": "205788004",
            "description": "Fetal alcohol syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "206188000",
            "description": "Subdural and cerebral hemorrhage due to birth trauma (disorder)",
            "attributes": null
          },
          {
            "code": "206191000",
            "description": "Local intracranial subdural hematoma due to birth trauma (disorder)",
            "attributes": null
          },
          {
            "code": "206192007",
            "description": "Tentorial tear due to birth trauma (disorder)",
            "attributes": null
          },
          {
            "code": "206195009",
            "description": "Extradural intracranial hemorrhage in fetus or newborn (disorder)",
            "attributes": null
          },
          {
            "code": "206196005",
            "description": "Cerebral hemorrhage due to birth injury (disorder)",
            "attributes": null
          },
          {
            "code": "206397006",
            "description": "Intraventricular (nontraumatic) hemorrhage, grade 3, of fetus and newborn (disorder)",
            "attributes": null
          },
          {
            "code": "206398001",
            "description": "Intraventricular hemorrhage due to birth injury (disorder)",
            "attributes": null
          },
          {
            "code": "206399009",
            "description": "Intracranial subarachnoid hemorrhage due to birth injury (disorder)",
            "attributes": null
          },
          {
            "code": "206417009",
            "description": "Intracranial nontraumatic hemorrhage of fetus and newborn (disorder)",
            "attributes": null
          },
          {
            "code": "206419007",
            "description": "Cerebellar (nontraumatic) and posterior fossa hemorrhage of fetus and newborn (disorder)",
            "attributes": null
          },
          {
            "code": "21202004",
            "description": "Perinatal intracranial subarachnoid hemorrhage (disorder)",
            "attributes": null
          },
          {
            "code": "21350002",
            "description": "Colloid cyst of third ventricle (disorder)",
            "attributes": null
          },
          {
            "code": "21601000119103",
            "description": "Hypoxic ischemic encephalopathy due to birth trauma (disorder)",
            "attributes": null
          },
          {
            "code": "22133005",
            "description": "Congenital anomaly of the peripheral nervous system (disorder)",
            "attributes": null
          },
          {
            "code": "22471005",
            "description": "Hemispheric cerebellar agenesis (disorder)",
            "attributes": null
          },
          {
            "code": "23024003",
            "description": "Macrogyria (disorder)",
            "attributes": null
          },
          {
            "code": "230306001",
            "description": "Benign hereditary chorea (disorder)",
            "attributes": null
          },
          {
            "code": "230530003",
            "description": "Congenital nuclear ophthalmoplegia (disorder)",
            "attributes": null
          },
          {
            "code": "230541001",
            "description": "Congenital disorder of facial nerve (disorder)",
            "attributes": null
          },
          {
            "code": "230779009",
            "description": "Congenital spastic foot (disorder)",
            "attributes": null
          },
          {
            "code": "230785002",
            "description": "Congenital dysarthria (disorder)",
            "attributes": null
          },
          {
            "code": "230786001",
            "description": "Congenital dysphasia (disorder)",
            "attributes": null
          },
          {
            "code": "230787005",
            "description": "Congenital expressive dysphasia (disorder)",
            "attributes": null
          },
          {
            "code": "230788000",
            "description": "Congenital receptive dysphasia (disorder)",
            "attributes": null
          },
          {
            "code": "230794008",
            "description": "Neuronal choristoma (disorder)",
            "attributes": null
          },
          {
            "code": "233717003",
            "description": "Diffuse pulmonary neurofibromatosis (disorder)",
            "attributes": null
          },
          {
            "code": "233718008",
            "description": "Pulmonary tuberous sclerosis (disorder)",
            "attributes": null
          },
          {
            "code": "234638009",
            "description": "Microcephaly, normal intelligence and immunodeficiency (disorder)",
            "attributes": null
          },
          {
            "code": "23880008",
            "description": "Congenital anomaly of peripheral nerve (disorder)",
            "attributes": null
          },
          {
            "code": "23931000119104",
            "description": "Hydrocephalus due to Arnold Chiari malformation type 2 (disorder)",
            "attributes": null
          },
          {
            "code": "23941000119108",
            "description": "Arnold Chiari type 2 without hydrocephalus (disorder)",
            "attributes": null
          },
          {
            "code": "240312009",
            "description": "Cerebral injury due to birth trauma (disorder)",
            "attributes": null
          },
          {
            "code": "25004000",
            "description": "Subdural hemorrhage due to intrapartum anoxia AND/OR hypoxia (disorder)",
            "attributes": null
          },
          {
            "code": "25129008",
            "description": "Hydromeningocele (disorder)",
            "attributes": null
          },
          {
            "code": "253098009",
            "description": "Neural tube defect (disorder)",
            "attributes": null
          },
          {
            "code": "253101008",
            "description": "Congenital cerebral hernia (disorder)",
            "attributes": null
          },
          {
            "code": "253103006",
            "description": "Frontal encephalocele (disorder)",
            "attributes": null
          },
          {
            "code": "253104000",
            "description": "Frontoethmoidal encephalocele (disorder)",
            "attributes": null
          },
          {
            "code": "253106003",
            "description": "Nasofrontal encephalocele (disorder)",
            "attributes": null
          },
          {
            "code": "253107007",
            "description": "Nasopharyngeal encephalocele (disorder)",
            "attributes": null
          },
          {
            "code": "253108002",
            "description": "Temporal encephalocele (disorder)",
            "attributes": null
          },
          {
            "code": "253109005",
            "description": "Parietal encephalocele (disorder)",
            "attributes": null
          },
          {
            "code": "253111001",
            "description": "Thoracolumbar spina bifida without hydrocephalus - closed (disorder)",
            "attributes": null
          },
          {
            "code": "253113003",
            "description": "Rachischisis with hydrocephalus (disorder)",
            "attributes": null
          },
          {
            "code": "253114009",
            "description": "Myelocele with hydrocephalus (disorder)",
            "attributes": null
          },
          {
            "code": "253115005",
            "description": "Hydromyelocele with hydrocephalus (disorder)",
            "attributes": null
          },
          {
            "code": "253117002",
            "description": "Closed spina bifida with Arnold-Chiari malformation (disorder)",
            "attributes": null
          },
          {
            "code": "253118007",
            "description": "Thoracolumbar spina bifida with hydrocephalus - closed (disorder)",
            "attributes": null
          },
          {
            "code": "253119004",
            "description": "Hemimyelocele (disorder)",
            "attributes": null
          },
          {
            "code": "253120005",
            "description": "Lipomeningocele (disorder)",
            "attributes": null
          },
          {
            "code": "253124001",
            "description": "Myelodysplasia of spinal cord (disorder)",
            "attributes": null
          },
          {
            "code": "253128003",
            "description": "Abnormality of neurogenesis (disorder)",
            "attributes": null
          },
          {
            "code": "253130001",
            "description": "Secondary microcephaly (disorder)",
            "attributes": null
          },
          {
            "code": "253133004",
            "description": "Hydrocephalus with anomaly of aqueduct of Sylvius (disorder)",
            "attributes": null
          },
          {
            "code": "253135006",
            "description": "Defect of telencephalic division (disorder)",
            "attributes": null
          },
          {
            "code": "253136007",
            "description": "Lobar holoprosencephaly (disorder)",
            "attributes": null
          },
          {
            "code": "253137003",
            "description": "Alobar holoprosencephaly (disorder)",
            "attributes": null
          },
          {
            "code": "253138008",
            "description": "Semi-lobar holoprosencephaly (disorder)",
            "attributes": null
          },
          {
            "code": "253139000",
            "description": "Agenesis of corpus callosum with lipoma (disorder)",
            "attributes": null
          },
          {
            "code": "253140003",
            "description": "Partial agenesis of corpus callosum (disorder)",
            "attributes": null
          },
          {
            "code": "253142006",
            "description": "Atrophy of corpus callosum (disorder)",
            "attributes": null
          },
          {
            "code": "253143001",
            "description": "Absence of septum pellucidum (disorder)",
            "attributes": null
          },
          {
            "code": "253145008",
            "description": "Reduction anomaly of hypothalamus (disorder)",
            "attributes": null
          },
          {
            "code": "253146009",
            "description": "Disorder of neuronal migration and differentiation (disorder)",
            "attributes": null
          },
          {
            "code": "253147000",
            "description": "Type 1 lissencephaly (disorder)",
            "attributes": null
          },
          {
            "code": "253148005",
            "description": "Miller Dieker syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "253149002",
            "description": "Type 2 lissencephaly (disorder)",
            "attributes": null
          },
          {
            "code": "253150002",
            "description": "Neuronal heterotopia (disorder)",
            "attributes": null
          },
          {
            "code": "253151003",
            "description": "Nodular heterotopia (disorder)",
            "attributes": null
          },
          {
            "code": "253152005",
            "description": "Laminar heterotopia (disorder)",
            "attributes": null
          },
          {
            "code": "253153000",
            "description": "Cortical dysplasia (disorder)",
            "attributes": null
          },
          {
            "code": "253154006",
            "description": "Localized cortical dysplasia (disorder)",
            "attributes": null
          },
          {
            "code": "253156008",
            "description": "Cortical dysplasia with hemimegalencephaly (disorder)",
            "attributes": null
          },
          {
            "code": "253158009",
            "description": "Hydranencephaly with proliferative vasculopathy (disorder)",
            "attributes": null
          },
          {
            "code": "253159001",
            "description": "Schizencephaly (disorder)",
            "attributes": null
          },
          {
            "code": "253160006",
            "description": "Colpocephaly (disorder)",
            "attributes": null
          },
          {
            "code": "253166000",
            "description": "Lateral meningocele (disorder)",
            "attributes": null
          },
          {
            "code": "253167009",
            "description": "Microdysgenesis (disorder)",
            "attributes": null
          },
          {
            "code": "253171007",
            "description": "Dysgenesis of the cerebellum (disorder)",
            "attributes": null
          },
          {
            "code": "253172000",
            "description": "Agenesis of cerebellum (disorder)",
            "attributes": null
          },
          {
            "code": "253173005",
            "description": "Unilateral agenesis of cerebellum (situation)",
            "attributes": null
          },
          {
            "code": "253174004",
            "description": "Aplasia of the vermis (disorder)",
            "attributes": null
          },
          {
            "code": "253175003",
            "description": "Familial aplasia of the vermis (disorder)",
            "attributes": null
          },
          {
            "code": "253176002",
            "description": "Gillespie syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "253177006",
            "description": "Absence of the vermis (disorder)",
            "attributes": null
          },
          {
            "code": "253178001",
            "description": "Granular cell hypoplasia (disorder)",
            "attributes": null
          },
          {
            "code": "253179009",
            "description": "Cerebellar cortical dysplasia (disorder)",
            "attributes": null
          },
          {
            "code": "253180007",
            "description": "Dysgenesis of the brainstem (disorder)",
            "attributes": null
          },
          {
            "code": "253181006",
            "description": "Olive dysplasia (disorder)",
            "attributes": null
          },
          {
            "code": "253182004",
            "description": "Dentate dysplasia (disorder)",
            "attributes": null
          },
          {
            "code": "253183009",
            "description": "Olivary heterotopia (disorder)",
            "attributes": null
          },
          {
            "code": "253184003",
            "description": "Chiari malformation (disorder)",
            "attributes": null
          },
          {
            "code": "253185002",
            "description": "Chiari malformation type I (disorder)",
            "attributes": null
          },
          {
            "code": "253186001",
            "description": "Chiari malformation type III (disorder)",
            "attributes": null
          },
          {
            "code": "253187005",
            "description": "Chiari malformation type IV (disorder)",
            "attributes": null
          },
          {
            "code": "253188000",
            "description": "Abnormality of canalization and retrogressive differentiation (disorder)",
            "attributes": null
          },
          {
            "code": "253192007",
            "description": "Fibrolipoma of filum terminale (disorder)",
            "attributes": null
          },
          {
            "code": "253199003",
            "description": "Congenital malformation of the meninges (disorder)",
            "attributes": null
          },
          {
            "code": "253203003",
            "description": "Hypoplasia of brain gyri (disorder)",
            "attributes": null
          },
          {
            "code": "25397008",
            "description": "Aqueduct of Sylvius anomaly (disorder)",
            "attributes": null
          },
          {
            "code": "254241004",
            "description": "Segmental neurofibromatosis (disorder)",
            "attributes": null
          },
          {
            "code": "254242006",
            "description": "Diffuse neurofibroma (disorder)",
            "attributes": null
          },
          {
            "code": "254243001",
            "description": "Ash leaf spot, tuberous sclerosis (disorder)",
            "attributes": null
          },
          {
            "code": "254249002",
            "description": "Fetal carbamazepine syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "254250002",
            "description": "Fetal cocaine syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "254254006",
            "description": "Fetal toluene syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "255581000119100",
            "description": "Simple craniosynostosis (disorder)",
            "attributes": null
          },
          {
            "code": "26568002",
            "description": "Faun tail syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "26595007",
            "description": "Congenital absence of part of brain (disorder)",
            "attributes": null
          },
          {
            "code": "266673001",
            "description": "Ectopic neuronal tissue (disorder)",
            "attributes": null
          },
          {
            "code": "268143001",
            "description": "Spina bifida with hydrocephalus - open (disorder)",
            "attributes": null
          },
          {
            "code": "268146009",
            "description": "Spina bifida without hydrocephalus - open (disorder)",
            "attributes": null
          },
          {
            "code": "276588003",
            "description": "Perinatal intracranial laceration (disorder)",
            "attributes": null
          },
          {
            "code": "276589006",
            "description": "Perinatal tentorial laceration (disorder)",
            "attributes": null
          },
          {
            "code": "276593000",
            "description": "Perinatal falx laceration (disorder)",
            "attributes": null
          },
          {
            "code": "276594006",
            "description": "Perinatal rupture of superficial cerebral vein (disorder)",
            "attributes": null
          },
          {
            "code": "276647007",
            "description": "Perinatal intracranial hemorrhage (disorder)",
            "attributes": null
          },
          {
            "code": "276648002",
            "description": "Intraventricular hemorrhage of prematurity (disorder)",
            "attributes": null
          },
          {
            "code": "276652002",
            "description": "Perinatal subependymal hemorrhage with intraventricular and intracerebral extension (disorder)",
            "attributes": null
          },
          {
            "code": "277921008",
            "description": "Atelencephaly (disorder)",
            "attributes": null
          },
          {
            "code": "277922001",
            "description": "Aprosencephaly (disorder)",
            "attributes": null
          },
          {
            "code": "277949001",
            "description": "Combined malformation of central nervous system and skeletal muscle (disorder)",
            "attributes": null
          },
          {
            "code": "277950001",
            "description": "Muscle eye brain disease (disorder)",
            "attributes": null
          },
          {
            "code": "28534004",
            "description": "Spastic paralysis due to intracranial birth injury (disorder)",
            "attributes": null
          },
          {
            "code": "287080001",
            "description": "Congenital anomaly of nervous system of head/neck (disorder)",
            "attributes": null
          },
          {
            "code": "288276001",
            "description": "Fetal cerebral hemorrhage (disorder)",
            "attributes": null
          },
          {
            "code": "28861008",
            "description": "Crouzon syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "29956001",
            "description": "Myelatelia (disorder)",
            "attributes": null
          },
          {
            "code": "30023002",
            "description": "Hydranencephaly (disorder)",
            "attributes": null
          },
          {
            "code": "302882002",
            "description": "Hydrocephalus associated with congenital aqueduct stenosis (disorder)",
            "attributes": null
          },
          {
            "code": "30620003",
            "description": "Spina bifida of dorsal region (disorder)",
            "attributes": null
          },
          {
            "code": "307359001",
            "description": "Congenital agenesis of brainstem nuclei (disorder)",
            "attributes": null
          },
          {
            "code": "307670000",
            "description": "Congenital nystagmus with sensory abnormality (disorder)",
            "attributes": null
          },
          {
            "code": "30915001",
            "description": "Holoprosencephaly sequence (disorder)",
            "attributes": null
          },
          {
            "code": "31076000",
            "description": "Congenital ischemic atrophy of central nervous system structure (disorder)",
            "attributes": null
          },
          {
            "code": "31429000",
            "description": "Cerebral cortical dysgenesis (disorder)",
            "attributes": null
          },
          {
            "code": "32219008",
            "description": "Craniorachischisis (disorder)",
            "attributes": null
          },
          {
            "code": "32232003",
            "description": "Spina bifida of cervical region (disorder)",
            "attributes": null
          },
          {
            "code": "330041000119103",
            "description": "Congenital porencephalic cyst (disorder)",
            "attributes": null
          },
          {
            "code": "35111000119109",
            "description": "Cystic malformation of posterior fossa (disorder)",
            "attributes": null
          },
          {
            "code": "359007",
            "description": "Kernicterus due to isoimmunization (disorder)",
            "attributes": null
          },
          {
            "code": "359824007",
            "description": "Incomplete anencephaly (disorder)",
            "attributes": null
          },
          {
            "code": "36010004",
            "description": "Congenital cerebral meningocele (disorder)",
            "attributes": null
          },
          {
            "code": "36025004",
            "description": "Fibrous skin tumor of tuberous sclerosis (disorder)",
            "attributes": null
          },
          {
            "code": "360527003",
            "description": "Diplomyelia (disorder)",
            "attributes": null
          },
          {
            "code": "360530005",
            "description": "Myeloschisis (disorder)",
            "attributes": null
          },
          {
            "code": "363034005",
            "description": "Congenital anomaly of neural structure of trunk (disorder)",
            "attributes": null
          },
          {
            "code": "371107004",
            "description": "Seizures complicating intracranial hemorrhage in the newborn (disorder)",
            "attributes": null
          },
          {
            "code": "373587001",
            "description": "Chiari malformation type II (disorder)",
            "attributes": null
          },
          {
            "code": "38116000",
            "description": "Hydromyelocele (disorder)",
            "attributes": null
          },
          {
            "code": "38353004",
            "description": "Congenital porencephaly (disorder)",
            "attributes": null
          },
          {
            "code": "39150004",
            "description": "Congenital anomaly of spinal meninges (disorder)",
            "attributes": null
          },
          {
            "code": "39574006",
            "description": "Congenital hypoplasia of inner granular layer of cerebellum (disorder)",
            "attributes": null
          },
          {
            "code": "40130009",
            "description": "Spina bifida without hydrocephalus (disorder)",
            "attributes": null
          },
          {
            "code": "403559003",
            "description": "Cutaneous lesion resulting from spinal dysraphism (disorder)",
            "attributes": null
          },
          {
            "code": "403560008",
            "description": "Port-wine stain associated with spinal dysraphism (disorder)",
            "attributes": null
          },
          {
            "code": "403561007",
            "description": "Cutaneous lesion resulting from spina bifida (disorder)",
            "attributes": null
          },
          {
            "code": "403815003",
            "description": "Axillary freckling due to neurofibromatosis (disorder)",
            "attributes": null
          },
          {
            "code": "403816002",
            "description": "Multiple cafÃ©-au-lait macules due to neurofibromatosis (disorder)",
            "attributes": null
          },
          {
            "code": "403817006",
            "description": "Multiple neurofibromas in neurofibromatosis (disorder)",
            "attributes": null
          },
          {
            "code": "403819009",
            "description": "Elephantiasis neurofibromatosa (disorder)",
            "attributes": null
          },
          {
            "code": "403820003",
            "description": "CafÃ©-au-lait macules with pulmonary stenosis (disorder)",
            "attributes": null
          },
          {
            "code": "403821004",
            "description": "CafÃ©-au-lait macules with temporal dysrhythmia (disorder)",
            "attributes": null
          },
          {
            "code": "403823001",
            "description": "Periungual fibroma in tuberous sclerosis (disorder)",
            "attributes": null
          },
          {
            "code": "4061000119104",
            "description": "Myelomeningocele without hydrocephalus (disorder)",
            "attributes": null
          },
          {
            "code": "410060009",
            "description": "Hydrencephalomeningocele (disorder)",
            "attributes": null
          },
          {
            "code": "413808003",
            "description": "Cerebral ventriculomegaly (disorder)",
            "attributes": null
          },
          {
            "code": "414667000",
            "description": "Meningomyelocele (disorder)",
            "attributes": null
          },
          {
            "code": "415713009",
            "description": "Thoracic hydromeningocele (disorder)",
            "attributes": null
          },
          {
            "code": "417658006",
            "description": "Holoanencephaly (disorder)",
            "attributes": null
          },
          {
            "code": "422474003",
            "description": "Partial absence of septum pellucidum (disorder)",
            "attributes": null
          },
          {
            "code": "42376006",
            "description": "Occipital encephalocele (disorder)",
            "attributes": null
          },
          {
            "code": "425687007",
            "description": "Spina bifida aperta of cervical spine (disorder)",
            "attributes": null
          },
          {
            "code": "427216002",
            "description": "Spina bifida aperta of thoracic spine (disorder)",
            "attributes": null
          },
          {
            "code": "428190001",
            "description": "Neurogenic bladder due to spina bifida (disorder)",
            "attributes": null
          },
          {
            "code": "428241007",
            "description": "Ventricular hemorrhage of fetus (disorder)",
            "attributes": null
          },
          {
            "code": "429466000",
            "description": "Spina bifida aperta of lumbar spine (disorder)",
            "attributes": null
          },
          {
            "code": "431265009",
            "description": "Fetal microcephaly (disorder)",
            "attributes": null
          },
          {
            "code": "43427008",
            "description": "Ectopic glial tissue (disorder)",
            "attributes": null
          },
          {
            "code": "43602006",
            "description": "Subdural intracranial hemorrhage in fetus or newborn (disorder)",
            "attributes": null
          },
          {
            "code": "438583008",
            "description": "Congenital bilateral perisylvian syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "442300000",
            "description": "Rhombencephalosynapsis (disorder)",
            "attributes": null
          },
          {
            "code": "444860006",
            "description": "Meningomyelocele of lumbosacral spine (disorder)",
            "attributes": null
          },
          {
            "code": "444978000",
            "description": "Meningocele of vertex (disorder)",
            "attributes": null
          },
          {
            "code": "445116003",
            "description": "Encephalocele of vertex (disorder)",
            "attributes": null
          },
          {
            "code": "445307009",
            "description": "Spina bifida of sacral region (disorder)",
            "attributes": null
          },
          {
            "code": "445308004",
            "description": "Split spinal cord malformation (disorder)",
            "attributes": null
          },
          {
            "code": "445468002",
            "description": "Occipital meningocele (disorder)",
            "attributes": null
          },
          {
            "code": "448227009",
            "description": "X-linked periventricular heterotopia (disorder)",
            "attributes": null
          },
          {
            "code": "45163000",
            "description": "Congenital pontocerebellar hypoplasia (disorder)",
            "attributes": null
          },
          {
            "code": "462165005",
            "description": "Fetal choroid plexus cyst (disorder)",
            "attributes": null
          },
          {
            "code": "46829007",
            "description": "Developmental displacement of brachial plexus (disorder)",
            "attributes": null
          },
          {
            "code": "47032000",
            "description": "Congenital hydrocephalus (disorder)",
            "attributes": null
          },
          {
            "code": "48376004",
            "description": "Congenital pseudoporencephaly (disorder)",
            "attributes": null
          },
          {
            "code": "4945003",
            "description": "Microgyria (disorder)",
            "attributes": null
          },
          {
            "code": "49946005",
            "description": "Podencephalus (disorder)",
            "attributes": null
          },
          {
            "code": "50143004",
            "description": "Kernicterus of newborn (disorder)",
            "attributes": null
          },
          {
            "code": "50429003",
            "description": "Congenital stenosis of aqueduct of Sylvius (disorder)",
            "attributes": null
          },
          {
            "code": "50751005",
            "description": "Sinus pericranii (disorder)",
            "attributes": null
          },
          {
            "code": "5102002",
            "description": "Agenesis of corpus callosum (disorder)",
            "attributes": null
          },
          {
            "code": "52330001",
            "description": "Meningoencephalocele (disorder)",
            "attributes": null
          },
          {
            "code": "52713000",
            "description": "Infantile neuroaxonal dystrophy (disorder)",
            "attributes": null
          },
          {
            "code": "53318002",
            "description": "Spina bifida with hydrocephalus (disorder)",
            "attributes": null
          },
          {
            "code": "53776005",
            "description": "Encephalocystocele (disorder)",
            "attributes": null
          },
          {
            "code": "54794009",
            "description": "Ectopic gray matter in centrum ovale (disorder)",
            "attributes": null
          },
          {
            "code": "55999004",
            "description": "Encephalocele (disorder)",
            "attributes": null
          },
          {
            "code": "56155002",
            "description": "Hemispheric cerebral agenesis (disorder)",
            "attributes": null
          },
          {
            "code": "56531003",
            "description": "Ulegyria (disorder)",
            "attributes": null
          },
          {
            "code": "57148006",
            "description": "Congenital anomaly of brain (disorder)",
            "attributes": null
          },
          {
            "code": "57284007",
            "description": "Severe birth asphyxia (disorder)",
            "attributes": null
          },
          {
            "code": "57544002",
            "description": "Multiple malformation syndrome due to non-infectious environmental agents (disorder)",
            "attributes": null
          },
          {
            "code": "5842009",
            "description": "Spinal cord dysplasia (disorder)",
            "attributes": null
          },
          {
            "code": "58557008",
            "description": "Spina bifida aperta (disorder)",
            "attributes": null
          },
          {
            "code": "609417004",
            "description": "Fetal anencephaly (disorder)",
            "attributes": null
          },
          {
            "code": "609437000",
            "description": "Fetal Alcohol Spectrum Disorder (disorder)",
            "attributes": null
          },
          {
            "code": "609528003",
            "description": "Posterior fossa arachnoid cyst (disorder)",
            "attributes": null
          },
          {
            "code": "609529006",
            "description": "Persistent Blake's pouch cyst (disorder)",
            "attributes": null
          },
          {
            "code": "61819007",
            "description": "Rachischisis (disorder)",
            "attributes": null
          },
          {
            "code": "62110005",
            "description": "Fetal methyl mercury syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "62158001",
            "description": "Status marmoratus (disorder)",
            "attributes": null
          },
          {
            "code": "65144005",
            "description": "Congenital spinal meningocele (disorder)",
            "attributes": null
          },
          {
            "code": "65455002",
            "description": "Nasal encephalocele (disorder)",
            "attributes": null
          },
          {
            "code": "65986000",
            "description": "Fetal aminopterin syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "66038001",
            "description": "Miller syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "66351003",
            "description": "Fetal trimethadione syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "67531005",
            "description": "Spina bifida (disorder)",
            "attributes": null
          },
          {
            "code": "67876003",
            "description": "Congenital obstruction of aqueduct of Sylvius (disorder)",
            "attributes": null
          },
          {
            "code": "67944007",
            "description": "Lhermitte-Duclos disease (disorder)",
            "attributes": null
          },
          {
            "code": "697924002",
            "description": "Pulmonary hypertension in neurofibromatosis (disorder)",
            "attributes": null
          },
          {
            "code": "698999002",
            "description": "Congenital atresia of aqueduct of Sylvius (disorder)",
            "attributes": null
          },
          {
            "code": "699812002",
            "description": "Subependymal nodular heterotopia (disorder)",
            "attributes": null
          },
          {
            "code": "70065001",
            "description": "Fetal hydantoin syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "702361006",
            "description": "Crouzon syndrome with acanthosis nigricans (disorder)",
            "attributes": null
          },
          {
            "code": "702410002",
            "description": "Iris coloboma with ptosis, hypertelorism, and mental retardation (disorder)",
            "attributes": null
          },
          {
            "code": "702437000",
            "description": "Amish lethal microcephaly (disorder)",
            "attributes": null
          },
          {
            "code": "702450004",
            "description": "FOXG1 syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "702611008",
            "description": "Congenital brain aplasia (disorder)",
            "attributes": null
          },
          {
            "code": "702628006",
            "description": "Congenital anomaly of cerebrum (disorder)",
            "attributes": null
          },
          {
            "code": "703389002",
            "description": "Calcium/calmodulin-dependent serine protein kinase related intellectual disability (disorder)",
            "attributes": null
          },
          {
            "code": "70534000",
            "description": "Occult spinal dysraphism sequence (disorder)",
            "attributes": null
          },
          {
            "code": "70611002",
            "description": "Perinatal intraventricular hemorrhage (disorder)",
            "attributes": null
          },
          {
            "code": "707433009",
            "description": "Lymphangioleiomyomatosis due to tuberous sclerosis syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "711153001",
            "description": "Bowen-Conradi syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "71178008",
            "description": "Congenital spinal hydromeningocele (disorder)",
            "attributes": null
          },
          {
            "code": "715344006",
            "description": "Neurofibromatosis Noonan syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "715406003",
            "description": "Isolated lissencephaly type 1 without known genetic defect (disorder)",
            "attributes": null
          },
          {
            "code": "715422002",
            "description": "Craniotelencephalic dysplasia (disorder)",
            "attributes": null
          },
          {
            "code": "715430001",
            "description": "Embryofetopathy caused by indomethacin (disorder)",
            "attributes": null
          },
          {
            "code": "715431002",
            "description": "Embryopathy caused by phenobarbital (disorder)",
            "attributes": null
          },
          {
            "code": "715434005",
            "description": "Holoprosencephaly craniosynostosis syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "715436007",
            "description": "Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration (disorder)",
            "attributes": null
          },
          {
            "code": "715462003",
            "description": "Microcephalus co-occurrent with cervical spine fusion anomaly (disorder)",
            "attributes": null
          },
          {
            "code": "715463008",
            "description": "Congenital pontocerebellar hypoplasia type 2 (disorder)",
            "attributes": null
          },
          {
            "code": "715780008",
            "description": "Lissencephaly type 1 due to doublecortin gene mutation (disorder)",
            "attributes": null
          },
          {
            "code": "715817007",
            "description": "Lissencephaly co-occurrent with congenital cerebellar hypoplasia (disorder)",
            "attributes": null
          },
          {
            "code": "715819005",
            "description": "Lissencephaly co-occurrent with congenital cerebellar hypoplasia type B (disorder)",
            "attributes": null
          },
          {
            "code": "715820004",
            "description": "Lissencephaly co-occurrent with congenital cerebellar hypoplasia type C (disorder)",
            "attributes": null
          },
          {
            "code": "715821000",
            "description": "Lissencephaly co-occurrent with congenital cerebellar hypoplasia type D (disorder)",
            "attributes": null
          },
          {
            "code": "715822007",
            "description": "Lissencephaly co-occurrent with congenital cerebellar hypoplasia type F (disorder)",
            "attributes": null
          },
          {
            "code": "715905006",
            "description": "Unilateral polymicrogyria (disorder)",
            "attributes": null
          },
          {
            "code": "715981004",
            "description": "Autosomal recessive primary microcephaly (disorder)",
            "attributes": null
          },
          {
            "code": "715990006",
            "description": "Agenesis of cerebellum and hydrocephalus syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "716005004",
            "description": "Fetal diethylstilbestrol syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "716996008",
            "description": "Hypoplasia of corpus callosum and mental retardation with adducted thumbs and spasticity and hydrocephalus syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "716997004",
            "description": "Joubert syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "716998009",
            "description": "Joubert syndrome with ocular defect (disorder)",
            "attributes": null
          },
          {
            "code": "716999001",
            "description": "Joubert syndrome with renal defect (disorder)",
            "attributes": null
          },
          {
            "code": "717632002",
            "description": "X-linked lissencephaly with agenesis of corpus callosum and genital anomaly syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "71779008",
            "description": "X-linked hydrocephalus syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "717939009",
            "description": "Anencephaly without rachischisis (disorder)",
            "attributes": null
          },
          {
            "code": "717977003",
            "description": "Lissencephaly syndrome Norman Roberts type (disorder)",
            "attributes": null
          },
          {
            "code": "718228001",
            "description": "Fetal iodine syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "718573009",
            "description": "Achalasia microcephaly syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "718605009",
            "description": "Congenital pontocerebellar hypoplasia type 7 (disorder)",
            "attributes": null
          },
          {
            "code": "718606005",
            "description": "Congenital pontocerebellar hypoplasia type 6 (disorder)",
            "attributes": null
          },
          {
            "code": "718607001",
            "description": "Congenital pontocerebellar hypoplasia type 5 (disorder)",
            "attributes": null
          },
          {
            "code": "718608006",
            "description": "Congenital pontocerebellar hypoplasia type 4 (disorder)",
            "attributes": null
          },
          {
            "code": "718609003",
            "description": "Congenital pontocerebellar hypoplasia type 3 (disorder)",
            "attributes": null
          },
          {
            "code": "718610008",
            "description": "Congenital pontocerebellar hypoplasia type 1 (disorder)",
            "attributes": null
          },
          {
            "code": "718611007",
            "description": "Congenital pontocerebellar hypoplasia type 8 (disorder)",
            "attributes": null
          },
          {
            "code": "718719001",
            "description": "Lissencephaly type 3 familial fetal akinesia sequence syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "718720007",
            "description": "Lissencephaly type 3 metacarpal bone dysplasia syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "718759003",
            "description": "Lissencephaly due to tubulin alpha 1A mutation (disorder)",
            "attributes": null
          },
          {
            "code": "719136005",
            "description": "X-linked intellectual disability with cerebellar hypoplasia syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "719139003",
            "description": "X-linked Dandy-Walker malformation with intellectual disability, basal ganglia disease and seizure syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "719162001",
            "description": "Radioulnar synostosis with microcephaly and scoliosis syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "719377004",
            "description": "Microcephalus with albinism and digital anomaly syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "719813003",
            "description": "X-linked mandibulofacial dysostosis (disorder)",
            "attributes": null
          },
          {
            "code": "7199000",
            "description": "Tuberous sclerosis syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "720408003",
            "description": "Acrofrontofacionasal dysostosis (disorder)",
            "attributes": null
          },
          {
            "code": "720518006",
            "description": "Athabaskan brainstem dysgenesis syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "720632004",
            "description": "Central bilateral macrogyria (disorder)",
            "attributes": null
          },
          {
            "code": "720813007",
            "description": "Craniosynostosis with Dandy-Walker malformation and hydrocephalus syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "721231007",
            "description": "Hydrocephalus with obesity and hypogonadism syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "721297008",
            "description": "Galloway Mowat syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "721845005",
            "description": "Hypomandibular faciocranial dysostosis (disorder)",
            "attributes": null
          },
          {
            "code": "721847002",
            "description": "Joubert syndrome with congenital hepatic fibrosis (disorder)",
            "attributes": null
          },
          {
            "code": "721862000",
            "description": "Joubert syndrome with oculorenal defect (disorder)",
            "attributes": null
          },
          {
            "code": "721873007",
            "description": "Joubert syndrome with orofaciodigital defect (disorder)",
            "attributes": null
          },
          {
            "code": "722036008",
            "description": "Megalencephaly, polymicrogyria, postaxial polydactyly, hydrocephalus syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "722385008",
            "description": "Cerebral dysgenesis, neuropathy, ichthyosis, palmoplantar keratoderma syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "722451006",
            "description": "Gomez Lopez Hernandez syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "722575008",
            "description": "Traumatic hemorrhage of cerebellum due to birth trauma (disorder)",
            "attributes": null
          },
          {
            "code": "722576009",
            "description": "Injury of brain stem due to birth trauma (disorder)",
            "attributes": null
          },
          {
            "code": "722580004",
            "description": "Fetal or neonatal intraventricular non-traumatic hemorrhage grade 4 (disorder)",
            "attributes": null
          },
          {
            "code": "722581000",
            "description": "Fetal or neonatal non-traumatic intraventricular hemorrhage (disorder)",
            "attributes": null
          },
          {
            "code": "722583002",
            "description": "Fetal or neonatal non-traumatic hemorrhage of subarachnoid space of brain (disorder)",
            "attributes": null
          },
          {
            "code": "722584008",
            "description": "Fetal or neonatal non-traumatic hemorrhage of subdural space of brain (disorder)",
            "attributes": null
          },
          {
            "code": "722905003",
            "description": "Intracranial laceration due to birth trauma (disorder)",
            "attributes": null
          },
          {
            "code": "722906002",
            "description": "Intracranial hemorrhage due to birth trauma (disorder)",
            "attributes": null
          },
          {
            "code": "722909009",
            "description": "Traumatic hemorrhage of intracranial epidural space due to birth trauma (disorder)",
            "attributes": null
          },
          {
            "code": "722989007",
            "description": "Aplasia of optic nerve (disorder)",
            "attributes": null
          },
          {
            "code": "722990003",
            "description": "Congenital atrophy of optic nerve (disorder)",
            "attributes": null
          },
          {
            "code": "722992006",
            "description": "Communicating hydrocephalus co-occurrent and due to congenital agenesis of arachnoid villi (disorder)",
            "attributes": null
          },
          {
            "code": "722996009",
            "description": "Congenital malformation of autonomic nervous system (disorder)",
            "attributes": null
          },
          {
            "code": "723405001",
            "description": "Microlissencephaly micromelia syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "723406000",
            "description": "Embryopathy caused by mycophenolate mofetil (disorder)",
            "attributes": null
          },
          {
            "code": "723612001",
            "description": "Spinal muscular atrophy, Dandy-Walker malformation, cataract syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "724067006",
            "description": "Permanent neonatal diabetes mellitus with cerebellar agenesis syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "724144006",
            "description": "Embryofetopathy caused by methimazole (disorder)",
            "attributes": null
          },
          {
            "code": "724999003",
            "description": "Isolated optic nerve hypoplasia (disorder)",
            "attributes": null
          },
          {
            "code": "725287006",
            "description": "Embryopathy caused by retinoid (disorder)",
            "attributes": null
          },
          {
            "code": "726031001",
            "description": "Cerebellar ataxia, intellectual disability, optic atrophy, skin abnormalities syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "726704006",
            "description": "Cataract, congenital heart disease, neural tube defect syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "733049004",
            "description": "Encephalopathy, intracerebral calcification, retinal degeneration syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "733068001",
            "description": "Absent tibia, polydactyly, arachnoid cyst syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "733072002",
            "description": "Alaninuria, microcephaly, dwarfism, enamel hypoplasia, diabetes mellitus syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "733092009",
            "description": "Microcephalus, hypergonadotropic hypogonadism, short stature syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "73331006",
            "description": "Hemimyelia (disorder)",
            "attributes": null
          },
          {
            "code": "733418003",
            "description": "Joubert syndrome with Jeune asphyxiating thoracic dystrophy (disorder)",
            "attributes": null
          },
          {
            "code": "735749005",
            "description": "Myelomeningocele co-occurrent with hydrocephalus (disorder)",
            "attributes": null
          },
          {
            "code": "75076004",
            "description": "Amyelencephalus (disorder)",
            "attributes": null
          },
          {
            "code": "7611002",
            "description": "Septo-optic dysplasia sequence (disorder)",
            "attributes": null
          },
          {
            "code": "762295002",
            "description": "Congenital obstructive hydrocephalus (disorder)",
            "attributes": null
          },
          {
            "code": "763350002",
            "description": "Intellectual disability, obesity, brain malformation, facial dysmorphism syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "763366000",
            "description": "Leukoencephalopathy, thalamus and brainstem anomalies, high lactate syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "763717004",
            "description": "Sporadic fetal brain disruption sequence (disorder)",
            "attributes": null
          },
          {
            "code": "763830009",
            "description": "Oculomaxillofacial dysostosis (disorder)",
            "attributes": null
          },
          {
            "code": "763861000",
            "description": "Pachygyria, intellectual disability, epilepsy syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "763889002",
            "description": "Spina bifida and hypospadias syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "76481000119102",
            "description": "Pressure ulcer due to spina bifida (disorder)",
            "attributes": null
          },
          {
            "code": "765089003",
            "description": "Focal epilepsy, intellectual disability, cerebro-cerebellar malformation syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "765331004",
            "description": "Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis (disorder)",
            "attributes": null
          },
          {
            "code": "765757003",
            "description": "Bilateral polymicrogyria (disorder)",
            "attributes": null
          },
          {
            "code": "766709000",
            "description": "Isolated hypoplasia of cerebellar vermis (disorder)",
            "attributes": null
          },
          {
            "code": "766710005",
            "description": "Isolated focal cortical dysplasia (disorder)",
            "attributes": null
          },
          {
            "code": "766871009",
            "description": "Diencephalic mesencephalic junction dysplasia (disorder)",
            "attributes": null
          },
          {
            "code": "766934006",
            "description": "Isolated unilateral hemispheric cerebellar hypoplasia (disorder)",
            "attributes": null
          },
          {
            "code": "768939009",
            "description": "Primary tethered cord syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "770408001",
            "description": "Congenital stenosis of cervical spinal canal (disorder)",
            "attributes": null
          },
          {
            "code": "770560008",
            "description": "Lissencephaly due to LIS1 mutation (disorder)",
            "attributes": null
          },
          {
            "code": "770725000",
            "description": "Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly (disorder)",
            "attributes": null
          },
          {
            "code": "771076003",
            "description": "Leptomyelolipoma (disorder)",
            "attributes": null
          },
          {
            "code": "771142009",
            "description": "Cortical dysplasia with focal epilepsy syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "771146007",
            "description": "Holoprosencephaly with caudal dysgenesis syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "771147003",
            "description": "Isolated arhinencephaly (disorder)",
            "attributes": null
          },
          {
            "code": "771234002",
            "description": "Isolated bilateral hemispheric cerebellar hypoplasia (disorder)",
            "attributes": null
          },
          {
            "code": "771303004",
            "description": "Severe neonatal onset encephalopathy with microcephaly (disorder)",
            "attributes": null
          },
          {
            "code": "771336003",
            "description": "Polymicrogyria with optic nerve hypoplasia (disorder)",
            "attributes": null
          },
          {
            "code": "77224008",
            "description": "Spina bifida of lumbar region (disorder)",
            "attributes": null
          },
          {
            "code": "773305003",
            "description": "Microcephaly, polymicrogyria, corpus callosum agenesis syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "773394007",
            "description": "Autosomal recessive frontotemporal pachygyria (disorder)",
            "attributes": null
          },
          {
            "code": "773497001",
            "description": "Partial corpus callosum agenesis, cerebellar vermis hypoplasia with posterior fossa cysts syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "773610007",
            "description": "Chudley McCullough syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "773627004",
            "description": "Porencephaly, microcephaly, bilateral congenital cataract syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "775907000",
            "description": "Congenital pontocerebellar hypoplasia type 9 (disorder)",
            "attributes": null
          },
          {
            "code": "778070003",
            "description": "Autosomal dominant primary microcephaly (disorder)",
            "attributes": null
          },
          {
            "code": "77817004",
            "description": "Neu-Laxova syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "78071008",
            "description": "Hydromicrocephaly (disorder)",
            "attributes": null
          },
          {
            "code": "781641005",
            "description": "Schwannomatosis (disorder)",
            "attributes": null
          },
          {
            "code": "782720005",
            "description": "Congenital pontocerebellar hypoplasia type 10 (disorder)",
            "attributes": null
          },
          {
            "code": "782879004",
            "description": "Occipital pachygyria and polymicrogyria (disorder)",
            "attributes": null
          },
          {
            "code": "782884005",
            "description": "Pontine tegmental cap dysplasia (disorder)",
            "attributes": null
          },
          {
            "code": "783724009",
            "description": "Fetal spina bifida (disorder)",
            "attributes": null
          },
          {
            "code": "783726006",
            "description": "Fetal hydrocephalus (disorder)",
            "attributes": null
          },
          {
            "code": "784344009",
            "description": "Cortical dysgenesis with pontocerebellar hypoplasia due to tubulin beta 3 class III mutation (disorder)",
            "attributes": null
          },
          {
            "code": "785299009",
            "description": "Cobblestone lissencephaly without muscular or ocular involvement (disorder)",
            "attributes": null
          },
          {
            "code": "785306007",
            "description": "Lissencephaly co-occurrent with congenital cerebellar hypoplasia type E (disorder)",
            "attributes": null
          },
          {
            "code": "785307003",
            "description": "Lissencephaly co-occurrent with congenital cerebellar hypoplasia type A (disorder)",
            "attributes": null
          },
          {
            "code": "78693004",
            "description": "Congenital hypoplasia of part of brain (disorder)",
            "attributes": null
          },
          {
            "code": "78784005",
            "description": "Amyelia (disorder)",
            "attributes": null
          },
          {
            "code": "789120001",
            "description": "Neurenteric cyst (disorder)",
            "attributes": null
          },
          {
            "code": "80651009",
            "description": "Aicardi's syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "81042008",
            "description": "Congenital anomaly of spinal cord (disorder)",
            "attributes": null
          },
          {
            "code": "81526008",
            "description": "Hydromeningomyelocele (disorder)",
            "attributes": null
          },
          {
            "code": "816068000",
            "description": "Periventricular nodular heterotopia (disorder)",
            "attributes": null
          },
          {
            "code": "82058009",
            "description": "Myelocele (disorder)",
            "attributes": null
          },
          {
            "code": "82203000",
            "description": "Treacher Collins syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "838339009",
            "description": "Basal encephalocele (disorder)",
            "attributes": null
          },
          {
            "code": "840471002",
            "description": "Hydrocephalus due to Dandy-Walker malformation (disorder)",
            "attributes": null
          },
          {
            "code": "840487004",
            "description": "Congenital stenosis of spinal canal (disorder)",
            "attributes": null
          },
          {
            "code": "84873005",
            "description": "Dural arteriovenous malformation (disorder)",
            "attributes": null
          },
          {
            "code": "85641006",
            "description": "Hemianencephaly (disorder)",
            "attributes": null
          },
          {
            "code": "860951008",
            "description": "Congenital anomaly of cauda equina (disorder)",
            "attributes": null
          },
          {
            "code": "8611000119100",
            "description": "Complex craniosynostosis (disorder)",
            "attributes": null
          },
          {
            "code": "866053004",
            "description": "Middle interhemispheric variant of holoprosencephaly (disorder)",
            "attributes": null
          },
          {
            "code": "88425004",
            "description": "Congenital anomaly of nervous system (disorder)",
            "attributes": null
          },
          {
            "code": "89369001",
            "description": "Anencephalus (disorder)",
            "attributes": null
          },
          {
            "code": "91848009",
            "description": "Acephaly (disorder)",
            "attributes": null
          },
          {
            "code": "91849001",
            "description": "Acephalostomia (disorder)",
            "attributes": null
          },
          {
            "code": "92503002",
            "description": "Neurofibromatosis type 2 (disorder)",
            "attributes": null
          },
          {
            "code": "92824003",
            "description": "Neurofibromatosis type 1 (disorder)",
            "attributes": null
          },
          {
            "code": "92904001",
            "description": "Congenital abnormal shape of cerebellum (disorder)",
            "attributes": null
          },
          {
            "code": "92905000",
            "description": "Congenital abnormal shape of cerebrum (disorder)",
            "attributes": null
          },
          {
            "code": "93249003",
            "description": "Congenital hypoplasia of cerebrum (disorder)",
            "attributes": null
          },
          {
            "code": "93557001",
            "description": "Holorachischisis (disorder)",
            "attributes": null
          },
          {
            "code": "95477007",
            "description": "Congenital degeneration of nervous system (disorder)",
            "attributes": null
          },
          {
            "code": "95478002",
            "description": "Congenital sacral meningocele (disorder)",
            "attributes": null
          },
          {
            "code": "95499004",
            "description": "Hypoplasia of the optic nerve (disorder)",
            "attributes": null
          },
          {
            "code": "95502000",
            "description": "Congenital anomaly of optic nerve (disorder)",
            "attributes": null
          },
          {
            "code": "95610008",
            "description": "Congenital brain damage (disorder)",
            "attributes": null
          },
          {
            "code": "95659007",
            "description": "Hindbrain hernia headache (disorder)",
            "attributes": null
          },
          {
            "code": "9721000119107",
            "description": "Malformation of central nervous system of fetus (disorder)",
            "attributes": null
          },
          {
            "code": "9740002",
            "description": "Macroencephaly (disorder)",
            "attributes": null
          }
        ]
      },
      {
        "concept_id": 4122,
        "concept_version_id": 11482,
        "concept_name": "Other neurological - other neurological condition (ICD-10)",
        "coding_system": {
          "id": 4,
          "name": "ICD10 codes",
          "description": "ICD10 Codes"
        },
        "phenotype_id": "PH1701",
        "phenotype_version_id": 3627,
        "phenotype_name": "Chronic paediatric conditions: Other neurological (excluding epilepsy and headaches)",
        "code_attribute_header": null,
        "codes": [
          {
            "code": "G040",
            "description": "Acute disseminated encephalitis",
            "attributes": null
          },
          {
            "code": "G041",
            "description": "Tropical spastic paraplegia",
            "attributes": null
          },
          {
            "code": "G08",
            "description": "Intracranial and intraspinal phlebitis and thrombophlebitis",
            "attributes": null
          },
          {
            "code": "G09",
            "description": "Sequelae of inflammatory diseases of central nervous system",
            "attributes": null
          },
          {
            "code": "G10",
            "description": "Huntington disease",
            "attributes": null
          },
          {
            "code": "G110",
            "description": "Congenital nonprogressive ataxia",
            "attributes": null
          },
          {
            "code": "G111",
            "description": "Early-onset cerebellar ataxia",
            "attributes": null
          },
          {
            "code": "G113",
            "description": "Cerebellar ataxia with defective DNA repair",
            "attributes": null
          },
          {
            "code": "G114",
            "description": "Hereditary spastic paraplegia",
            "attributes": null
          },
          {
            "code": "G118",
            "description": "Other hereditary ataxias",
            "attributes": null
          },
          {
            "code": "G119",
            "description": "Hereditary ataxia, unspecified",
            "attributes": null
          },
          {
            "code": "G12",
            "description": "Spinal muscular atrophy and related syndromes",
            "attributes": null
          },
          {
            "code": "G120",
            "description": "Infantile spinal muscular atrophy, type I [Werdnig-Hoffman]",
            "attributes": null
          },
          {
            "code": "G121",
            "description": "Other inherited spinal muscular atrophy",
            "attributes": null
          },
          {
            "code": "G122",
            "description": "Motor neuron disease",
            "attributes": null
          },
          {
            "code": "G128",
            "description": "Other spinal muscular atrophies and related syndromes",
            "attributes": null
          },
          {
            "code": "G129",
            "description": "Spinal muscular atrophy, unspecified",
            "attributes": null
          },
          {
            "code": "G13",
            "description": "Systemic atrophies primarily affecting central nervous system in diseases classified elsewhere",
            "attributes": null
          },
          {
            "code": "G130",
            "description": "Paraneoplastic neuromyopathy and neuropathy",
            "attributes": null
          },
          {
            "code": "G131",
            "description": "Other systemic atrophy primarily affecting central nervous system in neoplastic disease",
            "attributes": null
          },
          {
            "code": "G132",
            "description": "Systemic atrophy primarily affecting central nervous system in myxoedema",
            "attributes": null
          },
          {
            "code": "G138",
            "description": "Systemic atrophy primarily affecting central nervous system in other diseases classified elsewhere",
            "attributes": null
          },
          {
            "code": "G14",
            "description": "Postpolio syndrome",
            "attributes": null
          },
          {
            "code": "G20",
            "description": "Parkinson disease",
            "attributes": null
          },
          {
            "code": "G212",
            "description": "Secondary parkinsonism due to other external agents",
            "attributes": null
          },
          {
            "code": "G213",
            "description": "Postencephalitic parkinsonism",
            "attributes": null
          },
          {
            "code": "G214",
            "description": "Vascular parkinsonism",
            "attributes": null
          },
          {
            "code": "G218",
            "description": "Other secondary parkinsonism",
            "attributes": null
          },
          {
            "code": "G219",
            "description": "Secondary parkinsonism, unspecified",
            "attributes": null
          },
          {
            "code": "G22",
            "description": "Parkinsonism in diseases classified elsewhere",
            "attributes": null
          },
          {
            "code": "G23",
            "description": "Other degenerative diseases of basal ganglia",
            "attributes": null
          },
          {
            "code": "G230",
            "description": "Hallervorden-Spatz disease",
            "attributes": null
          },
          {
            "code": "G231",
            "description": "Progressive supranuclear ophthalmoplegia [Steele-Richardson-Olszewski]",
            "attributes": null
          },
          {
            "code": "G232",
            "description": "Striatonigral degeneration",
            "attributes": null
          },
          {
            "code": "G233",
            "description": "Multiple system atrophy, cerebellar type [MSA-C]",
            "attributes": null
          },
          {
            "code": "G238",
            "description": "Other specified degenerative diseases of basal ganglia",
            "attributes": null
          },
          {
            "code": "G239",
            "description": "Degenerative disease of basal ganglia, unspecified",
            "attributes": null
          },
          {
            "code": "G241",
            "description": "Idiopathic familial dystonia",
            "attributes": null
          },
          {
            "code": "G242",
            "description": "Idiopathic nonfamilial dystonia",
            "attributes": null
          },
          {
            "code": "G244",
            "description": "Idiopathic orofacial dystonia",
            "attributes": null
          },
          {
            "code": "G248",
            "description": "Other dystonia",
            "attributes": null
          },
          {
            "code": "G249",
            "description": "Dystonia, unspecified",
            "attributes": null
          },
          {
            "code": "G25",
            "description": "Other extrapyramidal and movement disorders",
            "attributes": null
          },
          {
            "code": "G250",
            "description": "Essential tremor",
            "attributes": null
          },
          {
            "code": "G252",
            "description": "Other specified forms of tremor",
            "attributes": null
          },
          {
            "code": "G253",
            "description": "Myoclonus",
            "attributes": null
          },
          {
            "code": "G255",
            "description": "Other chorea",
            "attributes": null
          },
          {
            "code": "G256",
            "description": "Drug-induced tics and other tics of organic origin",
            "attributes": null
          },
          {
            "code": "G258",
            "description": "Other specified extrapyramidal and movement disorders",
            "attributes": null
          },
          {
            "code": "G259",
            "description": "Extrapyramidal and movement disorder, unspecified",
            "attributes": null
          },
          {
            "code": "G26",
            "description": "Extrapyramidal and movement disorders in diseases classified elsewhere",
            "attributes": null
          },
          {
            "code": "G30",
            "description": "Alzheimer disease",
            "attributes": null
          },
          {
            "code": "G300",
            "description": "Alzheimer disease with early onset",
            "attributes": null
          },
          {
            "code": "G301",
            "description": "Alzheimer disease with late onset",
            "attributes": null
          },
          {
            "code": "G308",
            "description": "Other Alzheimer disease",
            "attributes": null
          },
          {
            "code": "G309",
            "description": "Alzheimer disease, unspecified",
            "attributes": null
          },
          {
            "code": "G31",
            "description": "Other degenerative diseases of nervous system, not elsewhere classified",
            "attributes": null
          },
          {
            "code": "G310",
            "description": "Circumscribed brain atrophy",
            "attributes": null
          },
          {
            "code": "G311",
            "description": "Senile degeneration of brain, not elsewhere classified",
            "attributes": null
          },
          {
            "code": "G312",
            "description": "Degeneration of nervous system due to alcohol",
            "attributes": null
          },
          {
            "code": "G318",
            "description": "Other specified degenerative diseases of nervous system",
            "attributes": null
          },
          {
            "code": "G319",
            "description": "Degenerative disease of nervous system, unspecified",
            "attributes": null
          },
          {
            "code": "G32",
            "description": "Other degenerative disorders of nervous system in diseases classified elsewhere",
            "attributes": null
          },
          {
            "code": "G320",
            "description": "Subacute combined degeneration of spinal cord in diseases classified elsewhere",
            "attributes": null
          },
          {
            "code": "G328",
            "description": "Other specified degenerative disorders of nervous system in diseases classified elsewhere",
            "attributes": null
          },
          {
            "code": "G35",
            "description": "Multiple sclerosis",
            "attributes": null
          },
          {
            "code": "G36",
            "description": "Other acute disseminated demyelination",
            "attributes": null
          },
          {
            "code": "G360",
            "description": "Neuromyelitis optica [Devic]",
            "attributes": null
          },
          {
            "code": "G361",
            "description": "Acute and subacute haemorrhagic leukoencephalitis [Hurst]",
            "attributes": null
          },
          {
            "code": "G368",
            "description": "Other specified acute disseminated demyelination",
            "attributes": null
          },
          {
            "code": "G369",
            "description": "Acute disseminated demyelination, unspecified",
            "attributes": null
          },
          {
            "code": "G37",
            "description": "Other demyelinating diseases of central nervous system",
            "attributes": null
          },
          {
            "code": "G370",
            "description": "Diffuse sclerosis",
            "attributes": null
          },
          {
            "code": "G371",
            "description": "Central demyelination of corpus callosum",
            "attributes": null
          },
          {
            "code": "G372",
            "description": "Central pontine myelinolysis",
            "attributes": null
          },
          {
            "code": "G373",
            "description": "Acute transverse myelitis in demyelinating disease of central nervous system",
            "attributes": null
          },
          {
            "code": "G374",
            "description": "Subacute necrotizing myelitis",
            "attributes": null
          },
          {
            "code": "G375",
            "description": "Concentric sclerosis [BalÃ³]",
            "attributes": null
          },
          {
            "code": "G378",
            "description": "Other specified demyelinating diseases of central nervous system",
            "attributes": null
          },
          {
            "code": "G379",
            "description": "Demyelinating disease of central nervous system, unspecified",
            "attributes": null
          },
          {
            "code": "G45",
            "description": "Transient cerebral ischaemic attacks and related syndromes",
            "attributes": null
          },
          {
            "code": "G450",
            "description": "Vertebro-basilar artery syndrome",
            "attributes": null
          },
          {
            "code": "G451",
            "description": "Carotid artery syndrome (hemispheric)",
            "attributes": null
          },
          {
            "code": "G452",
            "description": "Multiple and bilateral precerebral artery syndromes",
            "attributes": null
          },
          {
            "code": "G453",
            "description": "Amaurosis fugax",
            "attributes": null
          },
          {
            "code": "G454",
            "description": "Transient global amnesia",
            "attributes": null
          },
          {
            "code": "G458",
            "description": "Other transient cerebral ischaemic attacks and related syndromes",
            "attributes": null
          },
          {
            "code": "G459",
            "description": "Transient cerebral ischaemic attack, unspecified",
            "attributes": null
          },
          {
            "code": "G46",
            "description": "Vascular syndromes of brain in cerebrovascular diseases",
            "attributes": null
          },
          {
            "code": "G460",
            "description": "Middle cerebral artery syndrome",
            "attributes": null
          },
          {
            "code": "G461",
            "description": "Anterior cerebral artery syndrome",
            "attributes": null
          },
          {
            "code": "G462",
            "description": "Posterior cerebral artery syndrome",
            "attributes": null
          },
          {
            "code": "G463",
            "description": "Brain stem stroke syndrome",
            "attributes": null
          },
          {
            "code": "G464",
            "description": "Cerebellar stroke syndrome",
            "attributes": null
          },
          {
            "code": "G465",
            "description": "Pure motor lacunar syndrome",
            "attributes": null
          },
          {
            "code": "G466",
            "description": "Pure sensory lacunar syndrome",
            "attributes": null
          },
          {
            "code": "G467",
            "description": "Other lacunar syndromes",
            "attributes": null
          },
          {
            "code": "G468",
            "description": "Other vascular syndromes of brain in cerebrovascular diseases",
            "attributes": null
          },
          {
            "code": "G47",
            "description": "Sleep disorders",
            "attributes": null
          },
          {
            "code": "G473",
            "description": "Sleep apnoea",
            "attributes": null
          },
          {
            "code": "G474",
            "description": "Narcolepsy and cataplexy",
            "attributes": null
          },
          {
            "code": "G50",
            "description": "Disorders of trigeminal nerve",
            "attributes": null
          },
          {
            "code": "G500",
            "description": "Trigeminal neuralgia",
            "attributes": null
          },
          {
            "code": "G501",
            "description": "Atypical facial pain",
            "attributes": null
          },
          {
            "code": "G508",
            "description": "Other disorders of trigeminal nerve",
            "attributes": null
          },
          {
            "code": "G509",
            "description": "Disorder of trigeminal nerve, unspecified",
            "attributes": null
          },
          {
            "code": "G51",
            "description": "Facial nerve disorders",
            "attributes": null
          },
          {
            "code": "G510",
            "description": "Bell palsy",
            "attributes": null
          },
          {
            "code": "G511",
            "description": "Geniculate ganglionitis",
            "attributes": null
          },
          {
            "code": "G512",
            "description": "Melkersson syndrome",
            "attributes": null
          },
          {
            "code": "G513",
            "description": "Clonic hemifacial spasm",
            "attributes": null
          },
          {
            "code": "G514",
            "description": "Facial myokymia",
            "attributes": null
          },
          {
            "code": "G518",
            "description": "Other disorders of facial nerve",
            "attributes": null
          },
          {
            "code": "G519",
            "description": "Disorder of facial nerve, unspecified",
            "attributes": null
          },
          {
            "code": "G52",
            "description": "Disorders of other cranial nerves",
            "attributes": null
          },
          {
            "code": "G520",
            "description": "Disorders of olfactory nerve",
            "attributes": null
          },
          {
            "code": "G521",
            "description": "Disorders of glossopharyngeal nerve",
            "attributes": null
          },
          {
            "code": "G522",
            "description": "Disorders of vagus nerve",
            "attributes": null
          },
          {
            "code": "G523",
            "description": "Disorders of hypoglossal nerve",
            "attributes": null
          },
          {
            "code": "G527",
            "description": "Disorders of multiple cranial nerves",
            "attributes": null
          },
          {
            "code": "G528",
            "description": "Disorders of other specified cranial nerves",
            "attributes": null
          },
          {
            "code": "G529",
            "description": "Cranial nerve disorder, unspecified",
            "attributes": null
          },
          {
            "code": "G53",
            "description": "Cranial nerve disorders in diseases classified elsewhere",
            "attributes": null
          },
          {
            "code": "G530",
            "description": "Postzoster neuralgia",
            "attributes": null
          },
          {
            "code": "G531",
            "description": "Multiple cranial nerve palsies in infectious and parasitic diseases classified elsewhere",
            "attributes": null
          },
          {
            "code": "G532",
            "description": "Multiple cranial nerve palsies in sarcoidosis",
            "attributes": null
          },
          {
            "code": "G533",
            "description": "Multiple cranial nerve palsies in neoplastic disease",
            "attributes": null
          },
          {
            "code": "G538",
            "description": "Other cranial nerve disorders in other diseases classified elsewhere",
            "attributes": null
          },
          {
            "code": "G545",
            "description": "Neuralgic amyotrophy",
            "attributes": null
          },
          {
            "code": "G546",
            "description": "Phantom limb syndrome with pain",
            "attributes": null
          },
          {
            "code": "G547",
            "description": "Phantom limb syndrome without pain",
            "attributes": null
          },
          {
            "code": "G548",
            "description": "Other nerve root and plexus disorders",
            "attributes": null
          },
          {
            "code": "G55",
            "description": "Nerve root and plexus compressions in diseases classified elsewhere",
            "attributes": null
          },
          {
            "code": "G550",
            "description": "Nerve root and plexus compressions in neoplastic disease",
            "attributes": null
          },
          {
            "code": "G551",
            "description": "Nerve root and plexus compressions in intervertebral disc disorders",
            "attributes": null
          },
          {
            "code": "G552",
            "description": "Nerve root and plexus compressions in spondylosis",
            "attributes": null
          },
          {
            "code": "G553",
            "description": "Nerve root and plexus compressions in other dorsopathies",
            "attributes": null
          },
          {
            "code": "G558",
            "description": "Nerve root and plexus compressions in other diseases classified elsewhere",
            "attributes": null
          },
          {
            "code": "G580",
            "description": "Intercostal neuropathy",
            "attributes": null
          },
          {
            "code": "G587",
            "description": "Mononeuritis multiplex",
            "attributes": null
          },
          {
            "code": "G588",
            "description": "Other specified mononeuropathies",
            "attributes": null
          },
          {
            "code": "G589",
            "description": "Mononeuropathy, unspecified",
            "attributes": null
          },
          {
            "code": "G59",
            "description": "Mononeuropathy in diseases classified elsewhere",
            "attributes": null
          },
          {
            "code": "G590",
            "description": "Diabetic mononeuropathy",
            "attributes": null
          },
          {
            "code": "G598",
            "description": "Other mononeuropathies in diseases classified elsewhere",
            "attributes": null
          },
          {
            "code": "G60",
            "description": "Hereditary and idiopathic neuropathy",
            "attributes": null
          },
          {
            "code": "G600",
            "description": "Hereditary motor and sensory neuropathy",
            "attributes": null
          },
          {
            "code": "G601",
            "description": "Refsum disease",
            "attributes": null
          },
          {
            "code": "G602",
            "description": "Neuropathy in association with hereditary ataxia",
            "attributes": null
          },
          {
            "code": "G603",
            "description": "Idiopathic progressive neuropathy",
            "attributes": null
          },
          {
            "code": "G608",
            "description": "Other hereditary and idiopathic neuropathies",
            "attributes": null
          },
          {
            "code": "G609",
            "description": "Hereditary and idiopathic neuropathy, unspecified",
            "attributes": null
          },
          {
            "code": "G61",
            "description": "Inflammatory polyneuropathy",
            "attributes": null
          },
          {
            "code": "G610",
            "description": "Guillain-BarrÃ© syndrome",
            "attributes": null
          },
          {
            "code": "G611",
            "description": "Serum neuropathy",
            "attributes": null
          },
          {
            "code": "G618",
            "description": "Other inflammatory polyneuropathies",
            "attributes": null
          },
          {
            "code": "G619",
            "description": "Inflammatory polyneuropathy, unspecified",
            "attributes": null
          },
          {
            "code": "G62",
            "description": "Other polyneuropathies",
            "attributes": null
          },
          {
            "code": "G621",
            "description": "Alcoholic polyneuropathy",
            "attributes": null
          },
          {
            "code": "G622",
            "description": "Polyneuropathy due to other toxic agents",
            "attributes": null
          },
          {
            "code": "G628",
            "description": "Other specified polyneuropathies",
            "attributes": null
          },
          {
            "code": "G629",
            "description": "Polyneuropathy, unspecified",
            "attributes": null
          },
          {
            "code": "G631",
            "description": "Polyneuropathy in neoplastic disease",
            "attributes": null
          },
          {
            "code": "G632",
            "description": "Diabetic polyneuropathy",
            "attributes": null
          },
          {
            "code": "G633",
            "description": "Polyneuropathy in other endocrine and metabolic diseases",
            "attributes": null
          },
          {
            "code": "G635",
            "description": "Polyneuropathy in systemic connective tissue disorders",
            "attributes": null
          },
          {
            "code": "G636",
            "description": "Polyneuropathy in other musculoskeletal disorders",
            "attributes": null
          },
          {
            "code": "G638",
            "description": "Polyneuropathy in other diseases classified elsewhere",
            "attributes": null
          },
          {
            "code": "G64",
            "description": "Other disorders of peripheral nervous system",
            "attributes": null
          },
          {
            "code": "G70",
            "description": "Myasthenia gravis and other myoneural disorders",
            "attributes": null
          },
          {
            "code": "G700",
            "description": "Myasthenia gravis",
            "attributes": null
          },
          {
            "code": "G701",
            "description": "Toxic myoneural disorders",
            "attributes": null
          },
          {
            "code": "G702",
            "description": "Congenital and developmental myasthenia",
            "attributes": null
          },
          {
            "code": "G708",
            "description": "Other specified myoneural disorders",
            "attributes": null
          },
          {
            "code": "G709",
            "description": "Myoneural disorder, unspecified",
            "attributes": null
          },
          {
            "code": "G71",
            "description": "Primary disorders of muscles",
            "attributes": null
          },
          {
            "code": "G710",
            "description": "Muscular dystrophy",
            "attributes": null
          },
          {
            "code": "G711",
            "description": "Myotonic disorders",
            "attributes": null
          },
          {
            "code": "G712",
            "description": "Congenital myopathies",
            "attributes": null
          },
          {
            "code": "G713",
            "description": "Mitochondrial myopathy, not elsewhere classified",
            "attributes": null
          },
          {
            "code": "G718",
            "description": "Other primary disorders of muscles",
            "attributes": null
          },
          {
            "code": "G719",
            "description": "Primary disorder of muscle, unspecified",
            "attributes": null
          },
          {
            "code": "G72",
            "description": "Other myopathies",
            "attributes": null
          },
          {
            "code": "G721",
            "description": "Alcoholic myopathy",
            "attributes": null
          },
          {
            "code": "G722",
            "description": "Myopathy due to other toxic agents",
            "attributes": null
          },
          {
            "code": "G723",
            "description": "Periodic paralysis",
            "attributes": null
          },
          {
            "code": "G724",
            "description": "Inflammatory myopathy, not elsewhere classified",
            "attributes": null
          },
          {
            "code": "G728",
            "description": "Other specified myopathies",
            "attributes": null
          },
          {
            "code": "G729",
            "description": "Myopathy, unspecified",
            "attributes": null
          },
          {
            "code": "G730",
            "description": "Myasthenic syndromes in endocrine diseases",
            "attributes": null
          },
          {
            "code": "G731",
            "description": "Lambert-Eaton syndrome",
            "attributes": null
          },
          {
            "code": "G732",
            "description": "Other myasthenic syndromes in neoplastic disease",
            "attributes": null
          },
          {
            "code": "G733",
            "description": "Myasthenic syndromes in other diseases classified elsewhere",
            "attributes": null
          },
          {
            "code": "G735",
            "description": "Myopathy in endocrine diseases",
            "attributes": null
          },
          {
            "code": "G736",
            "description": "Myopathy in metabolic diseases",
            "attributes": null
          },
          {
            "code": "G737",
            "description": "Myopathy in other diseases classified elsewhere",
            "attributes": null
          },
          {
            "code": "G90",
            "description": "Disorders of autonomic nervous system",
            "attributes": null
          },
          {
            "code": "G900",
            "description": "Idiopathic peripheral autonomic neuropathy",
            "attributes": null
          },
          {
            "code": "G901",
            "description": "Familial dysautonomia [Riley-Day]",
            "attributes": null
          },
          {
            "code": "G902",
            "description": "Horner syndrome",
            "attributes": null
          },
          {
            "code": "G904",
            "description": "Autonomic dysreflexia",
            "attributes": null
          },
          {
            "code": "G905",
            "description": "Complex regional pain syndrome type I",
            "attributes": null
          },
          {
            "code": "G906",
            "description": "Complex regional pain syndrome type II",
            "attributes": null
          },
          {
            "code": "G908",
            "description": "Other disorders of autonomic nervous system",
            "attributes": null
          },
          {
            "code": "G909",
            "description": "Disorder of autonomic nervous system, unspecified",
            "attributes": null
          },
          {
            "code": "G91",
            "description": "Hydrocephalus",
            "attributes": null
          },
          {
            "code": "G910",
            "description": "Communicating hydrocephalus",
            "attributes": null
          },
          {
            "code": "G911",
            "description": "Obstructive hydrocephalus",
            "attributes": null
          },
          {
            "code": "G912",
            "description": "Normal-pressure hydrocephalus",
            "attributes": null
          },
          {
            "code": "G913",
            "description": "Post-traumatic hydrocephalus, unspecified",
            "attributes": null
          },
          {
            "code": "G918",
            "description": "Other hydrocephalus",
            "attributes": null
          },
          {
            "code": "G919",
            "description": "Hydrocephalus, unspecified",
            "attributes": null
          },
          {
            "code": "G92",
            "description": "Toxic encephalopathy",
            "attributes": null
          },
          {
            "code": "G930",
            "description": "Cerebral cysts",
            "attributes": null
          },
          {
            "code": "G931",
            "description": "Anoxic brain damage, not elsewhere classified",
            "attributes": null
          },
          {
            "code": "G932",
            "description": "Benign intracranial hypertension",
            "attributes": null
          },
          {
            "code": "G933",
            "description": "Postviral fatigue syndrome",
            "attributes": null
          },
          {
            "code": "G934",
            "description": "Encephalopathy, unspecified",
            "attributes": null
          },
          {
            "code": "G935",
            "description": "Compression of brain",
            "attributes": null
          },
          {
            "code": "G936",
            "description": "Cerebral oedema",
            "attributes": null
          },
          {
            "code": "G938",
            "description": "Other specified disorders of brain",
            "attributes": null
          },
          {
            "code": "G939",
            "description": "Disorder of brain, unspecified",
            "attributes": null
          },
          {
            "code": "G941",
            "description": "Hydrocephalus in neoplastic disease",
            "attributes": null
          },
          {
            "code": "G942",
            "description": "Hydrocephalus in other diseases classified elsewhere",
            "attributes": null
          },
          {
            "code": "G948",
            "description": "Other specified disorders of brain in diseases classified elsewhere",
            "attributes": null
          },
          {
            "code": "G95",
            "description": "Other diseases of spinal cord",
            "attributes": null
          },
          {
            "code": "G950",
            "description": "Syringomyelia and syringobulbia",
            "attributes": null
          },
          {
            "code": "G951",
            "description": "Vascular myelopathies",
            "attributes": null
          },
          {
            "code": "G952",
            "description": "Cord compression, unspecified",
            "attributes": null
          },
          {
            "code": "G958",
            "description": "Other specified diseases of spinal cord",
            "attributes": null
          },
          {
            "code": "G959",
            "description": "Disease of spinal cord, unspecified",
            "attributes": null
          },
          {
            "code": "G96",
            "description": "Other disorders of central nervous system",
            "attributes": null
          },
          {
            "code": "G961",
            "description": "Disorders of meninges, not elsewhere classified",
            "attributes": null
          },
          {
            "code": "G968",
            "description": "Other specified disorders of central nervous system",
            "attributes": null
          },
          {
            "code": "G969",
            "description": "Disorder of central nervous system, unspecified",
            "attributes": null
          },
          {
            "code": "G98",
            "description": "Other disorders of nervous system, not elsewhere classified",
            "attributes": null
          },
          {
            "code": "G99",
            "description": "Other disorders of nervous system in diseases classified elsewhere",
            "attributes": null
          },
          {
            "code": "G990",
            "description": "Autonomic neuropathy in endocrine and metabolic diseases",
            "attributes": null
          },
          {
            "code": "G991",
            "description": "Other disorders of autonomic nervous system in other diseases classified elsewhere",
            "attributes": null
          },
          {
            "code": "G992",
            "description": "Myelopathy in diseases classified elsewhere",
            "attributes": null
          },
          {
            "code": "G998",
            "description": "Other specified disorders of nervous system in diseases classified elsewhere",
            "attributes": null
          },
          {
            "code": "I60",
            "description": "Subarachnoid haemorrhage",
            "attributes": null
          },
          {
            "code": "I600",
            "description": "Subarachnoid haemorrhage from carotid siphon and bifurcation",
            "attributes": null
          },
          {
            "code": "I601",
            "description": "Subarachnoid haemorrhage from middle cerebral artery",
            "attributes": null
          },
          {
            "code": "I602",
            "description": "Subarachnoid haemorrhage from anterior communicating artery",
            "attributes": null
          },
          {
            "code": "I603",
            "description": "Subarachnoid haemorrhage from posterior communicating artery",
            "attributes": null
          },
          {
            "code": "I604",
            "description": "Subarachnoid haemorrhage from basilar artery",
            "attributes": null
          },
          {
            "code": "I605",
            "description": "Subarachnoid haemorrhage from vertebral artery",
            "attributes": null
          },
          {
            "code": "I606",
            "description": "Subarachnoid haemorrhage from other intracranial arteries",
            "attributes": null
          },
          {
            "code": "I607",
            "description": "Subarachnoid haemorrhage from intracranial artery, unspecified",
            "attributes": null
          },
          {
            "code": "I608",
            "description": "Other subarachnoid haemorrhage",
            "attributes": null
          },
          {
            "code": "I609",
            "description": "Subarachnoid haemorrhage, unspecified",
            "attributes": null
          },
          {
            "code": "I61",
            "description": "Intracerebral haemorrhage",
            "attributes": null
          },
          {
            "code": "I610",
            "description": "Intracerebral haemorrhage in hemisphere, subcortical",
            "attributes": null
          },
          {
            "code": "I611",
            "description": "Intracerebral haemorrhage in hemisphere, cortical",
            "attributes": null
          },
          {
            "code": "I612",
            "description": "Intracerebral haemorrhage in hemisphere, unspecified",
            "attributes": null
          },
          {
            "code": "I613",
            "description": "Intracerebral haemorrhage in brain stem",
            "attributes": null
          },
          {
            "code": "I614",
            "description": "Intracerebral haemorrhage in cerebellum",
            "attributes": null
          },
          {
            "code": "I615",
            "description": "Intracerebral haemorrhage, intraventricular",
            "attributes": null
          },
          {
            "code": "I616",
            "description": "Intracerebral haemorrhage, multiple localized",
            "attributes": null
          },
          {
            "code": "I618",
            "description": "Other intracerebral haemorrhage",
            "attributes": null
          },
          {
            "code": "I619",
            "description": "Intracerebral haemorrhage, unspecified",
            "attributes": null
          },
          {
            "code": "I62",
            "description": "Other nontraumatic intracranial haemorrhage",
            "attributes": null
          },
          {
            "code": "I620",
            "description": "Nontraumatic subdural haemorrhage",
            "attributes": null
          },
          {
            "code": "I621",
            "description": "Nontraumatic extradural haemorrhage",
            "attributes": null
          },
          {
            "code": "I629",
            "description": "Intracranial haemorrhage (nontraumatic), unspecified",
            "attributes": null
          },
          {
            "code": "I63",
            "description": "Cerebral infarction",
            "attributes": null
          },
          {
            "code": "I630",
            "description": "Cerebral infarction due to thrombosis of precerebral arteries",
            "attributes": null
          },
          {
            "code": "I631",
            "description": "Cerebral infarction due to embolism of precerebral arteries",
            "attributes": null
          },
          {
            "code": "I632",
            "description": "Cerebral infarction due to unspecified occlusion or stenosis of precerebral arteries",
            "attributes": null
          },
          {
            "code": "I633",
            "description": "Cerebral infarction due to thrombosis of cerebral arteries",
            "attributes": null
          },
          {
            "code": "I634",
            "description": "Cerebral infarction due to embolism of cerebral arteries",
            "attributes": null
          },
          {
            "code": "I635",
            "description": "Cerebral infarction due to unspecified occlusion or stenosis of cerebral arteries",
            "attributes": null
          },
          {
            "code": "I636",
            "description": "Cerebral infarction due to cerebral venous thrombosis, nonpyogenic",
            "attributes": null
          },
          {
            "code": "I638",
            "description": "Other cerebral infarction",
            "attributes": null
          },
          {
            "code": "I639",
            "description": "Cerebral infarction, unspecified",
            "attributes": null
          },
          {
            "code": "I64",
            "description": "Stroke, not specified as haemorrhage or infarction",
            "attributes": null
          },
          {
            "code": "I65",
            "description": "Occlusion and stenosis of precerebral arteries, not resulting in cerebral infarction",
            "attributes": null
          },
          {
            "code": "I650",
            "description": "Occlusion and stenosis of vertebral artery",
            "attributes": null
          },
          {
            "code": "I651",
            "description": "Occlusion and stenosis of basilar artery",
            "attributes": null
          },
          {
            "code": "I652",
            "description": "Occlusion and stenosis of carotid artery",
            "attributes": null
          },
          {
            "code": "I653",
            "description": "Occlusion and stenosis of multiple and bilateral precerebral arteries",
            "attributes": null
          },
          {
            "code": "I658",
            "description": "Occlusion and stenosis of other precerebral artery",
            "attributes": null
          },
          {
            "code": "I659",
            "description": "Occlusion and stenosis of unspecified precerebral artery",
            "attributes": null
          },
          {
            "code": "I66",
            "description": "Occlusion and stenosis of cerebral arteries, not resulting in cerebral infarction",
            "attributes": null
          },
          {
            "code": "I660",
            "description": "Occlusion and stenosis of middle cerebral artery",
            "attributes": null
          },
          {
            "code": "I661",
            "description": "Occlusion and stenosis of anterior cerebral artery",
            "attributes": null
          },
          {
            "code": "I662",
            "description": "Occlusion and stenosis of posterior cerebral artery",
            "attributes": null
          },
          {
            "code": "I663",
            "description": "Occlusion and stenosis of cerebellar arteries",
            "attributes": null
          },
          {
            "code": "I664",
            "description": "Occlusion and stenosis of multiple and bilateral cerebral arteries",
            "attributes": null
          },
          {
            "code": "I668",
            "description": "Occlusion and stenosis of other cerebral artery",
            "attributes": null
          },
          {
            "code": "I669",
            "description": "Occlusion and stenosis of unspecified cerebral artery",
            "attributes": null
          },
          {
            "code": "I67",
            "description": "Other cerebrovascular diseases",
            "attributes": null
          },
          {
            "code": "I670",
            "description": "Dissection of cerebral arteries, nonruptured",
            "attributes": null
          },
          {
            "code": "I671",
            "description": "Cerebral aneurysm, nonruptured",
            "attributes": null
          },
          {
            "code": "I672",
            "description": "Cerebral atherosclerosis",
            "attributes": null
          },
          {
            "code": "I673",
            "description": "Progressive vascular leukoencephalopathy",
            "attributes": null
          },
          {
            "code": "I674",
            "description": "Hypertensive encephalopathy",
            "attributes": null
          },
          {
            "code": "I675",
            "description": "Moyamoya disease",
            "attributes": null
          },
          {
            "code": "I676",
            "description": "Nonpyogenic thrombosis of intracranial venous system",
            "attributes": null
          },
          {
            "code": "I677",
            "description": "Cerebral arteritis, not elsewhere classified",
            "attributes": null
          },
          {
            "code": "I678",
            "description": "Other specified cerebrovascular diseases",
            "attributes": null
          },
          {
            "code": "I679",
            "description": "Cerebrovascular disease, unspecified",
            "attributes": null
          },
          {
            "code": "I68",
            "description": "Cerebrovascular disorders in diseases classified elsewhere",
            "attributes": null
          },
          {
            "code": "I680",
            "description": "Cerebral amyloid angiopathy E85.-",
            "attributes": null
          },
          {
            "code": "I682",
            "description": "Cerebral arteritis in other diseases classified elsewhere",
            "attributes": null
          },
          {
            "code": "I688",
            "description": "Other cerebrovascular disorders in diseases classified elsewhere",
            "attributes": null
          },
          {
            "code": "I69",
            "description": "Sequelae of cerebrovascular disease",
            "attributes": null
          },
          {
            "code": "I690",
            "description": "Sequelae of subarachnoid haemorrhage",
            "attributes": null
          },
          {
            "code": "I691",
            "description": "Sequelae of intracerebral haemorrhage",
            "attributes": null
          },
          {
            "code": "I692",
            "description": "Sequelae of other nontraumatic intracranial haemorrhage",
            "attributes": null
          },
          {
            "code": "I693",
            "description": "Sequelae of cerebral infarction",
            "attributes": null
          },
          {
            "code": "I694",
            "description": "Sequelae of stroke, not specified as haemorrhage or infarction",
            "attributes": null
          },
          {
            "code": "I698",
            "description": "Sequelae of other and unspecified cerebrovascular diseases",
            "attributes": null
          }
        ]
      },
      {
        "concept_id": 4123,
        "concept_version_id": 11483,
        "concept_name": "Other neurological - other neurological condition (Read v2)",
        "coding_system": {
          "id": 5,
          "name": "Read codes v2",
          "description": "Read codes v2"
        },
        "phenotype_id": "PH1701",
        "phenotype_version_id": 3627,
        "phenotype_name": "Chronic paediatric conditions: Other neurological (excluding epilepsy and headaches)",
        "code_attribute_header": null,
        "codes": [
          {
            "code": "A531.11",
            "description": "Post-herpetic neuralgia",
            "attributes": null
          },
          {
            "code": "A531200",
            "description": "Postherpetic trigeminal neuralgia",
            "attributes": null
          },
          {
            "code": "A531500",
            "description": "Postzoster neuralgia",
            "attributes": null
          },
          {
            "code": "A531511",
            "description": "Postherpetic neuralgia",
            "attributes": null
          },
          {
            "code": "A560.00",
            "description": "Rubella with neurological complication",
            "attributes": null
          },
          {
            "code": "A560000",
            "description": "Rubella with unspecified neurological complication",
            "attributes": null
          },
          {
            "code": "A560z00",
            "description": "Rubella with neurological complication NOS",
            "attributes": null
          },
          {
            "code": "A788400",
            "description": "Human immunodeficiency virus with neurological disease",
            "attributes": null
          },
          {
            "code": "A94y100",
            "description": "Syphilitic parkinsonism",
            "attributes": null
          },
          {
            "code": "AyuA800",
            "description": "[X]Rubella with neurological complications",
            "attributes": null
          },
          {
            "code": "C106000",
            "description": "Diabetes mellitus, juvenile type, with neurological manifestation",
            "attributes": null
          },
          {
            "code": "C106100",
            "description": "Diabetes mellitus, adult onset, with neurological manifestation",
            "attributes": null
          },
          {
            "code": "C106.11",
            "description": "Diabetic amyotrophy",
            "attributes": null
          },
          {
            "code": "C106.12",
            "description": "Diabetes mellitus with neuropathy",
            "attributes": null
          },
          {
            "code": "C106.13",
            "description": "Diabetes mellitus with polyneuropathy",
            "attributes": null
          },
          {
            "code": "C108211",
            "description": "Type I diabetes mellitus with neurological complications",
            "attributes": null
          },
          {
            "code": "C108212",
            "description": "Type 1 diabetes mellitus with neurological complications",
            "attributes": null
          },
          {
            "code": "C108B00",
            "description": "Insulin dependent diabetes mellitus with mononeuropathy",
            "attributes": null
          },
          {
            "code": "C108B11",
            "description": "Type I diabetes mellitus with mononeuropathy",
            "attributes": null
          },
          {
            "code": "C108B12",
            "description": "Type 1 diabetes mellitus with mononeuropathy",
            "attributes": null
          },
          {
            "code": "C108C00",
            "description": "Insulin dependent diabetes mellitus with polyneuropathy",
            "attributes": null
          },
          {
            "code": "C108C11",
            "description": "Type I diabetes mellitus with polyneuropathy",
            "attributes": null
          },
          {
            "code": "C108C12",
            "description": "Type 1 diabetes mellitus with polyneuropathy",
            "attributes": null
          },
          {
            "code": "C109200",
            "description": "Non-insulin-dependent diabetes mellitus with neurological complications",
            "attributes": null
          },
          {
            "code": "C109211",
            "description": "Type II diabetes mellitus with neurological complications",
            "attributes": null
          },
          {
            "code": "C109212",
            "description": "Type 2 diabetes mellitus with neurological complications",
            "attributes": null
          },
          {
            "code": "C109A00",
            "description": "Non-insulin dependent diabetes mellitus with mononeuropathy",
            "attributes": null
          },
          {
            "code": "C109A11",
            "description": "Type II diabetes mellitus with mononeuropathy",
            "attributes": null
          },
          {
            "code": "C109A12",
            "description": "Type 2 diabetes mellitus with mononeuropathy",
            "attributes": null
          },
          {
            "code": "C109B00",
            "description": "Non-insulin dependent diabetes mellitus with polyneuropathy",
            "attributes": null
          },
          {
            "code": "C109B11",
            "description": "Type II diabetes mellitus with polyneuropathy",
            "attributes": null
          },
          {
            "code": "C109B12",
            "description": "Type 2 diabetes mellitus with polyneuropathy",
            "attributes": null
          },
          {
            "code": "C10E200",
            "description": "Type 1 diabetes mellitus with neurological complications",
            "attributes": null
          },
          {
            "code": "C10E211",
            "description": "Type I diabetes mellitus with neurological complications",
            "attributes": null
          },
          {
            "code": "C10EB00",
            "description": "Type 1 diabetes mellitus with mononeuropathy",
            "attributes": null
          },
          {
            "code": "C10EB11",
            "description": "Type I diabetes mellitus with mononeuropathy",
            "attributes": null
          },
          {
            "code": "C10EB12",
            "description": "Insulin dependent diabetes mellitus with mononeuropathy",
            "attributes": null
          },
          {
            "code": "C10EC00",
            "description": "Type 1 diabetes mellitus with polyneuropathy",
            "attributes": null
          },
          {
            "code": "C10EC11",
            "description": "Type I diabetes mellitus with polyneuropathy",
            "attributes": null
          },
          {
            "code": "C10EC12",
            "description": "Insulin dependent diabetes mellitus with polyneuropathy",
            "attributes": null
          },
          {
            "code": "C10F200",
            "description": "Type 2 diabetes mellitus with neurological complications",
            "attributes": null
          },
          {
            "code": "C10F211",
            "description": "Type II diabetes mellitus with neurological complications",
            "attributes": null
          },
          {
            "code": "C10FA00",
            "description": "Type 2 diabetes mellitus with mononeuropathy",
            "attributes": null
          },
          {
            "code": "C10FA11",
            "description": "Type II diabetes mellitus with mononeuropathy",
            "attributes": null
          },
          {
            "code": "C10FB00",
            "description": "Type 2 diabetes mellitus with polyneuropathy",
            "attributes": null
          },
          {
            "code": "C10FB11",
            "description": "Type II diabetes mellitus with polyneuropathy",
            "attributes": null
          },
          {
            "code": "C315100",
            "description": "Mitochondrial encephalopathy, lactic acidosis and stroke-like episodes",
            "attributes": null
          },
          {
            "code": "C34y400",
            "description": "Gouty neuritis",
            "attributes": null
          },
          {
            "code": "C37z.11",
            "description": "Marinesco-Sjogren syndrome",
            "attributes": null
          },
          {
            "code": "C39A.00",
            "description": "Retinocochleocerebral vasculopathy",
            "attributes": null
          },
          {
            "code": "C39A.11",
            "description": "Susac's syndrome",
            "attributes": null
          },
          {
            "code": "E011100",
            "description": "Korsakov's alcoholic psychosis with peripheral neuritis",
            "attributes": null
          },
          {
            "code": "E030400",
            "description": "Acute confusional state, of cerebrovascular origin",
            "attributes": null
          },
          {
            "code": "Eu00.00",
            "description": "[X]Dementia in Alzheimer's disease",
            "attributes": null
          },
          {
            "code": "Eu00000",
            "description": "[X]Dementia in Alzheimer's disease with early onset",
            "attributes": null
          },
          {
            "code": "Eu00011",
            "description": "[X]Presenile dementia,Alzheimer's type",
            "attributes": null
          },
          {
            "code": "Eu00012",
            "description": "[X] Primary degenerative dementia of Alzheimer's type, presenile onset",
            "attributes": null
          },
          {
            "code": "Eu00013",
            "description": "[X]Alzheimer's disease type 2",
            "attributes": null
          },
          {
            "code": "Eu00100",
            "description": "[X]Dementia in Alzheimer's disease with late onset",
            "attributes": null
          },
          {
            "code": "Eu00111",
            "description": "[X]Alzheimer's disease type 1",
            "attributes": null
          },
          {
            "code": "Eu00112",
            "description": "[X]Senile dementia,Alzheimer's type",
            "attributes": null
          },
          {
            "code": "Eu00113",
            "description": "[X]Primary degenerative dementia of Alzheimer's type, senile onset",
            "attributes": null
          },
          {
            "code": "Eu00200",
            "description": "[X]Dementia in Alzheimer's dis, atypical or mixed type",
            "attributes": null
          },
          {
            "code": "Eu00z00",
            "description": "[X]Dementia in Alzheimer's disease, unspecified",
            "attributes": null
          },
          {
            "code": "Eu00z11",
            "description": "[X]Alzheimer's dementia unspec",
            "attributes": null
          },
          {
            "code": "Eu02000",
            "description": "[X]Dementia in Pick's disease",
            "attributes": null
          },
          {
            "code": "Eu02200",
            "description": "[X]Dementia in Huntington's disease",
            "attributes": null
          },
          {
            "code": "Eu02300",
            "description": "[X]Dementia in Parkinson's disease",
            "attributes": null
          },
          {
            "code": "Eu02500",
            "description": "[X]Lewy body dementia",
            "attributes": null
          },
          {
            "code": "Eu02z13",
            "description": "[X] Primary degenerative dementia NOS",
            "attributes": null
          },
          {
            "code": "F03..13",
            "description": "Transverse myelitis",
            "attributes": null
          },
          {
            "code": "F036000",
            "description": "Toxic encephalitis due to lead",
            "attributes": null
          },
          {
            "code": "F036100",
            "description": "Toxic encephalitis due to mercury",
            "attributes": null
          },
          {
            "code": "F036200",
            "description": "Toxic encephalitis due to thallium",
            "attributes": null
          },
          {
            "code": "F037.00",
            "description": "Transverse myelitis",
            "attributes": null
          },
          {
            "code": "F037000",
            "description": "Varicella transverse myelitis",
            "attributes": null
          },
          {
            "code": "F038.00",
            "description": "Tropical spastic paraplegia",
            "attributes": null
          },
          {
            "code": "F03y.12",
            "description": "Myalgic encephalomyelitis",
            "attributes": null
          },
          {
            "code": "F05..00",
            "description": "Phlebitis and thrombophlebitis of intracranial sinuses",
            "attributes": null
          },
          {
            "code": "F050.00",
            "description": "Embolism of central nervous system venous sinus",
            "attributes": null
          },
          {
            "code": "F050100",
            "description": "Embolism superior longitudinal sinus",
            "attributes": null
          },
          {
            "code": "F050.11",
            "description": "Embolus of central nervous system venous sinus",
            "attributes": null
          },
          {
            "code": "F050z00",
            "description": "Embolism central nervous system venous sinus NOS",
            "attributes": null
          },
          {
            "code": "F051.00",
            "description": "Thrombosis of central nervous system venous sinuses",
            "attributes": null
          },
          {
            "code": "F051000",
            "description": "Thrombosis cavernous sinus",
            "attributes": null
          },
          {
            "code": "F051100",
            "description": "Thrombosis of superior longitudinal sinus",
            "attributes": null
          },
          {
            "code": "F051200",
            "description": "Thrombosis lateral sinus",
            "attributes": null
          },
          {
            "code": "F051300",
            "description": "Thrombosis transverse sinus",
            "attributes": null
          },
          {
            "code": "F051z00",
            "description": "Thrombosis of central nervous system venous sinus NOS",
            "attributes": null
          },
          {
            "code": "F052000",
            "description": "Phlebitis cavernous sinus",
            "attributes": null
          },
          {
            "code": "F052100",
            "description": "Phlebitis of superior longitudinal sinus",
            "attributes": null
          },
          {
            "code": "F053.00",
            "description": "Thrombophlebitis of central nervous system venous sinuses",
            "attributes": null
          },
          {
            "code": "F053000",
            "description": "Thrombophlebitis of cavernous sinus",
            "attributes": null
          },
          {
            "code": "F053100",
            "description": "Thrombophlebitis of superior longitudinal venous sinus",
            "attributes": null
          },
          {
            "code": "F053200",
            "description": "Thrombophlebitis lateral venous sinus",
            "attributes": null
          },
          {
            "code": "F053z00",
            "description": "Thrombophlebitis of central nervous system venous sinus NOS",
            "attributes": null
          },
          {
            "code": "F05z.00",
            "description": "Phlebitis or thrombophlebitis of central nervous system venous sinus NOS",
            "attributes": null
          },
          {
            "code": "F06..00",
            "description": "Late effects of intracranial abscess or pyogenic infection",
            "attributes": null
          },
          {
            "code": "F06X.00",
            "description": "Sequelae of inflammatory diseases of the central nervous system",
            "attributes": null
          },
          {
            "code": "F10..00",
            "description": "Cerebral degenerations usually manifest in childhood",
            "attributes": null
          },
          {
            "code": "F101z00",
            "description": "Cerebral lipidoses NOS",
            "attributes": null
          },
          {
            "code": "F102.00",
            "description": "Cerebral degeneration in lipidoses EC",
            "attributes": null
          },
          {
            "code": "F102000",
            "description": "Cerebral degeneration in Gaucher's disease",
            "attributes": null
          },
          {
            "code": "F102100",
            "description": "Cerebral degeneration in Niemann-Pick disease",
            "attributes": null
          },
          {
            "code": "F102z00",
            "description": "Cerebral degeneration in lipidosis NOS",
            "attributes": null
          },
          {
            "code": "F103.00",
            "description": "Cerebral degeneration in diseases EC",
            "attributes": null
          },
          {
            "code": "F103100",
            "description": "Cerebral degeneration in mucopolysaccharidoses",
            "attributes": null
          },
          {
            "code": "F103z00",
            "description": "Cerebral degeneration in disease NOS",
            "attributes": null
          },
          {
            "code": "F10y.00",
            "description": "Other cerebral degenerations in childhood",
            "attributes": null
          },
          {
            "code": "F10y000",
            "description": "Alper's disease",
            "attributes": null
          },
          {
            "code": "F10y100",
            "description": "Leigh's disease",
            "attributes": null
          },
          {
            "code": "F10yz00",
            "description": "Other cerebral degenerations in childhood NOS",
            "attributes": null
          },
          {
            "code": "F10z.00",
            "description": "Childhood cerebral degenerations NOS",
            "attributes": null
          },
          {
            "code": "F11..00",
            "description": "Other cerebral degenerations",
            "attributes": null
          },
          {
            "code": "F110.00",
            "description": "Alzheimer's disease",
            "attributes": null
          },
          {
            "code": "F110000",
            "description": "Alzheimer's disease with early onset",
            "attributes": null
          },
          {
            "code": "F110100",
            "description": "Alzheimer's disease with late onset",
            "attributes": null
          },
          {
            "code": "F112.00",
            "description": "Senile degeneration of brain",
            "attributes": null
          },
          {
            "code": "F113.00",
            "description": "Acquired communicating hydrocephalus",
            "attributes": null
          },
          {
            "code": "F113000",
            "description": "Normal pressure hydrocephalus",
            "attributes": null
          },
          {
            "code": "F113011",
            "description": "Low pressure hydrocephalus",
            "attributes": null
          },
          {
            "code": "F113z00",
            "description": "Communicating hydrocephalus - acquired NOS",
            "attributes": null
          },
          {
            "code": "F114.00",
            "description": "Acquired obstructive hydrocephalus",
            "attributes": null
          },
          {
            "code": "F115.00",
            "description": "Hydrocephalus",
            "attributes": null
          },
          {
            "code": "F116.00",
            "description": "Lewy body disease",
            "attributes": null
          },
          {
            "code": "F118.00",
            "description": "Frontotemporal degeneration",
            "attributes": null
          },
          {
            "code": "F11x.00",
            "description": "Cerebral degeneration in other disease EC",
            "attributes": null
          },
          {
            "code": "F11X.00",
            "description": "Post-traumatic hydrocephalus, unspecified",
            "attributes": null
          },
          {
            "code": "F11x000",
            "description": "Cerebral degeneration due to alcoholism",
            "attributes": null
          },
          {
            "code": "F11x011",
            "description": "Alcoholic encephalopathy",
            "attributes": null
          },
          {
            "code": "F11x200",
            "description": "Cerebral degeneration due to cerebrovascular disease",
            "attributes": null
          },
          {
            "code": "F11x400",
            "description": "Cerebral degeneration due to neoplastic disease",
            "attributes": null
          },
          {
            "code": "F11x500",
            "description": "Cerebral degeneration due to myxoedema",
            "attributes": null
          },
          {
            "code": "F11x600",
            "description": "Cerebral degeneration due to vitamin B12 deficiency",
            "attributes": null
          },
          {
            "code": "F11xz00",
            "description": "Cerebral degeneration other disease NOS",
            "attributes": null
          },
          {
            "code": "F11y.00",
            "description": "Other cerebral degeneration",
            "attributes": null
          },
          {
            "code": "F11y100",
            "description": "Cerebral ataxia",
            "attributes": null
          },
          {
            "code": "F11y200",
            "description": "Corticobasal degeneration",
            "attributes": null
          },
          {
            "code": "F11yz00",
            "description": "Other cerebral degeneration NOS",
            "attributes": null
          },
          {
            "code": "F11z.00",
            "description": "Cerebral degeneration NOS",
            "attributes": null
          },
          {
            "code": "F11z.11",
            "description": "Cerebral atrophy",
            "attributes": null
          },
          {
            "code": "F....12",
            "description": "Nervous system diseases",
            "attributes": null
          },
          {
            "code": "F12..00",
            "description": "Parkinson's disease",
            "attributes": null
          },
          {
            "code": "F120.00",
            "description": "Paralysis agitans",
            "attributes": null
          },
          {
            "code": "F123.00",
            "description": "Postencephalitic parkinsonism",
            "attributes": null
          },
          {
            "code": "F124.00",
            "description": "Vascular parkinsonism",
            "attributes": null
          },
          {
            "code": "F12W.00",
            "description": "Secondary parkinsonism due to other external agents",
            "attributes": null
          },
          {
            "code": "F12X.00",
            "description": "Secondary parkinsonism, unspecified",
            "attributes": null
          },
          {
            "code": "F12z.00",
            "description": "Parkinson's disease NOS",
            "attributes": null
          },
          {
            "code": "F13..00",
            "description": "Other extrapyramidal disease and abnormal movement disorders",
            "attributes": null
          },
          {
            "code": "F130.00",
            "description": "Other basal ganglia degenerative diseases",
            "attributes": null
          },
          {
            "code": "F130000",
            "description": "Dejerine-Thomas syndrome",
            "attributes": null
          },
          {
            "code": "F130100",
            "description": "Hallervorden-Spatz disease",
            "attributes": null
          },
          {
            "code": "F130200",
            "description": "Striatonigral degeneration",
            "attributes": null
          },
          {
            "code": "F130300",
            "description": "Parkinsonism with orthostatic hypotension",
            "attributes": null
          },
          {
            "code": "F130400",
            "description": "Progressive supranuclear ophthalmoplegia",
            "attributes": null
          },
          {
            "code": "F130500",
            "description": "Shy-Drager syndrome",
            "attributes": null
          },
          {
            "code": "F130600",
            "description": "Aicardi Goutieres syndrome",
            "attributes": null
          },
          {
            "code": "F130z00",
            "description": "Other basal ganglia degenerative disease NOS",
            "attributes": null
          },
          {
            "code": "F131000",
            "description": "Benign essential tremor",
            "attributes": null
          },
          {
            "code": "F13..11",
            "description": "Extrapyramidal disease excluding Parkinson's disease",
            "attributes": null
          },
          {
            "code": "F131100",
            "description": "Familial tremor",
            "attributes": null
          },
          {
            "code": "F132.00",
            "description": "Myoclonus",
            "attributes": null
          },
          {
            "code": "F132000",
            "description": "Familial essential myoclonus",
            "attributes": null
          },
          {
            "code": "F132y00",
            "description": "Other specified myoclonus",
            "attributes": null
          },
          {
            "code": "F132y11",
            "description": "Paramyoclonus multiplex",
            "attributes": null
          },
          {
            "code": "F132z00",
            "description": "Myoclonus NOS",
            "attributes": null
          },
          {
            "code": "F134.00",
            "description": "Huntington's chorea",
            "attributes": null
          },
          {
            "code": "F135.00",
            "description": "Other choreas",
            "attributes": null
          },
          {
            "code": "F135000",
            "description": "Hemiballismus",
            "attributes": null
          },
          {
            "code": "F135100",
            "description": "Paroxysmal choreo-athetosis",
            "attributes": null
          },
          {
            "code": "F135z00",
            "description": "Other choreas NOS",
            "attributes": null
          },
          {
            "code": "F136.00",
            "description": "Idiopathic torsion dystonia",
            "attributes": null
          },
          {
            "code": "F136000",
            "description": "Idiopathic familial dystonia",
            "attributes": null
          },
          {
            "code": "F137.00",
            "description": "Symptomatic torsion dystonia",
            "attributes": null
          },
          {
            "code": "F137y00",
            "description": "Other specified symptomatic torsion dystonia",
            "attributes": null
          },
          {
            "code": "F137z00",
            "description": "Symptomatic torsion dystonia NOS",
            "attributes": null
          },
          {
            "code": "F138.00",
            "description": "Fragments of torsion dystonia",
            "attributes": null
          },
          {
            "code": "F138100",
            "description": "Orofacial dyskinesia",
            "attributes": null
          },
          {
            "code": "F138z00",
            "description": "Fragments of torsion dystonia NOS",
            "attributes": null
          },
          {
            "code": "F139100",
            "description": "Paroxysmal kinesigenic dyskinesia",
            "attributes": null
          },
          {
            "code": "F13A.00",
            "description": "Paroxysmal dystonia",
            "attributes": null
          },
          {
            "code": "F13B.00",
            "description": "Myoclonic dystonia",
            "attributes": null
          },
          {
            "code": "F13C.00",
            "description": "Segawa syndrome",
            "attributes": null
          },
          {
            "code": "F13z.00",
            "description": "Other and unspecified extrapyramidal diseases and abnormal movement disorders",
            "attributes": null
          },
          {
            "code": "F13z000",
            "description": "Unspecified extrapyramidal disease",
            "attributes": null
          },
          {
            "code": "F13z100",
            "description": "Stiff-man syndrome",
            "attributes": null
          },
          {
            "code": "F13z111",
            "description": "Stiff person syndrome",
            "attributes": null
          },
          {
            "code": "F13z300",
            "description": "Akinetic rigid syndrome",
            "attributes": null
          },
          {
            "code": "F13z600",
            "description": "Neuroferritinopathy",
            "attributes": null
          },
          {
            "code": "F13zz00",
            "description": "Extrapyramidal disease and abnormal movement disorder NOS",
            "attributes": null
          },
          {
            "code": "F14..00",
            "description": "Spinocerebellar disease",
            "attributes": null
          },
          {
            "code": "F141.00",
            "description": "Hereditary spastic paraplegia",
            "attributes": null
          },
          {
            "code": "F14..11",
            "description": "Cerebellar disease",
            "attributes": null
          },
          {
            "code": "F142.00",
            "description": "Primary cerebellar degeneration",
            "attributes": null
          },
          {
            "code": "F142200",
            "description": "Dyssynergia cerebellaris myoclonica",
            "attributes": null
          },
          {
            "code": "F142z00",
            "description": "Primary cerebellar degeneration NOS",
            "attributes": null
          },
          {
            "code": "F143.00",
            "description": "Cerebellar ataxia NOS",
            "attributes": null
          },
          {
            "code": "F143.11",
            "description": "Roussy-Levy syndrome",
            "attributes": null
          },
          {
            "code": "F144.00",
            "description": "Cerebellar ataxia in diseases EC",
            "attributes": null
          },
          {
            "code": "F144000",
            "description": "Cerebellar ataxia due to alcoholism",
            "attributes": null
          },
          {
            "code": "F144100",
            "description": "Cerebellar ataxia due to myxoedema",
            "attributes": null
          },
          {
            "code": "F144200",
            "description": "Cerebellar ataxia due to neoplasia",
            "attributes": null
          },
          {
            "code": "F144z00",
            "description": "Cerebellar ataxia in disease NOS",
            "attributes": null
          },
          {
            "code": "F145.00",
            "description": "Congenital nonprogressive ataxia",
            "attributes": null
          },
          {
            "code": "F146.00",
            "description": "Early onset cerebellar ataxia with hypogonadism",
            "attributes": null
          },
          {
            "code": "F14y.00",
            "description": "Other spinocerebellar diseases",
            "attributes": null
          },
          {
            "code": "F14y000",
            "description": "Ataxia-telangiectasia",
            "attributes": null
          },
          {
            "code": "F14y011",
            "description": "Louis - Bar syndrome",
            "attributes": null
          },
          {
            "code": "F14y100",
            "description": "Corticostriatal-spinal degeneration",
            "attributes": null
          },
          {
            "code": "F14yz00",
            "description": "Other spinocerebellar disease NOS",
            "attributes": null
          },
          {
            "code": "F14z.00",
            "description": "Spinocerebellar disease NOS",
            "attributes": null
          },
          {
            "code": "F15..00",
            "description": "Anterior horn cell disease",
            "attributes": null
          },
          {
            "code": "F150.00",
            "description": "Werdnig - Hoffmann disease",
            "attributes": null
          },
          {
            "code": "F150.11",
            "description": "Infantile spinal muscular atrophy",
            "attributes": null
          },
          {
            "code": "F151.00",
            "description": "Spinal muscular atrophy",
            "attributes": null
          },
          {
            "code": "F151000",
            "description": "Unspecified spinal muscular atrophy",
            "attributes": null
          },
          {
            "code": "F151100",
            "description": "Kugelberg - Welander disease",
            "attributes": null
          },
          {
            "code": "F151111",
            "description": "Juvenile spinal muscular atrophy",
            "attributes": null
          },
          {
            "code": "F151200",
            "description": "Adult spinal muscular atrophy",
            "attributes": null
          },
          {
            "code": "F151300",
            "description": "X-linked bulbo-spinal atrophy",
            "attributes": null
          },
          {
            "code": "F151z00",
            "description": "Spinal muscular atrophy NOS",
            "attributes": null
          },
          {
            "code": "F152.00",
            "description": "Motor neurone disease",
            "attributes": null
          },
          {
            "code": "F152000",
            "description": "Amyotrophic lateral sclerosis",
            "attributes": null
          },
          {
            "code": "F152100",
            "description": "Progressive muscular atrophy",
            "attributes": null
          },
          {
            "code": "F152111",
            "description": "Duchenne Aran muscular atrophy",
            "attributes": null
          },
          {
            "code": "F152200",
            "description": "Progressive bulbar palsy",
            "attributes": null
          },
          {
            "code": "F152300",
            "description": "Pseudobulbar palsy",
            "attributes": null
          },
          {
            "code": "F152400",
            "description": "Primary lateral sclerosis",
            "attributes": null
          },
          {
            "code": "F152z00",
            "description": "Motor neurone disease NOS",
            "attributes": null
          },
          {
            "code": "F15y.00",
            "description": "Other anterior horn cell disease",
            "attributes": null
          },
          {
            "code": "F15z.00",
            "description": "Anterior horn cell disease NOS",
            "attributes": null
          },
          {
            "code": "F16..00",
            "description": "Other diseases of spinal cord",
            "attributes": null
          },
          {
            "code": "F160.00",
            "description": "Syringomyelia and syringobulbia",
            "attributes": null
          },
          {
            "code": "F160000",
            "description": "Syringomyelia",
            "attributes": null
          },
          {
            "code": "F160100",
            "description": "Syringobulbia",
            "attributes": null
          },
          {
            "code": "F160z00",
            "description": "Syringomyelia or syringobulbia NOS",
            "attributes": null
          },
          {
            "code": "F161.00",
            "description": "Vascular myelopathies",
            "attributes": null
          },
          {
            "code": "F161000",
            "description": "Myelopathy due to acute infarction of spinal cord",
            "attributes": null
          },
          {
            "code": "F161100",
            "description": "Myelopathy due to arterial thrombosis of spinal cord",
            "attributes": null
          },
          {
            "code": "F161200",
            "description": "Myelopathy due to oedema of spinal cord",
            "attributes": null
          },
          {
            "code": "F161300",
            "description": "Myelopathy due to haematomyelia",
            "attributes": null
          },
          {
            "code": "F161400",
            "description": "Subacute necrotic myelopathy",
            "attributes": null
          },
          {
            "code": "F161500",
            "description": "Anterior spinal artery thrombosis",
            "attributes": null
          },
          {
            "code": "F161z00",
            "description": "Vascular myelopathy NOS",
            "attributes": null
          },
          {
            "code": "F162.00",
            "description": "Subacute combined degeneration of spinal cord",
            "attributes": null
          },
          {
            "code": "F163.00",
            "description": "Myelopathy due to disease EC",
            "attributes": null
          },
          {
            "code": "F163000",
            "description": "Myelopathy due to intervertebral disc disease",
            "attributes": null
          },
          {
            "code": "F163100",
            "description": "Myelopathy due to neoplastic disease",
            "attributes": null
          },
          {
            "code": "F163200",
            "description": "Myelopathy due to spondylosis",
            "attributes": null
          },
          {
            "code": "F163z00",
            "description": "Myelopathy due to disease NOS",
            "attributes": null
          },
          {
            "code": "F16y.00",
            "description": "Other myelopathy",
            "attributes": null
          },
          {
            "code": "F16y100",
            "description": "Myelopathy - radiation induced",
            "attributes": null
          },
          {
            "code": "F16yz00",
            "description": "Other myelopathy NOS",
            "attributes": null
          },
          {
            "code": "F16z.00",
            "description": "Myelopathy NOS",
            "attributes": null
          },
          {
            "code": "F16z.11",
            "description": "Cord compression NOS",
            "attributes": null
          },
          {
            "code": "F16z.12",
            "description": "Spinal cord compression NOS",
            "attributes": null
          },
          {
            "code": "F17..00",
            "description": "Autonomic nervous system disorders",
            "attributes": null
          },
          {
            "code": "F170.00",
            "description": "Idiopathic peripheral autonomic neuropathy",
            "attributes": null
          },
          {
            "code": "F170000",
            "description": "Carotid sinus syndrome",
            "attributes": null
          },
          {
            "code": "F170100",
            "description": "Cervical sympathetic paralysis",
            "attributes": null
          },
          {
            "code": "F170z00",
            "description": "Idiopathic peripheral autonomic neuropathy NOS",
            "attributes": null
          },
          {
            "code": "F171.00",
            "description": "Peripheral autonomic neuropathy disease EC",
            "attributes": null
          },
          {
            "code": "F171000",
            "description": "Autonomic neuropathy due to amyloid",
            "attributes": null
          },
          {
            "code": "F171100",
            "description": "Autonomic neuropathy due to diabetes",
            "attributes": null
          },
          {
            "code": "F172.00",
            "description": "[X] Horners syndrome",
            "attributes": null
          },
          {
            "code": "F173.00",
            "description": "Shoulder-hand syndrome",
            "attributes": null
          },
          {
            "code": "F174.00",
            "description": "Multiple system atrophy",
            "attributes": null
          },
          {
            "code": "F174000",
            "description": "Multiple system atrophy, cerebellar variant",
            "attributes": null
          },
          {
            "code": "F174100",
            "description": "Multiple system atrophy, Parkinson variant",
            "attributes": null
          },
          {
            "code": "F175.00",
            "description": "Autonomic dysreflexia",
            "attributes": null
          },
          {
            "code": "F17z.00",
            "description": "Autonomic nervous system disorder NOS",
            "attributes": null
          },
          {
            "code": "F17z.11",
            "description": "Horner's syndrome",
            "attributes": null
          },
          {
            "code": "F17z.12",
            "description": "Autonomic failure",
            "attributes": null
          },
          {
            "code": "F1z..00",
            "description": "Hereditary and degenerative diseases of the central nervous system NOS",
            "attributes": null
          },
          {
            "code": "F2...00",
            "description": "Other central nervous system disorders",
            "attributes": null
          },
          {
            "code": "F20..00",
            "description": "Multiple sclerosis",
            "attributes": null
          },
          {
            "code": "F200.00",
            "description": "Multiple sclerosis of the brain stem",
            "attributes": null
          },
          {
            "code": "F201.00",
            "description": "Multiple sclerosis of the spinal cord",
            "attributes": null
          },
          {
            "code": "F20..11",
            "description": "Disseminated sclerosis",
            "attributes": null
          },
          {
            "code": "F203.00",
            "description": "Exacerbation of multiple sclerosis",
            "attributes": null
          },
          {
            "code": "F204.00",
            "description": "Benign multiple sclerosis",
            "attributes": null
          },
          {
            "code": "F205.00",
            "description": "Malignant multiple sclerosis",
            "attributes": null
          },
          {
            "code": "F206.00",
            "description": "Primary progressive multiple sclerosis",
            "attributes": null
          },
          {
            "code": "F207.00",
            "description": "Relapsing and remitting multiple sclerosis",
            "attributes": null
          },
          {
            "code": "F208.00",
            "description": "Secondary progressive multiple sclerosis",
            "attributes": null
          },
          {
            "code": "F20z.00",
            "description": "Multiple sclerosis NOS",
            "attributes": null
          },
          {
            "code": "F21..00",
            "description": "Other central nervous system demyelinating diseases",
            "attributes": null
          },
          {
            "code": "F210.00",
            "description": "Neuromyelitis optica",
            "attributes": null
          },
          {
            "code": "F210.11",
            "description": "Devic's disease",
            "attributes": null
          },
          {
            "code": "F211.00",
            "description": "Schilder's disease",
            "attributes": null
          },
          {
            "code": "F211.11",
            "description": "Balo's concentric sclerosis",
            "attributes": null
          },
          {
            "code": "F213.00",
            "description": "Clinically isolated syndrome",
            "attributes": null
          },
          {
            "code": "F21X.00",
            "description": "Acute disseminated demyelination, unspecified",
            "attributes": null
          },
          {
            "code": "F21y.00",
            "description": "Other specified central nervous system demyelinating disease",
            "attributes": null
          },
          {
            "code": "F21y000",
            "description": "Marchiafava-Bignami disease",
            "attributes": null
          },
          {
            "code": "F21y100",
            "description": "Central pontine myelinosis",
            "attributes": null
          },
          {
            "code": "F21y200",
            "description": "Binswanger's disease",
            "attributes": null
          },
          {
            "code": "F21y211",
            "description": "Binswanger's encephalopathy",
            "attributes": null
          },
          {
            "code": "F21y300",
            "description": "Central demyelination of corpus callosum",
            "attributes": null
          },
          {
            "code": "F21y400",
            "description": "Subacute necrotizing myelitis",
            "attributes": null
          },
          {
            "code": "F21y500",
            "description": "Concentric sclerosis",
            "attributes": null
          },
          {
            "code": "F21y600",
            "description": "Vanishing white matter disease",
            "attributes": null
          },
          {
            "code": "F21yz00",
            "description": "Other specified central nervous system demyelination NOS",
            "attributes": null
          },
          {
            "code": "F21z.00",
            "description": "Central nervous system demyelination NOS",
            "attributes": null
          },
          {
            "code": "F24y000",
            "description": "Progressive supranuclear palsy",
            "attributes": null
          },
          {
            "code": "F24y011",
            "description": "Steele Richardson Olszewsk syn",
            "attributes": null
          },
          {
            "code": "F24y012",
            "description": "Steele - Richardson Oszewski syndrome",
            "attributes": null
          },
          {
            "code": "F24y200",
            "description": "Steele-Richardson-Olszewski syndrome",
            "attributes": null
          },
          {
            "code": "F27..00",
            "description": "Cataplexy and narcolepsy",
            "attributes": null
          },
          {
            "code": "F270.00",
            "description": "Cataplexy",
            "attributes": null
          },
          {
            "code": "F271.00",
            "description": "Narcolepsy",
            "attributes": null
          },
          {
            "code": "F27z.00",
            "description": "Cataplexy or narcolepsy NOS",
            "attributes": null
          },
          {
            "code": "F28..00",
            "description": "Other conditions of brain",
            "attributes": null
          },
          {
            "code": "F280.00",
            "description": "Cerebral cysts",
            "attributes": null
          },
          {
            "code": "F280000",
            "description": "Arachnoid cyst",
            "attributes": null
          },
          {
            "code": "F280100",
            "description": "Porencephalic cyst",
            "attributes": null
          },
          {
            "code": "F280111",
            "description": "Porencephaly",
            "attributes": null
          },
          {
            "code": "F280200",
            "description": "Pseudoporencephaly",
            "attributes": null
          },
          {
            "code": "F280y00",
            "description": "Other specified cerebral cyst",
            "attributes": null
          },
          {
            "code": "F280z00",
            "description": "Cerebral cyst NOS",
            "attributes": null
          },
          {
            "code": "F280z11",
            "description": "Intracerebral cyst NOS",
            "attributes": null
          },
          {
            "code": "F281.00",
            "description": "Anoxic brain damage",
            "attributes": null
          },
          {
            "code": "F281000",
            "description": "Persistent vegetative state",
            "attributes": null
          },
          {
            "code": "F281.11",
            "description": "Anoxic - ischaemic encephalopathy",
            "attributes": null
          },
          {
            "code": "F282.00",
            "description": "Benign intracranial hypertension",
            "attributes": null
          },
          {
            "code": "F282.11",
            "description": "Pseudotumour cerebri",
            "attributes": null
          },
          {
            "code": "F283.00",
            "description": "Unspecified encephalopathy",
            "attributes": null
          },
          {
            "code": "F284.00",
            "description": "Compression of brain",
            "attributes": null
          },
          {
            "code": "F284000",
            "description": "Brain stem compression",
            "attributes": null
          },
          {
            "code": "F284011",
            "description": "Herniation of brain stem",
            "attributes": null
          },
          {
            "code": "F284012",
            "description": "Posterior fossa compression syndrome",
            "attributes": null
          },
          {
            "code": "F284013",
            "description": "Medullary cone",
            "attributes": null
          },
          {
            "code": "F284z00",
            "description": "Compression of brain NOS",
            "attributes": null
          },
          {
            "code": "F285.00",
            "description": "Cerebral oedema",
            "attributes": null
          },
          {
            "code": "F286.00",
            "description": "Chronic fatigue syndrome",
            "attributes": null
          },
          {
            "code": "F286.11",
            "description": "CFS - Chronic fatigue syndrome",
            "attributes": null
          },
          {
            "code": "F286.12",
            "description": "Postviral fatigue syndrome",
            "attributes": null
          },
          {
            "code": "F286.13",
            "description": "PVFS - Postviral fatigue syn",
            "attributes": null
          },
          {
            "code": "F286.14",
            "description": "Post-viral fatigue syndrome",
            "attributes": null
          },
          {
            "code": "F286.15",
            "description": "Myalgic encephalomyelitis",
            "attributes": null
          },
          {
            "code": "F286.16",
            "description": "ME - Myalgic encephalomyelitis",
            "attributes": null
          },
          {
            "code": "F288.00",
            "description": "Alien limb phenomenon",
            "attributes": null
          },
          {
            "code": "F28y.00",
            "description": "Other conditions of brain OS",
            "attributes": null
          },
          {
            "code": "F28y000",
            "description": "Cerebral calcification",
            "attributes": null
          },
          {
            "code": "F28y400",
            "description": "GLUT1 deficiency syndrome",
            "attributes": null
          },
          {
            "code": "F28y411",
            "description": "Glucose transporter protein type 1 deficiency syndrome",
            "attributes": null
          },
          {
            "code": "F28yz00",
            "description": "Other conditions of brain NOS",
            "attributes": null
          },
          {
            "code": "F28yz11",
            "description": "Ondine's curse",
            "attributes": null
          },
          {
            "code": "F28z.00",
            "description": "Brain conditions NOS",
            "attributes": null
          },
          {
            "code": "F29..00",
            "description": "Other nervous system disorders",
            "attributes": null
          },
          {
            "code": "F292.00",
            "description": "Meninges disorder NEC",
            "attributes": null
          },
          {
            "code": "F292000",
            "description": "Adhesions - cerebral meninges",
            "attributes": null
          },
          {
            "code": "F292011",
            "description": "Cerebral meningeal adhesions",
            "attributes": null
          },
          {
            "code": "F292100",
            "description": "Adhesions - spinal meninges",
            "attributes": null
          },
          {
            "code": "F292111",
            "description": "Spinal meningeal adhesions",
            "attributes": null
          },
          {
            "code": "F292300",
            "description": "Cyst of the spinal meninges",
            "attributes": null
          },
          {
            "code": "F292z00",
            "description": "Meninges disorder NOS",
            "attributes": null
          },
          {
            "code": "F29X.00",
            "description": "Disorder of central nervous system, unspecified",
            "attributes": null
          },
          {
            "code": "F29y.00",
            "description": "Other and unspecified disorders of the nervous system",
            "attributes": null
          },
          {
            "code": "F29y100",
            "description": "Postpolio syndrome",
            "attributes": null
          },
          {
            "code": "F29y300",
            "description": "Toxic encephalopathy",
            "attributes": null
          },
          {
            "code": "F29y400",
            "description": "Cord compression",
            "attributes": null
          },
          {
            "code": "F29y411",
            "description": "Spinal cord compression",
            "attributes": null
          },
          {
            "code": "F29yz00",
            "description": "Other and unspecified disorders of the nervous system NOS",
            "attributes": null
          },
          {
            "code": "F29z.00",
            "description": "Other nervous system disorders NOS",
            "attributes": null
          },
          {
            "code": "F2y..00",
            "description": "Other specified disorders of central nervous system",
            "attributes": null
          },
          {
            "code": "F2z..00",
            "description": "Other central nervous system disorders NOS",
            "attributes": null
          },
          {
            "code": "F3...00",
            "description": "Peripheral nervous system disorders",
            "attributes": null
          },
          {
            "code": "F30..00",
            "description": "Trigeminal nerve disorders",
            "attributes": null
          },
          {
            "code": "F300.00",
            "description": "Post-herpetic trigeminal neuralgia",
            "attributes": null
          },
          {
            "code": "F301.00",
            "description": "Other specified trigeminal neuralgia",
            "attributes": null
          },
          {
            "code": "F301000",
            "description": "Tic douloureux",
            "attributes": null
          },
          {
            "code": "F301z00",
            "description": "Trigeminal neuralgia NOS",
            "attributes": null
          },
          {
            "code": "F30y.00",
            "description": "Other trigeminal nerve disorder",
            "attributes": null
          },
          {
            "code": "F30z.00",
            "description": "Trigeminal nerve disorder NOS",
            "attributes": null
          },
          {
            "code": "F31..00",
            "description": "Facial nerve disorders",
            "attributes": null
          },
          {
            "code": "F310.00",
            "description": "Bell's (facial) palsy",
            "attributes": null
          },
          {
            "code": "F311.00",
            "description": "Geniculate ganglionitis",
            "attributes": null
          },
          {
            "code": "F312.00",
            "description": "Clonic hemifacial spasm",
            "attributes": null
          },
          {
            "code": "F31y.00",
            "description": "Other facial nerve disorders",
            "attributes": null
          },
          {
            "code": "F31y100",
            "description": "Melkersson's syndrome",
            "attributes": null
          },
          {
            "code": "F31yz00",
            "description": "Other facial nerve disorder NOS",
            "attributes": null
          },
          {
            "code": "F31z.00",
            "description": "Facial nerve disorder NOS",
            "attributes": null
          },
          {
            "code": "F32..00",
            "description": "Other cranial nerve disorders",
            "attributes": null
          },
          {
            "code": "F320.00",
            "description": "Olfactory nerve disorders",
            "attributes": null
          },
          {
            "code": "F321.00",
            "description": "Glossopharyngeal neuralgia",
            "attributes": null
          },
          {
            "code": "F322.00",
            "description": "Other glossopharyngeal nerve disorder",
            "attributes": null
          },
          {
            "code": "F323.00",
            "description": "Vagus nerve disorders",
            "attributes": null
          },
          {
            "code": "F323000",
            "description": "Recurrent laryngeal nerve palsy",
            "attributes": null
          },
          {
            "code": "F324.00",
            "description": "Accessory nerve disorders",
            "attributes": null
          },
          {
            "code": "F325.00",
            "description": "Hypoglossal nerve disorders",
            "attributes": null
          },
          {
            "code": "F326.00",
            "description": "Multiple cranial nerve palsies",
            "attributes": null
          },
          {
            "code": "F326000",
            "description": "Collet-Sicard syndrome",
            "attributes": null
          },
          {
            "code": "F326100",
            "description": "Polyneuritis cranialis",
            "attributes": null
          },
          {
            "code": "F326300",
            "description": "Multiple cranial nerve palsies in sarcoidosis",
            "attributes": null
          },
          {
            "code": "F326400",
            "description": "Multiple cranial nerve palsies in neoplastic disease",
            "attributes": null
          },
          {
            "code": "F326z00",
            "description": "Multiple cranial nerve palsies NOS",
            "attributes": null
          },
          {
            "code": "F32z.00",
            "description": "Cranial nerve disorder NOS",
            "attributes": null
          },
          {
            "code": "F335.00",
            "description": "Neuralgic amyotrophy",
            "attributes": null
          },
          {
            "code": "F335.11",
            "description": "Parsonage - Aldren - Turner syndrome",
            "attributes": null
          },
          {
            "code": "F336.00",
            "description": "Phantom limb syndrome",
            "attributes": null
          },
          {
            "code": "F336000",
            "description": "Phantom limb syndrome with pain",
            "attributes": null
          },
          {
            "code": "F336100",
            "description": "Phantom limb syndrome without pain",
            "attributes": null
          },
          {
            "code": "F337000",
            "description": "Nerve root and plexus compressions in neoplastic disease",
            "attributes": null
          },
          {
            "code": "F337100",
            "description": "Nerve root and plexus compressions in intervertebral disc disorders",
            "attributes": null
          },
          {
            "code": "F337200",
            "description": "Nerve root and plexus compressions in spondylosis",
            "attributes": null
          },
          {
            "code": "F344.00",
            "description": "Causalgia",
            "attributes": null
          },
          {
            "code": "F345.00",
            "description": "Mononeuritis multiplex",
            "attributes": null
          },
          {
            "code": "F345000",
            "description": "Diabetic mononeuritis multiplex",
            "attributes": null
          },
          {
            "code": "F347.00",
            "description": "Complex regional pain syndrome type II",
            "attributes": null
          },
          {
            "code": "F35z.00",
            "description": "Mononeuritis of unspecified site NOS",
            "attributes": null
          },
          {
            "code": "F35z000",
            "description": "Diabetic mononeuritis NOS",
            "attributes": null
          },
          {
            "code": "F35z.11",
            "description": "Peripheral neuropathy - hereditary or idiopathic",
            "attributes": null
          },
          {
            "code": "F36..00",
            "description": "Hereditary and idiopathic peripheral neuropathy",
            "attributes": null
          },
          {
            "code": "F360.00",
            "description": "Hereditary peripheral neuropathy",
            "attributes": null
          },
          {
            "code": "F360000",
            "description": "Dejerine-Sottas disease",
            "attributes": null
          },
          {
            "code": "F360z00",
            "description": "Hereditary peripheral neuropathy NOS",
            "attributes": null
          },
          {
            "code": "F361.00",
            "description": "Peroneal muscular atrophy",
            "attributes": null
          },
          {
            "code": "F361000",
            "description": "Charcot-Marie-Tooth disease",
            "attributes": null
          },
          {
            "code": "F361011",
            "description": "Charcot's atrophy",
            "attributes": null
          },
          {
            "code": "F361012",
            "description": "Charcot-Marie-Tooth syndrome",
            "attributes": null
          },
          {
            "code": "F361z00",
            "description": "Peroneal muscular atrophy NOS",
            "attributes": null
          },
          {
            "code": "F362.00",
            "description": "Hereditary sensory neuropathy",
            "attributes": null
          },
          {
            "code": "F363.00",
            "description": "Refsum's disease",
            "attributes": null
          },
          {
            "code": "F364.00",
            "description": "Idiopathic progressive polyneuropathy",
            "attributes": null
          },
          {
            "code": "F365.00",
            "description": "Neuropathy in association with hereditary ataxia",
            "attributes": null
          },
          {
            "code": "F366.00",
            "description": "Polyneuropathy",
            "attributes": null
          },
          {
            "code": "F367.00",
            "description": "Peripheral neuropathy",
            "attributes": null
          },
          {
            "code": "F368.00",
            "description": "Hereditary motor and sensory neuropathy",
            "attributes": null
          },
          {
            "code": "F368000",
            "description": "Hereditary motor and sensory neuropathy type I",
            "attributes": null
          },
          {
            "code": "F368100",
            "description": "Hereditary motor and sensory neuropathy type II",
            "attributes": null
          },
          {
            "code": "F368200",
            "description": "Hereditary motor and sensory neuropathy type III",
            "attributes": null
          },
          {
            "code": "F368300",
            "description": "Hereditary motor and sensory neuropathy type IV",
            "attributes": null
          },
          {
            "code": "F369.00",
            "description": "Complex regional pain syndrome",
            "attributes": null
          },
          {
            "code": "F369.11",
            "description": "Chronic regional pain syndrome",
            "attributes": null
          },
          {
            "code": "F36y.00",
            "description": "Other idiopathic peripheral neuropathy",
            "attributes": null
          },
          {
            "code": "F36y000",
            "description": "Supranuclear paralysis",
            "attributes": null
          },
          {
            "code": "F36yz00",
            "description": "Other idiopathic peripheral neuropathy NOS",
            "attributes": null
          },
          {
            "code": "F36z.00",
            "description": "Hereditary or idiopathic peripheral neuropathy NOS",
            "attributes": null
          },
          {
            "code": "F37..00",
            "description": "Inflammatory and toxic neuropathy",
            "attributes": null
          },
          {
            "code": "F370000",
            "description": "Guillain-Barre syndrome",
            "attributes": null
          },
          {
            "code": "F370100",
            "description": "Postinfectious polyneuritis",
            "attributes": null
          },
          {
            "code": "F370200",
            "description": "Miller-Fisher syndrome",
            "attributes": null
          },
          {
            "code": "F371.00",
            "description": "Polyneuropathy in collagen vascular disease",
            "attributes": null
          },
          {
            "code": "F371000",
            "description": "Polyneuropathy in disseminated lupus erythematosus",
            "attributes": null
          },
          {
            "code": "F37..11",
            "description": "Toxic neuropathy",
            "attributes": null
          },
          {
            "code": "F371100",
            "description": "Polyneuropathy in polyarteritis nodosa",
            "attributes": null
          },
          {
            "code": "F371200",
            "description": "Polyneuropathy in rheumatoid arthritis",
            "attributes": null
          },
          {
            "code": "F371z00",
            "description": "Polyneuropathy in collagen vascular disease NOS",
            "attributes": null
          },
          {
            "code": "F372.00",
            "description": "Polyneuropathy in diabetes",
            "attributes": null
          },
          {
            "code": "F372000",
            "description": "Acute painful diabetic neuropathy",
            "attributes": null
          },
          {
            "code": "F372100",
            "description": "Chronic painful diabetic neuropathy",
            "attributes": null
          },
          {
            "code": "F372.11",
            "description": "Diabetic polyneuropathy",
            "attributes": null
          },
          {
            "code": "F372.12",
            "description": "Diabetic neuropathy",
            "attributes": null
          },
          {
            "code": "F372200",
            "description": "Asymptomatic diabetic neuropathy",
            "attributes": null
          },
          {
            "code": "F373.00",
            "description": "Polyneuropathy in malignant disease",
            "attributes": null
          },
          {
            "code": "F374.00",
            "description": "Polyneuropathy in disease EC",
            "attributes": null
          },
          {
            "code": "F374000",
            "description": "Polyneuropathy in amyloidosis",
            "attributes": null
          },
          {
            "code": "F374500",
            "description": "Polyneuropathy in hypoglycaemia",
            "attributes": null
          },
          {
            "code": "F374800",
            "description": "Polyneuropathy in porphyria",
            "attributes": null
          },
          {
            "code": "F374900",
            "description": "Polyneuropathy in sarcoidosis",
            "attributes": null
          },
          {
            "code": "F374A00",
            "description": "Polyneuropathy in uraemia",
            "attributes": null
          },
          {
            "code": "F374z00",
            "description": "Polyneuropathy in disease NOS",
            "attributes": null
          },
          {
            "code": "F375.00",
            "description": "Alcoholic polyneuropathy",
            "attributes": null
          },
          {
            "code": "F377.00",
            "description": "Other toxic agent polyneuropathy",
            "attributes": null
          },
          {
            "code": "F378.00",
            "description": "Intercostal neuropathy",
            "attributes": null
          },
          {
            "code": "F37X.00",
            "description": "Inflammatory polyneuropathy, unspecified",
            "attributes": null
          },
          {
            "code": "F37y.00",
            "description": "Other toxic or inflammatory neuropathy",
            "attributes": null
          },
          {
            "code": "F37y000",
            "description": "Serum neuropathy",
            "attributes": null
          },
          {
            "code": "F37y100",
            "description": "Axonal sensorimotor neuropathy",
            "attributes": null
          },
          {
            "code": "F37z.00",
            "description": "Toxic or inflammatory neuropathy NOS",
            "attributes": null
          },
          {
            "code": "F37z.11",
            "description": "Polyneuropathy unspecified",
            "attributes": null
          },
          {
            "code": "F38..00",
            "description": "Myoneural disorders",
            "attributes": null
          },
          {
            "code": "F380.00",
            "description": "Myasthenia gravis",
            "attributes": null
          },
          {
            "code": "F380100",
            "description": "Juvenile or adult myasthenia gravis",
            "attributes": null
          },
          {
            "code": "F380z00",
            "description": "Myasthenia gravis NOS",
            "attributes": null
          },
          {
            "code": "F381.00",
            "description": "Myasthenic syndrome due to disease EC",
            "attributes": null
          },
          {
            "code": "F381000",
            "description": "Eaton-Lambert syndrome",
            "attributes": null
          },
          {
            "code": "F381011",
            "description": "Lambert-Eaton syndrome",
            "attributes": null
          },
          {
            "code": "F38..11",
            "description": "Neuromuscular disease",
            "attributes": null
          },
          {
            "code": "F381100",
            "description": "Myasthenic syndrome due to other malignancy",
            "attributes": null
          },
          {
            "code": "F381300",
            "description": "Myasthenic syndrome due to diabetic amyotrophy",
            "attributes": null
          },
          {
            "code": "F381311",
            "description": "Diabetic amyotrophy",
            "attributes": null
          },
          {
            "code": "F381400",
            "description": "Myasthenic syndrome due to hypothyroidism",
            "attributes": null
          },
          {
            "code": "F381500",
            "description": "Myasthenic syndrome due to pernicious anaemia",
            "attributes": null
          },
          {
            "code": "F381600",
            "description": "Myasthenic syndrome due to thyrotoxicosis",
            "attributes": null
          },
          {
            "code": "F381z00",
            "description": "Myasthenic syndrome due to disease NOS",
            "attributes": null
          },
          {
            "code": "F382.00",
            "description": "Toxic myoneural disorder",
            "attributes": null
          },
          {
            "code": "F38y.00",
            "description": "Other specific myoneural disorder",
            "attributes": null
          },
          {
            "code": "F38y.11",
            "description": "Amyotonia congenita",
            "attributes": null
          },
          {
            "code": "F38y.12",
            "description": "Oppenheim's amyotonia",
            "attributes": null
          },
          {
            "code": "F38z.00",
            "description": "Myoneural disorder NOS",
            "attributes": null
          },
          {
            "code": "F390.00",
            "description": "Congenital hereditary muscular dystrophy",
            "attributes": null
          },
          {
            "code": "F390000",
            "description": "Benign congenital myopathy",
            "attributes": null
          },
          {
            "code": "F390100",
            "description": "Central core disease",
            "attributes": null
          },
          {
            "code": "F390200",
            "description": "Centronuclear myopathy",
            "attributes": null
          },
          {
            "code": "F390300",
            "description": "Myotubular myopathy",
            "attributes": null
          },
          {
            "code": "F390400",
            "description": "Nemaline body disease",
            "attributes": null
          },
          {
            "code": "F390z00",
            "description": "Congenital hereditary muscular dystrophy NOS",
            "attributes": null
          },
          {
            "code": "F391.00",
            "description": "Hereditary progressive muscular dystrophy",
            "attributes": null
          },
          {
            "code": "F391000",
            "description": "Duchenne muscular dystrophy",
            "attributes": null
          },
          {
            "code": "F391011",
            "description": "Pseudohypertrophic dystrophy",
            "attributes": null
          },
          {
            "code": "F391100",
            "description": "Erb's muscular dystrophy",
            "attributes": null
          },
          {
            "code": "F391200",
            "description": "Pelvic muscular dystrophy",
            "attributes": null
          },
          {
            "code": "F391400",
            "description": "Facioscapulohumeral muscular dystrophy",
            "attributes": null
          },
          {
            "code": "F391411",
            "description": "Facioscapulohumeral atrophy",
            "attributes": null
          },
          {
            "code": "F391500",
            "description": "Distal (Gower's) muscular dystrophy",
            "attributes": null
          },
          {
            "code": "F391600",
            "description": "Ocular muscular dystrophy",
            "attributes": null
          },
          {
            "code": "F391700",
            "description": "Oculopharyngeal muscular dystrophy",
            "attributes": null
          },
          {
            "code": "F391800",
            "description": "Becker muscular dystrophy",
            "attributes": null
          },
          {
            "code": "F391900",
            "description": "Hauptmann-Thannhauser muscular dystrophy",
            "attributes": null
          },
          {
            "code": "F391A00",
            "description": "Emery-Dreifuss muscular dystrophy",
            "attributes": null
          },
          {
            "code": "F391B00",
            "description": "Cardiomyopathy in Duchenne muscular dystrophy",
            "attributes": null
          },
          {
            "code": "F391y00",
            "description": "Other specified hereditary progressive muscular dystrophy",
            "attributes": null
          },
          {
            "code": "F391y11",
            "description": "Distal dystrophy",
            "attributes": null
          },
          {
            "code": "F391z00",
            "description": "Hereditary progressive muscular dystrophy NOS",
            "attributes": null
          },
          {
            "code": "F392.00",
            "description": "Myotonic disorders",
            "attributes": null
          },
          {
            "code": "F392000",
            "description": "Dystrophia myotonica (Steinert's disease)",
            "attributes": null
          },
          {
            "code": "F392011",
            "description": "Steinert's disease",
            "attributes": null
          },
          {
            "code": "F392100",
            "description": "Myotonia congenita (Thomsen's disease)",
            "attributes": null
          },
          {
            "code": "F392111",
            "description": "Thomsen's disease",
            "attributes": null
          },
          {
            "code": "F392200",
            "description": "Paramyotonia congenita (Eulenburg's disease)",
            "attributes": null
          },
          {
            "code": "F392211",
            "description": "Eulenburg's disease",
            "attributes": null
          },
          {
            "code": "F392300",
            "description": "Infantile myotonia",
            "attributes": null
          },
          {
            "code": "F392400",
            "description": "Neuromyotonia",
            "attributes": null
          },
          {
            "code": "F392500",
            "description": "Proximal myotonic myopathy",
            "attributes": null
          },
          {
            "code": "F392y00",
            "description": "Other specified myotonic disorder",
            "attributes": null
          },
          {
            "code": "F392z00",
            "description": "Myotonic disorder NOS",
            "attributes": null
          },
          {
            "code": "F393.00",
            "description": "Familial periodic paralysis",
            "attributes": null
          },
          {
            "code": "F393.11",
            "description": "Familial hypokalaemic periodic paralysis",
            "attributes": null
          },
          {
            "code": "F394.00",
            "description": "Toxic myopathy",
            "attributes": null
          },
          {
            "code": "F394100",
            "description": "Alcoholic myopathy",
            "attributes": null
          },
          {
            "code": "F395.00",
            "description": "Myopathy due to endocrine disease EC",
            "attributes": null
          },
          {
            "code": "F395000",
            "description": "Myopathy due to Addison's disease",
            "attributes": null
          },
          {
            "code": "F395100",
            "description": "Myopathy due to Cushing's syndrome",
            "attributes": null
          },
          {
            "code": "F395200",
            "description": "Myopathy due to hypopituitarism",
            "attributes": null
          },
          {
            "code": "F395300",
            "description": "Myopathy due to myxoedema",
            "attributes": null
          },
          {
            "code": "F395400",
            "description": "Myopathy due to thyrotoxicosis",
            "attributes": null
          },
          {
            "code": "F395z00",
            "description": "Myopathy due to endocrine disease NOS",
            "attributes": null
          },
          {
            "code": "F396.00",
            "description": "Symptomatic inflammatory myopathy in disease EC",
            "attributes": null
          },
          {
            "code": "F396000",
            "description": "Myopathy due to amyloid",
            "attributes": null
          },
          {
            "code": "F396100",
            "description": "Myopathy due to disseminated lupus erythematosus",
            "attributes": null
          },
          {
            "code": "F396300",
            "description": "Myopathy due to polyarteritis nodosa",
            "attributes": null
          },
          {
            "code": "F396400",
            "description": "Myopathy due to rheumatoid arthritis",
            "attributes": null
          },
          {
            "code": "F396500",
            "description": "Myopathy due to sarcoidosis",
            "attributes": null
          },
          {
            "code": "F396600",
            "description": "Myopathy due to scleroderma",
            "attributes": null
          },
          {
            "code": "F396700",
            "description": "Myopathy due to Sjogren's disease",
            "attributes": null
          },
          {
            "code": "F396z00",
            "description": "Symptomatic inflammatory myopathy in disease NOS",
            "attributes": null
          },
          {
            "code": "F397.00",
            "description": "Proximal myopathy",
            "attributes": null
          },
          {
            "code": "F398.00",
            "description": "Myopathy in metabolic diseases",
            "attributes": null
          },
          {
            "code": "F39B.00",
            "description": "Muscular dystrophy",
            "attributes": null
          },
          {
            "code": "F39X.00",
            "description": "Mitochondrial myopathy, not elsewhere classified",
            "attributes": null
          },
          {
            "code": "F3y..00",
            "description": "Other specified disorders of peripheral nervous system",
            "attributes": null
          },
          {
            "code": "F3y0.00",
            "description": "Diabetic mononeuropathy",
            "attributes": null
          },
          {
            "code": "F3z..00",
            "description": "Peripheral nervous system disorder NOS",
            "attributes": null
          },
          {
            "code": "F423600",
            "description": "Amaurosis fugax",
            "attributes": null
          },
          {
            "code": "F464200",
            "description": "Myotonic cataract",
            "attributes": null
          },
          {
            "code": "F4H0000",
            "description": "Papilloedema, unspecified",
            "attributes": null
          },
          {
            "code": "F4H0100",
            "description": "Papilloedema due to raised intracranial pressure",
            "attributes": null
          },
          {
            "code": "F4H0400",
            "description": "Foster-Kennedy syndrome",
            "attributes": null
          },
          {
            "code": "Fy...00",
            "description": "Other specified diseases of nervous system or sense organ",
            "attributes": null
          },
          {
            "code": "Fy03.00",
            "description": "Sleep apnoea",
            "attributes": null
          },
          {
            "code": "Fy03.11",
            "description": "Obstructive sleep apnoea",
            "attributes": null
          },
          {
            "code": "Fy04.00",
            "description": "Sleep-related respiratory failure",
            "attributes": null
          },
          {
            "code": "Fy04.11",
            "description": "Ondine's curse",
            "attributes": null
          },
          {
            "code": "Fyu0C00",
            "description": "[X]Sequelae of inflammatory diseases of the central nervous system",
            "attributes": null
          },
          {
            "code": "Fyu1.00",
            "description": "[X]Systemic atrophies primarily affecting the central nervous system",
            "attributes": null
          },
          {
            "code": "Fyu1000",
            "description": "[X]Other hereditary ataxias",
            "attributes": null
          },
          {
            "code": "Fyu1100",
            "description": "[X]Other inherited spinal muscular atrophy",
            "attributes": null
          },
          {
            "code": "Fyu1200",
            "description": "[X]Other spinal muscular atrophies and related syndromes",
            "attributes": null
          },
          {
            "code": "Fyu1300",
            "description": "[X]Paraneoplastic neuromyopathy and neuropathy",
            "attributes": null
          },
          {
            "code": "Fyu1400",
            "description": "[X]Other systemic atrophy affecting the central nervous system in neoplastic disease classified elsewhere",
            "attributes": null
          },
          {
            "code": "Fyu1500",
            "description": "[X]Systemic atrophy affecting the central nervous system in myxoedema",
            "attributes": null
          },
          {
            "code": "Fyu1600",
            "description": "[X]Systemic atrophy affecting the central nervous system in other diseases classified elsewhere",
            "attributes": null
          },
          {
            "code": "Fyu2.00",
            "description": "[X]Extrapyramidal and movement disorders",
            "attributes": null
          },
          {
            "code": "Fyu2100",
            "description": "[X]Other secondary parkinsonism",
            "attributes": null
          },
          {
            "code": "Fyu2200",
            "description": "[X]Parkinsonism in diseases classified elsewhere",
            "attributes": null
          },
          {
            "code": "Fyu2500",
            "description": "[X]Other specified forms of tremor",
            "attributes": null
          },
          {
            "code": "Fyu2600",
            "description": "[X]Other chorea",
            "attributes": null
          },
          {
            "code": "Fyu2700",
            "description": "[X]Other specified extrapyramidal and movement disorders",
            "attributes": null
          },
          {
            "code": "Fyu2800",
            "description": "[X]Extrapyramidal and movement disorders in diseases classified elsewhere",
            "attributes": null
          },
          {
            "code": "Fyu2900",
            "description": "[X]Secondary parkinsonism, unspecified",
            "attributes": null
          },
          {
            "code": "Fyu2B00",
            "description": "[X]Secondary parkinsonism due to other external agents",
            "attributes": null
          },
          {
            "code": "Fyu3.00",
            "description": "[X]Other degenerative diseases of the nervous system",
            "attributes": null
          },
          {
            "code": "Fyu3000",
            "description": "[X]Other Alzheimer's disease",
            "attributes": null
          },
          {
            "code": "Fyu3100",
            "description": "[X]Other specified degenerative diseases of the nervous system",
            "attributes": null
          },
          {
            "code": "Fyu3200",
            "description": "[X]Subacute combined degeneration of the spinal cord in diseases classified elsewhere",
            "attributes": null
          },
          {
            "code": "Fyu3400",
            "description": "[X]Other specified degenerative disorders of the nervous system in diseases classified elsewhere",
            "attributes": null
          },
          {
            "code": "Fyu4.00",
            "description": "[X]Demyelinating diseases of the central nervous system",
            "attributes": null
          },
          {
            "code": "Fyu4000",
            "description": "[X]Other specified acute disseminated demyelination",
            "attributes": null
          },
          {
            "code": "Fyu4100",
            "description": "[X]Other specified demyelinating diseases of the central nervous system",
            "attributes": null
          },
          {
            "code": "Fyu4200",
            "description": "[X]Acute disseminated demyelination, unspecified",
            "attributes": null
          },
          {
            "code": "Fyu5.00",
            "description": "[X]Episodic and paroxysmal disorders",
            "attributes": null
          },
          {
            "code": "Fyu5500",
            "description": "[X]Other transient cerebral ischaemic attacks and related syndromes",
            "attributes": null
          },
          {
            "code": "Fyu5600",
            "description": "[X]Other lacunar syndromes",
            "attributes": null
          },
          {
            "code": "Fyu5700",
            "description": "[X]Other vascular syndromes of the brain in cerebrovascular diseases",
            "attributes": null
          },
          {
            "code": "Fyu6000",
            "description": "[X]Other disorders of trigeminal nerve",
            "attributes": null
          },
          {
            "code": "Fyu6100",
            "description": "[X]Other disorders of facial nerve",
            "attributes": null
          },
          {
            "code": "Fyu6200",
            "description": "[X]Multiple cranial nerve palsies in infectious and parasitic diseases classified elsewhere",
            "attributes": null
          },
          {
            "code": "Fyu6300",
            "description": "[X]Multiple cranial nerve palsies in neoplastic disease classified elsewhere",
            "attributes": null
          },
          {
            "code": "Fyu6400",
            "description": "[X]Other cranial nerve disorders in other diseases classified elsewhere",
            "attributes": null
          },
          {
            "code": "Fyu6600",
            "description": "[X]Nerve root and plexus compressions in neoplastic disease classified elsewhere",
            "attributes": null
          },
          {
            "code": "Fyu6800",
            "description": "[X]Nerve root and plexus compressions in other diseases classified elsewhere",
            "attributes": null
          },
          {
            "code": "Fyu6C00",
            "description": "[X]Other specified mononeuropathies",
            "attributes": null
          },
          {
            "code": "Fyu6D00",
            "description": "[X]Other mononeuropathies in diseases classified elsewhere",
            "attributes": null
          },
          {
            "code": "Fyu6E00",
            "description": "[X]Ilio-inguinal nerve entrapment",
            "attributes": null
          },
          {
            "code": "Fyu7.00",
            "description": "[X]Polyneuropathies and other disorders of the peripheral nervous system",
            "attributes": null
          },
          {
            "code": "Fyu7000",
            "description": "[X]Other hereditary and idiopathic neuropathies",
            "attributes": null
          },
          {
            "code": "Fyu7100",
            "description": "[X]Other inflammatory polyneuropathies",
            "attributes": null
          },
          {
            "code": "Fyu7200",
            "description": "[X]Other specified polyneuropathies",
            "attributes": null
          },
          {
            "code": "Fyu7400",
            "description": "[X]Polyneuropathy in neoplastic disease classified elsewhere",
            "attributes": null
          },
          {
            "code": "Fyu7500",
            "description": "[X]Polyneuropathy in other endocrine and metabolic diseases classified elsewhere",
            "attributes": null
          },
          {
            "code": "Fyu7700",
            "description": "[X]Polyneuropathy in systemic connective tissue disorders classified elsewhere",
            "attributes": null
          },
          {
            "code": "Fyu7800",
            "description": "[X]Polyneuropathy in other musculoskeletal disorders classified elsewhere",
            "attributes": null
          },
          {
            "code": "Fyu7900",
            "description": "[X]Polyneuropathy in other diseases classified elsewhere",
            "attributes": null
          },
          {
            "code": "Fyu7A00",
            "description": "[X]Other disorders of the peripheral nervous system",
            "attributes": null
          },
          {
            "code": "Fyu7B00",
            "description": "[X]Inflammatory polyneuropathy, unspecified",
            "attributes": null
          },
          {
            "code": "Fyu7C00",
            "description": "[X] Polyneuropathy, unspecified",
            "attributes": null
          },
          {
            "code": "Fyu8.00",
            "description": "[X]Diseases of myoneural junction and muscle",
            "attributes": null
          },
          {
            "code": "Fyu8000",
            "description": "[X]Other specified myoneural disorders",
            "attributes": null
          },
          {
            "code": "Fyu8300",
            "description": "[X]Myasthenic syndromes in endocrine diseases classified elsewhere",
            "attributes": null
          },
          {
            "code": "Fyu8400",
            "description": "[X]Other myasthenic syndromes in neoplastic disease classified elsewhere",
            "attributes": null
          },
          {
            "code": "Fyu8500",
            "description": "[X]Myasthenic syndromes in other diseases classified elsewhere",
            "attributes": null
          },
          {
            "code": "Fyu8800",
            "description": "[X]Myopathy in metabolic diseases classified elsewhere",
            "attributes": null
          },
          {
            "code": "Fyu8A00",
            "description": "[X]Mitochondrial myopathy, not elsewhere classified",
            "attributes": null
          },
          {
            "code": "Fyu9100",
            "description": "[X]Other specified paralytic syndromes",
            "attributes": null
          },
          {
            "code": "FyuA.00",
            "description": "[X]Other disorders of the nervous system",
            "attributes": null
          },
          {
            "code": "FyuA000",
            "description": "[X]Other disorders of the autonomic nervous system",
            "attributes": null
          },
          {
            "code": "FyuA100",
            "description": "[X]Other hydrocephalus",
            "attributes": null
          },
          {
            "code": "FyuA200",
            "description": "[X]Other specified disorders of brain",
            "attributes": null
          },
          {
            "code": "FyuA300",
            "description": "[X]Hydrocephalus in infectious and parasitic diseases classified elsewhere",
            "attributes": null
          },
          {
            "code": "FyuA400",
            "description": "[X]Hydrocephalus in neoplastic disease classified elsewhere",
            "attributes": null
          },
          {
            "code": "FyuA500",
            "description": "[X]Hydrocephalus in other diseases classified elsewhere",
            "attributes": null
          },
          {
            "code": "FyuA600",
            "description": "[X]Other specified disorders of brain in diseases classified elsewhere",
            "attributes": null
          },
          {
            "code": "FyuA700",
            "description": "[X]Other specified diseases of spinal cord",
            "attributes": null
          },
          {
            "code": "FyuA800",
            "description": "[X]Other specified disorders of the central nervous system",
            "attributes": null
          },
          {
            "code": "FyuAA00",
            "description": "[X]Other postprocedural disorders of the nervous system",
            "attributes": null
          },
          {
            "code": "FyuAB00",
            "description": "[X]Other disorders of the nervous system, not elsewhere classified",
            "attributes": null
          },
          {
            "code": "FyuAC00",
            "description": "[X]Autonomic neuropathy in endocrine and metabolic diseases classified elsewhere",
            "attributes": null
          },
          {
            "code": "FyuAD00",
            "description": "[X]Other disorders of the autonomic nervous system in other diseases classified elsewhere",
            "attributes": null
          },
          {
            "code": "FyuAE00",
            "description": "[X]Myelopathy in diseases classified elsewhere",
            "attributes": null
          },
          {
            "code": "FyuAF00",
            "description": "[X]Other specified disorders of the nervous system in diseases classified elsewhere",
            "attributes": null
          },
          {
            "code": "FyuAG00",
            "description": "[X]Post-traumatic hydrocephalus, unspecified",
            "attributes": null
          },
          {
            "code": "FyuAH00",
            "description": "[X]Disorder of central nervous system, unspecified",
            "attributes": null
          },
          {
            "code": "G552.11",
            "description": "Becker's disease",
            "attributes": null
          },
          {
            "code": "G558000",
            "description": "Cardiomyopathy in Friedreich's ataxia",
            "attributes": null
          },
          {
            "code": "G558100",
            "description": "Cardiomyopathy in myotonic dystrophy",
            "attributes": null
          },
          {
            "code": "G6...00",
            "description": "Cerebrovascular disease",
            "attributes": null
          },
          {
            "code": "G60..00",
            "description": "Subarachnoid haemorrhage",
            "attributes": null
          },
          {
            "code": "G600.00",
            "description": "Ruptured berry aneurysm",
            "attributes": null
          },
          {
            "code": "G601.00",
            "description": "Subarachnoid haemorrhage from carotid siphon and bifurcation",
            "attributes": null
          },
          {
            "code": "G602.00",
            "description": "Subarachnoid haemorrhage from middle cerebral artery",
            "attributes": null
          },
          {
            "code": "G603.00",
            "description": "Subarachnoid haemorrhage from anterior communicating artery",
            "attributes": null
          },
          {
            "code": "G604.00",
            "description": "Subarachnoid haemorrhage from posterior communicating artery",
            "attributes": null
          },
          {
            "code": "G605.00",
            "description": "Subarachnoid haemorrhage from basilar artery",
            "attributes": null
          },
          {
            "code": "G60X.00",
            "description": "Subarachnoid haemorrhage from intracranial artery, unspecified",
            "attributes": null
          },
          {
            "code": "G60z.00",
            "description": "Subarachnoid haemorrhage NOS",
            "attributes": null
          },
          {
            "code": "G61..00",
            "description": "Intracerebral haemorrhage",
            "attributes": null
          },
          {
            "code": "G610.00",
            "description": "Cortical haemorrhage",
            "attributes": null
          },
          {
            "code": "G611.00",
            "description": "Internal capsule haemorrhage",
            "attributes": null
          },
          {
            "code": "G61..11",
            "description": "CVA - cerebrovascular accident due to intracerebral haemorrhage",
            "attributes": null
          },
          {
            "code": "G61..12",
            "description": "Stroke due to intracerebral haemorrhage",
            "attributes": null
          },
          {
            "code": "G612.00",
            "description": "Basal nucleus haemorrhage",
            "attributes": null
          },
          {
            "code": "G613.00",
            "description": "Cerebellar haemorrhage",
            "attributes": null
          },
          {
            "code": "G614.00",
            "description": "Pontine haemorrhage",
            "attributes": null
          },
          {
            "code": "G615.00",
            "description": "Bulbar haemorrhage",
            "attributes": null
          },
          {
            "code": "G616.00",
            "description": "External capsule haemorrhage",
            "attributes": null
          },
          {
            "code": "G617.00",
            "description": "Intracerebral haemorrhage, intraventricular",
            "attributes": null
          },
          {
            "code": "G618.00",
            "description": "Intracerebral haemorrhage, multiple localized",
            "attributes": null
          },
          {
            "code": "G619.00",
            "description": "Lobar cerebral haemorrhage",
            "attributes": null
          },
          {
            "code": "G61X.00",
            "description": "Intracerebral haemorrhage in hemisphere, unspecified",
            "attributes": null
          },
          {
            "code": "G61X000",
            "description": "Left sided intracerebral haemorrhage, unspecified",
            "attributes": null
          },
          {
            "code": "G61X100",
            "description": "Right sided intracerebral haemorrhage, unspecified",
            "attributes": null
          },
          {
            "code": "G61z.00",
            "description": "Intracerebral haemorrhage NOS",
            "attributes": null
          },
          {
            "code": "G62..00",
            "description": "Other and unspecified intracranial haemorrhage",
            "attributes": null
          },
          {
            "code": "G620.00",
            "description": "Extradural haemorrhage - nontraumatic",
            "attributes": null
          },
          {
            "code": "G621.00",
            "description": "Subdural haemorrhage - nontraumatic",
            "attributes": null
          },
          {
            "code": "G622.00",
            "description": "Subdural haematoma - nontraumatic",
            "attributes": null
          },
          {
            "code": "G62z.00",
            "description": "Intracranial haemorrhage NOS",
            "attributes": null
          },
          {
            "code": "G63..00",
            "description": "Precerebral arterial occlusion",
            "attributes": null
          },
          {
            "code": "G630.00",
            "description": "Basilar artery occlusion",
            "attributes": null
          },
          {
            "code": "G631.00",
            "description": "Carotid artery occlusion",
            "attributes": null
          },
          {
            "code": "G63..11",
            "description": "Infarction - precerebral",
            "attributes": null
          },
          {
            "code": "G631.11",
            "description": "Stenosis, carotid artery",
            "attributes": null
          },
          {
            "code": "G631.12",
            "description": "Thrombosis, carotid artery",
            "attributes": null
          },
          {
            "code": "G63..12",
            "description": "Stenosis of precerebral arteries",
            "attributes": null
          },
          {
            "code": "G632.00",
            "description": "Vertebral artery occlusion",
            "attributes": null
          },
          {
            "code": "G633.00",
            "description": "Multiple and bilateral precerebral arterial occlusion",
            "attributes": null
          },
          {
            "code": "G634.00",
            "description": "Carotid artery stenosis",
            "attributes": null
          },
          {
            "code": "G63y.00",
            "description": "Other precerebral artery occlusion",
            "attributes": null
          },
          {
            "code": "G63y000",
            "description": "Cerebral infarct due to thrombosis of precerebral arteries",
            "attributes": null
          },
          {
            "code": "G63y100",
            "description": "Cerebral infarction due to embolism of precerebral arteries",
            "attributes": null
          },
          {
            "code": "G63z.00",
            "description": "Precerebral artery occlusion NOS",
            "attributes": null
          },
          {
            "code": "G64..00",
            "description": "Cerebral arterial occlusion",
            "attributes": null
          },
          {
            "code": "G640000",
            "description": "Cerebral infarction due to thrombosis of cerebral arteries",
            "attributes": null
          },
          {
            "code": "G641000",
            "description": "Cerebral infarction due to embolism of cerebral arteries",
            "attributes": null
          },
          {
            "code": "G64..11",
            "description": "CVA - cerebrovascular accident due to cerebral artery occlusion",
            "attributes": null
          },
          {
            "code": "G64..12",
            "description": "Infarction - cerebral",
            "attributes": null
          },
          {
            "code": "G64..13",
            "description": "Stroke due to cerebral arterial occlusion",
            "attributes": null
          },
          {
            "code": "G64z.00",
            "description": "Cerebral infarction NOS",
            "attributes": null
          },
          {
            "code": "G64z000",
            "description": "Brainstem infarction",
            "attributes": null
          },
          {
            "code": "G64z100",
            "description": "Wallenberg syndrome",
            "attributes": null
          },
          {
            "code": "G64z.11",
            "description": "Brainstem infarction NOS",
            "attributes": null
          },
          {
            "code": "G64z111",
            "description": "Lateral medullary syndrome",
            "attributes": null
          },
          {
            "code": "G64z.12",
            "description": "Cerebellar infarction",
            "attributes": null
          },
          {
            "code": "G64z200",
            "description": "Left sided cerebral infarction",
            "attributes": null
          },
          {
            "code": "G64z300",
            "description": "Right sided cerebral infarction",
            "attributes": null
          },
          {
            "code": "G64z400",
            "description": "Infarction of basal ganglia",
            "attributes": null
          },
          {
            "code": "G65..00",
            "description": "Transient cerebral ischaemia",
            "attributes": null
          },
          {
            "code": "G650.00",
            "description": "Basilar artery syndrome",
            "attributes": null
          },
          {
            "code": "G650.11",
            "description": "Insufficiency - basilar artery",
            "attributes": null
          },
          {
            "code": "G651.00",
            "description": "Vertebral artery syndrome",
            "attributes": null
          },
          {
            "code": "G651000",
            "description": "Vertebro-basilar artery syndrome",
            "attributes": null
          },
          {
            "code": "G65..12",
            "description": "Transient ischaemic attack",
            "attributes": null
          },
          {
            "code": "G65..13",
            "description": "Vertebro-basilar insufficiency",
            "attributes": null
          },
          {
            "code": "G652.00",
            "description": "Subclavian steal syndrome",
            "attributes": null
          },
          {
            "code": "G653.00",
            "description": "Carotid artery syndrome hemispheric",
            "attributes": null
          },
          {
            "code": "G656.00",
            "description": "Vertebrobasilar insufficiency",
            "attributes": null
          },
          {
            "code": "G657.00",
            "description": "Carotid territory transient ischaemic attack",
            "attributes": null
          },
          {
            "code": "G65y.00",
            "description": "Other transient cerebral ischaemia",
            "attributes": null
          },
          {
            "code": "G65z.00",
            "description": "Transient cerebral ischaemia NOS",
            "attributes": null
          },
          {
            "code": "G65z100",
            "description": "Intermittent cerebral ischaemia",
            "attributes": null
          },
          {
            "code": "G65zz00",
            "description": "Transient cerebral ischaemia NOS",
            "attributes": null
          },
          {
            "code": "G66..00",
            "description": "Stroke and cerebrovascular accident unspecified",
            "attributes": null
          },
          {
            "code": "G660.00",
            "description": "Middle cerebral artery syndrome",
            "attributes": null
          },
          {
            "code": "G661.00",
            "description": "Anterior cerebral artery syndrome",
            "attributes": null
          },
          {
            "code": "G66..11",
            "description": "CVA unspecified",
            "attributes": null
          },
          {
            "code": "G66..12",
            "description": "Stroke unspecified",
            "attributes": null
          },
          {
            "code": "G66..13",
            "description": "CVA - Cerebrovascular accident unspecified",
            "attributes": null
          },
          {
            "code": "G662.00",
            "description": "Posterior cerebral artery syndrome",
            "attributes": null
          },
          {
            "code": "G663.00",
            "description": "Brain stem stroke syndrome",
            "attributes": null
          },
          {
            "code": "G664.00",
            "description": "Cerebellar stroke syndrome",
            "attributes": null
          },
          {
            "code": "G665.00",
            "description": "Pure motor lacunar syndrome",
            "attributes": null
          },
          {
            "code": "G666.00",
            "description": "Pure sensory lacunar syndrome",
            "attributes": null
          },
          {
            "code": "G667.00",
            "description": "Left sided CVA",
            "attributes": null
          },
          {
            "code": "G668.00",
            "description": "Right sided CVA",
            "attributes": null
          },
          {
            "code": "G67..00",
            "description": "Other cerebrovascular disease",
            "attributes": null
          },
          {
            "code": "G670.00",
            "description": "Cerebral atherosclerosis",
            "attributes": null
          },
          {
            "code": "G670.11",
            "description": "Precerebral atherosclerosis",
            "attributes": null
          },
          {
            "code": "G671.00",
            "description": "Generalised ischaemic cerebrovascular disease NOS",
            "attributes": null
          },
          {
            "code": "G671000",
            "description": "Acute cerebrovascular insufficiency NOS",
            "attributes": null
          },
          {
            "code": "G671100",
            "description": "Chronic cerebral ischaemia",
            "attributes": null
          },
          {
            "code": "G671z00",
            "description": "Generalised ischaemic cerebrovascular disease NOS",
            "attributes": null
          },
          {
            "code": "G672.00",
            "description": "Hypertensive encephalopathy",
            "attributes": null
          },
          {
            "code": "G672.11",
            "description": "Hypertensive crisis",
            "attributes": null
          },
          {
            "code": "G673100",
            "description": "Carotico-cavernous sinus fistula",
            "attributes": null
          },
          {
            "code": "G674.00",
            "description": "Cerebral arteritis",
            "attributes": null
          },
          {
            "code": "G674000",
            "description": "Cerebral amyloid angiopathy",
            "attributes": null
          },
          {
            "code": "G675.00",
            "description": "Moyamoya disease",
            "attributes": null
          },
          {
            "code": "G676.00",
            "description": "Nonpyogenic venous sinus thrombosis",
            "attributes": null
          },
          {
            "code": "G676000",
            "description": "Cerebral infarction due to cerebral venous thrombosis, nonpyogenic",
            "attributes": null
          },
          {
            "code": "G677000",
            "description": "Occlusion and stenosis of middle cerebral artery",
            "attributes": null
          },
          {
            "code": "G677100",
            "description": "Occlusion and stenosis of anterior cerebral artery",
            "attributes": null
          },
          {
            "code": "G677200",
            "description": "Occlusion and stenosis of posterior cerebral artery",
            "attributes": null
          },
          {
            "code": "G677300",
            "description": "Occlusion and stenosis of cerebellar arteries",
            "attributes": null
          },
          {
            "code": "G677400",
            "description": "Occlusion and stenosis of multiple and bilateral cerebral arteries",
            "attributes": null
          },
          {
            "code": "G678.00",
            "description": "Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy",
            "attributes": null
          },
          {
            "code": "G679.00",
            "description": "Small vessel cerebrovascular disease",
            "attributes": null
          },
          {
            "code": "G67A.00",
            "description": "Cerebral vein thrombosis",
            "attributes": null
          },
          {
            "code": "G67B.00",
            "description": "Reversible cerebral vasoconstriction syndrome",
            "attributes": null
          },
          {
            "code": "G67B.11",
            "description": "Call-Fleming syndrome",
            "attributes": null
          },
          {
            "code": "G67y.00",
            "description": "Other cerebrovascular disease OS",
            "attributes": null
          },
          {
            "code": "G67z.00",
            "description": "Other cerebrovascular disease NOS",
            "attributes": null
          },
          {
            "code": "G68..00",
            "description": "Late effects of cerebrovascular disease",
            "attributes": null
          },
          {
            "code": "G680.00",
            "description": "Sequelae of subarachnoid haemorrhage",
            "attributes": null
          },
          {
            "code": "G681.00",
            "description": "Sequelae of intracerebral haemorrhage",
            "attributes": null
          },
          {
            "code": "G683.00",
            "description": "Sequelae of cerebral infarction",
            "attributes": null
          },
          {
            "code": "G68W.00",
            "description": "Sequelae of other and unspecified cerebrovascular diseases",
            "attributes": null
          },
          {
            "code": "G68X.00",
            "description": "Sequelae of stroke, not specified as haemorrhage or infarction",
            "attributes": null
          },
          {
            "code": "G6W..00",
            "description": "Cerebral infarction due to unspecified occlusion or stenosis of precerebral arteries",
            "attributes": null
          },
          {
            "code": "G6X..00",
            "description": "Cerebral infarction due to unspecified occlusion or stenosis of cerebral arteries",
            "attributes": null
          },
          {
            "code": "G6y..00",
            "description": "Other specified cerebrovascular disease",
            "attributes": null
          },
          {
            "code": "G6z..00",
            "description": "Cerebrovascular disease NOS",
            "attributes": null
          },
          {
            "code": "G70y000",
            "description": "Carotid artery atherosclerosis",
            "attributes": null
          },
          {
            "code": "G70y011",
            "description": "Carotid artery disease",
            "attributes": null
          },
          {
            "code": "G769.00",
            "description": "Anterior spinal and vertebral artery compression syndromes",
            "attributes": null
          },
          {
            "code": "G79..00",
            "description": "Steal syndrome of hand",
            "attributes": null
          },
          {
            "code": "Gyu6.00",
            "description": "[X]Cerebrovascular diseases",
            "attributes": null
          },
          {
            "code": "Gyu6000",
            "description": "[X]Subarachnoid haemorrhage from other intracranial arteries",
            "attributes": null
          },
          {
            "code": "Gyu6100",
            "description": "[X]Other subarachnoid haemorrhage",
            "attributes": null
          },
          {
            "code": "Gyu6200",
            "description": "[X]Other intracerebral haemorrhage",
            "attributes": null
          },
          {
            "code": "Gyu6300",
            "description": "[X]Cerebral infarction due to unspecified occlusion or stenosis of cerebral arteries",
            "attributes": null
          },
          {
            "code": "Gyu6400",
            "description": "[X]Other cerebral infarction",
            "attributes": null
          },
          {
            "code": "Gyu6500",
            "description": "[X]Occlusion and stenosis of other precerebral arteries",
            "attributes": null
          },
          {
            "code": "Gyu6700",
            "description": "[X]Other specified cerebrovascular diseases",
            "attributes": null
          },
          {
            "code": "Gyu6900",
            "description": "[X]Cerebral arteritis in other diseases classified elsewhere",
            "attributes": null
          },
          {
            "code": "Gyu6A00",
            "description": "[X]Other cerebrovascular disorders in diseases classified elsewhere",
            "attributes": null
          },
          {
            "code": "Gyu6C00",
            "description": "[X]Sequelae of stroke, not specified as haemorrhage or infarction",
            "attributes": null
          },
          {
            "code": "Gyu6D00",
            "description": "[X]Sequelae of other and unspecified cerebrovascular diseases",
            "attributes": null
          },
          {
            "code": "Gyu6E00",
            "description": "[X]Subarachnoid haemorrhage from intracranial artery, unspecified",
            "attributes": null
          },
          {
            "code": "Gyu6F00",
            "description": "[X]Intracerebral haemorrhage in hemisphere, unspecified",
            "attributes": null
          },
          {
            "code": "Gyu6G00",
            "description": "[X]Cerebral infarction due to unspecified occlusion or stenosis of precerebral arteries",
            "attributes": null
          },
          {
            "code": "H5B..00",
            "description": "Sleep apnoea",
            "attributes": null
          },
          {
            "code": "H5B0.00",
            "description": "Obstructive sleep apnoea",
            "attributes": null
          },
          {
            "code": "M21yD00",
            "description": "Hemifacial atrophy",
            "attributes": null
          },
          {
            "code": "M21yD11",
            "description": "Romberg's syndrome",
            "attributes": null
          },
          {
            "code": "N035.11",
            "description": "Charcot's arthropathy",
            "attributes": null
          },
          {
            "code": "N111.00",
            "description": "Cervical spondylosis with myelopathy",
            "attributes": null
          },
          {
            "code": "N111000",
            "description": "Single-level cervical spondylosis with myelopathy",
            "attributes": null
          },
          {
            "code": "N111100",
            "description": "Two-level cervical spondylosis with myelopathy",
            "attributes": null
          },
          {
            "code": "N111.11",
            "description": "Vertebral artery compression syndrome",
            "attributes": null
          },
          {
            "code": "N111200",
            "description": "Multiple-level cervical spondylosis with myelopathy",
            "attributes": null
          },
          {
            "code": "N111300",
            "description": "Cervical myelopathy",
            "attributes": null
          },
          {
            "code": "N113.00",
            "description": "Thoracic spondylosis with myelopathy",
            "attributes": null
          },
          {
            "code": "N113000",
            "description": "Single-level thoracic spondylosis with myelopathy",
            "attributes": null
          },
          {
            "code": "N113100",
            "description": "Two-level thoracic spondylosis with myelopathy",
            "attributes": null
          },
          {
            "code": "N113200",
            "description": "Multiple-level thoracic spondylosis with myelopathy",
            "attributes": null
          },
          {
            "code": "N115.00",
            "description": "Lumbosacral spondylosis with myelopathy",
            "attributes": null
          },
          {
            "code": "N115000",
            "description": "Single-level lumbosacral spondylosis with myelopathy",
            "attributes": null
          },
          {
            "code": "N115100",
            "description": "Two-level lumbosacral spondylosis with myelopathy",
            "attributes": null
          },
          {
            "code": "N115200",
            "description": "Multiple-level lumbosacral spondylosis with myelopathy",
            "attributes": null
          },
          {
            "code": "N119.00",
            "description": "Cervical spondylosis with radiculopathy",
            "attributes": null
          },
          {
            "code": "N119000",
            "description": "Single-level cervical spondylosis with radiculopathy",
            "attributes": null
          },
          {
            "code": "N119100",
            "description": "Two-level cervical spondylosis with radiculopathy",
            "attributes": null
          },
          {
            "code": "N119200",
            "description": "Multiple-level cervical spondylosis with radiculopathy",
            "attributes": null
          },
          {
            "code": "N11z100",
            "description": "Spondylosis with myelopathy, NOS",
            "attributes": null
          },
          {
            "code": "N129.11",
            "description": "Prolapsed intervertebral disc with associated myelopathy",
            "attributes": null
          },
          {
            "code": "N12B.00",
            "description": "Disc prolapse with myelopathy",
            "attributes": null
          },
          {
            "code": "N12B000",
            "description": "Cervical disc prolapse with myelopathy",
            "attributes": null
          },
          {
            "code": "N12B100",
            "description": "Thoracic disc prolapse with myelopathy",
            "attributes": null
          },
          {
            "code": "N12B200",
            "description": "Lumbar disc prolapse with myelopathy",
            "attributes": null
          },
          {
            "code": "N12C.00",
            "description": "Disc prolapse with radiculopathy",
            "attributes": null
          },
          {
            "code": "N12C000",
            "description": "Cervical disc prolapse with radiculopathy",
            "attributes": null
          },
          {
            "code": "N12C100",
            "description": "Thoracic disc prolapse with radiculopathy",
            "attributes": null
          },
          {
            "code": "N12C200",
            "description": "Lumbar disc prolapse with radiculopathy",
            "attributes": null
          },
          {
            "code": "N12C400",
            "description": "Prolapsed lumbar intervertebral disc with sciatica",
            "attributes": null
          },
          {
            "code": "N337.00",
            "description": "Algoneurodystrophy",
            "attributes": null
          },
          {
            "code": "N337.11",
            "description": "Algodystrophy",
            "attributes": null
          },
          {
            "code": "N337111",
            "description": "Reflex sympathetic dystrophy",
            "attributes": null
          },
          {
            "code": "N337.12",
            "description": "Reflex sympathetic dystrophy",
            "attributes": null
          },
          {
            "code": "N337300",
            "description": "Algodystrophy of knee",
            "attributes": null
          },
          {
            "code": "N337z00",
            "description": "Algoneurodystrophy NOS",
            "attributes": null
          },
          {
            "code": "N33C.00",
            "description": "Complex regional pain syndrome type I",
            "attributes": null
          },
          {
            "code": "Nyu7400",
            "description": "[X]Lumbar and other intervertebral disc disorders with radiculopathy",
            "attributes": null
          },
          {
            "code": "P230.11",
            "description": "Hydrocephauls with anomaly of aqueduct of Sylvius",
            "attributes": null
          },
          {
            "code": "P243.00",
            "description": "Porencephaly",
            "attributes": null
          },
          {
            "code": "P2x2.00",
            "description": "Familial dysautonomia",
            "attributes": null
          },
          {
            "code": "P2x5.00",
            "description": "Riley - Day syndrome",
            "attributes": null
          },
          {
            "code": "PH02.11",
            "description": "Meige's disease",
            "attributes": null
          },
          {
            "code": "R007400",
            "description": "[D]Postviral (asthenic) syndrome",
            "attributes": null
          },
          {
            "code": "R007411",
            "description": "[D]Post viral debility",
            "attributes": null
          },
          {
            "code": "R008500",
            "description": "[D]Frey's syndrome",
            "attributes": null
          },
          {
            "code": "R042600",
            "description": "[D]Intracranial lesion",
            "attributes": null
          },
          {
            "code": "S630.11",
            "description": "Cerebral compression due to injury",
            "attributes": null
          },
          {
            "code": "SJ41200",
            "description": "Splanchnic nerve injury",
            "attributes": null
          },
          {
            "code": "SJ41300",
            "description": "Inferior mesenteric plexus injury",
            "attributes": null
          },
          {
            "code": "SJ41400",
            "description": "Stellate ganglion injury",
            "attributes": null
          },
          {
            "code": "SJ42.00",
            "description": "Intercostal nerve injury",
            "attributes": null
          },
          {
            "code": "SP10000",
            "description": "Anoxic brain damage complication",
            "attributes": null
          },
          {
            "code": "SP10100",
            "description": "Cerebral anoxia complication",
            "attributes": null
          },
          {
            "code": "SP3y800",
            "description": "Dysequilibrium syndrome",
            "attributes": null
          }
        ]
      },
      {
        "concept_id": 4124,
        "concept_version_id": 11484,
        "concept_name": "Other neurological - other neurological condition (SNOMED-CT)",
        "coding_system": {
          "id": 9,
          "name": "SNOMED  CT codes",
          "description": "SNOMED CT codes"
        },
        "phenotype_id": "PH1701",
        "phenotype_version_id": 3627,
        "phenotype_name": "Chronic paediatric conditions: Other neurological (excluding epilepsy and headaches)",
        "code_attribute_header": null,
        "codes": [
          {
            "code": "100491000119103",
            "description": "Myelopathy co-occurrent and due to spinal stenosis of lumbar region (disorder)",
            "attributes": null
          },
          {
            "code": "100511000119108",
            "description": "Myelopathy co-occurrent and due to spinal stenosis of thoracic region (disorder)",
            "attributes": null
          },
          {
            "code": "10068001",
            "description": "Sensory somatic cortical disorder (disorder)",
            "attributes": null
          },
          {
            "code": "101301000119106",
            "description": "Acute hypercapnic respiratory failure due to obstructive sleep apnea (disorder)",
            "attributes": null
          },
          {
            "code": "101421000119107",
            "description": "Dementia due to Parkinson's disease (disorder)",
            "attributes": null
          },
          {
            "code": "102781000119107",
            "description": "Sensory neuropathy due to type 1 diabetes mellitus (disorder)",
            "attributes": null
          },
          {
            "code": "102831000119104",
            "description": "Paralytic syndrome of both lower limbs as sequela of stroke (disorder)",
            "attributes": null
          },
          {
            "code": "103761000119107",
            "description": "Paralytic syndrome of all four limbs as sequela of stroke (disorder)",
            "attributes": null
          },
          {
            "code": "103851000119100",
            "description": "Restrictive lung disease due to amyotrophic lateral sclerosis (disorder)",
            "attributes": null
          },
          {
            "code": "103871000119109",
            "description": "Restrictive lung disease due to Parkinson disease (disorder)",
            "attributes": null
          },
          {
            "code": "10394003",
            "description": "Friedreich's ataxia (disorder)",
            "attributes": null
          },
          {
            "code": "104471000119105",
            "description": "Charcot arthropathy due to syphilis (disorder)",
            "attributes": null
          },
          {
            "code": "10481000119108",
            "description": "Colloid brain cyst (disorder)",
            "attributes": null
          },
          {
            "code": "105191000119100",
            "description": "Acquired central alveolar hypoventilation (disorder)",
            "attributes": null
          },
          {
            "code": "10532003",
            "description": "Primary degenerative dementia of the Alzheimer type, presenile onset, with depression (disorder)",
            "attributes": null
          },
          {
            "code": "105421000119105",
            "description": "Early onset Alzheimer's disease with behavioral disturbance (disorder)",
            "attributes": null
          },
          {
            "code": "1055001",
            "description": "Stenosis of precerebral artery (disorder)",
            "attributes": null
          },
          {
            "code": "106018006",
            "description": "Hereditary degenerative disease of central nervous system (disorder)",
            "attributes": null
          },
          {
            "code": "106021000119105",
            "description": "Multi-infarct dementia due to atherosclerosis (disorder)",
            "attributes": null
          },
          {
            "code": "108691000119102",
            "description": "Spasticity as sequela of stroke (disorder)",
            "attributes": null
          },
          {
            "code": "1091000119108",
            "description": "Obstructive sleep apnea of child (disorder)",
            "attributes": null
          },
          {
            "code": "10948005",
            "description": "Thoracic spondylosis with myelopathy (disorder)",
            "attributes": null
          },
          {
            "code": "109903009",
            "description": "Late effects of pyogenic intracranial abscess (disorder)",
            "attributes": null
          },
          {
            "code": "109904003",
            "description": "Acquired meningocele (disorder)",
            "attributes": null
          },
          {
            "code": "1101000119103",
            "description": "Obstructive sleep apnea of adult (disorder)",
            "attributes": null
          },
          {
            "code": "110181000119105",
            "description": "Peripheral sensory neuropathy due to type 2 diabetes mellitus (disorder)",
            "attributes": null
          },
          {
            "code": "11045000",
            "description": "Supranuclear facial nerve paralysis (disorder)",
            "attributes": null
          },
          {
            "code": "110997000",
            "description": "Fahr's syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "111028009",
            "description": "Arteriopathic granular atrophy of cerebral cortex (disorder)",
            "attributes": null
          },
          {
            "code": "111033008",
            "description": "Circumscribed atrophy of brain (disorder)",
            "attributes": null
          },
          {
            "code": "11104006",
            "description": "Dilated cardiomyopathy secondary to Refsum's disease (disorder)",
            "attributes": null
          },
          {
            "code": "111296006",
            "description": "Basilar artery embolism (disorder)",
            "attributes": null
          },
          {
            "code": "111297002",
            "description": "Nonparalytic stroke (disorder)",
            "attributes": null
          },
          {
            "code": "111298007",
            "description": "Chronic cerebral ischemia (disorder)",
            "attributes": null
          },
          {
            "code": "111299004",
            "description": "Atheroma of cerebral arteries (disorder)",
            "attributes": null
          },
          {
            "code": "111337001",
            "description": "Dyke-Davidoff-Masson syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "111406002",
            "description": "Diffuse mesangial sclerosis (disorder)",
            "attributes": null
          },
          {
            "code": "111489007",
            "description": "Breathing-related sleep disorder (disorder)",
            "attributes": null
          },
          {
            "code": "111496009",
            "description": "Syringomyelia (disorder)",
            "attributes": null
          },
          {
            "code": "111497000",
            "description": "Arterial thrombosis of spinal cord (disorder)",
            "attributes": null
          },
          {
            "code": "111499002",
            "description": "DÃ©jÃ©rine-Sottas disease (disorder)",
            "attributes": null
          },
          {
            "code": "111500006",
            "description": "Muscular dystrophy-deafmutism syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "111501005",
            "description": "Congenital hereditary muscular dystrophy (disorder)",
            "attributes": null
          },
          {
            "code": "111502003",
            "description": "Fukuyama congenital muscular dystrophy (disorder)",
            "attributes": null
          },
          {
            "code": "111503008",
            "description": "Merosin deficient congenital muscular dystrophy (disorder)",
            "attributes": null
          },
          {
            "code": "111505001",
            "description": "Muscle-eye-brain disease, congenital muscular dystrophy (disorder)",
            "attributes": null
          },
          {
            "code": "111506000",
            "description": "Distal muscular dystrophy, Miyoshi type (disorder)",
            "attributes": null
          },
          {
            "code": "111508004",
            "description": "Emery-Dreifuss muscular dystrophy (disorder)",
            "attributes": null
          },
          {
            "code": "111532006",
            "description": "Strabismus in neuromuscular disorder (disorder)",
            "attributes": null
          },
          {
            "code": "11265003",
            "description": "Hemichorea (disorder)",
            "attributes": null
          },
          {
            "code": "1131000119105",
            "description": "Sequela of cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "11442006",
            "description": "Hereditary sensory neuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "116288000",
            "description": "Paralytic stroke (disorder)",
            "attributes": null
          },
          {
            "code": "118940003",
            "description": "Disorder of nervous system (disorder)",
            "attributes": null
          },
          {
            "code": "12056002",
            "description": "Seventh cranial nerve autonomic disorder (disorder)",
            "attributes": null
          },
          {
            "code": "12237911000119109",
            "description": "Amaurosis fugax of left eye (disorder)",
            "attributes": null
          },
          {
            "code": "12237951000119105",
            "description": "Amaurosis fugax of right eye (disorder)",
            "attributes": null
          },
          {
            "code": "12242711000119109",
            "description": "Weakness of left facial muscle due to and following cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "12242751000119105",
            "description": "Weakness of right facial muscle due to and following cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "12265261000119102",
            "description": "Benign extra-axial hygroma (disorder)",
            "attributes": null
          },
          {
            "code": "12367511000119101",
            "description": "Paraplegia due to and following cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "125081000119106",
            "description": "Cerebral infarction due to occlusion of precerebral artery (disorder)",
            "attributes": null
          },
          {
            "code": "126011000119107",
            "description": "Acquired caroticocavernous sinus fistula (disorder)",
            "attributes": null
          },
          {
            "code": "126534007",
            "description": "Mixed sensorimotor polyneuropathy due to diabetes mellitus (disorder)",
            "attributes": null
          },
          {
            "code": "126535008",
            "description": "Motor polyneuropathy due to diabetes mellitus (disorder)",
            "attributes": null
          },
          {
            "code": "126944002",
            "description": "Brain disorder resulting from a period of impaired oxygen delivery to the brain (disorder)",
            "attributes": null
          },
          {
            "code": "126979000",
            "description": "Neoplasm of autonomic nerve (disorder)",
            "attributes": null
          },
          {
            "code": "127011001",
            "description": "Sensory neuropathy due to diabetes mellitus (disorder)",
            "attributes": null
          },
          {
            "code": "127324008",
            "description": "Myoclonic disorder (disorder)",
            "attributes": null
          },
          {
            "code": "128078004",
            "description": "Polyradiculoneuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "128123007",
            "description": "Disorder of peripheral autonomic nervous system (disorder)",
            "attributes": null
          },
          {
            "code": "128128003",
            "description": "Disorder of cerebral cortex (disorder)",
            "attributes": null
          },
          {
            "code": "128171000119104",
            "description": "Spontaneous caroticocavernous sinus fistula (disorder)",
            "attributes": null
          },
          {
            "code": "128189008",
            "description": "Mononeuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "128192007",
            "description": "Peripheral neuritis (disorder)",
            "attributes": null
          },
          {
            "code": "128193002",
            "description": "Phrenic nerve disorder (disorder)",
            "attributes": null
          },
          {
            "code": "128200000",
            "description": "Complex regional pain syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "128203003",
            "description": "Hereditary motor and sensory neuropathy with optic atrophy (disorder)",
            "attributes": null
          },
          {
            "code": "128204009",
            "description": "Hereditary motor and sensory neuropathy with retinitis pigmentosa (disorder)",
            "attributes": null
          },
          {
            "code": "128205005",
            "description": "Hereditary sensory and autonomic neuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "128206006",
            "description": "Congenital sensory neuropathy with selective loss of small myelinated fibers (disorder)",
            "attributes": null
          },
          {
            "code": "128207002",
            "description": "Giant axonal neuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "128208007",
            "description": "Peripheral axonal neuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "128209004",
            "description": "Chronic inflammatory demyelinating polyradiculoneuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "128212001",
            "description": "Spinal muscular atrophy, type II (disorder)",
            "attributes": null
          },
          {
            "code": "128213006",
            "description": "Neuromuscular junction disorder (disorder)",
            "attributes": null
          },
          {
            "code": "128218002",
            "description": "Disorder of intracranial venous sinus (disorder)",
            "attributes": null
          },
          {
            "code": "128283000",
            "description": "Chronic nervous system disorder (disorder)",
            "attributes": null
          },
          {
            "code": "128328009",
            "description": "Suprasellar syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "128431009",
            "description": "Internal hydrocephalus (disorder)",
            "attributes": null
          },
          {
            "code": "12853006",
            "description": "Embolism of torcular Herophili (disorder)",
            "attributes": null
          },
          {
            "code": "128608001",
            "description": "Cerebral arterial aneurysm (disorder)",
            "attributes": null
          },
          {
            "code": "128609009",
            "description": "Intracranial aneurysm (disorder)",
            "attributes": null
          },
          {
            "code": "129131007",
            "description": "Acute infective polyneuritis (disorder)",
            "attributes": null
          },
          {
            "code": "129593003",
            "description": "Entrapment syndrome due to amyloid (disorder)",
            "attributes": null
          },
          {
            "code": "129596006",
            "description": "Menopausal muscular dystrophy syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "129608008",
            "description": "Progressive pyramidopallidal degeneration (disorder)",
            "attributes": null
          },
          {
            "code": "129609000",
            "description": "Spinocerebellar ataxia (disorder)",
            "attributes": null
          },
          {
            "code": "129611009",
            "description": "Ischemic peripheral neuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "129612002",
            "description": "Anterior ethmoidal nerve syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "129613007",
            "description": "Tympanic plexus neuralgia syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "129615000",
            "description": "Nucleus ambiguus-hypoglossal nerve syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "129616004",
            "description": "Porphyric polyneuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "129617008",
            "description": "Hepatic neuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "129618003",
            "description": "Autonomic dysreflexia (disorder)",
            "attributes": null
          },
          {
            "code": "129620000",
            "description": "Scapuloperoneal muscular dystrophy (disorder)",
            "attributes": null
          },
          {
            "code": "129621001",
            "description": "Nemaline myopathy, early onset type (disorder)",
            "attributes": null
          },
          {
            "code": "129622008",
            "description": "Nemaline myopathy, late onset type (disorder)",
            "attributes": null
          },
          {
            "code": "133301000119102",
            "description": "Degenerative brain disorder caused by alcohol (disorder)",
            "attributes": null
          },
          {
            "code": "133951000119104",
            "description": "Temporal lobe sclerosis (disorder)",
            "attributes": null
          },
          {
            "code": "133981000119106",
            "description": "Dysarthria as late effects of cerebrovascular disease (disorder)",
            "attributes": null
          },
          {
            "code": "133991000119109",
            "description": "Fluency disorder as sequela of cerebrovascular disease (disorder)",
            "attributes": null
          },
          {
            "code": "134771000119108",
            "description": "Alteration of sensation as late effect of stroke (disorder)",
            "attributes": null
          },
          {
            "code": "135491000119100",
            "description": "Myelopathy due to benign neoplastic disease (disorder)",
            "attributes": null
          },
          {
            "code": "135511000119105",
            "description": "Myelopathy due to malignant neoplastic disease (disorder)",
            "attributes": null
          },
          {
            "code": "135761000119101",
            "description": "Cerebral degeneration due to alcoholism (disorder)",
            "attributes": null
          },
          {
            "code": "135781000119105",
            "description": "Cerebral degeneration due to hypothyroidism (disorder)",
            "attributes": null
          },
          {
            "code": "135801000119109",
            "description": "Compression of brain due to focal lesion (disorder)",
            "attributes": null
          },
          {
            "code": "135811000119107",
            "description": "Lewy body dementia with behavioral disturbance (disorder)",
            "attributes": null
          },
          {
            "code": "13601000119109",
            "description": "Necrosis of central nervous system caused by exposure to ionizing radiation (disorder)",
            "attributes": null
          },
          {
            "code": "13694005",
            "description": "Sensory polyneuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "137991000119103",
            "description": "Seizure disorder as sequela of stroke (disorder)",
            "attributes": null
          },
          {
            "code": "1386000",
            "description": "Intracranial hemorrhage (disorder)",
            "attributes": null
          },
          {
            "code": "13950001",
            "description": "Bergeron's chorea (disorder)",
            "attributes": null
          },
          {
            "code": "140281000119108",
            "description": "Hemiparesis as late effect of cerebrovascular disease (disorder)",
            "attributes": null
          },
          {
            "code": "14055002",
            "description": "Hydrocephalus ex vacuo (disorder)",
            "attributes": null
          },
          {
            "code": "140881000119109",
            "description": "Compression of brain co-occurrent and due to spontaneous cerebral hemorrhage (disorder)",
            "attributes": null
          },
          {
            "code": "140911000119109",
            "description": "Ischemic stroke with coma (disorder)",
            "attributes": null
          },
          {
            "code": "140921000119102",
            "description": "Ischemic stroke without coma (disorder)",
            "attributes": null
          },
          {
            "code": "141091000119105",
            "description": "Compression of brain co-occurrent and due to nontraumatic subarachnoid hemorrhage (disorder)",
            "attributes": null
          },
          {
            "code": "141151000119101",
            "description": "Nontraumatic subdural hematoma with brain compression (disorder)",
            "attributes": null
          },
          {
            "code": "141991000119109",
            "description": "Delusions in Alzheimer's disease (disorder)",
            "attributes": null
          },
          {
            "code": "142001000119106",
            "description": "Depressed mood in Alzheimer's disease (disorder)",
            "attributes": null
          },
          {
            "code": "142011000119109",
            "description": "Alzheimer's disease co-occurrent with delirium (disorder)",
            "attributes": null
          },
          {
            "code": "142031000119104",
            "description": "Visual field defect due to and following cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "14246007",
            "description": "Embolism of intracranial venous sinus (disorder)",
            "attributes": null
          },
          {
            "code": "142851000119103",
            "description": "Spontaneous cerebellar hemorrhage (disorder)",
            "attributes": null
          },
          {
            "code": "14289006",
            "description": "Myopathy in hypopituitarism (disorder)",
            "attributes": null
          },
          {
            "code": "142971000119102",
            "description": "Encephalopathy caused by H1N1 influenza (disorder)",
            "attributes": null
          },
          {
            "code": "14309005",
            "description": "Anterior choroidal artery syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "143521000119103",
            "description": "Nontraumatic intraparenchymal cerebral hemorrhage (disorder)",
            "attributes": null
          },
          {
            "code": "14363008",
            "description": "Anterior spinal artery compression syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "14415006",
            "description": "Pneumocephalus (disorder)",
            "attributes": null
          },
          {
            "code": "145741000119101",
            "description": "Apraxia as late effect of cerebrovascular disease (disorder)",
            "attributes": null
          },
          {
            "code": "148871000119109",
            "description": "Weakness as a late effect of cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "14977000",
            "description": "Multiple AND bilateral precerebral artery thrombosis (disorder)",
            "attributes": null
          },
          {
            "code": "149821000119103",
            "description": "Cerebral infarction due to carotid artery occlusion (disorder)",
            "attributes": null
          },
          {
            "code": "15080006",
            "description": "Myotubular myopathy with type I atrophy (disorder)",
            "attributes": null
          },
          {
            "code": "1511000119107",
            "description": "Peripheral neuropathy due to type 2 diabetes mellitus (disorder)",
            "attributes": null
          },
          {
            "code": "15139001",
            "description": "Chronic brain-hydrocephalus syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "15241006",
            "description": "Disorder of autonomic nervous system (disorder)",
            "attributes": null
          },
          {
            "code": "15258001",
            "description": "Subclavian steal syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "15705007",
            "description": "Phlebitis of basilar sinus (disorder)",
            "attributes": null
          },
          {
            "code": "15732002",
            "description": "Secondary taste disorder (disorder)",
            "attributes": null
          },
          {
            "code": "15742000",
            "description": "Thrombosis of inferior sagittal sinus (disorder)",
            "attributes": null
          },
          {
            "code": "15758002",
            "description": "Disorder of meninges (disorder)",
            "attributes": null
          },
          {
            "code": "15782007",
            "description": "1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine-induced parkinsonism (disorder)",
            "attributes": null
          },
          {
            "code": "15802004",
            "description": "Dystonia (disorder)",
            "attributes": null
          },
          {
            "code": "1581000119101",
            "description": "Dementia of the Alzheimer type with behavioral disturbance (disorder)",
            "attributes": null
          },
          {
            "code": "15967141000119103",
            "description": "Steal syndrome of left subclavian artery (disorder)",
            "attributes": null
          },
          {
            "code": "15967181000119108",
            "description": "Subclavian steal syndrome of right subclavian artery (disorder)",
            "attributes": null
          },
          {
            "code": "15972821000119108",
            "description": "Radiculopathy of lumbosacral spine due to disc disorder (disorder)",
            "attributes": null
          },
          {
            "code": "15978431000119106",
            "description": "Thrombosis of right vertebral artery (disorder)",
            "attributes": null
          },
          {
            "code": "15978471000119109",
            "description": "Thrombosis of left vertebral artery (disorder)",
            "attributes": null
          },
          {
            "code": "15978551000119104",
            "description": "Myelopathy of thoracolumbar spine due to disc disorder (disorder)",
            "attributes": null
          },
          {
            "code": "15978631000119109",
            "description": "Occlusion of bilateral vertebral arteries (disorder)",
            "attributes": null
          },
          {
            "code": "15982271000119104",
            "description": "Weakness of right facial muscle due to and following cerebrovascular disease (disorder)",
            "attributes": null
          },
          {
            "code": "15982311000119104",
            "description": "Weakness of left facial muscle due to and following cerebrovascular disease (disorder)",
            "attributes": null
          },
          {
            "code": "15985791000119101",
            "description": "Dystonia of right hand (disorder)",
            "attributes": null
          },
          {
            "code": "15985831000119107",
            "description": "Dystonia of left hand (disorder)",
            "attributes": null
          },
          {
            "code": "15988351000119101",
            "description": "Acquired right carotid cavernous fistula (disorder)",
            "attributes": null
          },
          {
            "code": "15988391000119106",
            "description": "Acquired left carotid cavernous fistula (disorder)",
            "attributes": null
          },
          {
            "code": "16000351000119109",
            "description": "Cerebrovascular accident due to occlusion of left posterior cerebral artery (disorder)",
            "attributes": null
          },
          {
            "code": "16000391000119104",
            "description": "Cerebrovascular accident due to occlusion of right posterior cerebral artery (disorder)",
            "attributes": null
          },
          {
            "code": "16000431000119109",
            "description": "Cerebrovascular accident due to occlusion of right middle cerebral artery (disorder)",
            "attributes": null
          },
          {
            "code": "16000511000119103",
            "description": "Cerebrovascular accident due to occlusion of left middle cerebral artery (disorder)",
            "attributes": null
          },
          {
            "code": "16002031000119102",
            "description": "Cerebrovascular accident due to thrombus of right middle cerebral artery (disorder)",
            "attributes": null
          },
          {
            "code": "16002111000119106",
            "description": "Cerebrovascular accident due to thrombus of left middle cerebral artery (disorder)",
            "attributes": null
          },
          {
            "code": "16005191000119106",
            "description": "Neuralgic amyotrophy of left brachial plexus (disorder)",
            "attributes": null
          },
          {
            "code": "16005231000119102",
            "description": "Neuralgic amyotrophy of right brachial plexus (disorder)",
            "attributes": null
          },
          {
            "code": "16023911000119108",
            "description": "Cerebrovascular accident due to occlusion of right carotid artery (disorder)",
            "attributes": null
          },
          {
            "code": "16023991000119104",
            "description": "Cerebrovascular accident due to occlusion of left pontine artery (disorder)",
            "attributes": null
          },
          {
            "code": "16024031000119100",
            "description": "Cerebrovascular accident due to occlusion of right pontine artery (disorder)",
            "attributes": null
          },
          {
            "code": "16024111000119109",
            "description": "Cerebrovascular accident due to occlusion of left carotid artery (disorder)",
            "attributes": null
          },
          {
            "code": "16024151000119105",
            "description": "Cerebrovascular accident due to occlusion of left cerebellar artery (disorder)",
            "attributes": null
          },
          {
            "code": "16024271000119107",
            "description": "Cerebrovascular accident due to occlusion of right cerebellar artery (disorder)",
            "attributes": null
          },
          {
            "code": "16026471000119103",
            "description": "Disorder of right suprascapular nerve (disorder)",
            "attributes": null
          },
          {
            "code": "16026511000119107",
            "description": "Disorder of peripheral nerve of bilateral upper limbs (disorder)",
            "attributes": null
          },
          {
            "code": "16026551000119108",
            "description": "Peripheral neuropathy of bilateral lower limbs (disorder)",
            "attributes": null
          },
          {
            "code": "16026591000119103",
            "description": "Auriculotemporal syndrome of right auriculotemporal nerve (disorder)",
            "attributes": null
          },
          {
            "code": "16026631000119103",
            "description": "Auriculotemporal syndrome of left auriculotemporal nerve (disorder)",
            "attributes": null
          },
          {
            "code": "16026751000119100",
            "description": "Radiculopathy of thoracolumbar spine due to disc disorder (disorder)",
            "attributes": null
          },
          {
            "code": "16026871000119101",
            "description": "Disorder of left suprascapular nerve (disorder)",
            "attributes": null
          },
          {
            "code": "16026951000119102",
            "description": "Cerebrovascular accident due to stenosis of right carotid artery (disorder)",
            "attributes": null
          },
          {
            "code": "16026991000119107",
            "description": "Cerebrovascular accident due to stenosis of left carotid artery (disorder)",
            "attributes": null
          },
          {
            "code": "16053951000119108",
            "description": "Polyneuropathy caused by ionizing radiation (disorder)",
            "attributes": null
          },
          {
            "code": "16057431000119103",
            "description": "Disorder of right facial nerve (disorder)",
            "attributes": null
          },
          {
            "code": "16057951000119104",
            "description": "Disorder of left facial nerve (disorder)",
            "attributes": null
          },
          {
            "code": "16057991000119109",
            "description": "Disorder of left trigeminal nerve (disorder)",
            "attributes": null
          },
          {
            "code": "16058031000119107",
            "description": "Disorder of right trigeminal nerve (disorder)",
            "attributes": null
          },
          {
            "code": "16058431000119104",
            "description": "White matter disease (disorder)",
            "attributes": null
          },
          {
            "code": "16061002",
            "description": "Endophlebitis of lateral venous sinus (disorder)",
            "attributes": null
          },
          {
            "code": "16206981000119106",
            "description": "Entrapment of bilateral ilioinguinal nerves (disorder)",
            "attributes": null
          },
          {
            "code": "16218291000119100",
            "description": "Acute cerebral ischemia (disorder)",
            "attributes": null
          },
          {
            "code": "16219201000119101",
            "description": "Behavioral disturbance co-occurrent and due to late onset Alzheimer dementia (disorder)",
            "attributes": null
          },
          {
            "code": "16219341000119105",
            "description": "Myelopathy due to spinal cord compression (disorder)",
            "attributes": null
          },
          {
            "code": "16260551000119106",
            "description": "Dysphasia due to and following cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "16275741000119100",
            "description": "Severe pediatric obstructive sleep apnea (disorder)",
            "attributes": null
          },
          {
            "code": "163672003",
            "description": "On examination - Parkinsonian tremor (finding)",
            "attributes": null
          },
          {
            "code": "16371781000119100",
            "description": "Cerebellar stroke (disorder)",
            "attributes": null
          },
          {
            "code": "164018003",
            "description": "On examination - Horner's syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "164103002",
            "description": "On examination - cranial nerve 5 - palsy (disorder)",
            "attributes": null
          },
          {
            "code": "164109003",
            "description": "On examination - cranial nerve -palsy -upper motor neuron (disorder)",
            "attributes": null
          },
          {
            "code": "164110008",
            "description": "On examination - cranial 7 -paralysis-upper motor neuron (disorder)",
            "attributes": null
          },
          {
            "code": "164122006",
            "description": "On examination - cranial nerve 12 paralysis (disorder)",
            "attributes": null
          },
          {
            "code": "16418006",
            "description": "Embolism of basilar sinus (disorder)",
            "attributes": null
          },
          {
            "code": "16419651000119103",
            "description": "Dependence on biphasic positive airway pressure ventilation due to central sleep apnea syndrome (finding)",
            "attributes": null
          },
          {
            "code": "16476641000119100",
            "description": "Acquired arteriovenous fistula of dura of cerebrum (disorder)",
            "attributes": null
          },
          {
            "code": "16561007",
            "description": "Acute anoxic encephalopathy (disorder)",
            "attributes": null
          },
          {
            "code": "16576004",
            "description": "Shy-Drager syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "16631009",
            "description": "Transverse myelopathy syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "16644681000119102",
            "description": "Cerebrovascular accident due to occlusion of bilateral pontine arteries (disorder)",
            "attributes": null
          },
          {
            "code": "16661931000119102",
            "description": "Cerebrovascular accident due to stenosis of bilateral vertebral arteries (disorder)",
            "attributes": null
          },
          {
            "code": "16661971000119104",
            "description": "Cerebrovascular accident due to stenosis of bilateral carotid arteries (disorder)",
            "attributes": null
          },
          {
            "code": "16703551000119107",
            "description": "Memory deficit due to and following cerebrovascular disease (disorder)",
            "attributes": null
          },
          {
            "code": "16703661000119105",
            "description": "Memory deficit due to and following cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "16703761000119102",
            "description": "Memory deficit due to and following ischemic cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "16703821000119100",
            "description": "Memory deficit due to and following hemorrhagic cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "16709811000119106",
            "description": "Spontaneous hemorrhage of subarachnoid space from anterior communicating artery (disorder)",
            "attributes": null
          },
          {
            "code": "16818591000119108",
            "description": "Calcification of basal ganglia (disorder)",
            "attributes": null
          },
          {
            "code": "16851005",
            "description": "Mitochondrial myopathy (disorder)",
            "attributes": null
          },
          {
            "code": "16931000119102",
            "description": "Neurologic disorder due to degeneration of lumbar intervertebral disc (disorder)",
            "attributes": null
          },
          {
            "code": "17258002",
            "description": "Chronic anoxic encephalopathy (disorder)",
            "attributes": null
          },
          {
            "code": "1767005",
            "description": "Fisher's syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "17940001",
            "description": "Toxic neuromuscular junction disorder (disorder)",
            "attributes": null
          },
          {
            "code": "17944005",
            "description": "Cerebral calcification (disorder)",
            "attributes": null
          },
          {
            "code": "17974002",
            "description": "Post-herpetic trigeminal neuralgia (disorder)",
            "attributes": null
          },
          {
            "code": "180234006",
            "description": "Infectious disorder of the peripheral nervous system (disorder)",
            "attributes": null
          },
          {
            "code": "18058007",
            "description": "Phlebitis of intracranial venous sinus (disorder)",
            "attributes": null
          },
          {
            "code": "182747006",
            "description": "Westphal disease (disorder)",
            "attributes": null
          },
          {
            "code": "18322005",
            "description": "Thrombosis of torcular Herophili (disorder)",
            "attributes": null
          },
          {
            "code": "186567003",
            "description": "Rubella with neurological complication (disorder)",
            "attributes": null
          },
          {
            "code": "186707002",
            "description": "Human immunodeficiency virus infection with neurological disease (disorder)",
            "attributes": null
          },
          {
            "code": "186791009",
            "description": "Plasmodium falciparum malaria with cerebral complications (disorder)",
            "attributes": null
          },
          {
            "code": "186831000119104",
            "description": "Apraxia due to and following cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "18708008",
            "description": "Hypertrophic interstitial neuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "187331000119105",
            "description": "Arthropathy of pelvis due to neurological disorder (disorder)",
            "attributes": null
          },
          {
            "code": "18751000119106",
            "description": "Monoplegia of leg dominant side as sequela of cerebrovascular disease (disorder)",
            "attributes": null
          },
          {
            "code": "18761000119108",
            "description": "Monoplegia of arm dominant side as sequela of cerebrovascular disease (disorder)",
            "attributes": null
          },
          {
            "code": "18801000119100",
            "description": "Multiple cranial neuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "18842008",
            "description": "Corticobasal degeneration (disorder)",
            "attributes": null
          },
          {
            "code": "19091006",
            "description": "Pallidoluysian degeneration (disorder)",
            "attributes": null
          },
          {
            "code": "19109004",
            "description": "Syringomyelobulbia (disorder)",
            "attributes": null
          },
          {
            "code": "191471000",
            "description": "Korsakov's alcoholic psychosis with peripheral neuritis (disorder)",
            "attributes": null
          },
          {
            "code": "191505005",
            "description": "Acute confusional state, of cerebrovascular origin (disorder)",
            "attributes": null
          },
          {
            "code": "192730008",
            "description": "Toxic encephalitis (disorder)",
            "attributes": null
          },
          {
            "code": "192753009",
            "description": "Phlebitis and thrombophlebitis of intracranial sinuses (disorder)",
            "attributes": null
          },
          {
            "code": "192755002",
            "description": "Embolism superior longitudinal sinus (disorder)",
            "attributes": null
          },
          {
            "code": "192759008",
            "description": "Cerebral venous sinus thrombosis (disorder)",
            "attributes": null
          },
          {
            "code": "192760003",
            "description": "Thrombosis of superior longitudinal sinus (disorder)",
            "attributes": null
          },
          {
            "code": "192761004",
            "description": "Thrombosis transverse sinus (disorder)",
            "attributes": null
          },
          {
            "code": "192764007",
            "description": "Phlebitis cavernous sinus (disorder)",
            "attributes": null
          },
          {
            "code": "192765008",
            "description": "Phlebitis of superior longitudinal sinus (disorder)",
            "attributes": null
          },
          {
            "code": "192769002",
            "description": "Thrombophlebitis of central nervous system venous sinuses (disorder)",
            "attributes": null
          },
          {
            "code": "192770001",
            "description": "Thrombophlebitis of cavernous sinus (disorder)",
            "attributes": null
          },
          {
            "code": "192771002",
            "description": "Thrombophlebitis of superior longitudinal venous sinus (disorder)",
            "attributes": null
          },
          {
            "code": "192772009",
            "description": "Thrombophlebitis lateral venous sinus (disorder)",
            "attributes": null
          },
          {
            "code": "192775006",
            "description": "Late effects of intracranial abscess or pyogenic infection (disorder)",
            "attributes": null
          },
          {
            "code": "192791009",
            "description": "Cerebral degeneration in Gaucher's disease (disorder)",
            "attributes": null
          },
          {
            "code": "192792002",
            "description": "Cerebral degeneration in Niemann-Pick disease (disorder)",
            "attributes": null
          },
          {
            "code": "192794001",
            "description": "Cerebral degeneration associated with another disorder (disorder)",
            "attributes": null
          },
          {
            "code": "192796004",
            "description": "Cerebral degeneration in mucopolysaccharidosis (disorder)",
            "attributes": null
          },
          {
            "code": "192805000",
            "description": "Acquired communicating hydrocephalus (disorder)",
            "attributes": null
          },
          {
            "code": "192811002",
            "description": "Alcoholic encephalopathy (disorder)",
            "attributes": null
          },
          {
            "code": "192813004",
            "description": "Cerebral degeneration due to cerebrovascular disease (disorder)",
            "attributes": null
          },
          {
            "code": "192815006",
            "description": "Cerebral degeneration due to neoplastic disease (disorder)",
            "attributes": null
          },
          {
            "code": "192816007",
            "description": "Myxedema encephalopathy (disorder)",
            "attributes": null
          },
          {
            "code": "192817003",
            "description": "Cerebral degeneration due to vitamin B12 deficiency (disorder)",
            "attributes": null
          },
          {
            "code": "192859002",
            "description": "Fragments of torsion dystonia (disorder)",
            "attributes": null
          },
          {
            "code": "192871008",
            "description": "Early onset cerebellar ataxia with myoclonus (disorder)",
            "attributes": null
          },
          {
            "code": "192874000",
            "description": "Cerebellar ataxia associated with another disorder (disorder)",
            "attributes": null
          },
          {
            "code": "192876003",
            "description": "Myxedema cerebellar degeneration (disorder)",
            "attributes": null
          },
          {
            "code": "192877007",
            "description": "Paraneoplastic cerebellar degeneration (disorder)",
            "attributes": null
          },
          {
            "code": "192894009",
            "description": "Syringomyelia and syringobulbia (disorder)",
            "attributes": null
          },
          {
            "code": "192897002",
            "description": "Myelopathy due to acute infarction of spinal cord (disorder)",
            "attributes": null
          },
          {
            "code": "192898007",
            "description": "Myelopathy due to arterial thrombosis of spinal cord (disorder)",
            "attributes": null
          },
          {
            "code": "192899004",
            "description": "Myelopathy due to edema of spinal cord (disorder)",
            "attributes": null
          },
          {
            "code": "192900009",
            "description": "Myelopathy due to hematomyelia (disorder)",
            "attributes": null
          },
          {
            "code": "192904000",
            "description": "Myelopathy due to another disorder (disorder)",
            "attributes": null
          },
          {
            "code": "192905004",
            "description": "Myelopathy due to intervertebral disc disease (disorder)",
            "attributes": null
          },
          {
            "code": "192906003",
            "description": "Myelopathy due to neoplastic disease (disorder)",
            "attributes": null
          },
          {
            "code": "192907007",
            "description": "Myelopathy due to spondylosis (disorder)",
            "attributes": null
          },
          {
            "code": "192915005",
            "description": "Cervical sympathetic paralysis (disorder)",
            "attributes": null
          },
          {
            "code": "192918007",
            "description": "Autonomic neuropathy due to amyloidosis (disorder)",
            "attributes": null
          },
          {
            "code": "192926004",
            "description": "Multiple sclerosis of the brainstem (disorder)",
            "attributes": null
          },
          {
            "code": "192927008",
            "description": "Multiple sclerosis of the spinal cord (disorder)",
            "attributes": null
          },
          {
            "code": "192929006",
            "description": "Exacerbation of multiple sclerosis (disorder)",
            "attributes": null
          },
          {
            "code": "192976002",
            "description": "Progressive supranuclear palsy (disorder)",
            "attributes": null
          },
          {
            "code": "19303008",
            "description": "Alcohol myopathy (disorder)",
            "attributes": null
          },
          {
            "code": "193042000",
            "description": "Cataplexy and narcolepsy (disorder)",
            "attributes": null
          },
          {
            "code": "193071004",
            "description": "Adhesions - cerebral meninges (disorder)",
            "attributes": null
          },
          {
            "code": "193072006",
            "description": "Adhesions - spinal meninges (disorder)",
            "attributes": null
          },
          {
            "code": "193073001",
            "description": "Cyst of spinal meninges (disorder)",
            "attributes": null
          },
          {
            "code": "193093009",
            "description": "Bell's palsy (disorder)",
            "attributes": null
          },
          {
            "code": "193101001",
            "description": "Multiple cranial nerve palsies in sarcoidosis (disorder)",
            "attributes": null
          },
          {
            "code": "193102008",
            "description": "Multiple cranial nerve palsies in neoplastic disease (disorder)",
            "attributes": null
          },
          {
            "code": "193114000",
            "description": "Phantom limb (disorder)",
            "attributes": null
          },
          {
            "code": "193116003",
            "description": "Phantom limb syndrome without pain (disorder)",
            "attributes": null
          },
          {
            "code": "193118002",
            "description": "Nerve root and plexus compressions in neoplastic disease (disorder)",
            "attributes": null
          },
          {
            "code": "193119005",
            "description": "Nerve root and plexus compressions in intervertebral disc disorders (disorder)",
            "attributes": null
          },
          {
            "code": "193120004",
            "description": "Nerve root and plexus compressions in spondylosis (disorder)",
            "attributes": null
          },
          {
            "code": "193141005",
            "description": "Mononeuritis multiplex due to diabetes mellitus (disorder)",
            "attributes": null
          },
          {
            "code": "193165008",
            "description": "Neuropathy in association with hereditary ataxia (disorder)",
            "attributes": null
          },
          {
            "code": "193174005",
            "description": "Post-infectious polyneuritis (disorder)",
            "attributes": null
          },
          {
            "code": "193177003",
            "description": "Polyneuropathy in collagen vascular disease (disorder)",
            "attributes": null
          },
          {
            "code": "193178008",
            "description": "Polyneuropathy in disseminated lupus erythematosus (disorder)",
            "attributes": null
          },
          {
            "code": "193179000",
            "description": "Polyneuropathy in polyarteritis nodosa (disorder)",
            "attributes": null
          },
          {
            "code": "193180002",
            "description": "Polyneuropathy in rheumatoid arthritis (disorder)",
            "attributes": null
          },
          {
            "code": "193183000",
            "description": "Acute painful neuropathy due to diabetes mellitus (disorder)",
            "attributes": null
          },
          {
            "code": "193184006",
            "description": "Chronic painful neuropathy due to diabetes mellitus (disorder)",
            "attributes": null
          },
          {
            "code": "193185007",
            "description": "Asymptomatic neuropathy due to diabetes mellitus (disorder)",
            "attributes": null
          },
          {
            "code": "193186008",
            "description": "Polyneuropathy associated with another disorder (disorder)",
            "attributes": null
          },
          {
            "code": "193187004",
            "description": "Polyneuropathy due to amyloidosis (disorder)",
            "attributes": null
          },
          {
            "code": "193191009",
            "description": "Neuropathy associated with hypoglycemia (disorder)",
            "attributes": null
          },
          {
            "code": "193195000",
            "description": "Sarcoid neuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "193196004",
            "description": "Uremic polyneuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "193203006",
            "description": "Serum neuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "193207007",
            "description": "Juvenile or adult myasthenia gravis (disorder)",
            "attributes": null
          },
          {
            "code": "193209005",
            "description": "Myasthenic syndrome due to another disorder (disorder)",
            "attributes": null
          },
          {
            "code": "193212008",
            "description": "Myasthenic syndrome due to hypothyroidism (disorder)",
            "attributes": null
          },
          {
            "code": "193213003",
            "description": "Myasthenic syndrome due to pernicious anemia (disorder)",
            "attributes": null
          },
          {
            "code": "193214009",
            "description": "Myasthenic syndrome due to thyrotoxicosis (disorder)",
            "attributes": null
          },
          {
            "code": "193222002",
            "description": "Benign congenital myopathy (disorder)",
            "attributes": null
          },
          {
            "code": "193225000",
            "description": "Hereditary progressive muscular dystrophy (disorder)",
            "attributes": null
          },
          {
            "code": "193227008",
            "description": "Pelvic muscular dystrophy (disorder)",
            "attributes": null
          },
          {
            "code": "193230001",
            "description": "Distal muscular dystrophy with juvenile onset (disorder)",
            "attributes": null
          },
          {
            "code": "193237003",
            "description": "Myotonic disorder (disorder)",
            "attributes": null
          },
          {
            "code": "193238008",
            "description": "Infantile myotonia (disorder)",
            "attributes": null
          },
          {
            "code": "193246009",
            "description": "Symptomatic inflammatory myopathy associated with another disorder (disorder)",
            "attributes": null
          },
          {
            "code": "193247000",
            "description": "Amyloid myopathy (disorder)",
            "attributes": null
          },
          {
            "code": "193248005",
            "description": "Myopathy due to disseminated lupus erythematosus (disorder)",
            "attributes": null
          },
          {
            "code": "193249002",
            "description": "Myopathy due to polyarteritis nodosa (disorder)",
            "attributes": null
          },
          {
            "code": "193250002",
            "description": "Myopathy due to rheumatoid arthritis (disorder)",
            "attributes": null
          },
          {
            "code": "193251003",
            "description": "Sarcoid myopathy (disorder)",
            "attributes": null
          },
          {
            "code": "193252005",
            "description": "Myopathy due to scleroderma (disorder)",
            "attributes": null
          },
          {
            "code": "193253000",
            "description": "Myopathy due to SjÃ¶gren's disease (disorder)",
            "attributes": null
          },
          {
            "code": "193255007",
            "description": "Proximal myopathy (disorder)",
            "attributes": null
          },
          {
            "code": "19378003",
            "description": "Pseudotabes due to diabetes mellitus (disorder)",
            "attributes": null
          },
          {
            "code": "193950006",
            "description": "Sensory disorder of eyelid (disorder)",
            "attributes": null
          },
          {
            "code": "194457007",
            "description": "Sequelae of inflammatory diseases of the central nervous system (disorder)",
            "attributes": null
          },
          {
            "code": "195030007",
            "description": "Cardiomyopathy in Friedreich's ataxia (disorder)",
            "attributes": null
          },
          {
            "code": "195031006",
            "description": "Cardiomyopathy in myotonic dystrophy (disorder)",
            "attributes": null
          },
          {
            "code": "195154000",
            "description": "Ruptured berry aneurysm (disorder)",
            "attributes": null
          },
          {
            "code": "195155004",
            "description": "Subarachnoid hemorrhage from carotid siphon and bifurcation (disorder)",
            "attributes": null
          },
          {
            "code": "195165005",
            "description": "Basal ganglia hemorrhage (disorder)",
            "attributes": null
          },
          {
            "code": "195167002",
            "description": "External capsule hemorrhage (disorder)",
            "attributes": null
          },
          {
            "code": "195168007",
            "description": "Intracerebral hemorrhage with intraventricular hemorrhage (disorder)",
            "attributes": null
          },
          {
            "code": "195169004",
            "description": "Intracerebral hemorrhage, multiple localized (disorder)",
            "attributes": null
          },
          {
            "code": "195176009",
            "description": "Non-traumatic intracranial subdural hemorrhage (disorder)",
            "attributes": null
          },
          {
            "code": "195180004",
            "description": "Basilar artery occlusion (disorder)",
            "attributes": null
          },
          {
            "code": "195182007",
            "description": "Vertebral artery occlusion (disorder)",
            "attributes": null
          },
          {
            "code": "195183002",
            "description": "Multiple and bilateral precerebral arterial occlusion (disorder)",
            "attributes": null
          },
          {
            "code": "195185009",
            "description": "Cerebral infarct due to thrombosis of precerebral arteries (disorder)",
            "attributes": null
          },
          {
            "code": "195186005",
            "description": "Cerebral infarction due to embolism of precerebral arteries (disorder)",
            "attributes": null
          },
          {
            "code": "195189003",
            "description": "Cerebral infarction due to thrombosis of cerebral arteries (disorder)",
            "attributes": null
          },
          {
            "code": "195190007",
            "description": "Cerebral infarction due to embolism of cerebral arteries (disorder)",
            "attributes": null
          },
          {
            "code": "195199008",
            "description": "Vertebrobasilar artery syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "195200006",
            "description": "Carotid artery syndrome hemispheric (disorder)",
            "attributes": null
          },
          {
            "code": "195206000",
            "description": "Intermittent cerebral ischemia (disorder)",
            "attributes": null
          },
          {
            "code": "195209007",
            "description": "Middle cerebral artery syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "195210002",
            "description": "Anterior cerebral artery syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "195211003",
            "description": "Posterior cerebral artery syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "195212005",
            "description": "Brainstem stroke syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "195213000",
            "description": "Cerebellar stroke syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "195216008",
            "description": "Left sided cerebral hemisphere cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "195217004",
            "description": "Right sided cerebral hemisphere cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "195229008",
            "description": "Non-pyogenic venous sinus thrombosis (disorder)",
            "attributes": null
          },
          {
            "code": "195230003",
            "description": "Cerebral infarction due to cerebral venous thrombosis, non-pyogenic (disorder)",
            "attributes": null
          },
          {
            "code": "195232006",
            "description": "Occlusion and stenosis of middle cerebral artery (disorder)",
            "attributes": null
          },
          {
            "code": "195233001",
            "description": "Occlusion and stenosis of anterior cerebral artery (disorder)",
            "attributes": null
          },
          {
            "code": "195234007",
            "description": "Occlusion and stenosis of posterior cerebral artery (disorder)",
            "attributes": null
          },
          {
            "code": "195235008",
            "description": "Occlusion and stenosis of cerebellar arteries (disorder)",
            "attributes": null
          },
          {
            "code": "195236009",
            "description": "Occlusion and stenosis of multiple and bilateral cerebral arteries (disorder)",
            "attributes": null
          },
          {
            "code": "195239002",
            "description": "Late effects of cerebrovascular disease (disorder)",
            "attributes": null
          },
          {
            "code": "195240000",
            "description": "Sequelae of subarachnoid hemorrhage (disorder)",
            "attributes": null
          },
          {
            "code": "195241001",
            "description": "Sequelae of intracerebral hemorrhage (disorder)",
            "attributes": null
          },
          {
            "code": "195243003",
            "description": "Sequelae of cerebral infarction (disorder)",
            "attributes": null
          },
          {
            "code": "195373009",
            "description": "Anterior spinal and vertebral artery compression syndromes (disorder)",
            "attributes": null
          },
          {
            "code": "19557000",
            "description": "Hyperexplexia (finding)",
            "attributes": null
          },
          {
            "code": "19972008",
            "description": "Postencephalitic parkinsonism (disorder)",
            "attributes": null
          },
          {
            "code": "20059004",
            "description": "Occlusion of cerebral artery (disorder)",
            "attributes": null
          },
          {
            "code": "202661006",
            "description": "Single-level cervical spondylosis with myelopathy (disorder)",
            "attributes": null
          },
          {
            "code": "202662004",
            "description": "Two-level cervical spondylosis with myelopathy (disorder)",
            "attributes": null
          },
          {
            "code": "202663009",
            "description": "Multiple-level cervical spondylosis with myelopathy (disorder)",
            "attributes": null
          },
          {
            "code": "202664003",
            "description": "Cervical myelopathy (disorder)",
            "attributes": null
          },
          {
            "code": "202670009",
            "description": "Single-level thoracic spondylosis with myelopathy (disorder)",
            "attributes": null
          },
          {
            "code": "202671008",
            "description": "Two-level thoracic spondylosis with myelopathy (disorder)",
            "attributes": null
          },
          {
            "code": "202672001",
            "description": "Multiple-level thoracic spondylosis with myelopathy (disorder)",
            "attributes": null
          },
          {
            "code": "202677007",
            "description": "Lumbosacral spondylosis with myelopathy (disorder)",
            "attributes": null
          },
          {
            "code": "202678002",
            "description": "Single-level lumbosacral spondylosis with myelopathy (disorder)",
            "attributes": null
          },
          {
            "code": "202679005",
            "description": "Two-level lumbosacral spondylosis with myelopathy (disorder)",
            "attributes": null
          },
          {
            "code": "202680008",
            "description": "Multiple-level lumbosacral spondylosis with myelopathy (disorder)",
            "attributes": null
          },
          {
            "code": "202683005",
            "description": "Cervical spondylosis with radiculopathy (disorder)",
            "attributes": null
          },
          {
            "code": "202684004",
            "description": "Single-level cervical spondylosis with radiculopathy (disorder)",
            "attributes": null
          },
          {
            "code": "202685003",
            "description": "Two-level cervical spondylosis with radiculopathy (disorder)",
            "attributes": null
          },
          {
            "code": "202686002",
            "description": "Multiple-level cervical spondylosis with radiculopathy (disorder)",
            "attributes": null
          },
          {
            "code": "202728009",
            "description": "Disc prolapse with myelopathy (disorder)",
            "attributes": null
          },
          {
            "code": "202729001",
            "description": "Cervical disc prolapse with myelopathy (disorder)",
            "attributes": null
          },
          {
            "code": "202730006",
            "description": "Thoracic disc prolapse with myelopathy (disorder)",
            "attributes": null
          },
          {
            "code": "202731005",
            "description": "Lumbar disc prolapse with myelopathy (disorder)",
            "attributes": null
          },
          {
            "code": "202732003",
            "description": "Disc prolapse with radiculopathy (disorder)",
            "attributes": null
          },
          {
            "code": "202733008",
            "description": "Cervical disc prolapse with radiculopathy (disorder)",
            "attributes": null
          },
          {
            "code": "202734002",
            "description": "Thoracic disc prolapse with radiculopathy (disorder)",
            "attributes": null
          },
          {
            "code": "202735001",
            "description": "Lumbar disc prolapse with radiculopathy (disorder)",
            "attributes": null
          },
          {
            "code": "20305008",
            "description": "Congenital myotonia, autosomal recessive form (disorder)",
            "attributes": null
          },
          {
            "code": "2032001",
            "description": "Cerebral edema (disorder)",
            "attributes": null
          },
          {
            "code": "20415001",
            "description": "Progressive sclerosing poliodystrophy (disorder)",
            "attributes": null
          },
          {
            "code": "20447006",
            "description": "Plasma cell dyscrasia with polyneuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "20725005",
            "description": "Familial visceral neuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "20801005",
            "description": "Secondary acid taste disorder (disorder)",
            "attributes": null
          },
          {
            "code": "20908003",
            "description": "Subcortical cerebral hemorrhage (disorder)",
            "attributes": null
          },
          {
            "code": "21018002",
            "description": "Inflammatory neuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "21201006",
            "description": "Sporadic cerebellar degeneration (disorder)",
            "attributes": null
          },
          {
            "code": "212239002",
            "description": "Cervical sympathetic nerve injury (disorder)",
            "attributes": null
          },
          {
            "code": "212242008",
            "description": "Injury of celiac ganglion (disorder)",
            "attributes": null
          },
          {
            "code": "212243003",
            "description": "Injury of celiac plexus (disorder)",
            "attributes": null
          },
          {
            "code": "212244009",
            "description": "Injury of thoracic sympathetic nerves (disorder)",
            "attributes": null
          },
          {
            "code": "212246006",
            "description": "Intercostal nerve injury (disorder)",
            "attributes": null
          },
          {
            "code": "21233002",
            "description": "Meningeal hemorrhage (disorder)",
            "attributes": null
          },
          {
            "code": "21258007",
            "description": "Thrombosis of lateral venous sinus (disorder)",
            "attributes": null
          },
          {
            "code": "213208008",
            "description": "Anoxic brain damage complication (disorder)",
            "attributes": null
          },
          {
            "code": "213209000",
            "description": "Cerebral anoxia complication (disorder)",
            "attributes": null
          },
          {
            "code": "21361000119109",
            "description": "Paraneoplastic peripheral neuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "21454007",
            "description": "Subarachnoid intracranial hemorrhage (disorder)",
            "attributes": null
          },
          {
            "code": "2177002",
            "description": "Postherpetic neuralgia (disorder)",
            "attributes": null
          },
          {
            "code": "21921000119103",
            "description": "Dementia co-occurrent and due to Pick's disease (disorder)",
            "attributes": null
          },
          {
            "code": "22126005",
            "description": "Hereditary neuraxial edema (disorder)",
            "attributes": null
          },
          {
            "code": "224186005",
            "description": "Cerebellar deficiency syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "22443004",
            "description": "Vestibulocerebellar ataxia (disorder)",
            "attributes": null
          },
          {
            "code": "22451001",
            "description": "Idiopathic torsion dystonia (disorder)",
            "attributes": null
          },
          {
            "code": "22722001",
            "description": "Idiopathic peripheral neuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "22811006",
            "description": "Leukoencephalopathy (disorder)",
            "attributes": null
          },
          {
            "code": "229221000119103",
            "description": "Myopathy due to Cushing's syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "229692002",
            "description": "Oral dystonia (disorder)",
            "attributes": null
          },
          {
            "code": "229694001",
            "description": "Oral dyskinesia (disorder)",
            "attributes": null
          },
          {
            "code": "230197009",
            "description": "Acute viral transverse myelitis (disorder)",
            "attributes": null
          },
          {
            "code": "230198004",
            "description": "Varicella transverse myelitis (disorder)",
            "attributes": null
          },
          {
            "code": "230202002",
            "description": "Vacuolar myelopathy (disorder)",
            "attributes": null
          },
          {
            "code": "230220006",
            "description": "Intracranial septic embolism (disorder)",
            "attributes": null
          },
          {
            "code": "230221005",
            "description": "Intracranial arterial septic embolism (disorder)",
            "attributes": null
          },
          {
            "code": "230222003",
            "description": "Septic thrombophlebitis of straight sinus (disorder)",
            "attributes": null
          },
          {
            "code": "230224002",
            "description": "Septic thrombophlebitis of cortical vein (disorder)",
            "attributes": null
          },
          {
            "code": "230225001",
            "description": "Septic thrombophlebitis of great cerebral vein (disorder)",
            "attributes": null
          },
          {
            "code": "230226000",
            "description": "System disorder of the nervous system (disorder)",
            "attributes": null
          },
          {
            "code": "230227009",
            "description": "Early onset cerebellar ataxia (disorder)",
            "attributes": null
          },
          {
            "code": "230228004",
            "description": "Early onset cerebellar ataxia with retained tendon reflexes (disorder)",
            "attributes": null
          },
          {
            "code": "230229007",
            "description": "Early onset cerebellar ataxia with hypogonadism (disorder)",
            "attributes": null
          },
          {
            "code": "230230002",
            "description": "Early onset cerebellar ataxia with retinitis pigmentosa and optic atrophy (disorder)",
            "attributes": null
          },
          {
            "code": "230231003",
            "description": "Early onset cerebellar ataxia with essential tremor (disorder)",
            "attributes": null
          },
          {
            "code": "230233000",
            "description": "Progressive cerebellar ataxia (disorder)",
            "attributes": null
          },
          {
            "code": "230234006",
            "description": "Periodic ataxia (disorder)",
            "attributes": null
          },
          {
            "code": "230235007",
            "description": "Olivopontocerebellar atrophy with slow eye movement (disorder)",
            "attributes": null
          },
          {
            "code": "230236008",
            "description": "Olivopontocerebellar atrophy with blindness (disorder)",
            "attributes": null
          },
          {
            "code": "230237004",
            "description": "Progressive spinocerebellar ataxia with decreased tendon reflexes (disorder)",
            "attributes": null
          },
          {
            "code": "230240004",
            "description": "Progressive cerebellar ataxia with hypogonadism (disorder)",
            "attributes": null
          },
          {
            "code": "230241000",
            "description": "Secondary cerebellar degeneration (disorder)",
            "attributes": null
          },
          {
            "code": "230246005",
            "description": "Progressive bulbar palsy of childhood (disorder)",
            "attributes": null
          },
          {
            "code": "230247001",
            "description": "Distal spinal muscular atrophy (disorder)",
            "attributes": null
          },
          {
            "code": "230248006",
            "description": "Scapuloperoneal spinal muscular atrophy (disorder)",
            "attributes": null
          },
          {
            "code": "230249003",
            "description": "Facioscapulohumeral spinal muscular atrophy (disorder)",
            "attributes": null
          },
          {
            "code": "230250003",
            "description": "Facioscapulohumeral spinal muscular atrophy with sensory loss (disorder)",
            "attributes": null
          },
          {
            "code": "230251004",
            "description": "Scapulohumeral spinal muscular atrophy (disorder)",
            "attributes": null
          },
          {
            "code": "230252006",
            "description": "Oculopharyngeal spinal muscular atrophy (disorder)",
            "attributes": null
          },
          {
            "code": "230253001",
            "description": "Bulbospinal neuronopathy (disorder)",
            "attributes": null
          },
          {
            "code": "230254007",
            "description": "Western Pacific motor neurone disease (disorder)",
            "attributes": null
          },
          {
            "code": "230255008",
            "description": "Madras-type motor neurone disease (disorder)",
            "attributes": null
          },
          {
            "code": "230256009",
            "description": "Benign monomelic amyotrophy (disorder)",
            "attributes": null
          },
          {
            "code": "230257000",
            "description": "Paraneoplastic motor neurone disease (disorder)",
            "attributes": null
          },
          {
            "code": "230258005",
            "description": "Amyotrophic lateral sclerosis with dementia (disorder)",
            "attributes": null
          },
          {
            "code": "230260007",
            "description": "Pure hereditary spastic paraplegia (disorder)",
            "attributes": null
          },
          {
            "code": "230261006",
            "description": "Complicated hereditary spastic paraplegia (disorder)",
            "attributes": null
          },
          {
            "code": "230264003",
            "description": "Troyer syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "230265002",
            "description": "Familial Alzheimer's disease of early onset (disorder)",
            "attributes": null
          },
          {
            "code": "230266001",
            "description": "Non-familial Alzheimer's disease of early onset (disorder)",
            "attributes": null
          },
          {
            "code": "230267005",
            "description": "Familial Alzheimer's disease of late onset (disorder)",
            "attributes": null
          },
          {
            "code": "230268000",
            "description": "Non-familial Alzheimer's disease of late onset (disorder)",
            "attributes": null
          },
          {
            "code": "230269008",
            "description": "Focal Alzheimer's disease (disorder)",
            "attributes": null
          },
          {
            "code": "230271008",
            "description": "Pick's disease with Pick bodies (disorder)",
            "attributes": null
          },
          {
            "code": "230272001",
            "description": "Pick's disease with Pick cells and no Pick bodies (disorder)",
            "attributes": null
          },
          {
            "code": "230273006",
            "description": "Frontotemporal degeneration (disorder)",
            "attributes": null
          },
          {
            "code": "230274000",
            "description": "Frontal lobe degeneration with motor neurone disease (disorder)",
            "attributes": null
          },
          {
            "code": "230278002",
            "description": "Progressive aphasia (disorder)",
            "attributes": null
          },
          {
            "code": "230279005",
            "description": "Non-Alzheimer's progressive dysphasia (disorder)",
            "attributes": null
          },
          {
            "code": "230280008",
            "description": "Progressive aphasia in Alzheimer's disease (disorder)",
            "attributes": null
          },
          {
            "code": "230281007",
            "description": "Argyrophilic grain disease (disorder)",
            "attributes": null
          },
          {
            "code": "230291001",
            "description": "Juvenile Parkinson's disease (disorder)",
            "attributes": null
          },
          {
            "code": "230292008",
            "description": "Secondary parkinsonism (disorder)",
            "attributes": null
          },
          {
            "code": "230293003",
            "description": "Carbon monoxide-induced parkinsonism (disorder)",
            "attributes": null
          },
          {
            "code": "230294009",
            "description": "Manganese-induced parkinsonism (disorder)",
            "attributes": null
          },
          {
            "code": "230295005",
            "description": "Parkinsonism with calcification of basal ganglia (disorder)",
            "attributes": null
          },
          {
            "code": "230296006",
            "description": "Vascular parkinsonism (disorder)",
            "attributes": null
          },
          {
            "code": "230297002",
            "description": "Multiple system atrophy (disorder)",
            "attributes": null
          },
          {
            "code": "230298007",
            "description": "Disorder presenting primarily with chorea (disorder)",
            "attributes": null
          },
          {
            "code": "230299004",
            "description": "Juvenile onset Huntington's disease (disorder)",
            "attributes": null
          },
          {
            "code": "230300007",
            "description": "Late onset Huntington's disease (disorder)",
            "attributes": null
          },
          {
            "code": "230301006",
            "description": "Akinetic-rigid form of Huntington's disease (disorder)",
            "attributes": null
          },
          {
            "code": "230302004",
            "description": "Pallidal degeneration (disorder)",
            "attributes": null
          },
          {
            "code": "230305002",
            "description": "Chronic hepatocerebral degeneration (disorder)",
            "attributes": null
          },
          {
            "code": "230306001",
            "description": "Benign hereditary chorea (disorder)",
            "attributes": null
          },
          {
            "code": "230307005",
            "description": "Chorea in systemic lupus erythematosus (disorder)",
            "attributes": null
          },
          {
            "code": "230309008",
            "description": "Kinesiogenic choreoathetosis (disorder)",
            "attributes": null
          },
          {
            "code": "230310003",
            "description": "Paroxysmal dystonia (disorder)",
            "attributes": null
          },
          {
            "code": "230311004",
            "description": "Basal ganglia degeneration with calcification (disorder)",
            "attributes": null
          },
          {
            "code": "230312006",
            "description": "Aicardi Goutieres syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "230313001",
            "description": "Autosomal dominant late onset basal ganglia degeneration (disorder)",
            "attributes": null
          },
          {
            "code": "230318005",
            "description": "Idiopathic familial dystonia (disorder)",
            "attributes": null
          },
          {
            "code": "230319002",
            "description": "Autosomal dominant idiopathic familial dystonia (disorder)",
            "attributes": null
          },
          {
            "code": "230320008",
            "description": "Autosomal recessive idiopathic familial dystonia (disorder)",
            "attributes": null
          },
          {
            "code": "230321007",
            "description": "Idiopathic non-familial dystonia (disorder)",
            "attributes": null
          },
          {
            "code": "230322000",
            "description": "Isolated cervical dystonia (disorder)",
            "attributes": null
          },
          {
            "code": "230325003",
            "description": "Meige syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "230326002",
            "description": "Idiopathic orofacial dystonia (disorder)",
            "attributes": null
          },
          {
            "code": "230327006",
            "description": "Edentulous orofacial dystonia (disorder)",
            "attributes": null
          },
          {
            "code": "230328001",
            "description": "Isolated oromandibular dystonia (disorder)",
            "attributes": null
          },
          {
            "code": "230329009",
            "description": "Posthemiplegic dystonia (disorder)",
            "attributes": null
          },
          {
            "code": "230330004",
            "description": "Occupational dystonia (disorder)",
            "attributes": null
          },
          {
            "code": "230332007",
            "description": "Diurnal dystonia (disorder)",
            "attributes": null
          },
          {
            "code": "230343004",
            "description": "Symptomatic myoclonus (disorder)",
            "attributes": null
          },
          {
            "code": "230344005",
            "description": "Post-anoxic myoclonus (disorder)",
            "attributes": null
          },
          {
            "code": "230345006",
            "description": "Postencephalitic myoclonus (disorder)",
            "attributes": null
          },
          {
            "code": "230347003",
            "description": "Segmental cord myoclonus (disorder)",
            "attributes": null
          },
          {
            "code": "230348008",
            "description": "Palatal-tympanic myoclonus (disorder)",
            "attributes": null
          },
          {
            "code": "230349000",
            "description": "Hyoid myoclonus (disorder)",
            "attributes": null
          },
          {
            "code": "230350000",
            "description": "Opsoclonus-myoclonus syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "230352008",
            "description": "Encephalopathy due to vitamin deficiency (disorder)",
            "attributes": null
          },
          {
            "code": "230353003",
            "description": "Morel laminar sclerosis (disorder)",
            "attributes": null
          },
          {
            "code": "230355005",
            "description": "Encephalopathy caused by heavy metal (disorder)",
            "attributes": null
          },
          {
            "code": "230357002",
            "description": "Urate encephalopathy (disorder)",
            "attributes": null
          },
          {
            "code": "230358007",
            "description": "Hyponatremic encephalopathy (disorder)",
            "attributes": null
          },
          {
            "code": "230359004",
            "description": "Secondary amyloid encephalopathy (disorder)",
            "attributes": null
          },
          {
            "code": "230360009",
            "description": "Encephalopathy caused by radiation damage (disorder)",
            "attributes": null
          },
          {
            "code": "230363006",
            "description": "Progressive neuronal degeneration of childhood (disorder)",
            "attributes": null
          },
          {
            "code": "230364000",
            "description": "Progressive neuronal degeneration without liver cirrhosis (disorder)",
            "attributes": null
          },
          {
            "code": "230365004",
            "description": "Neuroaxonal dystrophy (disorder)",
            "attributes": null
          },
          {
            "code": "230366003",
            "description": "Late infantile and juvenile neuroaxonal dystrophy (disorder)",
            "attributes": null
          },
          {
            "code": "230372003",
            "description": "Acute relapsing multiple sclerosis (disorder)",
            "attributes": null
          },
          {
            "code": "230377009",
            "description": "Extrapontine myelinolysis (disorder)",
            "attributes": null
          },
          {
            "code": "230378004",
            "description": "Acute non-infective transverse myelitis (disorder)",
            "attributes": null
          },
          {
            "code": "230379007",
            "description": "Subacute necrotizing myelitis (disorder)",
            "attributes": null
          },
          {
            "code": "230380005",
            "description": "Balo concentric sclerosis (disorder)",
            "attributes": null
          },
          {
            "code": "230493001",
            "description": "Mixed sleep apnea (disorder)",
            "attributes": null
          },
          {
            "code": "230494007",
            "description": "Alveolar sleep apnea (disorder)",
            "attributes": null
          },
          {
            "code": "230499002",
            "description": "Sleep-related respiratory failure (disorder)",
            "attributes": null
          },
          {
            "code": "230525002",
            "description": "Compression of optic radiation (disorder)",
            "attributes": null
          },
          {
            "code": "230526001",
            "description": "Compression of visual cortex (disorder)",
            "attributes": null
          },
          {
            "code": "230534007",
            "description": "Trigeminal nerve compression (disorder)",
            "attributes": null
          },
          {
            "code": "230535008",
            "description": "Trigeminal nerve inflammation (disorder)",
            "attributes": null
          },
          {
            "code": "230537000",
            "description": "Idiopathic trigeminal neuralgia (disorder)",
            "attributes": null
          },
          {
            "code": "230538005",
            "description": "Secondary trigeminal neuralgia (disorder)",
            "attributes": null
          },
          {
            "code": "230539002",
            "description": "Cluster tic syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "230540000",
            "description": "Idiopathic trigeminal neuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "230545005",
            "description": "Compression facial neuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "230546006",
            "description": "Familial facial nerve palsy (disorder)",
            "attributes": null
          },
          {
            "code": "230549004",
            "description": "Multiple cranial nerve palsies of ocular motor nerves (disorder)",
            "attributes": null
          },
          {
            "code": "230552007",
            "description": "X-linked hereditary motor and sensory neuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "230553002",
            "description": "Autosomal dominant sensory neuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "230556005",
            "description": "X-linked recessive sensory neuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "230557001",
            "description": "Hereditary dysautonomia with motor neuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "230558006",
            "description": "Hereditary liability to pressure palsies (disorder)",
            "attributes": null
          },
          {
            "code": "230559003",
            "description": "Hereditary hypertrophic neuropathy with paraproteinemia (disorder)",
            "attributes": null
          },
          {
            "code": "230560008",
            "description": "Congenital polyneuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "230561007",
            "description": "Congenital neuropathy with arthrogryposis multiplex congenita (disorder)",
            "attributes": null
          },
          {
            "code": "230562000",
            "description": "Congenital hypomyelinating neuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "230564004",
            "description": "Chronic inflammatory demyelinating polyradiculoneuropathy with central nervous system demyelination (disorder)",
            "attributes": null
          },
          {
            "code": "230567006",
            "description": "Neuropathy due to folic acid deficiency (disorder)",
            "attributes": null
          },
          {
            "code": "230571009",
            "description": "Neuropathy associated with endocrine disorder (disorder)",
            "attributes": null
          },
          {
            "code": "230572002",
            "description": "Neuropathy due to diabetes mellitus (disorder)",
            "attributes": null
          },
          {
            "code": "230574001",
            "description": "Acute painful polyneuropathy due to diabetes mellitus (disorder)",
            "attributes": null
          },
          {
            "code": "230575000",
            "description": "Chronic painful polyneuropathy due to diabetes mellitus (disorder)",
            "attributes": null
          },
          {
            "code": "230576004",
            "description": "Asymmetric polyneuropathy due to diabetes mellitus (disorder)",
            "attributes": null
          },
          {
            "code": "230577008",
            "description": "Mononeuropathy due to diabetes mellitus (disorder)",
            "attributes": null
          },
          {
            "code": "230579006",
            "description": "Thoracic radiculopathy due to diabetes mellitus (disorder)",
            "attributes": null
          },
          {
            "code": "230580009",
            "description": "Myxedema neuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "230581008",
            "description": "Neuropathy in acromegaly (disorder)",
            "attributes": null
          },
          {
            "code": "230586003",
            "description": "Neuropathy due to multiple myeloma (disorder)",
            "attributes": null
          },
          {
            "code": "230587007",
            "description": "Neuropathy in macroglobulinemia (disorder)",
            "attributes": null
          },
          {
            "code": "230589005",
            "description": "Neuropathy in cryoglobulinemia (disorder)",
            "attributes": null
          },
          {
            "code": "230590001",
            "description": "Neuropathy in benign monoclonal gammopathy (disorder)",
            "attributes": null
          },
          {
            "code": "230591002",
            "description": "Motor neuropathy with multiple conduction block (disorder)",
            "attributes": null
          },
          {
            "code": "230593004",
            "description": "Anoxic neuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "230594005",
            "description": "Critical illness polyneuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "230597003",
            "description": "Intercostal post-herpetic neuralgia (disorder)",
            "attributes": null
          },
          {
            "code": "230598008",
            "description": "Neuropathy caused by human immunodeficiency virus (disorder)",
            "attributes": null
          },
          {
            "code": "230599000",
            "description": "Ischemic neuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "230600002",
            "description": "Neuropathy in arteriosclerotic occlusive disease (disorder)",
            "attributes": null
          },
          {
            "code": "230601003",
            "description": "Neuropathy in thromboangiitis obliterans (disorder)",
            "attributes": null
          },
          {
            "code": "230602005",
            "description": "Embolic infarction of nerve trunk (disorder)",
            "attributes": null
          },
          {
            "code": "230603000",
            "description": "Hemorrhage into nerve trunk (disorder)",
            "attributes": null
          },
          {
            "code": "230605007",
            "description": "Lyme mononeuritis multiplex (disorder)",
            "attributes": null
          },
          {
            "code": "230606008",
            "description": "Ischemic neuropathy due to arterial steal (disorder)",
            "attributes": null
          },
          {
            "code": "230607004",
            "description": "Neuropathy caused by chemical substance (disorder)",
            "attributes": null
          },
          {
            "code": "230608009",
            "description": "Neuropathy caused by organic substance (disorder)",
            "attributes": null
          },
          {
            "code": "230609001",
            "description": "Neuropathy caused by heavy metal (disorder)",
            "attributes": null
          },
          {
            "code": "230610006",
            "description": "Lead neuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "230618004",
            "description": "Injury of abdominal sympathetic plexus (disorder)",
            "attributes": null
          },
          {
            "code": "230635000",
            "description": "Suprascapular nerve compression (disorder)",
            "attributes": null
          },
          {
            "code": "230645003",
            "description": "Compression neuropathy of trunk (disorder)",
            "attributes": null
          },
          {
            "code": "230646002",
            "description": "Intercostal neuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "230647006",
            "description": "Abdominal neuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "230648001",
            "description": "Abdominal cutaneous nerve entrapment syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "230649009",
            "description": "Multiple entrapment syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "230651008",
            "description": "Disorders of spinal neurones manifest by hyperactivity (disorder)",
            "attributes": null
          },
          {
            "code": "230655004",
            "description": "Idiopathic chronic neuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "230656003",
            "description": "Demyelinating sensorimotor neuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "230657007",
            "description": "Axonal sensorimotor neuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "230658002",
            "description": "Chronic idiopathic ataxic neuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "230659005",
            "description": "Segmental autonomic dysfunction (disorder)",
            "attributes": null
          },
          {
            "code": "230660000",
            "description": "Segmental hyperhidrosis (disorder)",
            "attributes": null
          },
          {
            "code": "230661001",
            "description": "Segmental hypohidrosis (disorder)",
            "attributes": null
          },
          {
            "code": "230662008",
            "description": "Ross syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "230664009",
            "description": "Sympathotonic orthostatic hypotension (disorder)",
            "attributes": null
          },
          {
            "code": "230666006",
            "description": "Paraneoplastic autonomic dysfunction (disorder)",
            "attributes": null
          },
          {
            "code": "230667002",
            "description": "Chronic idiopathic anhidrosis (disorder)",
            "attributes": null
          },
          {
            "code": "230668007",
            "description": "Idiopathic diffuse hyperhidrosis (disorder)",
            "attributes": null
          },
          {
            "code": "230669004",
            "description": "Genetically determined myasthenia (disorder)",
            "attributes": null
          },
          {
            "code": "230670003",
            "description": "Familial infantile myasthenia (disorder)",
            "attributes": null
          },
          {
            "code": "230671004",
            "description": "Acetylcholine resynthesis deficiency (disorder)",
            "attributes": null
          },
          {
            "code": "230672006",
            "description": "Congenital myasthenic syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "230673001",
            "description": "Congenital end-plate acetylcholine receptor deficiency (disorder)",
            "attributes": null
          },
          {
            "code": "230674007",
            "description": "Pseudomyopathic myasthenia (disorder)",
            "attributes": null
          },
          {
            "code": "230675008",
            "description": "Slow channel syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "230676009",
            "description": "Putative defect in acetylcholine synthesis or packaging (disorder)",
            "attributes": null
          },
          {
            "code": "230677000",
            "description": "Congenital end-plate acetylcholinesterase deficiency (disorder)",
            "attributes": null
          },
          {
            "code": "230678005",
            "description": "Decrease of motor end-plate potential amplitude without acetylcholine receptor deficiency (disorder)",
            "attributes": null
          },
          {
            "code": "230679002",
            "description": "Abnormality of synaptic vesicles (disorder)",
            "attributes": null
          },
          {
            "code": "230684008",
            "description": "Ocular myasthenia (disorder)",
            "attributes": null
          },
          {
            "code": "230685009",
            "description": "Myasthenia gravis associated with thymoma (disorder)",
            "attributes": null
          },
          {
            "code": "230686005",
            "description": "Generalized myasthenia (disorder)",
            "attributes": null
          },
          {
            "code": "230687001",
            "description": "Myopathy in myasthenia gravis (disorder)",
            "attributes": null
          },
          {
            "code": "230689003",
            "description": "Cerebrovascular and spinal vascular disorders (disorder)",
            "attributes": null
          },
          {
            "code": "230690007",
            "description": "Cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "230691006",
            "description": "Cerebrovascular accident due to occlusion of cerebral artery (disorder)",
            "attributes": null
          },
          {
            "code": "230692004",
            "description": "Infarction - precerebral (disorder)",
            "attributes": null
          },
          {
            "code": "230693009",
            "description": "Anterior cerebral circulation infarction (disorder)",
            "attributes": null
          },
          {
            "code": "230694003",
            "description": "Total anterior cerebral circulation infarction (disorder)",
            "attributes": null
          },
          {
            "code": "230695002",
            "description": "Partial anterior cerebral circulation infarction (disorder)",
            "attributes": null
          },
          {
            "code": "230696001",
            "description": "Posterior cerebral circulation infarction (disorder)",
            "attributes": null
          },
          {
            "code": "230698000",
            "description": "Lacunar infarction (disorder)",
            "attributes": null
          },
          {
            "code": "230699008",
            "description": "Pure motor lacunar infarction (disorder)",
            "attributes": null
          },
          {
            "code": "230700009",
            "description": "Pure sensory lacunar infarction (disorder)",
            "attributes": null
          },
          {
            "code": "230701008",
            "description": "Pure sensorimotor lacunar infarction (disorder)",
            "attributes": null
          },
          {
            "code": "230702001",
            "description": "Lacunar ataxic hemiparesis (disorder)",
            "attributes": null
          },
          {
            "code": "230703006",
            "description": "Dysarthria-clumsy hand syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "230706003",
            "description": "Hemorrhagic cerebral infarction (disorder)",
            "attributes": null
          },
          {
            "code": "230707007",
            "description": "Anterior cerebral circulation hemorrhagic infarction (disorder)",
            "attributes": null
          },
          {
            "code": "230708002",
            "description": "Posterior cerebral circulation hemorrhagic infarction (disorder)",
            "attributes": null
          },
          {
            "code": "230709005",
            "description": "Massive supratentorial cerebral hemorrhage (disorder)",
            "attributes": null
          },
          {
            "code": "230710000",
            "description": "Lobar cerebral hemorrhage (disorder)",
            "attributes": null
          },
          {
            "code": "230711001",
            "description": "Thalamic hemorrhage (disorder)",
            "attributes": null
          },
          {
            "code": "230712008",
            "description": "Lacunar hemorrhage (disorder)",
            "attributes": null
          },
          {
            "code": "230713003",
            "description": "Stroke of uncertain pathology (disorder)",
            "attributes": null
          },
          {
            "code": "230714009",
            "description": "Anterior circulation stroke of uncertain pathology (disorder)",
            "attributes": null
          },
          {
            "code": "230715005",
            "description": "Posterior circulation stroke of uncertain pathology (disorder)",
            "attributes": null
          },
          {
            "code": "230716006",
            "description": "Carotid territory transient ischemic attack (disorder)",
            "attributes": null
          },
          {
            "code": "230717002",
            "description": "Vertebrobasilar territory transient ischemic attack (disorder)",
            "attributes": null
          },
          {
            "code": "230718007",
            "description": "Subarachnoid hemorrhage due to ruptured arteriovenous malformation (disorder)",
            "attributes": null
          },
          {
            "code": "230719004",
            "description": "Intracranial subarachnoid hemorrhage due to ruptured aneurysm (disorder)",
            "attributes": null
          },
          {
            "code": "230720005",
            "description": "Cerebral venous thrombosis of straight sinus (disorder)",
            "attributes": null
          },
          {
            "code": "230721009",
            "description": "Cerebral venous thrombosis of sigmoid sinus (disorder)",
            "attributes": null
          },
          {
            "code": "230722002",
            "description": "Cerebral venous thrombosis of cortical vein (disorder)",
            "attributes": null
          },
          {
            "code": "230723007",
            "description": "Cerebral venous thrombosis of great cerebral vein (disorder)",
            "attributes": null
          },
          {
            "code": "230724001",
            "description": "Cerebral amyloid angiopathy (disorder)",
            "attributes": null
          },
          {
            "code": "230725000",
            "description": "Sporadic cerebral amyloid angiopathy (disorder)",
            "attributes": null
          },
          {
            "code": "230728003",
            "description": "Dissection of cervicocerebral artery (disorder)",
            "attributes": null
          },
          {
            "code": "230731002",
            "description": "Cerebral arteritis in systemic vasculitis (disorder)",
            "attributes": null
          },
          {
            "code": "230732009",
            "description": "Cerebral arteritis in giant cell arteritis (disorder)",
            "attributes": null
          },
          {
            "code": "230738008",
            "description": "Asymptomatic cerebrovascular disease (disorder)",
            "attributes": null
          },
          {
            "code": "230739000",
            "description": "Spinal cord stroke (disorder)",
            "attributes": null
          },
          {
            "code": "230740003",
            "description": "Anterior spinal artery thrombosis (disorder)",
            "attributes": null
          },
          {
            "code": "230741004",
            "description": "Venous infarction of spinal cord (disorder)",
            "attributes": null
          },
          {
            "code": "230745008",
            "description": "Hydrocephalus (disorder)",
            "attributes": null
          },
          {
            "code": "230746009",
            "description": "Obstructive hydrocephalus (disorder)",
            "attributes": null
          },
          {
            "code": "230747000",
            "description": "Isolated fourth ventricle hydrocephalus (disorder)",
            "attributes": null
          },
          {
            "code": "230748005",
            "description": "Intermittently raised pressure hydrocephalus (disorder)",
            "attributes": null
          },
          {
            "code": "230749002",
            "description": "Postmeningitic hydrocephalus (disorder)",
            "attributes": null
          },
          {
            "code": "230751003",
            "description": "Post-traumatic hydrocephalus (disorder)",
            "attributes": null
          },
          {
            "code": "230752005",
            "description": "Hydrocephalus due to cerebrospinal fluid absorption defect (disorder)",
            "attributes": null
          },
          {
            "code": "230753000",
            "description": "Hydrocephalus due to cerebrospinal fluid overproduction (disorder)",
            "attributes": null
          },
          {
            "code": "230754006",
            "description": "Uncinate herniation (disorder)",
            "attributes": null
          },
          {
            "code": "230755007",
            "description": "Upwards herniation of cerebellum (disorder)",
            "attributes": null
          },
          {
            "code": "230756008",
            "description": "Transtentorial herniation (disorder)",
            "attributes": null
          },
          {
            "code": "230757004",
            "description": "Transtentorial herniation downwards (disorder)",
            "attributes": null
          },
          {
            "code": "230758009",
            "description": "Transtentorial herniation upwards (disorder)",
            "attributes": null
          },
          {
            "code": "230759001",
            "description": "Vasogenic cerebral edema (disorder)",
            "attributes": null
          },
          {
            "code": "230760006",
            "description": "Cytotoxic cerebral edema (disorder)",
            "attributes": null
          },
          {
            "code": "230761005",
            "description": "Periventricular cerebrospinal fluid edema (disorder)",
            "attributes": null
          },
          {
            "code": "230762003",
            "description": "High altitude cerebral edema (disorder)",
            "attributes": null
          },
          {
            "code": "230766000",
            "description": "Multicystic encephalomalacia (disorder)",
            "attributes": null
          },
          {
            "code": "230782004",
            "description": "Dysequilibrium syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "230784003",
            "description": "Congenital pseudobulbar palsy (disorder)",
            "attributes": null
          },
          {
            "code": "230790004",
            "description": "Choroid plexus cyst (disorder)",
            "attributes": null
          },
          {
            "code": "230792007",
            "description": "Ependymal cyst (disorder)",
            "attributes": null
          },
          {
            "code": "230793002",
            "description": "Neuroglial cyst (disorder)",
            "attributes": null
          },
          {
            "code": "230802007",
            "description": "Brainstem death (disorder)",
            "attributes": null
          },
          {
            "code": "23096007",
            "description": "Cranial neuralgia (disorder)",
            "attributes": null
          },
          {
            "code": "232267001",
            "description": "Inflammatory facial neuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "232269003",
            "description": "Acute mastoiditis with facial paralysis (disorder)",
            "attributes": null
          },
          {
            "code": "23276006",
            "description": "Ventricular hemorrhage (disorder)",
            "attributes": null
          },
          {
            "code": "233964008",
            "description": "Internal carotid artery stenosis (disorder)",
            "attributes": null
          },
          {
            "code": "233983001",
            "description": "Ruptured cerebral aneurysm (disorder)",
            "attributes": null
          },
          {
            "code": "234025000",
            "description": "Steal syndrome of hand (disorder)",
            "attributes": null
          },
          {
            "code": "234028003",
            "description": "Cerebral steal syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "23414001",
            "description": "Peripheral demyelinating neuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "234530009",
            "description": "Chronic sarcoid myopathy (disorder)",
            "attributes": null
          },
          {
            "code": "23671000119107",
            "description": "Sequela of ischemic cerebral infarction (disorder)",
            "attributes": null
          },
          {
            "code": "23732000",
            "description": "Primary cerebellar degeneration (disorder)",
            "attributes": null
          },
          {
            "code": "237717004",
            "description": "Arachnoid cyst of pituitary (disorder)",
            "attributes": null
          },
          {
            "code": "237873000",
            "description": "Primary familial amyloid myopathy (disorder)",
            "attributes": null
          },
          {
            "code": "237874006",
            "description": "Primary sporadic amyloid myopathy (disorder)",
            "attributes": null
          },
          {
            "code": "237995002",
            "description": "Depletion of mitochondrial deoxyribonucleic acid (disorder)",
            "attributes": null
          },
          {
            "code": "238062008",
            "description": "Infantile Refsum's disease (disorder)",
            "attributes": null
          },
          {
            "code": "238065005",
            "description": "Pseudoinfantile Refsum's disease (disorder)",
            "attributes": null
          },
          {
            "code": "23819000",
            "description": "Embolism of cavernous venous sinus (disorder)",
            "attributes": null
          },
          {
            "code": "23820006",
            "description": "Fingerprint myopathy (disorder)",
            "attributes": null
          },
          {
            "code": "23853001",
            "description": "Disorder of the central nervous system (disorder)",
            "attributes": null
          },
          {
            "code": "23882000",
            "description": "Neuritis AND/OR radiculitis due to rupture of lumbar intervertebral disc (disorder)",
            "attributes": null
          },
          {
            "code": "240046001",
            "description": "Muscular dystrophy with predominantly proximal limb girdle distribution (disorder)",
            "attributes": null
          },
          {
            "code": "240047005",
            "description": "X-linked muscular dystrophy with limb girdle distribution (disorder)",
            "attributes": null
          },
          {
            "code": "240048000",
            "description": "X-linked muscular dystrophy with abnormal dystrophin (disorder)",
            "attributes": null
          },
          {
            "code": "240049008",
            "description": "Intermediate X-linked muscular dystrophy (disorder)",
            "attributes": null
          },
          {
            "code": "240050008",
            "description": "Manifesting female carrier of X-linked muscular dystrophy (disorder)",
            "attributes": null
          },
          {
            "code": "240051007",
            "description": "X-linked limb girdle muscular dystrophy with normal dystrophin (disorder)",
            "attributes": null
          },
          {
            "code": "240052000",
            "description": "Ji muscular dystrophy (disorder)",
            "attributes": null
          },
          {
            "code": "240053005",
            "description": "Hereditary myopathy limited to females (disorder)",
            "attributes": null
          },
          {
            "code": "240054004",
            "description": "Autosomal recessive muscular dystrophy with limb girdle distribution (disorder)",
            "attributes": null
          },
          {
            "code": "240055003",
            "description": "Autosomal recessive muscular dystrophy with abnormal dystrophin-associated glycoprotein (disorder)",
            "attributes": null
          },
          {
            "code": "240058001",
            "description": "Reunion-Indiana Amish type muscular dystrophy (disorder)",
            "attributes": null
          },
          {
            "code": "240060004",
            "description": "Western type of congenital muscular dystrophy (disorder)",
            "attributes": null
          },
          {
            "code": "240061000",
            "description": "Congenital muscular dystrophy with arthrogryposis multiplex congenita (disorder)",
            "attributes": null
          },
          {
            "code": "240062007",
            "description": "Ullrich congenital muscular dystrophy (disorder)",
            "attributes": null
          },
          {
            "code": "240063002",
            "description": "Eichsfeld type congenital muscular dystrophy (disorder)",
            "attributes": null
          },
          {
            "code": "240064008",
            "description": "Hutterite type of muscular dystrophy (disorder)",
            "attributes": null
          },
          {
            "code": "240065009",
            "description": "Adult onset autosomal recessive muscular dystrophy with normal dystrophin (disorder)",
            "attributes": null
          },
          {
            "code": "240067001",
            "description": "Autosomal dominant muscular dystrophy with limb girdle distribution (disorder)",
            "attributes": null
          },
          {
            "code": "240068006",
            "description": "Autosomal dominant muscular dystrophy with gene located at 5q31 (disorder)",
            "attributes": null
          },
          {
            "code": "240069003",
            "description": "Late onset proximal muscular dystrophy with dysarthria (disorder)",
            "attributes": null
          },
          {
            "code": "240070002",
            "description": "Muscular dystrophy not predominantly limb girdle in distribution (disorder)",
            "attributes": null
          },
          {
            "code": "240071003",
            "description": "X-linked muscular dystrophy not predominantly limb girdle (disorder)",
            "attributes": null
          },
          {
            "code": "240072005",
            "description": "Benign scapuloperoneal muscular dystrophy with cardiomyopathy (disorder)",
            "attributes": null
          },
          {
            "code": "240073000",
            "description": "Autosomal recessive muscular dystrophy not predominantly limb girdle (disorder)",
            "attributes": null
          },
          {
            "code": "240074006",
            "description": "Scapulohumeral muscular dystrophy (disorder)",
            "attributes": null
          },
          {
            "code": "240075007",
            "description": "Autosomal dominant muscular dystrophy not predominantly limb girdle (disorder)",
            "attributes": null
          },
          {
            "code": "240076008",
            "description": "Benign scapuloperoneal muscular dystrophy (disorder)",
            "attributes": null
          },
          {
            "code": "240077004",
            "description": "Severe scapuloperoneal muscular dystrophy with cardiomyopathy (disorder)",
            "attributes": null
          },
          {
            "code": "240078009",
            "description": "Benign congenital muscular dystrophy with finger flexion contractures (disorder)",
            "attributes": null
          },
          {
            "code": "240081004",
            "description": "Autosomal recessive centronuclear myopathy (disorder)",
            "attributes": null
          },
          {
            "code": "240082006",
            "description": "Myopathy with abnormality of histochemical fiber type (disorder)",
            "attributes": null
          },
          {
            "code": "240083001",
            "description": "Myopathy with type I hypotrophy (disorder)",
            "attributes": null
          },
          {
            "code": "240084007",
            "description": "Congenital myopathy with fiber type disproportion (disorder)",
            "attributes": null
          },
          {
            "code": "240085008",
            "description": "Congenital myopathy with uniform fiber type (disorder)",
            "attributes": null
          },
          {
            "code": "240086009",
            "description": "Myopathy with cytoplasmic inclusions (disorder)",
            "attributes": null
          },
          {
            "code": "240087000",
            "description": "Myopathy with tubular aggregates (disorder)",
            "attributes": null
          },
          {
            "code": "240089002",
            "description": "Myopathy in acromegaly (disorder)",
            "attributes": null
          },
          {
            "code": "240090006",
            "description": "Myopathy in hyperparathyroidism (disorder)",
            "attributes": null
          },
          {
            "code": "240091005",
            "description": "Myopathy in hypoparathyroidism (disorder)",
            "attributes": null
          },
          {
            "code": "240092003",
            "description": "Myopathy in osteomalacia (disorder)",
            "attributes": null
          },
          {
            "code": "240096000",
            "description": "Mitochondrial cytopathy (disorder)",
            "attributes": null
          },
          {
            "code": "240098004",
            "description": "Protein deficiency myopathy (disorder)",
            "attributes": null
          },
          {
            "code": "240099007",
            "description": "Potassium depletion myopathy (disorder)",
            "attributes": null
          },
          {
            "code": "240100004",
            "description": "Myopathy caused by snake bite (disorder)",
            "attributes": null
          },
          {
            "code": "240103002",
            "description": "Human immunodeficiency virus myopathy (disorder)",
            "attributes": null
          },
          {
            "code": "240104008",
            "description": "Congenital myotonic dystrophy (disorder)",
            "attributes": null
          },
          {
            "code": "2432006",
            "description": "Cerebrospinal fluid circulation disorder (disorder)",
            "attributes": null
          },
          {
            "code": "243338005",
            "description": "Nerve root compression syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "24473007",
            "description": "Persistent vegetative state (disorder)",
            "attributes": null
          },
          {
            "code": "24654003",
            "description": "Weber-Gubler syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "246781001",
            "description": "Superior oblique myokymia (disorder)",
            "attributes": null
          },
          {
            "code": "246826003",
            "description": "Aberrant III nerve regeneration (disorder)",
            "attributes": null
          },
          {
            "code": "24700007",
            "description": "Multiple sclerosis (disorder)",
            "attributes": null
          },
          {
            "code": "247390002",
            "description": "Sciatic nerve palsy (disorder)",
            "attributes": null
          },
          {
            "code": "24777009",
            "description": "Disorder of hypoglossal nerve (disorder)",
            "attributes": null
          },
          {
            "code": "24825006",
            "description": "Central alveolar hypoventilation syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "24861000119103",
            "description": "Symptomatic inflammatory myopathy (disorder)",
            "attributes": null
          },
          {
            "code": "24956004",
            "description": "Loculation syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "249892007",
            "description": "Progressive pseudobulbar palsy (disorder)",
            "attributes": null
          },
          {
            "code": "24991000119103",
            "description": "Thoracic myelopathy (disorder)",
            "attributes": null
          },
          {
            "code": "25044007",
            "description": "Neuromyelitis optica (disorder)",
            "attributes": null
          },
          {
            "code": "25133001",
            "description": "Completed stroke (disorder)",
            "attributes": null
          },
          {
            "code": "253131002",
            "description": "Hydrocephalus associated with late onset aqueduct stenosis (disorder)",
            "attributes": null
          },
          {
            "code": "253132009",
            "description": "External hydrocephalus (disorder)",
            "attributes": null
          },
          {
            "code": "253133004",
            "description": "Hydrocephalus with anomaly of aqueduct of Sylvius (disorder)",
            "attributes": null
          },
          {
            "code": "253144007",
            "description": "Cyst of septum pellucidum (disorder)",
            "attributes": null
          },
          {
            "code": "253162003",
            "description": "Cerebral arachnoid cyst (disorder)",
            "attributes": null
          },
          {
            "code": "253163008",
            "description": "Spinal arachnoid cyst (disorder)",
            "attributes": null
          },
          {
            "code": "253164002",
            "description": "Intradural spinal arachnoid cyst (disorder)",
            "attributes": null
          },
          {
            "code": "253165001",
            "description": "Extradural spinal arachnoid cyst (disorder)",
            "attributes": null
          },
          {
            "code": "253194008",
            "description": "Aneurysm of the vein of Galen (disorder)",
            "attributes": null
          },
          {
            "code": "25362006",
            "description": "Phytanic acid storage disease (disorder)",
            "attributes": null
          },
          {
            "code": "255522009",
            "description": "Neuromyopathy (disorder)",
            "attributes": null
          },
          {
            "code": "256321009",
            "description": "Disorder of neuromuscular transmission (disorder)",
            "attributes": null
          },
          {
            "code": "257277002",
            "description": "Combined disorder of muscle AND peripheral nerve (disorder)",
            "attributes": null
          },
          {
            "code": "25816005",
            "description": "Brain stem compression (disorder)",
            "attributes": null
          },
          {
            "code": "2584003",
            "description": "Cerebral degeneration in childhood (disorder)",
            "attributes": null
          },
          {
            "code": "26016002",
            "description": "Cerebrospinal nematodiasis (disorder)",
            "attributes": null
          },
          {
            "code": "26021000119107",
            "description": "Vertigo as sequela of cerebrovascular disease (disorder)",
            "attributes": null
          },
          {
            "code": "26037005",
            "description": "Radiation-induced myelopathy (disorder)",
            "attributes": null
          },
          {
            "code": "26111005",
            "description": "Metabolic myopathy (disorder)",
            "attributes": null
          },
          {
            "code": "26261000119109",
            "description": "Acute inflammatory demyelinating polyneuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "262701006",
            "description": "Edema of cervical cord (disorder)",
            "attributes": null
          },
          {
            "code": "262703009",
            "description": "Edema of lumbar cord (disorder)",
            "attributes": null
          },
          {
            "code": "262704003",
            "description": "Edema of sacral cord (disorder)",
            "attributes": null
          },
          {
            "code": "264556007",
            "description": "Occult neuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "265377002",
            "description": "Symptomatic parkinsonism (disorder)",
            "attributes": null
          },
          {
            "code": "26554009",
            "description": "Nuclear facial nerve paralysis (disorder)",
            "attributes": null
          },
          {
            "code": "26594006",
            "description": "Syringobulbia (disorder)",
            "attributes": null
          },
          {
            "code": "26609002",
            "description": "Neuralgic amyotrophy (disorder)",
            "attributes": null
          },
          {
            "code": "266253001",
            "description": "Precerebral arterial occlusion (disorder)",
            "attributes": null
          },
          {
            "code": "266254007",
            "description": "Occlusion of carotid artery (disorder)",
            "attributes": null
          },
          {
            "code": "266257000",
            "description": "Transient ischemic attack (disorder)",
            "attributes": null
          },
          {
            "code": "267390005",
            "description": "Post-infarction hypopituitarism (disorder)",
            "attributes": null
          },
          {
            "code": "267601009",
            "description": "Inflammatory and toxic neuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "267602002",
            "description": "Neuropathy in renal failure (disorder)",
            "attributes": null
          },
          {
            "code": "267604001",
            "description": "Myasthenic syndrome due to diabetic mellitus (disorder)",
            "attributes": null
          },
          {
            "code": "267607008",
            "description": "Familial periodic paralysis (disorder)",
            "attributes": null
          },
          {
            "code": "26848004",
            "description": "Chorea acanthocytosis syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "26852004",
            "description": "Primary degenerative dementia of the Alzheimer type, senile onset, with depression (disorder)",
            "attributes": null
          },
          {
            "code": "26929004",
            "description": "Alzheimer's disease (disorder)",
            "attributes": null
          },
          {
            "code": "26954004",
            "description": "Thrombophlebitis of superior sagittal sinus (disorder)",
            "attributes": null
          },
          {
            "code": "270907008",
            "description": "Spontaneous intracranial subarachnoid hemorrhage (disorder)",
            "attributes": null
          },
          {
            "code": "27148008",
            "description": "Hereditary motor end-plate disease (disorder)",
            "attributes": null
          },
          {
            "code": "271569006",
            "description": "Communicating hydrocephalus (disorder)",
            "attributes": null
          },
          {
            "code": "271730003",
            "description": "Horner's syndrome pupil (disorder)",
            "attributes": null
          },
          {
            "code": "27358001",
            "description": "Sylvian aqueduct syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "27405005",
            "description": "Central sleep apnea syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "274100004",
            "description": "Cerebral hemorrhage (disorder)",
            "attributes": null
          },
          {
            "code": "275363001",
            "description": "Rupture of superficial cerebral vein (disorder)",
            "attributes": null
          },
          {
            "code": "275470000",
            "description": "Post-cardiorespiratory arrest coma (disorder)",
            "attributes": null
          },
          {
            "code": "276219001",
            "description": "Occipital cerebral infarction (disorder)",
            "attributes": null
          },
          {
            "code": "276220007",
            "description": "Foville syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "276221006",
            "description": "Millard-Gubler syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "276222004",
            "description": "Top of basilar syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "276277008",
            "description": "Subarachnoid hemorrhage from multiple aneurysms (disorder)",
            "attributes": null
          },
          {
            "code": "276278003",
            "description": "Subarachnoid hemorrhage from anterior cerebral artery aneurysm (disorder)",
            "attributes": null
          },
          {
            "code": "276280009",
            "description": "Subarachnoid hemorrhage from middle cerebral artery aneurysm (disorder)",
            "attributes": null
          },
          {
            "code": "276281008",
            "description": "Subarachnoid hemorrhage from posterior cerebral artery aneurysm (disorder)",
            "attributes": null
          },
          {
            "code": "276282001",
            "description": "Subarachnoid hemorrhage from anterior communicating artery aneurysm (disorder)",
            "attributes": null
          },
          {
            "code": "276283006",
            "description": "Subarachnoid hemorrhage from posterior communicating artery aneurysm (disorder)",
            "attributes": null
          },
          {
            "code": "276284000",
            "description": "Subarachnoid hemorrhage from basilar artery aneurysm (disorder)",
            "attributes": null
          },
          {
            "code": "276285004",
            "description": "Subarachnoid hemorrhage from posterior inferior cerebellar artery aneurysm (disorder)",
            "attributes": null
          },
          {
            "code": "276286003",
            "description": "Subarachnoid hemorrhage from carotid artery aneurysm (disorder)",
            "attributes": null
          },
          {
            "code": "276722003",
            "description": "Intracerebellar and posterior fossa hemorrhage (disorder)",
            "attributes": null
          },
          {
            "code": "276837006",
            "description": "Epidermoid cyst of brain (disorder)",
            "attributes": null
          },
          {
            "code": "277189006",
            "description": "Subacute inflammatory demyelinating polyradiculoneuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "277190002",
            "description": "Pelagic paralysis (disorder)",
            "attributes": null
          },
          {
            "code": "277196008",
            "description": "Berry aneurysm (disorder)",
            "attributes": null
          },
          {
            "code": "277299009",
            "description": "Ruptured cerebral arteriovenous malformation (disorder)",
            "attributes": null
          },
          {
            "code": "277303004",
            "description": "Angiogram-negative intracranial subarachnoid hemorrhage (disorder)",
            "attributes": null
          },
          {
            "code": "277315000",
            "description": "Ruptured aneurysm of anterior cerebral artery (disorder)",
            "attributes": null
          },
          {
            "code": "277316004",
            "description": "Ruptured aneurysm of middle cerebral artery (disorder)",
            "attributes": null
          },
          {
            "code": "277319006",
            "description": "Ruptured aneurysm of posterior cerebral artery (disorder)",
            "attributes": null
          },
          {
            "code": "277320000",
            "description": "Ruptured aneurysm of anterior communicating artery (disorder)",
            "attributes": null
          },
          {
            "code": "277321001",
            "description": "Phrenic nerve lesion (disorder)",
            "attributes": null
          },
          {
            "code": "277322008",
            "description": "Ruptured aneurysm of posterior communicating artery (disorder)",
            "attributes": null
          },
          {
            "code": "277324009",
            "description": "Ruptured aneurysm of basilar artery (disorder)",
            "attributes": null
          },
          {
            "code": "277325005",
            "description": "Ruptured aneurysm of posterior inferior cerebellar artery (disorder)",
            "attributes": null
          },
          {
            "code": "277328007",
            "description": "Ruptured internal carotid-anterior communicating artery zone aneurysm (disorder)",
            "attributes": null
          },
          {
            "code": "277329004",
            "description": "Ruptured internal carotid-posterior communicating artery zone aneurysm (disorder)",
            "attributes": null
          },
          {
            "code": "277330009",
            "description": "Ruptured internal carotid bifurcation aneurysm (disorder)",
            "attributes": null
          },
          {
            "code": "277333006",
            "description": "Cyst of central nervous system (disorder)",
            "attributes": null
          },
          {
            "code": "277339005",
            "description": "Spinal epidermoid cyst (disorder)",
            "attributes": null
          },
          {
            "code": "277340007",
            "description": "Tension pneumocephalus (disorder)",
            "attributes": null
          },
          {
            "code": "277373000",
            "description": "Severe childhood autosomal recessive muscular dystrophy (disorder)",
            "attributes": null
          },
          {
            "code": "277476007",
            "description": "Cerebral ventricular distension (disorder)",
            "attributes": null
          },
          {
            "code": "277478008",
            "description": "Post-asphyxial encephalopathy (disorder)",
            "attributes": null
          },
          {
            "code": "277532002",
            "description": "Meningeal melanosis (disorder)",
            "attributes": null
          },
          {
            "code": "277802001",
            "description": "Notalgia paresthetica (disorder)",
            "attributes": null
          },
          {
            "code": "277879009",
            "description": "Autonomic neuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "277939004",
            "description": "Chronic myopathy with hypocalcemia and hypophosphatemia (disorder)",
            "attributes": null
          },
          {
            "code": "278509004",
            "description": "Congenital non-progressive ataxia (disorder)",
            "attributes": null
          },
          {
            "code": "27873005",
            "description": "Spinopontine degeneration (disorder)",
            "attributes": null
          },
          {
            "code": "278849000",
            "description": "Cerebral atrophy (disorder)",
            "attributes": null
          },
          {
            "code": "278855005",
            "description": "Frontal lobe degeneration (disorder)",
            "attributes": null
          },
          {
            "code": "278857002",
            "description": "Dementia of frontal lobe type (disorder)",
            "attributes": null
          },
          {
            "code": "279982005",
            "description": "Cerebral degeneration presenting primarily with dementia (disorder)",
            "attributes": null
          },
          {
            "code": "28007006",
            "description": "Trigeminal nerve sensory disorder (disorder)",
            "attributes": null
          },
          {
            "code": "280816001",
            "description": "Facial palsy (disorder)",
            "attributes": null
          },
          {
            "code": "281222009",
            "description": "Postoperative meningocele (disorder)",
            "attributes": null
          },
          {
            "code": "281223004",
            "description": "Traumatic meningocele (disorder)",
            "attributes": null
          },
          {
            "code": "281240008",
            "description": "Extension of cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "281509000",
            "description": "Hypoxic-ischemic coma (disorder)",
            "attributes": null
          },
          {
            "code": "2816000",
            "description": "Dilated cardiomyopathy secondary to myotonic dystrophy (disorder)",
            "attributes": null
          },
          {
            "code": "281864001",
            "description": "Non-traumatic intracranial subdural hematoma (disorder)",
            "attributes": null
          },
          {
            "code": "281865000",
            "description": "Non-traumatic extradural intracranial hematoma (disorder)",
            "attributes": null
          },
          {
            "code": "282742004",
            "description": "Intercostal post-herpetic neuritis (disorder)",
            "attributes": null
          },
          {
            "code": "282746001",
            "description": "Autonomic nerve injury (disorder)",
            "attributes": null
          },
          {
            "code": "282747005",
            "description": "Sympathetic nervous structure injury (disorder)",
            "attributes": null
          },
          {
            "code": "282748000",
            "description": "Parasympathetic nerve injury (disorder)",
            "attributes": null
          },
          {
            "code": "282792003",
            "description": "Sympathetic nerve injury (disorder)",
            "attributes": null
          },
          {
            "code": "282793008",
            "description": "Sympathetic ganglion injury (disorder)",
            "attributes": null
          },
          {
            "code": "282794002",
            "description": "Sympathetic plexus injury (disorder)",
            "attributes": null
          },
          {
            "code": "282795001",
            "description": "Sympathetic trunk injury (disorder)",
            "attributes": null
          },
          {
            "code": "282796000",
            "description": "Parasympathetic ganglion injury (disorder)",
            "attributes": null
          },
          {
            "code": "282797009",
            "description": "Sacral parasympathetic nerve injury (disorder)",
            "attributes": null
          },
          {
            "code": "282799007",
            "description": "Injury of ciliary ganglion (disorder)",
            "attributes": null
          },
          {
            "code": "282800006",
            "description": "Injury of pterygopalatine ganglion (disorder)",
            "attributes": null
          },
          {
            "code": "282801005",
            "description": "Injury of submandibular ganglion (disorder)",
            "attributes": null
          },
          {
            "code": "282803008",
            "description": "Injury of otic ganglion (disorder)",
            "attributes": null
          },
          {
            "code": "28318001",
            "description": "Basilar hemorrhage (disorder)",
            "attributes": null
          },
          {
            "code": "28366008",
            "description": "Cerebral arteritis (disorder)",
            "attributes": null
          },
          {
            "code": "28394000",
            "description": "Toxic encephalopathy (disorder)",
            "attributes": null
          },
          {
            "code": "284861000119104",
            "description": "Atherosclerosis of bilateral carotid arteries (disorder)",
            "attributes": null
          },
          {
            "code": "284871000119105",
            "description": "Atherosclerosis of left carotid artery (disorder)",
            "attributes": null
          },
          {
            "code": "284881000119108",
            "description": "Atherosclerosis of right carotid artery (disorder)",
            "attributes": null
          },
          {
            "code": "285145004",
            "description": "Akathisia (disorder)",
            "attributes": null
          },
          {
            "code": "285161000119105",
            "description": "Occlusion of left carotid artery (disorder)",
            "attributes": null
          },
          {
            "code": "285171000119104",
            "description": "Occlusion of right carotid artery (disorder)",
            "attributes": null
          },
          {
            "code": "285191000119103",
            "description": "Stenosis of left carotid artery (disorder)",
            "attributes": null
          },
          {
            "code": "285201000119100",
            "description": "Stenosis of right carotid artery (disorder)",
            "attributes": null
          },
          {
            "code": "285599002",
            "description": "Trunk nerve lesion (disorder)",
            "attributes": null
          },
          {
            "code": "28634005",
            "description": "Cerebral ataxia (disorder)",
            "attributes": null
          },
          {
            "code": "286742002",
            "description": "Impending cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "287731003",
            "description": "Cerebral ischemia (disorder)",
            "attributes": null
          },
          {
            "code": "28790007",
            "description": "Obstruction of precerebral artery (disorder)",
            "attributes": null
          },
          {
            "code": "288581000119102",
            "description": "Sleep related hypoxemia (disorder)",
            "attributes": null
          },
          {
            "code": "28869005",
            "description": "Dilated cardiomyopathy secondary to muscular dystrophy (disorder)",
            "attributes": null
          },
          {
            "code": "288723005",
            "description": "Acute ill-defined cerebrovascular disease (disorder)",
            "attributes": null
          },
          {
            "code": "28978003",
            "description": "Progressive supranuclear ophthalmoplegia (disorder)",
            "attributes": null
          },
          {
            "code": "290391000119106",
            "description": "Multisystem degeneration of autonomic nervous system (disorder)",
            "attributes": null
          },
          {
            "code": "290581000119101",
            "description": "Ataxia due to and following cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "290621000119101",
            "description": "Cognitive deficit due to and following cerebrovascular disease (disorder)",
            "attributes": null
          },
          {
            "code": "290631000119103",
            "description": "Dysarthria due to and following cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "290641000119107",
            "description": "Dysphagia due to and following non-traumatic intracerebral hemorrhage (disorder)",
            "attributes": null
          },
          {
            "code": "290791000119105",
            "description": "Fluency disorder due to and following cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "290931000119108",
            "description": "Monoplegia of lower limb due to and following cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "291091000119102",
            "description": "Monoplegia of left nondominant upper limb due to and following cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "291111000119105",
            "description": "Monoplegia of right nondominant upper limb due to and following cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "291121000119103",
            "description": "Monoplegia of upper limb due to and following cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "291351000119109",
            "description": "Spontaneous hemorrhage of subarachnoid space from basilar artery (disorder)",
            "attributes": null
          },
          {
            "code": "291371000119100",
            "description": "Spontaneous hemorrhage of subarachnoid space from intracranial artery (disorder)",
            "attributes": null
          },
          {
            "code": "291411000119104",
            "description": "Spontaneous hemorrhage of subarachnoid space from left posterior communicating artery (disorder)",
            "attributes": null
          },
          {
            "code": "291481000119105",
            "description": "Spontaneous haemorrhage of subarachnoid space from right posterior communicating artery (disorder)",
            "attributes": null
          },
          {
            "code": "291511000119103",
            "description": "Spontaneous hemorrhage of deep cerebral hemisphere (disorder)",
            "attributes": null
          },
          {
            "code": "291521000119105",
            "description": "Spontaneous hemorrhage of cortical intracerebral hemisphere (disorder)",
            "attributes": null
          },
          {
            "code": "291531000119108",
            "description": "Spontaneous hemorrhage of cerebral hemisphere (disorder)",
            "attributes": null
          },
          {
            "code": "291541000119104",
            "description": "Spontaneous hemorrhage of brain stem (disorder)",
            "attributes": null
          },
          {
            "code": "291571000119106",
            "description": "Spontaneous cerebral hemorrhage (disorder)",
            "attributes": null
          },
          {
            "code": "291581000119109",
            "description": "Acute nontraumatic subdural hemorrhage (disorder)",
            "attributes": null
          },
          {
            "code": "29159009",
            "description": "Familial dysautonomia (disorder)",
            "attributes": null
          },
          {
            "code": "291591000119107",
            "description": "Subacute non-traumatic intracranial subdural hemorrhage (disorder)",
            "attributes": null
          },
          {
            "code": "291621000119109",
            "description": "Cognitive deficit due to and following nontraumatic subarachnoid hemorrhage (disorder)",
            "attributes": null
          },
          {
            "code": "291631000119107",
            "description": "Aphasia due to and following non-traumatic subarachnoid hemorrhage (disorder)",
            "attributes": null
          },
          {
            "code": "291681000119108",
            "description": "Dysphagia due to and following non-traumatic subarachnoid hemorrhage (disorder)",
            "attributes": null
          },
          {
            "code": "291711000119109",
            "description": "Cognitive deficit due to and following nontraumatic intracerebral hemorrhage (disorder)",
            "attributes": null
          },
          {
            "code": "291721000119102",
            "description": "Aphasia due to and following non-traumatic intracerebral hemorrhage (disorder)",
            "attributes": null
          },
          {
            "code": "292621000119100",
            "description": "Occlusion of right vertebral artery (disorder)",
            "attributes": null
          },
          {
            "code": "292631000119102",
            "description": "Occlusion of left vertebral artery (disorder)",
            "attributes": null
          },
          {
            "code": "292661000119105",
            "description": "Cerebrovascular accident due to stenosis of right vertebral artery (disorder)",
            "attributes": null
          },
          {
            "code": "292671000119104",
            "description": "Cerebrovascular accident due to stenosis of left vertebral artery (disorder)",
            "attributes": null
          },
          {
            "code": "292681000119101",
            "description": "Cerebrovascular accident due to occlusion of right vertebral artery (disorder)",
            "attributes": null
          },
          {
            "code": "292691000119103",
            "description": "Cerebrovascular accident due to occlusion of left vertebral artery (disorder)",
            "attributes": null
          },
          {
            "code": "292851000119109",
            "description": "Lacunar ataxic hemiparesis of right dominant side (disorder)",
            "attributes": null
          },
          {
            "code": "292861000119106",
            "description": "Lacunar ataxic hemiparesis of left dominant side (disorder)",
            "attributes": null
          },
          {
            "code": "292871000119100",
            "description": "Acquired pseudoporencephaly (disorder)",
            "attributes": null
          },
          {
            "code": "292991000119106",
            "description": "Eaton Lambert syndrome without underlying malignancy (disorder)",
            "attributes": null
          },
          {
            "code": "29322000",
            "description": "Acute cerebrovascular insufficiency (disorder)",
            "attributes": null
          },
          {
            "code": "293811000119100",
            "description": "Cerebral infarction due to vertebral artery stenosis (disorder)",
            "attributes": null
          },
          {
            "code": "293831000119105",
            "description": "Cerebral infarction due to stenosis of precerebral artery (disorder)",
            "attributes": null
          },
          {
            "code": "293921000119104",
            "description": "Complex regional pain syndrome type I of bilateral upper limbs (disorder)",
            "attributes": null
          },
          {
            "code": "293931000119101",
            "description": "Complex regional pain syndrome type I of left lower limb (disorder)",
            "attributes": null
          },
          {
            "code": "293941000119105",
            "description": "Complex regional pain syndrome type I of left upper limb (disorder)",
            "attributes": null
          },
          {
            "code": "293951000119107",
            "description": "Complex regional pain syndrome type I of bilateral lower limbs (disorder)",
            "attributes": null
          },
          {
            "code": "293961000119109",
            "description": "Complex regional pain syndrome type I of right lower limb (disorder)",
            "attributes": null
          },
          {
            "code": "293971000119103",
            "description": "Complex regional pain syndrome type I of right upper limb (disorder)",
            "attributes": null
          },
          {
            "code": "294011000119108",
            "description": "Spontaneous rupture of dura mater (disorder)",
            "attributes": null
          },
          {
            "code": "29570005",
            "description": "Leigh's disease (disorder)",
            "attributes": null
          },
          {
            "code": "29618004",
            "description": "Striatonigral degeneration (disorder)",
            "attributes": null
          },
          {
            "code": "297138001",
            "description": "Embolus of circle of Willis (disorder)",
            "attributes": null
          },
          {
            "code": "297157005",
            "description": "Intracranial venous thrombosis (disorder)",
            "attributes": null
          },
          {
            "code": "29774004",
            "description": "Vascular myelopathy (disorder)",
            "attributes": null
          },
          {
            "code": "298118004",
            "description": "Suprascapular nerve lesion (disorder)",
            "attributes": null
          },
          {
            "code": "298119007",
            "description": "Long thoracic nerve lesion (disorder)",
            "attributes": null
          },
          {
            "code": "298137008",
            "description": "Thoracoabdominal neuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "2992000",
            "description": "Pigmentary pallidal degeneration (disorder)",
            "attributes": null
          },
          {
            "code": "29941000119105",
            "description": "Ataxia as sequela of cerebrovascular disease (disorder)",
            "attributes": null
          },
          {
            "code": "299966003",
            "description": "Compression of lumbar nerve root (disorder)",
            "attributes": null
          },
          {
            "code": "299967007",
            "description": "Compression of sacral nerve root (disorder)",
            "attributes": null
          },
          {
            "code": "300920004",
            "description": "Carotid atherosclerosis (disorder)",
            "attributes": null
          },
          {
            "code": "300992002",
            "description": "Alcohol-induced cerebellar ataxia (disorder)",
            "attributes": null
          },
          {
            "code": "301765007",
            "description": "Cerebellar hematoma (disorder)",
            "attributes": null
          },
          {
            "code": "302213007",
            "description": "Caroticocavernous sinus fistula (disorder)",
            "attributes": null
          },
          {
            "code": "302225005",
            "description": "Polyneuropathy and mononeuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "302226006",
            "description": "Peripheral nerve disease (disorder)",
            "attributes": null
          },
          {
            "code": "302878004",
            "description": "Intracranial septic thrombophlebitis (disorder)",
            "attributes": null
          },
          {
            "code": "302879007",
            "description": "Septic thrombophlebitis of cavernous sinus (disorder)",
            "attributes": null
          },
          {
            "code": "302880005",
            "description": "Septic thrombophlebitis of sagittal sinus (disorder)",
            "attributes": null
          },
          {
            "code": "302881009",
            "description": "Septic thrombophlebitis of lateral sinus (disorder)",
            "attributes": null
          },
          {
            "code": "302883007",
            "description": "Meningeal cyst (disorder)",
            "attributes": null
          },
          {
            "code": "302884001",
            "description": "Multiple cranial nerve lesions and linked syndromes (disorder)",
            "attributes": null
          },
          {
            "code": "302909007",
            "description": "Diffuse cerebrovascular disease (disorder)",
            "attributes": null
          },
          {
            "code": "30292005",
            "description": "Mononeuritis multiplex (disorder)",
            "attributes": null
          },
          {
            "code": "304535004",
            "description": "Parkinsonian features (finding)",
            "attributes": null
          },
          {
            "code": "304737009",
            "description": "Familial hyperkalemic periodic paralysis (disorder)",
            "attributes": null
          },
          {
            "code": "305719002",
            "description": "Neuromyotonia (disorder)",
            "attributes": null
          },
          {
            "code": "30736009",
            "description": "Dysphonia of palatopharyngolaryngeal myoclonus (disorder)",
            "attributes": null
          },
          {
            "code": "307362003",
            "description": "Intracranial venous septic embolism (disorder)",
            "attributes": null
          },
          {
            "code": "307363008",
            "description": "Multiple lacunar infarcts (disorder)",
            "attributes": null
          },
          {
            "code": "307405000",
            "description": "Hypoglossal nerve palsy (disorder)",
            "attributes": null
          },
          {
            "code": "30753002",
            "description": "Normal pressure hydrocephalus (disorder)",
            "attributes": null
          },
          {
            "code": "307672008",
            "description": "Oculopalatal myoclonus (disorder)",
            "attributes": null
          },
          {
            "code": "307693006",
            "description": "Vertical myoclonus (disorder)",
            "attributes": null
          },
          {
            "code": "307766002",
            "description": "Left sided cerebral infarction (disorder)",
            "attributes": null
          },
          {
            "code": "307767006",
            "description": "Right sided cerebral infarction (disorder)",
            "attributes": null
          },
          {
            "code": "308634000",
            "description": "Spinal demyelination (disorder)",
            "attributes": null
          },
          {
            "code": "308909003",
            "description": "Parkinsonian tremor (finding)",
            "attributes": null
          },
          {
            "code": "309255002",
            "description": "Charcot's joint of foot (disorder)",
            "attributes": null
          },
          {
            "code": "309520003",
            "description": "Symmetrical sensory neuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "30967002",
            "description": "Thyrotoxic periodic paralysis (disorder)",
            "attributes": null
          },
          {
            "code": "31097004",
            "description": "Post poliomyelitis syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "311191000119109",
            "description": "Myelopathy co-occurrent and due to lumbosacral intervertebral disc disorder (disorder)",
            "attributes": null
          },
          {
            "code": "311211000119105",
            "description": "Radiculopathy due to lumbar intervertebral disc disorder (disorder)",
            "attributes": null
          },
          {
            "code": "311221000119103",
            "description": "Radiculopathy co-occurrent and due to lumbosacral intervertebral disc disorder (disorder)",
            "attributes": null
          },
          {
            "code": "311231000119100",
            "description": "Radiculopathy co-occurrent and due to thoracic intervertebral disc disorder (disorder)",
            "attributes": null
          },
          {
            "code": "311804006",
            "description": "Prolapsed lumbar intervertebral disc with sciatica (disorder)",
            "attributes": null
          },
          {
            "code": "312586003",
            "description": "Intracranial thrombophlebitis (disorder)",
            "attributes": null
          },
          {
            "code": "312594005",
            "description": "Head and neck arterial thrombosis (disorder)",
            "attributes": null
          },
          {
            "code": "312991009",
            "description": "Senile dementia of the Lewy body type (disorder)",
            "attributes": null
          },
          {
            "code": "313304007",
            "description": "Non-traumatic spinal subdural hematoma (disorder)",
            "attributes": null
          },
          {
            "code": "31382008",
            "description": "Jugular foramen syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "315056009",
            "description": "Pudendal nerve neuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "315608004",
            "description": "Cardiomyopathy in Duchenne muscular dystrophy (disorder)",
            "attributes": null
          },
          {
            "code": "3168002",
            "description": "Thrombophlebitis of intracranial venous sinus (disorder)",
            "attributes": null
          },
          {
            "code": "31681005",
            "description": "Trigeminal neuralgia (disorder)",
            "attributes": null
          },
          {
            "code": "31785008",
            "description": "Collet-Sicard syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "31839002",
            "description": "Myasthenia gravis, adult form (disorder)",
            "attributes": null
          },
          {
            "code": "32112006",
            "description": "Phlebitis of inferior sagittal sinus (disorder)",
            "attributes": null
          },
          {
            "code": "322461000119108",
            "description": "Polyneuropathy due to systemic sclerosis (disorder)",
            "attributes": null
          },
          {
            "code": "32595002",
            "description": "Mononeuritis (disorder)",
            "attributes": null
          },
          {
            "code": "32728005",
            "description": "Hemorrhage due to ruptured congenital cerebral aneurysm (disorder)",
            "attributes": null
          },
          {
            "code": "32798002",
            "description": "Parkinsonism (disorder)",
            "attributes": null
          },
          {
            "code": "329361000119107",
            "description": "Cerebrovascular accident due to occlusion of right middle cerebral artery by embolus (disorder)",
            "attributes": null
          },
          {
            "code": "329371000119101",
            "description": "Cerebrovascular accident due to occlusion of left middle cerebral artery by embolus (disorder)",
            "attributes": null
          },
          {
            "code": "329421000119107",
            "description": "Cerebrovascular accident due to occlusion of right posterior cerebral artery by embolus (disorder)",
            "attributes": null
          },
          {
            "code": "329431000119105",
            "description": "Cerebrovascular accident due to occlusion of left posterior cerebral artery by embolus (disorder)",
            "attributes": null
          },
          {
            "code": "329451000119104",
            "description": "Cerebrovascular accident due to occlusion of right cerebellar artery by embolus (disorder)",
            "attributes": null
          },
          {
            "code": "329461000119102",
            "description": "Cerebrovascular accident due to occlusion of left cerebellar artery by embolus (disorder)",
            "attributes": null
          },
          {
            "code": "329481000119106",
            "description": "Occlusion of right middle cerebral artery (disorder)",
            "attributes": null
          },
          {
            "code": "329491000119109",
            "description": "Occlusion of left middle cerebral artery (disorder)",
            "attributes": null
          },
          {
            "code": "329561000119101",
            "description": "Occlusion of right posterior cerebral artery (disorder)",
            "attributes": null
          },
          {
            "code": "329571000119107",
            "description": "Occlusion of left posterior cerebral artery (disorder)",
            "attributes": null
          },
          {
            "code": "329641000119104",
            "description": "Cerebrovascular accident due to thrombus of basilar artery (disorder)",
            "attributes": null
          },
          {
            "code": "329651000119102",
            "description": "Cerebrovascular accident due to thrombus of right carotid artery (disorder)",
            "attributes": null
          },
          {
            "code": "330011000119102",
            "description": "Non-traumatic cerebral edema (disorder)",
            "attributes": null
          },
          {
            "code": "330061000119104",
            "description": "Acquired cerebral ventriculomegaly (disorder)",
            "attributes": null
          },
          {
            "code": "330411000119109",
            "description": "Lacunar ataxic hemiparesis of left nondominant side (disorder)",
            "attributes": null
          },
          {
            "code": "330421000119102",
            "description": "Lacunar ataxic hemiparesis of right nondominant side (disorder)",
            "attributes": null
          },
          {
            "code": "330791000119108",
            "description": "Cerebrovascular accident due to thrombus of left carotid artery (disorder)",
            "attributes": null
          },
          {
            "code": "33209009",
            "description": "Idiopathic progressive polyneuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "33301000119105",
            "description": "Sequela of cardioembolic stroke (disorder)",
            "attributes": null
          },
          {
            "code": "3331000119108",
            "description": "Laryngeal dystonia (disorder)",
            "attributes": null
          },
          {
            "code": "33331000119103",
            "description": "Sequela of lacunar stroke (disorder)",
            "attributes": null
          },
          {
            "code": "33595009",
            "description": "Arachnoid cyst (disorder)",
            "attributes": null
          },
          {
            "code": "33772003",
            "description": "Myelomalacia (disorder)",
            "attributes": null
          },
          {
            "code": "33832002",
            "description": "Third division of fifth cranial nerve disorder (disorder)",
            "attributes": null
          },
          {
            "code": "34101000119105",
            "description": "Nocturnal myoclonus (disorder)",
            "attributes": null
          },
          {
            "code": "34139004",
            "description": "Intervertebral disc disorder of lumbar region with myelopathy (disorder)",
            "attributes": null
          },
          {
            "code": "34181000119102",
            "description": "Cerebral infarction due to occlusion of basilar artery (disorder)",
            "attributes": null
          },
          {
            "code": "34184002",
            "description": "Corpus callosum syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "34191000119104",
            "description": "Cerebral infarction due to vertebral artery occlusion (disorder)",
            "attributes": null
          },
          {
            "code": "34253008",
            "description": "Myopathy in Addison's disease (disorder)",
            "attributes": null
          },
          {
            "code": "34513009",
            "description": "Zebra body myopathy (disorder)",
            "attributes": null
          },
          {
            "code": "3456001",
            "description": "Chronic progressive non-hereditary chorea (disorder)",
            "attributes": null
          },
          {
            "code": "347079002",
            "description": "Chorda tympani disorder (disorder)",
            "attributes": null
          },
          {
            "code": "34781003",
            "description": "Vertebral artery syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "348051000119102",
            "description": "Atrophy of right optic nerve following inflammation (disorder)",
            "attributes": null
          },
          {
            "code": "348501000119108",
            "description": "Atrophy of left optic nerve following inflammation (disorder)",
            "attributes": null
          },
          {
            "code": "350471000119102",
            "description": "Idiopathic small fiber peripheral neuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "35145002",
            "description": "Uremic encephalopathy (disorder)",
            "attributes": null
          },
          {
            "code": "35386004",
            "description": "Cavernous sinus syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "35491000119107",
            "description": "Restrictive lung mechanics due to neuromuscular disease (disorder)",
            "attributes": null
          },
          {
            "code": "35777006",
            "description": "Mononeuropathy multiplex due to diabetes mellitus (disorder)",
            "attributes": null
          },
          {
            "code": "359554008",
            "description": "Charcot's arthropathy (disorder)",
            "attributes": null
          },
          {
            "code": "359611005",
            "description": "Neuropathy with neurologic complication due to diabetes mellitus (disorder)",
            "attributes": null
          },
          {
            "code": "361000119103",
            "description": "Paralytic syndrome on one side of the body as late effect of cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "361216007",
            "description": "Femoral mononeuropathy due to diabetes mellitus (disorder)",
            "attributes": null
          },
          {
            "code": "361272001",
            "description": "Cerebellar ataxia due to alcoholism (disorder)",
            "attributes": null
          },
          {
            "code": "361273006",
            "description": "Alcoholic cerebellar degeneration (disorder)",
            "attributes": null
          },
          {
            "code": "36179005",
            "description": "Reversible ischemic neurologic deficit syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "365258000",
            "description": "Tibial nerve palsy (disorder)",
            "attributes": null
          },
          {
            "code": "368521000119107",
            "description": "Disorder of nerve co-occurrent and due to type 1 diabetes mellitus (disorder)",
            "attributes": null
          },
          {
            "code": "368581000119106",
            "description": "Neuropathy due to type 2 diabetes mellitus (disorder)",
            "attributes": null
          },
          {
            "code": "36905001",
            "description": "Secondary bitter taste disorder (disorder)",
            "attributes": null
          },
          {
            "code": "370502006",
            "description": "Encephalomyelopathy (disorder)",
            "attributes": null
          },
          {
            "code": "371029002",
            "description": "Ischemic disorder of spinal cord (disorder)",
            "attributes": null
          },
          {
            "code": "371040005",
            "description": "Thrombotic stroke (disorder)",
            "attributes": null
          },
          {
            "code": "371041009",
            "description": "Embolic stroke (disorder)",
            "attributes": null
          },
          {
            "code": "371076006",
            "description": "Congenital syringomyelia (disorder)",
            "attributes": null
          },
          {
            "code": "371109001",
            "description": "Immature autonomic system (disorder)",
            "attributes": null
          },
          {
            "code": "371114002",
            "description": "Seizures complicating intracranial hemorrhage (disorder)",
            "attributes": null
          },
          {
            "code": "371116000",
            "description": "Posthemorrhagic hydrocephalus (disorder)",
            "attributes": null
          },
          {
            "code": "371158002",
            "description": "Disorder of basilar artery (disorder)",
            "attributes": null
          },
          {
            "code": "371313002",
            "description": "Congenital cerebellar cortical atrophy (disorder)",
            "attributes": null
          },
          {
            "code": "372477008",
            "description": "Post-traumatic syrinx (disorder)",
            "attributes": null
          },
          {
            "code": "37340000",
            "description": "Motor neuron disease (disorder)",
            "attributes": null
          },
          {
            "code": "373606000",
            "description": "Occlusive stroke (disorder)",
            "attributes": null
          },
          {
            "code": "37481009",
            "description": "Anterior tongue taste disorder (disorder)",
            "attributes": null
          },
          {
            "code": "37650008",
            "description": "Hereditary cerebellar degeneration (disorder)",
            "attributes": null
          },
          {
            "code": "37770007",
            "description": "Melkersson's syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "37934003",
            "description": "Mitochondrial-lipid-glycogen storage myopathy (disorder)",
            "attributes": null
          },
          {
            "code": "37943007",
            "description": "Multiple AND bilateral precerebral artery embolism (disorder)",
            "attributes": null
          },
          {
            "code": "38073003",
            "description": "Neuritis AND/OR radiculitis due to displacement of intervertebral disc (disorder)",
            "attributes": null
          },
          {
            "code": "384993003",
            "description": "Periventricular hemorrhagic venous infarct (disorder)",
            "attributes": null
          },
          {
            "code": "385006",
            "description": "Secondary peripheral neuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "38523005",
            "description": "Syphilitic parkinsonism (disorder)",
            "attributes": null
          },
          {
            "code": "386033004",
            "description": "Neuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "386766007",
            "description": "Marchiafava-Bignami disease (disorder)",
            "attributes": null
          },
          {
            "code": "386781001",
            "description": "Spastic syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "387732009",
            "description": "Becker muscular dystrophy (disorder)",
            "attributes": null
          },
          {
            "code": "38837006",
            "description": "Acquired porencephaly (disorder)",
            "attributes": null
          },
          {
            "code": "389088001",
            "description": "Hypoxia of brain (disorder)",
            "attributes": null
          },
          {
            "code": "389089009",
            "description": "Anoxia of brain (disorder)",
            "attributes": null
          },
          {
            "code": "389098007",
            "description": "Anoxic encephalopathy (disorder)",
            "attributes": null
          },
          {
            "code": "389100007",
            "description": "Ischemic encephalopathy (disorder)",
            "attributes": null
          },
          {
            "code": "389101006",
            "description": "Anoxic-ischemic encephalopathy (disorder)",
            "attributes": null
          },
          {
            "code": "3900008",
            "description": "Mixed sensory-motor polyneuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "39058009",
            "description": "Lumbosacral radiculoplexus neuropathy due to diabetes mellitus (disorder)",
            "attributes": null
          },
          {
            "code": "390936003",
            "description": "Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (disorder)",
            "attributes": null
          },
          {
            "code": "39127005",
            "description": "Symmetric proximal motor neuropathy due to diabetes mellitus (disorder)",
            "attributes": null
          },
          {
            "code": "39134007",
            "description": "Hematomyelia (disorder)",
            "attributes": null
          },
          {
            "code": "39181008",
            "description": "Radiculoplexus neuropathy due to diabetes mellitus (disorder)",
            "attributes": null
          },
          {
            "code": "39510005",
            "description": "Neurogenic ossifying arthropathy (disorder)",
            "attributes": null
          },
          {
            "code": "397734008",
            "description": "Hereditary sensory and autonomic neuropathy type I (disorder)",
            "attributes": null
          },
          {
            "code": "397809001",
            "description": "Nontraumatic extradural intracranial hemorrhage (disorder)",
            "attributes": null
          },
          {
            "code": "398040009",
            "description": "Charcot-Marie-Tooth disease, type I (disorder)",
            "attributes": null
          },
          {
            "code": "398100001",
            "description": "Hereditary motor and sensory neuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "398148000",
            "description": "Hereditary sensory and autonomic neuropathy type II (disorder)",
            "attributes": null
          },
          {
            "code": "398187000",
            "description": "Charcot-Marie-Tooth disease, type II (disorder)",
            "attributes": null
          },
          {
            "code": "398432008",
            "description": "Bulbar weakness (disorder)",
            "attributes": null
          },
          {
            "code": "399040002",
            "description": "Congenital central hypoventilation (disorder)",
            "attributes": null
          },
          {
            "code": "399041003",
            "description": "Chastek paralysis (disorder)",
            "attributes": null
          },
          {
            "code": "399091004",
            "description": "Facioscapulohumeral muscular dystrophy (disorder)",
            "attributes": null
          },
          {
            "code": "39912006",
            "description": "Hereditary spastic paraplegia (disorder)",
            "attributes": null
          },
          {
            "code": "39925003",
            "description": "Juvenile myopathy, encephalopathy, lactic acidosis AND stroke (disorder)",
            "attributes": null
          },
          {
            "code": "400983004",
            "description": "Ilio-inguinal nerve entrapment (disorder)",
            "attributes": null
          },
          {
            "code": "40161000119102",
            "description": "Weakness of face muscles as sequela of stroke (disorder)",
            "attributes": null
          },
          {
            "code": "402615009",
            "description": "Hypermelanosis due to nervous system disorder (disorder)",
            "attributes": null
          },
          {
            "code": "402740007",
            "description": "Dermatosis due to peripheral nerve disorder (disorder)",
            "attributes": null
          },
          {
            "code": "402742004",
            "description": "Skin damage resulting from acquired nerve disorder (disorder)",
            "attributes": null
          },
          {
            "code": "40276003",
            "description": "Embolism of precerebral artery (disorder)",
            "attributes": null
          },
          {
            "code": "403602005",
            "description": "Trigeminal trophic syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "403603000",
            "description": "Neurotrophic damage to skin (disorder)",
            "attributes": null
          },
          {
            "code": "40381009",
            "description": "Familial normokalemic periodic paralysis (disorder)",
            "attributes": null
          },
          {
            "code": "404188001",
            "description": "Sequelae of meningitis (disorder)",
            "attributes": null
          },
          {
            "code": "40450001",
            "description": "Embolism of superior sagittal sinus (disorder)",
            "attributes": null
          },
          {
            "code": "40632002",
            "description": "Charcot-Marie-Tooth disease, type IA (disorder)",
            "attributes": null
          },
          {
            "code": "406564009",
            "description": "Brucella infection of the central nervous system (disorder)",
            "attributes": null
          },
          {
            "code": "40720005",
            "description": "Cerebral cyst (disorder)",
            "attributes": null
          },
          {
            "code": "408664007",
            "description": "Pontine artery occlusion (disorder)",
            "attributes": null
          },
          {
            "code": "408665008",
            "description": "Pontine artery thrombosis (disorder)",
            "attributes": null
          },
          {
            "code": "408751001",
            "description": "Complex regional pain syndrome, type II (disorder)",
            "attributes": null
          },
          {
            "code": "4088009",
            "description": "Acquired hydrocephalus (disorder)",
            "attributes": null
          },
          {
            "code": "40956001",
            "description": "Guillain-BarrÃ© syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "410014007",
            "description": "Post-traumatic communicating hydrocephalus (disorder)",
            "attributes": null
          },
          {
            "code": "410015008",
            "description": "Post-traumatic non-communicating hydrocephalus (disorder)",
            "attributes": null
          },
          {
            "code": "41009006",
            "description": "Progressive cerebellar tremor (disorder)",
            "attributes": null
          },
          {
            "code": "41022003",
            "description": "Intervertebral disc disorder of thoracic region with myelopathy (disorder)",
            "attributes": null
          },
          {
            "code": "4113009",
            "description": "Arrested hydrocephalus (disorder)",
            "attributes": null
          },
          {
            "code": "413100008",
            "description": "Akinetic rigid syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "413102000",
            "description": "Infarction of basal ganglia (disorder)",
            "attributes": null
          },
          {
            "code": "41362007",
            "description": "Ossifying pachymeningitis (disorder)",
            "attributes": null
          },
          {
            "code": "413758000",
            "description": "Cardioembolic stroke (disorder)",
            "attributes": null
          },
          {
            "code": "413807008",
            "description": "Cerebellar hernia (disorder)",
            "attributes": null
          },
          {
            "code": "414400006",
            "description": "Hernia of cerebellar tonsil into foramen magnum (disorder)",
            "attributes": null
          },
          {
            "code": "414927004",
            "description": "Ocular myasthenia with strabismus (disorder)",
            "attributes": null
          },
          {
            "code": "41574007",
            "description": "Paramyotonia congenita (disorder)",
            "attributes": null
          },
          {
            "code": "416123004",
            "description": "Complaining of akathisia (disorder)",
            "attributes": null
          },
          {
            "code": "416780008",
            "description": "Primary degenerative dementia of the Alzheimer type, presenile onset (disorder)",
            "attributes": null
          },
          {
            "code": "416975007",
            "description": "Primary degenerative dementia of the Alzheimer type, senile onset (disorder)",
            "attributes": null
          },
          {
            "code": "417017003",
            "description": "Acute cerebellar syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "41713005",
            "description": "Benedikt's syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "41733009",
            "description": "Neuritis AND/OR radiculitis due to rupture of intervertebral disc (disorder)",
            "attributes": null
          },
          {
            "code": "418072004",
            "description": "Central nervous system depression (disorder)",
            "attributes": null
          },
          {
            "code": "418143002",
            "description": "Cerebral degeneration (disorder)",
            "attributes": null
          },
          {
            "code": "4183003",
            "description": "Charcot-Marie-Tooth disease, type IC (disorder)",
            "attributes": null
          },
          {
            "code": "418763003",
            "description": "Periodic limb movement disorder (disorder)",
            "attributes": null
          },
          {
            "code": "418856006",
            "description": "Paraneoplastic optic neuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "41964001",
            "description": "Hypertrophic cardiomyopathy secondary to neuromuscular disorder (disorder)",
            "attributes": null
          },
          {
            "code": "41975002",
            "description": "Insomnia with sleep apnea (disorder)",
            "attributes": null
          },
          {
            "code": "420146005",
            "description": "Cerebral degeneration associated with generalized lipidosis (disorder)",
            "attributes": null
          },
          {
            "code": "420436000",
            "description": "Mononeuropathy due to type 2 diabetes mellitus (disorder)",
            "attributes": null
          },
          {
            "code": "420718004",
            "description": "Central nervous system demyelinating disease associated with acquired immunodeficiency syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "420918009",
            "description": "Mononeuropathy due to type 1 diabetes mellitus (disorder)",
            "attributes": null
          },
          {
            "code": "420932006",
            "description": "Episodic ataxia type 2 (disorder)",
            "attributes": null
          },
          {
            "code": "421182009",
            "description": "Episodic ataxia type 1 (disorder)",
            "attributes": null
          },
          {
            "code": "421326000",
            "description": "Disorder of nervous system due to type 2 diabetes mellitus (disorder)",
            "attributes": null
          },
          {
            "code": "421455009",
            "description": "Episodic ataxia (disorder)",
            "attributes": null
          },
          {
            "code": "421468001",
            "description": "Disorder of nervous system due to type 1 diabetes mellitus (disorder)",
            "attributes": null
          },
          {
            "code": "421998001",
            "description": "Central nervous disorder associated with acquired immunodeficiency syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "422348008",
            "description": "Andersen Tawil syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "422426003",
            "description": "Facial nerve disorder (disorder)",
            "attributes": null
          },
          {
            "code": "422504002",
            "description": "Ischemic stroke (disorder)",
            "attributes": null
          },
          {
            "code": "423144007",
            "description": "Multifactorial encephalopathy (disorder)",
            "attributes": null
          },
          {
            "code": "42345000",
            "description": "Polyneuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "423488006",
            "description": "Papilledema - optic disc edema due to raised intracranial pressure (disorder)",
            "attributes": null
          },
          {
            "code": "423582009",
            "description": "Traumatic arachnoid cyst (disorder)",
            "attributes": null
          },
          {
            "code": "42369001",
            "description": "Pallidopontonigral degeneration (disorder)",
            "attributes": null
          },
          {
            "code": "424054000",
            "description": "Nerve entrapment due to scar (disorder)",
            "attributes": null
          },
          {
            "code": "424271007",
            "description": "Hysterical cataplexy (disorder)",
            "attributes": null
          },
          {
            "code": "42429001",
            "description": "Cerebromeningeal hemorrhage (disorder)",
            "attributes": null
          },
          {
            "code": "424736006",
            "description": "Peripheral neuropathy due to diabetes mellitus (disorder)",
            "attributes": null
          },
          {
            "code": "425390006",
            "description": "Dementia associated with Parkinson's Disease (disorder)",
            "attributes": null
          },
          {
            "code": "425420004",
            "description": "Thrombosis of internal carotid artery (disorder)",
            "attributes": null
          },
          {
            "code": "425492002",
            "description": "Generalized dystonia (disorder)",
            "attributes": null
          },
          {
            "code": "425500002",
            "description": "Secondary progressive multiple sclerosis (disorder)",
            "attributes": null
          },
          {
            "code": "425522009",
            "description": "Hyperammonemic encephalopathy (disorder)",
            "attributes": null
          },
          {
            "code": "425576009",
            "description": "Traumatic cyst of leptomeninges (disorder)",
            "attributes": null
          },
          {
            "code": "425642008",
            "description": "Monoplegia of dominant lower limb as a late effect of cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "425659003",
            "description": "Vasculitic neuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "425756000",
            "description": "Idiopathic transverse myelitis (disorder)",
            "attributes": null
          },
          {
            "code": "425882004",
            "description": "Paralytic syndrome as late effect of stroke (disorder)",
            "attributes": null
          },
          {
            "code": "425892007",
            "description": "Baroreflex failure syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "425932008",
            "description": "Thrombosis of posterior communicating artery (disorder)",
            "attributes": null
          },
          {
            "code": "425957003",
            "description": "Non-traumatic intracerebral ventricular hemorrhage (disorder)",
            "attributes": null
          },
          {
            "code": "425988004",
            "description": "Sensory integration disorder (disorder)",
            "attributes": null
          },
          {
            "code": "426033005",
            "description": "Dysphagia as a late effect of cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "426107000",
            "description": "Acute lacunar infarction (disorder)",
            "attributes": null
          },
          {
            "code": "426187002",
            "description": "Myoclonus of stapedius muscle (disorder)",
            "attributes": null
          },
          {
            "code": "4262001",
            "description": "Phlebitis of superior sagittal sinus (disorder)",
            "attributes": null
          },
          {
            "code": "426293000",
            "description": "Sural neuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "426373005",
            "description": "Relapsing remitting multiple sclerosis (disorder)",
            "attributes": null
          },
          {
            "code": "426542005",
            "description": "Sleep hypoventilation due to lower airway obstruction (disorder)",
            "attributes": null
          },
          {
            "code": "42658009",
            "description": "Disorder of the peripheral nervous system (disorder)",
            "attributes": null
          },
          {
            "code": "426651005",
            "description": "Occlusion of bilateral carotid arteries (disorder)",
            "attributes": null
          },
          {
            "code": "426788002",
            "description": "Vertigo as late effect of stroke (disorder)",
            "attributes": null
          },
          {
            "code": "426814001",
            "description": "Transient cerebral ischemia due to atrial fibrillation (disorder)",
            "attributes": null
          },
          {
            "code": "426983002",
            "description": "Infarction of medulla oblongata (disorder)",
            "attributes": null
          },
          {
            "code": "427020007",
            "description": "Cerebral vasculitis (disorder)",
            "attributes": null
          },
          {
            "code": "427027005",
            "description": "Lumbosacral radiculoplexus neuropathy due to type 2 diabetes mellitus (disorder)",
            "attributes": null
          },
          {
            "code": "427065003",
            "description": "Monoplegia of dominant upper limb as a late effect of cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "427086003",
            "description": "Bickerstaff's brainstem encephalitis (disorder)",
            "attributes": null
          },
          {
            "code": "427111000",
            "description": "Non-epileptic myoclonus (disorder)",
            "attributes": null
          },
          {
            "code": "427232004",
            "description": "Hemidystonia (disorder)",
            "attributes": null
          },
          {
            "code": "427296003",
            "description": "Thalamic infarction (disorder)",
            "attributes": null
          },
          {
            "code": "427432001",
            "description": "Paralytic syndrome as late effect of thalamic stroke (disorder)",
            "attributes": null
          },
          {
            "code": "427488005",
            "description": "On - off phenomenon (disorder)",
            "attributes": null
          },
          {
            "code": "427571000",
            "description": "Lumbosacral radiculoplexus neuropathy due to type 1 diabetes mellitus (disorder)",
            "attributes": null
          },
          {
            "code": "42769004",
            "description": "Diffuse Lewy body disease with spongiform cortical change (disorder)",
            "attributes": null
          },
          {
            "code": "427777003",
            "description": "Restrictive lung disease due to muscular dystrophy (disorder)",
            "attributes": null
          },
          {
            "code": "427789001",
            "description": "Myoclonus of tensor tympani muscle (disorder)",
            "attributes": null
          },
          {
            "code": "427878002",
            "description": "Arthropathy of the hand associated with a neurological disorder (disorder)",
            "attributes": null
          },
          {
            "code": "427925000",
            "description": "Arthropathy of the wrist associated with a neurological disorder (disorder)",
            "attributes": null
          },
          {
            "code": "427945008",
            "description": "Segmental dystonia (disorder)",
            "attributes": null
          },
          {
            "code": "428106000",
            "description": "Arthropathy of multiple joints associated with a neurological disorder (disorder)",
            "attributes": null
          },
          {
            "code": "428259005",
            "description": "Acquired tethered cord syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "428359008",
            "description": "Ilioinguinal nerve neuritis (disorder)",
            "attributes": null
          },
          {
            "code": "428700003",
            "description": "Primary progressive multiple sclerosis (disorder)",
            "attributes": null
          },
          {
            "code": "428779003",
            "description": "Arthropathy of the knee associated with a neurological disorder (disorder)",
            "attributes": null
          },
          {
            "code": "429438008",
            "description": "Sequela of infectious meningitis (disorder)",
            "attributes": null
          },
          {
            "code": "429456008",
            "description": "Hypoventilation during sleep due to neuromuscular disorder (disorder)",
            "attributes": null
          },
          {
            "code": "429643006",
            "description": "Arthropathy of the elbow associated with a neurological disorder (disorder)",
            "attributes": null
          },
          {
            "code": "42970005",
            "description": "Nonpyogenic thrombosis of intracranial venous sinus (disorder)",
            "attributes": null
          },
          {
            "code": "42986003",
            "description": "Charcot-Marie-Tooth disease, type IB (disorder)",
            "attributes": null
          },
          {
            "code": "42998008",
            "description": "Vagus nerve laryngeal paralysis (disorder)",
            "attributes": null
          },
          {
            "code": "430042004",
            "description": "Acute panautonomic neuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "430397002",
            "description": "Disorder of nervous system caused by West Nile virus (disorder)",
            "attributes": null
          },
          {
            "code": "430428000",
            "description": "Arthropathy of the ankle AND/OR foot associated with a neurological disorder (disorder)",
            "attributes": null
          },
          {
            "code": "430893009",
            "description": "Sleep related rhythmic movement disorder (disorder)",
            "attributes": null
          },
          {
            "code": "430947007",
            "description": "Paralytic syndrome of nondominant side as late effect of stroke (disorder)",
            "attributes": null
          },
          {
            "code": "430959006",
            "description": "Paralytic syndrome of dominant side as late effect of stroke (disorder)",
            "attributes": null
          },
          {
            "code": "431034009",
            "description": "Torsion dystonia (disorder)",
            "attributes": null
          },
          {
            "code": "43105007",
            "description": "Choreoathetosis (disorder)",
            "attributes": null
          },
          {
            "code": "431520004",
            "description": "Inflammation of spinal cord caused by toxin (disorder)",
            "attributes": null
          },
          {
            "code": "43152001",
            "description": "Central core disease (disorder)",
            "attributes": null
          },
          {
            "code": "432249006",
            "description": "Infarction of spinal cord (disorder)",
            "attributes": null
          },
          {
            "code": "43226001",
            "description": "Sarcotubular myopathy (disorder)",
            "attributes": null
          },
          {
            "code": "432504007",
            "description": "Cerebral infarction (disorder)",
            "attributes": null
          },
          {
            "code": "433183000",
            "description": "Neurogenic bladder as late effect of cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "433493000",
            "description": "Acquired torsion dystonia (disorder)",
            "attributes": null
          },
          {
            "code": "433691000124104",
            "description": "Intracranial hypotension (disorder)",
            "attributes": null
          },
          {
            "code": "4338008",
            "description": "Arnold's nerve reflex cough syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "43647007",
            "description": "Juvenile paralysis agitans of Hunt (disorder)",
            "attributes": null
          },
          {
            "code": "43658003",
            "description": "Vertebral artery obstruction (disorder)",
            "attributes": null
          },
          {
            "code": "438481007",
            "description": "Postoperative tethered cord syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "438511000",
            "description": "Benign multiple sclerosis (disorder)",
            "attributes": null
          },
          {
            "code": "438513002",
            "description": "Cerebral degeneration due to Parkinson's disease (disorder)",
            "attributes": null
          },
          {
            "code": "43898003",
            "description": "Brachial neuritis AND/OR radiculitis due to rupture of cervical intervertebral disc (disorder)",
            "attributes": null
          },
          {
            "code": "439567002",
            "description": "Malignant multiple sclerosis (disorder)",
            "attributes": null
          },
          {
            "code": "439732004",
            "description": "Myoclonic dystonia (disorder)",
            "attributes": null
          },
          {
            "code": "43977004",
            "description": "Corticostriatal-spinal degeneration (disorder)",
            "attributes": null
          },
          {
            "code": "440140008",
            "description": "History of cerebrovascular accident with residual deficit (situation)",
            "attributes": null
          },
          {
            "code": "441526008",
            "description": "Infarct of cerebrum due to iatrogenic cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "441529001",
            "description": "Dysphasia as late effect of cerebrovascular disease (disorder)",
            "attributes": null
          },
          {
            "code": "441630004",
            "description": "Aphasia as late effect of cerebrovascular disease (disorder)",
            "attributes": null
          },
          {
            "code": "441735003",
            "description": "Sensory disorder as a late effect of cerebrovascular disease (disorder)",
            "attributes": null
          },
          {
            "code": "441759008",
            "description": "Abnormal vision as a late effect of cerebrovascular disease (disorder)",
            "attributes": null
          },
          {
            "code": "441894009",
            "description": "Monoplegia of nondominant lower limb as a late effect of cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "441910000",
            "description": "Idiopathic sleep related non-obstructive alveolar hypoventilation (disorder)",
            "attributes": null
          },
          {
            "code": "441960006",
            "description": "Speech and language deficit as late effect of cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "441991000",
            "description": "Hemiparesis as late effect of cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "442024001",
            "description": "Hemiplegia as late effect of cerebrovascular disease (disorder)",
            "attributes": null
          },
          {
            "code": "442164004",
            "description": "Organic sleep apnea (disorder)",
            "attributes": null
          },
          {
            "code": "442181008",
            "description": "Monoplegia of nondominant upper limb as a late effect of cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "442212003",
            "description": "Residual cognitive deficit as late effect of cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "442344002",
            "description": "Dementia due to Huntington chorea (disorder)",
            "attributes": null
          },
          {
            "code": "44248001",
            "description": "Raymond-Cestan syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "442511009",
            "description": "Progressive encephalopathy with edema, hypsarrhythmia and optic atrophy syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "44253006",
            "description": "Nutritional myopathy (disorder)",
            "attributes": null
          },
          {
            "code": "442617003",
            "description": "Aphasia as late effect of cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "442668000",
            "description": "Hemiplegia of nondominant side as late effect of cerebrovascular disease (disorder)",
            "attributes": null
          },
          {
            "code": "442676003",
            "description": "Hemiplegia of dominant side as late effect of cerebrovascular disease (disorder)",
            "attributes": null
          },
          {
            "code": "442733008",
            "description": "Hemiplegia as late effect of cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "442964000",
            "description": "Conus medullaris syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "443153007",
            "description": "Inflammation of brain and spinal cord caused by toxic substance (disorder)",
            "attributes": null
          },
          {
            "code": "443352005",
            "description": "Dystonia of head (disorder)",
            "attributes": null
          },
          {
            "code": "443353000",
            "description": "Entrapment of genitofemoral nerve (disorder)",
            "attributes": null
          },
          {
            "code": "443490000",
            "description": "Entrapment of plantar nerve (disorder)",
            "attributes": null
          },
          {
            "code": "443760008",
            "description": "Sleep hypoventilation (disorder)",
            "attributes": null
          },
          {
            "code": "443819006",
            "description": "Critical illness myopathy (disorder)",
            "attributes": null
          },
          {
            "code": "443929000",
            "description": "Small vessel cerebrovascular disease (disorder)",
            "attributes": null
          },
          {
            "code": "444024002",
            "description": "Multiple system atrophy, cerebellar variant (disorder)",
            "attributes": null
          },
          {
            "code": "444172003",
            "description": "Recurrent transient cerebral ischemic attack (disorder)",
            "attributes": null
          },
          {
            "code": "444197004",
            "description": "Multiple system atrophy, Parkinson variant (disorder)",
            "attributes": null
          },
          {
            "code": "444657001",
            "description": "Superior cerebellar artery syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "444980006",
            "description": "Sporadic olivopontocerebellar atrophy (disorder)",
            "attributes": null
          },
          {
            "code": "445006008",
            "description": "Focal dystonia (disorder)",
            "attributes": null
          },
          {
            "code": "445166009",
            "description": "Cystic degeneration of brain (disorder)",
            "attributes": null
          },
          {
            "code": "445252005",
            "description": "Glucose transporter protein type 1 deficiency syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "445339002",
            "description": "Neuropathy caused by ionizing radiation (disorder)",
            "attributes": null
          },
          {
            "code": "445423005",
            "description": "Paraneoplastic subacute necrotic myelopathy (disorder)",
            "attributes": null
          },
          {
            "code": "445475001",
            "description": "Paraneoplastic sensorimotor neuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "445967004",
            "description": "Clinically isolated syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "446495002",
            "description": "Ependymal cyst of spinal meninges (disorder)",
            "attributes": null
          },
          {
            "code": "446712002",
            "description": "Thromboembolus of precerebral artery (disorder)",
            "attributes": null
          },
          {
            "code": "446940004",
            "description": "Ependymal cyst of spinal cord (disorder)",
            "attributes": null
          },
          {
            "code": "446995005",
            "description": "Shuddering attacks (disorder)",
            "attributes": null
          },
          {
            "code": "447232008",
            "description": "Ependymal cyst of ventricle of brain (disorder)",
            "attributes": null
          },
          {
            "code": "447292006",
            "description": "Mitochondrial encephalomyopathy (disorder)",
            "attributes": null
          },
          {
            "code": "447351004",
            "description": "Vanishing white matter disease (disorder)",
            "attributes": null
          },
          {
            "code": "4477007",
            "description": "Juvenile myopathy AND lactate acidosis (disorder)",
            "attributes": null
          },
          {
            "code": "447739003",
            "description": "Mega cisterna magna (finding)",
            "attributes": null
          },
          {
            "code": "448705004",
            "description": "Mesial temporal lobe sclerosis (disorder)",
            "attributes": null
          },
          {
            "code": "449020009",
            "description": "Intraparenchymal hemorrhage of brain (disorder)",
            "attributes": null
          },
          {
            "code": "449305009",
            "description": "Paraneoplastic sensory neuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "449793009",
            "description": "Hemorrhage into subdural space of neuraxis (disorder)",
            "attributes": null
          },
          {
            "code": "449795002",
            "description": "Hemorrhage into subdural space of spine (disorder)",
            "attributes": null
          },
          {
            "code": "449797005",
            "description": "Non-traumatic hematoma of subdural space of neuraxis (disorder)",
            "attributes": null
          },
          {
            "code": "44983007",
            "description": "Intervertebral disc disorder with myelopathy (disorder)",
            "attributes": null
          },
          {
            "code": "449899001",
            "description": "Dropped head syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "449916008",
            "description": "Peripheral facial palsy (disorder)",
            "attributes": null
          },
          {
            "code": "44997004",
            "description": "Quail myopathy of Lesbos (disorder)",
            "attributes": null
          },
          {
            "code": "450362008",
            "description": "Hemorrhage into subarachnoid space of neuraxis (disorder)",
            "attributes": null
          },
          {
            "code": "450363003",
            "description": "Hemorrhage into subarachnoid space of spine (disorder)",
            "attributes": null
          },
          {
            "code": "450376009",
            "description": "Hemorrhage of intracranial meningeal space (disorder)",
            "attributes": null
          },
          {
            "code": "450377000",
            "description": "Hemorrhage into meningeal space of neuraxis (disorder)",
            "attributes": null
          },
          {
            "code": "450425005",
            "description": "Intracranial hematoma (disorder)",
            "attributes": null
          },
          {
            "code": "450886002",
            "description": "Posterior reversible encephalopathy syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "451034003",
            "description": "Hemorrhage into subpial space of neuraxis (disorder)",
            "attributes": null
          },
          {
            "code": "451035002",
            "description": "Subpial intracranial hemorrhage (disorder)",
            "attributes": null
          },
          {
            "code": "451036001",
            "description": "Hemorrhage into subpial space of spinal cord (disorder)",
            "attributes": null
          },
          {
            "code": "451037005",
            "description": "Hemorrhage in globus pallidus (disorder)",
            "attributes": null
          },
          {
            "code": "451038000",
            "description": "Hemorrhage in caudate nucleus (disorder)",
            "attributes": null
          },
          {
            "code": "451039008",
            "description": "Hemorrhage in putamen (disorder)",
            "attributes": null
          },
          {
            "code": "45294007",
            "description": "Auriculotemporal syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "45299002",
            "description": "Intestinal autonomic neuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "45600000",
            "description": "Toxic polyneuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "45639009",
            "description": "Hereditary cerebral amyloid angiopathy, Icelandic type (disorder)",
            "attributes": null
          },
          {
            "code": "45655002",
            "description": "Vagal hoarseness (disorder)",
            "attributes": null
          },
          {
            "code": "45781009",
            "description": "Peripheral nerve entrapment syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "45814002",
            "description": "Birnbaum's syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "45853006",
            "description": "Roussy-LÃ©vy syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "45864009",
            "description": "Senile degeneration of brain (disorder)",
            "attributes": null
          },
          {
            "code": "45897005",
            "description": "Jervis' syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "46091002",
            "description": "Disorder of parasympathetic nervous system (disorder)",
            "attributes": null
          },
          {
            "code": "46138007",
            "description": "Tropical ataxic neuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "46251005",
            "description": "Corticospinal motor disease (disorder)",
            "attributes": null
          },
          {
            "code": "46263000",
            "description": "Cataplexy (disorder)",
            "attributes": null
          },
          {
            "code": "46421000119102",
            "description": "Behavior disorder as sequela of cerebral infarction (disorder)",
            "attributes": null
          },
          {
            "code": "4645000",
            "description": "Senile brain amyloidosis (disorder)",
            "attributes": null
          },
          {
            "code": "46804001",
            "description": "Severe x-linked myotubular myopathy (disorder)",
            "attributes": null
          },
          {
            "code": "46960006",
            "description": "Lumbago-sciatica due to displacement of lumbar intervertebral disc (disorder)",
            "attributes": null
          },
          {
            "code": "46963008",
            "description": "Compression of brain (disorder)",
            "attributes": null
          },
          {
            "code": "46966000",
            "description": "Cerebral compression due to injury (disorder)",
            "attributes": null
          },
          {
            "code": "47000000",
            "description": "Acute transverse myelitis (disorder)",
            "attributes": null
          },
          {
            "code": "471846004",
            "description": "Cardiomyopathy due to neuromuscular disorder (disorder)",
            "attributes": null
          },
          {
            "code": "472697007",
            "description": "Type I paratrigeminal syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "472698002",
            "description": "Type II paratrigeminal syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "472746006",
            "description": "Cerebrovascular disorder due to paradoxical embolus (disorder)",
            "attributes": null
          },
          {
            "code": "472916000",
            "description": "Toxic metabolic encephalopathy (disorder)",
            "attributes": null
          },
          {
            "code": "47311000119103",
            "description": "Static encephalopathy (disorder)",
            "attributes": null
          },
          {
            "code": "47339000",
            "description": "Secondary sweet taste disorder (disorder)",
            "attributes": null
          },
          {
            "code": "47351000119102",
            "description": "Post-traumatic nerve entrapment (disorder)",
            "attributes": null
          },
          {
            "code": "47924005",
            "description": "Motor cortical disorder (disorder)",
            "attributes": null
          },
          {
            "code": "4817008",
            "description": "Primary degenerative dementia of the Alzheimer type, senile onset, with delirium (disorder)",
            "attributes": null
          },
          {
            "code": "48248005",
            "description": "Thrombophlebitis of inferior sagittal sinus (disorder)",
            "attributes": null
          },
          {
            "code": "48522003",
            "description": "Spinal cord disorder (disorder)",
            "attributes": null
          },
          {
            "code": "48601000119107",
            "description": "Paralytic syndrome on one side of the body as effect of cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "48601002",
            "description": "Thrombosis of precerebral artery (disorder)",
            "attributes": null
          },
          {
            "code": "49049000",
            "description": "Parkinson's disease (disorder)",
            "attributes": null
          },
          {
            "code": "49386006",
            "description": "Orofacial dyskinesia (disorder)",
            "attributes": null
          },
          {
            "code": "49422009",
            "description": "Cortical hemorrhage (disorder)",
            "attributes": null
          },
          {
            "code": "49453006",
            "description": "Cerebral herniation (disorder)",
            "attributes": null
          },
          {
            "code": "49455004",
            "description": "Polyneuropathy due to diabetes mellitus (disorder)",
            "attributes": null
          },
          {
            "code": "49692006",
            "description": "Schilder's disease (disorder)",
            "attributes": null
          },
          {
            "code": "49793008",
            "description": "Hereditary motor neuron disease (disorder)",
            "attributes": null
          },
          {
            "code": "49949003",
            "description": "Paroxysmal choreoathetosis (disorder)",
            "attributes": null
          },
          {
            "code": "50122000",
            "description": "Metabolic encephalopathy (disorder)",
            "attributes": null
          },
          {
            "code": "50270004",
            "description": "Dilated cardiomyopathy secondary to Friedreich's ataxia (disorder)",
            "attributes": null
          },
          {
            "code": "50330009",
            "description": "Disorder of sympathetic nervous system (disorder)",
            "attributes": null
          },
          {
            "code": "50366005",
            "description": "Mandibular neuropraxia (disorder)",
            "attributes": null
          },
          {
            "code": "50490005",
            "description": "Hypertensive encephalopathy (disorder)",
            "attributes": null
          },
          {
            "code": "50620007",
            "description": "Autonomic neuropathy due to diabetes mellitus (disorder)",
            "attributes": null
          },
          {
            "code": "50639002",
            "description": "Vagus nerve palate paralysis (disorder)",
            "attributes": null
          },
          {
            "code": "51004007",
            "description": "Herniation under falx cerebri (disorder)",
            "attributes": null
          },
          {
            "code": "5134006",
            "description": "Familial amyloid polyneuropathy, type VI (disorder)",
            "attributes": null
          },
          {
            "code": "51399001",
            "description": "Toxic encephalopathy caused by lead (disorder)",
            "attributes": null
          },
          {
            "code": "51723007",
            "description": "Carotid sinus syncope (disorder)",
            "attributes": null
          },
          {
            "code": "51771007",
            "description": "Postviral fatigue syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "5181000119108",
            "description": "Cervical plexopathy (disorder)",
            "attributes": null
          },
          {
            "code": "51881002",
            "description": "Injury of splanchnic nerve (disorder)",
            "attributes": null
          },
          {
            "code": "5217008",
            "description": "Stiff-man syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "52201006",
            "description": "Internal capsule hemorrhage (disorder)",
            "attributes": null
          },
          {
            "code": "52274002",
            "description": "Dystonia lenticularis (disorder)",
            "attributes": null
          },
          {
            "code": "52522001",
            "description": "Degenerative brain disorder (disorder)",
            "attributes": null
          },
          {
            "code": "5262007",
            "description": "Spinal muscular atrophy (disorder)",
            "attributes": null
          },
          {
            "code": "52702003",
            "description": "Chronic fatigue syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "52713000",
            "description": "Infantile neuroaxonal dystrophy (disorder)",
            "attributes": null
          },
          {
            "code": "52723009",
            "description": "Injury of stellate ganglion (disorder)",
            "attributes": null
          },
          {
            "code": "53322007",
            "description": "Hypertrophic cardiomyopathy secondary to Friedreich's ataxia (disorder)",
            "attributes": null
          },
          {
            "code": "53387004",
            "description": "Hereditary myopathy associated with hydrocephalus (disorder)",
            "attributes": null
          },
          {
            "code": "53509000",
            "description": "Myopathy in Cushing's disease (disorder)",
            "attributes": null
          },
          {
            "code": "53622003",
            "description": "Cerebral malaria (disorder)",
            "attributes": null
          },
          {
            "code": "54280009",
            "description": "Kugelberg-Welander disease (disorder)",
            "attributes": null
          },
          {
            "code": "54304004",
            "description": "Progressive bulbar palsy (disorder)",
            "attributes": null
          },
          {
            "code": "54502004",
            "description": "Primary degenerative dementia of the Alzheimer type, presenile onset, with delusions (disorder)",
            "attributes": null
          },
          {
            "code": "54519002",
            "description": "Basilar artery stenosis (disorder)",
            "attributes": null
          },
          {
            "code": "54593000",
            "description": "Trigemino-sympathetic syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "55009008",
            "description": "Primary degenerative dementia of the Alzheimer type, senile onset, with delusions (disorder)",
            "attributes": null
          },
          {
            "code": "55051001",
            "description": "Myasthenia gravis, juvenile form (disorder)",
            "attributes": null
          },
          {
            "code": "55133004",
            "description": "Multi-core congenital myopathy (disorder)",
            "attributes": null
          },
          {
            "code": "55382008",
            "description": "Cerebral atherosclerosis (disorder)",
            "attributes": null
          },
          {
            "code": "55481000",
            "description": "Limbic disorder (disorder)",
            "attributes": null
          },
          {
            "code": "55623006",
            "description": "Toxic encephalopathy caused by mercury (disorder)",
            "attributes": null
          },
          {
            "code": "55637002",
            "description": "Spinal hemiplegia (disorder)",
            "attributes": null
          },
          {
            "code": "55734000",
            "description": "Endophlebitis of basilar sinus (disorder)",
            "attributes": null
          },
          {
            "code": "55776008",
            "description": "Symptomatic torsion dystonia (disorder)",
            "attributes": null
          },
          {
            "code": "5582005",
            "description": "Posterior fossa compression syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "56120004",
            "description": "A. Schmidt's syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "56384000",
            "description": "Embolism of inferior sagittal sinus (disorder)",
            "attributes": null
          },
          {
            "code": "56453003",
            "description": "Hereditary cerebral amyloid angiopathy, Dutch type (disorder)",
            "attributes": null
          },
          {
            "code": "56795008",
            "description": "Polyneuritis cranialis (disorder)",
            "attributes": null
          },
          {
            "code": "56989000",
            "description": "Eaton-Lambert syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "5771000119106",
            "description": "Phantom limb syndrome with pain (disorder)",
            "attributes": null
          },
          {
            "code": "57938005",
            "description": "Congenital myotonia, autosomal dominant form (disorder)",
            "attributes": null
          },
          {
            "code": "57958006",
            "description": "Endocrine myopathy (disorder)",
            "attributes": null
          },
          {
            "code": "57981008",
            "description": "Progressing stroke (disorder)",
            "attributes": null
          },
          {
            "code": "5855005",
            "description": "Trigeminal nerve motor disorder (disorder)",
            "attributes": null
          },
          {
            "code": "58638006",
            "description": "Pseudoporencephaly (disorder)",
            "attributes": null
          },
          {
            "code": "58756001",
            "description": "Huntington's chorea (disorder)",
            "attributes": null
          },
          {
            "code": "58762006",
            "description": "Encephalomalacia (disorder)",
            "attributes": null
          },
          {
            "code": "58795000",
            "description": "Distal muscular dystrophy (disorder)",
            "attributes": null
          },
          {
            "code": "59103002",
            "description": "Cerebral paralysis with homolateral ataxia (disorder)",
            "attributes": null
          },
          {
            "code": "59798009",
            "description": "Vagus nerve sensory disorder (disorder)",
            "attributes": null
          },
          {
            "code": "59979003",
            "description": "Second division of fifth cranial nerve disorder (disorder)",
            "attributes": null
          },
          {
            "code": "60146005",
            "description": "Bailey-Cushing syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "60342002",
            "description": "Movement disorder (disorder)",
            "attributes": null
          },
          {
            "code": "60380001",
            "description": "Narcolepsy (disorder)",
            "attributes": null
          },
          {
            "code": "60490008",
            "description": "Brachial neuritis AND/OR radiculitis due to displacement of cervical intervertebral disc (disorder)",
            "attributes": null
          },
          {
            "code": "60576007",
            "description": "Subacute combined degeneration of spinal cord (disorder)",
            "attributes": null
          },
          {
            "code": "60703000",
            "description": "Axonal neuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "60706008",
            "description": "Phlebitis of torcular Herophili (disorder)",
            "attributes": null
          },
          {
            "code": "60738003",
            "description": "Secondary myopathy (disorder)",
            "attributes": null
          },
          {
            "code": "608874000",
            "description": "Eaton Lambert syndrome with underlying malignancy (disorder)",
            "attributes": null
          },
          {
            "code": "609218006",
            "description": "Paroxysmal nonkinesigenic dyskinesia (disorder)",
            "attributes": null
          },
          {
            "code": "609221008",
            "description": "Paroxysmal kinesigenic dyskinesia (disorder)",
            "attributes": null
          },
          {
            "code": "60935008",
            "description": "Paramyoclonus multiplex (disorder)",
            "attributes": null
          },
          {
            "code": "609382000",
            "description": "Chronic non-traumatic intracranial subdural hemorrhage (disorder)",
            "attributes": null
          },
          {
            "code": "609558009",
            "description": "Essential tremor (disorder)",
            "attributes": null
          },
          {
            "code": "609559001",
            "description": "Hereditary essential tremor (disorder)",
            "attributes": null
          },
          {
            "code": "609601001",
            "description": "Suprascapular neuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "609640006",
            "description": "Compression neuropathy of genitofemoral nerve (disorder)",
            "attributes": null
          },
          {
            "code": "609641005",
            "description": "Compression neuropathy of ilioinguinal nerve (disorder)",
            "attributes": null
          },
          {
            "code": "6118003",
            "description": "Demyelinating disease of central nervous system (disorder)",
            "attributes": null
          },
          {
            "code": "61200008",
            "description": "Pallidonigroluysian degeneration (disorder)",
            "attributes": null
          },
          {
            "code": "61291000119103",
            "description": "Disorder of central nervous system co-occurrent and due to acute lymphoid leukemia in remission (disorder)",
            "attributes": null
          },
          {
            "code": "61301000119102",
            "description": "Disorder of central nervous system co-occurrent and due to acute lymphoid leukemia (disorder)",
            "attributes": null
          },
          {
            "code": "61337004",
            "description": "Electric chorea (disorder)",
            "attributes": null
          },
          {
            "code": "61687004",
            "description": "Endophlebitis of inferior sagittal sinus (disorder)",
            "attributes": null
          },
          {
            "code": "62266001",
            "description": "Luft's hypermetabolic myopathy (disorder)",
            "attributes": null
          },
          {
            "code": "62732009",
            "description": "Alien limb phenomenon (disorder)",
            "attributes": null
          },
          {
            "code": "62914000",
            "description": "Cerebrovascular disease (disorder)",
            "attributes": null
          },
          {
            "code": "62985007",
            "description": "Hereditary insensitivity to pain with anhidrosis (disorder)",
            "attributes": null
          },
          {
            "code": "63081009",
            "description": "Acute infarction of spinal cord (disorder)",
            "attributes": null
          },
          {
            "code": "63135006",
            "description": "Amyotonia congenita (disorder)",
            "attributes": null
          },
          {
            "code": "63684002",
            "description": "Hereditary hollow viscus myopathy (disorder)",
            "attributes": null
          },
          {
            "code": "63864004",
            "description": "Tongue protrusion disorder of twelfth cranial nerve (disorder)",
            "attributes": null
          },
          {
            "code": "63900005",
            "description": "Alajouanine's syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "63986002",
            "description": "Brain stem herniation (disorder)",
            "attributes": null
          },
          {
            "code": "64009001",
            "description": "Basilar artery syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "64309007",
            "description": "Trigeminal nerve disorder (disorder)",
            "attributes": null
          },
          {
            "code": "64370005",
            "description": "Aganglionosis of parasympathetic nerve ganglia (disorder)",
            "attributes": null
          },
          {
            "code": "64383006",
            "description": "Werdnig-Hoffmann disease (disorder)",
            "attributes": null
          },
          {
            "code": "64465004",
            "description": "Hypernasality syndrome due to neurologic disease (disorder)",
            "attributes": null
          },
          {
            "code": "64518008",
            "description": "Paratrigeminal syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "64586002",
            "description": "Carotid artery stenosis (disorder)",
            "attributes": null
          },
          {
            "code": "64624009",
            "description": "Hypoglycemic encephalopathy (disorder)",
            "attributes": null
          },
          {
            "code": "64741003",
            "description": "Myotonic cataract (disorder)",
            "attributes": null
          },
          {
            "code": "6475002",
            "description": "Primary degenerative dementia of the Alzheimer type, presenile onset, uncomplicated (disorder)",
            "attributes": null
          },
          {
            "code": "64775002",
            "description": "Vertebral artery thrombosis (disorder)",
            "attributes": null
          },
          {
            "code": "65017003",
            "description": "Hereditary peripheral neuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "65084004",
            "description": "Vertebral artery embolism (disorder)",
            "attributes": null
          },
          {
            "code": "65096006",
            "description": "Primary degenerative dementia of the Alzheimer type, presenile onset, with delirium (disorder)",
            "attributes": null
          },
          {
            "code": "65260001",
            "description": "Cervical spondylosis with myelopathy (disorder)",
            "attributes": null
          },
          {
            "code": "65312002",
            "description": "Cerebral arteriosclerosis (disorder)",
            "attributes": null
          },
          {
            "code": "65605001",
            "description": "Edema of spinal cord (disorder)",
            "attributes": null
          },
          {
            "code": "65705009",
            "description": "Porencephalic cyst (disorder)",
            "attributes": null
          },
          {
            "code": "66010009",
            "description": "Supranuclear paralysis (disorder)",
            "attributes": null
          },
          {
            "code": "6607004",
            "description": "Syringoencephalomyelia (disorder)",
            "attributes": null
          },
          {
            "code": "66073004",
            "description": "Glossopharyngeal taste disorder (disorder)",
            "attributes": null
          },
          {
            "code": "66108005",
            "description": "Primary degenerative dementia of the Alzheimer type, senile onset, uncomplicated (disorder)",
            "attributes": null
          },
          {
            "code": "66637005",
            "description": "Hemiballism (disorder)",
            "attributes": null
          },
          {
            "code": "66952001",
            "description": "Toxic myopathy (disorder)",
            "attributes": null
          },
          {
            "code": "672441000119103",
            "description": "Hemiplegia of nondominant side due to and following ischemic cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "672461000119104",
            "description": "Hemiplegia of dominant side due to and following ischemic cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "672501000119104",
            "description": "Dysarthria due to and following ischemic cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "672511000119101",
            "description": "Dysarthria due to and following hemorrhagic cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "672521000119108",
            "description": "Dysphasia due to and following ischemic cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "672531000119106",
            "description": "Dysphasia due to and following hemorrhagic cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "672541000119102",
            "description": "Aphasia due to and following ischemic cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "672551000119100",
            "description": "Aphasia due to and following hemorrhagic cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "672561000119103",
            "description": "Cognitive deficit due to and following ischemic cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "672571000119109",
            "description": "Cognitive deficit due to and following hemorrhagic cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "674091000119108",
            "description": "Vertigo due to and following ischemic cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "674111000119100",
            "description": "Ataxia due to and following ischemic cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "674121000119107",
            "description": "Ataxia due to and following hemorrhagic cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "674161000119102",
            "description": "Monoplegia of upper limb due to and following ischemic cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "674361000119104",
            "description": "Apraxia due to and following ischemic cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "67437007",
            "description": "Lumbar spondylosis with myelopathy (disorder)",
            "attributes": null
          },
          {
            "code": "674381000119108",
            "description": "Weakness of facial muscle due to and following ischemic cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "674391000119106",
            "description": "Speech and language deficit due to and following hemorrhagic cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "674401000119108",
            "description": "Speech and language deficit due to and following ischemic cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "674481000119100",
            "description": "Spontaneous hematoma of spinal cord (disorder)",
            "attributes": null
          },
          {
            "code": "67724008",
            "description": "Secondary salt taste disorder (disorder)",
            "attributes": null
          },
          {
            "code": "67747009",
            "description": "Ocular muscular dystrophy (disorder)",
            "attributes": null
          },
          {
            "code": "67761004",
            "description": "Olivopontocerebellar degeneration (disorder)",
            "attributes": null
          },
          {
            "code": "67930001",
            "description": "Syringoencephalia (disorder)",
            "attributes": null
          },
          {
            "code": "67975003",
            "description": "Fibrocartilagenous emboli of spinal cord (disorder)",
            "attributes": null
          },
          {
            "code": "67992007",
            "description": "Multiple AND bilateral precerebral artery obstruction (disorder)",
            "attributes": null
          },
          {
            "code": "6807001",
            "description": "Central pontine myelinolysis (disorder)",
            "attributes": null
          },
          {
            "code": "680991000119108",
            "description": "Atrophy of bilateral optic nerves following inflammation (disorder)",
            "attributes": null
          },
          {
            "code": "68116008",
            "description": "Dentatorubropallidoluysian degeneration (disorder)",
            "attributes": null
          },
          {
            "code": "68121000119103",
            "description": "Facial palsy House-Brackmann grade II (disorder)",
            "attributes": null
          },
          {
            "code": "68131000119100",
            "description": "Facial palsy House-Brackmann grade III (disorder)",
            "attributes": null
          },
          {
            "code": "68141000119109",
            "description": "Facial palsy House-Brackmann grade IV (disorder)",
            "attributes": null
          },
          {
            "code": "68151000119106",
            "description": "Facial palsy House-Brackmann grade V (disorder)",
            "attributes": null
          },
          {
            "code": "68186003",
            "description": "Congenital myopathy with abnormal subcellular organelles (disorder)",
            "attributes": null
          },
          {
            "code": "68267002",
            "description": "Benign intracranial hypertension (disorder)",
            "attributes": null
          },
          {
            "code": "68437005",
            "description": "Thyrotoxic myopathy (disorder)",
            "attributes": null
          },
          {
            "code": "68504005",
            "description": "Ataxia-telangiectasia syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "68577004",
            "description": "Acute necrotizing myelitis (disorder)",
            "attributes": null
          },
          {
            "code": "68711000119109",
            "description": "Genitofemoral neuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "68721000119102",
            "description": "Ilioinguinal neuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "68982002",
            "description": "Disorder of olfactory nerve (disorder)",
            "attributes": null
          },
          {
            "code": "690171000119105",
            "description": "Weakness of facial muscle due to and following embolic cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "690201000119109",
            "description": "Ataxia due to and following embolic cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "690271000119104",
            "description": "Hemiplegia of nondominant side due to and following embolic cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "690311000119104",
            "description": "Dysarthria due to and following embolic cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "690321000119106",
            "description": "Aphasia due to and following embolic cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "690331000119109",
            "description": "Speech and language deficit due to and following embolic cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "690341000119100",
            "description": "Cognitive deficit due to and following embolic cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "690351000119103",
            "description": "Dysphasia due to and following embolic cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "69116000",
            "description": "Moyamoya disease (disorder)",
            "attributes": null
          },
          {
            "code": "69131009",
            "description": "Spinal ataxia (disorder)",
            "attributes": null
          },
          {
            "code": "691461000119103",
            "description": "Acquired cerebral atrophy (disorder)",
            "attributes": null
          },
          {
            "code": "69233001",
            "description": "Paradoxical facial movements (disorder)",
            "attributes": null
          },
          {
            "code": "69501006",
            "description": "Facial nerve motor disorder (disorder)",
            "attributes": null
          },
          {
            "code": "697914005",
            "description": "Pulmonary hypertension due to sleep-disordered breathing (disorder)",
            "attributes": null
          },
          {
            "code": "69798007",
            "description": "Carotid artery obstruction (disorder)",
            "attributes": null
          },
          {
            "code": "698279003",
            "description": "X-linked dystonia parkinsonism (disorder)",
            "attributes": null
          },
          {
            "code": "698363002",
            "description": "Postoperative thromboembolus of precerebral artery (disorder)",
            "attributes": null
          },
          {
            "code": "698623009",
            "description": "Arthropathy associated with syringomyelia (disorder)",
            "attributes": null
          },
          {
            "code": "698625002",
            "description": "Dementia associated with normal pressure hydrocephalus (disorder)",
            "attributes": null
          },
          {
            "code": "698626001",
            "description": "Dementia associated with multiple sclerosis (disorder)",
            "attributes": null
          },
          {
            "code": "698736001",
            "description": "Postoperative communicating hydrocephalus (disorder)",
            "attributes": null
          },
          {
            "code": "698737005",
            "description": "Postmeningitic obstructive hydrocephalus (disorder)",
            "attributes": null
          },
          {
            "code": "698738000",
            "description": "Brainstem myoclonus (disorder)",
            "attributes": null
          },
          {
            "code": "698767004",
            "description": "Post-cerebrovascular accident epilepsy (disorder)",
            "attributes": null
          },
          {
            "code": "698781002",
            "description": "Dementia associated with cerebral anoxia (disorder)",
            "attributes": null
          },
          {
            "code": "698835006",
            "description": "Cerebral cortex myoclonus (disorder)",
            "attributes": null
          },
          {
            "code": "698836007",
            "description": "Spinal cord myoclonus (disorder)",
            "attributes": null
          },
          {
            "code": "698837003",
            "description": "Posttraumatic porencephalic cyst of brain (disorder)",
            "attributes": null
          },
          {
            "code": "698839000",
            "description": "Benign intracranial hypertension due to hypervitaminosis A (disorder)",
            "attributes": null
          },
          {
            "code": "698846009",
            "description": "Tibial muscular dystrophy (disorder)",
            "attributes": null
          },
          {
            "code": "698954005",
            "description": "Primary degenerative dementia of the Alzheimer type, senile onset in remission (disorder)",
            "attributes": null
          },
          {
            "code": "698955006",
            "description": "Primary degenerative dementia of the Alzheimer type, presenile onset in remission (disorder)",
            "attributes": null
          },
          {
            "code": "699184009",
            "description": "Perry syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "699190008",
            "description": "Paroxysmal extreme pain disorder (disorder)",
            "attributes": null
          },
          {
            "code": "699267007",
            "description": "Myosin storage myopathy (disorder)",
            "attributes": null
          },
          {
            "code": "699268002",
            "description": "Myopathy with deficiency of iron-sulfur cluster assembly enzyme (disorder)",
            "attributes": null
          },
          {
            "code": "699269005",
            "description": "Myofibrillar myopathy (disorder)",
            "attributes": null
          },
          {
            "code": "699299001",
            "description": "Neuroferritinopathy (disorder)",
            "attributes": null
          },
          {
            "code": "699315005",
            "description": "Neutral lipid storage disease with myopathy (disorder)",
            "attributes": null
          },
          {
            "code": "699328003",
            "description": "Myoclonic epilepsy myopathy sensory ataxia (disorder)",
            "attributes": null
          },
          {
            "code": "699706000",
            "description": "Embolism of middle cerebral artery (disorder)",
            "attributes": null
          },
          {
            "code": "699866005",
            "description": "Progressive bulbar palsy with sensorineural deafness (disorder)",
            "attributes": null
          },
          {
            "code": "700058006",
            "description": "Ataxia-telangiectasia-like disorder (disorder)",
            "attributes": null
          },
          {
            "code": "700077008",
            "description": "Charcot arthropathy of joint of ankle (disorder)",
            "attributes": null
          },
          {
            "code": "700437007",
            "description": "Charcot arthropathy of midfoot (disorder)",
            "attributes": null
          },
          {
            "code": "700438002",
            "description": "Charcot arthropathy of hindfoot (disorder)",
            "attributes": null
          },
          {
            "code": "700467001",
            "description": "Reversible cerebral vasoconstriction syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "700507000",
            "description": "Supernumerary phantom limb (disorder)",
            "attributes": null
          },
          {
            "code": "702323008",
            "description": "Rapid onset dystonia parkinsonism (disorder)",
            "attributes": null
          },
          {
            "code": "702343002",
            "description": "Early onset myopathy with fatal cardiomyopathy (disorder)",
            "attributes": null
          },
          {
            "code": "702349003",
            "description": "Actin accumulation myopathy (disorder)",
            "attributes": null
          },
          {
            "code": "702363009",
            "description": "Cold-induced sweating syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "702373006",
            "description": "Hereditary myopathy with early respiratory failure (disorder)",
            "attributes": null
          },
          {
            "code": "702376003",
            "description": "Huntington disease-like syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "702379005",
            "description": "Hypomyelination and congenital cataract (disorder)",
            "attributes": null
          },
          {
            "code": "702380008",
            "description": "Idiopathic inflammatory myopathy (disorder)",
            "attributes": null
          },
          {
            "code": "702382000",
            "description": "Inclusion body myopathy 2 (disorder)",
            "attributes": null
          },
          {
            "code": "702383005",
            "description": "Distal myopathy 2 (disorder)",
            "attributes": null
          },
          {
            "code": "702393003",
            "description": "Frontotemporal dementia with gene located on 3p11 (disorder)",
            "attributes": null
          },
          {
            "code": "702419001",
            "description": "Fatty acid hydroxylase associated neurodegeneration (disorder)",
            "attributes": null
          },
          {
            "code": "702421006",
            "description": "Familial encephalopathy with neuroserpin inclusion bodies (disorder)",
            "attributes": null
          },
          {
            "code": "702426001",
            "description": "GRN-related frontotemporal dementia (disorder)",
            "attributes": null
          },
          {
            "code": "702427005",
            "description": "Hereditary diffuse leukoencephalopathy with spheroids (disorder)",
            "attributes": null
          },
          {
            "code": "702429008",
            "description": "Frontotemporal dementia with parkinsonism-17 (disorder)",
            "attributes": null
          },
          {
            "code": "702433001",
            "description": "Congenital cataracts, facial dysmorphism and neuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "702439002",
            "description": "Agenesis of corpus callosum with peripheral neuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "702442008",
            "description": "Ataxia with vitamin E deficiency (disorder)",
            "attributes": null
          },
          {
            "code": "702445005",
            "description": "Autosomal recessive spastic ataxia of Charlevoix-Saguenay (disorder)",
            "attributes": null
          },
          {
            "code": "702448007",
            "description": "Dystonia 6 (disorder)",
            "attributes": null
          },
          {
            "code": "702575003",
            "description": "Retinocochleocerebral vasculopathy (disorder)",
            "attributes": null
          },
          {
            "code": "703156006",
            "description": "Deep hemispheric cerebral hemorrhage (disorder)",
            "attributes": null
          },
          {
            "code": "703158007",
            "description": "Embolism of internal auditory artery (disorder)",
            "attributes": null
          },
          {
            "code": "703161008",
            "description": "Occlusion of internal auditory artery (disorder)",
            "attributes": null
          },
          {
            "code": "703163006",
            "description": "Secondary cerebrovascular disease (disorder)",
            "attributes": null
          },
          {
            "code": "703174002",
            "description": "Subarachnoid hemorrhage from vertebral artery aneurysm (disorder)",
            "attributes": null
          },
          {
            "code": "703180005",
            "description": "Asymptomatic occlusion of extracranial carotid artery (disorder)",
            "attributes": null
          },
          {
            "code": "703184001",
            "description": "Asymptomatic occlusion of intracranial carotid artery (disorder)",
            "attributes": null
          },
          {
            "code": "703205008",
            "description": "Asymptomatic occlusion of posterior cerebral artery (disorder)",
            "attributes": null
          },
          {
            "code": "703206009",
            "description": "Asymptomatic occlusion of basilar artery (disorder)",
            "attributes": null
          },
          {
            "code": "703207000",
            "description": "Asymptomatic occlusion of anterior cerebral artery (disorder)",
            "attributes": null
          },
          {
            "code": "703208005",
            "description": "Asymptomatic occlusion of middle cerebral artery (disorder)",
            "attributes": null
          },
          {
            "code": "703215002",
            "description": "Non-aneurysmal subarachnoid intracranial hemorrhage (disorder)",
            "attributes": null
          },
          {
            "code": "703216001",
            "description": "Perimesencephalic subarachnoid hemorrhage (disorder)",
            "attributes": null
          },
          {
            "code": "703217005",
            "description": "Convexal subarachnoid hemorrhage (disorder)",
            "attributes": null
          },
          {
            "code": "703218000",
            "description": "Cerebral vasoconstriction syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "703219008",
            "description": "Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (disorder)",
            "attributes": null
          },
          {
            "code": "703226008",
            "description": "Familial cerebral saccular aneurysm (disorder)",
            "attributes": null
          },
          {
            "code": "703300001",
            "description": "Hypoxic ischemic encephalopathy (disorder)",
            "attributes": null
          },
          {
            "code": "703301002",
            "description": "Mild hypoxic ischemic encephalopathy (disorder)",
            "attributes": null
          },
          {
            "code": "703302009",
            "description": "Moderate hypoxic ischemic encephalopathy (disorder)",
            "attributes": null
          },
          {
            "code": "703303004",
            "description": "Severe hypoxic ischemic encephalopathy (disorder)",
            "attributes": null
          },
          {
            "code": "703304005",
            "description": "Hypoxic ischemic encephalopathy due to strangulation (disorder)",
            "attributes": null
          },
          {
            "code": "703305006",
            "description": "Hypoxic ischemic encephalopathy due to cardiac arrest (disorder)",
            "attributes": null
          },
          {
            "code": "703312002",
            "description": "Primary cerebral arteritis (disorder)",
            "attributes": null
          },
          {
            "code": "703313007",
            "description": "Cerebral amyloid angiopathy associated with systemic amyloidosis (disorder)",
            "attributes": null
          },
          {
            "code": "70350007",
            "description": "Degenerative myelopathy (disorder)",
            "attributes": null
          },
          {
            "code": "703522009",
            "description": "Biotin-thiamine-responsive basal ganglia disease (disorder)",
            "attributes": null
          },
          {
            "code": "703524005",
            "description": "Spinal muscular atrophy with progressive myoclonic epilepsy (disorder)",
            "attributes": null
          },
          {
            "code": "703530005",
            "description": "Brody myopathy (disorder)",
            "attributes": null
          },
          {
            "code": "703532002",
            "description": "Cap myopathy (disorder)",
            "attributes": null
          },
          {
            "code": "703543005",
            "description": "Infantile ascending hereditary spastic paralysis (disorder)",
            "attributes": null
          },
          {
            "code": "703544004",
            "description": "Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia (disorder)",
            "attributes": null
          },
          {
            "code": "703621006",
            "description": "Multifocal clinically isolated syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "703622004",
            "description": "Monofocal clinically isolated syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "703862003",
            "description": "Spinal subdural hematoma (disorder)",
            "attributes": null
          },
          {
            "code": "704079000",
            "description": "Non-aneurysmal perimesencephalic subarachnoid hemorrhage (disorder)",
            "attributes": null
          },
          {
            "code": "705058008",
            "description": "Charcot arthropathy of forefoot (disorder)",
            "attributes": null
          },
          {
            "code": "705128004",
            "description": "Cerebral infarction due to embolism of middle cerebral artery (disorder)",
            "attributes": null
          },
          {
            "code": "705129007",
            "description": "Thrombosis of middle cerebral artery (disorder)",
            "attributes": null
          },
          {
            "code": "705130002",
            "description": "Cerebral infarction due to thrombosis of middle cerebral artery (disorder)",
            "attributes": null
          },
          {
            "code": "70607008",
            "description": "Thrombosis of superior sagittal sinus (disorder)",
            "attributes": null
          },
          {
            "code": "706891008",
            "description": "Neuropathy due to unstable diabetes mellitus type 1 (disorder)",
            "attributes": null
          },
          {
            "code": "70835005",
            "description": "Disorder of basal ganglia (disorder)",
            "attributes": null
          },
          {
            "code": "709012003",
            "description": "Minimally conscious state (disorder)",
            "attributes": null
          },
          {
            "code": "709143008",
            "description": "Peripheral neuropathy caused by toxin (disorder)",
            "attributes": null
          },
          {
            "code": "709144002",
            "description": "Peripheral neuropathy of upper limb caused by toxin (disorder)",
            "attributes": null
          },
          {
            "code": "709145001",
            "description": "Peripheral neuropathy due to inflammation (disorder)",
            "attributes": null
          },
          {
            "code": "709415008",
            "description": "Mitochondrial membrane protein associated neurodegeneration (disorder)",
            "attributes": null
          },
          {
            "code": "709489006",
            "description": "Small fiber neuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "710110008",
            "description": "Phantom pain (disorder)",
            "attributes": null
          },
          {
            "code": "710349003",
            "description": "Peripheral neuropathy of upper limb due to metabolic disorder (disorder)",
            "attributes": null
          },
          {
            "code": "710357000",
            "description": "Peripheral neuropathy of upper limb due to inflammatory disease (disorder)",
            "attributes": null
          },
          {
            "code": "710360007",
            "description": "Peripheral neuropathy due to metabolic disorder (disorder)",
            "attributes": null
          },
          {
            "code": "710575003",
            "description": "Transient ischemic attack due to embolism (disorder)",
            "attributes": null
          },
          {
            "code": "711055006",
            "description": "Phantom pain following excision of eye (disorder)",
            "attributes": null
          },
          {
            "code": "711056007",
            "description": "Phantom pain following amputation of penis (disorder)",
            "attributes": null
          },
          {
            "code": "711057003",
            "description": "Phantom pain following amputation of lower limb (disorder)",
            "attributes": null
          },
          {
            "code": "711058008",
            "description": "Phantom pain following amputation of upper limb (disorder)",
            "attributes": null
          },
          {
            "code": "711158005",
            "description": "Spinocerebellar ataxia type 36 (disorder)",
            "attributes": null
          },
          {
            "code": "711265009",
            "description": "Caveolin 3 related distal myopathy (disorder)",
            "attributes": null
          },
          {
            "code": "711403001",
            "description": "Cerebral folate transport deficiency (disorder)",
            "attributes": null
          },
          {
            "code": "711406009",
            "description": "Autosomal recessive axonal neuropathy with neuromyotonia (disorder)",
            "attributes": null
          },
          {
            "code": "711443006",
            "description": "Aphasia due to brain damage (disorder)",
            "attributes": null
          },
          {
            "code": "711483003",
            "description": "Spinal muscular atrophy with respiratory distress type 1 (disorder)",
            "attributes": null
          },
          {
            "code": "712537009",
            "description": "Complex regional pain syndrome of upper limb (disorder)",
            "attributes": null
          },
          {
            "code": "712644005",
            "description": "Inflammation of obturator nerve (disorder)",
            "attributes": null
          },
          {
            "code": "712820006",
            "description": "Cerebral pseudoatrophy (disorder)",
            "attributes": null
          },
          {
            "code": "71286001",
            "description": "Spinal cord compression (disorder)",
            "attributes": null
          },
          {
            "code": "712882000",
            "description": "Autonomic neuropathy due to type 1 diabetes mellitus (disorder)",
            "attributes": null
          },
          {
            "code": "712883005",
            "description": "Autonomic neuropathy due to type 2 diabetes mellitus (disorder)",
            "attributes": null
          },
          {
            "code": "713081000",
            "description": "Dissection of cerebral artery (disorder)",
            "attributes": null
          },
          {
            "code": "713265001",
            "description": "Nontraumatic ruptured cerebral aneurysm (disorder)",
            "attributes": null
          },
          {
            "code": "713425003",
            "description": "Spinal cord compression due to metastasis to spine (disorder)",
            "attributes": null
          },
          {
            "code": "713489006",
            "description": "Polyneuropathy co-occurrent with human immunodeficiency virus infection (disorder)",
            "attributes": null
          },
          {
            "code": "713503007",
            "description": "Disorder of spinal cord co-occurrent with human immunodeficiency virus infection (disorder)",
            "attributes": null
          },
          {
            "code": "713527009",
            "description": "Disorder of peripheral nervous system co-occurrent with human immunodeficiency virus infection (disorder)",
            "attributes": null
          },
          {
            "code": "713543002",
            "description": "Demyelinating disease of central nervous system co-occurrent with human immunodeficiency virus infection (disorder)",
            "attributes": null
          },
          {
            "code": "713571008",
            "description": "Disorder of central nervous system co-occurrent with human immunodeficiency virus infection (disorder)",
            "attributes": null
          },
          {
            "code": "713705003",
            "description": "Polyneuropathy due to type 1 diabetes mellitus (disorder)",
            "attributes": null
          },
          {
            "code": "713706002",
            "description": "Polyneuropathy due to type 2 diabetes mellitus (disorder)",
            "attributes": null
          },
          {
            "code": "713829001",
            "description": "Postinfective intercostal neuralgia (disorder)",
            "attributes": null
          },
          {
            "code": "713831005",
            "description": "Postinfective peripheral neuralgia (disorder)",
            "attributes": null
          },
          {
            "code": "713837009",
            "description": "Postinfective segmental peripheral neuralgia (disorder)",
            "attributes": null
          },
          {
            "code": "713839007",
            "description": "Intercostal neuralgia as late effect of trauma (disorder)",
            "attributes": null
          },
          {
            "code": "713847007",
            "description": "Post-surgery obturator neuralgia (disorder)",
            "attributes": null
          },
          {
            "code": "713911007",
            "description": "Lumbosacral spondylosis co-occurrent with root compression (disorder)",
            "attributes": null
          },
          {
            "code": "714027006",
            "description": "Trigeminal nerve palsy (disorder)",
            "attributes": null
          },
          {
            "code": "714279000",
            "description": "Myelopathy caused by Human T-lymphotropic virus 1 (disorder)",
            "attributes": null
          },
          {
            "code": "71444005",
            "description": "Cerebral arterial thrombosis (disorder)",
            "attributes": null
          },
          {
            "code": "715317001",
            "description": "Proximal myotonic myopathy (disorder)",
            "attributes": null
          },
          {
            "code": "715340002",
            "description": "Autosomal recessive limb girdle muscular dystrophy type 2D (disorder)",
            "attributes": null
          },
          {
            "code": "715341003",
            "description": "Autosomal recessive limb girdle muscular dystrophy type 2A (disorder)",
            "attributes": null
          },
          {
            "code": "715345007",
            "description": "Young onset Parkinson disease (disorder)",
            "attributes": null
          },
          {
            "code": "715366004",
            "description": "Autosomal recessive cerebellar ataxia with oculomotor apraxia type 1 (disorder)",
            "attributes": null
          },
          {
            "code": "715369006",
            "description": "Autosomal recessive cerebelloparenchymal disorder type 3 (disorder)",
            "attributes": null
          },
          {
            "code": "715371006",
            "description": "Cerebellar ataxia co-occurrent with ectodermal dysplasia (disorder)",
            "attributes": null
          },
          {
            "code": "715415005",
            "description": "Richards-Rundle syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "715429006",
            "description": "Congenital muscular dystrophy with infantile cataract and hypogonadism syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "715437003",
            "description": "Neuronal intranuclear inclusion disease (disorder)",
            "attributes": null
          },
          {
            "code": "715465001",
            "description": "Spinocerebellar degeneration co-occurrent with macular corneal dystrophy (disorder)",
            "attributes": null
          },
          {
            "code": "715483009",
            "description": "Olivopontocerebellar atrophy co-occurrent with sensorineural hearing loss (disorder)",
            "attributes": null
          },
          {
            "code": "715491000",
            "description": "Autosomal recessive spastic paraplegia type 11 (disorder)",
            "attributes": null
          },
          {
            "code": "715504003",
            "description": "Spastic paraparesis co-occurrent with deafness (disorder)",
            "attributes": null
          },
          {
            "code": "715564000",
            "description": "Paroxysmal dystonic choreoathetosis with episodic ataxia and spasticity (disorder)",
            "attributes": null
          },
          {
            "code": "715565004",
            "description": "Lethal arthrogryposis co-occurrent with anterior horn cell disease (disorder)",
            "attributes": null
          },
          {
            "code": "715574002",
            "description": "Posterior cortical atrophy syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "715624006",
            "description": "Chronic ataxic neuropathy, ophthalmoplegia, monoclonal immunoglobulin M protein, cold agglutinin and disialosyl antibody syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "715627004",
            "description": "Primary progressive freezing gait syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "715645004",
            "description": "Hereditary thermosensitive neuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "715646003",
            "description": "Desmin related myopathy with Mallory body-like inclusions (disorder)",
            "attributes": null
          },
          {
            "code": "715665006",
            "description": "Hereditary motor and sensory neuropathy Okinawa type (disorder)",
            "attributes": null
          },
          {
            "code": "715666007",
            "description": "Charcot-Marie-Tooth disease type IE (disorder)",
            "attributes": null
          },
          {
            "code": "715726000",
            "description": "Spinocerebellar ataxia type 7 (disorder)",
            "attributes": null
          },
          {
            "code": "715737004",
            "description": "Parkinsonism co-occurrent with dementia of Guadeloupe (disorder)",
            "attributes": null
          },
          {
            "code": "715748006",
            "description": "Spinocerebellar ataxia type 1 (disorder)",
            "attributes": null
          },
          {
            "code": "715751004",
            "description": "Spinocerebellar ataxia type 2 (disorder)",
            "attributes": null
          },
          {
            "code": "715752006",
            "description": "Spinocerebellar ataxia type 6 (disorder)",
            "attributes": null
          },
          {
            "code": "715753001",
            "description": "Spinocerebellar ataxia type 8 (disorder)",
            "attributes": null
          },
          {
            "code": "715754007",
            "description": "Spinocerebellar ataxia type 10 (disorder)",
            "attributes": null
          },
          {
            "code": "715755008",
            "description": "Spinocerebellar ataxia type 4 (disorder)",
            "attributes": null
          },
          {
            "code": "715768000",
            "description": "Autosomal dominant dopa responsive dystonia (disorder)",
            "attributes": null
          },
          {
            "code": "715770009",
            "description": "Acute motor axonal neuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "715776003",
            "description": "Spastic paraplegia type 7 (disorder)",
            "attributes": null
          },
          {
            "code": "715777007",
            "description": "Primary dystonia type 2 (disorder)",
            "attributes": null
          },
          {
            "code": "715788001",
            "description": "Myotonia fluctuans (disorder)",
            "attributes": null
          },
          {
            "code": "715789009",
            "description": "Myotonia permanens (disorder)",
            "attributes": null
          },
          {
            "code": "715793003",
            "description": "Acetazolamide responsive myotonia (disorder)",
            "attributes": null
          },
          {
            "code": "715795005",
            "description": "Charcot-Marie-Tooth disease type 4 (disorder)",
            "attributes": null
          },
          {
            "code": "715796006",
            "description": "Charcot-Marie-Tooth disease type 4A (disorder)",
            "attributes": null
          },
          {
            "code": "715797002",
            "description": "Charcot-Marie-Tooth disease type 4C (disorder)",
            "attributes": null
          },
          {
            "code": "715798007",
            "description": "Charcot-Marie-Tooth disease type 4D (disorder)",
            "attributes": null
          },
          {
            "code": "715799004",
            "description": "Charcot-Marie-Tooth disease type 4G (disorder)",
            "attributes": null
          },
          {
            "code": "715800000",
            "description": "Charcot-Marie-Tooth disease type 4B2 (disorder)",
            "attributes": null
          },
          {
            "code": "715801001",
            "description": "Charcot-Marie-Tooth disease type 4F (disorder)",
            "attributes": null
          },
          {
            "code": "715802008",
            "description": "Charcot-Marie-Tooth disease type 4H (disorder)",
            "attributes": null
          },
          {
            "code": "715803003",
            "description": "Charcot-Marie-Tooth disease type 4B1 (disorder)",
            "attributes": null
          },
          {
            "code": "715824008",
            "description": "Spinocerebellar ataxia type 28 (disorder)",
            "attributes": null
          },
          {
            "code": "715825009",
            "description": "Spinocerebellar ataxia type 29 (disorder)",
            "attributes": null
          },
          {
            "code": "715826005",
            "description": "Spinocerebellar ataxia type 31 (disorder)",
            "attributes": null
          },
          {
            "code": "715827001",
            "description": "Autosomal recessive dopa responsive dystonia (disorder)",
            "attributes": null
          },
          {
            "code": "715863001",
            "description": "Autoimmune necrotizing myopathy (disorder)",
            "attributes": null
          },
          {
            "code": "715902009",
            "description": "Primary orthostatic tremor (disorder)",
            "attributes": null
          },
          {
            "code": "715984007",
            "description": "Cerebellar ataxia with hypogonadism and choroidal dystrophy syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "716051003",
            "description": "Cerebrovascular accident during surgery (disorder)",
            "attributes": null
          },
          {
            "code": "716107009",
            "description": "Early onset parkinsonism and intellectual disability syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "716200002",
            "description": "Nephrogenic diabetes insipidus and intracranial calcification syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "716281000",
            "description": "Primary progressive non fluent aphasia (disorder)",
            "attributes": null
          },
          {
            "code": "716338001",
            "description": "Muscular pseudohypertrophy and hypothyroidism syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "716380002",
            "description": "Logopenic progressive aphasia (disorder)",
            "attributes": null
          },
          {
            "code": "716662004",
            "description": "Autosomal dominant late onset Parkinson disease (disorder)",
            "attributes": null
          },
          {
            "code": "716664003",
            "description": "Primary dystonia 21 (disorder)",
            "attributes": null
          },
          {
            "code": "716667005",
            "description": "Right temporal atrophy variant frontotemporal dementia (disorder)",
            "attributes": null
          },
          {
            "code": "716696006",
            "description": "Autosomal dominant centronuclear myopathy (disorder)",
            "attributes": null
          },
          {
            "code": "716722005",
            "description": "Acute motor sensory axonal Guillain-BarrÃ© syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "716723000",
            "description": "Guillain-BarrÃ© syndrome acute inflammatory demyelinating polyradiculoneuropathic form (disorder)",
            "attributes": null
          },
          {
            "code": "716724006",
            "description": "Spinocerebellar ataxia type 15/16 (disorder)",
            "attributes": null
          },
          {
            "code": "716994006",
            "description": "Behavioral variant of frontotemporal dementia (disorder)",
            "attributes": null
          },
          {
            "code": "717008005",
            "description": "Autosomal dominant Charcot-Marie-Tooth disease type 2B (disorder)",
            "attributes": null
          },
          {
            "code": "717010007",
            "description": "Autosomal dominant Charcot-Marie-Tooth disease type 2C (disorder)",
            "attributes": null
          },
          {
            "code": "717011006",
            "description": "Autosomal dominant Charcot-Marie-Tooth disease type 2D (disorder)",
            "attributes": null
          },
          {
            "code": "717012004",
            "description": "Autosomal dominant Charcot-Marie-Tooth disease type 2E (disorder)",
            "attributes": null
          },
          {
            "code": "717013009",
            "description": "Autosomal dominant Charcot-Marie-Tooth disease type 2I (disorder)",
            "attributes": null
          },
          {
            "code": "717014003",
            "description": "Autosomal dominant Charcot-Marie-Tooth disease type 2J (disorder)",
            "attributes": null
          },
          {
            "code": "717016001",
            "description": "Autosomal dominant Charcot-Marie-Tooth disease type 2A1 (disorder)",
            "attributes": null
          },
          {
            "code": "717054001",
            "description": "Maternally inherited mitochondrial dystonia (disorder)",
            "attributes": null
          },
          {
            "code": "717266001",
            "description": "Sensory ataxic neuropathy with dysarthria and ophthalmoparesis syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "717332007",
            "description": "Cerebellar ataxia Cayman type (disorder)",
            "attributes": null
          },
          {
            "code": "717825008",
            "description": "Hereditary sensory and autonomic neuropathy type 1B (disorder)",
            "attributes": null
          },
          {
            "code": "717826009",
            "description": "Hereditary sensory and autonomic neuropathy with deafness and global delay (disorder)",
            "attributes": null
          },
          {
            "code": "717827000",
            "description": "Hereditary sensory and autonomic neuropathy with spastic paraplegia (disorder)",
            "attributes": null
          },
          {
            "code": "71791000119104",
            "description": "Peripheral neuropathy due to type 1 diabetes mellitus (disorder)",
            "attributes": null
          },
          {
            "code": "717942003",
            "description": "Brain dopamine-serotonin vesicular transport disease (disorder)",
            "attributes": null
          },
          {
            "code": "717964007",
            "description": "Juvenile primary lateral sclerosis (disorder)",
            "attributes": null
          },
          {
            "code": "717975006",
            "description": "Autosomal dominant optic atrophy and peripheral neuropathy syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "718103001",
            "description": "Hereditary geniospasm (disorder)",
            "attributes": null
          },
          {
            "code": "718124006",
            "description": "Fatal infantile cytochrome C oxidase deficiency (disorder)",
            "attributes": null
          },
          {
            "code": "718174008",
            "description": "Infantile striatonigral degeneration (disorder)",
            "attributes": null
          },
          {
            "code": "718176005",
            "description": "Autosomal recessive limb girdle muscular dystrophy type 2C (disorder)",
            "attributes": null
          },
          {
            "code": "718177001",
            "description": "Autosomal recessive limb girdle muscular dystrophy type 2F (disorder)",
            "attributes": null
          },
          {
            "code": "718178006",
            "description": "Autosomal dominant limb girdle muscular dystrophy type 1B (disorder)",
            "attributes": null
          },
          {
            "code": "718179003",
            "description": "Autosomal recessive limb girdle muscular dystrophy type 2B (disorder)",
            "attributes": null
          },
          {
            "code": "718180000",
            "description": "Autosomal recessive limb girdle muscular dystrophy type 2I (disorder)",
            "attributes": null
          },
          {
            "code": "718212006",
            "description": "Mitochondrial encephalocardiomyopathy due to transmembrane protein 70 mutation (disorder)",
            "attributes": null
          },
          {
            "code": "718213001",
            "description": "Polyneuropathy associated with monoclonal immunoglobulin M antibodies to myelin-associated glycoprotein (disorder)",
            "attributes": null
          },
          {
            "code": "718214007",
            "description": "Mitochondrial neurogastrointestinal encephalomyopathy syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "718219002",
            "description": "Congenital lactic acidosis Saguenay-Lac-Saint-Jean type (disorder)",
            "attributes": null
          },
          {
            "code": "718362003",
            "description": "Functional movement disorder (disorder)",
            "attributes": null
          },
          {
            "code": "718551002",
            "description": "Moyamoya disease with early onset achalasia (disorder)",
            "attributes": null
          },
          {
            "code": "718555006",
            "description": "Juvenile amyotrophic lateral sclerosis (disorder)",
            "attributes": null
          },
          {
            "code": "718572004",
            "description": "Bethlem myopathy (disorder)",
            "attributes": null
          },
          {
            "code": "718685006",
            "description": "Orthostatic hypotension co-occurrent and due to Parkinson's disease (disorder)",
            "attributes": null
          },
          {
            "code": "718713000",
            "description": "Hypertrophic cardiomyopathy with hypotonia and lactic acidosis syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "718752007",
            "description": "Episodic ataxia type 7 (disorder)",
            "attributes": null
          },
          {
            "code": "718753002",
            "description": "Episodic ataxia type 6 (disorder)",
            "attributes": null
          },
          {
            "code": "718754008",
            "description": "Episodic ataxia type 4 (disorder)",
            "attributes": null
          },
          {
            "code": "718755009",
            "description": "Episodic ataxia type 3 (disorder)",
            "attributes": null
          },
          {
            "code": "718756005",
            "description": "Episodic ataxia type 5 (disorder)",
            "attributes": null
          },
          {
            "code": "718770005",
            "description": "Spinocerebellar ataxia type 25 (disorder)",
            "attributes": null
          },
          {
            "code": "718774001",
            "description": "Spinocerebellar ataxia type 21 (disorder)",
            "attributes": null
          },
          {
            "code": "718845002",
            "description": "X-linked intellectual disability with ataxia and apraxia syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "718847005",
            "description": "X-linked neurodegenerative syndrome Hamel type (disorder)",
            "attributes": null
          },
          {
            "code": "718849008",
            "description": "X-linked neurodegenerative syndrome Bertini type (disorder)",
            "attributes": null
          },
          {
            "code": "718850008",
            "description": "Autosomal recessive limb girdle muscular dystrophy type 2E (disorder)",
            "attributes": null
          },
          {
            "code": "719103009",
            "description": "Autosomal recessive spastic paraplegia type 39 (disorder)",
            "attributes": null
          },
          {
            "code": "719164000",
            "description": "Symmetrical thalamic calcification (disorder)",
            "attributes": null
          },
          {
            "code": "719207000",
            "description": "Spinocerebellar ataxia type 11 (disorder)",
            "attributes": null
          },
          {
            "code": "719210007",
            "description": "Spinocerebellar ataxia type 14 (disorder)",
            "attributes": null
          },
          {
            "code": "719249005",
            "description": "Spinocerebellar ataxia type 17 (disorder)",
            "attributes": null
          },
          {
            "code": "719250005",
            "description": "Spinocerebellar ataxia type 18 (disorder)",
            "attributes": null
          },
          {
            "code": "719252002",
            "description": "Spinocerebellar ataxia type 27 (disorder)",
            "attributes": null
          },
          {
            "code": "719254001",
            "description": "Spinocerebellar ataxia type 32 (disorder)",
            "attributes": null
          },
          {
            "code": "719255000",
            "description": "Spinocerebellar ataxia type 34 (disorder)",
            "attributes": null
          },
          {
            "code": "719276005",
            "description": "Primary dystonia type 4 (disorder)",
            "attributes": null
          },
          {
            "code": "719278006",
            "description": "Primary dystonia type 13 (disorder)",
            "attributes": null
          },
          {
            "code": "719300001",
            "description": "Spinocerebellar ataxia type 35 (disorder)",
            "attributes": null
          },
          {
            "code": "719301002",
            "description": "Spinocerebellar ataxia type 37 (disorder)",
            "attributes": null
          },
          {
            "code": "719405005",
            "description": "Leukoencephalopathy with metaphyseal chondrodysplasia syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "719510006",
            "description": "Autosomal dominant Charcot-Marie-Tooth disease type 2F (disorder)",
            "attributes": null
          },
          {
            "code": "719511005",
            "description": "Autosomal dominant Charcot-Marie-Tooth disease type 2G (disorder)",
            "attributes": null
          },
          {
            "code": "719512003",
            "description": "Autosomal dominant Charcot-Marie-Tooth disease type 2K (disorder)",
            "attributes": null
          },
          {
            "code": "719513008",
            "description": "Autosomal dominant Charcot-Marie-Tooth disease type 2L (disorder)",
            "attributes": null
          },
          {
            "code": "719514002",
            "description": "Autosomal dominant Charcot-Marie-Tooth disease type 2M (disorder)",
            "attributes": null
          },
          {
            "code": "719515001",
            "description": "Autosomal dominant Charcot-Marie-Tooth disease type 2N (disorder)",
            "attributes": null
          },
          {
            "code": "719516000",
            "description": "Autosomal dominant focal dystonia DYT25 type (disorder)",
            "attributes": null
          },
          {
            "code": "719717006",
            "description": "Psychosis co-occurrent and due to Parkinson's disease (disorder)",
            "attributes": null
          },
          {
            "code": "719815005",
            "description": "X-linked myopathy with excessive autophagy (disorder)",
            "attributes": null
          },
          {
            "code": "719816006",
            "description": "X-linked sideroblastic anemia with spinocerebellar ataxia (disorder)",
            "attributes": null
          },
          {
            "code": "719817002",
            "description": "X-linked spinocerebellar ataxia type 3 (disorder)",
            "attributes": null
          },
          {
            "code": "719818007",
            "description": "X-linked spinocerebellar ataxia type 4 (disorder)",
            "attributes": null
          },
          {
            "code": "719838008",
            "description": "X-linked hereditary sensory and autonomic neuropathy with deafness (disorder)",
            "attributes": null
          },
          {
            "code": "719972004",
            "description": "Haddad syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "719976001",
            "description": "Glaucoma and sleep apnea syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "719979008",
            "description": "Charcot-Marie-Tooth disease type ID (disorder)",
            "attributes": null
          },
          {
            "code": "719980006",
            "description": "Charcot-Marie-Tooth disease type IF (disorder)",
            "attributes": null
          },
          {
            "code": "719981005",
            "description": "Charcot-Marie-Tooth disease type 2B2 (disorder)",
            "attributes": null
          },
          {
            "code": "719985001",
            "description": "Autosomal dominant limb girdle muscular dystrophy type 1A (disorder)",
            "attributes": null
          },
          {
            "code": "719986000",
            "description": "Autosomal dominant limb girdle muscular dystrophy type 1C (disorder)",
            "attributes": null
          },
          {
            "code": "719987009",
            "description": "Autosomal dominant limb girdle muscular dystrophy type 1D (disorder)",
            "attributes": null
          },
          {
            "code": "719988004",
            "description": "Autosomal dominant limb girdle muscular dystrophy type 1E (disorder)",
            "attributes": null
          },
          {
            "code": "719989007",
            "description": "Autosomal dominant limb girdle muscular dystrophy type 1F (disorder)",
            "attributes": null
          },
          {
            "code": "719990003",
            "description": "Autosomal dominant limb girdle muscular dystrophy type 1G (disorder)",
            "attributes": null
          },
          {
            "code": "720010009",
            "description": "Microphthalmia with brain atrophy syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "720466001",
            "description": "Adult-onset dystonia parkinsonism (disorder)",
            "attributes": null
          },
          {
            "code": "720517001",
            "description": "Ataxia with deafness and intellectual disability syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "720522001",
            "description": "Autosomal recessive limb girdle muscular dystrophy type 2G (disorder)",
            "attributes": null
          },
          {
            "code": "720523006",
            "description": "Autosomal recessive limb girdle muscular dystrophy type 2K (disorder)",
            "attributes": null
          },
          {
            "code": "720576001",
            "description": "Brain calcification Rajab type (disorder)",
            "attributes": null
          },
          {
            "code": "720637005",
            "description": "Charcot-Marie-Tooth disease type 2H (disorder)",
            "attributes": null
          },
          {
            "code": "720638000",
            "description": "Charcot-Marie-Tooth disease type 4J (disorder)",
            "attributes": null
          },
          {
            "code": "720750004",
            "description": "Spinocerebellar degeneration and corneal dystrophy syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "720956003",
            "description": "Foix Chavany Marie syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "721190004",
            "description": "Myopathy due to magnesium deficiency (disorder)",
            "attributes": null
          },
          {
            "code": "721197001",
            "description": "Polyneuropathy due to classical cystic fibrosis (disorder)",
            "attributes": null
          },
          {
            "code": "721211008",
            "description": "Encephalopathy caused by methylmercury (disorder)",
            "attributes": null
          },
          {
            "code": "721228006",
            "description": "Huntington disease-like 2 (disorder)",
            "attributes": null
          },
          {
            "code": "721254003",
            "description": "Infection of cranial nerve (disorder)",
            "attributes": null
          },
          {
            "code": "721536001",
            "description": "Autonomic disorder caused by toxin (disorder)",
            "attributes": null
          },
          {
            "code": "721537005",
            "description": "Acquired Horner syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "721846006",
            "description": "Hypomyelination, hypogonadotropic hypogonadism, hypodontia syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "722060007",
            "description": "Oculogastrointestinal muscular dystrophy (disorder)",
            "attributes": null
          },
          {
            "code": "722212004",
            "description": "Severe X-linked mitochondrial encephalomyopathy (disorder)",
            "attributes": null
          },
          {
            "code": "722293005",
            "description": "Autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "722294004",
            "description": "Autosomal dominant intermediate Charcot-Marie-Tooth disease type E (disorder)",
            "attributes": null
          },
          {
            "code": "722386009",
            "description": "Celiac disease with epilepsy and cerebral calcification syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "722435003",
            "description": "Dystonia 16 (disorder)",
            "attributes": null
          },
          {
            "code": "722557007",
            "description": "Parkinsonism due to human immunodeficiency virus infection (disorder)",
            "attributes": null
          },
          {
            "code": "722558002",
            "description": "Parkinsonism following infection (disorder)",
            "attributes": null
          },
          {
            "code": "722599008",
            "description": "Parkinsonism due to hereditary spastic paraplegia (disorder)",
            "attributes": null
          },
          {
            "code": "722600006",
            "description": "Non-amnestic Alzheimer disease (disorder)",
            "attributes": null
          },
          {
            "code": "722601005",
            "description": "White matter disorder caused by infection (disorder)",
            "attributes": null
          },
          {
            "code": "722602003",
            "description": "White matter disorder caused by toxin (disorder)",
            "attributes": null
          },
          {
            "code": "722763000",
            "description": "Infantile dystonia parkinsonism (disorder)",
            "attributes": null
          },
          {
            "code": "722964001",
            "description": "Atypical Parkinsonism (disorder)",
            "attributes": null
          },
          {
            "code": "722965000",
            "description": "Parkinsonism due to heredodegenerative disorder (disorder)",
            "attributes": null
          },
          {
            "code": "722966004",
            "description": "Chorea due to heredodegenerative disorder (disorder)",
            "attributes": null
          },
          {
            "code": "722967008",
            "description": "Ataxia due to mitochondrial mutations (disorder)",
            "attributes": null
          },
          {
            "code": "722969006",
            "description": "Tremor due to metabolic disorder (disorder)",
            "attributes": null
          },
          {
            "code": "722970007",
            "description": "Tremor due to substance abuse (disorder)",
            "attributes": null
          },
          {
            "code": "722974003",
            "description": "Segmental myoclonus (disorder)",
            "attributes": null
          },
          {
            "code": "722984002",
            "description": "Myelopathy due to metabolic disorder (disorder)",
            "attributes": null
          },
          {
            "code": "722985001",
            "description": "Acute venous infarction of spinal cord (disorder)",
            "attributes": null
          },
          {
            "code": "722986000",
            "description": "Chronic venous infarction of spinal cord (disorder)",
            "attributes": null
          },
          {
            "code": "722987009",
            "description": "Amyotrophic lateral sclerosis plus syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "722988004",
            "description": "Compression of olfactory nerve (disorder)",
            "attributes": null
          },
          {
            "code": "722991004",
            "description": "Autoimmune myopathy (disorder)",
            "attributes": null
          },
          {
            "code": "722997000",
            "description": "Inherited autonomic nervous system disorder (disorder)",
            "attributes": null
          },
          {
            "code": "722998005",
            "description": "Autonomic nervous system hyperactivity (disorder)",
            "attributes": null
          },
          {
            "code": "723000001",
            "description": "Generalized hyperhidrosis due to neurological disorder (disorder)",
            "attributes": null
          },
          {
            "code": "723082006",
            "description": "Silent cerebral infarct (disorder)",
            "attributes": null
          },
          {
            "code": "723083001",
            "description": "Late effects of cerebral ischemic stroke (disorder)",
            "attributes": null
          },
          {
            "code": "723084007",
            "description": "Sequela of non-traumatic intracerebral hemorrhage (disorder)",
            "attributes": null
          },
          {
            "code": "723085008",
            "description": "Sequela of non-traumatic intracranial subarachnoid hemorrhage (disorder)",
            "attributes": null
          },
          {
            "code": "723122006",
            "description": "Primary tic disorder (disorder)",
            "attributes": null
          },
          {
            "code": "723129002",
            "description": "Spinal cord compression due to degenerative disorder of spinal column (disorder)",
            "attributes": null
          },
          {
            "code": "723147008",
            "description": "Autonomic disorder co-occurrent and due to Chagas disease (disorder)",
            "attributes": null
          },
          {
            "code": "723148003",
            "description": "Syncope due to autonomic failure (disorder)",
            "attributes": null
          },
          {
            "code": "723151005",
            "description": "Permanent vegetative state (disorder)",
            "attributes": null
          },
          {
            "code": "723152003",
            "description": "Minimally conscious state plus (disorder)",
            "attributes": null
          },
          {
            "code": "723153008",
            "description": "Minimally conscious state minus (disorder)",
            "attributes": null
          },
          {
            "code": "723306004",
            "description": "Facial onset sensory and motor neuronopathy syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "723308003",
            "description": "Epidermolysis bullosa simplex with muscular dystrophy (disorder)",
            "attributes": null
          },
          {
            "code": "723359002",
            "description": "Familial acute necrotizing encephalopathy (disorder)",
            "attributes": null
          },
          {
            "code": "723407009",
            "description": "Muscular dystrophy Selcen type (disorder)",
            "attributes": null
          },
          {
            "code": "723439002",
            "description": "Native American myopathy (disorder)",
            "attributes": null
          },
          {
            "code": "723441001",
            "description": "Non-progressive cerebellar ataxia with intellectual disability (disorder)",
            "attributes": null
          },
          {
            "code": "723452007",
            "description": "Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "723497003",
            "description": "Peripheral neuropathy with sensorineural hearing impairment syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "723557004",
            "description": "Thiamine-responsive encephalopathy (disorder)",
            "attributes": null
          },
          {
            "code": "723612001",
            "description": "Spinal muscular atrophy, Dandy-Walker malformation, cataract syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "723622007",
            "description": "X-linked spastic paraplegia type 2 (disorder)",
            "attributes": null
          },
          {
            "code": "723644002",
            "description": "Microvascular cranial nerve palsy (disorder)",
            "attributes": null
          },
          {
            "code": "723666009",
            "description": "Length-dependent peripheral neuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "723721007",
            "description": "Sensorineural hearing loss, early graying, essential tremor syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "723819007",
            "description": "Autosomal dominant spastic paraplegia type 36 (disorder)",
            "attributes": null
          },
          {
            "code": "723820001",
            "description": "Autosomal dominant spastic paraplegia type 4 (disorder)",
            "attributes": null
          },
          {
            "code": "723821002",
            "description": "Autosomal recessive spastic paraplegia type 44 (disorder)",
            "attributes": null
          },
          {
            "code": "723822009",
            "description": "Autosomal recessive spastic paraplegia type 46 (disorder)",
            "attributes": null
          },
          {
            "code": "723823004",
            "description": "Autosomal recessive spastic paraplegia type 53 (disorder)",
            "attributes": null
          },
          {
            "code": "723824005",
            "description": "Autosomal recessive spastic paraplegia type 54 (disorder)",
            "attributes": null
          },
          {
            "code": "723825006",
            "description": "Autosomal recessive spastic paraplegia type 55 (disorder)",
            "attributes": null
          },
          {
            "code": "723826007",
            "description": "Autosomal recessive spastic paraplegia type 57 (disorder)",
            "attributes": null
          },
          {
            "code": "723857007",
            "description": "Silent micro-hemorrhage of brain (disorder)",
            "attributes": null
          },
          {
            "code": "723940009",
            "description": "Hypohidrosis co-occurrent and due to disorder of sympathetic nervous system (disorder)",
            "attributes": null
          },
          {
            "code": "723992000",
            "description": "Kufor Rakeb syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "724002003",
            "description": "Retinal ischemia, digestive tract small vessel hyalinosis, diffuse cerebral calcification syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "724065003",
            "description": "Autosomal recessive posterior column ataxia and retinitis pigmentosa (disorder)",
            "attributes": null
          },
          {
            "code": "724072002",
            "description": "Paroxysmal exertion-induced dyskinesia (disorder)",
            "attributes": null
          },
          {
            "code": "724095006",
            "description": "Myopathy due to calsequestrin and sarcoplasmic/endoplasmic reticulum calcium ATPase 1 protein overload (disorder)",
            "attributes": null
          },
          {
            "code": "724097003",
            "description": "Moyamoya angiopathy, short stature, facial dysmorphism, hypergonadotropic hypogonadism syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "724138007",
            "description": "Mitochondrial myopathy with sideroblastic anemia syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "724172004",
            "description": "McLeod neuroacanthocytosis syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "724227000",
            "description": "Infantile onset spinocerebellar ataxia (disorder)",
            "attributes": null
          },
          {
            "code": "724228005",
            "description": "Infantile choroidocerebral calcification syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "724283004",
            "description": "Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum (disorder)",
            "attributes": null
          },
          {
            "code": "724349009",
            "description": "Hereditary inclusion body myopathy, joint contracture, ophthalmoplegia syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "724351008",
            "description": "Hereditary hyperekplexia (disorder)",
            "attributes": null
          },
          {
            "code": "724357007",
            "description": "Hereditary cerebral hemorrhage with amyloidosis (disorder)",
            "attributes": null
          },
          {
            "code": "724383002",
            "description": "Hemidystonia hemiatrophy syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "724424009",
            "description": "Cerebral ischemic stroke due to small artery occlusion (disorder)",
            "attributes": null
          },
          {
            "code": "724425005",
            "description": "Cerebral ischemic stroke due to intracranial large artery atherosclerosis (disorder)",
            "attributes": null
          },
          {
            "code": "724426006",
            "description": "Cerebral ischemic stroke due to extracranial large artery atherosclerosis (disorder)",
            "attributes": null
          },
          {
            "code": "724427002",
            "description": "Asymptomatic stenosis of intracranial artery (disorder)",
            "attributes": null
          },
          {
            "code": "724428007",
            "description": "Asymptomatic stenosis of extracranial artery (disorder)",
            "attributes": null
          },
          {
            "code": "724429004",
            "description": "Stroke co-occurrent with migraine (disorder)",
            "attributes": null
          },
          {
            "code": "724504007",
            "description": "Central sleep apnea caused by substance (disorder)",
            "attributes": null
          },
          {
            "code": "724506009",
            "description": "Central sleep apnea co-occurrent with Cheyne Stokes respiration (disorder)",
            "attributes": null
          },
          {
            "code": "724507000",
            "description": "Central sleep apnea without Cheyne-Stokes respiration (disorder)",
            "attributes": null
          },
          {
            "code": "724508005",
            "description": "Late-onset central hypoventilation co-occurrent and due to hypothalamic dysfunction (disorder)",
            "attributes": null
          },
          {
            "code": "724509002",
            "description": "Sleep-related hypoventilation caused by substance (disorder)",
            "attributes": null
          },
          {
            "code": "724544000",
            "description": "Infection causing tic (disorder)",
            "attributes": null
          },
          {
            "code": "724545004",
            "description": "Tic due to and following infection (disorder)",
            "attributes": null
          },
          {
            "code": "724546003",
            "description": "Infection causing parkinsonism (disorder)",
            "attributes": null
          },
          {
            "code": "724547007",
            "description": "Infection causing chorea (disorder)",
            "attributes": null
          },
          {
            "code": "724548002",
            "description": "Chorea due to and following infective disorder (disorder)",
            "attributes": null
          },
          {
            "code": "724558003",
            "description": "Peripheral neuropathy due to hypervitaminosis B6 (disorder)",
            "attributes": null
          },
          {
            "code": "724559006",
            "description": "Myopathy co-occurrent and due to hypercalcemia (disorder)",
            "attributes": null
          },
          {
            "code": "724560001",
            "description": "Neurological disorder due to nutrient deficiency (disorder)",
            "attributes": null
          },
          {
            "code": "724561002",
            "description": "Encephalopathy due to nutritional deficiency (disorder)",
            "attributes": null
          },
          {
            "code": "724562009",
            "description": "Myelopathy due to nutritional deficiency (disorder)",
            "attributes": null
          },
          {
            "code": "724565006",
            "description": "White matter disorder due to nutritional deficiency (disorder)",
            "attributes": null
          },
          {
            "code": "724566007",
            "description": "Neurological disorder due to excess intake of micronutrients (disorder)",
            "attributes": null
          },
          {
            "code": "724567003",
            "description": "Neurological disorder due to excess intake of macronutrients (disorder)",
            "attributes": null
          },
          {
            "code": "724572007",
            "description": "Neuromuscular junction disorder caused by organic phosphorus compound ingestion (disorder)",
            "attributes": null
          },
          {
            "code": "724574008",
            "description": "Neurological disorder caused by ingestible alcohol (disorder)",
            "attributes": null
          },
          {
            "code": "724761004",
            "description": "Sporadic Parkinson disease (disorder)",
            "attributes": null
          },
          {
            "code": "724762006",
            "description": "Parkinsonism due to and following injury of head (disorder)",
            "attributes": null
          },
          {
            "code": "724763001",
            "description": "Parkinsonism due to mass lesion of brain (disorder)",
            "attributes": null
          },
          {
            "code": "724764007",
            "description": "Chorea co-occurrent and due to Huntington disease-like condition (disorder)",
            "attributes": null
          },
          {
            "code": "724765008",
            "description": "Chorea co-occurrent and due to dentatorubropallidoluysian degeneration (disorder)",
            "attributes": null
          },
          {
            "code": "724766009",
            "description": "Chorea co-occurrent and due to Wilson disease (disorder)",
            "attributes": null
          },
          {
            "code": "724767000",
            "description": "Chorea co-occurrent and due to systemic lupus erythematosus (disorder)",
            "attributes": null
          },
          {
            "code": "724769002",
            "description": "Ataxia co-occurrent and due to phytanic acid storage disease (disorder)",
            "attributes": null
          },
          {
            "code": "724775006",
            "description": "X-linked hereditary spastic paraplegia (disorder)",
            "attributes": null
          },
          {
            "code": "724776007",
            "description": "Dementia due to disorder of central nervous system (disorder)",
            "attributes": null
          },
          {
            "code": "724778008",
            "description": "Progressive relapsing multiple sclerosis (disorder)",
            "attributes": null
          },
          {
            "code": "724779000",
            "description": "White matter disorder co-occurrent and due to cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (disorder)",
            "attributes": null
          },
          {
            "code": "724780002",
            "description": "Demyelination of central nervous system co-occurrent and due to neurosarcoidosis (disorder)",
            "attributes": null
          },
          {
            "code": "724781003",
            "description": "Demyelination of central nervous system co-occurrent and due to systemic lupus erythematosus (disorder)",
            "attributes": null
          },
          {
            "code": "724782005",
            "description": "Demyelination of central nervous system co-occurrent and due to Sjogren disease (disorder)",
            "attributes": null
          },
          {
            "code": "724783000",
            "description": "Demyelination of central nervous system co-occurrent and due to Behcet disease (disorder)",
            "attributes": null
          },
          {
            "code": "724784006",
            "description": "Demyelination of central nervous system co-occurrent and due to mitochondrial disease (disorder)",
            "attributes": null
          },
          {
            "code": "724785007",
            "description": "Epilepsy due to perinatal stroke (disorder)",
            "attributes": null
          },
          {
            "code": "724787004",
            "description": "Epilepsy due to cerebrovascular accident (disorder)",
            "attributes": null
          },
          {
            "code": "724811002",
            "description": "Disorder of autonomic nervous system due to infectious disease (disorder)",
            "attributes": null
          },
          {
            "code": "724812009",
            "description": "Disorder of autonomic nervous system caused by substance (disorder)",
            "attributes": null
          },
          {
            "code": "724813004",
            "description": "Autonomic nervous system disorder co-occurrent and due to neurodegenerative disorder (disorder)",
            "attributes": null
          },
          {
            "code": "724814005",
            "description": "Autonomic neuropathy due to sodium channelopathy (disorder)",
            "attributes": null
          },
          {
            "code": "724815006",
            "description": "Autonomic neuropathy due to disorder of immune function (disorder)",
            "attributes": null
          },
          {
            "code": "724816007",
            "description": "Acquired anhidrosis co-occurrent and due to primary autonomic disorder (disorder)",
            "attributes": null
          },
          {
            "code": "724821005",
            "description": "Functional chorea (disorder)",
            "attributes": null
          },
          {
            "code": "724822003",
            "description": "Functional dystonia (disorder)",
            "attributes": null
          },
          {
            "code": "724823008",
            "description": "Functional parkinsonism (disorder)",
            "attributes": null
          },
          {
            "code": "724844008",
            "description": "Pruritus due to neurological disorder (disorder)",
            "attributes": null
          },
          {
            "code": "724988000",
            "description": "Epilepsy co-occurrent and due to degenerative brain disorder (disorder)",
            "attributes": null
          },
          {
            "code": "724989008",
            "description": "Epilepsy co-occurrent and due to mesial temporal sclerosis (disorder)",
            "attributes": null
          },
          {
            "code": "724991000",
            "description": "Epilepsy co-occurrent and due to demyelinating disorder (disorder)",
            "attributes": null
          },
          {
            "code": "724993002",
            "description": "Cerebral ischemic stroke due to occlusion of extracranial large artery (disorder)",
            "attributes": null
          },
          {
            "code": "724994008",
            "description": "Cerebral ischemic stroke due to stenosis of extracranial large artery (disorder)",
            "attributes": null
          },
          {
            "code": "724998006",
            "description": "Polyneuropathy co-occurrent and due to systemic connective tissue disorder (disorder)",
            "attributes": null
          },
          {
            "code": "725000003",
            "description": "Secondary intracranial hypotension (disorder)",
            "attributes": null
          },
          {
            "code": "725001004",
            "description": "Idiopathic syringomyelia (disorder)",
            "attributes": null
          },
          {
            "code": "725042001",
            "description": "Autosomal recessive limb girdle muscular dystrophy type 2J (disorder)",
            "attributes": null
          },
          {
            "code": "725043006",
            "description": "Autosomal recessive limb girdle muscular dystrophy type 2O (disorder)",
            "attributes": null
          },
          {
            "code": "725047007",
            "description": "Autosomal recessive Charcot-Marie-Tooth disease with hoarseness (disorder)",
            "attributes": null
          },
          {
            "code": "725048002",
            "description": "Charcot-Marie-Tooth disease type 2B1 (disorder)",
            "attributes": null
          },
          {
            "code": "725097006",
            "description": "Crisponi syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "725132001",
            "description": "Ischemic stroke without residual deficits (disorder)",
            "attributes": null
          },
          {
            "code": "725139005",
            "description": "Spastic paraplegia, optic atrophy, neuropathy syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "725146001",
            "description": "Atypical juvenile parkinsonism (disorder)",
            "attributes": null
          },
          {
            "code": "725392005",
            "description": "Autosomal dominant striatal neurodegeneration (disorder)",
            "attributes": null
          },
          {
            "code": "725394006",
            "description": "Autosomal recessive ataxia due to ubiquinone deficiency (disorder)",
            "attributes": null
          },
          {
            "code": "725408001",
            "description": "Autosomal recessive cerebellar ataxia with oculomotor apraxia type 2 (disorder)",
            "attributes": null
          },
          {
            "code": "725420009",
            "description": "Congenital muscular dystrophy Paradas type (disorder)",
            "attributes": null
          },
          {
            "code": "725464001",
            "description": "Adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy (disorder)",
            "attributes": null
          },
          {
            "code": "72585000",
            "description": "Parkinsonian syndrome associated with idiopathic orthostatic hypotension (disorder)",
            "attributes": null
          },
          {
            "code": "725903003",
            "description": "Autosomal dominant myoglobinuria (disorder)",
            "attributes": null
          },
          {
            "code": "725907002",
            "description": "Autosomal recessive limb girdle muscular dystrophy type 2Y (disorder)",
            "attributes": null
          },
          {
            "code": "725958000",
            "description": "Chronic cerebrospinal venous insufficiency (disorder)",
            "attributes": null
          },
          {
            "code": "726031001",
            "description": "Cerebellar ataxia, intellectual disability, optic atrophy, skin abnormalities syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "726051002",
            "description": "Myotonia congenita (disorder)",
            "attributes": null
          },
          {
            "code": "726107008",
            "description": "Distal myopathy Welander type (disorder)",
            "attributes": null
          },
          {
            "code": "72655000",
            "description": "Alternating hypoglossal hemiplegia (disorder)",
            "attributes": null
          },
          {
            "code": "726606003",
            "description": "Autosomal recessive spastic paraplegia type 32 (disorder)",
            "attributes": null
          },
          {
            "code": "726607007",
            "description": "Autosomal recessive spastic paraplegia type 26 (disorder)",
            "attributes": null
          },
          {
            "code": "726608002",
            "description": "Autosomal recessive spastic paraplegia type 23 (disorder)",
            "attributes": null
          },
          {
            "code": "726609005",
            "description": "Autosomal recessive spastic paraplegia type 64 (disorder)",
            "attributes": null
          },
          {
            "code": "726610000",
            "description": "Autosomal recessive spastic paraplegia type 63 (disorder)",
            "attributes": null
          },
          {
            "code": "726611001",
            "description": "Autosomal recessive spastic paraplegia type 61 (disorder)",
            "attributes": null
          },
          {
            "code": "726614009",
            "description": "Autosomal recessive limb girdle muscular dystrophy type 2P (disorder)",
            "attributes": null
          },
          {
            "code": "726615005",
            "description": "Autosomal recessive limb girdle muscular dystrophy type 2Q (disorder)",
            "attributes": null
          },
          {
            "code": "726616006",
            "description": "Autosomal recessive limb girdle muscular dystrophy type 2L (disorder)",
            "attributes": null
          },
          {
            "code": "726617002",
            "description": "Autosomal recessive limb girdle muscular dystrophy type 2N (disorder)",
            "attributes": null
          },
          {
            "code": "726618007",
            "description": "Autosomal recessive limb girdle muscular dystrophy type 2M (disorder)",
            "attributes": null
          },
          {
            "code": "726622002",
            "description": "Spastic paraplegia with Paget disease of bone syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "726669007",
            "description": "Central nervous system calcification, deafness, tubular acidosis, anemia syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "72839009",
            "description": "Geniculate ganglionitis (disorder)",
            "attributes": null
          },
          {
            "code": "72858000",
            "description": "Speech cortex disorder (disorder)",
            "attributes": null
          },
          {
            "code": "72986009",
            "description": "Acute hemorrhagic leukoencephalitis (disorder)",
            "attributes": null
          },
          {
            "code": "73013002",
            "description": "Cranial nerve disorder (disorder)",
            "attributes": null
          },
          {
            "code": "73020009",
            "description": "Cerebral hemisphere hemorrhage (disorder)",
            "attributes": null
          },
          {
            "code": "73119000",
            "description": "Retinitis pigmentosa-deafness-ataxia syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "73173006",
            "description": "Spasm of cerebral arteries (disorder)",
            "attributes": null
          },
          {
            "code": "73192008",
            "description": "Multiple AND bilateral precerebral artery stenosis (disorder)",
            "attributes": null
          },
          {
            "code": "732245008",
            "description": "Pure mitochondrial myopathy (disorder)",
            "attributes": null
          },
          {
            "code": "732264002",
            "description": "Coenzyme A synthase protein associated neurodegeneration (disorder)",
            "attributes": null
          },
          {
            "code": "732923001",
            "description": "Hemorrhage of medulla oblongata (disorder)",
            "attributes": null
          },
          {
            "code": "732929002",
            "description": "Autosomal recessive limb girdle muscular dystrophy type 2S (disorder)",
            "attributes": null
          },
          {
            "code": "732930007",
            "description": "Autosomal recessive limb girdle muscular dystrophy type 2T (disorder)",
            "attributes": null
          },
          {
            "code": "732931006",
            "description": "Autosomal recessive limb girdle muscular dystrophy type 2R (disorder)",
            "attributes": null
          },
          {
            "code": "732932004",
            "description": "Autosomal recessive spastic paraplegia type 18 (disorder)",
            "attributes": null
          },
          {
            "code": "732933009",
            "description": "Autosomal recessive spastic paraplegia type 25 (disorder)",
            "attributes": null
          },
          {
            "code": "732948003",
            "description": "Autosomal dominant spastic paraplegia type 10 (disorder)",
            "attributes": null
          },
          {
            "code": "732949006",
            "description": "Autosomal dominant spastic paraplegia type 6 (disorder)",
            "attributes": null
          },
          {
            "code": "732951005",
            "description": "Mitochondrial myopathy, lactic acidosis, deafness syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "732958004",
            "description": "Spastic paraplegia with precocious puberty syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "732959007",
            "description": "Beta-propeller protein-associated neurodegeneration (disorder)",
            "attributes": null
          },
          {
            "code": "73297009",
            "description": "Muscular dystrophy (disorder)",
            "attributes": null
          },
          {
            "code": "733028000",
            "description": "Multiple sclerosis, ichthyosis, factor VIII deficiency syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "733029008",
            "description": "Autosomal dominant spastic paraplegia type 29 (disorder)",
            "attributes": null
          },
          {
            "code": "733033001",
            "description": "Spinocerebellar ataxia dysmorphism syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "733065003",
            "description": "Myoclonus, cerebellar ataxia, deafness syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "733071009",
            "description": "Deafness, small bowel diverticulosis, neuropathy syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "733089005",
            "description": "Spastic paraplegia, nephritis, deafness syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "733191004",
            "description": "Dementia due to chronic subdural hematoma (disorder)",
            "attributes": null
          },
          {
            "code": "733198005",
            "description": "Encephalopathy due to and following cardiopulmonary bypass (disorder)",
            "attributes": null
          },
          {
            "code": "733199002",
            "description": "Multifocal cerebral infarction due to and following procedure on cardiovascular system (disorder)",
            "attributes": null
          },
          {
            "code": "733200004",
            "description": "Superficial siderosis of central nervous system (disorder)",
            "attributes": null
          },
          {
            "code": "733455003",
            "description": "Spastic paraplegia, glaucoma, intellectual disability syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "733489002",
            "description": "Distal myopathy with posterior leg and anterior hand involvement (disorder)",
            "attributes": null
          },
          {
            "code": "733599009",
            "description": "Adult-onset multiple mitochondrial deoxyribonucleic acid deletion syndrome due to deoxyguanosine kinase deficiency (disorder)",
            "attributes": null
          },
          {
            "code": "73390009",
            "description": "Endophlebitis of cavernous venous sinus (disorder)",
            "attributes": null
          },
          {
            "code": "734020000",
            "description": "Spinocerebellar ataxia type 40 (disorder)",
            "attributes": null
          },
          {
            "code": "734021001",
            "description": "Spinocerebellar ataxia type 38 (disorder)",
            "attributes": null
          },
          {
            "code": "734023003",
            "description": "Sporadic adult-onset ataxia of unknown etiology (disorder)",
            "attributes": null
          },
          {
            "code": "73430006",
            "description": "Sleep apnea (disorder)",
            "attributes": null
          },
          {
            "code": "734326000",
            "description": "Stenosis of left vertebral artery (disorder)",
            "attributes": null
          },
          {
            "code": "734327009",
            "description": "Stenosis of right vertebral artery (disorder)",
            "attributes": null
          },
          {
            "code": "734374000",
            "description": "Thrombosis of left carotid artery (disorder)",
            "attributes": null
          },
          {
            "code": "734382000",
            "description": "Thrombosis of right carotid artery (disorder)",
            "attributes": null
          },
          {
            "code": "734383005",
            "description": "Thrombosis of left middle cerebral artery (disorder)",
            "attributes": null
          },
          {
            "code": "734384004",
            "description": "Thrombosis of right middle cerebral artery (disorder)",
            "attributes": null
          },
          {
            "code": "734396006",
            "description": "Spontaneous rupture of left posterior communicating artery (disorder)",
            "attributes": null
          },
          {
            "code": "734397002",
            "description": "Spontaneous rupture of right posterior communicating artery (disorder)",
            "attributes": null
          },
          {
            "code": "73466007",
            "description": "Parasympathetic cardiovascular function disorder (disorder)",
            "attributes": null
          },
          {
            "code": "734879002",
            "description": "Ruptured aneurysm of right posterior communicating artery (disorder)",
            "attributes": null
          },
          {
            "code": "734880004",
            "description": "Ruptured aneurysm of left posterior communicating artery (disorder)",
            "attributes": null
          },
          {
            "code": "734947007",
            "description": "Complex regional pain syndrome type I (disorder)",
            "attributes": null
          },
          {
            "code": "73495003",
            "description": "Dyssynergia cerebellaris myoclonica (disorder)",
            "attributes": null
          },
          {
            "code": "734959006",
            "description": "Embolus of left cerebellar artery (disorder)",
            "attributes": null
          },
          {
            "code": "734960001",
            "description": "Embolus of right cerebellar artery (disorder)",
            "attributes": null
          },
          {
            "code": "734961002",
            "description": "Embolus of left posterior cerebral artery (disorder)",
            "attributes": null
          },
          {
            "code": "734963004",
            "description": "Embolus of right posterior cerebral artery (disorder)",
            "attributes": null
          },
          {
            "code": "734964005",
            "description": "Embolus of left middle cerebral artery (disorder)",
            "attributes": null
          },
          {
            "code": "734965006",
            "description": "Embolus of right middle cerebral artery (disorder)",
            "attributes": null
          },
          {
            "code": "734986006",
            "description": "Complex regional pain syndrome of lower limb (disorder)",
            "attributes": null
          },
          {
            "code": "734988007",
            "description": "Complex regional pain syndrome of knee (disorder)",
            "attributes": null
          },
          {
            "code": "735114006",
            "description": "Occlusion of right pontine artery (disorder)",
            "attributes": null
          },
          {
            "code": "735115007",
            "description": "Occlusion of left pontine artery (disorder)",
            "attributes": null
          },
          {
            "code": "735131004",
            "description": "Occlusion of left cerebellar artery (disorder)",
            "attributes": null
          },
          {
            "code": "735132006",
            "description": "Occlusion of right cerebellar artery (disorder)",
            "attributes": null
          },
          {
            "code": "735206008",
            "description": "Communicating hydrocephalus due to and following traumatic hemorrhage (disorder)",
            "attributes": null
          },
          {
            "code": "735676003",
            "description": "Narcolepsy type 1 (disorder)",
            "attributes": null
          },
          {
            "code": "737227004",
            "description": "Autosomal dominant hereditary spastic paraplegia (disorder)",
            "attributes": null
          },
          {
            "code": "737228009",
            "description": "Progressive focal cortical atrophy (disorder)",
            "attributes": null
          },
          {
            "code": "737229001",
            "description": "White matter disorder due to vascular abnormality (disorder)",
            "attributes": null
          },
          {
            "code": "737230006",
            "description": "White matter disorder due to ischemia (disorder)",
            "attributes": null
          },
          {
            "code": "737240009",
            "description": "Autonomic neuropathy due to endocrine disease (disorder)",
            "attributes": null
          },
          {
            "code": "737241008",
            "description": "Autonomic neuropathy due to metabolic disease (disorder)",
            "attributes": null
          },
          {
            "code": "737582007",
            "description": "Hemiparkinsonism hemiatrophy syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "73765005",
            "description": "Disorder of vagus nerve (disorder)",
            "attributes": null
          },
          {
            "code": "73782007",
            "description": "Megaconial myopathy (disorder)",
            "attributes": null
          },
          {
            "code": "7379000",
            "description": "Pseudobulbar palsy (disorder)",
            "attributes": null
          },
          {
            "code": "738779002",
            "description": "Spontaneous intracranial hemorrhage (disorder)",
            "attributes": null
          },
          {
            "code": "73935008",
            "description": "Toxic encephalopathy caused by hydroxyquinoline (disorder)",
            "attributes": null
          },
          {
            "code": "7409003",
            "description": "Secondary periodic paralysis (disorder)",
            "attributes": null
          },
          {
            "code": "74231003",
            "description": "Retrosphenoidal space syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "74267005",
            "description": "Toxic encephalopathy caused by carbon tetrachloride (disorder)",
            "attributes": null
          },
          {
            "code": "74644004",
            "description": "Influenza with encephalopathy (disorder)",
            "attributes": null
          },
          {
            "code": "74810008",
            "description": "Premotor cortex syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "75038005",
            "description": "Cerebellar hemorrhage (disorder)",
            "attributes": null
          },
          {
            "code": "75046006",
            "description": "Combined pyramidal-extrapyramidal syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "75072002",
            "description": "Nemaline myopathy (disorder)",
            "attributes": null
          },
          {
            "code": "75138007",
            "description": "Endophlebitis of superior sagittal sinus (disorder)",
            "attributes": null
          },
          {
            "code": "75143000",
            "description": "Toxic encephalitis caused by thallium (disorder)",
            "attributes": null
          },
          {
            "code": "75467001",
            "description": "Intervertebral disc disorder of cervical region with myelopathy (disorder)",
            "attributes": null
          },
          {
            "code": "75543006",
            "description": "Cerebral embolism (disorder)",
            "attributes": null
          },
          {
            "code": "75572007",
            "description": "Polyradiculopathy (disorder)",
            "attributes": null
          },
          {
            "code": "75853001",
            "description": "Central nervous system disorder of water regulation (disorder)",
            "attributes": null
          },
          {
            "code": "75962003",
            "description": "First division of fifth cranial nerve disorder (disorder)",
            "attributes": null
          },
          {
            "code": "75983009",
            "description": "Vidian neuralgia (disorder)",
            "attributes": null
          },
          {
            "code": "76156000",
            "description": "Juvenile cerebellar degeneration AND myoclonus (disorder)",
            "attributes": null
          },
          {
            "code": "762297005",
            "description": "White matter disorder due to vitamin B12 deficiency (disorder)",
            "attributes": null
          },
          {
            "code": "762299008",
            "description": "Myelopathy due to toxicity of substance (disorder)",
            "attributes": null
          },
          {
            "code": "762352004",
            "description": "Demyelination due to systemic vasculitis (disorder)",
            "attributes": null
          },
          {
            "code": "762598004",
            "description": "Chronic musculoskeletal pain due to disease of nervous system (disorder)",
            "attributes": null
          },
          {
            "code": "762629007",
            "description": "Occlusion of right middle cerebral artery by embolus (disorder)",
            "attributes": null
          },
          {
            "code": "762630002",
            "description": "Occlusion of left middle cerebral artery by embolus (disorder)",
            "attributes": null
          },
          {
            "code": "762632005",
            "description": "Occlusion of left cerebellar artery by embolus (disorder)",
            "attributes": null
          },
          {
            "code": "762633000",
            "description": "Occlusion of right cerebellar artery by embolus (disorder)",
            "attributes": null
          },
          {
            "code": "762648006",
            "description": "Stenosis of right cerebellar artery (disorder)",
            "attributes": null
          },
          {
            "code": "762649003",
            "description": "Stenosis of left cerebellar artery (disorder)",
            "attributes": null
          },
          {
            "code": "762651004",
            "description": "Occlusion of right posterior cerebral artery by embolus (disorder)",
            "attributes": null
          },
          {
            "code": "762652006",
            "description": "Occlusion of left posterior cerebral artery by embolus (disorder)",
            "attributes": null
          },
          {
            "code": "763065008",
            "description": "Ataxia telangiectasia variant (disorder)",
            "attributes": null
          },
          {
            "code": "763067000",
            "description": "Autosomal dominant congenital benign spinal muscular atrophy (disorder)",
            "attributes": null
          },
          {
            "code": "763068005",
            "description": "Autosomal dominant spastic paraplegia type 31 (disorder)",
            "attributes": null
          },
          {
            "code": "763069002",
            "description": "Autosomal dominant spastic paraplegia type 41 (disorder)",
            "attributes": null
          },
          {
            "code": "763070001",
            "description": "Autosomal dominant spastic paraplegia type 42 (disorder)",
            "attributes": null
          },
          {
            "code": "763110007",
            "description": "Combined oxidative phosphorylation defect type 13 (disorder)",
            "attributes": null
          },
          {
            "code": "763127004",
            "description": "Benign paroxysmal tonic upgaze of childhood with ataxia (disorder)",
            "attributes": null
          },
          {
            "code": "763135001",
            "description": "Charcot-Marie-Tooth disease type 4E (disorder)",
            "attributes": null
          },
          {
            "code": "763136000",
            "description": "Charcot-Marie-Tooth disease, deafness, intellectual disability syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "763218005",
            "description": "Congenital trigeminal anesthesia (disorder)",
            "attributes": null
          },
          {
            "code": "763310000",
            "description": "Acute necrotizing encephalopathy of childhood (disorder)",
            "attributes": null
          },
          {
            "code": "763312008",
            "description": "Autosomal recessive cerebellar ataxia, pyramidal signs, nystagmus, oculomotor apraxia syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "763314009",
            "description": "Congenital muscular dystrophy with hyperlaxity (disorder)",
            "attributes": null
          },
          {
            "code": "763315005",
            "description": "Congenital myopathy with myasthenic-like onset (disorder)",
            "attributes": null
          },
          {
            "code": "763344007",
            "description": "Cerebellar ataxia, intellectual disability, oculomotor apraxia, cerebellar cysts syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "763345008",
            "description": "Charcot-Marie-Tooth disease type 4B3 (disorder)",
            "attributes": null
          },
          {
            "code": "763346009",
            "description": "Fetal akinesia, cerebral and retinal hemorrhage syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "763347000",
            "description": "X-linked Charcot-Marie-Tooth disease type 6 (disorder)",
            "attributes": null
          },
          {
            "code": "763348005",
            "description": "Autosomal recessive cerebellar ataxia with late-onset spasticity (disorder)",
            "attributes": null
          },
          {
            "code": "763349002",
            "description": "Progressive myoclonic epilepsy with dystonia (disorder)",
            "attributes": null
          },
          {
            "code": "763351003",
            "description": "Spectrin-associated autosomal recessive cerebellar ataxia (disorder)",
            "attributes": null
          },
          {
            "code": "763352005",
            "description": "Familial dyskinesia and facial myokymia (disorder)",
            "attributes": null
          },
          {
            "code": "763366000",
            "description": "Leukoencephalopathy, thalamus and brainstem anomalies, high lactate syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "763367009",
            "description": "Autosomal recessive spastic paraplegia type 48 (disorder)",
            "attributes": null
          },
          {
            "code": "763369007",
            "description": "Autosomal dominant spastic paraplegia type 37 (disorder)",
            "attributes": null
          },
          {
            "code": "763370008",
            "description": "X-linked spastic paraplegia type 34 (disorder)",
            "attributes": null
          },
          {
            "code": "763373005",
            "description": "Autosomal recessive spastic paraplegia type 5A (disorder)",
            "attributes": null
          },
          {
            "code": "763374004",
            "description": "Autosomal dominant spastic paraplegia type 12 (disorder)",
            "attributes": null
          },
          {
            "code": "763375003",
            "description": "Autosomal dominant spastic paraplegia type 19 (disorder)",
            "attributes": null
          },
          {
            "code": "763376002",
            "description": "Autosomal recessive spastic paraplegia type 28 (disorder)",
            "attributes": null
          },
          {
            "code": "763377006",
            "description": "Autosomal spastic paraplegia type 30 (disorder)",
            "attributes": null
          },
          {
            "code": "763400005",
            "description": "X-linked Charcot-Marie-Tooth disease type 4 (disorder)",
            "attributes": null
          },
          {
            "code": "763402002",
            "description": "Spastic paraplegia, neuropathy, poikiloderma syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "763455008",
            "description": "X-linked Charcot-Marie-Tooth disease type 1 (disorder)",
            "attributes": null
          },
          {
            "code": "763457000",
            "description": "X-linked Charcot-Marie-Tooth disease type 2 (disorder)",
            "attributes": null
          },
          {
            "code": "763458005",
            "description": "X-linked Charcot-Marie-Tooth disease type 3 (disorder)",
            "attributes": null
          },
          {
            "code": "763460007",
            "description": "X-linked Charcot-Marie-Tooth disease type 5 (disorder)",
            "attributes": null
          },
          {
            "code": "76349003",
            "description": "Extrapyramidal disease (disorder)",
            "attributes": null
          },
          {
            "code": "763533003",
            "description": "Distal hereditary motor neuropathy Jerash type (disorder)",
            "attributes": null
          },
          {
            "code": "763597000",
            "description": "Hereditary ataxia (disorder)",
            "attributes": null
          },
          {
            "code": "763669001",
            "description": "Spastic ataxia with congenital miosis (disorder)",
            "attributes": null
          },
          {
            "code": "763718009",
            "description": "Finnish upper limb onset distal myopathy (disorder)",
            "attributes": null
          },
          {
            "code": "763721006",
            "description": "Hypermethioninemia encephalopathy due to deficiency of adenosine kinase (disorder)",
            "attributes": null
          },
          {
            "code": "763770005",
            "description": "Familial myoclonus of cerebral cortex (disorder)",
            "attributes": null
          },
          {
            "code": "763776004",
            "description": "Kelch like family member 9 related early-onset distal myopathy (disorder)",
            "attributes": null
          },
          {
            "code": "763798008",
            "description": "Microcephalus, complex motor and sensory axonal neuropathy syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "763803004",
            "description": "Morvan syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "763829004",
            "description": "Oculopharyngodistal myopathy (disorder)",
            "attributes": null
          },
          {
            "code": "763895001",
            "description": "Myosclerosis (disorder)",
            "attributes": null
          },
          {
            "code": "76402003",
            "description": "Carotid artery insufficiency syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "764525006",
            "description": "Cylindrical spirals myopathy (disorder)",
            "attributes": null
          },
          {
            "code": "764686003",
            "description": "Autosomal recessive spastic paraplegia type 15 (disorder)",
            "attributes": null
          },
          {
            "code": "764688002",
            "description": "Autosomal recessive spastic paraplegia type 35 (disorder)",
            "attributes": null
          },
          {
            "code": "764730007",
            "description": "Autosomal dominant Charcot-Marie-Tooth disease type 2 due to kinesin family member 5A mutation (disorder)",
            "attributes": null
          },
          {
            "code": "764733009",
            "description": "Progressive external ophthalmoplegia, myopathy, emaciation syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "764734003",
            "description": "Autosomal recessive spastic paraplegia type 21 (disorder)",
            "attributes": null
          },
          {
            "code": "764736001",
            "description": "Autosomal recessive spastic paraplegia type 43 (disorder)",
            "attributes": null
          },
          {
            "code": "764850002",
            "description": "Autosomal dominant Charcot-Marie-Tooth disease type 2A2 (disorder)",
            "attributes": null
          },
          {
            "code": "764854006",
            "description": "Autosomal dominant slowed nerve conduction velocity (disorder)",
            "attributes": null
          },
          {
            "code": "764859001",
            "description": "Laing early-onset distal myopathy (disorder)",
            "attributes": null
          },
          {
            "code": "76492009",
            "description": "Minimal change myopathy (disorder)",
            "attributes": null
          },
          {
            "code": "764944006",
            "description": "Congenital muscular dystrophy type 1B (disorder)",
            "attributes": null
          },
          {
            "code": "764945007",
            "description": "Congenital myopathy with internal nuclei and atypical cores (disorder)",
            "attributes": null
          },
          {
            "code": "764957003",
            "description": "King Denborough syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "764992006",
            "description": "Muscle filaminopathy (disorder)",
            "attributes": null
          },
          {
            "code": "764994007",
            "description": "Myopathy with hexagonally cross-linked tubular arrays (disorder)",
            "attributes": null
          },
          {
            "code": "765045003",
            "description": "Autosomal recessive spastic paraplegia type 62 (disorder)",
            "attributes": null
          },
          {
            "code": "765046002",
            "description": "Autosomal dominant Charcot-Marie-Tooth disease type 2U (disorder)",
            "attributes": null
          },
          {
            "code": "765047006",
            "description": "SURF1, cytochrome c oxidase assembly factor related Charcot-Marie-Tooth disease type 4 (disorder)",
            "attributes": null
          },
          {
            "code": "765091006",
            "description": "Spinocerebellar ataxia with axonal neuropathy type 1 (disorder)",
            "attributes": null
          },
          {
            "code": "765092004",
            "description": "Spheroid body myopathy (disorder)",
            "attributes": null
          },
          {
            "code": "765100000",
            "description": "Ribonucleotide reductase regulatory TP53 inducible subunit M2B-related mitochondrial deoxyribonucleic acid depletion syndrome encephalomyopathic form with renal tubulopathy (disorder)",
            "attributes": null
          },
          {
            "code": "765170001",
            "description": "Sodium voltage-gated channel alpha subunit 8-related epilepsy with encephalopathy (disorder)",
            "attributes": null
          },
          {
            "code": "765196004",
            "description": "Distal myotilinopathy (disorder)",
            "attributes": null
          },
          {
            "code": "765197008",
            "description": "Symptomatic form of muscular dystrophy of Duchenne and Becker in female carrier (disorder)",
            "attributes": null
          },
          {
            "code": "765403009",
            "description": "F-box and leucine rich repeat protein 4 related mitochondrial deoxyribonucleic acid depletion syndrome encephalomyopathic form (disorder)",
            "attributes": null
          },
          {
            "code": "765744006",
            "description": "Autosomal dominant intermediate Charcot-Marie-Tooth disease type A (disorder)",
            "attributes": null
          },
          {
            "code": "765745007",
            "description": "Autosomal dominant intermediate Charcot-Marie-Tooth disease type B (disorder)",
            "attributes": null
          },
          {
            "code": "765746008",
            "description": "Autosomal dominant intermediate Charcot-Marie-Tooth disease type C (disorder)",
            "attributes": null
          },
          {
            "code": "765747004",
            "description": "Autosomal dominant intermediate Charcot-Marie-Tooth disease type D (disorder)",
            "attributes": null
          },
          {
            "code": "765751002",
            "description": "Autoimmune encephalopathy with parasomnia and obstructive sleep apnea (disorder)",
            "attributes": null
          },
          {
            "code": "765753004",
            "description": "Autosomal recessive spastic paraplegia type 45 (disorder)",
            "attributes": null
          },
          {
            "code": "766049000",
            "description": "Acute sensory ataxic neuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "766246000",
            "description": "Marburg acute multiple sclerosis (disorder)",
            "attributes": null
          },
          {
            "code": "766251006",
            "description": "Lethal infantile mitochondrial myopathy (disorder)",
            "attributes": null
          },
          {
            "code": "76628006",
            "description": "Post-hemiplegic chorea (disorder)",
            "attributes": null
          },
          {
            "code": "76670001",
            "description": "Duchenne muscular dystrophy (disorder)",
            "attributes": null
          },
          {
            "code": "766706007",
            "description": "Inflammatory myopathy with abundant macrophages (disorder)",
            "attributes": null
          },
          {
            "code": "766715000",
            "description": "Metabolic myopathy due to lactate transporter defect (disorder)",
            "attributes": null
          },
          {
            "code": "766722008",
            "description": "Paraparetic variant of Guillain-BarrÃ© syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "766752000",
            "description": "Neurolymphomatosis (disorder)",
            "attributes": null
          },
          {
            "code": "766764008",
            "description": "X-linked distal spinal muscular atrophy type 3 (disorder)",
            "attributes": null
          },
          {
            "code": "766767001",
            "description": "Autosomal recessive spastic paraplegia type 67 (disorder)",
            "attributes": null
          },
          {
            "code": "766814006",
            "description": "Autosomal recessive cerebellar ataxia with saccadic intrusion syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "766818009",
            "description": "X-linked non progressive cerebellar ataxia (disorder)",
            "attributes": null
          },
          {
            "code": "766931003",
            "description": "Hypomyelination neuropathy arthrogryposis syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "766977007",
            "description": "Severe early-onset axonal neuropathy due to mitofusin 2 deficiency (disorder)",
            "attributes": null
          },
          {
            "code": "76762001",
            "description": "Eosinophilic myopathy (disorder)",
            "attributes": null
          },
          {
            "code": "768553002",
            "description": "Hypermanganesemia with dystonia (disorder)",
            "attributes": null
          },
          {
            "code": "768554008",
            "description": "Hypermanganesemia with dystonia 2 (disorder)",
            "attributes": null
          },
          {
            "code": "76886005",
            "description": "Polyneuritis (disorder)",
            "attributes": null
          },
          {
            "code": "76896001",
            "description": "Subpial siderosis (disorder)",
            "attributes": null
          },
          {
            "code": "770094004",
            "description": "Cervical radiculoplexus neuropathy due to diabetes mellitus (disorder)",
            "attributes": null
          },
          {
            "code": "770095003",
            "description": "Cranial nerve palsy due to diabetes mellitus (disorder)",
            "attributes": null
          },
          {
            "code": "770098001",
            "description": "Cranial nerve palsy due to type 1 diabetes mellitus (disorder)",
            "attributes": null
          },
          {
            "code": "770430000",
            "description": "Autosomal recessive distal spinal muscular atrophy type 3 (disorder)",
            "attributes": null
          },
          {
            "code": "770558006",
            "description": "Late-onset distal myopathy Markesbery Griggs type (disorder)",
            "attributes": null
          },
          {
            "code": "770596007",
            "description": "Rippling muscle disease with myasthenia gravis (disorder)",
            "attributes": null
          },
          {
            "code": "770626007",
            "description": "Congenital Horner syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "770627003",
            "description": "Desmin-related myofibrillar myopathy (disorder)",
            "attributes": null
          },
          {
            "code": "770630005",
            "description": "Distal hereditary motor neuropathy type 1 (disorder)",
            "attributes": null
          },
          {
            "code": "770655004",
            "description": "Microcephalus, brain defect, spasticity, hypernatremia syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "770678005",
            "description": "Progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy-like syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "770683002",
            "description": "Secondary syringomyelia (disorder)",
            "attributes": null
          },
          {
            "code": "770720005",
            "description": "Autosomal recessive spastic paraplegia type 58 (disorder)",
            "attributes": null
          },
          {
            "code": "770722002",
            "description": "Proximal myopathy with extrapyramidal signs (disorder)",
            "attributes": null
          },
          {
            "code": "770724001",
            "description": "Autosomal recessive spastic paraplegia type 70 (disorder)",
            "attributes": null
          },
          {
            "code": "770727008",
            "description": "Spinal muscular atrophy with respiratory distress type 2 (disorder)",
            "attributes": null
          },
          {
            "code": "770757004",
            "description": "X-linked parkinsonism with spasticity syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "770759001",
            "description": "Autosomal dominant intermediate Charcot-Marie-Tooth disease type F (disorder)",
            "attributes": null
          },
          {
            "code": "770786001",
            "description": "Hereditary inclusion body myopathy type 4 (disorder)",
            "attributes": null
          },
          {
            "code": "770787005",
            "description": "Benign Samaritan congenital myopathy (disorder)",
            "attributes": null
          },
          {
            "code": "770792007",
            "description": "Adult-onset distal myopathy due to valosin containing protein mutation (disorder)",
            "attributes": null
          },
          {
            "code": "770898002",
            "description": "Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to WW domain containing oxidoreductase deficiency (disorder)",
            "attributes": null
          },
          {
            "code": "770939009",
            "description": "Huntington disease-like 3 (disorder)",
            "attributes": null
          },
          {
            "code": "77097004",
            "description": "Oculopharyngeal muscular dystrophy (disorder)",
            "attributes": null
          },
          {
            "code": "771081007",
            "description": "Distal hereditary motor neuropathy type 7 (disorder)",
            "attributes": null
          },
          {
            "code": "771143004",
            "description": "Hereditary motor and sensory neuropathy type 5 (disorder)",
            "attributes": null
          },
          {
            "code": "771144005",
            "description": "Hereditary motor and sensory neuropathy with acrodystrophy (disorder)",
            "attributes": null
          },
          {
            "code": "771184001",
            "description": "Leukoencephalopathy, palmoplantar keratoderma syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "771238004",
            "description": "Spinal atrophy, ophthalmoplegia, pyramidal syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "771267003",
            "description": "Congenital muscular dystrophy with integrin alpha-7 deficiency (disorder)",
            "attributes": null
          },
          {
            "code": "771272007",
            "description": "Congenital muscular dystrophy due to lamin A/C mutation (disorder)",
            "attributes": null
          },
          {
            "code": "7713009",
            "description": "Intrapontine hemorrhage (disorder)",
            "attributes": null
          },
          {
            "code": "771302009",
            "description": "Autosomal recessive lower motor neuron disease with childhood onset (disorder)",
            "attributes": null
          },
          {
            "code": "771305006",
            "description": "Progressive polyneuropathy with bilateral striatal necrosis (disorder)",
            "attributes": null
          },
          {
            "code": "771307003",
            "description": "Charcot-Marie-Tooth disease type 2B5 (disorder)",
            "attributes": null
          },
          {
            "code": "771334000",
            "description": "Autosomal dominant limb-girdle muscular dystrophy type 1H (disorder)",
            "attributes": null
          },
          {
            "code": "771469002",
            "description": "Early-onset spastic ataxia, myoclonic epilepsy, neuropathy syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "771475006",
            "description": "Young adult-onset distal hereditary motor neuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "771514002",
            "description": "Early-onset progressive neurodegeneration, blindness, ataxia, spasticity syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "772129007",
            "description": "Autosomal dominant childhood-onset proximal spinal muscular atrophy (disorder)",
            "attributes": null
          },
          {
            "code": "773306002",
            "description": "Congenital lethal myopathy Compton North type (disorder)",
            "attributes": null
          },
          {
            "code": "773308001",
            "description": "Autosomal recessive intermediate Charcot-Marie-Tooth disease type A (disorder)",
            "attributes": null
          },
          {
            "code": "773330000",
            "description": "Autosomal recessive intermediate Charcot-Marie-Tooth disease type B (disorder)",
            "attributes": null
          },
          {
            "code": "773393001",
            "description": "Autosomal dominant Charcot-Marie-Tooth disease type 2Q (disorder)",
            "attributes": null
          },
          {
            "code": "773398005",
            "description": "Congenital cataract, progressive muscular hypotonia, hearing loss, developmental delay syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "773414009",
            "description": "Autosomal recessive intermediate Charcot-Marie-Tooth disease type C (disorder)",
            "attributes": null
          },
          {
            "code": "773425000",
            "description": "Autosomal recessive spastic paraplegia type 59 (disorder)",
            "attributes": null
          },
          {
            "code": "773495009",
            "description": "Episodic ataxia with slurred speech (disorder)",
            "attributes": null
          },
          {
            "code": "773498006",
            "description": "Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to TUD deficiency (disorder)",
            "attributes": null
          },
          {
            "code": "773555005",
            "description": "Severe neurodegenerative syndrome with lipodystrophy (disorder)",
            "attributes": null
          },
          {
            "code": "773663004",
            "description": "Rapid-onset childhood obesity, hypothalamic dysfunction, hypoventilation, autonomic dysregulation syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "773668008",
            "description": "Childhood encephalopathy due to thiamine pyrophosphokinase deficiency (disorder)",
            "attributes": null
          },
          {
            "code": "773729007",
            "description": "X-linked myopathy with postural muscle atrophy (disorder)",
            "attributes": null
          },
          {
            "code": "774069007",
            "description": "Protein kinase cAMP-dependent type I regulatory subunit beta-related neurodegenerative dementia with intermediate filaments (disorder)",
            "attributes": null
          },
          {
            "code": "774147002",
            "description": "Charcot-Marie-Tooth disease type 2R (disorder)",
            "attributes": null
          },
          {
            "code": "774151000",
            "description": "Ferro-cerebro-cutaneous syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "774153002",
            "description": "Periodic paralysis with transient compartment-like syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "774154008",
            "description": "Periodic paralysis with later-onset distal motor neuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "77436004",
            "description": "Paroxysmal ocular dyskinesia (disorder)",
            "attributes": null
          },
          {
            "code": "77461000119109",
            "description": "Myasthenia gravis with exacerbation (disorder)",
            "attributes": null
          },
          {
            "code": "77471000119103",
            "description": "Myasthenia gravis without exacerbation (disorder)",
            "attributes": null
          },
          {
            "code": "77553008",
            "description": "Opticocochleodentate degeneration (disorder)",
            "attributes": null
          },
          {
            "code": "77600008",
            "description": "Bing-Neel syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "776087007",
            "description": "Autosomal recessive cerebral atrophy (disorder)",
            "attributes": null
          },
          {
            "code": "77659000",
            "description": "Paraneoplastic neuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "778002005",
            "description": "Sodium voltage-gated channel alpha subunit 2 encephalopathy (disorder)",
            "attributes": null
          },
          {
            "code": "778003000",
            "description": "Autosomal dominant intermediate Charcot-Marie-Tooth disease with neuropathic pain (disorder)",
            "attributes": null
          },
          {
            "code": "778011005",
            "description": "Severe intellectual disability and progressive spastic paraplegia (disorder)",
            "attributes": null
          },
          {
            "code": "778029000",
            "description": "FAST kinase domains 2-related infantile mitochondrial encephalomyopathy (disorder)",
            "attributes": null
          },
          {
            "code": "778030005",
            "description": "Autosomal recessive spastic paraplegia type 27 (disorder)",
            "attributes": null
          },
          {
            "code": "778048001",
            "description": "Mitochondrially encoded ATP synthase membrane subunit 6-related mitochondrial spastic paraplegia (disorder)",
            "attributes": null
          },
          {
            "code": "778060000",
            "description": "Collagen type IV alpha 1 chain related familial vascular leukoencephalopathy (disorder)",
            "attributes": null
          },
          {
            "code": "77956009",
            "description": "Steinert myotonic dystrophy syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "78152008",
            "description": "Multiple cranial nerve palsy (disorder)",
            "attributes": null
          },
          {
            "code": "782309008",
            "description": "Immune-mediated neuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "782670003",
            "description": "Autosomal dominant spastic paraplegia type 3 (disorder)",
            "attributes": null
          },
          {
            "code": "782675008",
            "description": "Distal myopathy with anterior tibial onset (disorder)",
            "attributes": null
          },
          {
            "code": "782690007",
            "description": "Gemignani syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "782695002",
            "description": "Primary dystonia DYT17 type (disorder)",
            "attributes": null
          },
          {
            "code": "782696001",
            "description": "Recessive mitochondrial ataxia syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "782718007",
            "description": "Dystonia aphonia syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "782719004",
            "description": "Autosomal recessive cerebellar ataxia due to STIP1 homology and U-box containing protein 1 deficiency (disorder)",
            "attributes": null
          },
          {
            "code": "782721009",
            "description": "Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to RUN and cysteine rich domain containing beclin 1 interacting protein deficiency (disorder)",
            "attributes": null
          },
          {
            "code": "782723007",
            "description": "Severe intellectual disability, progressive spastic diplegia syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "782725000",
            "description": "Autosomal recessive spastic paraplegia type 69 (disorder)",
            "attributes": null
          },
          {
            "code": "782726004",
            "description": "Autosomal recessive spastic paraplegia type 71 (disorder)",
            "attributes": null
          },
          {
            "code": "782727008",
            "description": "Autosomal spastic paraplegia type 72 (disorder)",
            "attributes": null
          },
          {
            "code": "782737003",
            "description": "Diffuse cerebral and cerebellar atrophy, intractable seizures, progressive microcephaly syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "782742006",
            "description": "Autosomal dominant Charcot-Marie-Tooth disease type 2 with giant axons (disorder)",
            "attributes": null
          },
          {
            "code": "782743001",
            "description": "Huntington disease-like syndrome due to chromosome 9 open reading frame 72 expansions (disorder)",
            "attributes": null
          },
          {
            "code": "782746009",
            "description": "Autosomal recessive spastic paraplegia type 60 (disorder)",
            "attributes": null
          },
          {
            "code": "782747000",
            "description": "Autosomal recessive spastic paraplegia type 66 (disorder)",
            "attributes": null
          },
          {
            "code": "78275009",
            "description": "Obstructive sleep apnea syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "782752005",
            "description": "Peripheral neuropathy, myopathy, hoarseness, hearing loss syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "782824007",
            "description": "Sodium channelopathy-related small fiber neuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "782826009",
            "description": "Charcot-Marie-Tooth disease type 2P (disorder)",
            "attributes": null
          },
          {
            "code": "782829002",
            "description": "Autosomal dominant Charcot-Marie-Tooth disease type 2O (disorder)",
            "attributes": null
          },
          {
            "code": "782881002",
            "description": "Hereditary sensorimotor neuropathy with hyperelastic skin (disorder)",
            "attributes": null
          },
          {
            "code": "782883004",
            "description": "Fatal infantile hypertonic myofibrillar myopathy (disorder)",
            "attributes": null
          },
          {
            "code": "782886007",
            "description": "Infantile spasms, psychomotor retardation, progressive brain atrophy, basal ganglia disease syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "782887003",
            "description": "Inherited congenital spastic tetraplegia (disorder)",
            "attributes": null
          },
          {
            "code": "782935003",
            "description": "Tremor, nystagmus, duodenal ulcer syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "783010003",
            "description": "Pharyngeal-cervical-brachial variant of Guillain-BarrÃ© syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "783012006",
            "description": "Parkinsonian pyramidal syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "783060009",
            "description": "Autosomal recessive cerebellar ataxia, psychomotor delay syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "783094006",
            "description": "Autosomal recessive spastic paraplegia type 14 (disorder)",
            "attributes": null
          },
          {
            "code": "783148005",
            "description": "Distal nebulin myopathy (disorder)",
            "attributes": null
          },
          {
            "code": "783161005",
            "description": "Familial dementia British type (disorder)",
            "attributes": null
          },
          {
            "code": "783166000",
            "description": "Distal anoctaminopathy (disorder)",
            "attributes": null
          },
          {
            "code": "783174004",
            "description": "Congenital muscular dystrophy with intellectual disability (disorder)",
            "attributes": null
          },
          {
            "code": "783175003",
            "description": "Congenital muscular dystrophy without intellectual disability (disorder)",
            "attributes": null
          },
          {
            "code": "783176002",
            "description": "Congenital muscular dystrophy with cerebellar involvement (disorder)",
            "attributes": null
          },
          {
            "code": "783179009",
            "description": "Cranio-cervical dystonia with laryngeal and upper limb involvement (disorder)",
            "attributes": null
          },
          {
            "code": "783180007",
            "description": "Combined hyperactive dysfunction syndrome of cranial nerves (disorder)",
            "attributes": null
          },
          {
            "code": "783198006",
            "description": "Hereditary sensory and autonomic neuropathy due to tectonin beta-propeller repeat containing 2 mutation (disorder)",
            "attributes": null
          },
          {
            "code": "783203003",
            "description": "Ataxia with tapetoretinal degeneration syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "783242003",
            "description": "Adult-onset cervical dystonia DYT23 type (disorder)",
            "attributes": null
          },
          {
            "code": "783244002",
            "description": "Acute pure sensory neuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "783257005",
            "description": "Familial recurrent peripheral facial palsy (disorder)",
            "attributes": null
          },
          {
            "code": "783258000",
            "description": "Familial dementia Danish type (disorder)",
            "attributes": null
          },
          {
            "code": "783413008",
            "description": "Multiple aneurysms of cerebral artery (disorder)",
            "attributes": null
          },
          {
            "code": "783416000",
            "description": "Aneurysm of anterior cerebral artery (disorder)",
            "attributes": null
          },
          {
            "code": "783417009",
            "description": "Aneurysm of posterior inferior cerebellar artery (disorder)",
            "attributes": null
          },
          {
            "code": "783418004",
            "description": "Aneurysm of anterior communicating artery (disorder)",
            "attributes": null
          },
          {
            "code": "783419007",
            "description": "Aneurysm of posterior cerebral artery (disorder)",
            "attributes": null
          },
          {
            "code": "783420001",
            "description": "Aneurysm of middle cerebral artery (disorder)",
            "attributes": null
          },
          {
            "code": "783421002",
            "description": "Aneurysm of posterior communicating artery (disorder)",
            "attributes": null
          },
          {
            "code": "783550006",
            "description": "Hereditary sensory and autonomic neuropathy type 7 (disorder)",
            "attributes": null
          },
          {
            "code": "783554002",
            "description": "Autosomal recessive limb girdle muscular dystrophy type 2U (disorder)",
            "attributes": null
          },
          {
            "code": "783618006",
            "description": "Lower motor neuron syndrome with late-adult onset (disorder)",
            "attributes": null
          },
          {
            "code": "783622001",
            "description": "Autosomal dominant spastic paraplegia type 38 (disorder)",
            "attributes": null
          },
          {
            "code": "783697000",
            "description": "X-linked spastic paraplegia type 16 (disorder)",
            "attributes": null
          },
          {
            "code": "783698005",
            "description": "Autosomal dominant spastic paraplegia type 13 (disorder)",
            "attributes": null
          },
          {
            "code": "783705006",
            "description": "Sporadic hyperekplexia (disorder)",
            "attributes": null
          },
          {
            "code": "783707003",
            "description": "Cerebral aneurysm due to dissection of cerebral artery (disorder)",
            "attributes": null
          },
          {
            "code": "783716004",
            "description": "Acquired aneurysm of cerebral artery (disorder)",
            "attributes": null
          },
          {
            "code": "783722008",
            "description": "Myopathy and diabetes mellitus (disorder)",
            "attributes": null
          },
          {
            "code": "783734000",
            "description": "Mitochondrial deoxyribonucleic acid depletion syndrome, hepatocerebral form due to deoxyguanosine kinase deficiency (disorder)",
            "attributes": null
          },
          {
            "code": "783764008",
            "description": "Autosomal recessive spastic paraplegia type 56 (disorder)",
            "attributes": null
          },
          {
            "code": "783770002",
            "description": "Alpha-B crystallin-related late-onset myopathy (disorder)",
            "attributes": null
          },
          {
            "code": "783787000",
            "description": "Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations (disorder)",
            "attributes": null
          },
          {
            "code": "784201008",
            "description": "Acquired hydromeningocele (disorder)",
            "attributes": null
          },
          {
            "code": "784289008",
            "description": "Nerve palsy (disorder)",
            "attributes": null
          },
          {
            "code": "784341001",
            "description": "Amyotrophic lateral sclerosis type 4 (disorder)",
            "attributes": null
          },
          {
            "code": "784343003",
            "description": "Autosomal recessive spastic ataxia with leukoencephalopathy (disorder)",
            "attributes": null
          },
          {
            "code": "784347002",
            "description": "Autosomal recessive spastic ataxia, optic atrophy, dysarthria syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "784348007",
            "description": "Familial congenital mirror movements (disorder)",
            "attributes": null
          },
          {
            "code": "784352007",
            "description": "X-linked scapuloperoneal muscular dystrophy (disorder)",
            "attributes": null
          },
          {
            "code": "784370005",
            "description": "Mitochondrial myopathy with reversible cytochrome C oxidase deficiency (disorder)",
            "attributes": null
          },
          {
            "code": "784371009",
            "description": "Huntington disease-like 1 (disorder)",
            "attributes": null
          },
          {
            "code": "784380009",
            "description": "Autosomal dominant spastic ataxia type 1 (disorder)",
            "attributes": null
          },
          {
            "code": "784391002",
            "description": "Autosomal dominant adult-onset proximal spinal muscular atrophy (disorder)",
            "attributes": null
          },
          {
            "code": "78468005",
            "description": "Erb's muscular dystrophy (disorder)",
            "attributes": null
          },
          {
            "code": "785298001",
            "description": "Muscle eye brain disease with bilateral multicystic leukodystrophy (disorder)",
            "attributes": null
          },
          {
            "code": "785300001",
            "description": "Infantile-onset autosomal recessive non progressive cerebellar ataxia (disorder)",
            "attributes": null
          },
          {
            "code": "785301002",
            "description": "Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia (disorder)",
            "attributes": null
          },
          {
            "code": "785304005",
            "description": "Autosomal recessive spastic paraplegia type 24 (disorder)",
            "attributes": null
          },
          {
            "code": "785305006",
            "description": "Autosomal dominant spastic paraplegia type 8 (disorder)",
            "attributes": null
          },
          {
            "code": "78569004",
            "description": "Posterior inferior cerebellar artery syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "785723001",
            "description": "Persistent idiopathic facial pain (disorder)",
            "attributes": null
          },
          {
            "code": "785726009",
            "description": "Hyperekplexia epilepsy syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "785810000",
            "description": "Synucleinopathy (disorder)",
            "attributes": null
          },
          {
            "code": "78689005",
            "description": "Chronic brain syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "787037000",
            "description": "Congenital muscular dystrophy type 1A (disorder)",
            "attributes": null
          },
          {
            "code": "787044009",
            "description": "Stenosis of bilateral carotid arteries (disorder)",
            "attributes": null
          },
          {
            "code": "787172004",
            "description": "Childhood-onset autosomal recessive myopathy with external ophthalmoplegia (disorder)",
            "attributes": null
          },
          {
            "code": "787174003",
            "description": "Intellectual disability, hyperkinetic movement, truncal ataxia syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "787175002",
            "description": "Ankyrin 3 related intellectual disability, sleep disturbance syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "787932009",
            "description": "Disorder of gastric branch of vagus nerve (disorder)",
            "attributes": null
          },
          {
            "code": "788454002",
            "description": "Stenosis of bilateral vertebral arteries (disorder)",
            "attributes": null
          },
          {
            "code": "788455001",
            "description": "Occlusion of bilateral pontine arteries (disorder)",
            "attributes": null
          },
          {
            "code": "788880006",
            "description": "Cerebral ischemic stroke due to dissection of artery (disorder)",
            "attributes": null
          },
          {
            "code": "788881005",
            "description": "Cerebral ischemic stroke due to aortic arch embolism (disorder)",
            "attributes": null
          },
          {
            "code": "788882003",
            "description": "Cerebral ischemic stroke due to global hypoperfusion with watershed infarct (disorder)",
            "attributes": null
          },
          {
            "code": "788883008",
            "description": "Cerebral ischemic stroke due to hypercoagulable state (disorder)",
            "attributes": null
          },
          {
            "code": "788884002",
            "description": "Cerebral ischemic stroke due to subarachnoid hemorrhage (disorder)",
            "attributes": null
          },
          {
            "code": "788907005",
            "description": "Dissociative neurological symptom disorder co-occurrent with chorea (disorder)",
            "attributes": null
          },
          {
            "code": "788908000",
            "description": "Dissociative neurological symptom disorder co-occurrent with dystonia (disorder)",
            "attributes": null
          },
          {
            "code": "788909008",
            "description": "Dissociative neurological symptom disorder co-occurrent with facial spasm (disorder)",
            "attributes": null
          },
          {
            "code": "788910003",
            "description": "Dissociative neurological symptom disorder co-occurrent with myoclonus (disorder)",
            "attributes": null
          },
          {
            "code": "788911004",
            "description": "Dissociative neurological symptom disorder co-occurrent with Parkinsonism (disorder)",
            "attributes": null
          },
          {
            "code": "788916009",
            "description": "Encephalopathy caused by ammonia (disorder)",
            "attributes": null
          },
          {
            "code": "789017006",
            "description": "Radiculopathy due to intervertebral disc disorder (disorder)",
            "attributes": null
          },
          {
            "code": "789018001",
            "description": "Radiculopathy due to metabolic disorder (disorder)",
            "attributes": null
          },
          {
            "code": "789019009",
            "description": "Radiculopathy due to neoplastic disease (disorder)",
            "attributes": null
          },
          {
            "code": "789021004",
            "description": "Radiculopathy due to spondylosis (disorder)",
            "attributes": null
          },
          {
            "code": "789055001",
            "description": "Treatment-emergent central sleep apnea (disorder)",
            "attributes": null
          },
          {
            "code": "789430001",
            "description": "Acquired right-sided Horner syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "789431002",
            "description": "Acquired left-sided Horner syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "789542009",
            "description": "Neuropathy due to type 1 diabetes mellitus (disorder)",
            "attributes": null
          },
          {
            "code": "789585000",
            "description": "Sensory polyneuropathy due to diabetes mellitus (disorder)",
            "attributes": null
          },
          {
            "code": "789588003",
            "description": "Peripheral sensory neuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "789674008",
            "description": "Spastic paraplegia, optic atrophy, neuropathy and spastic paraplegia, optic atrophy neuropathy-related disorder (disorder)",
            "attributes": null
          },
          {
            "code": "79152002",
            "description": "Dilated cardiomyopathy secondary to neuromuscular disorder (disorder)",
            "attributes": null
          },
          {
            "code": "7916009",
            "description": "Alcoholic polyneuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "79280005",
            "description": "Hypersomnia with sleep apnea (disorder)",
            "attributes": null
          },
          {
            "code": "7931000119101",
            "description": "Anterior choroidal artery thrombosis (disorder)",
            "attributes": null
          },
          {
            "code": "79341000119107",
            "description": "Mixed dementia (disorder)",
            "attributes": null
          },
          {
            "code": "79366000",
            "description": "Injury of inferior mesenteric plexus (disorder)",
            "attributes": null
          },
          {
            "code": "79554005",
            "description": "Asymmetric proximal motor neuropathy due to diabetes mellitus (disorder)",
            "attributes": null
          },
          {
            "code": "80098002",
            "description": "Diffuse Lewy body disease (disorder)",
            "attributes": null
          },
          {
            "code": "80138003",
            "description": "Isaacs syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "80180004",
            "description": "Pallidonigral degeneration (disorder)",
            "attributes": null
          },
          {
            "code": "80606009",
            "description": "Carotid artery embolism (disorder)",
            "attributes": null
          },
          {
            "code": "80690008",
            "description": "Degenerative disease of the central nervous system (disorder)",
            "attributes": null
          },
          {
            "code": "80734006",
            "description": "Marinesco-SjÃ¶gren syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "80758005",
            "description": "Embolism of lateral venous sinus (disorder)",
            "attributes": null
          },
          {
            "code": "80901002",
            "description": "Endophlebitis of torcular Herophili (disorder)",
            "attributes": null
          },
          {
            "code": "80962007",
            "description": "Disorder of glossopharyngeal nerve (disorder)",
            "attributes": null
          },
          {
            "code": "80976008",
            "description": "Myasthenic crisis (disorder)",
            "attributes": null
          },
          {
            "code": "81211007",
            "description": "Primary lateral sclerosis (disorder)",
            "attributes": null
          },
          {
            "code": "81308009",
            "description": "Disorder of brain (disorder)",
            "attributes": null
          },
          {
            "code": "81391000119106",
            "description": "Charcot arthropathy due to syringomyelia (disorder)",
            "attributes": null
          },
          {
            "code": "81634008",
            "description": "Perineurial cyst (disorder)",
            "attributes": null
          },
          {
            "code": "8166000",
            "description": "Thrombophlebitis of basilar sinus (disorder)",
            "attributes": null
          },
          {
            "code": "81682002",
            "description": "Functional disease of the central nervous system with neuroendocrine disturbance (disorder)",
            "attributes": null
          },
          {
            "code": "816984002",
            "description": "Progressive multiple sclerosis (disorder)",
            "attributes": null
          },
          {
            "code": "81750007",
            "description": "Glossopharyngeal nerve sensory disorder (disorder)",
            "attributes": null
          },
          {
            "code": "81830002",
            "description": "Mononeuropathy simplex due to diabetes mellitus (disorder)",
            "attributes": null
          },
          {
            "code": "8191000119104",
            "description": "Arthropathy of wrist due to neurological disorder (disorder)",
            "attributes": null
          },
          {
            "code": "82077006",
            "description": "Myotubular myopathy (disorder)",
            "attributes": null
          },
          {
            "code": "82088000",
            "description": "Eleventh cranial nerve motor disorder (disorder)",
            "attributes": null
          },
          {
            "code": "82331007",
            "description": "Neuritis AND/OR radiculitis due to displacement of lumbar intervertebral disc (disorder)",
            "attributes": null
          },
          {
            "code": "82346000",
            "description": "Acquired obstructive hydrocephalus (disorder)",
            "attributes": null
          },
          {
            "code": "82351000119105",
            "description": "Altered behavior co-occurrent and due to Pick's disease (disorder)",
            "attributes": null
          },
          {
            "code": "82361000119107",
            "description": "Altered behavior in dementia due to Huntington chorea (disorder)",
            "attributes": null
          },
          {
            "code": "82371000119101",
            "description": "Dementia due to multiple sclerosis with altered behavior (disorder)",
            "attributes": null
          },
          {
            "code": "8269002",
            "description": "Cerebrospinal angiopathy (disorder)",
            "attributes": null
          },
          {
            "code": "827047007",
            "description": "Palsy of vagus nerve (disorder)",
            "attributes": null
          },
          {
            "code": "827048002",
            "description": "Palsy of accessory nerve (disorder)",
            "attributes": null
          },
          {
            "code": "827049005",
            "description": "Palsy of upper motor nerve (disorder)",
            "attributes": null
          },
          {
            "code": "827050005",
            "description": "Palsy of glossopharyngeal nerve (disorder)",
            "attributes": null
          },
          {
            "code": "827172005",
            "description": "X-linked progressive cerebellar ataxia (disorder)",
            "attributes": null
          },
          {
            "code": "82732003",
            "description": "Familial hypokalemic periodic paralysis (disorder)",
            "attributes": null
          },
          {
            "code": "83090005",
            "description": "Dural ossification (disorder)",
            "attributes": null
          },
          {
            "code": "83304000",
            "description": "Dubini's chorea (disorder)",
            "attributes": null
          },
          {
            "code": "838275008",
            "description": "Stenosis of cerebral artery (disorder)",
            "attributes": null
          },
          {
            "code": "838276009",
            "description": "Amyotrophic lateral sclerosis, parkinsonism, dementia complex (disorder)",
            "attributes": null
          },
          {
            "code": "838309004",
            "description": "Cerebrovascular abnormality due to Takayasu disease (disorder)",
            "attributes": null
          },
          {
            "code": "838319005",
            "description": "Autonomic neuropathy due to Fabry disease (disorder)",
            "attributes": null
          },
          {
            "code": "838320004",
            "description": "Autonomic neuropathy due to medication induced hypoglycemia (disorder)",
            "attributes": null
          },
          {
            "code": "838321000",
            "description": "Autonomic ganglionopathy (disorder)",
            "attributes": null
          },
          {
            "code": "838322007",
            "description": "Autonomic neuropathy due to Allgrove syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "838323002",
            "description": "Autoimmune opsoclonus myoclonus (disorder)",
            "attributes": null
          },
          {
            "code": "838330008",
            "description": "Autoimmune ganglionopathy (disorder)",
            "attributes": null
          },
          {
            "code": "838347009",
            "description": "Autonomic neuropathy due to Refsum Disease (disorder)",
            "attributes": null
          },
          {
            "code": "838348004",
            "description": "Autonomic neuropathy due to Tangier disease (disorder)",
            "attributes": null
          },
          {
            "code": "838376007",
            "description": "Chronic myopathy caused by alcohol (disorder)",
            "attributes": null
          },
          {
            "code": "838381003",
            "description": "Chronic bilateral vestibulopathy due to and following meningitis (disorder)",
            "attributes": null
          },
          {
            "code": "838383000",
            "description": "Chorea caused by toxin (disorder)",
            "attributes": null
          },
          {
            "code": "838441009",
            "description": "Mental retardation, adducted thumbs, shuffling gait, aphasia syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "83982007",
            "description": "Subacute necrotic myelopathy (disorder)",
            "attributes": null
          },
          {
            "code": "840422007",
            "description": "Dissection of anterior cerebral artery (disorder)",
            "attributes": null
          },
          {
            "code": "840434004",
            "description": "Dissection of posterior cerebral artery (disorder)",
            "attributes": null
          },
          {
            "code": "840436002",
            "description": "Dissection of middle cerebral artery (disorder)",
            "attributes": null
          },
          {
            "code": "840437006",
            "description": "Dissection of multiple cerebral arteries (disorder)",
            "attributes": null
          },
          {
            "code": "840441005",
            "description": "Dissection of intracranial artery (disorder)",
            "attributes": null
          },
          {
            "code": "840459008",
            "description": "Cranial neuropathy due to sinusitis (disorder)",
            "attributes": null
          },
          {
            "code": "840461004",
            "description": "Cranial neuropathy due to petrous infection (disorder)",
            "attributes": null
          },
          {
            "code": "840501003",
            "description": "Dystonia caused by toxin (disorder)",
            "attributes": null
          },
          {
            "code": "840511005",
            "description": "Compression of spinal cord due to intraspinal abscess (disorder)",
            "attributes": null
          },
          {
            "code": "840721004",
            "description": "Incomplete spinal cord syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "843004",
            "description": "Poliomyelomalacia (disorder)",
            "attributes": null
          },
          {
            "code": "8443005",
            "description": "Facial nerve sensory disorder (disorder)",
            "attributes": null
          },
          {
            "code": "84438001",
            "description": "Pure autonomic failure (disorder)",
            "attributes": null
          },
          {
            "code": "84590007",
            "description": "Lower motor neuron disease (disorder)",
            "attributes": null
          },
          {
            "code": "84759007",
            "description": "Disorder of accessory nerve (disorder)",
            "attributes": null
          },
          {
            "code": "85102008",
            "description": "Cerebellar ataxia (disorder)",
            "attributes": null
          },
          {
            "code": "85423005",
            "description": "Motor polyneuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "85505000",
            "description": "Adult spinal muscular atrophy (disorder)",
            "attributes": null
          },
          {
            "code": "85592008",
            "description": "Primary progressive cerebellar degeneration (disorder)",
            "attributes": null
          },
          {
            "code": "8563000",
            "description": "Cholinergic crisis (disorder)",
            "attributes": null
          },
          {
            "code": "85672005",
            "description": "Anterior horn cell disease (disorder)",
            "attributes": null
          },
          {
            "code": "85972008",
            "description": "Sensory disorder (disorder)",
            "attributes": null
          },
          {
            "code": "86003009",
            "description": "Carotid artery thrombosis (disorder)",
            "attributes": null
          },
          {
            "code": "86044005",
            "description": "Amyotrophic lateral sclerosis (disorder)",
            "attributes": null
          },
          {
            "code": "860799000",
            "description": "Encephalopathy due to folate deficiency (disorder)",
            "attributes": null
          },
          {
            "code": "860804005",
            "description": "Epilepsy due to infectious encephalitis (disorder)",
            "attributes": null
          },
          {
            "code": "860806007",
            "description": "Epilepsy due to infectious meningitis (disorder)",
            "attributes": null
          },
          {
            "code": "860807003",
            "description": "Hereditary autonomic neuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "860809000",
            "description": "Hereditary sensory autonomic neuropathy type IIA (disorder)",
            "attributes": null
          },
          {
            "code": "860810005",
            "description": "Hereditary sensory autonomic neuropathy type IIB (disorder)",
            "attributes": null
          },
          {
            "code": "860811009",
            "description": "Hereditary sensory autonomic neuropathy type ID (disorder)",
            "attributes": null
          },
          {
            "code": "860812002",
            "description": "Hereditary sensory autonomic neuropathy type IE (disorder)",
            "attributes": null
          },
          {
            "code": "860813007",
            "description": "Hereditary sensory autonomic neuropathy type IA (disorder)",
            "attributes": null
          },
          {
            "code": "860814001",
            "description": "Hereditary sensory autonomic neuropathy type IC (disorder)",
            "attributes": null
          },
          {
            "code": "860815000",
            "description": "Epilepsy due to neonatal central nervous system infection (disorder)",
            "attributes": null
          },
          {
            "code": "860880003",
            "description": "Hyperhidrosis due to autonomic dysregulation (disorder)",
            "attributes": null
          },
          {
            "code": "860883001",
            "description": "Generalized autonomic neuropathy due to diabetes mellitus (disorder)",
            "attributes": null
          },
          {
            "code": "860922009",
            "description": "Erectile dysfunction due to neuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "8627007",
            "description": "Injury of celiac ganglion AND/OR plexus (disorder)",
            "attributes": null
          },
          {
            "code": "86489003",
            "description": "Idiopathic peripheral autonomic neuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "86558004",
            "description": "Cerebellar pressure cone (disorder)",
            "attributes": null
          },
          {
            "code": "866047004",
            "description": "Multiple mononeuropathy due to perinuclear antineutrophil cytoplasmic associated antibody associated vasculitis (disorder)",
            "attributes": null
          },
          {
            "code": "866051002",
            "description": "Motor neuron disease due to lead intoxication (disorder)",
            "attributes": null
          },
          {
            "code": "866104001",
            "description": "Intracranial hypotension due to cerebrospinal fluid fistula (disorder)",
            "attributes": null
          },
          {
            "code": "86695008",
            "description": "Dying back phenomenon (disorder)",
            "attributes": null
          },
          {
            "code": "870290001",
            "description": "Myelopathy due to vitamin B12 deficiency (disorder)",
            "attributes": null
          },
          {
            "code": "870291002",
            "description": "Myelopathy due to lathyrism (disorder)",
            "attributes": null
          },
          {
            "code": "870297003",
            "description": "Myopathy due to chronic alcoholism (disorder)",
            "attributes": null
          },
          {
            "code": "870299000",
            "description": "Myopathy due to calcium deficiency (disorder)",
            "attributes": null
          },
          {
            "code": "870342005",
            "description": "Compression of spinal cord due to granulomatous disorder (disorder)",
            "attributes": null
          },
          {
            "code": "870345007",
            "description": "Compression of spinal cord due to cavernous hemangioma (disorder)",
            "attributes": null
          },
          {
            "code": "870544005",
            "description": "Occlusion of distal basilar artery (disorder)",
            "attributes": null
          },
          {
            "code": "870564000",
            "description": "Occlusion of spinal vein (disorder)",
            "attributes": null
          },
          {
            "code": "870566003",
            "description": "Occlusion of anterior choroidal artery (disorder)",
            "attributes": null
          },
          {
            "code": "870579007",
            "description": "Occlusion of branch of basilar artery (disorder)",
            "attributes": null
          },
          {
            "code": "87058001",
            "description": "Vagus nerve motor disorder (disorder)",
            "attributes": null
          },
          {
            "code": "871637001",
            "description": "Thrombosis of multiple cerebral veins (disorder)",
            "attributes": null
          },
          {
            "code": "871842007",
            "description": "Intracranial hemorrhage due to leptospirosis (disorder)",
            "attributes": null
          },
          {
            "code": "87536007",
            "description": "Central nervous system complication (disorder)",
            "attributes": null
          },
          {
            "code": "87551000119101",
            "description": "Visual disturbance as sequela of cerebrovascular disease (disorder)",
            "attributes": null
          },
          {
            "code": "87555007",
            "description": "Claude's syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "87651000119100",
            "description": "Facial palsy House-Brackmann grade VI (disorder)",
            "attributes": null
          },
          {
            "code": "87764000",
            "description": "Foster-Kennedy syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "87844004",
            "description": "Hypothyroid myopathy (disorder)",
            "attributes": null
          },
          {
            "code": "87921000119104",
            "description": "Cranial nerve palsy due to type 2 diabetes mellitus (disorder)",
            "attributes": null
          },
          {
            "code": "87937009",
            "description": "Endophlebitis of intracranial venous sinus (disorder)",
            "attributes": null
          },
          {
            "code": "88032003",
            "description": "Amaurosis fugax (disorder)",
            "attributes": null
          },
          {
            "code": "88125005",
            "description": "Henoch's chorea (disorder)",
            "attributes": null
          },
          {
            "code": "88174006",
            "description": "Basilar artery thrombosis (disorder)",
            "attributes": null
          },
          {
            "code": "88219000",
            "description": "Celiac plexus syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "88269008",
            "description": "Thalamic syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "88755007",
            "description": "Phlebitis of lateral venous sinus (disorder)",
            "attributes": null
          },
          {
            "code": "88922007",
            "description": "Thrombosis of basilar sinus (disorder)",
            "attributes": null
          },
          {
            "code": "88923002",
            "description": "Progressive muscular atrophy (disorder)",
            "attributes": null
          },
          {
            "code": "89142007",
            "description": "Progressive intracranial arterial occlusion (disorder)",
            "attributes": null
          },
          {
            "code": "89511000119106",
            "description": "Subdural hygroma (disorder)",
            "attributes": null
          },
          {
            "code": "89576007",
            "description": "Pallidonigrospinal degeneration (disorder)",
            "attributes": null
          },
          {
            "code": "8960007",
            "description": "Myotonia levior (disorder)",
            "attributes": null
          },
          {
            "code": "89601008",
            "description": "Tic of organic origin (disorder)",
            "attributes": null
          },
          {
            "code": "89742000",
            "description": "Vagus nerve autonomic disorder (disorder)",
            "attributes": null
          },
          {
            "code": "89911000119102",
            "description": "Sleep related hypoventilation or hypoxemia (disorder)",
            "attributes": null
          },
          {
            "code": "89980009",
            "description": "Thrombosis of cavernous venous sinus (disorder)",
            "attributes": null
          },
          {
            "code": "90011000119105",
            "description": "Organic sleep related movement disorder (disorder)",
            "attributes": null
          },
          {
            "code": "90099008",
            "description": "Subcortical leukoencephalopathy (disorder)",
            "attributes": null
          },
          {
            "code": "90162006",
            "description": "Syringopontia (disorder)",
            "attributes": null
          },
          {
            "code": "90253000",
            "description": "Progressive subcortical gliosis (disorder)",
            "attributes": null
          },
          {
            "code": "90520006",
            "description": "Vertebral artery stenosis (disorder)",
            "attributes": null
          },
          {
            "code": "91502009",
            "description": "Spinocerebellar disease (disorder)",
            "attributes": null
          },
          {
            "code": "91521000119104",
            "description": "Narcolepsy without cataplexy (disorder)",
            "attributes": null
          },
          {
            "code": "91601000119109",
            "description": "Sequela of thrombotic stroke (disorder)",
            "attributes": null
          },
          {
            "code": "91637004",
            "description": "Myasthenia gravis (disorder)",
            "attributes": null
          },
          {
            "code": "91953003",
            "description": "Azorean disease, type I (disorder)",
            "attributes": null
          },
          {
            "code": "91954009",
            "description": "Azorean disease, type II (disorder)",
            "attributes": null
          },
          {
            "code": "91956006",
            "description": "Azorean disease, type IV (disorder)",
            "attributes": null
          },
          {
            "code": "92341000119107",
            "description": "Weakness of extremities as sequela of stroke (disorder)",
            "attributes": null
          },
          {
            "code": "9345005",
            "description": "Dialysis dementia (disorder)",
            "attributes": null
          },
          {
            "code": "9366002",
            "description": "Palatal myoclonus (disorder)",
            "attributes": null
          },
          {
            "code": "93681000119102",
            "description": "Insomnia co-occurrent and due to nocturnal myoclonus (disorder)",
            "attributes": null
          },
          {
            "code": "9386003",
            "description": "Gouty neuritis (disorder)",
            "attributes": null
          },
          {
            "code": "9412006",
            "description": "Tongue deviation disorder of twelfth cranial nerve (disorder)",
            "attributes": null
          },
          {
            "code": "95454007",
            "description": "Brain stem hemorrhage (disorder)",
            "attributes": null
          },
          {
            "code": "95455008",
            "description": "Thrombosis of cerebral veins (disorder)",
            "attributes": null
          },
          {
            "code": "95456009",
            "description": "Brain stem ischemia (disorder)",
            "attributes": null
          },
          {
            "code": "95457000",
            "description": "Brain stem infarction (disorder)",
            "attributes": null
          },
          {
            "code": "95458005",
            "description": "Cerebellar artery occlusion (disorder)",
            "attributes": null
          },
          {
            "code": "95459002",
            "description": "Cerebellar artery thrombosis (disorder)",
            "attributes": null
          },
          {
            "code": "95460007",
            "description": "Cerebellar infarction (disorder)",
            "attributes": null
          },
          {
            "code": "95461006",
            "description": "Thrombophlebitis of cerebral vein (disorder)",
            "attributes": null
          },
          {
            "code": "95638000",
            "description": "Localized cranial lesion (disorder)",
            "attributes": null
          },
          {
            "code": "95640005",
            "description": "Disorder of brain stem (disorder)",
            "attributes": null
          },
          {
            "code": "95641009",
            "description": "Disorder of midbrain (disorder)",
            "attributes": null
          },
          {
            "code": "95643007",
            "description": "Autoimmune encephalitis (disorder)",
            "attributes": null
          },
          {
            "code": "95646004",
            "description": "Cerebellar degeneration (disorder)",
            "attributes": null
          },
          {
            "code": "95647008",
            "description": "Upper motor neuron disease (disorder)",
            "attributes": null
          },
          {
            "code": "95662005",
            "description": "Sensory neuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "95663000",
            "description": "Peripheral motor neuropathy (disorder)",
            "attributes": null
          },
          {
            "code": "95670000",
            "description": "Nervus intermedius neuralgia (disorder)",
            "attributes": null
          },
          {
            "code": "95794005",
            "description": "Tolosa-Hunt syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "95834000",
            "description": "Facial hemiatrophy (disorder)",
            "attributes": null
          },
          {
            "code": "9611000119107",
            "description": "Symptomatic carotid artery stenosis (disorder)",
            "attributes": null
          },
          {
            "code": "9631000119102",
            "description": "Carotid sinus hypersensitivity (disorder)",
            "attributes": null
          },
          {
            "code": "9638002",
            "description": "Hypoglossal-pyramid syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "9741000119101",
            "description": "Primary central sleep apnea (disorder)",
            "attributes": null
          },
          {
            "code": "97751000119108",
            "description": "Altered behavior in Alzheimer's disease (disorder)",
            "attributes": null
          },
          {
            "code": "98071000119100",
            "description": "Arthropathy of shoulder due to neurological disorder (disorder)",
            "attributes": null
          },
          {
            "code": "9901000119100",
            "description": "Occlusion of cerebral artery with stroke (disorder)",
            "attributes": null
          },
          {
            "code": "99451000119105",
            "description": "Cerebral infarction due to stenosis of carotid artery (disorder)",
            "attributes": null
          },
          {
            "code": "9971000119105",
            "description": "Myelopathy co-occurrent and due to spinal stenosis of cervical region (disorder)",
            "attributes": null
          }
        ]
      },
      {
        "concept_id": 4125,
        "concept_version_id": 11485,
        "concept_name": "Other neurological - neurological devices (ICD-10)",
        "coding_system": {
          "id": 4,
          "name": "ICD10 codes",
          "description": "ICD10 Codes"
        },
        "phenotype_id": "PH1701",
        "phenotype_version_id": 3627,
        "phenotype_name": "Chronic paediatric conditions: Other neurological (excluding epilepsy and headaches)",
        "code_attribute_header": null,
        "codes": [
          {
            "code": "Z982",
            "description": "Presence of cerebrospinal fluid drainage device",
            "attributes": null
          }
        ]
      },
      {
        "concept_id": 4126,
        "concept_version_id": 11486,
        "concept_name": "Other neurological - neurological devices (Read v2)",
        "coding_system": {
          "id": 5,
          "name": "Read codes v2",
          "description": "Read codes v2"
        },
        "phenotype_id": "PH1701",
        "phenotype_version_id": 3627,
        "phenotype_name": "Chronic paediatric conditions: Other neurological (excluding epilepsy and headaches)",
        "code_attribute_header": null,
        "codes": [
          {
            "code": "ZV45S00",
            "description": "[V]Ventriculoperitoneal shunt catheter in situ",
            "attributes": null
          }
        ]
      },
      {
        "concept_id": 4127,
        "concept_version_id": 11487,
        "concept_name": "Other neurological - neurological devices (SNOMED-CT)",
        "coding_system": {
          "id": 9,
          "name": "SNOMED  CT codes",
          "description": "SNOMED CT codes"
        },
        "phenotype_id": "PH1701",
        "phenotype_version_id": 3627,
        "phenotype_name": "Chronic paediatric conditions: Other neurological (excluding epilepsy and headaches)",
        "code_attribute_header": null,
        "codes": [
          {
            "code": "137471000119107",
            "description": "Programmable ventricular shunt valve in situ (finding)",
            "attributes": null
          },
          {
            "code": "449886004",
            "description": "Hydrocephalic shunt catheter in situ (finding)",
            "attributes": null
          },
          {
            "code": "699006006",
            "description": "Ventricular shunt in situ (finding)",
            "attributes": null
          },
          {
            "code": "700132008",
            "description": "Ventriculoperitoneal shunt in situ (finding)",
            "attributes": null
          },
          {
            "code": "737289004",
            "description": "Cerebrospinal fluid drainage device in situ (finding)",
            "attributes": null
          }
        ]
      }
    ],
    "status": 1,
    "doi": "https://doi.org/10.48533/kpjt-f665",
    "is_deleted": false,
    "publish_status": 2,
    "owner": "farrellj",
    "template": {
      "id": 1,
      "name": "Clinical-Coded Phenotype",
      "description": "Phenotype definitions that are based on lists of clinical codes, or algorithms using clinical codes.",
      "version_id": 1
    },
    "versions": [
      {
        "version_id": 3627,
        "version_name": "Chronic paediatric conditions: Other neurological (excluding epilepsy and headaches)",
        "version_date": "2025-01-19T16:01:42.712650Z",
        "is_published": true,
        "is_latest": true
      },
      {
        "version_id": 3617,
        "version_name": "Other neurological (excluding epilepsy and headaches)",
        "version_date": "2025-01-18T20:07:42.614529Z",
        "is_published": true,
        "is_latest": false
      }
    ]
  }
]