[
  {
    "phenotype_id": "PH3859",
    "phenotype_version_id": 9012,
    "name": "Chronic Neurological Disease including Significant Learning Disorder",
    "definition": "This codelist was taken from [OpenCodelists](https://www.opencodelists.org/), created by [OpenSAFELY](https://www.opensafely.org/). We recommend viewing this Phenotype on the OpenCodelist website to view the most recent version.\n\n\nTaken from the `CNS_COV_COD` field in SARS\\-CoV2 COVID19 Vaccination Uptake Reporting Codes 20_21 v1, published by PRIMIS.\n\n\n© PRIMIS \\- the University of Nottingham 2021\n\n\n© University of Oxford for the Bennett Institute for Applied Data Science 2025\\. This work may be copied freely for non\\-commercial research and study.\n\n",
    "implementation": null,
    "publications": null,
    "validation": null,
    "citation_requirements": null,
    "created": "2026-01-26T23:37:32.895839Z",
    "author": "PRIMIS Covid Vaccination Uptake Reporting (old)",
    "collections": [
      {
        "name": "OpenCodelist",
        "value": 31
      },
      {
        "name": "Phenotype Library",
        "value": 18
      }
    ],
    "tags": null,
    "organisation": {
      "id": 1,
      "slug": "opensafely",
      "name": "OpenSAFELY"
    },
    "world_access": 1,
    "updated": "2026-01-26T23:37:32.886252Z",
    "references": [],
    "signed_off": [],
    "methodology": "",
    "coding_system": [
      {
        "name": "SNOMED  CT codes",
        "value": 9
      }
    ],
    "open_codelist_id": "primis-covid19-vacc-uptake-old/cns_cov_cod",
    "source_reference": "https://www.opencodelists.org/codelist/primis-covid19-vacc-uptake-old/cns_cov_cod/v1",
    "concept_information": [
      {
        "concept_id": 9189,
        "concept_version_id": 16674,
        "concept_name": "primis-covid19-vacc-uptake-old/cns_cov_cod/v1",
        "coding_system": {
          "id": 9,
          "name": "SNOMED  CT codes",
          "description": "SNOMED CT codes"
        },
        "phenotype_id": "PH3859",
        "phenotype_version_id": 9012,
        "phenotype_name": "Chronic Neurological Disease including Significant Learning Disorder",
        "code_attribute_header": [],
        "codes": [
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            "description": "Coffin-Siris syndrome",
            "attributes": null
          },
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            "description": "Myelopathy co-occurrent and due to spinal stenosis of lumbar region",
            "attributes": null
          },
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            "description": "Myelopathy co-occurrent and due to spinal stenosis of thoracic region",
            "attributes": null
          },
          {
            "code": "10068001",
            "description": "Sensory somatic cortical disorder",
            "attributes": null
          },
          {
            "code": "100721000119109",
            "description": "High grade astrocytoma of brain",
            "attributes": null
          },
          {
            "code": "100731000119107",
            "description": "Low grade astrocytoma of brain",
            "attributes": null
          },
          {
            "code": "10082001",
            "description": "Progressive rubella panencephalitis",
            "attributes": null
          },
          {
            "code": "100941000119100",
            "description": "Epilepsy in mother complicating pregnancy",
            "attributes": null
          },
          {
            "code": "101421000119107",
            "description": "Dementia due to Parkinson's disease",
            "attributes": null
          },
          {
            "code": "102448004",
            "description": "Drug-induced dyskinesia",
            "attributes": null
          },
          {
            "code": "102449007",
            "description": "Tardive dyskinesia",
            "attributes": null
          },
          {
            "code": "10256000",
            "description": "Brain stem laceration without open intracranial wound AND with loss of consciousness",
            "attributes": null
          },
          {
            "code": "10277002",
            "description": "Cerebellopontine angle syndrome",
            "attributes": null
          },
          {
            "code": "102831000119104",
            "description": "Paralytic syndrome of both lower limbs as sequela of stroke",
            "attributes": null
          },
          {
            "code": "10310006",
            "description": "Open fracture of C1-C4 level with incomplete spinal cord lesion",
            "attributes": null
          },
          {
            "code": "10327003",
            "description": "Cocaine-induced mood disorder",
            "attributes": null
          },
          {
            "code": "1032761000000105",
            "description": "Intraventricular (nontraumatic) haemorrhage, grade 4, of fetus and newborn",
            "attributes": null
          },
          {
            "code": "10340008",
            "description": "Isolated gonadotropin deficiency",
            "attributes": null
          },
          {
            "code": "10349009",
            "description": "Multi-infarct dementia with delirium",
            "attributes": null
          },
          {
            "code": "103761000119107",
            "description": "Paralytic syndrome of all four limbs as sequela of stroke",
            "attributes": null
          },
          {
            "code": "103931000119102",
            "description": "Hepatic coma due to hepatitis",
            "attributes": null
          },
          {
            "code": "10394003",
            "description": "Friedreich's ataxia",
            "attributes": null
          },
          {
            "code": "104431000119107",
            "description": "Lipomyelomeningocele",
            "attributes": null
          },
          {
            "code": "10481000119108",
            "description": "Colloid brain cyst",
            "attributes": null
          },
          {
            "code": "104981000119104",
            "description": "Oligodendroglioma of cerebrum",
            "attributes": null
          },
          {
            "code": "10532003",
            "description": "Primary degenerative dementia of the Alzheimer type, presenile onset, with depression",
            "attributes": null
          },
          {
            "code": "105421000119105",
            "description": "Early onset Alzheimer's disease with behavioral disturbance",
            "attributes": null
          },
          {
            "code": "105451000119102",
            "description": "Amnestic disorder associated with general medical condition",
            "attributes": null
          },
          {
            "code": "1055001",
            "description": "Stenosis of precerebral artery",
            "attributes": null
          },
          {
            "code": "10575009",
            "description": "Open fracture of vertebral column with spinal cord injury",
            "attributes": null
          },
          {
            "code": "106014008",
            "description": "Organic mental disorder of unknown etiology",
            "attributes": null
          },
          {
            "code": "106018006",
            "description": "Hereditary degenerative disease of central nervous system",
            "attributes": null
          },
          {
            "code": "106021000119105",
            "description": "Multi-infarct dementia due to atherosclerosis",
            "attributes": null
          },
          {
            "code": "106071000119106",
            "description": "Secondary hypothalamic insufficiency",
            "attributes": null
          },
          {
            "code": "10649000",
            "description": "Hyperpituitarism",
            "attributes": null
          },
          {
            "code": "10651001",
            "description": "Temporal lobectomy behavior syndrome",
            "attributes": null
          },
          {
            "code": "10677711000119101",
            "description": "Encephalopathy caused by Influenza A virus",
            "attributes": null
          },
          {
            "code": "10701000119109",
            "description": "Refractory complex partial seizure with impairment of consciousness",
            "attributes": null
          },
          {
            "code": "10736002",
            "description": "Isolated thyroliberin deficiency",
            "attributes": null
          },
          {
            "code": "10750951000119106",
            "description": "Epilepsy in mother complicating childbirth",
            "attributes": null
          },
          {
            "code": "10752641000119102",
            "description": "Eclampsia with pre-existing hypertension in childbirth",
            "attributes": null
          },
          {
            "code": "107581000119103",
            "description": "Astrocytoma of brain stem",
            "attributes": null
          },
          {
            "code": "1078001000000105",
            "description": "Haemorrhagic stroke",
            "attributes": null
          },
          {
            "code": "1082451000119102",
            "description": "Encephalitis caused by Actinomyces",
            "attributes": null
          },
          {
            "code": "1082511000119102",
            "description": "Hepatic coma due to acute hepatic failure",
            "attributes": null
          },
          {
            "code": "1082621000119108",
            "description": "Hepatic coma due to alcoholic liver failure",
            "attributes": null
          },
          {
            "code": "1084741000119103",
            "description": "Meningoencephalitis due to Blastomyces dermatitidis",
            "attributes": null
          },
          {
            "code": "1085091000119108",
            "description": "Hepatic coma due to chronic hepatic failure",
            "attributes": null
          },
          {
            "code": "1086061000119109",
            "description": "Diphtheria radiculomyelitis",
            "attributes": null
          },
          {
            "code": "108691000119102",
            "description": "Spasticity as sequela of stroke",
            "attributes": null
          },
          {
            "code": "1086991000119103",
            "description": "Gonococcal abscess of brain",
            "attributes": null
          },
          {
            "code": "1087451000000109",
            "description": "Late onset alcohol-induced psychosis",
            "attributes": null
          },
          {
            "code": "1087461000000107",
            "description": "Late onset substance-induced psychosis",
            "attributes": null
          },
          {
            "code": "1087481000000103",
            "description": "Late onset cocaine-induced psychosis",
            "attributes": null
          },
          {
            "code": "1087491000000101",
            "description": "Late onset lysergic acid diethylamide-induced psychosis",
            "attributes": null
          },
          {
            "code": "1087501000000107",
            "description": "Late onset cannabinoid-induced psychosis",
            "attributes": null
          },
          {
            "code": "1087511000000109",
            "description": "Late onset amphetamine-induced psychosis",
            "attributes": null
          },
          {
            "code": "10878002",
            "description": "Aneurysm of common carotid artery",
            "attributes": null
          },
          {
            "code": "1089411000000104",
            "description": "Cerebral infarction due to occlusion of cerebral artery",
            "attributes": null
          },
          {
            "code": "1089421000000105",
            "description": "Cerebral infarction due to stenosis of cerebral artery",
            "attributes": null
          },
          {
            "code": "1089501000000102",
            "description": "Presenile dementia with psychosis",
            "attributes": null
          },
          {
            "code": "1089521000000106",
            "description": "Predominantly cortical dementia",
            "attributes": null
          },
          {
            "code": "1089531000000108",
            "description": "Predominantly cortical vascular dementia",
            "attributes": null
          },
          {
            "code": "1089811000119106",
            "description": "Meningoencephalitis caused by Acanthamoeba",
            "attributes": null
          },
          {
            "code": "1089821000119104",
            "description": "Meningoencephalitis due to Chagas disease",
            "attributes": null
          },
          {
            "code": "1092691000119109",
            "description": "Hepatic coma due to subacute liver failure",
            "attributes": null
          },
          {
            "code": "10943311000119108",
            "description": "Contusion of right cerebrum",
            "attributes": null
          },
          {
            "code": "10943471000119107",
            "description": "Contusion of left cerebrum",
            "attributes": null
          },
          {
            "code": "109478007",
            "description": "Kohlschutter's syndrome",
            "attributes": null
          },
          {
            "code": "10948005",
            "description": "Thoracic spondylosis with myelopathy",
            "attributes": null
          },
          {
            "code": "109561000",
            "description": "Cerebrofacial dysplasia",
            "attributes": null
          },
          {
            "code": "109905002",
            "description": "Acquired myelocele",
            "attributes": null
          },
          {
            "code": "109911004",
            "description": "Overlapping malignant neoplasm of brain and other parts of the central nervous system",
            "attributes": null
          },
          {
            "code": "109912006",
            "description": "Overlapping malignant neoplasm of brain",
            "attributes": null
          },
          {
            "code": "109915008",
            "description": "Primary malignant neoplasm of meninges",
            "attributes": null
          },
          {
            "code": "110030002",
            "description": "Concussion injury of brain",
            "attributes": null
          },
          {
            "code": "110150000",
            "description": "Spinal cord concussion",
            "attributes": null
          },
          {
            "code": "11045000",
            "description": "Supranuclear facial nerve paralysis",
            "attributes": null
          },
          {
            "code": "1105051000000102",
            "description": "Subacute combined degeneration of spinal cord due to use of nitrous oxide",
            "attributes": null
          },
          {
            "code": "110997000",
            "description": "Fahr's syndrome",
            "attributes": null
          },
          {
            "code": "111028009",
            "description": "Arteriopathic granular atrophy of cerebral cortex",
            "attributes": null
          },
          {
            "code": "111033008",
            "description": "Circumscribed atrophy of brain",
            "attributes": null
          },
          {
            "code": "111296006",
            "description": "Basilar artery embolism",
            "attributes": null
          },
          {
            "code": "111297002",
            "description": "Nonparalytic stroke",
            "attributes": null
          },
          {
            "code": "111298007",
            "description": "Chronic cerebral ischemia",
            "attributes": null
          },
          {
            "code": "111299004",
            "description": "Atheroma of cerebral arteries",
            "attributes": null
          },
          {
            "code": "111337001",
            "description": "Dyke-Davidoff-Masson syndrome",
            "attributes": null
          },
          {
            "code": "111383007",
            "description": "Dysmorphic sialidosis, juvenile form",
            "attributes": null
          },
          {
            "code": "111385000",
            "description": "Tay-Sachs disease",
            "attributes": null
          },
          {
            "code": "111395007",
            "description": "Nephrogenic diabetes insipidus",
            "attributes": null
          },
          {
            "code": "111479008",
            "description": "Organic mental disorder",
            "attributes": null
          },
          {
            "code": "111480006",
            "description": "Psychoactive substance-induced organic dementia",
            "attributes": null
          },
          {
            "code": "111487009",
            "description": "Dream anxiety disorder",
            "attributes": null
          },
          {
            "code": "111488004",
            "description": "Kleine-Levin syndrome",
            "attributes": null
          },
          {
            "code": "111496009",
            "description": "Syringomyelia",
            "attributes": null
          },
          {
            "code": "111497000",
            "description": "Arterial thrombosis of spinal cord",
            "attributes": null
          },
          {
            "code": "111498005",
            "description": "Extratemporal epilepsy",
            "attributes": null
          },
          {
            "code": "111499002",
            "description": "Déjérine-Sottas disease",
            "attributes": null
          },
          {
            "code": "111500006",
            "description": "Muscular dystrophy-deafmutism syndrome",
            "attributes": null
          },
          {
            "code": "111501005",
            "description": "Congenital hereditary muscular dystrophy",
            "attributes": null
          },
          {
            "code": "111502003",
            "description": "Fukuyama congenital muscular dystrophy",
            "attributes": null
          },
          {
            "code": "111503008",
            "description": "Merosin deficient congenital muscular dystrophy",
            "attributes": null
          },
          {
            "code": "111504002",
            "description": "Walker-Warburg congenital muscular dystrophy",
            "attributes": null
          },
          {
            "code": "111505001",
            "description": "Muscle-eye-brain disease, congenital muscular dystrophy",
            "attributes": null
          },
          {
            "code": "111506000",
            "description": "Distal muscular dystrophy, Miyoshi type",
            "attributes": null
          },
          {
            "code": "111508004",
            "description": "Emery-Dreifuss muscular dystrophy",
            "attributes": null
          },
          {
            "code": "111548007",
            "description": "Syndrome of diencephalo-hypophyseal origin",
            "attributes": null
          },
          {
            "code": "111558006",
            "description": "Insulin coma",
            "attributes": null
          },
          {
            "code": "111568001",
            "description": "Hypothalamic syndrome",
            "attributes": null
          },
          {
            "code": "111633007",
            "description": "Open fracture of sacrum AND/OR coccyx with complete cauda equina lesion",
            "attributes": null
          },
          {
            "code": "111641000119102",
            "description": "Congenital choroid plexus cyst",
            "attributes": null
          },
          {
            "code": "111681000",
            "description": "Extradural hemorrhage following injury with open intracranial wound AND loss of consciousness",
            "attributes": null
          },
          {
            "code": "111851005",
            "description": "Subacute adenoviral encephalitis",
            "attributes": null
          },
          {
            "code": "111872008",
            "description": "Post measles encephalitis",
            "attributes": null
          },
          {
            "code": "111897007",
            "description": "Acute necrotizing encephalitis",
            "attributes": null
          },
          {
            "code": "111936002",
            "description": "Cerebral sarcoidosis",
            "attributes": null
          },
          {
            "code": "11197005",
            "description": "Hydromyelia",
            "attributes": null
          },
          {
            "code": "11265003",
            "description": "Hemichorea",
            "attributes": null
          },
          {
            "code": "1131000119105",
            "description": "Sequela of cerebrovascular accident",
            "attributes": null
          },
          {
            "code": "11387009",
            "description": "Psychoactive substance-induced organic mental disorder",
            "attributes": null
          },
          {
            "code": "11413003",
            "description": "Incomplete spinal cord lesion at T1-T6 level without bone injury",
            "attributes": null
          },
          {
            "code": "11442006",
            "description": "Hereditary sensory neuropathy",
            "attributes": null
          },
          {
            "code": "11471000224106",
            "description": "Diffuse intrinsic pontine glioma",
            "attributes": null
          },
          {
            "code": "11538006",
            "description": "Quadriplegia",
            "attributes": null
          },
          {
            "code": "116288000",
            "description": "Paralytic stroke",
            "attributes": null
          },
          {
            "code": "116401000119105",
            "description": "Recurrent complex partial epilepsy",
            "attributes": null
          },
          {
            "code": "116811000119106",
            "description": "Non-Hodgkin lymphoma of central nervous system metastatic to lymph node of lower limb",
            "attributes": null
          },
          {
            "code": "116821000119104",
            "description": "Non-Hodgkin lymphoma of central nervous system metastatic to lymph node of upper limb",
            "attributes": null
          },
          {
            "code": "11701009",
            "description": "Hemicephaly",
            "attributes": null
          },
          {
            "code": "117891000119100",
            "description": "Simple partial seizure",
            "attributes": null
          },
          {
            "code": "11807002",
            "description": "Injury at C5-C7 level with spinal cord injury AND without bone injury",
            "attributes": null
          },
          {
            "code": "11862006",
            "description": "Drug-induced myelopathy",
            "attributes": null
          },
          {
            "code": "118951003",
            "description": "Drug-induced nephrogenic diabetes insipidus",
            "attributes": null
          },
          {
            "code": "119001000119108",
            "description": "Intractable simple partial epilepsy",
            "attributes": null
          },
          {
            "code": "12237911000119109",
            "description": "Amaurosis fugax of left eye",
            "attributes": null
          },
          {
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            "description": "Amaurosis fugax of right eye",
            "attributes": null
          },
          {
            "code": "12242711000119109",
            "description": "Weakness of left facial muscle due to and following cerebrovascular accident",
            "attributes": null
          },
          {
            "code": "12242751000119105",
            "description": "Weakness of right facial muscle due to and following cerebrovascular accident",
            "attributes": null
          },
          {
            "code": "12246008",
            "description": "Acute neuronopathic Gaucher's disease",
            "attributes": null
          },
          {
            "code": "12275031000119106",
            "description": "Congenital cerebral ventriculomegaly",
            "attributes": null
          },
          {
            "code": "12331003",
            "description": "Gigantism due to somatostatin deficiency",
            "attributes": null
          },
          {
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            "description": "Presenile dementia",
            "attributes": null
          },
          {
            "code": "12367511000119101",
            "description": "Paraplegia due to and following cerebrovascular accident",
            "attributes": null
          },
          {
            "code": "123758004",
            "description": "Complex pituitary endocrine disorder",
            "attributes": null
          },
          {
            "code": "123759007",
            "description": "Prepuberal hyperpituitarism",
            "attributes": null
          },
          {
            "code": "123760002",
            "description": "Prepuberal panhypopituitarism",
            "attributes": null
          },
          {
            "code": "123763000",
            "description": "Houssay's syndrome",
            "attributes": null
          },
          {
            "code": "1239331000000100",
            "description": "Significant intellectual disability",
            "attributes": null
          },
          {
            "code": "12394009",
            "description": "Miscarriage with cerebral anoxia",
            "attributes": null
          },
          {
            "code": "123950001",
            "description": "Rheumatic chorea without heart involvement",
            "attributes": null
          },
          {
            "code": "123953004",
            "description": "Idiopathic hypogonadotropic hypogonadism",
            "attributes": null
          },
          {
            "code": "12398201000119102",
            "description": "Anxiety disorder caused by methamphetamine",
            "attributes": null
          },
          {
            "code": "12398281000119105",
            "description": "Methamphetamine withdrawal",
            "attributes": null
          },
          {
            "code": "124001000119104",
            "description": "Status migrainosus co-occurrent and due to migraine without aura",
            "attributes": null
          },
          {
            "code": "1240561000000108",
            "description": "Encephalopathy due to disease caused by Severe acute respiratory syndrome coronavirus 2",
            "attributes": null
          },
          {
            "code": "124081000119107",
            "description": "Menstrual status migrainosus",
            "attributes": null
          },
          {
            "code": "124171000119105",
            "description": "Chronic intractable migraine without aura",
            "attributes": null
          },
          {
            "code": "12454008",
            "description": "Cauda equina syndrome with neurogenic bladder",
            "attributes": null
          },
          {
            "code": "125081000119106",
            "description": "Cerebral infarction due to occlusion of precerebral artery",
            "attributes": null
          },
          {
            "code": "125501000119105",
            "description": "Fetus with complete trisomy 21 syndrome",
            "attributes": null
          },
          {
            "code": "125511000119108",
            "description": "Fetus with complete trisomy 18 syndrome",
            "attributes": null
          },
          {
            "code": "125521000119101",
            "description": "Fetus with complete trisomy 13 syndrome",
            "attributes": null
          },
          {
            "code": "125609005",
            "description": "Open fracture of cervical region with spinal cord injury",
            "attributes": null
          },
          {
            "code": "12589008",
            "description": "Brain stem laceration with open intracranial wound",
            "attributes": null
          },
          {
            "code": "125921000119106",
            "description": "Hepatic coma due to acute hepatitis C",
            "attributes": null
          },
          {
            "code": "126011000119107",
            "description": "Acquired caroticocavernous sinus fistula",
            "attributes": null
          },
          {
            "code": "12677003",
            "description": "Tuberculosis of brain",
            "attributes": null
          },
          {
            "code": "126944002",
            "description": "Brain disorder resulting from a period of impaired oxygen delivery to the brain",
            "attributes": null
          },
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            "description": "Acquired left carotid cavernous fistula",
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            "description": "Cerebrovascular accident due to occlusion of left posterior cerebral artery",
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            "description": "Cerebrovascular accident due to occlusion of right posterior cerebral artery",
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            "description": "Cerebrovascular accident due to occlusion of right middle cerebral artery",
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            "description": "Cerebrovascular accident due to thrombus of left middle cerebral artery",
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            "description": "Cerebrovascular accident due to occlusion of right carotid artery",
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            "description": "Cerebrovascular accident due to occlusion of left pontine artery",
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            "description": "Cerebrovascular accident due to occlusion of left carotid artery",
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            "description": "Cerebrovascular accident due to occlusion of left cerebellar artery",
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            "description": "Cerebrovascular accident due to occlusion of right cerebellar artery",
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            "code": "16026008",
            "description": "Congenital cerebellar hypoplasia",
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            "description": "Acute paralytic non-bulbar poliomyelitis",
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            "description": "Acute paralytic poliomyelitis, vaccine-associated",
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          {
            "code": "191454001",
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            "code": "191455000",
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          {
            "code": "191457008",
            "description": "Senile dementia with depressive or paranoid features",
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          {
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          {
            "code": "191459006",
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          {
            "code": "191461002",
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          {
            "code": "191463004",
            "description": "Uncomplicated arteriosclerotic dementia",
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          {
            "code": "191464005",
            "description": "Arteriosclerotic dementia with delirium",
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          {
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          {
            "code": "191466007",
            "description": "Arteriosclerotic dementia with depression",
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            "description": "Korsakov's alcoholic psychosis with peripheral neuritis",
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            "description": "Chronic alcoholic brain syndrome",
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            "description": "Alcohol withdrawal hallucinosis",
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            "code": "191478006",
            "description": "Alcoholic paranoia",
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          {
            "code": "191480000",
            "description": "Alcohol withdrawal syndrome",
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          {
            "code": "191492000",
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            "description": "Drug-induced amnestic syndrome",
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            "code": "191499009",
            "description": "Transient organic psychoses",
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            "code": "230297002",
            "description": "Multiple system atrophy",
            "attributes": null
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          {
            "code": "230298007",
            "description": "Disorder presenting primarily with chorea",
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          {
            "code": "230299004",
            "description": "Juvenile onset Huntington's disease",
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            "code": "230300007",
            "description": "Late onset Huntington's disease",
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            "code": "230301006",
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            "code": "230302004",
            "description": "Pallidal degeneration",
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            "code": "230305002",
            "description": "Chronic hepatocerebral degeneration",
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            "code": "230307005",
            "description": "Chorea in systemic lupus erythematosus",
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            "code": "230309008",
            "description": "Kinesiogenic choreoathetosis",
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            "code": "230310003",
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          {
            "code": "230311004",
            "description": "Basal ganglia degeneration with calcification",
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          {
            "code": "230312006",
            "description": "Aicardi Goutieres syndrome",
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            "code": "230313001",
            "description": "Autosomal dominant late onset basal ganglia degeneration",
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            "code": "230314007",
            "description": "Sandifer syndrome",
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            "code": "230315008",
            "description": "Drug-induced dystonia",
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            "code": "230316009",
            "description": "Drug-induced acute dystonia",
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            "code": "230317000",
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            "code": "230318005",
            "description": "Idiopathic familial dystonia",
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            "code": "230319002",
            "description": "Autosomal dominant idiopathic familial dystonia",
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            "code": "230320008",
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            "code": "230321007",
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            "code": "230322000",
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            "code": "230323005",
            "description": "Spasmodic retrocollis",
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            "code": "230324004",
            "description": "Isolated blepharospasm",
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            "code": "230325003",
            "description": "Meige syndrome",
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            "code": "230326002",
            "description": "Idiopathic orofacial dystonia",
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            "code": "230327006",
            "description": "Edentulous orofacial dystonia",
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            "code": "230328001",
            "description": "Isolated oromandibular dystonia",
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            "code": "230329009",
            "description": "Posthemiplegic dystonia",
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            "code": "230330004",
            "description": "Occupational dystonia",
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            "code": "230332007",
            "description": "Diurnal dystonia",
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            "code": "230333002",
            "description": "Drug-induced akathisia",
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            "code": "230334008",
            "description": "Drug-induced tic",
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            "code": "230335009",
            "description": "Facial tic disorder",
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            "code": "230336005",
            "description": "Vocal tic disorder",
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            "code": "230337001",
            "description": "Motor tic disorder",
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            "code": "230338006",
            "description": "Gestural tic disorder",
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            "code": "230343004",
            "description": "Symptomatic myoclonus",
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            "code": "230344005",
            "description": "Post-anoxic myoclonus",
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            "code": "230345006",
            "description": "Postencephalitic myoclonus",
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            "code": "230346007",
            "description": "Drug-induced myoclonus",
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            "code": "230347003",
            "description": "Segmental cord myoclonus",
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            "code": "230348008",
            "description": "Palatal-tympanic myoclonus",
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            "code": "230349000",
            "description": "Hyoid myoclonus",
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            "code": "230350000",
            "description": "Opsoclonus-myoclonus syndrome",
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            "code": "230352008",
            "description": "Encephalopathy due to vitamin deficiency",
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            "code": "230353003",
            "description": "Morel laminar sclerosis",
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            "code": "230354009",
            "description": "Drug-induced encephalopathy",
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            "description": "Encephalopathy caused by heavy metal",
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            "code": "230357002",
            "description": "Urate encephalopathy",
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            "code": "230359004",
            "description": "Secondary amyloid encephalopathy",
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            "code": "230360009",
            "description": "Encephalopathy caused by radiation damage",
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            "code": "230361008",
            "description": "Sepsis-associated encephalopathy",
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            "code": "230363006",
            "description": "Progressive neuronal degeneration of childhood",
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            "description": "Progressive neuronal degeneration without liver cirrhosis",
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            "description": "Neuroaxonal dystrophy",
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            "description": "Late infantile and juvenile neuroaxonal dystrophy",
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            "code": "230367007",
            "description": "Neuroaxonal leukodystrophy",
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            "code": "230368002",
            "description": "Type III transitional Pelizaeus-Merzbacher disease",
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            "code": "230369005",
            "description": "Type IV adult Pelizaeus-Merzbacher disease",
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            "code": "230370006",
            "description": "Type V atypical Pelizaeus-Merzbacher disease",
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            "code": "230371005",
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            "code": "230377009",
            "description": "Extrapontine myelinolysis",
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            "description": "Acute non-infective transverse myelitis",
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            "description": "Subacute necrotizing myelitis",
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            "code": "230380005",
            "description": "Balo concentric sclerosis",
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            "description": "Localization-related epilepsy",
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            "description": "Benign psychomotor epilepsy of childhood",
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            "code": "230384001",
            "description": "Benign atypical partial epilepsy in childhood",
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            "description": "Primary inherited reading epilepsy",
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            "description": "Frontal lobe epilepsy",
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            "description": "Supplementary motor epilepsy",
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            "description": "Cingulate epilepsy",
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            "description": "Anterior frontopolar epilepsy",
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            "description": "Orbitofrontal epilepsy",
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            "description": "Dorsolateral epilepsy",
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            "description": "Non-progressive Kozhevnikow syndrome",
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            "description": "Juvenile absence epilepsy",
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            "description": "Cryptogenic generalized epilepsy",
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            "description": "Cryptogenic West syndrome",
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            "description": "Lennox-Gastaut syndrome",
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            "description": "Lafora disease",
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            "description": "Secondary reading epilepsy",
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            "description": "Writing epilepsy",
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            "description": "Paraneoplastic autonomic dysfunction",
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            "description": "Genetically determined myasthenia",
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            "description": "Familial infantile myasthenia",
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            "description": "Acetylcholine resynthesis deficiency",
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            "description": "Congenital myasthenic syndrome",
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            "code": "230674007",
            "description": "Pseudomyopathic myasthenia",
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            "description": "Slow channel syndrome",
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            "description": "Myasthenia gravis associated with thymoma",
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            "description": "Generalized myasthenia",
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            "description": "Myopathy in myasthenia gravis",
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            "description": "Cerebrovascular accident",
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            "description": "Infarction - precerebral",
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            "description": "Anterior cerebral circulation infarction",
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            "description": "Total anterior cerebral circulation infarction",
            "attributes": null
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            "description": "Partial anterior cerebral circulation infarction",
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            "description": "Posterior cerebral circulation infarction",
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            "description": "Lacunar infarction",
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            "description": "Pure motor lacunar infarction",
            "attributes": null
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            "description": "Pure sensory lacunar infarction",
            "attributes": null
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            "code": "230701008",
            "description": "Pure sensorimotor lacunar infarction",
            "attributes": null
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            "description": "Lacunar ataxic hemiparesis",
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            "code": "230703006",
            "description": "Dysarthria-clumsy hand syndrome",
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            "description": "Hemorrhagic cerebral infarction",
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          {
            "code": "230707007",
            "description": "Anterior cerebral circulation hemorrhagic infarction",
            "attributes": null
          },
          {
            "code": "230708002",
            "description": "Posterior cerebral circulation hemorrhagic infarction",
            "attributes": null
          },
          {
            "code": "230709005",
            "description": "Massive supratentorial cerebral hemorrhage",
            "attributes": null
          },
          {
            "code": "230710000",
            "description": "Lobar cerebral hemorrhage",
            "attributes": null
          },
          {
            "code": "230711001",
            "description": "Thalamic hemorrhage",
            "attributes": null
          },
          {
            "code": "230712008",
            "description": "Lacunar hemorrhage",
            "attributes": null
          },
          {
            "code": "230713003",
            "description": "Stroke of uncertain pathology",
            "attributes": null
          },
          {
            "code": "230714009",
            "description": "Anterior circulation stroke of uncertain pathology",
            "attributes": null
          },
          {
            "code": "230715005",
            "description": "Posterior circulation stroke of uncertain pathology",
            "attributes": null
          },
          {
            "code": "230716006",
            "description": "Carotid territory transient ischemic attack",
            "attributes": null
          },
          {
            "code": "230717002",
            "description": "Vertebrobasilar territory transient ischemic attack",
            "attributes": null
          },
          {
            "code": "230720005",
            "description": "Cerebral venous thrombosis of straight sinus",
            "attributes": null
          },
          {
            "code": "230721009",
            "description": "Cerebral venous thrombosis of sigmoid sinus",
            "attributes": null
          },
          {
            "code": "230722002",
            "description": "Cerebral venous thrombosis of cortical vein",
            "attributes": null
          },
          {
            "code": "230723007",
            "description": "Cerebral venous thrombosis of great cerebral vein",
            "attributes": null
          },
          {
            "code": "230724001",
            "description": "Cerebral amyloid angiopathy",
            "attributes": null
          },
          {
            "code": "230725000",
            "description": "Sporadic cerebral amyloid angiopathy",
            "attributes": null
          },
          {
            "code": "230730001",
            "description": "Dissection of vertebral artery",
            "attributes": null
          },
          {
            "code": "230731002",
            "description": "Cerebral arteritis in systemic vasculitis",
            "attributes": null
          },
          {
            "code": "230732009",
            "description": "Cerebral arteritis in giant cell arteritis",
            "attributes": null
          },
          {
            "code": "230735006",
            "description": "Syphilitic cerebral arteritis",
            "attributes": null
          },
          {
            "code": "230738008",
            "description": "Asymptomatic cerebrovascular disease",
            "attributes": null
          },
          {
            "code": "230739000",
            "description": "Spinal cord stroke",
            "attributes": null
          },
          {
            "code": "230741004",
            "description": "Venous infarction of spinal cord",
            "attributes": null
          },
          {
            "code": "230745008",
            "description": "Hydrocephalus",
            "attributes": null
          },
          {
            "code": "230746009",
            "description": "Obstructive hydrocephalus",
            "attributes": null
          },
          {
            "code": "230747000",
            "description": "Isolated fourth ventricle hydrocephalus",
            "attributes": null
          },
          {
            "code": "230748005",
            "description": "Intermittently raised pressure hydrocephalus",
            "attributes": null
          },
          {
            "code": "230749002",
            "description": "Postmeningitic hydrocephalus",
            "attributes": null
          },
          {
            "code": "230751003",
            "description": "Post-traumatic hydrocephalus",
            "attributes": null
          },
          {
            "code": "230752005",
            "description": "Hydrocephalus due to cerebrospinal fluid absorption defect",
            "attributes": null
          },
          {
            "code": "230753000",
            "description": "Hydrocephalus due to cerebrospinal fluid overproduction",
            "attributes": null
          },
          {
            "code": "230754006",
            "description": "Uncinate herniation",
            "attributes": null
          },
          {
            "code": "230755007",
            "description": "Upwards herniation of cerebellum",
            "attributes": null
          },
          {
            "code": "230756008",
            "description": "Transtentorial herniation",
            "attributes": null
          },
          {
            "code": "230757004",
            "description": "Transtentorial herniation downwards",
            "attributes": null
          },
          {
            "code": "230758009",
            "description": "Transtentorial herniation upwards",
            "attributes": null
          },
          {
            "code": "230759001",
            "description": "Vasogenic cerebral edema",
            "attributes": null
          },
          {
            "code": "230760006",
            "description": "Cytotoxic cerebral edema",
            "attributes": null
          },
          {
            "code": "230761005",
            "description": "Periventricular cerebrospinal fluid edema",
            "attributes": null
          },
          {
            "code": "230762003",
            "description": "High altitude cerebral edema",
            "attributes": null
          },
          {
            "code": "230763008",
            "description": "Cerebral edema due to trauma",
            "attributes": null
          },
          {
            "code": "230766000",
            "description": "Multicystic encephalomalacia",
            "attributes": null
          },
          {
            "code": "230769007",
            "description": "Periventricular leukomalacia",
            "attributes": null
          },
          {
            "code": "230773005",
            "description": "Spastic cerebral palsy",
            "attributes": null
          },
          {
            "code": "230780007",
            "description": "Dyskinetic cerebral palsy",
            "attributes": null
          },
          {
            "code": "230781006",
            "description": "Dystonic/rigid cerebral palsy",
            "attributes": null
          },
          {
            "code": "230782004",
            "description": "Dysequilibrium syndrome",
            "attributes": null
          },
          {
            "code": "230784003",
            "description": "Congenital pseudobulbar palsy",
            "attributes": null
          },
          {
            "code": "230786001",
            "description": "Congenital dysphasia",
            "attributes": null
          },
          {
            "code": "230787005",
            "description": "Congenital expressive dysphasia",
            "attributes": null
          },
          {
            "code": "230788000",
            "description": "Congenital receptive dysphasia",
            "attributes": null
          },
          {
            "code": "230790004",
            "description": "Choroid plexus cyst",
            "attributes": null
          },
          {
            "code": "230791000",
            "description": "Hypothalamic neuronal hamartoma",
            "attributes": null
          },
          {
            "code": "230796005",
            "description": "Non-diabetic hypoglycemic coma",
            "attributes": null
          },
          {
            "code": "230801000",
            "description": "Post-ictal coma",
            "attributes": null
          },
          {
            "code": "230802007",
            "description": "Brainstem death",
            "attributes": null
          },
          {
            "code": "230806005",
            "description": "Brain ventricular shunt infection",
            "attributes": null
          },
          {
            "code": "230807001",
            "description": "Brain ventricular shunt displacement",
            "attributes": null
          },
          {
            "code": "230808006",
            "description": "Brain ventricular shunt obstruction",
            "attributes": null
          },
          {
            "code": "231439009",
            "description": "Toxic confusional state",
            "attributes": null
          },
          {
            "code": "231440006",
            "description": "Delirium of mixed origin",
            "attributes": null
          },
          {
            "code": "231442003",
            "description": "Organic catatonic disorder",
            "attributes": null
          },
          {
            "code": "231443008",
            "description": "Right hemispheric organic affective disorder",
            "attributes": null
          },
          {
            "code": "231444002",
            "description": "Organic bipolar disorder",
            "attributes": null
          },
          {
            "code": "231445001",
            "description": "Organic dissociative disorder",
            "attributes": null
          },
          {
            "code": "231446000",
            "description": "Organic emotionally labile disorder",
            "attributes": null
          },
          {
            "code": "231448004",
            "description": "Age-associated memory impairment",
            "attributes": null
          },
          {
            "code": "231449007",
            "description": "Epileptic psychosis",
            "attributes": null
          },
          {
            "code": "231450007",
            "description": "Psychosis associated with intensive care",
            "attributes": null
          },
          {
            "code": "231451006",
            "description": "Drug-induced intensive care psychosis",
            "attributes": null
          },
          {
            "code": "231452004",
            "description": "Limbic epilepsy personality syndrome",
            "attributes": null
          },
          {
            "code": "231453009",
            "description": "Lobotomy syndrome",
            "attributes": null
          },
          {
            "code": "231454003",
            "description": "Organic pseudopsychopathic personality",
            "attributes": null
          },
          {
            "code": "231455002",
            "description": "Organic pseudoretarded personality",
            "attributes": null
          },
          {
            "code": "231456001",
            "description": "Postleucotomy syndrome",
            "attributes": null
          },
          {
            "code": "23186000",
            "description": "Menstrual migraine",
            "attributes": null
          },
          {
            "code": "232036006",
            "description": "Cilioretinal artery occlusion",
            "attributes": null
          },
          {
            "code": "232059000",
            "description": "Laurence-Moon syndrome",
            "attributes": null
          },
          {
            "code": "23276006",
            "description": "Ventricular hemorrhage",
            "attributes": null
          },
          {
            "code": "23283004",
            "description": "Open fracture of T1-T6 level with incomplete spinal cord lesion",
            "attributes": null
          },
          {
            "code": "233718008",
            "description": "Pulmonary tuberous sclerosis",
            "attributes": null
          },
          {
            "code": "23374007",
            "description": "Atypical absence seizure",
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          },
          {
            "code": "233964008",
            "description": "Internal carotid artery stenosis",
            "attributes": null
          },
          {
            "code": "233983001",
            "description": "Ruptured cerebral aneurysm",
            "attributes": null
          },
          {
            "code": "233988005",
            "description": "Carotid artery aneurysm",
            "attributes": null
          },
          {
            "code": "234005004",
            "description": "Vertebral artery rupture",
            "attributes": null
          },
          {
            "code": "234006003",
            "description": "Carotid artery rupture",
            "attributes": null
          },
          {
            "code": "234142008",
            "description": "Cerebral arteriovenous malformation",
            "attributes": null
          },
          {
            "code": "234149004",
            "description": "Congenital arteriovenous fistula of brain",
            "attributes": null
          },
          {
            "code": "23501004",
            "description": "Arginase deficiency",
            "attributes": null
          },
          {
            "code": "2355008",
            "description": "Rud's syndrome",
            "attributes": null
          },
          {
            "code": "23645006",
            "description": "Organic mood disorder",
            "attributes": null
          },
          {
            "code": "236529001",
            "description": "Prune belly syndrome with pulmonic stenosis, mental retardation and deafness",
            "attributes": null
          },
          {
            "code": "23671000119107",
            "description": "Sequela of ischemic cerebral infarction",
            "attributes": null
          },
          {
            "code": "237120002",
            "description": "Hypothalamic amenorrhea",
            "attributes": null
          },
          {
            "code": "23713006",
            "description": "Contusion of cerebral cortex",
            "attributes": null
          },
          {
            "code": "23728006",
            "description": "Partial bilateral paralysis",
            "attributes": null
          },
          {
            "code": "237283007",
            "description": "Eclampsia in labor",
            "attributes": null
          },
          {
            "code": "23732000",
            "description": "Primary cerebellar degeneration",
            "attributes": null
          },
          {
            "code": "237349002",
            "description": "Mild postnatal depression",
            "attributes": null
          },
          {
            "code": "237351003",
            "description": "Mild postnatal psychosis",
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          },
          {
            "code": "23740006",
            "description": "Bilateral paralysis of tongue",
            "attributes": null
          },
          {
            "code": "237512007",
            "description": "Thyrotoxicosis due to thyrotropin-secreting pituitary adenoma",
            "attributes": null
          },
          {
            "code": "237577005",
            "description": "Abnormality of somatostatin secretion",
            "attributes": null
          },
          {
            "code": "237578000",
            "description": "Excessive somatostatin secretion",
            "attributes": null
          },
          {
            "code": "237595008",
            "description": "Abnormality of neurotensine secretion",
            "attributes": null
          },
          {
            "code": "237612000",
            "description": "Photomyoclonus, diabetes mellitus, deafness, nephropathy and cerebral dysfunction",
            "attributes": null
          },
          {
            "code": "237662005",
            "description": "Hyperprolactinemia",
            "attributes": null
          },
          {
            "code": "237663000",
            "description": "Idiopathic hyperprolactinemia",
            "attributes": null
          },
          {
            "code": "237664006",
            "description": "Pituitary stalk compression hyperprolactinemia",
            "attributes": null
          },
          {
            "code": "237665007",
            "description": "Drug-induced hyperprolactinemia",
            "attributes": null
          },
          {
            "code": "237666008",
            "description": "Physiological hyperprolactinemia",
            "attributes": null
          },
          {
            "code": "237667004",
            "description": "Lactation hyperprolactinemia",
            "attributes": null
          },
          {
            "code": "237668009",
            "description": "Pregnancy hyperprolactinemia",
            "attributes": null
          },
          {
            "code": "237669001",
            "description": "Adrenocorticotropic hormone hypersecretion",
            "attributes": null
          },
          {
            "code": "237670000",
            "description": "Adrenocorticotropic hormone hypersecretion not causing Cushing syndrome",
            "attributes": null
          },
          {
            "code": "237671001",
            "description": "Gonadotrophin hypersecretion",
            "attributes": null
          },
          {
            "code": "237672008",
            "description": "Luteinizing hormone hypersecretion",
            "attributes": null
          },
          {
            "code": "237673003",
            "description": "Follicle-stimulating hormone hypersecretion",
            "attributes": null
          },
          {
            "code": "237674009",
            "description": "Anterior pituitary hyperplasia",
            "attributes": null
          },
          {
            "code": "237675005",
            "description": "Somatotroph hyperplasia",
            "attributes": null
          },
          {
            "code": "237676006",
            "description": "Lactotroph hyperplasia",
            "attributes": null
          },
          {
            "code": "237677002",
            "description": "Gonadotroph hyperplasia",
            "attributes": null
          },
          {
            "code": "237678007",
            "description": "Thyrotroph hyperplasia",
            "attributes": null
          },
          {
            "code": "237680001",
            "description": "Corticotroph hyperplasia",
            "attributes": null
          },
          {
            "code": "237682009",
            "description": "Panhypopituitarism - anterior and posterior",
            "attributes": null
          },
          {
            "code": "237683004",
            "description": "Panhypopituitarism - X-linked",
            "attributes": null
          },
          {
            "code": "237684005",
            "description": "Sheehan's syndrome",
            "attributes": null
          },
          {
            "code": "237685006",
            "description": "Partial hypopituitarism",
            "attributes": null
          },
          {
            "code": "237687003",
            "description": "Isolated growth hormone deficiency - autosomal dominant",
            "attributes": null
          },
          {
            "code": "237688008",
            "description": "Idiopathic growth hormone deficiency",
            "attributes": null
          },
          {
            "code": "237689000",
            "description": "Growth hormone neurosecretory dysfunction",
            "attributes": null
          },
          {
            "code": "237691008",
            "description": "Psychosocial growth hormone deficiency",
            "attributes": null
          },
          {
            "code": "237692001",
            "description": "Adrenocorticotropic hormone deficiency",
            "attributes": null
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          {
            "code": "237693006",
            "description": "Idiopathic adrenocorticotropic hormone deficiency",
            "attributes": null
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          {
            "code": "237694000",
            "description": "Steroid suppression of adrenocorticotropic hormone secretion",
            "attributes": null
          },
          {
            "code": "237695004",
            "description": "Idiopathic thyroid stimulating hormone deficiency",
            "attributes": null
          },
          {
            "code": "237696003",
            "description": "Familial central diabetes insipidus",
            "attributes": null
          },
          {
            "code": "237697007",
            "description": "Oxytocin deficiency",
            "attributes": null
          },
          {
            "code": "237698002",
            "description": "Iatrogenic hypopituitarism",
            "attributes": null
          },
          {
            "code": "237699005",
            "description": "Post-traumatic hypopituitarism",
            "attributes": null
          },
          {
            "code": "237700006",
            "description": "Hypopituitarism due to iron overload",
            "attributes": null
          },
          {
            "code": "237701005",
            "description": "Pituitary apoplexy",
            "attributes": null
          },
          {
            "code": "237702003",
            "description": "Pituitary hemorrhage",
            "attributes": null
          },
          {
            "code": "237703008",
            "description": "Pituitary fibrosis",
            "attributes": null
          },
          {
            "code": "237704002",
            "description": "Pituitary fibrosis with midline fibrosis",
            "attributes": null
          },
          {
            "code": "237705001",
            "description": "Hypophysitis",
            "attributes": null
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          {
            "code": "237706000",
            "description": "Autoimmune hypophysitis",
            "attributes": null
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          {
            "code": "237707009",
            "description": "Lymphocytic hypophysitis of pregnancy",
            "attributes": null
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          {
            "code": "237708004",
            "description": "Granulomatous giant-cell hypophysitis",
            "attributes": null
          },
          {
            "code": "237709007",
            "description": "Granuloma of pituitary and hypothalamus",
            "attributes": null
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          {
            "code": "237710002",
            "description": "Pituitary granuloma",
            "attributes": null
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          {
            "code": "237711003",
            "description": "Hypothalamic granuloma",
            "attributes": null
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          {
            "code": "237714006",
            "description": "Hamartoma of hypothalamus",
            "attributes": null
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          {
            "code": "237716008",
            "description": "Pituitary cyst",
            "attributes": null
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          {
            "code": "237717004",
            "description": "Arachnoid cyst of pituitary",
            "attributes": null
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          {
            "code": "237718009",
            "description": "Pituitary gland enlarged",
            "attributes": null
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          {
            "code": "237719001",
            "description": "Pituitary adenoma with extrasellar extension",
            "attributes": null
          },
          {
            "code": "237720007",
            "description": "Hamartoma of pituitary and hypothalamus",
            "attributes": null
          },
          {
            "code": "23772009",
            "description": "Dysphonia of Gilles de la Tourette's syndrome",
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          {
            "code": "237721006",
            "description": "Tumor of pituitary and suprasellar region",
            "attributes": null
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          {
            "code": "237723009",
            "description": "Pituitary stalk compression",
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          {
            "code": "237724003",
            "description": "Hypothalamic disorder of appetite",
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          {
            "code": "237725002",
            "description": "Defective osmoregulation",
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          {
            "code": "237726001",
            "description": "Osmoregulation defect - absent thirst",
            "attributes": null
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          {
            "code": "237727005",
            "description": "Osmoregulation defect - excess thirst",
            "attributes": null
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          {
            "code": "237728000",
            "description": "Absent osmoregulation",
            "attributes": null
          },
          {
            "code": "237729008",
            "description": "Reset hypothalamic osmostat",
            "attributes": null
          },
          {
            "code": "237730003",
            "description": "Hypothalamic overactivity",
            "attributes": null
          },
          {
            "code": "237731004",
            "description": "Loss of hypothalamic inhibition",
            "attributes": null
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          {
            "code": "237733001",
            "description": "Diencephalic syndrome",
            "attributes": null
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          {
            "code": "237867001",
            "description": "Hereditary cerebrovascular amyloidosis",
            "attributes": null
          },
          {
            "code": "237960000",
            "description": "D-2-hydroxyglutaric aciduria",
            "attributes": null
          },
          {
            "code": "237961001",
            "description": "L-2-hydroxyglutaric aciduria",
            "attributes": null
          },
          {
            "code": "238018004",
            "description": "Total hexosaminidase deficiency - infantile",
            "attributes": null
          },
          {
            "code": "238019007",
            "description": "Total hexosaminidase deficiency - juvenile",
            "attributes": null
          },
          {
            "code": "238020001",
            "description": "Total hexosaminidase deficiency - adult",
            "attributes": null
          },
          {
            "code": "238021002",
            "description": "B variant hexosaminidase A deficiency - infantile",
            "attributes": null
          },
          {
            "code": "238022009",
            "description": "B variant hexosaminidase A deficiency - juvenile",
            "attributes": null
          },
          {
            "code": "238023004",
            "description": "B variant hexosaminidase A deficiency - adult",
            "attributes": null
          },
          {
            "code": "238024005",
            "description": "B1 variant hexosaminidase A deficiency",
            "attributes": null
          },
          {
            "code": "238025006",
            "description": "GM1 gangliosidosis",
            "attributes": null
          },
          {
            "code": "238026007",
            "description": "Infantile GM1 gangliosidosis",
            "attributes": null
          },
          {
            "code": "238027003",
            "description": "Adult GM1 gangliosidosis",
            "attributes": null
          },
          {
            "code": "238030005",
            "description": "Galactocerebroside beta-galactosidase deficiency - early onset",
            "attributes": null
          },
          {
            "code": "238031009",
            "description": "Arylsulfatase A deficiency",
            "attributes": null
          },
          {
            "code": "238048001",
            "description": "Alpha-N-acetylgalactosaminidase deficiency",
            "attributes": null
          },
          {
            "code": "23808003",
            "description": "Rolandic vein occlusion syndrome",
            "attributes": null
          },
          {
            "code": "23819000",
            "description": "Embolism of cavernous venous sinus",
            "attributes": null
          },
          {
            "code": "23849003",
            "description": "Sandhoff disease",
            "attributes": null
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          {
            "code": "23871000119106",
            "description": "Somnambulism co-occurrent with sleep terror disorder",
            "attributes": null
          },
          {
            "code": "238826008",
            "description": "de Barsy syndrome",
            "attributes": null
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          {
            "code": "238972008",
            "description": "Cutaneous monosymptomatic delusional psychosis",
            "attributes": null
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          {
            "code": "238973003",
            "description": "Delusions of parasitosis",
            "attributes": null
          },
          {
            "code": "238974009",
            "description": "Delusions of infestation",
            "attributes": null
          },
          {
            "code": "238975005",
            "description": "Delusion of foul odor",
            "attributes": null
          },
          {
            "code": "238977002",
            "description": "Delusional hyperhidrosis",
            "attributes": null
          },
          {
            "code": "238978007",
            "description": "Hyperschemazia",
            "attributes": null
          },
          {
            "code": "238979004",
            "description": "Hyposchemazia",
            "attributes": null
          },
          {
            "code": "239026002",
            "description": "Hypohidrosis-diabetes insipidus syndrome",
            "attributes": null
          },
          {
            "code": "23931000119104",
            "description": "Hydrocephalus due to Arnold Chiari malformation type 2",
            "attributes": null
          },
          {
            "code": "23941000119108",
            "description": "Arnold Chiari type 2 without hydrocephalus",
            "attributes": null
          },
          {
            "code": "240046001",
            "description": "Muscular dystrophy with predominantly proximal limb girdle distribution",
            "attributes": null
          },
          {
            "code": "240047005",
            "description": "X-linked muscular dystrophy with limb girdle distribution",
            "attributes": null
          },
          {
            "code": "240048000",
            "description": "X-linked muscular dystrophy with abnormal dystrophin",
            "attributes": null
          },
          {
            "code": "240049008",
            "description": "Intermediate X-linked muscular dystrophy",
            "attributes": null
          },
          {
            "code": "240050008",
            "description": "Manifesting female carrier of X-linked muscular dystrophy",
            "attributes": null
          },
          {
            "code": "240051007",
            "description": "X-linked limb girdle muscular dystrophy with normal dystrophin",
            "attributes": null
          },
          {
            "code": "240052000",
            "description": "Ji muscular dystrophy",
            "attributes": null
          },
          {
            "code": "240053005",
            "description": "Hereditary myopathy limited to females",
            "attributes": null
          },
          {
            "code": "240054004",
            "description": "Autosomal recessive muscular dystrophy with limb girdle distribution",
            "attributes": null
          },
          {
            "code": "240055003",
            "description": "Autosomal recessive muscular dystrophy with abnormal dystrophin-associated glycoprotein",
            "attributes": null
          },
          {
            "code": "240058001",
            "description": "Reunion-Indiana Amish type muscular dystrophy",
            "attributes": null
          },
          {
            "code": "240060004",
            "description": "Western type of congenital muscular dystrophy",
            "attributes": null
          },
          {
            "code": "240061000",
            "description": "Congenital muscular dystrophy with arthrogryposis multiplex congenita",
            "attributes": null
          },
          {
            "code": "240062007",
            "description": "Ullrich congenital muscular dystrophy",
            "attributes": null
          },
          {
            "code": "240063002",
            "description": "Eichsfeld type congenital muscular dystrophy",
            "attributes": null
          },
          {
            "code": "240064008",
            "description": "Hutterite type of muscular dystrophy",
            "attributes": null
          },
          {
            "code": "240065009",
            "description": "Adult onset autosomal recessive muscular dystrophy with normal dystrophin",
            "attributes": null
          },
          {
            "code": "240067001",
            "description": "Autosomal dominant muscular dystrophy with limb girdle distribution",
            "attributes": null
          },
          {
            "code": "240068006",
            "description": "Autosomal dominant muscular dystrophy with gene located at 5q31",
            "attributes": null
          },
          {
            "code": "240069003",
            "description": "Late onset proximal muscular dystrophy with dysarthria",
            "attributes": null
          },
          {
            "code": "240070002",
            "description": "Muscular dystrophy not predominantly limb girdle in distribution",
            "attributes": null
          },
          {
            "code": "240071003",
            "description": "X-linked muscular dystrophy not predominantly limb girdle",
            "attributes": null
          },
          {
            "code": "240072005",
            "description": "Benign scapuloperoneal muscular dystrophy with cardiomyopathy",
            "attributes": null
          },
          {
            "code": "240073000",
            "description": "Autosomal recessive muscular dystrophy not predominantly limb girdle",
            "attributes": null
          },
          {
            "code": "240074006",
            "description": "Scapulohumeral muscular dystrophy",
            "attributes": null
          },
          {
            "code": "240075007",
            "description": "Autosomal dominant muscular dystrophy not predominantly limb girdle",
            "attributes": null
          },
          {
            "code": "240076008",
            "description": "Benign scapuloperoneal muscular dystrophy",
            "attributes": null
          },
          {
            "code": "240077004",
            "description": "Severe scapuloperoneal muscular dystrophy with cardiomyopathy",
            "attributes": null
          },
          {
            "code": "240078009",
            "description": "Benign congenital muscular dystrophy with finger flexion contractures",
            "attributes": null
          },
          {
            "code": "240081004",
            "description": "Autosomal recessive centronuclear myopathy",
            "attributes": null
          },
          {
            "code": "240082006",
            "description": "Myopathy with abnormality of histochemical fiber type",
            "attributes": null
          },
          {
            "code": "240083001",
            "description": "Myopathy with type I hypotrophy",
            "attributes": null
          },
          {
            "code": "240084007",
            "description": "Congenital myopathy with fiber type disproportion",
            "attributes": null
          },
          {
            "code": "240085008",
            "description": "Congenital myopathy with uniform fiber type",
            "attributes": null
          },
          {
            "code": "240086009",
            "description": "Myopathy with cytoplasmic inclusions",
            "attributes": null
          },
          {
            "code": "240087000",
            "description": "Myopathy with tubular aggregates",
            "attributes": null
          },
          {
            "code": "240104008",
            "description": "Congenital myotonic dystrophy",
            "attributes": null
          },
          {
            "code": "240312009",
            "description": "Cerebral injury due to birth trauma",
            "attributes": null
          },
          {
            "code": "240393003",
            "description": "Listeria cerebritis",
            "attributes": null
          },
          {
            "code": "240448007",
            "description": "Legionella encephalopathy",
            "attributes": null
          },
          {
            "code": "240460008",
            "description": "Acute paralytic poliomyelitis",
            "attributes": null
          },
          {
            "code": "240464004",
            "description": "Rabies coma",
            "attributes": null
          },
          {
            "code": "24059009",
            "description": "Acute cerebellar ataxia caused by varicella",
            "attributes": null
          },
          {
            "code": "240845003",
            "description": "Cerebral loiasis",
            "attributes": null
          },
          {
            "code": "240875008",
            "description": "Cerebral gnathostomiasis",
            "attributes": null
          },
          {
            "code": "241006",
            "description": "Epilepsia partialis continua",
            "attributes": null
          },
          {
            "code": "241992009",
            "description": "Spinal cord decompression injury",
            "attributes": null
          },
          {
            "code": "241993004",
            "description": "Cerebral decompression injury",
            "attributes": null
          },
          {
            "code": "241994005",
            "description": "Cerebellar decompression injury",
            "attributes": null
          },
          {
            "code": "2421000119107",
            "description": "Hallucinations co-occurrent and due to late onset dementia",
            "attributes": null
          },
          {
            "code": "24326000",
            "description": "Metachromatic leukodystrophy, adult type",
            "attributes": null
          },
          {
            "code": "2438005",
            "description": "Iniencephaly",
            "attributes": null
          },
          {
            "code": "24392008",
            "description": "Injury at C1-C4 level with spinal cord injury AND without bone injury",
            "attributes": null
          },
          {
            "code": "24473007",
            "description": "Persistent vegetative state",
            "attributes": null
          },
          {
            "code": "24624008",
            "description": "Aneurysm of internal carotid artery",
            "attributes": null
          },
          {
            "code": "24630008",
            "description": "Listeria meningoencephalitis",
            "attributes": null
          },
          {
            "code": "246528007",
            "description": "Simple partial seizure with focal motor signs without march",
            "attributes": null
          },
          {
            "code": "246529004",
            "description": "Simple partial seizure with focal motor signs with march",
            "attributes": null
          },
          {
            "code": "246530009",
            "description": "Versive seizure",
            "attributes": null
          },
          {
            "code": "246531008",
            "description": "Postural seizure",
            "attributes": null
          },
          {
            "code": "246532001",
            "description": "Phonatory seizure",
            "attributes": null
          },
          {
            "code": "246533006",
            "description": "Simple partial seizure with somatosensory or special sensory dysfunction",
            "attributes": null
          },
          {
            "code": "246535004",
            "description": "Dysphasic seizure",
            "attributes": null
          },
          {
            "code": "246536003",
            "description": "Cognitive seizure",
            "attributes": null
          },
          {
            "code": "246537007",
            "description": "Affective seizure",
            "attributes": null
          },
          {
            "code": "246538002",
            "description": "Seizure causing illusions",
            "attributes": null
          },
          {
            "code": "246539005",
            "description": "Seizure with structured hallucinations",
            "attributes": null
          },
          {
            "code": "246540007",
            "description": "Simple partial seizure followed by impaired consciousness",
            "attributes": null
          },
          {
            "code": "24654003",
            "description": "Weber-Gubler syndrome",
            "attributes": null
          },
          {
            "code": "246541006",
            "description": "Simple partial onset of seizure with automatisms",
            "attributes": null
          },
          {
            "code": "246542004",
            "description": "Complex part seizure with impairment of consciousness only",
            "attributes": null
          },
          {
            "code": "246544003",
            "description": "Partial seizure evolving to secondary generalized seizure",
            "attributes": null
          },
          {
            "code": "246546001",
            "description": "Absence seizure with impairment of consciousness only",
            "attributes": null
          },
          {
            "code": "246548000",
            "description": "Absence seizure with mild clonic components",
            "attributes": null
          },
          {
            "code": "246549008",
            "description": "Absence seizure with atonic components",
            "attributes": null
          },
          {
            "code": "246550008",
            "description": "Absence seizure with tonic components",
            "attributes": null
          },
          {
            "code": "246551007",
            "description": "Absence seizure with automatisms",
            "attributes": null
          },
          {
            "code": "246552000",
            "description": "Absence seizure with autonomic components",
            "attributes": null
          },
          {
            "code": "24700007",
            "description": "Multiple sclerosis",
            "attributes": null
          },
          {
            "code": "247400008",
            "description": "Painful arms and moving fingers",
            "attributes": null
          },
          {
            "code": "248260009",
            "description": "Unrefreshed by sleep",
            "attributes": null
          },
          {
            "code": "2495006",
            "description": "Congenital cerebral arteriovenous aneurysm",
            "attributes": null
          },
          {
            "code": "249892007",
            "description": "Progressive pseudobulbar palsy",
            "attributes": null
          },
          {
            "code": "24991000119103",
            "description": "Thoracic myelopathy",
            "attributes": null
          },
          {
            "code": "25044007",
            "description": "Neuromyelitis optica",
            "attributes": null
          },
          {
            "code": "25133001",
            "description": "Completed stroke",
            "attributes": null
          },
          {
            "code": "25185004",
            "description": "Cerebellar contusion with open intracranial wound AND no loss of consciousness",
            "attributes": null
          },
          {
            "code": "25297005",
            "description": "Psychogenic adductor spastic dysphonia",
            "attributes": null
          },
          {
            "code": "253010003",
            "description": "Microprolactinoma",
            "attributes": null
          },
          {
            "code": "253011004",
            "description": "Macroprolactinoma",
            "attributes": null
          },
          {
            "code": "253098009",
            "description": "Neural tube defect",
            "attributes": null
          },
          {
            "code": "253101008",
            "description": "Congenital cerebral hernia",
            "attributes": null
          },
          {
            "code": "253103006",
            "description": "Frontal encephalocele",
            "attributes": null
          },
          {
            "code": "253104000",
            "description": "Frontoethmoidal encephalocele",
            "attributes": null
          },
          {
            "code": "253106003",
            "description": "Nasofrontal encephalocele",
            "attributes": null
          },
          {
            "code": "253107007",
            "description": "Nasopharyngeal encephalocele",
            "attributes": null
          },
          {
            "code": "253108002",
            "description": "Temporal encephalocele",
            "attributes": null
          },
          {
            "code": "253109005",
            "description": "Parietal encephalocele",
            "attributes": null
          },
          {
            "code": "253111001",
            "description": "Thoracolumbar spina bifida without hydrocephalus - closed",
            "attributes": null
          },
          {
            "code": "253113003",
            "description": "Rachischisis with hydrocephalus",
            "attributes": null
          },
          {
            "code": "253114009",
            "description": "Myelocele with hydrocephalus",
            "attributes": null
          },
          {
            "code": "253115005",
            "description": "Hydromyelocele with hydrocephalus",
            "attributes": null
          },
          {
            "code": "253117002",
            "description": "Closed spina bifida with Arnold-Chiari malformation",
            "attributes": null
          },
          {
            "code": "253118007",
            "description": "Thoracolumbar spina bifida with hydrocephalus - closed",
            "attributes": null
          },
          {
            "code": "253119004",
            "description": "Hemimyelocele",
            "attributes": null
          },
          {
            "code": "253120005",
            "description": "Lipomeningocele",
            "attributes": null
          },
          {
            "code": "253124001",
            "description": "Myelodysplasia of spinal cord",
            "attributes": null
          },
          {
            "code": "253125000",
            "description": "Spinal hamartoma",
            "attributes": null
          },
          {
            "code": "253130001",
            "description": "Secondary microcephaly",
            "attributes": null
          },
          {
            "code": "253131002",
            "description": "Hydrocephalus associated with late onset aqueduct stenosis",
            "attributes": null
          },
          {
            "code": "253132009",
            "description": "External hydrocephalus",
            "attributes": null
          },
          {
            "code": "253133004",
            "description": "Hydrocephalus with anomaly of aqueduct of Sylvius",
            "attributes": null
          },
          {
            "code": "253135006",
            "description": "Defect of telencephalic division",
            "attributes": null
          },
          {
            "code": "253136007",
            "description": "Lobar holoprosencephaly",
            "attributes": null
          },
          {
            "code": "253137003",
            "description": "Alobar holoprosencephaly",
            "attributes": null
          },
          {
            "code": "253138008",
            "description": "Semi-lobar holoprosencephaly",
            "attributes": null
          },
          {
            "code": "253139000",
            "description": "Agenesis of corpus callosum with lipoma",
            "attributes": null
          },
          {
            "code": "253140003",
            "description": "Partial agenesis of corpus callosum",
            "attributes": null
          },
          {
            "code": "253142006",
            "description": "Atrophy of corpus callosum",
            "attributes": null
          },
          {
            "code": "253143001",
            "description": "Absence of septum pellucidum",
            "attributes": null
          },
          {
            "code": "253144007",
            "description": "Cyst of septum pellucidum",
            "attributes": null
          },
          {
            "code": "253145008",
            "description": "Reduction anomaly of hypothalamus",
            "attributes": null
          },
          {
            "code": "253147000",
            "description": "Type 1 lissencephaly",
            "attributes": null
          },
          {
            "code": "253148005",
            "description": "Miller Dieker syndrome",
            "attributes": null
          },
          {
            "code": "253149002",
            "description": "Type 2 lissencephaly",
            "attributes": null
          },
          {
            "code": "253151003",
            "description": "Nodular heterotopia",
            "attributes": null
          },
          {
            "code": "253152005",
            "description": "Laminar heterotopia",
            "attributes": null
          },
          {
            "code": "253153000",
            "description": "Cortical dysplasia",
            "attributes": null
          },
          {
            "code": "253154006",
            "description": "Localized cortical dysplasia",
            "attributes": null
          },
          {
            "code": "253156008",
            "description": "Cortical dysplasia with hemimegalencephaly",
            "attributes": null
          },
          {
            "code": "253158009",
            "description": "Hydranencephaly with proliferative vasculopathy",
            "attributes": null
          },
          {
            "code": "253159001",
            "description": "Schizencephaly",
            "attributes": null
          },
          {
            "code": "253160006",
            "description": "Colpocephaly",
            "attributes": null
          },
          {
            "code": "253163008",
            "description": "Spinal arachnoid cyst",
            "attributes": null
          },
          {
            "code": "253164002",
            "description": "Intradural spinal arachnoid cyst",
            "attributes": null
          },
          {
            "code": "253165001",
            "description": "Extradural spinal arachnoid cyst",
            "attributes": null
          },
          {
            "code": "253167009",
            "description": "Microdysgenesis",
            "attributes": null
          },
          {
            "code": "253168004",
            "description": "Familial megalencephaly",
            "attributes": null
          },
          {
            "code": "253169007",
            "description": "Sporadic megalencephaly",
            "attributes": null
          },
          {
            "code": "253170008",
            "description": "Hemimegalencephaly",
            "attributes": null
          },
          {
            "code": "253171007",
            "description": "Dysgenesis of the cerebellum",
            "attributes": null
          },
          {
            "code": "253172000",
            "description": "Agenesis of cerebellum",
            "attributes": null
          },
          {
            "code": "253174004",
            "description": "Aplasia of the vermis",
            "attributes": null
          },
          {
            "code": "253175003",
            "description": "Familial aplasia of the vermis",
            "attributes": null
          },
          {
            "code": "253176002",
            "description": "Gillespie syndrome",
            "attributes": null
          },
          {
            "code": "253177006",
            "description": "Absence of the vermis",
            "attributes": null
          },
          {
            "code": "253178001",
            "description": "Granular cell hypoplasia",
            "attributes": null
          },
          {
            "code": "253179009",
            "description": "Cerebellar cortical dysplasia",
            "attributes": null
          },
          {
            "code": "253180007",
            "description": "Dysgenesis of the brainstem",
            "attributes": null
          },
          {
            "code": "253181006",
            "description": "Olive dysplasia",
            "attributes": null
          },
          {
            "code": "253182004",
            "description": "Dentate dysplasia",
            "attributes": null
          },
          {
            "code": "253183009",
            "description": "Olivary heterotopia",
            "attributes": null
          },
          {
            "code": "253184003",
            "description": "Chiari malformation",
            "attributes": null
          },
          {
            "code": "253185002",
            "description": "Chiari malformation type I",
            "attributes": null
          },
          {
            "code": "253186001",
            "description": "Chiari malformation type III",
            "attributes": null
          },
          {
            "code": "253187005",
            "description": "Chiari malformation type IV",
            "attributes": null
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          {
            "code": "253188000",
            "description": "Abnormality of canalization and retrogressive differentiation",
            "attributes": null
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          {
            "code": "253189008",
            "description": "Sacral dysgenesis",
            "attributes": null
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          {
            "code": "253190004",
            "description": "Lumbosacral agenesis",
            "attributes": null
          },
          {
            "code": "253192007",
            "description": "Fibrolipoma of filum terminale",
            "attributes": null
          },
          {
            "code": "253194008",
            "description": "Aneurysm of the vein of Galen",
            "attributes": null
          },
          {
            "code": "253203003",
            "description": "Hypoplasia of brain gyri",
            "attributes": null
          },
          {
            "code": "25331007",
            "description": "Injury at T7-T12 level with spinal cord injury AND without bone injury",
            "attributes": null
          },
          {
            "code": "25362006",
            "description": "Phytanic acid storage disease",
            "attributes": null
          },
          {
            "code": "253699002",
            "description": "Isolation of common carotid artery",
            "attributes": null
          },
          {
            "code": "25397008",
            "description": "Aqueduct of Sylvius anomaly",
            "attributes": null
          },
          {
            "code": "254092004",
            "description": "Saldino-Mainzer dysplasia",
            "attributes": null
          },
          {
            "code": "254243001",
            "description": "Ash leaf spot, tuberous sclerosis",
            "attributes": null
          },
          {
            "code": "254255007",
            "description": "Congenital malformation of anterior pituitary",
            "attributes": null
          },
          {
            "code": "254256008",
            "description": "Congenital malformation of posterior pituitary",
            "attributes": null
          },
          {
            "code": "254775002",
            "description": "Bregeat's syndrome",
            "attributes": null
          },
          {
            "code": "254936001",
            "description": "Glial tumor of brain",
            "attributes": null
          },
          {
            "code": "254938000",
            "description": "Astrocytoma of brain",
            "attributes": null
          },
          {
            "code": "254939008",
            "description": "Ependymoma of brain",
            "attributes": null
          },
          {
            "code": "254940005",
            "description": "Oligodendroglioma of brain",
            "attributes": null
          },
          {
            "code": "254941009",
            "description": "Mixed glial tumor of brain",
            "attributes": null
          },
          {
            "code": "254942002",
            "description": "Tumor of choroid plexus",
            "attributes": null
          },
          {
            "code": "254943007",
            "description": "Benign tumor of choroid plexus",
            "attributes": null
          },
          {
            "code": "254945000",
            "description": "Embryonal tumor of brain",
            "attributes": null
          },
          {
            "code": "254946004",
            "description": "Glial tumor of spinal cord",
            "attributes": null
          },
          {
            "code": "254947008",
            "description": "Glioma of spinal cord",
            "attributes": null
          },
          {
            "code": "254948003",
            "description": "Astrocytoma of spinal cord",
            "attributes": null
          },
          {
            "code": "254949006",
            "description": "Ependymoma of spinal cord",
            "attributes": null
          },
          {
            "code": "254950006",
            "description": "Oligodendroglioma of spinal cord",
            "attributes": null
          },
          {
            "code": "254951005",
            "description": "Mixed glial tumor of spinal cord",
            "attributes": null
          },
          {
            "code": "254954002",
            "description": "Embryonal tumor of spinal cord",
            "attributes": null
          },
          {
            "code": "254955001",
            "description": "Pituitary carcinoma",
            "attributes": null
          },
          {
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            "code": "28318001",
            "description": "Basilar hemorrhage",
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            "code": "28366008",
            "description": "Cerebral arteritis",
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            "code": "28368009",
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            "code": "284821000119109",
            "description": "Aneurysm of intracranial portion of internal carotid artery",
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            "code": "284861000119104",
            "description": "Atherosclerosis of bilateral carotid arteries",
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          {
            "code": "284871000119105",
            "description": "Atherosclerosis of left carotid artery",
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            "code": "284881000119108",
            "description": "Atherosclerosis of right carotid artery",
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            "code": "2851000119101",
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            "code": "285201000119100",
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            "code": "286742002",
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            "code": "286914008",
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            "code": "286933003",
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            "code": "28721000119108",
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            "code": "287731003",
            "description": "Cerebral ischemia",
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            "code": "28778005",
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            "code": "28790007",
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            "code": "288461000119105",
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            "code": "288723005",
            "description": "Acute ill-defined cerebrovascular disease",
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            "code": "288851000119106",
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            "code": "288861000119108",
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            "code": "29003001",
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            "code": "290401000119108",
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            "code": "290461000119109",
            "description": "Spastic hemiplegia of left dominant side",
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            "code": "290471000119103",
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            "code": "290653008",
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            "code": "290671000119100",
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            "code": "290681000119102",
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            "code": "290691000119104",
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            "code": "290711000119101",
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            "code": "290761000119103",
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            "code": "290791000119105",
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            "code": "290871000119101",
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            "code": "29093005",
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            "code": "291311000119108",
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            "code": "291351000119109",
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            "code": "291371000119100",
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            "code": "291411000119104",
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            "code": "291481000119105",
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            "code": "291511000119103",
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            "code": "291531000119108",
            "description": "Spontaneous hemorrhage of cerebral hemisphere",
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            "code": "291541000119104",
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            "code": "291571000119106",
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            "description": "Familial dysautonomia",
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            "description": "Meningoencephalomyelitis",
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            "description": "Alcohol-induced organic mental disorder",
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            "code": "292631000119102",
            "description": "Occlusion of left vertebral artery",
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            "description": "Cerebrovascular accident due to stenosis of right vertebral artery",
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            "code": "292671000119104",
            "description": "Cerebrovascular accident due to stenosis of left vertebral artery",
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            "description": "Cerebrovascular accident due to occlusion of right vertebral artery",
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            "code": "292851000119109",
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            "code": "292921000119109",
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            "code": "292931000119107",
            "description": "Intraspinal subdural granuloma",
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            "description": "Acute cerebrovascular insufficiency",
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            "description": "Cerebral infarction due to vertebral artery stenosis",
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            "description": "Cerebral infarction due to stenosis of precerebral artery",
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            "code": "294041000119107",
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          {
            "code": "294051000119109",
            "description": "Flaccid hemiplegia of left nondominant side",
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            "code": "294061000119106",
            "description": "Flaccid hemiplegia of right dominant side",
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          {
            "code": "294071000119100",
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          {
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            "description": "Paralytic syndrome",
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            "description": "Leigh's disease",
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            "description": "Striatonigral degeneration",
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            "description": "Aphasia-left parietal lobe syndrome",
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            "description": "Intracranial venous thrombosis",
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            "description": "Vertebral artery aneurysm",
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            "description": "Partial seizure",
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            "description": "Diffuse cerebrovascular disease",
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            "description": "Variant Creutzfeldt-Jakob disease",
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            "description": "Cocaine delusional disorder",
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            "description": "Spina bifida of dorsal region",
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            "description": "Hormone-induced hypopituitarism",
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            "description": "Brain ventricular shunt malfunction",
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          {
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            "description": "Congenital athetosis",
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            "description": "Motor epilepsy",
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            "code": "307357004",
            "description": "Jacksonian, focal or motor epilepsy",
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          {
            "code": "307359001",
            "description": "Congenital agenesis of brainstem nuclei",
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            "code": "30736009",
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            "description": "Intracranial venous septic embolism",
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            "description": "Multiple lacunar infarcts",
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          {
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            "description": "Microglioma",
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            "description": "Oculopalatal myoclonus",
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            "description": "Left sided cerebral infarction",
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            "description": "Right sided cerebral infarction",
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            "description": "Cerebellar laceration with open intracranial wound",
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            "description": "Spinal demyelination",
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            "description": "Flashbacks",
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          {
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            "description": "Congenital ischemic atrophy of central nervous system structure",
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            "description": "Post poliomyelitis syndrome",
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            "description": "Tuberculous meningoencephalitis",
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            "description": "Traumatic cerebral edema with open intracranial wound",
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            "description": "Brain stem laceration with open intracranial wound AND loss of consciousness",
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            "description": "Profound intellectual disability",
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            "description": "Infective ventriculitis, brain",
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          {
            "code": "31235003",
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            "description": "Intracranial thrombophlebitis",
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            "description": "Abductor spastic dysphonia",
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            "description": "Spinal dislocation with cervical cord lesion",
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            "description": "Spinal dislocation with thoracic cord lesion",
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            "description": "Spinal dislocation with lumbar cord lesion",
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            "description": "Senile dementia of the Lewy body type",
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            "description": "Non-traumatic spinal subdural hematoma",
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            "code": "313434001",
            "description": "Residual hemiplegia",
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            "code": "31367003",
            "description": "Postvaccinal encephalomyelitis",
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            "description": "Medication-induced postural tremor",
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            "code": "314950006",
            "description": "Migration of spinal cord stimulator",
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            "code": "315046005",
            "description": "Traumatic subdural hematoma without open intracranial wound",
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            "description": "Cardiomyopathy in Duchenne muscular dystrophy",
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            "description": "Mumps encephalitis",
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            "description": "Myasthenia gravis, adult form",
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            "description": "Hallucinogen hallucinosis",
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            "description": "Phlebitis of inferior sagittal sinus",
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            "description": "Facial hemiplegia",
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            "code": "322112361000132104",
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            "code": "32232003",
            "description": "Spina bifida of cervical region",
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            "code": "32358001",
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            "code": "32390006",
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            "description": "Psychoactive substance-induced organic delusional disorder",
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            "code": "32680009",
            "description": "Nothnagel's syndrome",
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            "description": "Hemorrhage due to ruptured congenital cerebral aneurysm",
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            "description": "Inhalant-induced persisting dementia",
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            "code": "329371000119101",
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            "code": "329431000119105",
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            "description": "Open fracture of C1-C4 level with posterior cord syndrome",
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            "description": "Reversible ischemic neurologic deficit syndrome",
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            "description": "Malignant neoplasm of temporal lobe",
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            "description": "Malignant tumor of spinal cord",
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            "description": "Malignant tumor of pineal gland",
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            "description": "Psychoactive substance-induced organic mood disorder",
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            "description": "Hereditary cerebellar degeneration",
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            "description": "Mood disorder due to a general medical condition",
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            "description": "Tuberculosis of spinal meninges",
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            "description": "Periventricular hemorrhagic venous infarct",
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            "code": "38576000",
            "description": "Nonfamilial hyperinsulinemic isolated somatotropin deficiency",
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            "code": "38632003",
            "description": "Pharyngeal pituitary tissue",
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          {
            "code": "386766007",
            "description": "Marchiafava-Bignami disease",
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          {
            "code": "386805003",
            "description": "Mild cognitive disorder",
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          {
            "code": "38742007",
            "description": "Central retinal artery occlusion",
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          {
            "code": "387732009",
            "description": "Becker muscular dystrophy",
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          {
            "code": "38795005",
            "description": "Sialidosis",
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          {
            "code": "38837006",
            "description": "Acquired porencephaly",
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          {
            "code": "389088001",
            "description": "Hypoxia of brain",
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          {
            "code": "389089009",
            "description": "Anoxia of brain",
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          {
            "code": "389098007",
            "description": "Anoxic encephalopathy",
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          {
            "code": "389100007",
            "description": "Ischemic encephalopathy",
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          {
            "code": "389101006",
            "description": "Anoxic-ischemic encephalopathy",
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          {
            "code": "389271000",
            "description": "Spondyloenchondromatosis with basal ganglia calcification",
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          },
          {
            "code": "38941006",
            "description": "Neuroleptic-induced tardive dyskinesia",
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          {
            "code": "39003006",
            "description": "Psychoactive substance-induced organic delirium",
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            "code": "39020005",
            "description": "Brain injury, without skull fracture",
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          },
          {
            "code": "390936003",
            "description": "Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy",
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          {
            "code": "39134007",
            "description": "Hematomyelia",
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          {
            "code": "39150004",
            "description": "Congenital anomaly of spinal meninges",
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          {
            "code": "39194005",
            "description": "Visual epilepsy",
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          {
            "code": "392662004",
            "description": "West Nile encephalitis",
            "attributes": null
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          {
            "code": "39390005",
            "description": "Niemann-Pick disease, type B",
            "attributes": null
          },
          {
            "code": "39574006",
            "description": "Congenital hypoplasia of inner granular layer of cerebellum",
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          {
            "code": "396338004",
            "description": "Metachromatic leucodystrophy",
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            "code": "39745004",
            "description": "Chronic progressive epilepsia partialis continua",
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          {
            "code": "397734008",
            "description": "Hereditary sensory and autonomic neuropathy type I",
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          },
          {
            "code": "397763006",
            "description": "Human immunodeficiency virus encephalopathy",
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          {
            "code": "397827003",
            "description": "Growth hormone deficiency",
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          {
            "code": "397961002",
            "description": "Encephalomyelitis caused by lymphocytic choriomeningitis virus",
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          {
            "code": "398040009",
            "description": "Charcot-Marie-Tooth disease, type I",
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          {
            "code": "39807006",
            "description": "Cannabis intoxication delirium",
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          {
            "code": "398100001",
            "description": "Hereditary motor and sensory neuropathy",
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          {
            "code": "398148000",
            "description": "Hereditary sensory and autonomic neuropathy type II",
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          },
          {
            "code": "398187000",
            "description": "Charcot-Marie-Tooth disease, type II",
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          {
            "code": "398229007",
            "description": "Amyloid polyneuropathy type I",
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          {
            "code": "398329009",
            "description": "Human immunodeficiency virus encephalitis",
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            "code": "398432008",
            "description": "Bulbar weakness",
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          {
            "code": "399041003",
            "description": "Chastek paralysis",
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          {
            "code": "399091004",
            "description": "Facioscapulohumeral muscular dystrophy",
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            "code": "399100005",
            "description": "Disorder of hypothalamus",
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          {
            "code": "39912006",
            "description": "Hereditary spastic paraplegia",
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            "code": "399244003",
            "description": "Disorder of pituitary gland",
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            "code": "39925003",
            "description": "Juvenile myopathy, encephalopathy, lactic acidosis AND stroke",
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            "code": "39951001",
            "description": "Cannabis-induced anxiety disorder",
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            "code": "39960009",
            "description": "Grimaces",
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          {
            "code": "40099009",
            "description": "Meningoencephalitis caused by mumps",
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            "code": "40130009",
            "description": "Spina bifida without hydrocephalus",
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            "code": "40135004",
            "description": "Subdural hemorrhage following injury without open intracranial wound AND with no loss of consciousness",
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            "code": "40230002",
            "description": "Encephalitis caused by Langat virus",
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            "code": "402460000",
            "description": "Familial amyloid polyneuropathy with cutaneous amyloidosis",
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            "code": "40259002",
            "description": "Progressive sensory ataxia of Charolais",
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            "code": "402732001",
            "description": "Habit tic",
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            "code": "402733006",
            "description": "Habit tic affecting skin",
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            "code": "402735004",
            "description": "Habit tic affecting hair",
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            "code": "40276003",
            "description": "Embolism of precerebral artery",
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          {
            "code": "40354009",
            "description": "De Lange syndrome",
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            "code": "403595006",
            "description": "Pinocchio syndrome",
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            "code": "403815003",
            "description": "Axillary freckling due to neurofibromatosis",
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            "code": "403816002",
            "description": "Multiple café-au-lait macules due to neurofibromatosis",
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            "code": "403817006",
            "description": "Multiple neurofibromas in neurofibromatosis",
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            "code": "403819009",
            "description": "Elephantiasis neurofibromatosa",
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            "code": "40405003",
            "description": "Illegal abortion with cerebral anoxia",
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            "code": "404235004",
            "description": "Jamestown Canyon virus encephalitis",
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            "code": "40425004",
            "description": "Postconcussion syndrome",
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            "code": "40450001",
            "description": "Embolism of superior sagittal sinus",
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            "code": "404664002",
            "description": "Malignant optic glioma",
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            "code": "404689008",
            "description": "Alternating hemiplegia",
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            "code": "404906000",
            "description": "Post-operative confusion",
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            "description": "Hallucinogen intoxication delirium",
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            "code": "405754008",
            "description": "Cervical spinal cord injury",
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            "code": "405755009",
            "description": "Anterior cervical spinal cord injury at C1-C4 level without spinal bone injury",
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            "code": "405756005",
            "description": "Anterior cervical spinal cord injury, without spinal bone injury, C5-7",
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          },
          {
            "code": "405757001",
            "description": "Central cervical cord injury, without spinal bony injury, C1-4",
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            "code": "405758006",
            "description": "Central cervical cord injury, without spinal bony injury, C5-7",
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          {
            "code": "405759003",
            "description": "Cervical spinal cord injury without spinal bone injury",
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          },
          {
            "code": "405760008",
            "description": "Complete cervical cord injury, without spinal bone injury, C1-4",
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            "code": "405761007",
            "description": "Complete cervical cord injury, without spinal bone injury, C5-7",
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            "description": "Posterior cervical spinal cord injury without spinal bone injury, C5-7",
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            "code": "405765003",
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            "code": "4061000119104",
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          {
            "code": "40632002",
            "description": "Charcot-Marie-Tooth disease, type IA",
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            "code": "406573001",
            "description": "Primary encephalitis",
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            "code": "40673001",
            "description": "Post-encephalitic syndrome",
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            "description": "Severe intellectual disability",
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            "description": "Cerebral cyst",
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            "code": "407472000",
            "description": "Nairoviral encephalitis",
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            "code": "407675009",
            "description": "Complex partial epileptic seizure",
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            "code": "40781006",
            "description": "Hypopituitarism due to pituitary tumor",
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            "code": "40802007",
            "description": "Metachromatic leukodystrophy, congenital type",
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            "code": "40816002",
            "description": "Retropulsion petit mal",
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            "code": "408664007",
            "description": "Pontine artery occlusion",
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            "description": "Pontine artery thrombosis",
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            "description": "Acquired hydrocephalus",
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            "code": "40946000",
            "description": "Hepatic coma due to viral hepatitis",
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            "code": "409556004",
            "description": "Q fever encephalitis",
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            "description": "Spastic paralysis due to birth injury",
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            "description": "Post-traumatic communicating hydrocephalus",
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            "description": "Complex partial seizure with impairment of consciousness",
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            "code": "41040004",
            "description": "Complete trisomy 21 syndrome",
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            "description": "Fungal infection of brain",
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            "description": "Alcohol-induced sleep disorder",
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            "description": "Globoid cell leukodystrophy, late-onset",
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            "description": "Cerebro-oculo-facio-skeletal syndrome",
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          {
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            "description": "Cyst of pineal gland",
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          {
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            "description": "Stress-induced epilepsy",
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            "description": "Benign neonatal sleep myoclonus",
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            "code": "41370002",
            "description": "Myelitis",
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            "code": "413758000",
            "description": "Cardioembolic stroke",
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            "code": "413807008",
            "description": "Cerebellar hernia",
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            "description": "Cerebral ventriculomegaly",
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            "description": "Cortical visual impairment",
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            "description": "Hernia of cerebellar tonsil into foramen magnum",
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            "description": "Ocular myasthenia with strabismus",
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          {
            "code": "415347009",
            "description": "Rio Bravo viral encephalitis",
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            "code": "415525005",
            "description": "Encephalitis caused by Siberian tick-borne encephalitis virus",
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            "description": "Paramyotonia congenita",
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            "description": "Familial amyloid polyneuropathy, Jewish type",
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            "description": "Complaining of akathisia",
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          {
            "code": "416265003",
            "description": "Tuberculoma of brain",
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            "description": "Primary degenerative dementia of the Alzheimer type, presenile onset",
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            "description": "Vein of Galen malformation",
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            "code": "416903004",
            "description": "Tuberculoma of spinal cord",
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            "code": "416975007",
            "description": "Primary degenerative dementia of the Alzheimer type, senile onset",
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            "code": "417017003",
            "description": "Acute cerebellar syndrome",
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            "description": "Neuroinvasive California encephalitis virus infection",
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            "description": "Benedikt's syndrome",
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            "description": "Duplicative flashbacks",
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            "description": "Tuberculous abscess of spinal cord",
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          {
            "code": "417607009",
            "description": "Neuroinvasive Saint Louis encephalitis virus infection",
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            "description": "Holoanencephaly",
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            "description": "Neuroinvasive Cache Valley encephalitis virus infection",
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            "description": "Cerebral degeneration",
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          {
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            "description": "Charcot-Marie-Tooth disease, type IC",
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            "code": "418455000",
            "description": "Encephalitis caused by protozoa",
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            "description": "Eosinophilic meningoencephalitis caused by Angiostrongylus cantonensis",
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            "description": "California serogroup virus neuroinvasive disease",
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            "description": "Encephalitis caused by rickettsia",
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            "description": "Neuronal ceroid lipofuscinosis",
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            "description": "Cerebral degeneration associated with generalized lipidosis",
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            "description": "Familial diabetes insipidus",
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            "description": "Encephalitis associated with acquired immunodeficiency syndrome",
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            "description": "Myelopathy associated with acquired immunodeficiency syndrome",
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            "description": "Progressive multifocal leukoencephalopathy associated with acquired immunodeficiency syndrome",
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            "description": "Organic dementia associated with acquired immunodeficiency syndrome",
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            "description": "Coma due to diabetes mellitus",
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            "description": "Supranuclear gaze palsy",
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            "code": "420718004",
            "description": "Central nervous system demyelinating disease associated with acquired immunodeficiency syndrome",
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            "description": "Organic brain syndrome associated with acquired immunodeficiency syndrome",
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            "description": "Intraocular non-Hodgkin malignant lymphoma",
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            "code": "421019006",
            "description": "Hypogonadotropic hypogonadism due to follicle-stimulating hormone deficiency",
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            "description": "Presenile dementia associated with acquired immunodeficiency syndrome",
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            "description": "Ketoacidotic coma due to type 1 diabetes mellitus",
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            "code": "421283008",
            "description": "Primary lymphoma of brain associated with acquired immunodeficiency syndrome",
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            "code": "421315006",
            "description": "Myelitis associated with acquired immunodeficiency syndrome",
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          {
            "code": "421415007",
            "description": "Subacute adenoviral encephalitis associated with acquired immunodeficiency syndrome",
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            "description": "Hypoglycemic coma due to type 1 diabetes mellitus",
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          {
            "code": "421529006",
            "description": "Dementia associated with acquired immunodeficiency syndrome",
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            "code": "421684006",
            "description": "Adult growth hormone deficiency",
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          {
            "code": "421725003",
            "description": "Hypoglycemic coma due to diabetes mellitus",
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          {
            "code": "421821002",
            "description": "Hypogonadotropic hypogonadism due to luteinizing hormone deficiency",
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          {
            "code": "421827003",
            "description": "Encephalopathy associated with acquired immunodeficiency syndrome",
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            "code": "421847006",
            "description": "Ketoacidotic coma due to type 2 diabetes mellitus",
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            "description": "Adult growth hormone deficiency with onset in childhood",
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            "code": "421966007",
            "description": "Non-ketotic non-hyperosmolar coma due to diabetes mellitus",
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          {
            "code": "421998001",
            "description": "Central nervous disorder associated with acquired immunodeficiency syndrome",
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          {
            "code": "422089004",
            "description": "Encephalomyelitis associated with acquired immunodeficiency syndrome",
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          {
            "code": "422126006",
            "description": "Hyperosmolar coma due to diabetes mellitus",
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          {
            "code": "422240004",
            "description": "Gonadotropin releasing factor deficiency",
            "attributes": null
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          {
            "code": "4223005",
            "description": "Parkinsonism caused by drug",
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            "description": "Partial absence of septum pellucidum",
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            "description": "Ischemic stroke",
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            "description": "Refractory infantile spasms",
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            "description": "Malignant neoplasm of brain",
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            "description": "Encephalitis caused by Herpesvirus",
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            "description": "Apraxia due to cerebrovascular accident",
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            "description": "Low grade glioma of cerebellum",
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            "description": "Low grade glioma of brainstem",
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            "description": "Low grade glioma of cerebrum",
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            "description": "Low grade glioma of thalamus",
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            "description": "Malignant neoplasm of cerebrum",
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            "description": "Benign neoplasm of spinal intradural intramedullary space",
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            "description": "Low grade glioma of brain",
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            "description": "Nelson syndrome",
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            "description": "Infection of spinal cord caused by Histoplasma",
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            "description": "Hemiplegia of dominant side as late effect of cerebrovascular disease",
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            "description": "Hemiplegia as late effect of cerebrovascular accident",
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            "description": "Glioma of brainstem",
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            "description": "Superior cerebellar artery syndrome",
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            "description": "Bacterial meningomyelitis",
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            "code": "444980006",
            "description": "Sporadic olivopontocerebellar atrophy",
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            "code": "445006008",
            "description": "Focal dystonia",
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            "code": "445014002",
            "description": "Paraneoplastic limbic encephalitis",
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            "code": "445109004",
            "description": "Isolation of left common carotid artery",
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            "code": "445116003",
            "description": "Encephalocele of vertex",
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            "code": "445158000",
            "description": "Colloid cyst of pituitary gland",
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            "code": "445166009",
            "description": "Cystic degeneration of brain",
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            "code": "445252005",
            "description": "Glucose transporter protein type 1 deficiency syndrome",
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            "code": "445307009",
            "description": "Spina bifida of sacral region",
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            "code": "445308004",
            "description": "Split spinal cord malformation",
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            "code": "445322004",
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            "code": "445349004",
            "description": "Isolation of right common carotid artery",
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            "code": "445355009",
            "description": "Refractory epilepsy",
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            "code": "445359003",
            "description": "Bacterial meningoencephalitis",
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            "code": "445423005",
            "description": "Paraneoplastic subacute necrotic myelopathy",
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            "code": "445475001",
            "description": "Paraneoplastic sensorimotor neuropathy",
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            "code": "445779008",
            "description": "Traumatic injury of spinal cord at T7-T12 level",
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            "code": "445897006",
            "description": "Incomplete transverse lesion of thoracic spinal cord",
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            "code": "4463009",
            "description": "Familial amyloid polyneuropathy, type II",
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            "code": "446311006",
            "description": "Acute bulbar poliomyelitis caused by Human poliovirus 2",
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            "code": "446495002",
            "description": "Ependymal cyst of spinal meninges",
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            "code": "446644006",
            "description": "Traumatic injury of spinal cord at T1-T6 level",
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            "code": "446712002",
            "description": "Thromboembolus of precerebral artery",
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            "code": "446835008",
            "description": "Traumatic injury of sacral spinal cord",
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            "code": "446940004",
            "description": "Ependymal cyst of spinal cord",
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            "code": "446945009",
            "description": "Invasive pituitary adenoma",
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          {
            "code": "446957000",
            "description": "Acute bulbar poliomyelitis caused by Human poliovirus 1",
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          {
            "code": "446958005",
            "description": "Acute paralytic poliomyelitis caused by Human poliovirus 1",
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            "code": "446995005",
            "description": "Shuddering attacks",
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            "code": "447012002",
            "description": "Tuberculosis of spinal cord",
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            "code": "447232008",
            "description": "Ependymal cyst of ventricle of brain",
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          {
            "code": "447262002",
            "description": "Acute paralytic poliomyelitis caused by Human poliovirus 2",
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            "code": "447292006",
            "description": "Mitochondrial encephalomyopathy",
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            "code": "4473006",
            "description": "Migraine with aura",
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            "code": "447351004",
            "description": "Vanishing white matter disease",
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          {
            "code": "447378002",
            "description": "Acute paralytic poliomyelitis caused by Human poliovirus 3",
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            "code": "447396006",
            "description": "Concussion injury of cerebrum",
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            "code": "447464004",
            "description": "Complete spinal cord injury at T7-T12 level",
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            "code": "447575003",
            "description": "Complete spinal cord injury at T1-T6 level",
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            "code": "447655002",
            "description": "Benign neoplastic cyst of brain",
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            "code": "4477007",
            "description": "Juvenile myopathy AND lactate acidosis",
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            "code": "448045004",
            "description": "Fragile X associated tremor ataxia syndrome",
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            "code": "448054001",
            "description": "Adult onset autosomal dominant leukodystrophy",
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            "code": "448135004",
            "description": "Benign teratoma of pineal region",
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            "code": "448148000",
            "description": "Functioning pituitary neoplasm",
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            "code": "448218008",
            "description": "Malignant neoplasm of cerebellopontine angle",
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            "code": "448227009",
            "description": "X-linked periventricular heterotopia",
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            "code": "448248006",
            "description": "Malignant neoplasm of axial suprasellar region of brain",
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            "code": "448250003",
            "description": "Malignant teratoma of pineal region",
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            "code": "448254007",
            "description": "Non-Hodgkin's lymphoma of central nervous system",
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            "code": "448314007",
            "description": "Malignant epithelial neoplasm of spinal cord",
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            "code": "448563005",
            "description": "Functionless pituitary neoplasm",
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            "code": "448705004",
            "description": "Mesial temporal lobe sclerosis",
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            "code": "448863000",
            "description": "Malignant epithelial neoplasm of pineal gland",
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            "code": "448989001",
            "description": "Malignant epithelial neoplasm of brain",
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            "code": "448995000",
            "description": "Follicular non-Hodgkin's lymphoma of central nervous system",
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            "code": "449020009",
            "description": "Intraparenchymal hemorrhage of brain",
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            "code": "44913001",
            "description": "Athetosis",
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            "code": "449203004",
            "description": "Focal seizure with experiential sensory symptoms",
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            "code": "449221001",
            "description": "Diffuse non-Hodgkin's lymphoma of central nervous system",
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            "code": "449253005",
            "description": "Malignant epithelial neoplasm of hypothalamus",
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            "code": "449305009",
            "description": "Paraneoplastic sensory neuropathy",
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            "code": "449420002",
            "description": "Malignant neoplasm of cerebellum",
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            "code": "449795002",
            "description": "Hemorrhage into subdural space of spine",
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            "code": "449799008",
            "description": "Subependymal giant cell astrocytoma",
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            "code": "44983007",
            "description": "Intervertebral disc disorder with myelopathy",
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            "code": "449901005",
            "description": "Hepatic encephalopathy in fulminant hepatic failure",
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            "code": "449902003",
            "description": "Portal systemic encephalopathy",
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            "code": "449903008",
            "description": "Dural arteriovenous fistula of spinal cord",
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            "description": "Intramedullary glomus arteriovenous malformation of spinal cord",
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            "description": "Intramedullary and extramedullary arteriovenous malformation of spinal cord",
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            "code": "449906000",
            "description": "Perimedullary arteriovenous fistula of spinal cord",
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            "code": "450363003",
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            "description": "Traumatic brain injury with loss of consciousness one hour or more",
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            "description": "Posterior reversible encephalopathy syndrome",
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            "code": "451036001",
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            "code": "451037005",
            "description": "Hemorrhage in globus pallidus",
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            "code": "451038000",
            "description": "Hemorrhage in caudate nucleus",
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            "description": "Hemorrhage in putamen",
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            "code": "45163000",
            "description": "Congenital pontocerebellar hypoplasia",
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            "description": "Encephalitis",
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            "code": "4523006",
            "description": "Babinski-Nageotte syndrome",
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            "description": "Neurohypophyseal diabetes insipidus",
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            "code": "45639009",
            "description": "Hereditary cerebral amyloid angiopathy, Icelandic type",
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            "description": "Diencephalic syndrome of infancy",
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            "code": "45814002",
            "description": "Birnbaum's syndrome",
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            "code": "45853006",
            "description": "Roussy-Lévy syndrome",
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            "code": "45864009",
            "description": "Senile degeneration of brain",
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            "code": "45897005",
            "description": "Jervis' syndrome",
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            "description": "Senile brain amyloidosis",
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            "description": "Von Hippel-Lindau syndrome",
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            "description": "Multi-infarct dementia",
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            "code": "66637005",
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            "code": "66751000",
            "description": "Niemann-Pick disease, type C",
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            "code": "66881004",
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            "code": "67155006",
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            "description": "Cerebral-retinal arteriovenous aneurysm",
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            "description": "Familial essential myoclonus",
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            "code": "674091000119108",
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            "code": "67437007",
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            "code": "674481000119100",
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            "code": "67531005",
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            "code": "67747009",
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            "code": "67761004",
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            "code": "67771000119102",
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            "code": "67854007",
            "description": "Maroteaux-Lamy syndrome, mild form",
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            "code": "67855008",
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            "code": "67873006",
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            "code": "67876003",
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            "code": "67930001",
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            "code": "68061000119109",
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            "code": "6807001",
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            "code": "68091000119102",
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            "code": "68107009",
            "description": "Cerebral paresis with homolateral ataxia",
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            "code": "68116008",
            "description": "Dentatorubropallidoluysian degeneration",
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            "code": "68186003",
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            "code": "68267002",
            "description": "Benign intracranial hypertension",
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            "code": "68390005",
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            "code": "684911000119105",
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            "code": "68504005",
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            "code": "68761002",
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            "description": "Maroteaux-Lamy syndrome",
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            "description": "Familial Creutzfeldt-Jakob",
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            "description": "Atherosclerosis, deafness, diabetes, epilepsy, nephropathy syndrome",
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            "code": "720522001",
            "description": "Autosomal recessive limb girdle muscular dystrophy type 2G",
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          {
            "code": "720523006",
            "description": "Autosomal recessive limb girdle muscular dystrophy type 2K",
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          {
            "code": "720576001",
            "description": "Brain calcification Rajab type",
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          {
            "code": "720626009",
            "description": "Dissection of carotid artery",
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          {
            "code": "720632004",
            "description": "Central bilateral macrogyria",
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          {
            "code": "720637005",
            "description": "Charcot-Marie-Tooth disease type 2H",
            "attributes": null
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          {
            "code": "720638000",
            "description": "Charcot-Marie-Tooth disease type 4J",
            "attributes": null
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          {
            "code": "720750004",
            "description": "Spinocerebellar degeneration and corneal dystrophy syndrome",
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            "code": "720809000",
            "description": "Dissection of external carotid artery",
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            "code": "720813007",
            "description": "Craniosynostosis with Dandy-Walker malformation and hydrocephalus syndrome",
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          {
            "code": "720815000",
            "description": "Capra DeMarco syndrome",
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          {
            "code": "720816004",
            "description": "Craniosynostosis and intracranial calcification syndrome",
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          {
            "code": "720819006",
            "description": "Curry Jones syndrome",
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            "code": "720825005",
            "description": "Cystic leukoencephalopathy without megalencephaly",
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          {
            "code": "720830009",
            "description": "Neuronal ceroid lipofuscinosis due to deficiency of cathepsin D",
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            "code": "720852000",
            "description": "Cervical hypertrichosis and peripheral neuropathy syndrome",
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          {
            "code": "720855003",
            "description": "Cerebrooculonasal syndrome",
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            "code": "720864008",
            "description": "Encephalopathy due to prosaposin deficiency",
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          {
            "code": "720954000",
            "description": "Filippi syndrome",
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          {
            "code": "721008000",
            "description": "Hall Riggs syndrome",
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            "code": "721015008",
            "description": "Hydrocephalus with endocardial fibroelastosis and cataract syndrome",
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            "code": "72103000",
            "description": "Simple partial seizure with special sensory symptoms",
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            "code": "721072003",
            "description": "Short stature, pituitary and cerebellar defect and small sella turcica syndrome",
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            "code": "721088003",
            "description": "Developmental delay, epilepsy, neonatal diabetes syndrome",
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            "code": "721092005",
            "description": "Developmental malformation, deafness, dystonia syndrome",
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            "code": "721165001",
            "description": "Variably protease sensitive prionopathy",
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          {
            "code": "721207002",
            "description": "Seizure, sensorineural deafness, ataxia, intellectual disability, electrolyte imbalance syndrome",
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          {
            "code": "721211008",
            "description": "Encephalopathy caused by methylmercury",
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          {
            "code": "721219005",
            "description": "Familial Alzheimer-like prion disease",
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          {
            "code": "721221000",
            "description": "Hirschsprung disease with deafness and polydactyly syndrome",
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          {
            "code": "721222007",
            "description": "Hirschsprung disease with type D brachydactyly syndrome",
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          {
            "code": "721223002",
            "description": "Hirschsprung disease with nail hypoplasia and dysmorphism",
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            "code": "721228006",
            "description": "Huntington disease-like 2",
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            "code": "721229003",
            "description": "Hydrocephalus, costovertebral dysplasia, Sprengel anomaly syndrome",
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          {
            "code": "721231007",
            "description": "Hydrocephalus with obesity and hypogonadism syndrome",
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            "code": "721244002",
            "description": "Infection causing myelitis",
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            "code": "721245001",
            "description": "Myelitis caused by bacterium",
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          {
            "code": "721246000",
            "description": "Myelitis caused by fungus",
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          {
            "code": "721247009",
            "description": "Parasitic infection causing myelitis",
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          {
            "code": "721248004",
            "description": "Myelitis caused by virus",
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          {
            "code": "721249007",
            "description": "Infection causing encephalomyelitis",
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            "code": "721250007",
            "description": "Abscess of spinal cord caused by bacterium",
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            "code": "721255002",
            "description": "Acquired prion disease",
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            "code": "721288009",
            "description": "Hypopituitarism following procedure",
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          {
            "code": "721297008",
            "description": "Galloway Mowat syndrome",
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            "code": "721330006",
            "description": "Diffuse injury of cerebrum",
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          {
            "code": "721331005",
            "description": "Diffuse injury of cerebellum",
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            "code": "721332003",
            "description": "Diffuse injury of brainstem",
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            "code": "721333008",
            "description": "Crush injury of brain",
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            "description": "Complete lesion of cervical spinal cord",
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            "code": "721363004",
            "description": "Complete lesion of spinal cord at first cervical level",
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            "code": "721364005",
            "description": "Complete lesion of spinal cord at second cervical level",
            "attributes": null
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          {
            "code": "721365006",
            "description": "Complete lesion of spinal cord at third cervical level",
            "attributes": null
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          {
            "code": "721366007",
            "description": "Complete lesion of spinal cord at fourth cervical level",
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          {
            "code": "721367003",
            "description": "Complete lesion of spinal cord at fifth cervical level",
            "attributes": null
          },
          {
            "code": "721368008",
            "description": "Complete lesion of spinal cord at sixth cervical level",
            "attributes": null
          },
          {
            "code": "721369000",
            "description": "Complete lesion of spinal cord at seventh cervical level",
            "attributes": null
          },
          {
            "code": "721370004",
            "description": "Complete lesion of spinal cord at eighth cervical level",
            "attributes": null
          },
          {
            "code": "721371000",
            "description": "Central cord syndrome of cervical spinal cord",
            "attributes": null
          },
          {
            "code": "721372007",
            "description": "Central cord syndrome of spinal cord at first cervical level",
            "attributes": null
          },
          {
            "code": "721373002",
            "description": "Central cord syndrome of spinal cord at second cervical level",
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          },
          {
            "code": "721374008",
            "description": "Central cord syndrome of spinal cord at third cervical level",
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          {
            "code": "721375009",
            "description": "Central cord syndrome of spinal cord at fourth cervical level",
            "attributes": null
          },
          {
            "code": "721376005",
            "description": "Central cord syndrome of spinal cord at fifth cervical level",
            "attributes": null
          },
          {
            "code": "721377001",
            "description": "Central cord syndrome of spinal cord at sixth cervical level",
            "attributes": null
          },
          {
            "code": "721378006",
            "description": "Central cord syndrome of spinal cord at seventh cervical level",
            "attributes": null
          },
          {
            "code": "721379003",
            "description": "Central cord syndrome of spinal cord at eighth cervical level",
            "attributes": null
          },
          {
            "code": "721380000",
            "description": "Anterior cord syndrome of cervical spinal cord",
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          },
          {
            "code": "721381001",
            "description": "Anterior cord syndrome of spinal cord at first cervical level",
            "attributes": null
          },
          {
            "code": "721382008",
            "description": "Anterior cord syndrome of spinal cord at second cervical level",
            "attributes": null
          },
          {
            "code": "721383003",
            "description": "Anterior cord syndrome of spinal cord at third cervical level",
            "attributes": null
          },
          {
            "code": "721384009",
            "description": "Anterior cord syndrome of spinal cord at fourth cervical level",
            "attributes": null
          },
          {
            "code": "721385005",
            "description": "Anterior cord syndrome of spinal cord at fifth cervical level",
            "attributes": null
          },
          {
            "code": "721386006",
            "description": "Anterior cord syndrome of spinal cord at sixth cervical level",
            "attributes": null
          },
          {
            "code": "721387002",
            "description": "Anterior cord syndrome of spinal cord at seventh cervical level",
            "attributes": null
          },
          {
            "code": "721388007",
            "description": "Anterior cord syndrome of spinal cord at eighth cervical level",
            "attributes": null
          },
          {
            "code": "721389004",
            "description": "Posterior cord syndrome of cervical spinal cord",
            "attributes": null
          },
          {
            "code": "721390008",
            "description": "Posterior cord syndrome of spinal cord at first cervical level",
            "attributes": null
          },
          {
            "code": "721391007",
            "description": "Posterior cord syndrome of spinal cord at second cervical level",
            "attributes": null
          },
          {
            "code": "721392000",
            "description": "Posterior cord syndrome of spinal cord at third cervical level",
            "attributes": null
          },
          {
            "code": "721393005",
            "description": "Posterior cord syndrome of spinal cord at fourth cervical level",
            "attributes": null
          },
          {
            "code": "721394004",
            "description": "Posterior cord syndrome of spinal cord at fifth cervical level",
            "attributes": null
          },
          {
            "code": "721395003",
            "description": "Posterior cord syndrome of spinal cord at sixth cervical level",
            "attributes": null
          },
          {
            "code": "721396002",
            "description": "Posterior cord syndrome of spinal cord at seventh cervical level",
            "attributes": null
          },
          {
            "code": "721397006",
            "description": "Posterior cord syndrome of spinal cord at eighth cervical level",
            "attributes": null
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          {
            "code": "721398001",
            "description": "Brown-Sequard syndrome of cervical spinal cord",
            "attributes": null
          },
          {
            "code": "721399009",
            "description": "Brown-Sequard syndrome at first cervical level",
            "attributes": null
          },
          {
            "code": "721400002",
            "description": "Brown-Sequard syndrome at second cervical level",
            "attributes": null
          },
          {
            "code": "721401003",
            "description": "Brown-Sequard syndrome at third cervical level",
            "attributes": null
          },
          {
            "code": "721402005",
            "description": "Brown-Sequard syndrome at fourth cervical level",
            "attributes": null
          },
          {
            "code": "721403000",
            "description": "Brown-Sequard syndrome at fifth cervical level",
            "attributes": null
          },
          {
            "code": "721404006",
            "description": "Brown-Sequard syndrome at sixth cervical level",
            "attributes": null
          },
          {
            "code": "721405007",
            "description": "Brown-Sequard syndrome at seventh cervical level",
            "attributes": null
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          {
            "code": "721406008",
            "description": "Brown-Sequard syndrome at eighth cervical level",
            "attributes": null
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          {
            "code": "721428008",
            "description": "Injury of thoracic spinal cord",
            "attributes": null
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          {
            "code": "721429000",
            "description": "Complete lesion of thoracic spinal cord",
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          {
            "code": "721430005",
            "description": "Complete lesion of spinal cord at first thoracic level",
            "attributes": null
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          {
            "code": "721431009",
            "description": "Complete lesion of spinal cord at second thoracic level",
            "attributes": null
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          {
            "code": "721432002",
            "description": "Complete lesion of spinal cord at third thoracic level",
            "attributes": null
          },
          {
            "code": "721433007",
            "description": "Complete lesion of spinal cord at fourth thoracic level",
            "attributes": null
          },
          {
            "code": "721434001",
            "description": "Complete lesion of spinal cord at fifth thoracic level",
            "attributes": null
          },
          {
            "code": "721435000",
            "description": "Complete lesion of spinal cord at sixth thoracic level",
            "attributes": null
          },
          {
            "code": "721436004",
            "description": "Complete lesion of spinal cord at seventh thoracic level",
            "attributes": null
          },
          {
            "code": "721437008",
            "description": "Complete lesion of spinal cord at eighth thoracic level",
            "attributes": null
          },
          {
            "code": "721438003",
            "description": "Complete lesion of spinal cord at ninth thoracic level",
            "attributes": null
          },
          {
            "code": "721439006",
            "description": "Complete lesion of spinal cord at tenth thoracic level",
            "attributes": null
          },
          {
            "code": "721440008",
            "description": "Complete lesion of spinal cord at eleventh thoracic level",
            "attributes": null
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          {
            "code": "721441007",
            "description": "Complete lesion of spinal cord at twelfth thoracic level",
            "attributes": null
          },
          {
            "code": "721442000",
            "description": "Central cord syndrome of thoracic spinal cord",
            "attributes": null
          },
          {
            "code": "721443005",
            "description": "Central cord syndrome of spinal cord at first thoracic level",
            "attributes": null
          },
          {
            "code": "721444004",
            "description": "Central cord syndrome of spinal cord at second thoracic level",
            "attributes": null
          },
          {
            "code": "721445003",
            "description": "Central cord syndrome of spinal cord at third thoracic level",
            "attributes": null
          },
          {
            "code": "721446002",
            "description": "Central cord syndrome of spinal cord at fourth thoracic level",
            "attributes": null
          },
          {
            "code": "721447006",
            "description": "Central cord syndrome of spinal cord at fifth thoracic level",
            "attributes": null
          },
          {
            "code": "721448001",
            "description": "Central cord syndrome of spinal cord at sixth thoracic level",
            "attributes": null
          },
          {
            "code": "721449009",
            "description": "Central cord syndrome of spinal cord at seventh thoracic level",
            "attributes": null
          },
          {
            "code": "721450009",
            "description": "Central cord syndrome of spinal cord at eighth thoracic level",
            "attributes": null
          },
          {
            "code": "721451008",
            "description": "Central cord syndrome of spinal cord at ninth thoracic level",
            "attributes": null
          },
          {
            "code": "721452001",
            "description": "Central cord syndrome of spinal cord at tenth thoracic level",
            "attributes": null
          },
          {
            "code": "721453006",
            "description": "Central cord syndrome of spinal cord at eleventh thoracic level",
            "attributes": null
          },
          {
            "code": "721454000",
            "description": "Central cord syndrome of spinal cord at twelfth thoracic level",
            "attributes": null
          },
          {
            "code": "721455004",
            "description": "Anterior cord syndrome of thoracic spinal cord",
            "attributes": null
          },
          {
            "code": "721456003",
            "description": "Anterior cord syndrome of spinal cord at first thoracic level",
            "attributes": null
          },
          {
            "code": "721457007",
            "description": "Anterior cord syndrome of spinal cord at second thoracic level",
            "attributes": null
          },
          {
            "code": "721458002",
            "description": "Anterior cord syndrome of spinal cord at third thoracic level",
            "attributes": null
          },
          {
            "code": "721459005",
            "description": "Anterior cord syndrome of spinal cord at fourth thoracic level",
            "attributes": null
          },
          {
            "code": "721460000",
            "description": "Anterior cord syndrome of spinal cord at fifth thoracic level",
            "attributes": null
          },
          {
            "code": "721461001",
            "description": "Anterior cord syndrome of spinal cord at sixth thoracic level",
            "attributes": null
          },
          {
            "code": "721462008",
            "description": "Anterior cord syndrome of spinal cord at seventh thoracic level",
            "attributes": null
          },
          {
            "code": "721463003",
            "description": "Anterior cord syndrome of spinal cord at eighth thoracic level",
            "attributes": null
          },
          {
            "code": "721464009",
            "description": "Anterior cord syndrome of spinal cord at ninth thoracic level",
            "attributes": null
          },
          {
            "code": "721465005",
            "description": "Anterior cord syndrome of spinal cord at tenth thoracic level",
            "attributes": null
          },
          {
            "code": "721466006",
            "description": "Anterior cord syndrome of spinal cord at eleventh thoracic level",
            "attributes": null
          },
          {
            "code": "721467002",
            "description": "Anterior cord syndrome of spinal cord at twelfth thoracic level",
            "attributes": null
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          {
            "code": "721468007",
            "description": "Posterior cord syndrome of thoracic spinal cord",
            "attributes": null
          },
          {
            "code": "721469004",
            "description": "Posterior cord syndrome of spinal cord at first thoracic level",
            "attributes": null
          },
          {
            "code": "721470003",
            "description": "Posterior cord syndrome of spinal cord at second thoracic level",
            "attributes": null
          },
          {
            "code": "721471004",
            "description": "Posterior cord syndrome of spinal cord at third thoracic level",
            "attributes": null
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          {
            "code": "721472006",
            "description": "Posterior cord syndrome of spinal cord at fourth thoracic level",
            "attributes": null
          },
          {
            "code": "721473001",
            "description": "Posterior cord syndrome of spinal cord at fifth thoracic level",
            "attributes": null
          },
          {
            "code": "721474007",
            "description": "Posterior cord syndrome of spinal cord at sixth thoracic level",
            "attributes": null
          },
          {
            "code": "721475008",
            "description": "Posterior cord syndrome of spinal cord at seventh thoracic level",
            "attributes": null
          },
          {
            "code": "721476009",
            "description": "Posterior cord syndrome of spinal cord at eighth thoracic level",
            "attributes": null
          },
          {
            "code": "721477000",
            "description": "Posterior cord syndrome of spinal cord at ninth thoracic level",
            "attributes": null
          },
          {
            "code": "721478005",
            "description": "Posterior cord syndrome of spinal cord at tenth thoracic level",
            "attributes": null
          },
          {
            "code": "721479002",
            "description": "Posterior cord syndrome of spinal cord at eleventh thoracic level",
            "attributes": null
          },
          {
            "code": "721480004",
            "description": "Posterior cord syndrome of spinal cord at twelfth thoracic level",
            "attributes": null
          },
          {
            "code": "721481000",
            "description": "Brown-Séquard syndrome of thoracic spinal cord",
            "attributes": null
          },
          {
            "code": "721482007",
            "description": "Brown-Séquard syndrome at first thoracic level",
            "attributes": null
          },
          {
            "code": "721483002",
            "description": "Brown-Séquard syndrome at second thoracic level",
            "attributes": null
          },
          {
            "code": "721484008",
            "description": "Brown-Séquard syndrome at third thoracic level",
            "attributes": null
          },
          {
            "code": "721485009",
            "description": "Brown-Séquard syndrome at fourth thoracic level",
            "attributes": null
          },
          {
            "code": "721486005",
            "description": "Brown-Séquard syndrome at fifth thoracic level",
            "attributes": null
          },
          {
            "code": "721487001",
            "description": "Brown-Séquard syndrome at sixth thoracic level",
            "attributes": null
          },
          {
            "code": "721488006",
            "description": "Brown-Séquard syndrome at seventh thoracic level",
            "attributes": null
          },
          {
            "code": "721489003",
            "description": "Brown-Séquard syndrome at eighth thoracic level",
            "attributes": null
          },
          {
            "code": "721490007",
            "description": "Brown-Séquard syndrome at ninth thoracic level",
            "attributes": null
          },
          {
            "code": "721491006",
            "description": "Brown-Séquard syndrome at tenth thoracic level",
            "attributes": null
          },
          {
            "code": "721492004",
            "description": "Brown-Séquard syndrome at eleventh thoracic level",
            "attributes": null
          },
          {
            "code": "721493009",
            "description": "Brown-Séquard syndrome at twelfth thoracic level",
            "attributes": null
          },
          {
            "code": "721499008",
            "description": "Complete lesion of lumbar spinal cord",
            "attributes": null
          },
          {
            "code": "721500004",
            "description": "Complete lesion of spinal cord at first lumbar level",
            "attributes": null
          },
          {
            "code": "721501000",
            "description": "Complete lesion of spinal cord at second lumbar level",
            "attributes": null
          },
          {
            "code": "721502007",
            "description": "Complete lesion of spinal cord at third lumbar level",
            "attributes": null
          },
          {
            "code": "721503002",
            "description": "Complete lesion of spinal cord at fourth lumbar level",
            "attributes": null
          },
          {
            "code": "721504008",
            "description": "Complete lesion of spinal cord at fifth lumbar level",
            "attributes": null
          },
          {
            "code": "721505009",
            "description": "Central cord syndrome of lumbar spinal cord",
            "attributes": null
          },
          {
            "code": "721506005",
            "description": "Central cord syndrome of spinal cord at first lumbar level",
            "attributes": null
          },
          {
            "code": "721507001",
            "description": "Central cord syndrome of spinal cord at second lumbar level",
            "attributes": null
          },
          {
            "code": "721508006",
            "description": "Central cord syndrome of spinal cord at third lumbar level",
            "attributes": null
          },
          {
            "code": "721509003",
            "description": "Central cord syndrome of spinal cord at fourth lumbar level",
            "attributes": null
          },
          {
            "code": "721510008",
            "description": "Central cord syndrome of spinal cord at fifth lumbar level",
            "attributes": null
          },
          {
            "code": "721511007",
            "description": "Anterior cord syndrome of lumbar spinal cord",
            "attributes": null
          },
          {
            "code": "721512000",
            "description": "Anterior cord syndrome of spinal cord at first lumbar level",
            "attributes": null
          },
          {
            "code": "721513005",
            "description": "Anterior cord syndrome of spinal cord at second lumbar level",
            "attributes": null
          },
          {
            "code": "721514004",
            "description": "Anterior cord syndrome of spinal cord at third lumbar level",
            "attributes": null
          },
          {
            "code": "721515003",
            "description": "Anterior cord syndrome of spinal cord at fourth lumbar level",
            "attributes": null
          },
          {
            "code": "721516002",
            "description": "Anterior cord syndrome of spinal cord at fifth lumbar level",
            "attributes": null
          },
          {
            "code": "721517006",
            "description": "Posterior cord syndrome of lumbar spinal cord",
            "attributes": null
          },
          {
            "code": "721518001",
            "description": "Posterior cord syndrome of spinal cord at first lumbar level",
            "attributes": null
          },
          {
            "code": "721519009",
            "description": "Posterior cord syndrome of spinal cord at second lumbar level",
            "attributes": null
          },
          {
            "code": "721520003",
            "description": "Posterior cord syndrome of spinal cord at third lumbar level",
            "attributes": null
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          {
            "code": "721521004",
            "description": "Posterior cord syndrome of spinal cord at fourth lumbar level",
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            "code": "721522006",
            "description": "Posterior cord syndrome of spinal cord at fifth lumbar level",
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            "code": "721523001",
            "description": "Brown-Séquard syndrome of lumbar spinal cord",
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            "code": "721524007",
            "description": "Brown-Séquard syndrome at first lumbar level",
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            "code": "721525008",
            "description": "Brown-Séquard syndrome at second lumbar level",
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            "code": "721526009",
            "description": "Brown-Séquard syndrome at third lumbar level",
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            "code": "721527000",
            "description": "Brown-Séquard syndrome at fourth lumbar level",
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            "code": "721528005",
            "description": "Brown-Séquard syndrome at fifth lumbar level",
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            "code": "721529002",
            "description": "Complete injury of sacral spinal cord",
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            "code": "721535002",
            "description": "Central neurocytoma of brain",
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            "code": "721766005",
            "description": "Encephalitis caused by Alphavirus",
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            "code": "721776008",
            "description": "Encephalitis caused by Polyoma virus",
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            "code": "721788005",
            "description": "Encephalitis caused by Rubulavirus",
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            "code": "721790006",
            "description": "Encephalitis caused by Hendra virus",
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            "code": "721791005",
            "description": "Encephalitis caused by Nipah virus",
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            "code": "721815007",
            "description": "Encephalitis caused by Trypanosoma brucei",
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            "code": "721818009",
            "description": "Encephalitis caused by Schistosoma",
            "attributes": null
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            "code": "721819001",
            "description": "Encephalitis caused by Schistosoma haematobium",
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            "code": "721820007",
            "description": "Encephalitis caused by Schistosoma mansoni",
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            "code": "721821006",
            "description": "Encephalitis caused by Schistosoma japonicum",
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            "code": "721823009",
            "description": "Encephalitis caused by Echinococcus granulosus",
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            "code": "721825002",
            "description": "Encephalitis caused by Taenia solium",
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            "code": "721826001",
            "description": "Encephalitis caused by Coenurus cerebralis",
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            "code": "721842008",
            "description": "Hypogonadotropic hypogonadism with frontoparietal alopecia syndrome",
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            "code": "721846006",
            "description": "Hypomyelination, hypogonadotropic hypogonadism, hypodontia syndrome",
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            "code": "721847002",
            "description": "Joubert syndrome with congenital hepatic fibrosis",
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            "code": "721862000",
            "description": "Joubert syndrome with oculorenal defect",
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            "code": "721873007",
            "description": "Joubert syndrome with orofaciodigital defect",
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            "code": "721903007",
            "description": "Microcephaly, hypogammaglobulinemia, abnormal immunity syndrome",
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            "code": "721974000",
            "description": "Lowry MacLean syndrome",
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            "code": "721975004",
            "description": "Epiphyseal dysplasia, microcephalus, nystagmus syndrome",
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            "code": "721979005",
            "description": "Lymphedema and cerebral arteriovenous anomaly syndrome",
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            "code": "722004001",
            "description": "Agenesis of internal carotid artery",
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            "code": "722006004",
            "description": "Isotretinoin embryopathy-like syndrome",
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            "code": "722033000",
            "description": "Macrocephaly, short stature, paraplegia syndrome",
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            "code": "722036008",
            "description": "Megalencephaly, polymicrogyria, postaxial polydactyly, hydrocephalus syndrome",
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            "code": "722055008",
            "description": "Oculopalatocerebral syndrome",
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            "code": "722056009",
            "description": "Oculocerebrofacial syndrome Kaufman type",
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            "code": "722064003",
            "description": "Odontoleukodystrophy",
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            "code": "722110003",
            "description": "Osteogenesis imperfecta, retinopathy, seizures, intellectual disability syndrome",
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            "code": "722201004",
            "description": "Median cleft of upper lip, corpus callosum lipoma, cutaneous polyp syndrome",
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            "code": "722209002",
            "description": "Spastic paraplegia, intellectual disability, palmoplantar hyperkeratosis syndrome",
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            "code": "722212004",
            "description": "Severe X-linked mitochondrial encephalomyopathy",
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            "code": "722281001",
            "description": "Agammaglobulinemia, microcephaly, craniosynostosis, severe dermatitis syndrome",
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            "code": "722282008",
            "description": "Agenesis of corpus callosum, intellectual disability, coloboma, micrognathia syndrome",
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            "code": "722283003",
            "description": "Agnathia, holoprosencephaly, situs inversus syndrome",
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            "code": "722293005",
            "description": "Autosomal dominant cerebellar ataxia, deafness and narcolepsy syndrome",
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            "code": "722294004",
            "description": "Autosomal dominant intermediate Charcot-Marie-Tooth disease type E",
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            "code": "722377004",
            "description": "Paraganglioma and gastric stromal sarcoma syndrome",
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            "description": "Congenital cataract with intellectual disability and hypogonadotropic hypogonadism syndrome",
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            "code": "722381004",
            "description": "Congenital cataract, nephropathy, encephalopathy syndrome",
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            "description": "Cerebral dysgenesis, neuropathy, ichthyosis, palmoplantar keratoderma syndrome",
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            "description": "Celiac disease with epilepsy and cerebral calcification syndrome",
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            "description": "Congenital hereditary facial paralysis with variable hearing loss syndrome",
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            "code": "722390006",
            "description": "Congenital intrauterine infection-like syndrome",
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            "code": "722432000",
            "description": "Duane anomaly, myopathy, scoliosis syndrome",
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            "code": "722435003",
            "description": "Dystonia 16",
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            "code": "722451006",
            "description": "Gomez Lopez Hernandez syndrome",
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            "code": "722453009",
            "description": "Cutaneous mastocytosis, short stature, hearing loss syndrome",
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            "code": "722455002",
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            "code": "722456001",
            "description": "Intellectual disability, developmental delay, contracture syndrome",
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            "code": "722488009",
            "description": "Neurodegeneration due to 3-hydroxyisobutyryl coenzyme A hydrolase deficiency",
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            "code": "722493007",
            "description": "Familial caudal dysgenesis",
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            "code": "722556003",
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            "code": "722557007",
            "description": "Parkinsonism due to human immunodeficiency virus infection",
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            "code": "722558002",
            "description": "Parkinsonism following infection",
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            "code": "722576009",
            "description": "Injury of brain stem due to birth trauma",
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            "code": "722599008",
            "description": "Parkinsonism due to hereditary spastic paraplegia",
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            "code": "722600006",
            "description": "Non-amnestic Alzheimer disease",
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            "code": "722601005",
            "description": "White matter disorder caused by infection",
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            "code": "722602003",
            "description": "White matter disorder caused by toxin",
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            "code": "722614006",
            "description": "Focal non-hemorrhagic contusion of cerebrum",
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            "code": "722615007",
            "description": "Focal hemorrhagic contusion of cerebrum",
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            "code": "722616008",
            "description": "Focal laceration of cerebrum",
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            "description": "Multiple focal injuries of cerebrum",
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            "code": "722618009",
            "description": "Focal non-hemorrhagic contusion of cerebellum",
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            "code": "722622004",
            "description": "Focal non-hemorrhagic contusion of brainstem",
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            "code": "722625002",
            "description": "Focal laceration of brainstem",
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            "code": "722626001",
            "description": "Multiple focal injuries of cerebellum",
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            "code": "722627005",
            "description": "Focal injury of brainstem",
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            "code": "722633001",
            "description": "Multiple traumatic hemorrhages of brain tissue",
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            "code": "722653002",
            "description": "Injury of lumbar spinal cord",
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            "description": "Incomplete injury of sacral spinal cord",
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            "code": "722660008",
            "description": "Radiation injury of brain caused by ionizing radiation following radiotherapy procedure",
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            "description": "Metastatic malignant neoplasm of meninges",
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            "description": "Focal laceration of cerebellum",
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            "code": "722718001",
            "description": "Primary malignant meningioma",
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            "code": "722762005",
            "description": "Ganglioside GM3 synthase deficiency",
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            "code": "722763000",
            "description": "Infantile dystonia parkinsonism",
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            "code": "722907006",
            "description": "Contusion of cerebellum due to birth trauma",
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            "code": "722908001",
            "description": "Contusion of brain due to birth trauma",
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            "code": "722914008",
            "description": "Central neonatal apnea",
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            "code": "722929005",
            "description": "Perinatal arterial ischemic stroke",
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            "code": "722931001",
            "description": "Neonatal compression of brain",
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            "code": "722943000",
            "description": "Macroprolactinemia",
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            "code": "722944006",
            "description": "Congenital hypogonadotropic hypogonadism",
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            "description": "Delirium caused by substance or medication",
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            "code": "722962002",
            "description": "Amnestic disorder caused by substance",
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            "code": "722964001",
            "description": "Atypical Parkinsonism",
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            "code": "722965000",
            "description": "Parkinsonism due to heredodegenerative disorder",
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            "code": "722966004",
            "description": "Chorea due to heredodegenerative disorder",
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            "code": "722967008",
            "description": "Ataxia due to mitochondrial mutations",
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            "code": "722968003",
            "description": "Acquired ataxia",
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            "code": "722969006",
            "description": "Tremor due to metabolic disorder",
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            "code": "722970007",
            "description": "Tremor due to substance abuse",
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            "description": "Secondary tic disorder",
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            "code": "722973009",
            "description": "Tic due to developmental disorder",
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            "code": "722974003",
            "description": "Segmental myoclonus",
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            "description": "Dementia co-occurrent and due to neurocysticercosis",
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            "code": "722978000",
            "description": "Dementia caused by toxin",
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            "code": "722979008",
            "description": "Dementia due to metabolic abnormality",
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            "description": "Dementia due to chromosomal anomaly",
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            "description": "Infrequent episodic tension-type headache",
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            "description": "Frequent episodic tension-type headache",
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            "code": "722984002",
            "description": "Myelopathy due to metabolic disorder",
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            "description": "Acute venous infarction of spinal cord",
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            "description": "Chronic venous infarction of spinal cord",
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            "description": "Amyotrophic lateral sclerosis plus syndrome",
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            "description": "Concussion of sacral spinal cord",
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            "description": "Inherited autonomic nervous system disorder",
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            "description": "Silent cerebral infarct",
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            "description": "Late effects of cerebral ischemic stroke",
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            "description": "Sequela of non-traumatic intracerebral hemorrhage",
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            "description": "Primary tic disorder",
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            "description": "Ischemic vascular dementia",
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            "description": "Primary progressive apraxia of speech",
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            "description": "Epileptic encephalopathy",
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            "description": "Spinal cord compression due to degenerative disorder of spinal column",
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            "description": "Crush injury of brain without coma",
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            "description": "Permanent vegetative state",
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            "description": "Injury of spinal cord caused by ionizing radiation following radiotherapy procedure",
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            "description": "Flaccid diplegia of upper limbs",
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            "description": "Spastic diplegia of upper limbs",
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            "description": "Diplegia of lower limbs",
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            "description": "Microcephaly, seizure, intellectual disability, heart disease syndrome",
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            "description": "Facial onset sensory and motor neuronopathy syndrome",
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            "description": "Ethylmalonic encephalopathy",
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            "description": "Epidermolysis bullosa simplex with muscular dystrophy",
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            "description": "Endocrine-cerebro-osteodysplasia syndrome",
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            "description": "Familial acute necrotizing encephalopathy",
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            "description": "Rapidly progressive dementia",
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            "description": "Microcephalic osteodysplastic dysplasia Saul Wilson type",
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            "code": "723405001",
            "description": "Microlissencephaly micromelia syndrome",
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            "description": "Non-progressive cerebellar ataxia with intellectual disability",
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            "description": "Polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract syndrome",
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            "description": "Peripheral neuropathy with sensorineural hearing impairment syndrome",
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          {
            "code": "723501008",
            "description": "Renier Gabreels Jasper syndrome",
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            "code": "723557004",
            "description": "Thiamine-responsive encephalopathy",
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            "description": "Spinal muscular atrophy, Dandy-Walker malformation, cataract syndrome",
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            "description": "Spastic tetraplegia, retinitis pigmentosa, intellectual disability syndrome",
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            "description": "Sialidosis type 1",
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            "description": "Severe intellectual disability, epilepsy, anal anomaly, distal phalangeal hypoplasia syndrome",
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            "description": "Autosomal dominant spastic paraplegia type 36",
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            "code": "723820001",
            "description": "Autosomal dominant spastic paraplegia type 4",
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            "code": "723821002",
            "description": "Autosomal recessive spastic paraplegia type 44",
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            "code": "723822009",
            "description": "Autosomal recessive spastic paraplegia type 46",
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            "description": "Autosomal recessive spastic paraplegia type 53",
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            "code": "723824005",
            "description": "Autosomal recessive spastic paraplegia type 54",
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            "description": "Keratosis follicularis, dwarfism, cerebral atrophy syndrome",
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            "description": "Silent micro-hemorrhage of brain",
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            "description": "Psychotic disorder caused by alcohol with schizophreniform symptoms",
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            "description": "Mood disorder with depressive symptoms caused by alcohol",
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            "description": "Mood disorder with manic symptoms caused by alcohol",
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            "description": "Mood disorder with mixed manic and depressive symptoms caused by alcohol",
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            "description": "Psychotic disorder caused by cannabis",
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            "description": "Sleep disorder caused by cannabis",
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            "description": "Kufor Rakeb syndrome",
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            "description": "Retinitis pigmentosa, hypopituitarism, nephronophthisis, skeletal dysplasia syndrome",
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            "description": "Retinal ischemia, digestive tract small vessel hyalinosis, diffuse cerebral calcification syndrome",
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            "description": "Autosomal recessive posterior column ataxia and retinitis pigmentosa",
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            "description": "Permanent neonatal diabetes mellitus with cerebellar agenesis syndrome",
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            "description": "Neuroectodermal melanolysosomal disease",
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            "description": "Moyamoya angiopathy, short stature, facial dysmorphism, hypergonadotropic hypogonadism syndrome",
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            "description": "Microcephalic primordial dwarfism due to zinc finger protein 335 deficiency",
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            "description": "McLeod neuroacanthocytosis syndrome",
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            "description": "Moebius syndrome, axonal neuropathy, hypogonadotropic hypogonadism syndrome",
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            "description": "Kleefstra syndrome",
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            "description": "Infantile osteopetrosis with neuroaxonal dysplasia syndrome",
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            "code": "724227000",
            "description": "Infantile onset spinocerebellar ataxia",
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            "code": "724228005",
            "description": "Infantile choroidocerebral calcification syndrome",
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            "code": "724281002",
            "description": "Hyposmia, nasal and ocular hypoplasia, hypogonadotropic hypogonadism syndrome",
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            "code": "724283004",
            "description": "Hypomyelinating leukodystrophy with atrophy of basal ganglia and cerebellum",
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            "code": "724351008",
            "description": "Hereditary hyperekplexia",
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            "code": "724357007",
            "description": "Hereditary cerebral hemorrhage with amyloidosis",
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            "code": "724383002",
            "description": "Hemidystonia hemiatrophy syndrome",
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            "code": "724385009",
            "description": "Growth delay due to insulin-like growth factor type 1 deficiency",
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            "code": "72442006",
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            "code": "724424009",
            "description": "Cerebral ischemic stroke due to small artery occlusion",
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            "code": "724425005",
            "description": "Cerebral ischemic stroke due to intracranial large artery atherosclerosis",
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            "description": "Cerebral ischemic stroke due to extracranial large artery atherosclerosis",
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            "description": "Asymptomatic stenosis of intracranial artery",
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            "description": "Asymptomatic stenosis of extracranial artery",
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            "description": "Stroke co-occurrent with migraine",
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            "description": "Late-onset central hypoventilation co-occurrent and due to hypothalamic dysfunction",
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            "code": "724542001",
            "description": "Encephalitis caused by Venezuelan equine encephalomyelitis virus",
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            "code": "724543006",
            "description": "Infection causing multiple abscesses of brain",
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            "code": "724544000",
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            "description": "Tic due to and following infection",
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            "code": "724546003",
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            "description": "Epilepsy due to infectious disease of central nervous system",
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            "code": "724561002",
            "description": "Encephalopathy due to nutritional deficiency",
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            "code": "724562009",
            "description": "Myelopathy due to nutritional deficiency",
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            "code": "724565006",
            "description": "White matter disorder due to nutritional deficiency",
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            "description": "Pyridoxal 5-phosphate dependent epilepsy",
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            "code": "724643004",
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            "description": "Myeloid leukemia co-occurrent with Down syndrome",
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            "description": "Psychotic disorder caused by hypnotic",
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            "description": "Psychotic disorder caused by anxiolytic",
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            "code": "724679007",
            "description": "Mood disorder with manic symptoms caused by sedative",
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            "code": "724680005",
            "description": "Mood disorder with manic symptoms caused by hypnotic",
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            "description": "Mood disorder with manic symptoms caused by anxiolytic",
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            "description": "Mood disorder with mixed depressive and manic symptoms caused by sedative",
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            "code": "724683007",
            "description": "Mood disorder with mixed depressive and manic symptoms caused by hypnotic",
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            "description": "Mood disorder with mixed depressive and manic symptoms caused by anxiolytic",
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            "description": "Amnestic disorder caused by sedative",
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            "description": "Amnestic disorder caused by hypnotic",
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            "code": "724687008",
            "description": "Amnestic disorder caused by anxiolytic",
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            "code": "724689006",
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            "code": "724690002",
            "description": "Mood disorder with depressive symptoms caused by cocaine",
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            "description": "Obsessive compulsive disorder caused by cocaine",
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            "description": "Psychotic disorder caused by volatile inhalant",
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            "code": "724705005",
            "description": "Delirium caused by methylenedioxymethamphetamine",
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            "code": "724706006",
            "description": "Psychotic disorder caused by methylenedioxymethamphetamine",
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            "code": "724707002",
            "description": "Mood disorder caused by methylenedioxymethamphetamine",
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            "description": "Anxiety disorder caused by methylenedioxymethamphetamine",
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            "code": "724716003",
            "description": "Delirium caused by ketamine",
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            "code": "724717007",
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            "code": "724718002",
            "description": "Psychotic disorder caused by dissociative drug",
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            "code": "724719005",
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            "code": "724720004",
            "description": "Mood disorder caused by dissociative drug",
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            "code": "724721000",
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            "code": "724722007",
            "description": "Anxiety disorder caused by dissociative drug",
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            "code": "724766009",
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            "code": "724786008",
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            "description": "Epilepsy due to cerebrovascular accident",
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            "description": "Charcot-Marie-Tooth disease type 2B1",
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            "description": "Autosomal recessive cerebellar ataxia with oculomotor apraxia type 2",
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            "description": "Congenital muscular dystrophy Paradas type",
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            "code": "725433003",
            "description": "Autosomal recessive cerebellar ataxia Beauce type",
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            "description": "Autosomal recessive limb girdle muscular dystrophy type 2Y",
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            "description": "Myotonia congenita",
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            "description": "Distal myopathy Welander type",
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            "description": "Alternating hypoglossal hemiplegia",
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            "description": "Autosomal recessive spastic paraplegia type 32",
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            "description": "Autosomal recessive spastic paraplegia type 26",
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            "description": "Autosomal recessive spastic paraplegia type 23",
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            "description": "Autosomal recessive spastic paraplegia type 64",
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            "description": "Autosomal recessive spastic paraplegia type 63",
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            "code": "726611001",
            "description": "Autosomal recessive spastic paraplegia type 61",
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            "code": "726614009",
            "description": "Autosomal recessive limb girdle muscular dystrophy type 2P",
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            "code": "726615005",
            "description": "Autosomal recessive limb girdle muscular dystrophy type 2Q",
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            "code": "726616006",
            "description": "Autosomal recessive limb girdle muscular dystrophy type 2L",
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            "code": "726617002",
            "description": "Autosomal recessive limb girdle muscular dystrophy type 2N",
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            "code": "726618007",
            "description": "Autosomal recessive limb girdle muscular dystrophy type 2M",
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            "description": "Speech cortex disorder",
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            "description": "Oropouche virus disease",
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            "description": "Multiple AND bilateral precerebral artery stenosis",
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            "description": "Pure mitochondrial myopathy",
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            "description": "Cortical blindness, intellectual disability, polydactyly syndrome",
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            "code": "732264002",
            "description": "Coenzyme A synthase protein associated neurodegeneration",
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            "code": "732923001",
            "description": "Hemorrhage of medulla oblongata",
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            "description": "Split hand, obstructive uropathy, spina bifida, diaphragmatic defect syndrome",
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            "code": "732929002",
            "description": "Autosomal recessive limb girdle muscular dystrophy type 2S",
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            "code": "732930007",
            "description": "Autosomal recessive limb girdle muscular dystrophy type 2T",
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            "code": "732931006",
            "description": "Autosomal recessive limb girdle muscular dystrophy type 2R",
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            "code": "732932004",
            "description": "Autosomal recessive spastic paraplegia type 18",
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            "code": "732933009",
            "description": "Autosomal recessive spastic paraplegia type 25",
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            "code": "732948003",
            "description": "Autosomal dominant spastic paraplegia type 10",
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            "code": "732949006",
            "description": "Autosomal dominant spastic paraplegia type 6",
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            "code": "732951005",
            "description": "Mitochondrial myopathy, lactic acidosis, deafness syndrome",
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            "code": "732958004",
            "description": "Spastic paraplegia with precocious puberty syndrome",
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            "description": "Beta-propeller protein-associated neurodegeneration",
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            "description": "Muscular dystrophy",
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            "description": "Multiple sclerosis, ichthyosis, factor VIII deficiency syndrome",
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            "code": "733029008",
            "description": "Autosomal dominant spastic paraplegia type 29",
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            "code": "733031004",
            "description": "Epilepsy, microcephaly, skeletal dysplasia syndrome",
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            "code": "733032006",
            "description": "Epilepsy telangiectasia syndrome",
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            "code": "733033001",
            "description": "Spinocerebellar ataxia dysmorphism syndrome",
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            "code": "733044009",
            "description": "Dermatoleukodystrophy",
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            "code": "733049004",
            "description": "Encephalopathy, intracerebral calcification, retinal degeneration syndrome",
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            "code": "733065003",
            "description": "Myoclonus, cerebellar ataxia, deafness syndrome",
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            "code": "733068001",
            "description": "Absent tibia, polydactyly, arachnoid cyst syndrome",
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            "code": "733071009",
            "description": "Deafness, small bowel diverticulosis, neuropathy syndrome",
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            "code": "733072002",
            "description": "Alaninuria, microcephaly, dwarfism, enamel hypoplasia, diabetes mellitus syndrome",
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            "code": "733082001",
            "description": "Early-onset Lafora body disease",
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            "code": "733086003",
            "description": "Pseudoprogeria syndrome",
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            "code": "733089005",
            "description": "Spastic paraplegia, nephritis, deafness syndrome",
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            "code": "733091002",
            "description": "Isolated hereditary congenital facial paralysis",
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            "code": "733092009",
            "description": "Microcephalus, hypergonadotropic hypogonadism, short stature syndrome",
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            "code": "733094005",
            "description": "Dandy-Walker malformation with postaxial polydactyly syndrome",
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            "code": "733096007",
            "description": "Thyrocerebrorenal syndrome",
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          {
            "code": "733113002",
            "description": "Hypogonadotropic hypogonadism retinitis pigmentosa syndrome",
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            "code": "733168003",
            "description": "Invasive aspergillosis of brain",
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            "code": "733184002",
            "description": "Dementia caused by heavy metal exposure",
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            "code": "733185001",
            "description": "Dementia following injury caused by exposure to ionizing radiation",
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            "code": "733190003",
            "description": "Dementia due to primary malignant neoplasm of brain",
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            "code": "733191004",
            "description": "Dementia due to chronic subdural hematoma",
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            "code": "733192006",
            "description": "Dementia due to herpes encephalitis",
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            "code": "733193001",
            "description": "Dementia co-occurrent and due to progressive multifocal leukoencephalopathy",
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            "code": "733194007",
            "description": "Dementia co-occurrent and due to Down syndrome",
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            "code": "733195008",
            "description": "Epilepsy of infancy with migrating focal seizures",
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            "code": "733198005",
            "description": "Encephalopathy due to and following cardiopulmonary bypass",
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            "code": "733199002",
            "description": "Multifocal cerebral infarction due to and following procedure on cardiovascular system",
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            "code": "73331006",
            "description": "Hemimyelia",
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            "code": "733417008",
            "description": "Facial dysmorphism, macrocephaly, myopia, Dandy-Walker malformation syndrome",
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            "code": "733418003",
            "description": "Joubert syndrome with Jeune asphyxiating thoracic dystrophy",
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            "code": "733422008",
            "description": "Prion protein systemic amyloidosis",
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            "code": "733452000",
            "description": "Leukoencephalopathy, dystonia, motor neuropathy syndrome",
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            "code": "733455003",
            "description": "Spastic paraplegia, glaucoma, intellectual disability syndrome",
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            "code": "733469003",
            "description": "Hereditary congenital hypomelanotic and hypermelanotic cutaneous macules, growth retardation, intellectual disability syndrome",
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            "code": "733472005",
            "description": "Microcephalus, glomerulonephritis, marfanoid habitus syndrome",
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            "code": "733489002",
            "description": "Distal myopathy with posterior leg and anterior hand involvement",
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            "code": "733599009",
            "description": "Adult-onset multiple mitochondrial deoxyribonucleic acid deletion syndrome due to deoxyguanosine kinase deficiency",
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            "code": "733604003",
            "description": "Microcephalus, lymphedema, chorioretinopathy syndrome",
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            "code": "733623005",
            "description": "Autism spectrum disorder, epilepsy, arthrogryposis syndrome",
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            "code": "733630004",
            "description": "Deficiency of alpha-ketoglutarate dehydrogenase",
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            "code": "733636005",
            "description": "3-phosphoglycerate dehydrogenase deficiency juvenile form",
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            "code": "733637001",
            "description": "3-phosphoglycerate dehydrogenase deficiency infantile form",
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            "code": "733650000",
            "description": "Adult familial nephronophthisis with spastic quadriparesia syndrome",
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            "code": "73390009",
            "description": "Endophlebitis of cavernous venous sinus",
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            "code": "733926004",
            "description": "Ganglioneuroblastoma of central nervous system",
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            "code": "734017008",
            "description": "Ectodermal dysplasia, intellectual disability, central nervous system malformation syndrome",
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            "code": "734020000",
            "description": "Spinocerebellar ataxia type 40",
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            "code": "734021001",
            "description": "Spinocerebellar ataxia type 38",
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            "description": "Sporadic adult-onset ataxia of unknown etiology",
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            "code": "734066005",
            "description": "Diffuse large B-cell lymphoma of central nervous system",
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            "code": "734099007",
            "description": "Neuroblastoma of central nervous system",
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            "code": "73413009",
            "description": "Cortex contusion with open intracranial wound AND concussion",
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            "code": "734326000",
            "description": "Stenosis of left vertebral artery",
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            "code": "734327009",
            "description": "Stenosis of right vertebral artery",
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            "code": "734374000",
            "description": "Thrombosis of left carotid artery",
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            "code": "734382000",
            "description": "Thrombosis of right carotid artery",
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            "code": "734383005",
            "description": "Thrombosis of left middle cerebral artery",
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            "code": "734384004",
            "description": "Thrombosis of right middle cerebral artery",
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            "code": "734396006",
            "description": "Spontaneous rupture of left posterior communicating artery",
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            "description": "Spontaneous rupture of right posterior communicating artery",
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            "description": "Pyridoxine-dependent epilepsy",
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            "description": "Chronic vocal tic disorder",
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            "code": "734879002",
            "description": "Ruptured aneurysm of right posterior communicating artery",
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            "description": "Ruptured aneurysm of left posterior communicating artery",
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            "description": "Dyssynergia cerebellaris myoclonica",
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            "code": "734959006",
            "description": "Embolus of left cerebellar artery",
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            "code": "734960001",
            "description": "Embolus of right cerebellar artery",
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            "code": "734961002",
            "description": "Embolus of left posterior cerebral artery",
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            "code": "734963004",
            "description": "Embolus of right posterior cerebral artery",
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            "code": "734964005",
            "description": "Embolus of left middle cerebral artery",
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            "code": "734965006",
            "description": "Embolus of right middle cerebral artery",
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            "code": "735114006",
            "description": "Occlusion of right pontine artery",
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            "code": "735115007",
            "description": "Occlusion of left pontine artery",
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            "code": "735131004",
            "description": "Occlusion of left cerebellar artery",
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            "code": "735132006",
            "description": "Occlusion of right cerebellar artery",
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            "description": "Communicating hydrocephalus due to and following traumatic hemorrhage",
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            "description": "Seizure co-occurrent and due to drug withdrawal",
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            "description": "Leukoencephalopathy with brain stem and spinal cord involvement and high lactate syndrome",
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            "description": "Deep abscess of cerebral hemisphere",
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            "description": "Abscess of corpus callosum",
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            "description": "Parasitic infection causing granuloma of cerebrum",
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            "description": "Infection causing granuloma of spinal cord",
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            "code": "735749005",
            "description": "Myelomeningocele co-occurrent with hydrocephalus",
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            "description": "Psychotic disorder with schizophreniform symptoms caused by cocaine",
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            "code": "735757008",
            "description": "Primary ganglioneuroblastoma of brain",
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            "code": "736321008",
            "description": "Injury of both visual cortices",
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            "code": "73663008",
            "description": "Neurologic xeroderma pigmentosum",
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            "code": "737159004",
            "description": "Aneurysm of basilar artery",
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            "description": "Dissection of basilar artery",
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            "code": "737225007",
            "description": "Secondary psychotic syndrome with hallucinations and delusions",
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            "code": "737227004",
            "description": "Autosomal dominant hereditary spastic paraplegia",
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            "code": "737228009",
            "description": "Progressive focal cortical atrophy",
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            "code": "737229001",
            "description": "White matter disorder due to vascular abnormality",
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            "description": "White matter disorder due to ischemia",
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            "description": "Traumatic hemorrhage of thalamus",
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            "description": "Traumatic hemorrhage of basal ganglia",
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            "description": "Concussion of cervical spinal cord",
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            "description": "Traumatic edema of cervical spinal cord",
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            "description": "Concussion of thoracic spinal cord",
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            "description": "Traumatic edema of thoracic spinal cord",
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            "description": "Concussion of lumbar spinal cord",
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            "description": "Traumatic edema of lumbar spinal cord",
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            "code": "737338002",
            "description": "Synthetic cannabinoid withdrawal",
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            "description": "Delirium caused by synthetic cannabinoid",
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            "description": "Anxiety disorder caused by synthetic cannabinoid",
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            "description": "Hemiparkinsonism hemiatrophy syndrome",
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            "description": "Toxic encephalopathy caused by hydroxyquinoline",
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            "description": "Complete spinal cord injury",
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            "description": "Incomplete spinal cord injury",
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            "description": "Congenital anomaly of pituitary gland",
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            "description": "Cerebellar hemangioblastomatosis",
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            "description": "Acromegaly",
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            "code": "74267005",
            "description": "Toxic encephalopathy caused by carbon tetrachloride",
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            "code": "74333002",
            "description": "Spasmodic torticollis",
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            "code": "74351001",
            "description": "Reye's syndrome",
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            "description": "Open fracture of C5-C7 level with central cord syndrome",
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            "description": "Simple partial seizure with autonomic dysfunction",
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          {
            "code": "74644004",
            "description": "Influenza with encephalopathy",
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            "code": "74728003",
            "description": "Hypopituitarism",
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            "description": "Complex partial seizure + impairment consciousness at onset",
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            "code": "74772000",
            "description": "Meningomyelitis",
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            "code": "74810008",
            "description": "Premotor cortex syndrome",
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            "code": "74934004",
            "description": "Psychoactive substance-induced withdrawal syndrome",
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            "description": "Athetoid cerebral palsy",
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            "description": "Post-traumatic epilepsy",
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            "description": "Cerebellar hemorrhage",
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            "description": "Combined pyramidal-extrapyramidal syndrome",
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            "code": "75072002",
            "description": "Nemaline myopathy",
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            "description": "Inhalant-induced psychotic disorder with delusions",
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            "description": "Personal history of transient ischaemic attack",
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            "description": "Endophlebitis of superior sagittal sinus",
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            "code": "75143000",
            "description": "Toxic encephalitis caused by thallium",
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            "description": "Spastic spinal syphilitic paralysis",
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            "description": "Intervertebral disc disorder of cervical region with myelopathy",
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            "description": "Amyotrophia congenita",
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            "description": "Subarachnoid hemorrhage following injury with open intracranial wound AND loss of consciousness",
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            "description": "Cerebral embolism",
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            "description": "Mood disorder with depressive features due to general medical condition",
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            "description": "Isolated follicle stimulating hormone deficiency",
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            "code": "75968004",
            "description": "Sotos' syndrome",
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            "description": "Septo-optic dysplasia sequence",
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            "description": "Juvenile cerebellar degeneration AND myoclonus",
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            "description": "Transient infantile hyperthyrotropinemia",
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            "description": "Congenital obstructive hydrocephalus",
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            "description": "White matter disorder due to vitamin B12 deficiency",
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            "description": "Myelopathy due to toxicity of substance",
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            "description": "Movement disorder due to toxicity of substance",
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            "description": "Mood disorder with manic symptoms caused by opioid",
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            "description": "Mood disorder with depressive symptoms caused by opioid",
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            "description": "Mood disorder with mixed depressive and manic symptoms caused by opioid",
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            "description": "Delirium caused by stimulant",
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            "code": "762325009",
            "description": "Psychotic disorder caused by stimulant",
            "attributes": null
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            "code": "762326005",
            "description": "Psychotic disorder with hallucinations caused by stimulant",
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            "description": "Psychotic disorder with delusions caused by stimulant",
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            "code": "762328006",
            "description": "Mood disorder caused by stimulant",
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            "code": "762329003",
            "description": "Mood disorder with depressive symptoms caused by stimulant",
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            "description": "Mood disorder with mixed depressive and manic symptoms caused by stimulant",
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            "description": "Anxiety disorder caused by stimulant",
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            "code": "762335003",
            "description": "Mood disorder with manic symptoms caused by hallucinogen",
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            "description": "Mood disorder with depressive symptoms caused by hallucinogen",
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            "description": "Mood disorder with mixed depressive and manic symptoms caused by hallucinogen",
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            "description": "Mood disorder with manic symptoms caused by volatile inhalant",
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            "description": "Mood disorder with depressive symptoms caused by volatile inhalant",
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            "description": "Mood disorder with mixed depressive and manic symptoms caused by volatile inhalant",
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            "description": "Mood disorder with manic symptoms caused by dissociative drug",
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            "description": "Mood disorder with depressive symptoms caused by dissociative drug",
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            "description": "Mood disorder with mixed depressive and manic symptoms caused by dissociative drug",
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            "description": "Dementia due to prion disease",
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            "description": "Dementia due to and following injury of head",
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            "description": "Demyelination due to systemic vasculitis",
            "attributes": null
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            "description": "Atypical tic disorder",
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            "code": "762436001",
            "description": "Injury of left visual cortex",
            "attributes": null
          },
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            "code": "762457009",
            "description": "Astroblastoma of brain",
            "attributes": null
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            "code": "762506007",
            "description": "Delirium caused by synthetic cathinone",
            "attributes": null
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            "description": "Psychotic disorder caused by synthetic cathinone",
            "attributes": null
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            "code": "762508008",
            "description": "Psychotic disorder with hallucinations caused by synthetic cathinone",
            "attributes": null
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          {
            "code": "762509000",
            "description": "Psychotic disorder with delusions caused by synthetic cathinone",
            "attributes": null
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            "description": "Psychotic disorder with schizophreniform symptoms caused by synthetic cathinone",
            "attributes": null
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            "code": "762511009",
            "description": "Mood disorder caused by synthetic cathinone",
            "attributes": null
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            "code": "762512002",
            "description": "Mood disorder with depressive symptoms caused by synthetic cathinone",
            "attributes": null
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          {
            "code": "762513007",
            "description": "Mood disorder with manic symptoms caused by synthetic cathinone",
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          },
          {
            "code": "762514001",
            "description": "Mood disorder with mixed depressive and manic symptoms caused by synthetic cathinone",
            "attributes": null
          },
          {
            "code": "762515000",
            "description": "Anxiety disorder caused by synthetic cathinone",
            "attributes": null
          },
          {
            "code": "762516004",
            "description": "Obsessive compulsive disorder caused by synthetic cathinone",
            "attributes": null
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          {
            "code": "762617003",
            "description": "Injury of right visual cortex",
            "attributes": null
          },
          {
            "code": "762629007",
            "description": "Occlusion of right middle cerebral artery by embolus",
            "attributes": null
          },
          {
            "code": "762630002",
            "description": "Occlusion of left middle cerebral artery by embolus",
            "attributes": null
          },
          {
            "code": "762632005",
            "description": "Occlusion of left cerebellar artery by embolus",
            "attributes": null
          },
          {
            "code": "762633000",
            "description": "Occlusion of right cerebellar artery by embolus",
            "attributes": null
          },
          {
            "code": "762648006",
            "description": "Stenosis of right cerebellar artery",
            "attributes": null
          },
          {
            "code": "762649003",
            "description": "Stenosis of left cerebellar artery",
            "attributes": null
          },
          {
            "code": "762651004",
            "description": "Occlusion of right posterior cerebral artery by embolus",
            "attributes": null
          },
          {
            "code": "762652006",
            "description": "Occlusion of left posterior cerebral artery by embolus",
            "attributes": null
          },
          {
            "code": "762663009",
            "description": "Mesencephalic light-near dissociation",
            "attributes": null
          },
          {
            "code": "762672001",
            "description": "Synthetic cathinone withdrawal",
            "attributes": null
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          {
            "code": "762707000",
            "description": "Subcortical dementia",
            "attributes": null
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          {
            "code": "763065008",
            "description": "Ataxia telangiectasia variant",
            "attributes": null
          },
          {
            "code": "763067000",
            "description": "Autosomal dominant congenital benign spinal muscular atrophy",
            "attributes": null
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            "code": "763068005",
            "description": "Autosomal dominant spastic paraplegia type 31",
            "attributes": null
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          {
            "code": "763069002",
            "description": "Autosomal dominant spastic paraplegia type 41",
            "attributes": null
          },
          {
            "code": "763070001",
            "description": "Autosomal dominant spastic paraplegia type 42",
            "attributes": null
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          {
            "code": "763127004",
            "description": "Benign paroxysmal tonic upgaze of childhood with ataxia",
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            "code": "763130006",
            "description": "Cleft palate, large ears, small head syndrome",
            "attributes": null
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          {
            "code": "763135001",
            "description": "Charcot-Marie-Tooth disease type 4E",
            "attributes": null
          },
          {
            "code": "763136000",
            "description": "Charcot-Marie-Tooth disease, deafness, intellectual disability syndrome",
            "attributes": null
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            "code": "763280005",
            "description": "Encephalopathy, hypertrophic cardiomyopathy, renal tubular disease syndrome",
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            "code": "763310000",
            "description": "Acute necrotizing encephalopathy of childhood",
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            "code": "763312008",
            "description": "Autosomal recessive cerebellar ataxia, pyramidal signs, nystagmus, oculomotor apraxia syndrome",
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            "code": "763314009",
            "description": "Congenital muscular dystrophy with hyperlaxity",
            "attributes": null
          },
          {
            "code": "763315005",
            "description": "Congenital myopathy with myasthenic-like onset",
            "attributes": null
          },
          {
            "code": "763344007",
            "description": "Cerebellar ataxia, intellectual disability, oculomotor apraxia, cerebellar cysts syndrome",
            "attributes": null
          },
          {
            "code": "763345008",
            "description": "Charcot-Marie-Tooth disease type 4B3",
            "attributes": null
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          {
            "code": "763347000",
            "description": "X-linked Charcot-Marie-Tooth disease type 6",
            "attributes": null
          },
          {
            "code": "763348005",
            "description": "Autosomal recessive cerebellar ataxia with late-onset spasticity",
            "attributes": null
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            "code": "763349002",
            "description": "Progressive myoclonic epilepsy with dystonia",
            "attributes": null
          },
          {
            "code": "763350002",
            "description": "Intellectual disability, obesity, brain malformation, facial dysmorphism syndrome",
            "attributes": null
          },
          {
            "code": "763351003",
            "description": "Spectrin-associated autosomal recessive cerebellar ataxia",
            "attributes": null
          },
          {
            "code": "763352005",
            "description": "Familial dyskinesia and facial myokymia",
            "attributes": null
          },
          {
            "code": "763366000",
            "description": "Leukoencephalopathy, thalamus and brainstem anomalies, high lactate syndrome",
            "attributes": null
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          {
            "code": "763367009",
            "description": "Autosomal recessive spastic paraplegia type 48",
            "attributes": null
          },
          {
            "code": "763369007",
            "description": "Autosomal dominant spastic paraplegia type 37",
            "attributes": null
          },
          {
            "code": "763370008",
            "description": "X-linked spastic paraplegia type 34",
            "attributes": null
          },
          {
            "code": "763373005",
            "description": "Autosomal recessive spastic paraplegia type 5A",
            "attributes": null
          },
          {
            "code": "763374004",
            "description": "Autosomal dominant spastic paraplegia type 12",
            "attributes": null
          },
          {
            "code": "763375003",
            "description": "Autosomal dominant spastic paraplegia type 19",
            "attributes": null
          },
          {
            "code": "763376002",
            "description": "Autosomal recessive spastic paraplegia type 28",
            "attributes": null
          },
          {
            "code": "763377006",
            "description": "Autosomal spastic paraplegia type 30",
            "attributes": null
          },
          {
            "code": "763400005",
            "description": "X-linked Charcot-Marie-Tooth disease type 4",
            "attributes": null
          },
          {
            "code": "763402002",
            "description": "Spastic paraplegia, neuropathy, poikiloderma syndrome",
            "attributes": null
          },
          {
            "code": "763403007",
            "description": "Spastic paraplegia, facial cutaneous lesion syndrome",
            "attributes": null
          },
          {
            "code": "763455008",
            "description": "X-linked Charcot-Marie-Tooth disease type 1",
            "attributes": null
          },
          {
            "code": "763457000",
            "description": "X-linked Charcot-Marie-Tooth disease type 2",
            "attributes": null
          },
          {
            "code": "763458005",
            "description": "X-linked Charcot-Marie-Tooth disease type 3",
            "attributes": null
          },
          {
            "code": "763460007",
            "description": "X-linked Charcot-Marie-Tooth disease type 5",
            "attributes": null
          },
          {
            "code": "76349003",
            "description": "Extrapyramidal disease",
            "attributes": null
          },
          {
            "code": "763533003",
            "description": "Distal hereditary motor neuropathy Jerash type",
            "attributes": null
          },
          {
            "code": "763534009",
            "description": "Hot water reflex epilepsy",
            "attributes": null
          },
          {
            "code": "763622006",
            "description": "Thinking epilepsy",
            "attributes": null
          },
          {
            "code": "763632004",
            "description": "Startle epilepsy",
            "attributes": null
          },
          {
            "code": "763669001",
            "description": "Spastic ataxia with congenital miosis",
            "attributes": null
          },
          {
            "code": "763688008",
            "description": "Deafness, encephaloneuropathy, obesity, valvulopathy syndrome",
            "attributes": null
          },
          {
            "code": "763715007",
            "description": "Familial hyperprolactinemia",
            "attributes": null
          },
          {
            "code": "763717004",
            "description": "Sporadic fetal brain disruption sequence",
            "attributes": null
          },
          {
            "code": "763718009",
            "description": "Finnish upper limb onset distal myopathy",
            "attributes": null
          },
          {
            "code": "763721006",
            "description": "Hypermethioninemia encephalopathy due to deficiency of adenosine kinase",
            "attributes": null
          },
          {
            "code": "763722004",
            "description": "Hypotonia, speech impairment, severe cognitive delay syndrome",
            "attributes": null
          },
          {
            "code": "763743003",
            "description": "Intellectual disability, spasticity, ectrodactyly syndrome",
            "attributes": null
          },
          {
            "code": "763770005",
            "description": "Familial myoclonus of cerebral cortex",
            "attributes": null
          },
          {
            "code": "763776004",
            "description": "Kelch like family member 9 related early-onset distal myopathy",
            "attributes": null
          },
          {
            "code": "763793004",
            "description": "Limbic encephalitis with contactin-associated protein-like 2 antibodies",
            "attributes": null
          },
          {
            "code": "763794005",
            "description": "Limbic encephalitis with leucine-rich glioma-inactivated 1 antibodies",
            "attributes": null
          },
          {
            "code": "763797003",
            "description": "Agenesis of corpus callosum and abnormal genitalia syndrome",
            "attributes": null
          },
          {
            "code": "763798008",
            "description": "Microcephalus, complex motor and sensory axonal neuropathy syndrome",
            "attributes": null
          },
          {
            "code": "763802009",
            "description": "Micturition induced epilepsy",
            "attributes": null
          },
          {
            "code": "763803004",
            "description": "Morvan syndrome",
            "attributes": null
          },
          {
            "code": "763821001",
            "description": "Porencephaly, cerebellar hypoplasia, internal malformations syndrome",
            "attributes": null
          },
          {
            "code": "763827002",
            "description": "Orgasm induced epilepsy",
            "attributes": null
          },
          {
            "code": "763829004",
            "description": "Oculopharyngodistal myopathy",
            "attributes": null
          },
          {
            "code": "763837007",
            "description": "Oro-facial digital syndrome type 14",
            "attributes": null
          },
          {
            "code": "763861000",
            "description": "Pachygyria, intellectual disability, epilepsy syndrome",
            "attributes": null
          },
          {
            "code": "763869003",
            "description": "Myelitis caused by ionizing radiation following radiotherapy",
            "attributes": null
          },
          {
            "code": "763889002",
            "description": "Spina bifida and hypospadias syndrome",
            "attributes": null
          },
          {
            "code": "763895001",
            "description": "Myosclerosis",
            "attributes": null
          },
          {
            "code": "76402003",
            "description": "Carotid artery insufficiency syndrome",
            "attributes": null
          },
          {
            "code": "764095005",
            "description": "Leukoencephalopathy, ataxia, hypodontia, hypomyelination syndrome",
            "attributes": null
          },
          {
            "code": "76418009",
            "description": "Concussion with mental confusion AND/OR disorientation without loss of consciousness",
            "attributes": null
          },
          {
            "code": "76435008",
            "description": "Open fracture of C1-C4 level with spinal cord injury",
            "attributes": null
          },
          {
            "code": "764453009",
            "description": "Action myoclonus renal failure syndrome",
            "attributes": null
          },
          {
            "code": "764456001",
            "description": "Hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency",
            "attributes": null
          },
          {
            "code": "764522009",
            "description": "Familial focal epilepsy with variable foci",
            "attributes": null
          },
          {
            "code": "764525006",
            "description": "Cylindrical spirals myopathy",
            "attributes": null
          },
          {
            "code": "764661000000103",
            "description": "Cervical spinal cord injury, without spinal bone injury, C5-7",
            "attributes": null
          },
          {
            "code": "764686003",
            "description": "Autosomal recessive spastic paraplegia type 15",
            "attributes": null
          },
          {
            "code": "764688002",
            "description": "Autosomal recessive spastic paraplegia type 35",
            "attributes": null
          },
          {
            "code": "764730007",
            "description": "Autosomal dominant Charcot-Marie-Tooth disease type 2 due to kinesin family member 5A mutation",
            "attributes": null
          },
          {
            "code": "764732004",
            "description": "Microcephalus, cerebellar hypoplasia, cardiac conduction defect syndrome",
            "attributes": null
          },
          {
            "code": "764734003",
            "description": "Autosomal recessive spastic paraplegia type 21",
            "attributes": null
          },
          {
            "code": "764736001",
            "description": "Autosomal recessive spastic paraplegia type 43",
            "attributes": null
          },
          {
            "code": "76474001",
            "description": "Herpetic acute necrotizing encephalitis",
            "attributes": null
          },
          {
            "code": "764812008",
            "description": "Autosomal recessive myogenic arthrogryposis multiplex congenita",
            "attributes": null
          },
          {
            "code": "764850002",
            "description": "Autosomal dominant Charcot-Marie-Tooth disease type 2A2",
            "attributes": null
          },
          {
            "code": "764854006",
            "description": "Autosomal dominant slowed nerve conduction velocity",
            "attributes": null
          },
          {
            "code": "764859001",
            "description": "Laing early-onset distal myopathy",
            "attributes": null
          },
          {
            "code": "764944006",
            "description": "Congenital muscular dystrophy type 1B",
            "attributes": null
          },
          {
            "code": "764945007",
            "description": "Congenital myopathy with internal nuclei and atypical cores",
            "attributes": null
          },
          {
            "code": "764959000",
            "description": "Intellectual disability, myopathy, short stature, endocrine defect syndrome",
            "attributes": null
          },
          {
            "code": "764962002",
            "description": "Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1",
            "attributes": null
          },
          {
            "code": "764993001",
            "description": "Encephalitis caused by Mycoplasma pneumoniae",
            "attributes": null
          },
          {
            "code": "764998005",
            "description": "Non-herpetic acute limbic encephalitis",
            "attributes": null
          },
          {
            "code": "765045003",
            "description": "Autosomal recessive spastic paraplegia type 62",
            "attributes": null
          },
          {
            "code": "765046002",
            "description": "Autosomal dominant Charcot-Marie-Tooth disease type 2U",
            "attributes": null
          },
          {
            "code": "765047006",
            "description": "SURF1, cytochrome c oxidase assembly factor related Charcot-Marie-Tooth disease type 4",
            "attributes": null
          },
          {
            "code": "765089003",
            "description": "Focal epilepsy, intellectual disability, cerebro-cerebellar malformation syndrome",
            "attributes": null
          },
          {
            "code": "765091006",
            "description": "Spinocerebellar ataxia with axonal neuropathy type 1",
            "attributes": null
          },
          {
            "code": "765093009",
            "description": "Rolandic epilepsy, speech dyspraxia syndrome",
            "attributes": null
          },
          {
            "code": "765100000",
            "description": "Ribonucleotide reductase regulatory TP53 inducible subunit M2B-related mitochondrial deoxyribonucleic acid depletion syndrome encephalomyopathic form with renal tubulopathy",
            "attributes": null
          },
          {
            "code": "765151006",
            "description": "Asphyxiophilia",
            "attributes": null
          },
          {
            "code": "765170001",
            "description": "Sodium voltage-gated channel alpha subunit 8-related epilepsy with encephalopathy",
            "attributes": null
          },
          {
            "code": "765197008",
            "description": "Symptomatic form of muscular dystrophy of Duchenne and Becker in female carrier",
            "attributes": null
          },
          {
            "code": "765202001",
            "description": "Familial multiple benign meningioma",
            "attributes": null
          },
          {
            "code": "765216006",
            "description": "Audiogenic epilepsy",
            "attributes": null
          },
          {
            "code": "765325002",
            "description": "Peripheral demyelinating neuropathy, central dysmyelinating leukodystrophy, Waardenburg syndrome, Hirschsprung disease",
            "attributes": null
          },
          {
            "code": "765331004",
            "description": "Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis",
            "attributes": null
          },
          {
            "code": "765401006",
            "description": "Mitochondrial deoxyribonucleic acid depletion syndrome encephalomyopathic form",
            "attributes": null
          },
          {
            "code": "765403009",
            "description": "F-box and leucine rich repeat protein 4 related mitochondrial deoxyribonucleic acid depletion syndrome encephalomyopathic form",
            "attributes": null
          },
          {
            "code": "765434008",
            "description": "Human immunodeficiency virus type I enhancer binding protein 2 related intellectual disability",
            "attributes": null
          },
          {
            "code": "765744006",
            "description": "Autosomal dominant intermediate Charcot-Marie-Tooth disease type A",
            "attributes": null
          },
          {
            "code": "765745007",
            "description": "Autosomal dominant intermediate Charcot-Marie-Tooth disease type B",
            "attributes": null
          },
          {
            "code": "765746008",
            "description": "Autosomal dominant intermediate Charcot-Marie-Tooth disease type C",
            "attributes": null
          },
          {
            "code": "765747004",
            "description": "Autosomal dominant intermediate Charcot-Marie-Tooth disease type D",
            "attributes": null
          },
          {
            "code": "765751002",
            "description": "Autoimmune encephalopathy with parasomnia and obstructive sleep apnea",
            "attributes": null
          },
          {
            "code": "765753004",
            "description": "Autosomal recessive spastic paraplegia type 45",
            "attributes": null
          },
          {
            "code": "765756007",
            "description": "Benign infantile seizure with mild gastroenteritis syndrome",
            "attributes": null
          },
          {
            "code": "765757003",
            "description": "Bilateral polymicrogyria",
            "attributes": null
          },
          {
            "code": "765758008",
            "description": "Microcephalic primordial dwarfism Montreal type",
            "attributes": null
          },
          {
            "code": "766032007",
            "description": "Holoprosencephaly, ectrodactyly, cleft lip, cleft palate syndrome",
            "attributes": null
          },
          {
            "code": "766044005",
            "description": "Acute encephalopathy with biphasic seizures and late reduced diffusion",
            "attributes": null
          },
          {
            "code": "766246000",
            "description": "Marburg acute multiple sclerosis",
            "attributes": null
          },
          {
            "code": "766251006",
            "description": "Lethal infantile mitochondrial myopathy",
            "attributes": null
          },
          {
            "code": "76628006",
            "description": "Post-hemiplegic chorea",
            "attributes": null
          },
          {
            "code": "76670001",
            "description": "Duchenne muscular dystrophy",
            "attributes": null
          },
          {
            "code": "766709000",
            "description": "Isolated hypoplasia of cerebellar vermis",
            "attributes": null
          },
          {
            "code": "766710005",
            "description": "Isolated focal cortical dysplasia",
            "attributes": null
          },
          {
            "code": "76675006",
            "description": "Cerebellar laceration without open intracranial wound AND with concussion",
            "attributes": null
          },
          {
            "code": "766752000",
            "description": "Neurolymphomatosis",
            "attributes": null
          },
          {
            "code": "766753005",
            "description": "Nijmegen breakage syndrome-like disorder",
            "attributes": null
          },
          {
            "code": "766764008",
            "description": "X-linked distal spinal muscular atrophy type 3",
            "attributes": null
          },
          {
            "code": "766767001",
            "description": "Autosomal recessive spastic paraplegia type 67",
            "attributes": null
          },
          {
            "code": "766814006",
            "description": "Autosomal recessive cerebellar ataxia with saccadic intrusion syndrome",
            "attributes": null
          },
          {
            "code": "766815007",
            "description": "Perioral myoclonia with absences",
            "attributes": null
          },
          {
            "code": "766818009",
            "description": "X-linked non progressive cerebellar ataxia",
            "attributes": null
          },
          {
            "code": "766871009",
            "description": "Diencephalic mesencephalic junction dysplasia",
            "attributes": null
          },
          {
            "code": "766872002",
            "description": "Parkinsonism caused by cyanide",
            "attributes": null
          },
          {
            "code": "766931003",
            "description": "Hypomyelination neuropathy arthrogryposis syndrome",
            "attributes": null
          },
          {
            "code": "766932005",
            "description": "Hypothalamic hamartoma with gelastic seizure",
            "attributes": null
          },
          {
            "code": "766934006",
            "description": "Isolated unilateral hemispheric cerebellar hypoplasia",
            "attributes": null
          },
          {
            "code": "766977007",
            "description": "Severe early-onset axonal neuropathy due to mitofusin 2 deficiency",
            "attributes": null
          },
          {
            "code": "766987006",
            "description": "Moebius syndrome",
            "attributes": null
          },
          {
            "code": "767254005",
            "description": "Recurrent benign focal seizures of childhood",
            "attributes": null
          },
          {
            "code": "767448007",
            "description": "Pineoblastoma",
            "attributes": null
          },
          {
            "code": "768473009",
            "description": "Purine rich element binding protein A syndrome",
            "attributes": null
          },
          {
            "code": "768553002",
            "description": "Hypermanganesemia with dystonia",
            "attributes": null
          },
          {
            "code": "768554008",
            "description": "Hypermanganesemia with dystonia 2",
            "attributes": null
          },
          {
            "code": "768555009",
            "description": "5q31.3 microdeletion syndrome",
            "attributes": null
          },
          {
            "code": "768556005",
            "description": "Ataxia pancytopenia syndrome",
            "attributes": null
          },
          {
            "code": "768663003",
            "description": "Leukoencephalopathy with mild cerebellar ataxia and white matter edema",
            "attributes": null
          },
          {
            "code": "768666006",
            "description": "Syntaxin binding protein 1 encephalopathy with epilepsy",
            "attributes": null
          },
          {
            "code": "76880004",
            "description": "Angelman syndrome",
            "attributes": null
          },
          {
            "code": "76889003",
            "description": "Failed attempted abortion with cerebral anoxia",
            "attributes": null
          },
          {
            "code": "768939009",
            "description": "Primary tethered cord syndrome",
            "attributes": null
          },
          {
            "code": "769065000",
            "description": "Tubulin beta 4A class IVa related leukodystrophy",
            "attributes": null
          },
          {
            "code": "76916001",
            "description": "Spina bifida occulta",
            "attributes": null
          },
          {
            "code": "76938004",
            "description": "Infantile encephalopathy AND lactic acidosis",
            "attributes": null
          },
          {
            "code": "77015008",
            "description": "Crossed hemiplegia",
            "attributes": null
          },
          {
            "code": "770404004",
            "description": "Autosomal recessive chorioretinopathy and microcephaly syndrome",
            "attributes": null
          },
          {
            "code": "770430000",
            "description": "Autosomal recessive distal spinal muscular atrophy type 3",
            "attributes": null
          },
          {
            "code": "770431001",
            "description": "Early-onset epileptic encephalopathy and intellectual disability due to glutamate receptor, ionotropic, N-methyl-D-aspartate, subunit 2A mutation",
            "attributes": null
          },
          {
            "code": "770438007",
            "description": "Infantile spasm and broad thumb syndrome",
            "attributes": null
          },
          {
            "code": "770560008",
            "description": "Lissencephaly due to LIS1 mutation",
            "attributes": null
          },
          {
            "code": "770564004",
            "description": "Microcephalic primordial dwarfism Alazami type",
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            "code": "770565003",
            "description": "Microcephalic primordial dwarfism Dauber type",
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            "code": "770596007",
            "description": "Rippling muscle disease with myasthenia gravis",
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            "code": "770604006",
            "description": "X-linked cerebral, cerebellar, coloboma syndrome",
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            "code": "770623004",
            "description": "Benign occipital lobe epilepsy",
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            "description": "Benign partial epilepsy of infancy with complex partial seizures",
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            "code": "770626007",
            "description": "Congenital Horner syndrome",
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            "code": "770627003",
            "description": "Desmin-related myofibrillar myopathy",
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            "code": "770630005",
            "description": "Distal hereditary motor neuropathy type 1",
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            "code": "770643005",
            "description": "Mesial temporal lobe epilepsy with hippocampal sclerosis",
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            "code": "770655004",
            "description": "Microcephalus, brain defect, spasticity, hypernatremia syndrome",
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            "code": "770664009",
            "description": "Neonatal brainstem dysfunction",
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            "code": "770678005",
            "description": "Progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy-like syndrome",
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            "code": "770680004",
            "description": "Prader-Willi-like syndrome",
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            "code": "770682007",
            "description": "Rosette-forming glioneuronal neoplasm",
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            "code": "770683002",
            "description": "Secondary syringomyelia",
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            "code": "770720005",
            "description": "Autosomal recessive spastic paraplegia type 58",
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            "code": "770721009",
            "description": "Microcephaly, thin corpus callosum, intellectual disability syndrome",
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            "description": "Proximal myopathy with extrapyramidal signs",
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            "code": "770724001",
            "description": "Autosomal recessive spastic paraplegia type 70",
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            "description": "Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly",
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            "code": "770727008",
            "description": "Spinal muscular atrophy with respiratory distress type 2",
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            "code": "770751003",
            "description": "Severe motor and intellectual disabilities, sensorineural deafness, dystonia syndrome",
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            "code": "770755007",
            "description": "Intellectual disability, seizures, hypotonia, ophthalmologic, skeletal anomalies syndrome",
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            "code": "770757004",
            "description": "X-linked parkinsonism with spasticity syndrome",
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            "code": "770758009",
            "description": "New-onset refractory status epilepticus",
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            "code": "770759001",
            "description": "Autosomal dominant intermediate Charcot-Marie-Tooth disease type F",
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            "code": "770786001",
            "description": "Hereditary inclusion body myopathy type 4",
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            "code": "770792007",
            "description": "Adult-onset distal myopathy due to valosin containing protein mutation",
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            "code": "770898002",
            "description": "Autosomal recessive cerebellar ataxia, epilepsy, intellectual disability syndrome due to WW domain containing oxidoreductase deficiency",
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            "code": "770939009",
            "description": "Huntington disease-like 3",
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            "code": "770941005",
            "description": "Alopecia, progressive neurological defect, endocrinopathy syndrome",
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            "code": "77097004",
            "description": "Oculopharyngeal muscular dystrophy",
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            "code": "771074000",
            "description": "Microcephaly, short stature, intellectual disability, facial dysmorphism syndrome",
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            "code": "771076003",
            "description": "Leptomyelolipoma",
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            "code": "771081007",
            "description": "Distal hereditary motor neuropathy type 7",
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            "code": "771141002",
            "description": "Benign partial epilepsy with secondarily generalized seizures in infancy",
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            "code": "771142009",
            "description": "Cortical dysplasia with focal epilepsy syndrome",
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            "code": "771143004",
            "description": "Hereditary motor and sensory neuropathy type 5",
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            "code": "771144005",
            "description": "Hereditary motor and sensory neuropathy with acrodystrophy",
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            "code": "771146007",
            "description": "Holoprosencephaly with caudal dysgenesis syndrome",
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            "code": "771147003",
            "description": "Isolated arhinencephaly",
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            "code": "771148008",
            "description": "X-linked colobomatous microphthalmia, microcephaly, intellectual disability, short stature syndrome",
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            "code": "771179007",
            "description": "Extrasystoles, short stature, hyperpigmentation, microcephaly syndrome",
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            "code": "771184001",
            "description": "Leukoencephalopathy, palmoplantar keratoderma syndrome",
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            "code": "771223000",
            "description": "Infantile epileptic dyskinetic encephalopathy",
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            "code": "771234002",
            "description": "Isolated bilateral hemispheric cerebellar hypoplasia",
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            "code": "771261002",
            "description": "Digital extensor muscle aplasia with polyneuropathy",
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            "code": "771263004",
            "description": "Ptosis and vocal cord paralysis syndrome",
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            "code": "771267003",
            "description": "Congenital muscular dystrophy with integrin alpha-7 deficiency",
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            "description": "Steroid-responsive encephalopathy associated with autoimmune thyroiditis",
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            "description": "Congenital muscular dystrophy due to lamin A/C mutation",
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            "description": "Intrapontine hemorrhage",
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            "description": "Autosomal recessive lower motor neuron disease with childhood onset",
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            "description": "Severe neonatal onset encephalopathy with microcephaly",
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            "description": "Benign nocturnal alternating hemiplegia of childhood",
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            "description": "Progressive polyneuropathy with bilateral striatal necrosis",
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            "code": "771307003",
            "description": "Charcot-Marie-Tooth disease type 2B5",
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            "description": "Non-acquired combined pituitary hormone deficiency, sensorineural hearing loss, spine abnormalities syndrome",
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            "description": "Autosomal dominant limb-girdle muscular dystrophy type 1H",
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            "description": "Delirium following surgical procedure",
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            "description": "Hyperactive delirium following surgical procedure",
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            "description": "Hypoactive delirium following surgical procedure",
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            "description": "Mixed hyperactive hypoactive delirium following surgical procedure",
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            "code": "771448004",
            "description": "Autism epilepsy syndrome due to branched chain ketoacid dehydrogenase kinase deficiency",
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            "description": "Early-onset spastic ataxia, myoclonic epilepsy, neuropathy syndrome",
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            "description": "Jawad syndrome",
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            "description": "Young adult-onset distal hereditary motor neuropathy",
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            "description": "Autosomal recessive leukoencephalopathy, ischemic stroke, retinitis pigmentosa syndrome",
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            "description": "Solute carrier family 35 member A2 congenital disorder of glycosylation",
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            "description": "Autosomal dominant childhood-onset proximal spinal muscular atrophy",
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            "code": "772224009",
            "description": "Warburg micro syndrome",
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            "description": "RAB18, member RAS oncogene family deficiency",
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            "description": "Spina bifida of lumbar region",
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            "code": "77274005",
            "description": "Idiopathic diabetes insipidus",
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            "description": "Cyclin-dependent kinase-like 5 deficiency",
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            "description": "Hydrocephalus, blue sclera, nephropathy syndrome",
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            "description": "Congenital lethal myopathy Compton North type",
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            "description": "Zechi Ceide syndrome",
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            "description": "Autosomal recessive intermediate Charcot-Marie-Tooth disease type A",
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            "description": "Autosomal recessive intermediate Charcot-Marie-Tooth disease type B",
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            "description": "Autosomal dominant Charcot-Marie-Tooth disease type 2Q",
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            "description": "Autosomal recessive frontotemporal pachygyria",
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            "description": "Autosomal recessive intermediate Charcot-Marie-Tooth disease type C",
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            "description": "Contiguous ABCD1 DXS1357E deletion syndrome",
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            "description": "Autosomal recessive spastic paraplegia type 59",
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            "description": "Childhood-onset spasticity with hyperglycinemia",
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            "description": "Chudley McCullough syndrome",
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            "description": "Bing-Neel syndrome",
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            "description": "FAST kinase domains 2-related infantile mitochondrial encephalomyopathy",
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            "description": "Neu-Laxova syndrome",
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            "description": "Steinert myotonic dystrophy syndrome",
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            "description": "Acquired hydrocephalus of newborn",
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            "description": "Autosomal dominant spastic paraplegia type 3",
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            "description": "Distal myopathy with anterior tibial onset",
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            "description": "Gemignani syndrome",
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            "description": "Primary dystonia DYT17 type",
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            "description": "Recessive mitochondrial ataxia syndrome",
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            "description": "Dystonia aphonia syndrome",
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            "description": "Congenital pontocerebellar hypoplasia type 10",
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            "description": "Autosomal recessive spastic paraplegia type 69",
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            "description": "Autosomal recessive spastic paraplegia type 71",
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            "description": "Autosomal spastic paraplegia type 72",
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            "code": "782744007",
            "description": "Lipoic acid synthetase deficiency",
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            "code": "782746009",
            "description": "Autosomal recessive spastic paraplegia type 60",
            "attributes": null
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            "code": "782747000",
            "description": "Autosomal recessive spastic paraplegia type 66",
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          {
            "code": "782752005",
            "description": "Peripheral neuropathy, myopathy, hoarseness, hearing loss syndrome",
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            "code": "782753000",
            "description": "Intellectual disability, coarse face, macrocephaly, cerebellar hypotrophy syndrome",
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            "code": "782754006",
            "description": "Foveal hypoplasia, optic nerve decussation defect, anterior segment dysgenesis syndrome",
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            "code": "782755007",
            "description": "Primary microcephaly, mild intellectual disability, young-onset diabetes syndrome",
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            "code": "782757004",
            "description": "Congenital microcephaly, severe encephalopathy, progressive cerebral atrophy syndrome",
            "attributes": null
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            "code": "782771007",
            "description": "Mitochondrial deoxyribonucleic acid depletion syndrome hepatocerebrorenal form",
            "attributes": null
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          {
            "code": "782772000",
            "description": "Congenital muscular dystrophy with intellectual disability and severe epilepsy",
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            "code": "782824007",
            "description": "Sodium channelopathy-related small fiber neuropathy",
            "attributes": null
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          {
            "code": "782825008",
            "description": "Primary microcephaly, epilepsy, permanent neonatal diabetes syndrome",
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          {
            "code": "782826009",
            "description": "Charcot-Marie-Tooth disease type 2P",
            "attributes": null
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          {
            "code": "782829002",
            "description": "Autosomal dominant Charcot-Marie-Tooth disease type 2O",
            "attributes": null
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            "code": "782879004",
            "description": "Occipital pachygyria and polymicrogyria",
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          {
            "code": "782881002",
            "description": "Hereditary sensorimotor neuropathy with hyperelastic skin",
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          {
            "code": "782884005",
            "description": "Pontine tegmental cap dysplasia",
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            "code": "782886007",
            "description": "Infantile spasms, psychomotor retardation, progressive brain atrophy, basal ganglia disease syndrome",
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            "code": "782887003",
            "description": "Inherited congenital spastic tetraplegia",
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            "code": "782917007",
            "description": "Familial adrenal hypoplasia with absent pituitary luteinizing hormone",
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          {
            "code": "782941005",
            "description": "Richieri Costa-da Silva syndrome",
            "attributes": null
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          {
            "code": "782951006",
            "description": "Thoracic dysplasia and hydrocephalus syndrome",
            "attributes": null
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          {
            "code": "783005002",
            "description": "Severe microbrachycephaly, intellectual disability, athetoid cerebral palsy syndrome",
            "attributes": null
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          {
            "code": "783008000",
            "description": "Pituitary dermoid and epidermoid cysts",
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          {
            "code": "783009008",
            "description": "Pituitary deficiency due to Rathke cleft cysts",
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          {
            "code": "783012006",
            "description": "Parkinsonian pyramidal syndrome",
            "attributes": null
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          {
            "code": "783016009",
            "description": "Panhypophysitis",
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          {
            "code": "783055005",
            "description": "Progressive myoclonic epilepsy type 5",
            "attributes": null
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          {
            "code": "783057002",
            "description": "DNA replication helicase/nuclease 2-related mitochondrial deoxyribonucleic acid deletion syndrome",
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            "code": "783060009",
            "description": "Autosomal recessive cerebellar ataxia, psychomotor delay syndrome",
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          {
            "code": "78306007",
            "description": "Epidural ascending spinal paralysis",
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          {
            "code": "783062001",
            "description": "Progressive myoclonic epilepsy type 6",
            "attributes": null
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            "code": "783064000",
            "description": "Progressive myoclonic epilepsy type 3",
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          {
            "code": "783091003",
            "description": "46,XY gonadal dysgenesis, motor and sensory neuropathy syndrome",
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            "code": "783094006",
            "description": "Autosomal recessive spastic paraplegia type 14",
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          {
            "code": "783139000",
            "description": "Progressive myoclonic epilepsy type 8",
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            "code": "783148005",
            "description": "Distal nebulin myopathy",
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          {
            "code": "783157004",
            "description": "Leigh syndrome with nephrotic syndrome",
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            "code": "783158009",
            "description": "Infundibulo neurohypophysitis",
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            "code": "783160006",
            "description": "Hereditary gelsolin amyloidosis",
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            "code": "783161005",
            "description": "Familial dementia British type",
            "attributes": null
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            "code": "783166000",
            "description": "Distal anoctaminopathy",
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            "code": "783174004",
            "description": "Congenital muscular dystrophy with intellectual disability",
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            "code": "783175003",
            "description": "Congenital muscular dystrophy without intellectual disability",
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            "code": "783176002",
            "description": "Congenital muscular dystrophy with cerebellar involvement",
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            "code": "783179009",
            "description": "Cranio-cervical dystonia with laryngeal and upper limb involvement",
            "attributes": null
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            "code": "783203003",
            "description": "Ataxia with tapetoretinal degeneration syndrome",
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            "code": "783242003",
            "description": "Adult-onset cervical dystonia DYT23 type",
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            "code": "783243008",
            "description": "Adenohypophysitis",
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            "code": "783258000",
            "description": "Familial dementia Danish type",
            "attributes": null
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            "code": "783413008",
            "description": "Multiple aneurysms of cerebral artery",
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            "code": "783415001",
            "description": "Aneurysm of internal carotid bifurcation",
            "attributes": null
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            "code": "783416000",
            "description": "Aneurysm of anterior cerebral artery",
            "attributes": null
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            "code": "783417009",
            "description": "Aneurysm of posterior inferior cerebellar artery",
            "attributes": null
          },
          {
            "code": "783418004",
            "description": "Aneurysm of anterior communicating artery",
            "attributes": null
          },
          {
            "code": "783419007",
            "description": "Aneurysm of posterior cerebral artery",
            "attributes": null
          },
          {
            "code": "783420001",
            "description": "Aneurysm of middle cerebral artery",
            "attributes": null
          },
          {
            "code": "783421002",
            "description": "Aneurysm of posterior communicating artery",
            "attributes": null
          },
          {
            "code": "783422009",
            "description": "Aneurysm of internal carotid-anterior communicating artery zone",
            "attributes": null
          },
          {
            "code": "783423004",
            "description": "Aneurysm of internal carotid-posterior communicating artery zone",
            "attributes": null
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            "code": "783550006",
            "description": "Hereditary sensory and autonomic neuropathy type 7",
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            "code": "783554002",
            "description": "Autosomal recessive limb girdle muscular dystrophy type 2U",
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            "code": "783558004",
            "description": "Combined oxidative phosphorylation defect type 11",
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          {
            "code": "78358001",
            "description": "Amphetamine withdrawal",
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          {
            "code": "783618006",
            "description": "Lower motor neuron syndrome with late-adult onset",
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            "code": "783622001",
            "description": "Autosomal dominant spastic paraplegia type 38",
            "attributes": null
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            "code": "783629005",
            "description": "Congenital aneurysm of cerebral artery",
            "attributes": null
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            "code": "783630000",
            "description": "Congenital aneurysm of precerebral artery",
            "attributes": null
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            "code": "783697000",
            "description": "X-linked spastic paraplegia type 16",
            "attributes": null
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            "code": "783698005",
            "description": "Autosomal dominant spastic paraplegia type 13",
            "attributes": null
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          {
            "code": "783701002",
            "description": "Port-wine nevi, mega cisterna magna, hydrocephalus syndrome",
            "attributes": null
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          {
            "code": "783703004",
            "description": "White matter hypoplasia, corpus callosum agenesis, intellectual disability syndrome",
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            "code": "783705006",
            "description": "Sporadic hyperekplexia",
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            "code": "783707003",
            "description": "Cerebral aneurysm due to dissection of cerebral artery",
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            "code": "783716004",
            "description": "Acquired aneurysm of cerebral artery",
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            "code": "783722008",
            "description": "Myopathy and diabetes mellitus",
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          {
            "code": "783731008",
            "description": "Fibromuscular dysplasia of wall of carotid artery",
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            "code": "783733006",
            "description": "Fibromuscular dysplasia of wall of bilateral carotid arteries",
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          {
            "code": "783734000",
            "description": "Mitochondrial deoxyribonucleic acid depletion syndrome, hepatocerebral form due to deoxyguanosine kinase deficiency",
            "attributes": null
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            "code": "783739005",
            "description": "Familial temporal lobe epilepsy",
            "attributes": null
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            "code": "783764008",
            "description": "Autosomal recessive spastic paraplegia type 56",
            "attributes": null
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            "code": "783787000",
            "description": "Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations",
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          {
            "code": "784341001",
            "description": "Amyotrophic lateral sclerosis type 4",
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            "code": "784342008",
            "description": "Familial infantile myoclonic epilepsy",
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            "code": "784343003",
            "description": "Autosomal recessive spastic ataxia with leukoencephalopathy",
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            "code": "784344009",
            "description": "Cortical dysgenesis with pontocerebellar hypoplasia due to tubulin beta 3 class III mutation",
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            "code": "784345005",
            "description": "Malignant migrating partial seizures of infancy",
            "attributes": null
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            "code": "784346006",
            "description": "Navajo neurohepatopathy",
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            "code": "784348007",
            "description": "Familial congenital mirror movements",
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            "code": "784352007",
            "description": "X-linked scapuloperoneal muscular dystrophy",
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            "code": "784370005",
            "description": "Mitochondrial myopathy with reversible cytochrome C oxidase deficiency",
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            "code": "784371009",
            "description": "Huntington disease-like 1",
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            "code": "784372002",
            "description": "Familial mesial temporal lobe epilepsy with febrile seizures",
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            "code": "784377008",
            "description": "Autosomal dominant epilepsy with auditory features",
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            "code": "784391002",
            "description": "Autosomal dominant adult-onset proximal spinal muscular atrophy",
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            "code": "78468005",
            "description": "Erb's muscular dystrophy",
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            "code": "785298001",
            "description": "Muscle eye brain disease with bilateral multicystic leukodystrophy",
            "attributes": null
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            "code": "785299009",
            "description": "Cobblestone lissencephaly without muscular or ocular involvement",
            "attributes": null
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            "code": "785300001",
            "description": "Infantile-onset autosomal recessive non progressive cerebellar ataxia",
            "attributes": null
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            "code": "785301002",
            "description": "Childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia",
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            "code": "785302009",
            "description": "Adult-onset autosomal recessive cerebellar ataxia",
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            "code": "785303004",
            "description": "Multiple congenital anomalies, hypotonia, seizures syndrome",
            "attributes": null
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            "code": "785304005",
            "description": "Autosomal recessive spastic paraplegia type 24",
            "attributes": null
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          {
            "code": "785305006",
            "description": "Autosomal dominant spastic paraplegia type 8",
            "attributes": null
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            "code": "785306007",
            "description": "Lissencephaly co-occurrent with congenital cerebellar hypoplasia type E",
            "attributes": null
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            "code": "785307003",
            "description": "Lissencephaly co-occurrent with congenital cerebellar hypoplasia type A",
            "attributes": null
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            "code": "78569004",
            "description": "Posterior inferior cerebellar artery syndrome",
            "attributes": null
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          {
            "code": "785726009",
            "description": "Hyperekplexia epilepsy syndrome",
            "attributes": null
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          {
            "code": "785809005",
            "description": "Mills syndrome",
            "attributes": null
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            "code": "785810000",
            "description": "Synucleinopathy",
            "attributes": null
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            "code": "78689005",
            "description": "Chronic brain syndrome",
            "attributes": null
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            "code": "78693004",
            "description": "Congenital hypoplasia of part of brain",
            "attributes": null
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          {
            "code": "787037000",
            "description": "Congenital muscular dystrophy type 1A",
            "attributes": null
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            "code": "787044009",
            "description": "Stenosis of bilateral carotid arteries",
            "attributes": null
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          {
            "code": "787174003",
            "description": "Intellectual disability, hyperkinetic movement, truncal ataxia syndrome",
            "attributes": null
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            "code": "78784005",
            "description": "Amyelia",
            "attributes": null
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            "code": "788417006",
            "description": "Alopecia, epilepsy, intellectual disability syndrome Moynahan type",
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            "code": "788454002",
            "description": "Stenosis of bilateral vertebral arteries",
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            "code": "788455001",
            "description": "Occlusion of bilateral pontine arteries",
            "attributes": null
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          {
            "code": "788756004",
            "description": "Spindle cell oncocytoma of posterior pituitary gland",
            "attributes": null
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          {
            "code": "788757008",
            "description": "Pituicytoma of posterior pituitary gland",
            "attributes": null
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          {
            "code": "788758003",
            "description": "Sellar ependymoma of posterior pituitary gland",
            "attributes": null
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            "code": "78879009",
            "description": "Intracranial hemorrhage following injury with open intracranial wound AND concussion",
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            "code": "788863007",
            "description": "Amnestic disorder caused by psychoactive substance",
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            "code": "788864001",
            "description": "Amnestic disorder caused by volatile solvent",
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            "code": "788880006",
            "description": "Cerebral ischemic stroke due to dissection of artery",
            "attributes": null
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            "code": "788881005",
            "description": "Cerebral ischemic stroke due to aortic arch embolism",
            "attributes": null
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          {
            "code": "788882003",
            "description": "Cerebral ischemic stroke due to global hypoperfusion with watershed infarct",
            "attributes": null
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            "code": "788883008",
            "description": "Cerebral ischemic stroke due to hypercoagulable state",
            "attributes": null
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            "code": "788884002",
            "description": "Cerebral ischemic stroke due to subarachnoid hemorrhage",
            "attributes": null
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            "code": "788898005",
            "description": "Dementia caused by volatile inhalant",
            "attributes": null
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            "code": "788899002",
            "description": "Dementia due to pellagra",
            "attributes": null
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            "code": "788908000",
            "description": "Dissociative neurological symptom disorder co-occurrent with dystonia",
            "attributes": null
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            "code": "788911004",
            "description": "Dissociative neurological symptom disorder co-occurrent with Parkinsonism",
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          {
            "code": "788915008",
            "description": "Encephalitis caused by Henipavirus",
            "attributes": null
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          {
            "code": "788916009",
            "description": "Encephalopathy caused by ammonia",
            "attributes": null
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          {
            "code": "788930004",
            "description": "Focal contusion of brain",
            "attributes": null
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            "code": "788931000",
            "description": "Focal contusion of occipital lobe",
            "attributes": null
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            "code": "788932007",
            "description": "Focal contusion of parietal lobe",
            "attributes": null
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          {
            "code": "788933002",
            "description": "Focal contusion of temporal lobe",
            "attributes": null
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          {
            "code": "788934008",
            "description": "Focal laceration of brain",
            "attributes": null
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            "code": "788983007",
            "description": "Mood disorder caused by cannabis",
            "attributes": null
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          {
            "code": "789005009",
            "description": "Paralysis of uvula after diphtheria",
            "attributes": null
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          {
            "code": "789046004",
            "description": "Sleep-related movement disorder caused by drug",
            "attributes": null
          },
          {
            "code": "789047008",
            "description": "Sleep-related movement disorder caused by substance",
            "attributes": null
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          {
            "code": "789053008",
            "description": "Transient motor tic",
            "attributes": null
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          {
            "code": "789063000",
            "description": "Primary hyperaldosteronism, seizures, neurological abnormalities syndrome",
            "attributes": null
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          {
            "code": "789120001",
            "description": "Neurenteric cyst",
            "attributes": null
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          {
            "code": "78914008",
            "description": "Laceration of brain",
            "attributes": null
          },
          {
            "code": "789187001",
            "description": "X-linked acrogigantism due to Xq26 microduplication",
            "attributes": null
          },
          {
            "code": "789657008",
            "description": "ATPase cation transporting 13A2 related juvenile neuronal ceroid lipofuscinosis",
            "attributes": null
          },
          {
            "code": "78968003",
            "description": "Brain stem contusion with open intracranial wound",
            "attributes": null
          },
          {
            "code": "791000124107",
            "description": "2-methyl-3-hydroxybutyric aciduria",
            "attributes": null
          },
          {
            "code": "792004",
            "description": "Jakob-Creutzfeldt disease",
            "attributes": null
          },
          {
            "code": "79220008",
            "description": "Brain stem contusion without open intracranial wound AND with concussion",
            "attributes": null
          },
          {
            "code": "79267007",
            "description": "Retinal migraine",
            "attributes": null
          },
          {
            "code": "7931000119101",
            "description": "Anterior choroidal artery thrombosis",
            "attributes": null
          },
          {
            "code": "79341000119107",
            "description": "Mixed dementia",
            "attributes": null
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          {
            "code": "79348005",
            "description": "Simple partial seizure, consciousness not impaired",
            "attributes": null
          },
          {
            "code": "79385002",
            "description": "Lowe syndrome",
            "attributes": null
          },
          {
            "code": "79591004",
            "description": "Spastic paralysis due to spinal birth injury",
            "attributes": null
          },
          {
            "code": "79631006",
            "description": "Absence seizure",
            "attributes": null
          },
          {
            "code": "79633009",
            "description": "Spastic hemiplegia",
            "attributes": null
          },
          {
            "code": "79745005",
            "description": "Reflex epilepsy",
            "attributes": null
          },
          {
            "code": "79897009",
            "description": "Cerebellar abscess",
            "attributes": null
          },
          {
            "code": "7990002",
            "description": "Immunoglobulinemia with isolated somatotropin deficiency",
            "attributes": null
          },
          {
            "code": "80098002",
            "description": "Diffuse Lewy body disease",
            "attributes": null
          },
          {
            "code": "80180004",
            "description": "Pallidonigral degeneration",
            "attributes": null
          },
          {
            "code": "80328002",
            "description": "Progressive cone-rod dystrophy",
            "attributes": null
          },
          {
            "code": "80381005",
            "description": "Adductor spastic dysphonia of dystonia",
            "attributes": null
          },
          {
            "code": "80495009",
            "description": "Sleep walking disorder",
            "attributes": null
          },
          {
            "code": "80544005",
            "description": "Spongy degeneration of central nervous system",
            "attributes": null
          },
          {
            "code": "80599001",
            "description": "Isolated corticotropin deficiency",
            "attributes": null
          },
          {
            "code": "80606009",
            "description": "Carotid artery embolism",
            "attributes": null
          },
          {
            "code": "80651009",
            "description": "Aicardi's syndrome",
            "attributes": null
          },
          {
            "code": "80690008",
            "description": "Degenerative disease of the central nervous system",
            "attributes": null
          },
          {
            "code": "80734006",
            "description": "Marinesco-Sjögren syndrome",
            "attributes": null
          },
          {
            "code": "80758005",
            "description": "Embolism of lateral venous sinus",
            "attributes": null
          },
          {
            "code": "80849007",
            "description": "Gigantism",
            "attributes": null
          },
          {
            "code": "80868005",
            "description": "Cocaine withdrawal",
            "attributes": null
          },
          {
            "code": "80901002",
            "description": "Endophlebitis of torcular Herophili",
            "attributes": null
          },
          {
            "code": "80935004",
            "description": "Flaccid hemiplegia",
            "attributes": null
          },
          {
            "code": "80976008",
            "description": "Myasthenic crisis",
            "attributes": null
          },
          {
            "code": "80980003",
            "description": "Open fracture of C5-C7 level with spinal cord injury",
            "attributes": null
          },
          {
            "code": "81042008",
            "description": "Congenital anomaly of spinal cord",
            "attributes": null
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            "code": "81211007",
            "description": "Primary lateral sclerosis",
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            "code": "81308009",
            "description": "Disorder of brain",
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            "code": "813921000000104",
            "description": "Spastic hemiplegic cerebral palsy",
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            "code": "81412002",
            "description": "Cortex contusion with open intracranial wound AND loss of consciousness",
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            "code": "81442004",
            "description": "Closed fracture of cervical region with spinal cord injury",
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            "code": "81475007",
            "description": "Acquired nephrogenic diabetes insipidus",
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          {
            "code": "81526008",
            "description": "Hydromeningomyelocele",
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          {
            "code": "816067005",
            "description": "Diabetes, hypogonadism, deafness, intellectual disability syndrome",
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            "code": "816068000",
            "description": "Periventricular nodular heterotopia",
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          {
            "code": "816205008",
            "description": "Malignant pituitary blastoma",
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          },
          {
            "code": "81642009",
            "description": "Late effect of spinal cord injury",
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          {
            "code": "8166000",
            "description": "Thrombophlebitis of basilar sinus",
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          },
          {
            "code": "816984002",
            "description": "Progressive multiple sclerosis",
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          },
          {
            "code": "81780002",
            "description": "Beckwith-Wiedemann syndrome",
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            "code": "8183009",
            "description": "Closed fracture of T7-T12 level with central cord syndrome",
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          {
            "code": "81854007",
            "description": "Alexander's disease",
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            "code": "81896006",
            "description": "Dysmorphic sialidosis with renal involvement",
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          {
            "code": "818967003",
            "description": "Medulloepithelioma of central nervous system",
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          },
          {
            "code": "82058009",
            "description": "Myelocele",
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          {
            "code": "82077006",
            "description": "Myotubular myopathy",
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            "code": "822021000000103",
            "description": "Acute encephalitis",
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            "code": "82339009",
            "description": "Amphetamine-induced anxiety disorder",
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            "code": "82344002",
            "description": "Cerebellar contusion with open intracranial wound",
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            "code": "82346000",
            "description": "Acquired obstructive hydrocephalus",
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          {
            "code": "82351000119105",
            "description": "Altered behavior co-occurrent and due to Pick's disease",
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            "code": "82361000119107",
            "description": "Altered behavior in dementia due to Huntington chorea",
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          {
            "code": "82371000119101",
            "description": "Dementia due to multiple sclerosis with altered behavior",
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            "code": "82381000119103",
            "description": "Epileptic dementia with behavioral disturbance",
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            "code": "82401000",
            "description": "Simple partial seizure with motor dysfunction",
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            "code": "82501000119102",
            "description": "Anaplastic astrocytoma of central nervous system",
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          {
            "code": "82547005",
            "description": "Acute adenoviral meningoencephalitis",
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            "code": "82598004",
            "description": "Secondary hypothyroidism",
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          {
            "code": "8269002",
            "description": "Cerebrospinal angiopathy",
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            "code": "827172005",
            "description": "X-linked progressive cerebellar ataxia",
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            "code": "82793005",
            "description": "Hypothalamic obesity",
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            "code": "82800008",
            "description": "Dipsogenic diabetes insipidus",
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            "code": "8291000119107",
            "description": "Atonic epilepsy",
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          {
            "code": "82959004",
            "description": "Dementia paralytica juvenilis",
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            "code": "830015009",
            "description": "Dermoid cyst of spinal cord",
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          },
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            "code": "830032008",
            "description": "Dermoid cyst of occipital lobe",
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          },
          {
            "code": "830033003",
            "description": "Dermoid cyst of brain",
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          {
            "code": "8301004",
            "description": "Caudal dysplasia sequence",
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            "code": "83157008",
            "description": "Fatal familial insomnia",
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          {
            "code": "83159006",
            "description": "Cytomegalovirus encephalitis",
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            "code": "83168008",
            "description": "Psychoactive substance-induced organic amnestic disorder",
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          {
            "code": "83304000",
            "description": "Dubini's chorea",
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          {
            "code": "833326008",
            "description": "Cortical vascular dementia",
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          {
            "code": "83351003",
            "description": "Basilar migraine",
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          },
          {
            "code": "83367009",
            "description": "Amphetamine-induced organic mental disorder",
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          {
            "code": "83465002",
            "description": "Neuroleptic-induced acute dystonia",
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            "code": "83501007",
            "description": "Organic mood disorder of mixed type",
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            "code": "836301008",
            "description": "Amnestic mild cognitive disorder",
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            "code": "83716008",
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          {
            "code": "83759003",
            "description": "Adductor spastic dysphonia of musculoskeletal tension reaction",
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            "code": "838275008",
            "description": "Stenosis of cerebral artery",
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          {
            "code": "838276009",
            "description": "Amyotrophic lateral sclerosis, parkinsonism, dementia complex",
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            "code": "838308007",
            "description": "Fibromuscular dysplasia of wall of intracranial artery",
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            "code": "838309004",
            "description": "Cerebrovascular abnormality due to Takayasu disease",
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          {
            "code": "838315004",
            "description": "Encephalomyelitis caused by Burkholderia",
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            "code": "83832001",
            "description": "Metachromatic leukodystrophy without arylsulfatase deficiency",
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          {
            "code": "838323002",
            "description": "Autoimmune opsoclonus myoclonus",
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            "code": "838331007",
            "description": "Ataxia due to chronic infection of central nervous system",
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            "code": "838332000",
            "description": "Abscess of brainstem",
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          {
            "code": "838339009",
            "description": "Basal encephalocele",
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            "code": "838351006",
            "description": "Acute seizure due to infection of central nervous system",
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            "code": "838371002",
            "description": "Abscess of cerebral hemisphere lobe",
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            "code": "838373004",
            "description": "Abscess of frontal lobe",
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            "code": "838383000",
            "description": "Chorea caused by toxin",
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          {
            "code": "838390005",
            "description": "Abscess of spinal cord caused by fungus",
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            "code": "838392002",
            "description": "Abscess of parietal lobe",
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          {
            "code": "838393007",
            "description": "Abscess of pons cerebri",
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            "code": "838394001",
            "description": "Abscess of midbrain",
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            "code": "838395000",
            "description": "Abscess of occipital lobe",
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            "description": "Mental retardation, adducted thumbs, shuffling gait, aphasia syndrome",
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            "code": "838528007",
            "description": "Mood disorder with manic symptoms caused by amfetamine and amfetamine derivative",
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            "code": "838529004",
            "description": "Mood disorder with mixed depressive and manic symptoms caused by amfetamine and amfetamine derivative",
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          {
            "code": "838530009",
            "description": "Mood disorder with depressive symptoms caused by amfetamine and amfetamine derivative",
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          {
            "code": "83942000",
            "description": "Acute disseminated encephalomyelitis",
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            "code": "83982007",
            "description": "Subacute necrotic myelopathy",
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          {
            "code": "83991006",
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          {
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            "description": "Dissection of extracranial carotid artery",
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            "code": "840420004",
            "description": "Dissection of extracranial vertebral artery",
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          {
            "code": "840422007",
            "description": "Dissection of anterior cerebral artery",
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          {
            "code": "840434004",
            "description": "Dissection of posterior cerebral artery",
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            "code": "840436002",
            "description": "Dissection of middle cerebral artery",
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            "description": "Dissection of multiple cerebral arteries",
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          {
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            "description": "Dissection of intracranial vertebral artery",
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          {
            "code": "840439009",
            "description": "Dissection of intracranial carotid artery",
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          {
            "code": "840440006",
            "description": "Encephalitis caused by Leptospira species",
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            "description": "Dissection of intracranial artery",
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          {
            "code": "840442003",
            "description": "Encephalitis caused by human immunodeficiency virus type 2",
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            "code": "840449007",
            "description": "Cognitive impairment caused by ingestible alcohol",
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            "code": "840452004",
            "description": "Classical sporadic Creutzfeldt-Jakob disease",
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            "code": "840454003",
            "description": "Cyst of spinal cord caused by parasite",
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            "code": "840464007",
            "description": "Dementia due to carbon monoxide poisoning",
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            "code": "840465008",
            "description": "Dementia due to iron deficiency",
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            "code": "840471002",
            "description": "Hydrocephalus due to Dandy-Walker malformation",
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          {
            "code": "840496004",
            "description": "Encephalitis caused by Borrelia species",
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          {
            "code": "840498003",
            "description": "Encephalitis caused by human immunodeficiency virus type 1",
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            "code": "840501003",
            "description": "Dystonia caused by toxin",
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            "code": "840505007",
            "description": "Down syndrome co-occurrent with leukemoid reaction associated transient neonatal pustulosis",
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            "description": "Compression of spinal cord due to intraspinal abscess",
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            "description": "Incomplete spinal cord syndrome",
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          {
            "code": "84160009",
            "description": "Laryngeal hemiplegia",
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            "description": "Contusion of brain with open intracranial wound",
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          {
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            "description": "Partial epileptic seizure of occipital lobe with impairment of consciousness",
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            "description": "Partial epileptic seizure of temporal lobe with impairment of consciousness",
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            "description": "Intractable partial temporal lobe epilepsy with impairment of consciousness",
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            "description": "Intractable partial parietal lobe epilepsy with impairment of consciousness",
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            "description": "Cerebral venous thrombosis of pregnancy AND/OR puerperium",
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            "code": "84221000119101",
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            "description": "Intractable partial occipital lobe epilepsy with impairment of consciousness",
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            "code": "843004",
            "description": "Poliomyelomalacia",
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            "code": "84455002",
            "description": "Spinal paraplegia",
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            "code": "84461004",
            "description": "Exencephaly",
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            "code": "84590007",
            "description": "Lower motor neuron disease",
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            "description": "Closed fracture of C1-C4 level with incomplete cord lesion",
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            "description": "Functional hypogonadotropic hypogonadism",
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            "description": "Epilepsy",
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            "description": "Cerebellar laceration with open intracranial wound AND loss of consciousness",
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          {
            "code": "85039006",
            "description": "Postpartum amenorrhea-galactorrhea syndrome",
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          {
            "code": "85102008",
            "description": "Cerebellar ataxia",
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          {
            "code": "8511007",
            "description": "Transient tic disorder, single episode",
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          {
            "code": "85262003",
            "description": "Open fracture of T1-T6 level with posterior cord syndrome",
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            "code": "8528005",
            "description": "Acute ascending myelitis",
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            "code": "85505000",
            "description": "Adult spinal muscular atrophy",
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          {
            "code": "8551000119100",
            "description": "Benign neoplasm of spinal intradural extramedullary space",
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          },
          {
            "code": "85561006",
            "description": "Uncomplicated alcohol withdrawal",
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          {
            "code": "85592008",
            "description": "Primary progressive cerebellar degeneration",
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            "code": "8563000",
            "description": "Cholinergic crisis",
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          {
            "code": "85641006",
            "description": "Hemianencephaly",
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          {
            "code": "85672005",
            "description": "Anterior horn cell disease",
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          {
            "code": "85821003",
            "description": "Acute non-psychotic brain syndrome",
            "attributes": null
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            "code": "85861002",
            "description": "Subchronic undifferentiated schizophrenia",
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            "code": "86003009",
            "description": "Carotid artery thrombosis",
            "attributes": null
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          {
            "code": "86044005",
            "description": "Amyotrophic lateral sclerosis",
            "attributes": null
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          {
            "code": "86073008",
            "description": "Hypersomatotropic gigantism",
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            "code": "860799000",
            "description": "Encephalopathy due to folate deficiency",
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            "code": "860802009",
            "description": "Ex-vacuo hydrocephalus due to infection",
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          {
            "code": "860803004",
            "description": "Hydrocephalus due to tuberculosis of brain",
            "attributes": null
          },
          {
            "code": "860804005",
            "description": "Epilepsy due to infectious encephalitis",
            "attributes": null
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          {
            "code": "860805006",
            "description": "Encephalomyelitis caused by Neisseria meningitidis",
            "attributes": null
          },
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            "code": "860806007",
            "description": "Epilepsy due to infectious meningitis",
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          {
            "code": "860807003",
            "description": "Hereditary autonomic neuropathy",
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          {
            "code": "860809000",
            "description": "Hereditary sensory autonomic neuropathy type IIA",
            "attributes": null
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            "code": "860810005",
            "description": "Hereditary sensory autonomic neuropathy type IIB",
            "attributes": null
          },
          {
            "code": "860811009",
            "description": "Hereditary sensory autonomic neuropathy type ID",
            "attributes": null
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          {
            "code": "860812002",
            "description": "Hereditary sensory autonomic neuropathy type IE",
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          {
            "code": "860813007",
            "description": "Hereditary sensory autonomic neuropathy type IA",
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          {
            "code": "860814001",
            "description": "Hereditary sensory autonomic neuropathy type IC",
            "attributes": null
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            "code": "860815000",
            "description": "Epilepsy due to neonatal central nervous system infection",
            "attributes": null
          },
          {
            "code": "860822008",
            "description": "Encephalitis caused by Nocardia",
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          },
          {
            "code": "860826006",
            "description": "Creutzfeldt-Jakob Disease caused by human growth hormone",
            "attributes": null
          },
          {
            "code": "860834000",
            "description": "Granuloma of brain caused by Schistosoma",
            "attributes": null
          },
          {
            "code": "860840007",
            "description": "Granuloma of brain caused by Schistosoma japonicum",
            "attributes": null
          },
          {
            "code": "860841006",
            "description": "Encephalomyelitis caused by bacterium",
            "attributes": null
          },
          {
            "code": "860842004",
            "description": "Encephalomyelitis caused by Coxiella burnetii",
            "attributes": null
          },
          {
            "code": "860849008",
            "description": "Granuloma of spinal cord caused by fungus",
            "attributes": null
          },
          {
            "code": "860851007",
            "description": "Granuloma of cerebral hemispheric lobe",
            "attributes": null
          },
          {
            "code": "860852000",
            "description": "Granuloma of brainstem",
            "attributes": null
          },
          {
            "code": "860864008",
            "description": "Granuloma of brain caused by Schistosoma haematobium",
            "attributes": null
          },
          {
            "code": "860865009",
            "description": "Encephalitis caused by Trypanosoma brucei gambiense",
            "attributes": null
          },
          {
            "code": "860866005",
            "description": "Encephalitis caused by Trypanosoma brucei rhodesiense",
            "attributes": null
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            "code": "860868006",
            "description": "Encephalitis caused by Me Tri virus",
            "attributes": null
          },
          {
            "code": "860881004",
            "description": "Flaccid diplegia of lower extremities",
            "attributes": null
          },
          {
            "code": "860886009",
            "description": "Granuloma of brain caused by Schistosoma mansoni",
            "attributes": null
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          {
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            "description": "Cerebellar contusion with open intracranial wound AND concussion",
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          {
            "code": "86188000",
            "description": "Kuru",
            "attributes": null
          },
          {
            "code": "8635005",
            "description": "Alcohol withdrawal delirium",
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          {
            "code": "864171000000103",
            "description": "Non-epileptic attack disorder",
            "attributes": null
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          {
            "code": "86444004",
            "description": "Niemann-Pick disease, type C, acute form",
            "attributes": null
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          {
            "code": "864471000000106",
            "description": "Anterior opercular syndrome",
            "attributes": null
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          {
            "code": "86558004",
            "description": "Cerebellar pressure cone",
            "attributes": null
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          {
            "code": "866045007",
            "description": "Myelitis caused by Actinomyces",
            "attributes": null
          },
          {
            "code": "866050001",
            "description": "Mixed germ cell neoplasm of central nervous system",
            "attributes": null
          },
          {
            "code": "866051002",
            "description": "Motor neuron disease due to lead intoxication",
            "attributes": null
          },
          {
            "code": "866053004",
            "description": "Middle interhemispheric variant of holoprosencephaly",
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          },
          {
            "code": "866055006",
            "description": "Myelitis caused by Enterovirus",
            "attributes": null
          },
          {
            "code": "866056007",
            "description": "Myelitis caused by Epstein-Barr virus",
            "attributes": null
          },
          {
            "code": "866057003",
            "description": "Myelitis caused by Dengue virus",
            "attributes": null
          },
          {
            "code": "866058008",
            "description": "Myelitis caused by Human echovirus",
            "attributes": null
          },
          {
            "code": "866059000",
            "description": "Myelitis caused by Human coxsackievirus A",
            "attributes": null
          },
          {
            "code": "866060005",
            "description": "Myelitis caused by Cytomegalovirus",
            "attributes": null
          },
          {
            "code": "866061009",
            "description": "Myelitis caused by Coccidioides",
            "attributes": null
          },
          {
            "code": "866062002",
            "description": "Myelitis caused by Coenurus cerebralis",
            "attributes": null
          },
          {
            "code": "866063007",
            "description": "Myelitis caused by Mycoplasma pneumoniae",
            "attributes": null
          },
          {
            "code": "866064001",
            "description": "Myelitis caused by Aspergillus",
            "attributes": null
          },
          {
            "code": "866065000",
            "description": "Myelitis caused by Schistosoma mansoni",
            "attributes": null
          },
          {
            "code": "866066004",
            "description": "Myelitis caused by Borrelia burgdorferi",
            "attributes": null
          },
          {
            "code": "866067008",
            "description": "Myelitis caused by Schistosoma japonicum",
            "attributes": null
          },
          {
            "code": "866090003",
            "description": "Meningomyelitis caused by Treponema pallidum",
            "attributes": null
          },
          {
            "code": "866121005",
            "description": "Myelitis caused by Schistosoma",
            "attributes": null
          },
          {
            "code": "866123008",
            "description": "Myelitis caused by Schistosoma haematobium",
            "attributes": null
          },
          {
            "code": "866124002",
            "description": "Myelitis caused by human poliovirus",
            "attributes": null
          },
          {
            "code": "866125001",
            "description": "Myelitis caused by Retroviridae",
            "attributes": null
          },
          {
            "code": "866126000",
            "description": "Myelitis caused by Influenza A virus",
            "attributes": null
          },
          {
            "code": "866127009",
            "description": "Myelitis caused by Plasmodium",
            "attributes": null
          },
          {
            "code": "866128004",
            "description": "Myelitis caused by Roseolovirus",
            "attributes": null
          },
          {
            "code": "866129007",
            "description": "Myelitis caused by human T-lymphotropic virus type 1",
            "attributes": null
          },
          {
            "code": "866130002",
            "description": "Myelitis caused by Herpes simplex type 2",
            "attributes": null
          },
          {
            "code": "866131003",
            "description": "Myelitis caused by Human herpes virus",
            "attributes": null
          },
          {
            "code": "866132005",
            "description": "Myelitis caused by Herpes simplex type 1",
            "attributes": null
          },
          {
            "code": "866251007",
            "description": "Myelitis caused by Human coxsackievirus B",
            "attributes": null
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          {
            "code": "86842008",
            "description": "Iatrogenic pituitary disorder",
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            "code": "870262000",
            "description": "Pervasive developmental disorder with disorder of intellectual development without loss of previously acquired skills",
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          {
            "code": "870264004",
            "description": "Pervasive developmental disorder with disorder of intellectual development and pervasive impairment of functional language without loss of previously acquired skills",
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            "code": "870265003",
            "description": "Pervasive developmental disorder with disorder of intellectual development with loss of previously acquired skills",
            "attributes": null
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          {
            "code": "870266002",
            "description": "Pervasive developmental disorder with disorder of intellectual development and marked impairment of functional language with loss of previously acquired skills",
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            "code": "870267006",
            "description": "Pervasive developmental disorder with disorder of intellectual development and marked impairment of functional language without loss of previously acquired skills",
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            "code": "870268001",
            "description": "Pervasive developmental disorder with disorder of intellectual development and complete impairment of functional language without loss of previously acquired skills",
            "attributes": null
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          {
            "code": "870269009",
            "description": "Pervasive developmental disorder with disorder of intellectual development and absence of functional language with loss of previously acquired skills",
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            "code": "870270005",
            "description": "Pervasive developmental disorder with disorder of intellectual development and complete impairment of functional language with loss of previously acquired skills",
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            "code": "870284000",
            "description": "Pelizaeus Merzbacher like disease due to HSPD1 mutation",
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          },
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            "code": "870285004",
            "description": "Pelizaeus Merzbacher like disease due to SLC16A2 mutation",
            "attributes": null
          },
          {
            "code": "870286003",
            "description": "Pelizaeus Merzbacher like disease due to AIMP1 mutation",
            "attributes": null
          },
          {
            "code": "870287007",
            "description": "Pelizaeus Merzbacher like disease due to GJC2 mutation",
            "attributes": null
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            "code": "870288002",
            "description": "Parkinsonism caused by methanol",
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            "code": "870290001",
            "description": "Myelopathy due to vitamin B12 deficiency",
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            "code": "870291002",
            "description": "Myelopathy due to lathyrism",
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            "code": "870293004",
            "description": "Myelitis caused by Treponema pallidum",
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            "code": "870294005",
            "description": "Myelitis caused by Toxoplasma gondii",
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            "code": "870295006",
            "description": "Parkinsonism caused by carbon disulfide",
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          },
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            "code": "870305003",
            "description": "Pervasive developmental disorder with cognitive developmental delay and marked impairment of functional language",
            "attributes": null
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            "code": "870308001",
            "description": "Pervasive developmental disorder with cognitive developmental delay and complete impairment of functional language",
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            "code": "870340002",
            "description": "Granuloma of spinal cord caused by Mycobacterium",
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            "code": "870341003",
            "description": "Granuloma of spinal cord caused by parasite",
            "attributes": null
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            "code": "870342005",
            "description": "Compression of spinal cord due to granulomatous disorder",
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          },
          {
            "code": "870343000",
            "description": "Granuloma of spinal cord caused by bacterium",
            "attributes": null
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            "code": "870345007",
            "description": "Compression of spinal cord due to cavernous hemangioma",
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            "code": "870364001",
            "description": "Traumatic anterior cord syndrome",
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            "code": "87043009",
            "description": "Cerebral anoxia after obstetrical surgery AND/OR other procedure including delivery",
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            "code": "870540001",
            "description": "Contusion of hindbrain",
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            "code": "870544005",
            "description": "Occlusion of distal basilar artery",
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            "code": "870548008",
            "description": "Closed fracture of skull with cerebral laceration",
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          },
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            "code": "870549000",
            "description": "Closed fracture of skull with cerebral contusion",
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            "code": "870550000",
            "description": "Closed fracture of base of skull with cerebral laceration",
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          },
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            "code": "870551001",
            "description": "Closed fracture of base of skull with cerebral contusion",
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          },
          {
            "code": "870553003",
            "description": "Open fracture of vault of skull with cerebral laceration",
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          },
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            "code": "870554009",
            "description": "Open fracture of vault of skull with cerebral contusion",
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            "code": "870555005",
            "description": "Open fracture of skull with cerebral contusion",
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          },
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            "code": "870556006",
            "description": "Open fracture of skull with cerebral laceration",
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            "code": "870563006",
            "description": "Contusion of cerebrum with open intracranial wound",
            "attributes": null
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          {
            "code": "870565004",
            "description": "Contusion of hindbrain with open intracranial wound",
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          },
          {
            "code": "870566003",
            "description": "Occlusion of anterior choroidal artery",
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          },
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            "code": "870579007",
            "description": "Occlusion of branch of basilar artery",
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          {
            "code": "870637009",
            "description": "Dissection of cervical artery",
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            "code": "87091000119101",
            "description": "Malignant glioma of cerebrum",
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            "code": "87095001",
            "description": "Olfactory seizure",
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          {
            "code": "87111000119109",
            "description": "Malignant glioma of hypothalamus",
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            "code": "87121000119102",
            "description": "Malignant glioma of cerebellum",
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            "code": "87132004",
            "description": "Opioid withdrawal",
            "attributes": null
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          {
            "code": "87151000119105",
            "description": "Malignant glioma of central nervous system",
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            "code": "871637001",
            "description": "Thrombosis of multiple cerebral veins",
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            "code": "87227007",
            "description": "Cerebral depression in newborn",
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            "code": "87235005",
            "description": "Dialysis disequilibrium syndrome",
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          {
            "code": "87476004",
            "description": "Convulsions in the newborn",
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          {
            "code": "87551000119101",
            "description": "Visual disturbance as sequela of cerebrovascular disease",
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          },
          {
            "code": "87555007",
            "description": "Claude's syndrome",
            "attributes": null
          },
          {
            "code": "87607002",
            "description": "Pelizaeus-Merzbacher disease, classic form",
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          },
          {
            "code": "87842000",
            "description": "Generalized neuromuscular exhaustion syndrome",
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          {
            "code": "87888006",
            "description": "Cortex contusion with open intracranial wound",
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          },
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            "code": "87937009",
            "description": "Endophlebitis of intracranial venous sinus",
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          {
            "code": "88032003",
            "description": "Amaurosis fugax",
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          {
            "code": "88174006",
            "description": "Basilar artery thrombosis",
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          {
            "code": "88269008",
            "description": "Thalamic syndrome",
            "attributes": null
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          {
            "code": "8829008",
            "description": "Isolated lutropin deficiency",
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            "code": "8837000",
            "description": "Amphetamine delirium",
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          {
            "code": "8840000",
            "description": "Closed fracture of C1-C4 level with spinal cord injury",
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          },
          {
            "code": "88405003",
            "description": "Open fracture of T7-T12 level with central cord syndrome",
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          },
          {
            "code": "88518009",
            "description": "Wilson's disease",
            "attributes": null
          },
          {
            "code": "885831000000109",
            "description": "Choreoathetoid cerebral palsy",
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            "code": "88755007",
            "description": "Phlebitis of lateral venous sinus",
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          {
            "code": "88845000",
            "description": "Explosive type organic personality disorder",
            "attributes": null
          },
          {
            "code": "88922007",
            "description": "Thrombosis of basilar sinus",
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          {
            "code": "88923002",
            "description": "Progressive muscular atrophy",
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          {
            "code": "89142007",
            "description": "Progressive intracranial arterial occlusion",
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          {
            "code": "89261000",
            "description": "Isolated thyrotropin deficiency",
            "attributes": null
          },
          {
            "code": "89369001",
            "description": "Anencephalus",
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          },
          {
            "code": "8939001",
            "description": "Incomplete spinal cord lesion at C1-C4 level without bone injury",
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          },
          {
            "code": "89392001",
            "description": "Prader-Willi syndrome",
            "attributes": null
          },
          {
            "code": "89437009",
            "description": "Cerebral paraparesis",
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          {
            "code": "89441000119109",
            "description": "Ventriculitis of the brain",
            "attributes": null
          },
          {
            "code": "89451009",
            "description": "Inhalant-induced mood disorder",
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          },
          {
            "code": "89476005",
            "description": "Pituitary cachexia",
            "attributes": null
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          {
            "code": "89525009",
            "description": "Gelastic seizure",
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          },
          {
            "code": "89576007",
            "description": "Pallidonigrospinal degeneration",
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          {
            "code": "89601008",
            "description": "Tic of organic origin",
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          {
            "code": "89980009",
            "description": "Thrombosis of cavernous venous sinus",
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          {
            "code": "90011000119105",
            "description": "Organic sleep related movement disorder",
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          {
            "code": "90099008",
            "description": "Subcortical leukoencephalopathy",
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            "code": "9015001",
            "description": "Brain injury without open intracranial wound",
            "attributes": null
          },
          {
            "code": "90162006",
            "description": "Syringopontia",
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          },
          {
            "code": "90182005",
            "description": "Hypophysectomy-induced hypopituitarism",
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          {
            "code": "90253000",
            "description": "Progressive subcortical gliosis",
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          {
            "code": "903741000000102",
            "description": "Uhthoff phenomenon",
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          {
            "code": "90429009",
            "description": "Cerebellar laceration without open intracranial wound AND with loss of consciousness",
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          },
          {
            "code": "904531000000100",
            "description": "Bilateral spastic cerebral palsy",
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          {
            "code": "90520006",
            "description": "Vertebral artery stenosis",
            "attributes": null
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          {
            "code": "90584004",
            "description": "Spinal cord injury",
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          {
            "code": "90755006",
            "description": "Nicotine withdrawal",
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          {
            "code": "90768003",
            "description": "Contusion of brain without open intracranial wound",
            "attributes": null
          },
          {
            "code": "90791004",
            "description": "Posthemiplegic ataxia",
            "attributes": null
          },
          {
            "code": "90811000119100",
            "description": "Low grade malignant glioma of brain",
            "attributes": null
          },
          {
            "code": "90831000119105",
            "description": "Grade 4 malignant glioma of brain",
            "attributes": null
          },
          {
            "code": "91012008",
            "description": "Repeated concussion of brain",
            "attributes": null
          },
          {
            "code": "91187007",
            "description": "Pituitary dwarfism with small sella turcica",
            "attributes": null
          },
          {
            "code": "91327001",
            "description": "Quadriparesis",
            "attributes": null
          },
          {
            "code": "9133005",
            "description": "Familial amyloid polyneuropathy, Iowa type",
            "attributes": null
          },
          {
            "code": "91377003",
            "description": "Transient hyperprolactinemia",
            "attributes": null
          },
          {
            "code": "91483004",
            "description": "Tuberculous encephalitis",
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          {
            "code": "91502009",
            "description": "Spinocerebellar disease",
            "attributes": null
          },
          {
            "code": "91601000119109",
            "description": "Sequela of thrombotic stroke",
            "attributes": null
          },
          {
            "code": "91637004",
            "description": "Myasthenia gravis",
            "attributes": null
          },
          {
            "code": "91952008",
            "description": "Azorean disease",
            "attributes": null
          },
          {
            "code": "91953003",
            "description": "Azorean disease, type I",
            "attributes": null
          },
          {
            "code": "91954009",
            "description": "Azorean disease, type II",
            "attributes": null
          },
          {
            "code": "91955005",
            "description": "Azorean disease, type III",
            "attributes": null
          },
          {
            "code": "91956006",
            "description": "Azorean disease, type IV",
            "attributes": null
          },
          {
            "code": "92029009",
            "description": "Benign neoplasm of brain stem",
            "attributes": null
          },
          {
            "code": "92030004",
            "description": "Benign neoplasm of brain",
            "attributes": null
          },
          {
            "code": "92050000",
            "description": "Benign neoplasm of cerebellum",
            "attributes": null
          },
          {
            "code": "92052008",
            "description": "Benign neoplasm of cerebral ventricle",
            "attributes": null
          },
          {
            "code": "92072003",
            "description": "Benign neoplasm of craniopharyngeal duct",
            "attributes": null
          },
          {
            "code": "92114009",
            "description": "Benign neoplasm of frontal lobe",
            "attributes": null
          },
          {
            "code": "92253009",
            "description": "Benign neoplasm of occipital lobe",
            "attributes": null
          },
          {
            "code": "92276007",
            "description": "Benign neoplasm of parietal lobe",
            "attributes": null
          },
          {
            "code": "92294001",
            "description": "Benign neoplasm of pineal gland",
            "attributes": null
          },
          {
            "code": "92296004",
            "description": "Benign neoplasm of pituitary gland",
            "attributes": null
          },
          {
            "code": "92341000119107",
            "description": "Weakness of extremities as sequela of stroke",
            "attributes": null
          },
          {
            "code": "92405007",
            "description": "Benign neoplasm of spinal cord",
            "attributes": null
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          {
            "code": "92406008",
            "description": "Benign neoplasm of spinal meninges",
            "attributes": null
          },
          {
            "code": "92427003",
            "description": "Benign neoplasm of temporal lobe",
            "attributes": null
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          {
            "code": "92503002",
            "description": "Neurofibromatosis type 2",
            "attributes": null
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          {
            "code": "92573003",
            "description": "Carcinoma in situ of craniopharyngeal duct",
            "attributes": null
          },
          {
            "code": "92682003",
            "description": "Carcinoma in situ of pineal gland",
            "attributes": null
          },
          {
            "code": "92683008",
            "description": "Carcinoma in situ of pituitary gland",
            "attributes": null
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          {
            "code": "92824003",
            "description": "Neurofibromatosis type 1",
            "attributes": null
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          {
            "code": "92904001",
            "description": "Congenital abnormal shape of cerebellum",
            "attributes": null
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            "code": "92905000",
            "description": "Congenital abnormal shape of cerebrum",
            "attributes": null
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          {
            "code": "92962004",
            "description": "Congenital absence of carotid artery",
            "attributes": null
          },
          {
            "code": "92997002",
            "description": "Congenital anomaly of carotid artery",
            "attributes": null
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          {
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            "description": "Congenital dilatation of carotid artery",
            "attributes": null
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            "code": "93249003",
            "description": "Congenital hypoplasia of cerebrum",
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            "code": "93312006",
            "description": "Congenital malposition of carotid artery",
            "attributes": null
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            "code": "93396008",
            "description": "Congenital stenosis of carotid artery",
            "attributes": null
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            "description": "Drug-induced dyskinesia, acute onset",
            "attributes": null
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            "description": "Dialysis dementia",
            "attributes": null
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          {
            "code": "93557001",
            "description": "Holorachischisis",
            "attributes": null
          },
          {
            "code": "936271000000100",
            "description": "Congenital anomaly of precerebral vessel",
            "attributes": null
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            "code": "9366002",
            "description": "Palatal myoclonus",
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          {
            "code": "93681000119102",
            "description": "Insomnia co-occurrent and due to nocturnal myoclonus",
            "attributes": null
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          {
            "code": "93726004",
            "description": "Primary malignant neoplasm of brain stem",
            "attributes": null
          },
          {
            "code": "93727008",
            "description": "Primary malignant neoplasm of brain",
            "attributes": null
          },
          {
            "code": "93744007",
            "description": "Primary malignant neoplasm of central nervous system",
            "attributes": null
          },
          {
            "code": "93746009",
            "description": "Primary malignant neoplasm of cerebellum",
            "attributes": null
          },
          {
            "code": "93747000",
            "description": "Primary malignant neoplasm of cerebral meninges",
            "attributes": null
          },
          {
            "code": "93748005",
            "description": "Primary malignant neoplasm of cerebral ventricle",
            "attributes": null
          },
          {
            "code": "93749002",
            "description": "Primary malignant neoplasm of cerebrum",
            "attributes": null
          },
          {
            "code": "93768004",
            "description": "Primary malignant neoplasm of craniopharyngeal duct",
            "attributes": null
          },
          {
            "code": "93807001",
            "description": "Primary malignant neoplasm of frontal lobe",
            "attributes": null
          },
          {
            "code": "93928006",
            "description": "Primary malignant neoplasm of occipital lobe",
            "attributes": null
          },
          {
            "code": "93931007",
            "description": "Primary malignant neoplasm of optic nerve",
            "attributes": null
          },
          {
            "code": "93946000",
            "description": "Primary malignant neoplasm of parietal lobe",
            "attributes": null
          },
          {
            "code": "93962006",
            "description": "Primary malignant neoplasm of pineal gland",
            "attributes": null
          },
          {
            "code": "93964007",
            "description": "Primary malignant neoplasm of pituitary gland",
            "attributes": null
          },
          {
            "code": "94068003",
            "description": "Primary malignant neoplasm of spinal cord",
            "attributes": null
          },
          {
            "code": "94069006",
            "description": "Primary malignant neoplasm of spinal meninges",
            "attributes": null
          },
          {
            "code": "94086000",
            "description": "Primary malignant neoplasm of temporal lobe",
            "attributes": null
          },
          {
            "code": "94224009",
            "description": "Secondary malignant neoplasm of brain stem",
            "attributes": null
          },
          {
            "code": "94225005",
            "description": "Secondary malignant neoplasm of brain",
            "attributes": null
          },
          {
            "code": "94243009",
            "description": "Secondary malignant neoplasm of central nervous system",
            "attributes": null
          },
          {
            "code": "94245002",
            "description": "Secondary malignant neoplasm of cerebellum",
            "attributes": null
          },
          {
            "code": "94246001",
            "description": "Secondary malignant neoplasm of cerebral meninges",
            "attributes": null
          },
          {
            "code": "94247005",
            "description": "Secondary malignant neoplasm of cerebral ventricle",
            "attributes": null
          },
          {
            "code": "94248000",
            "description": "Secondary malignant neoplasm of cerebrum",
            "attributes": null
          },
          {
            "code": "94267001",
            "description": "Secondary malignant neoplasm of craniopharyngeal duct",
            "attributes": null
          },
          {
            "code": "94309003",
            "description": "Secondary malignant neoplasm of frontal lobe",
            "attributes": null
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