{
  "concept_id": 4121,
  "concept_version_id": 11481,
  "coding_system": {
    "id": 9,
    "name": "SNOMED  CT codes",
    "description": "SNOMED CT codes"
  },
  "name": "Other neurological - congenital neurological condition (SNOMED-CT)",
  "description": null,
  "author": "",
  "entry_date": "2025-01-18",
  "validation_performed": false,
  "validation_description": null,
  "publication_doi": "",
  "publication_link": "",
  "secondary_publication_links": null,
  "paper_published": false,
  "source_reference": "",
  "citation_requirements": null,
  "owner_access": 3,
  "group_access": 1,
  "world_access": 1,
  "tags": null,
  "collections": null,
  "created_by": null,
  "modified_by": null,
  "owner": null,
  "group": null,
  "phenotype_owner": "PH1701",
  "phenotype_owner_history_id": 3617,
  "requested_entity_id": null,
  "components": [
    {
      "id": 9948,
      "name": "Inclusion 1",
      "logical_type": "INCLUDE",
      "source_type": "FILE_IMPORT",
      "source": "text/csv",
      "codes": [
        {
          "id": 518888,
          "code": "109411007",
          "description": "Fronto-naso-ethmoidal dysostosis (disorder)"
        },
        {
          "id": 518889,
          "code": "109415003",
          "description": "Spheno-frontal dysostosis (disorder)"
        },
        {
          "id": 518890,
          "code": "109561000",
          "description": "Cerebrofacial dysplasia (disorder)"
        },
        {
          "id": 518891,
          "code": "109905002",
          "description": "Acquired myelocele (disorder)"
        },
        {
          "id": 518892,
          "code": "111338006",
          "description": "Agenesis of nerve (disorder)"
        },
        {
          "id": 518893,
          "code": "111505001",
          "description": "Muscle-eye-brain disease, congenital muscular dystrophy (disorder)"
        },
        {
          "id": 518894,
          "code": "111641000119102",
          "description": "Congenital choroid plexus cyst (disorder)"
        },
        {
          "id": 518895,
          "code": "11197005",
          "description": "Hydromyelia (disorder)"
        },
        {
          "id": 518896,
          "code": "11701009",
          "description": "Hemicephaly (disorder)"
        },
        {
          "id": 518897,
          "code": "12275031000119106",
          "description": "Congenital cerebral ventriculomegaly (disorder)"
        },
        {
          "id": 518898,
          "code": "126941005",
          "description": "Subdural intracranial hemorrhage due to birth trauma (disorder)"
        },
        {
          "id": 518899,
          "code": "127329003",
          "description": "Congenital anomaly of visual system (disorder)"
        },
        {
          "id": 518900,
          "code": "127551000119100",
          "description": "Congenital hypoplasia of brain (disorder)"
        },
        {
          "id": 518901,
          "code": "128124001",
          "description": "Congenital anomaly of central nervous system (disorder)"
        },
        {
          "id": 518902,
          "code": "14061004",
          "description": "Derencephalus (disorder)"
        },
        {
          "id": 518903,
          "code": "14447001",
          "description": "Dandy-Walker syndrome (disorder)"
        },
        {
          "id": 518904,
          "code": "15552004",
          "description": "Osteogenesis imperfecta, recessive perinatal lethal, with microcephaly AND cataracts (disorder)"
        },
        {
          "id": 518905,
          "code": "15671007",
          "description": "Encephalocele of orbit (disorder)"
        },
        {
          "id": 518906,
          "code": "15985031000119102",
          "description": "Neonatal non-traumatic intraventricular hemorrhage (disorder)"
        },
        {
          "id": 518907,
          "code": "16026008",
          "description": "Congenital cerebellar hypoplasia (disorder)"
        },
        {
          "id": 518908,
          "code": "16054391000119102",
          "description": "Congenital hypoplasia of right optic nerve (disorder)"
        },
        {
          "id": 518909,
          "code": "16054431000119107",
          "description": "Congenital hypoplasia of left optic nerve (disorder)"
        },
        {
          "id": 518910,
          "code": "16054471000119105",
          "description": "Congenital hypoplasia of bilateral optic nerves (disorder)"
        },
        {
          "id": 518911,
          "code": "171131006",
          "description": "Meningocele (disorder)"
        },
        {
          "id": 518912,
          "code": "172069000",
          "description": "Congenital meningocele (disorder)"
        },
        {
          "id": 518913,
          "code": "17231009",
          "description": "Fetal valproate syndrome (disorder)"
        },
        {
          "id": 518914,
          "code": "17761000119109",
          "description": "High lumbar myelomeningocele (disorder)"
        },
        {
          "id": 518915,
          "code": "17771000119103",
          "description": "Low lumbar myelomeningocele (disorder)"
        },
        {
          "id": 518916,
          "code": "1829003",
          "description": "Microcephalus (disorder)"
        },
        {
          "id": 518917,
          "code": "19133005",
          "description": "Neurofibromatosis syndrome (disorder)"
        },
        {
          "id": 518918,
          "code": "19276002",
          "description": "Congenital cerebral cyst (disorder)"
        },
        {
          "id": 518919,
          "code": "192814005",
          "description": "Cerebral degeneration due to congenital hydrocephalus (disorder)"
        },
        {
          "id": 518920,
          "code": "203663000",
          "description": "Scoliosis in neurofibromatosis (disorder)"
        },
        {
          "id": 518921,
          "code": "203923004",
          "description": "Acrania (disorder)"
        },
        {
          "id": 518922,
          "code": "203934001",
          "description": "Cervical spina bifida with hydrocephalus (disorder)"
        },
        {
          "id": 518923,
          "code": "203935000",
          "description": "Thoracic spina bifida with hydrocephalus (disorder)"
        },
        {
          "id": 518924,
          "code": "203936004",
          "description": "Lumbar spina bifida with hydrocephalus (disorder)"
        },
        {
          "id": 518925,
          "code": "203941007",
          "description": "Cervical spina bifida with hydrocephalus - open (disorder)"
        },
        {
          "id": 518926,
          "code": "203942000",
          "description": "Thoracic spina bifida with hydrocephalus - open (disorder)"
        },
        {
          "id": 518927,
          "code": "203943005",
          "description": "Lumbar spina bifida with hydrocephalus - open (disorder)"
        },
        {
          "id": 518928,
          "code": "203944004",
          "description": "Sacral spina bifida with hydrocephalus - open (disorder)"
        },
        {
          "id": 518929,
          "code": "203946002",
          "description": "Spina bifida with hydrocephalus - closed (disorder)"
        },
        {
          "id": 518930,
          "code": "203948001",
          "description": "Cervical spina bifida with hydrocephalus - closed (disorder)"
        },
        {
          "id": 518931,
          "code": "203949009",
          "description": "Thoracic spina bifida with hydrocephalus - closed (disorder)"
        },
        {
          "id": 518932,
          "code": "203950009",
          "description": "Lumbar spina bifida with hydrocephalus - closed (disorder)"
        },
        {
          "id": 518933,
          "code": "203951008",
          "description": "Sacral spina bifida with hydrocephalus - closed (disorder)"
        },
        {
          "id": 518934,
          "code": "203954000",
          "description": "Spina bifida with hydrocephalus of late onset (disorder)"
        },
        {
          "id": 518935,
          "code": "203955004",
          "description": "Spina bifida with stenosis of aqueduct of Sylvius (disorder)"
        },
        {
          "id": 518936,
          "code": "203957007",
          "description": "Dandy-Walker syndrome with spina bifida (disorder)"
        },
        {
          "id": 518937,
          "code": "203967002",
          "description": "Spinal hydromeningocele (disorder)"
        },
        {
          "id": 518938,
          "code": "203969004",
          "description": "Cervical spinal hydromeningocele (disorder)"
        },
        {
          "id": 518939,
          "code": "203974007",
          "description": "Cervical hydromyelocele (disorder)"
        },
        {
          "id": 518940,
          "code": "203975008",
          "description": "Thoracic hydromyelocele (disorder)"
        },
        {
          "id": 518941,
          "code": "203976009",
          "description": "Lumbar hydromyelocele (disorder)"
        },
        {
          "id": 518942,
          "code": "203980004",
          "description": "Cervical spinal meningocele (disorder)"
        },
        {
          "id": 518943,
          "code": "203981000",
          "description": "Thoracic spinal meningocele (disorder)"
        },
        {
          "id": 518944,
          "code": "203982007",
          "description": "Lumbar spinal meningocele (disorder)"
        },
        {
          "id": 518945,
          "code": "203985009",
          "description": "Cervical meningomyelocele (disorder)"
        },
        {
          "id": 518946,
          "code": "203986005",
          "description": "Thoracic meningomyelocele (disorder)"
        },
        {
          "id": 518947,
          "code": "203987001",
          "description": "Lumbar meningomyelocele (disorder)"
        },
        {
          "id": 518948,
          "code": "203990007",
          "description": "Cervical myelocele (disorder)"
        },
        {
          "id": 518949,
          "code": "203991006",
          "description": "Thoracic myelocele (disorder)"
        },
        {
          "id": 518950,
          "code": "203992004",
          "description": "Lumbar myelocele (disorder)"
        },
        {
          "id": 518951,
          "code": "203994003",
          "description": "Myelocystocele (disorder)"
        },
        {
          "id": 518952,
          "code": "203996001",
          "description": "Cervical myelocystocele (disorder)"
        },
        {
          "id": 518953,
          "code": "203997005",
          "description": "Thoracic myelocystocele (disorder)"
        },
        {
          "id": 518954,
          "code": "203998000",
          "description": "Lumbar myelocystocele (disorder)"
        },
        {
          "id": 518955,
          "code": "204003007",
          "description": "Cervical spina bifida without hydrocephalus - open (disorder)"
        },
        {
          "id": 518956,
          "code": "204004001",
          "description": "Thoracic spina bifida without hydrocephalus - open (disorder)"
        },
        {
          "id": 518957,
          "code": "204005000",
          "description": "Lumbar spina bifida without hydrocephalus - open (disorder)"
        },
        {
          "id": 518958,
          "code": "204006004",
          "description": "Sacral spina bifida without hydrocephalus - open (disorder)"
        },
        {
          "id": 518959,
          "code": "204008003",
          "description": "Spina bifida without hydrocephalus - closed (disorder)"
        },
        {
          "id": 518960,
          "code": "204010001",
          "description": "Cervical spina bifida without hydrocephalus - closed (disorder)"
        },
        {
          "id": 518961,
          "code": "204011002",
          "description": "Thoracic spina bifida without hydrocephalus - closed (disorder)"
        },
        {
          "id": 518962,
          "code": "204012009",
          "description": "Lumbar spina bifida without hydrocephalus - closed (disorder)"
        },
        {
          "id": 518963,
          "code": "204013004",
          "description": "Sacral spina bifida without hydrocephalus - closed (disorder)"
        },
        {
          "id": 518964,
          "code": "204021005",
          "description": "Encephalomyelocele (disorder)"
        },
        {
          "id": 518965,
          "code": "204022003",
          "description": "Hydromeningocele - cranial (disorder)"
        },
        {
          "id": 518966,
          "code": "204036008",
          "description": "Lissencephaly (disorder)"
        },
        {
          "id": 518967,
          "code": "204040004",
          "description": "Agenesis of cerebrum (disorder)"
        },
        {
          "id": 518968,
          "code": "204042007",
          "description": "Congenital malformation of corpus callosum (disorder)"
        },
        {
          "id": 518969,
          "code": "204043002",
          "description": "Hypoplasia of corpus callosum (disorder)"
        },
        {
          "id": 518970,
          "code": "204044008",
          "description": "Aplasia of corpus callosum (disorder)"
        },
        {
          "id": 518971,
          "code": "204046005",
          "description": "Anomalies of hypothalamus (disorder)"
        },
        {
          "id": 518972,
          "code": "204047001",
          "description": "Anomalies of cerebellum (disorder)"
        },
        {
          "id": 518973,
          "code": "204049003",
          "description": "Aplasia of cerebellum (disorder)"
        },
        {
          "id": 518974,
          "code": "204052006",
          "description": "Cebocephaly (disorder)"
        },
        {
          "id": 518975,
          "code": "204061006",
          "description": "Foramen of Magendie atresia (disorder)"
        },
        {
          "id": 518976,
          "code": "204062004",
          "description": "Foramen of Luschka atresia (disorder)"
        },
        {
          "id": 518977,
          "code": "204067005",
          "description": "Single congenital cerebral cyst (disorder)"
        },
        {
          "id": 518978,
          "code": "204068000",
          "description": "Multiple congenital cerebral cysts (disorder)"
        },
        {
          "id": 518979,
          "code": "204072001",
          "description": "Congenital adhesions of cerebral meninges (disorder)"
        },
        {
          "id": 518980,
          "code": "204074000",
          "description": "Multiple brain anomalies (disorder)"
        },
        {
          "id": 518981,
          "code": "204081007",
          "description": "Spinal cord hypoplasia (disorder)"
        },
        {
          "id": 518982,
          "code": "204086002",
          "description": "Brachial plexus displacement (disorder)"
        },
        {
          "id": 518983,
          "code": "205788004",
          "description": "Fetal alcohol syndrome (disorder)"
        },
        {
          "id": 518984,
          "code": "206188000",
          "description": "Subdural and cerebral hemorrhage due to birth trauma (disorder)"
        },
        {
          "id": 518985,
          "code": "206191000",
          "description": "Local intracranial subdural hematoma due to birth trauma (disorder)"
        },
        {
          "id": 518986,
          "code": "206192007",
          "description": "Tentorial tear due to birth trauma (disorder)"
        },
        {
          "id": 518987,
          "code": "206195009",
          "description": "Extradural intracranial hemorrhage in fetus or newborn (disorder)"
        },
        {
          "id": 518988,
          "code": "206196005",
          "description": "Cerebral hemorrhage due to birth injury (disorder)"
        },
        {
          "id": 518989,
          "code": "206397006",
          "description": "Intraventricular (nontraumatic) hemorrhage, grade 3, of fetus and newborn (disorder)"
        },
        {
          "id": 518990,
          "code": "206398001",
          "description": "Intraventricular hemorrhage due to birth injury (disorder)"
        },
        {
          "id": 518991,
          "code": "206399009",
          "description": "Intracranial subarachnoid hemorrhage due to birth injury (disorder)"
        },
        {
          "id": 518992,
          "code": "206417009",
          "description": "Intracranial nontraumatic hemorrhage of fetus and newborn (disorder)"
        },
        {
          "id": 518993,
          "code": "206419007",
          "description": "Cerebellar (nontraumatic) and posterior fossa hemorrhage of fetus and newborn (disorder)"
        },
        {
          "id": 518994,
          "code": "21202004",
          "description": "Perinatal intracranial subarachnoid hemorrhage (disorder)"
        },
        {
          "id": 518995,
          "code": "21350002",
          "description": "Colloid cyst of third ventricle (disorder)"
        },
        {
          "id": 518996,
          "code": "21601000119103",
          "description": "Hypoxic ischemic encephalopathy due to birth trauma (disorder)"
        },
        {
          "id": 518997,
          "code": "22133005",
          "description": "Congenital anomaly of the peripheral nervous system (disorder)"
        },
        {
          "id": 518998,
          "code": "22471005",
          "description": "Hemispheric cerebellar agenesis (disorder)"
        },
        {
          "id": 518999,
          "code": "23024003",
          "description": "Macrogyria (disorder)"
        },
        {
          "id": 519000,
          "code": "230306001",
          "description": "Benign hereditary chorea (disorder)"
        },
        {
          "id": 519001,
          "code": "230530003",
          "description": "Congenital nuclear ophthalmoplegia (disorder)"
        },
        {
          "id": 519002,
          "code": "230541001",
          "description": "Congenital disorder of facial nerve (disorder)"
        },
        {
          "id": 519003,
          "code": "230779009",
          "description": "Congenital spastic foot (disorder)"
        },
        {
          "id": 519004,
          "code": "230785002",
          "description": "Congenital dysarthria (disorder)"
        },
        {
          "id": 519005,
          "code": "230786001",
          "description": "Congenital dysphasia (disorder)"
        },
        {
          "id": 519006,
          "code": "230787005",
          "description": "Congenital expressive dysphasia (disorder)"
        },
        {
          "id": 519007,
          "code": "230788000",
          "description": "Congenital receptive dysphasia (disorder)"
        },
        {
          "id": 519008,
          "code": "230794008",
          "description": "Neuronal choristoma (disorder)"
        },
        {
          "id": 519009,
          "code": "233717003",
          "description": "Diffuse pulmonary neurofibromatosis (disorder)"
        },
        {
          "id": 519010,
          "code": "233718008",
          "description": "Pulmonary tuberous sclerosis (disorder)"
        },
        {
          "id": 519011,
          "code": "234638009",
          "description": "Microcephaly, normal intelligence and immunodeficiency (disorder)"
        },
        {
          "id": 519012,
          "code": "23880008",
          "description": "Congenital anomaly of peripheral nerve (disorder)"
        },
        {
          "id": 519013,
          "code": "23931000119104",
          "description": "Hydrocephalus due to Arnold Chiari malformation type 2 (disorder)"
        },
        {
          "id": 519014,
          "code": "23941000119108",
          "description": "Arnold Chiari type 2 without hydrocephalus (disorder)"
        },
        {
          "id": 519015,
          "code": "240312009",
          "description": "Cerebral injury due to birth trauma (disorder)"
        },
        {
          "id": 519016,
          "code": "25004000",
          "description": "Subdural hemorrhage due to intrapartum anoxia AND/OR hypoxia (disorder)"
        },
        {
          "id": 519017,
          "code": "25129008",
          "description": "Hydromeningocele (disorder)"
        },
        {
          "id": 519018,
          "code": "253098009",
          "description": "Neural tube defect (disorder)"
        },
        {
          "id": 519019,
          "code": "253101008",
          "description": "Congenital cerebral hernia (disorder)"
        },
        {
          "id": 519020,
          "code": "253103006",
          "description": "Frontal encephalocele (disorder)"
        },
        {
          "id": 519021,
          "code": "253104000",
          "description": "Frontoethmoidal encephalocele (disorder)"
        },
        {
          "id": 519022,
          "code": "253106003",
          "description": "Nasofrontal encephalocele (disorder)"
        },
        {
          "id": 519023,
          "code": "253107007",
          "description": "Nasopharyngeal encephalocele (disorder)"
        },
        {
          "id": 519024,
          "code": "253108002",
          "description": "Temporal encephalocele (disorder)"
        },
        {
          "id": 519025,
          "code": "253109005",
          "description": "Parietal encephalocele (disorder)"
        },
        {
          "id": 519026,
          "code": "253111001",
          "description": "Thoracolumbar spina bifida without hydrocephalus - closed (disorder)"
        },
        {
          "id": 519027,
          "code": "253113003",
          "description": "Rachischisis with hydrocephalus (disorder)"
        },
        {
          "id": 519028,
          "code": "253114009",
          "description": "Myelocele with hydrocephalus (disorder)"
        },
        {
          "id": 519029,
          "code": "253115005",
          "description": "Hydromyelocele with hydrocephalus (disorder)"
        },
        {
          "id": 519030,
          "code": "253117002",
          "description": "Closed spina bifida with Arnold-Chiari malformation (disorder)"
        },
        {
          "id": 519031,
          "code": "253118007",
          "description": "Thoracolumbar spina bifida with hydrocephalus - closed (disorder)"
        },
        {
          "id": 519032,
          "code": "253119004",
          "description": "Hemimyelocele (disorder)"
        },
        {
          "id": 519033,
          "code": "253120005",
          "description": "Lipomeningocele (disorder)"
        },
        {
          "id": 519034,
          "code": "253124001",
          "description": "Myelodysplasia of spinal cord (disorder)"
        },
        {
          "id": 519035,
          "code": "253128003",
          "description": "Abnormality of neurogenesis (disorder)"
        },
        {
          "id": 519036,
          "code": "253130001",
          "description": "Secondary microcephaly (disorder)"
        },
        {
          "id": 519037,
          "code": "253133004",
          "description": "Hydrocephalus with anomaly of aqueduct of Sylvius (disorder)"
        },
        {
          "id": 519038,
          "code": "253135006",
          "description": "Defect of telencephalic division (disorder)"
        },
        {
          "id": 519039,
          "code": "253136007",
          "description": "Lobar holoprosencephaly (disorder)"
        },
        {
          "id": 519040,
          "code": "253137003",
          "description": "Alobar holoprosencephaly (disorder)"
        },
        {
          "id": 519041,
          "code": "253138008",
          "description": "Semi-lobar holoprosencephaly (disorder)"
        },
        {
          "id": 519042,
          "code": "253139000",
          "description": "Agenesis of corpus callosum with lipoma (disorder)"
        },
        {
          "id": 519043,
          "code": "253140003",
          "description": "Partial agenesis of corpus callosum (disorder)"
        },
        {
          "id": 519044,
          "code": "253142006",
          "description": "Atrophy of corpus callosum (disorder)"
        },
        {
          "id": 519045,
          "code": "253143001",
          "description": "Absence of septum pellucidum (disorder)"
        },
        {
          "id": 519046,
          "code": "253145008",
          "description": "Reduction anomaly of hypothalamus (disorder)"
        },
        {
          "id": 519047,
          "code": "253146009",
          "description": "Disorder of neuronal migration and differentiation (disorder)"
        },
        {
          "id": 519048,
          "code": "253147000",
          "description": "Type 1 lissencephaly (disorder)"
        },
        {
          "id": 519049,
          "code": "253148005",
          "description": "Miller Dieker syndrome (disorder)"
        },
        {
          "id": 519050,
          "code": "253149002",
          "description": "Type 2 lissencephaly (disorder)"
        },
        {
          "id": 519051,
          "code": "253150002",
          "description": "Neuronal heterotopia (disorder)"
        },
        {
          "id": 519052,
          "code": "253151003",
          "description": "Nodular heterotopia (disorder)"
        },
        {
          "id": 519053,
          "code": "253152005",
          "description": "Laminar heterotopia (disorder)"
        },
        {
          "id": 519054,
          "code": "253153000",
          "description": "Cortical dysplasia (disorder)"
        },
        {
          "id": 519055,
          "code": "253154006",
          "description": "Localized cortical dysplasia (disorder)"
        },
        {
          "id": 519056,
          "code": "253156008",
          "description": "Cortical dysplasia with hemimegalencephaly (disorder)"
        },
        {
          "id": 519057,
          "code": "253158009",
          "description": "Hydranencephaly with proliferative vasculopathy (disorder)"
        },
        {
          "id": 519058,
          "code": "253159001",
          "description": "Schizencephaly (disorder)"
        },
        {
          "id": 519059,
          "code": "253160006",
          "description": "Colpocephaly (disorder)"
        },
        {
          "id": 519060,
          "code": "253166000",
          "description": "Lateral meningocele (disorder)"
        },
        {
          "id": 519061,
          "code": "253167009",
          "description": "Microdysgenesis (disorder)"
        },
        {
          "id": 519062,
          "code": "253171007",
          "description": "Dysgenesis of the cerebellum (disorder)"
        },
        {
          "id": 519063,
          "code": "253172000",
          "description": "Agenesis of cerebellum (disorder)"
        },
        {
          "id": 519064,
          "code": "253173005",
          "description": "Unilateral agenesis of cerebellum (situation)"
        },
        {
          "id": 519065,
          "code": "253174004",
          "description": "Aplasia of the vermis (disorder)"
        },
        {
          "id": 519066,
          "code": "253175003",
          "description": "Familial aplasia of the vermis (disorder)"
        },
        {
          "id": 519067,
          "code": "253176002",
          "description": "Gillespie syndrome (disorder)"
        },
        {
          "id": 519068,
          "code": "253177006",
          "description": "Absence of the vermis (disorder)"
        },
        {
          "id": 519069,
          "code": "253178001",
          "description": "Granular cell hypoplasia (disorder)"
        },
        {
          "id": 519070,
          "code": "253179009",
          "description": "Cerebellar cortical dysplasia (disorder)"
        },
        {
          "id": 519071,
          "code": "253180007",
          "description": "Dysgenesis of the brainstem (disorder)"
        },
        {
          "id": 519072,
          "code": "253181006",
          "description": "Olive dysplasia (disorder)"
        },
        {
          "id": 519073,
          "code": "253182004",
          "description": "Dentate dysplasia (disorder)"
        },
        {
          "id": 519074,
          "code": "253183009",
          "description": "Olivary heterotopia (disorder)"
        },
        {
          "id": 519075,
          "code": "253184003",
          "description": "Chiari malformation (disorder)"
        },
        {
          "id": 519076,
          "code": "253185002",
          "description": "Chiari malformation type I (disorder)"
        },
        {
          "id": 519077,
          "code": "253186001",
          "description": "Chiari malformation type III (disorder)"
        },
        {
          "id": 519078,
          "code": "253187005",
          "description": "Chiari malformation type IV (disorder)"
        },
        {
          "id": 519079,
          "code": "253188000",
          "description": "Abnormality of canalization and retrogressive differentiation (disorder)"
        },
        {
          "id": 519080,
          "code": "253192007",
          "description": "Fibrolipoma of filum terminale (disorder)"
        },
        {
          "id": 519081,
          "code": "253199003",
          "description": "Congenital malformation of the meninges (disorder)"
        },
        {
          "id": 519082,
          "code": "253203003",
          "description": "Hypoplasia of brain gyri (disorder)"
        },
        {
          "id": 519083,
          "code": "25397008",
          "description": "Aqueduct of Sylvius anomaly (disorder)"
        },
        {
          "id": 519084,
          "code": "254241004",
          "description": "Segmental neurofibromatosis (disorder)"
        },
        {
          "id": 519085,
          "code": "254242006",
          "description": "Diffuse neurofibroma (disorder)"
        },
        {
          "id": 519086,
          "code": "254243001",
          "description": "Ash leaf spot, tuberous sclerosis (disorder)"
        },
        {
          "id": 519087,
          "code": "254249002",
          "description": "Fetal carbamazepine syndrome (disorder)"
        },
        {
          "id": 519088,
          "code": "254250002",
          "description": "Fetal cocaine syndrome (disorder)"
        },
        {
          "id": 519089,
          "code": "254254006",
          "description": "Fetal toluene syndrome (disorder)"
        },
        {
          "id": 519090,
          "code": "255581000119100",
          "description": "Simple craniosynostosis (disorder)"
        },
        {
          "id": 519091,
          "code": "26568002",
          "description": "Faun tail syndrome (disorder)"
        },
        {
          "id": 519092,
          "code": "26595007",
          "description": "Congenital absence of part of brain (disorder)"
        },
        {
          "id": 519093,
          "code": "266673001",
          "description": "Ectopic neuronal tissue (disorder)"
        },
        {
          "id": 519094,
          "code": "268143001",
          "description": "Spina bifida with hydrocephalus - open (disorder)"
        },
        {
          "id": 519095,
          "code": "268146009",
          "description": "Spina bifida without hydrocephalus - open (disorder)"
        },
        {
          "id": 519096,
          "code": "276588003",
          "description": "Perinatal intracranial laceration (disorder)"
        },
        {
          "id": 519097,
          "code": "276589006",
          "description": "Perinatal tentorial laceration (disorder)"
        },
        {
          "id": 519098,
          "code": "276593000",
          "description": "Perinatal falx laceration (disorder)"
        },
        {
          "id": 519099,
          "code": "276594006",
          "description": "Perinatal rupture of superficial cerebral vein (disorder)"
        },
        {
          "id": 519100,
          "code": "276647007",
          "description": "Perinatal intracranial hemorrhage (disorder)"
        },
        {
          "id": 519101,
          "code": "276648002",
          "description": "Intraventricular hemorrhage of prematurity (disorder)"
        },
        {
          "id": 519102,
          "code": "276652002",
          "description": "Perinatal subependymal hemorrhage with intraventricular and intracerebral extension (disorder)"
        },
        {
          "id": 519103,
          "code": "277921008",
          "description": "Atelencephaly (disorder)"
        },
        {
          "id": 519104,
          "code": "277922001",
          "description": "Aprosencephaly (disorder)"
        },
        {
          "id": 519105,
          "code": "277949001",
          "description": "Combined malformation of central nervous system and skeletal muscle (disorder)"
        },
        {
          "id": 519106,
          "code": "277950001",
          "description": "Muscle eye brain disease (disorder)"
        },
        {
          "id": 519107,
          "code": "28534004",
          "description": "Spastic paralysis due to intracranial birth injury (disorder)"
        },
        {
          "id": 519108,
          "code": "287080001",
          "description": "Congenital anomaly of nervous system of head/neck (disorder)"
        },
        {
          "id": 519109,
          "code": "288276001",
          "description": "Fetal cerebral hemorrhage (disorder)"
        },
        {
          "id": 519110,
          "code": "28861008",
          "description": "Crouzon syndrome (disorder)"
        },
        {
          "id": 519111,
          "code": "29956001",
          "description": "Myelatelia (disorder)"
        },
        {
          "id": 519112,
          "code": "30023002",
          "description": "Hydranencephaly (disorder)"
        },
        {
          "id": 519113,
          "code": "302882002",
          "description": "Hydrocephalus associated with congenital aqueduct stenosis (disorder)"
        },
        {
          "id": 519114,
          "code": "30620003",
          "description": "Spina bifida of dorsal region (disorder)"
        },
        {
          "id": 519115,
          "code": "307359001",
          "description": "Congenital agenesis of brainstem nuclei (disorder)"
        },
        {
          "id": 519116,
          "code": "307670000",
          "description": "Congenital nystagmus with sensory abnormality (disorder)"
        },
        {
          "id": 519117,
          "code": "30915001",
          "description": "Holoprosencephaly sequence (disorder)"
        },
        {
          "id": 519118,
          "code": "31076000",
          "description": "Congenital ischemic atrophy of central nervous system structure (disorder)"
        },
        {
          "id": 519119,
          "code": "31429000",
          "description": "Cerebral cortical dysgenesis (disorder)"
        },
        {
          "id": 519120,
          "code": "32219008",
          "description": "Craniorachischisis (disorder)"
        },
        {
          "id": 519121,
          "code": "32232003",
          "description": "Spina bifida of cervical region (disorder)"
        },
        {
          "id": 519122,
          "code": "330041000119103",
          "description": "Congenital porencephalic cyst (disorder)"
        },
        {
          "id": 519123,
          "code": "35111000119109",
          "description": "Cystic malformation of posterior fossa (disorder)"
        },
        {
          "id": 519124,
          "code": "359007",
          "description": "Kernicterus due to isoimmunization (disorder)"
        },
        {
          "id": 519125,
          "code": "359824007",
          "description": "Incomplete anencephaly (disorder)"
        },
        {
          "id": 519126,
          "code": "36010004",
          "description": "Congenital cerebral meningocele (disorder)"
        },
        {
          "id": 519127,
          "code": "36025004",
          "description": "Fibrous skin tumor of tuberous sclerosis (disorder)"
        },
        {
          "id": 519128,
          "code": "360527003",
          "description": "Diplomyelia (disorder)"
        },
        {
          "id": 519129,
          "code": "360530005",
          "description": "Myeloschisis (disorder)"
        },
        {
          "id": 519130,
          "code": "363034005",
          "description": "Congenital anomaly of neural structure of trunk (disorder)"
        },
        {
          "id": 519131,
          "code": "371107004",
          "description": "Seizures complicating intracranial hemorrhage in the newborn (disorder)"
        },
        {
          "id": 519132,
          "code": "373587001",
          "description": "Chiari malformation type II (disorder)"
        },
        {
          "id": 519133,
          "code": "38116000",
          "description": "Hydromyelocele (disorder)"
        },
        {
          "id": 519134,
          "code": "38353004",
          "description": "Congenital porencephaly (disorder)"
        },
        {
          "id": 519135,
          "code": "39150004",
          "description": "Congenital anomaly of spinal meninges (disorder)"
        },
        {
          "id": 519136,
          "code": "39574006",
          "description": "Congenital hypoplasia of inner granular layer of cerebellum (disorder)"
        },
        {
          "id": 519137,
          "code": "40130009",
          "description": "Spina bifida without hydrocephalus (disorder)"
        },
        {
          "id": 519138,
          "code": "403559003",
          "description": "Cutaneous lesion resulting from spinal dysraphism (disorder)"
        },
        {
          "id": 519139,
          "code": "403560008",
          "description": "Port-wine stain associated with spinal dysraphism (disorder)"
        },
        {
          "id": 519140,
          "code": "403561007",
          "description": "Cutaneous lesion resulting from spina bifida (disorder)"
        },
        {
          "id": 519141,
          "code": "403815003",
          "description": "Axillary freckling due to neurofibromatosis (disorder)"
        },
        {
          "id": 519142,
          "code": "403816002",
          "description": "Multiple café-au-lait macules due to neurofibromatosis (disorder)"
        },
        {
          "id": 519143,
          "code": "403817006",
          "description": "Multiple neurofibromas in neurofibromatosis (disorder)"
        },
        {
          "id": 519144,
          "code": "403819009",
          "description": "Elephantiasis neurofibromatosa (disorder)"
        },
        {
          "id": 519145,
          "code": "403820003",
          "description": "Café-au-lait macules with pulmonary stenosis (disorder)"
        },
        {
          "id": 519146,
          "code": "403821004",
          "description": "Café-au-lait macules with temporal dysrhythmia (disorder)"
        },
        {
          "id": 519147,
          "code": "403823001",
          "description": "Periungual fibroma in tuberous sclerosis (disorder)"
        },
        {
          "id": 519148,
          "code": "4061000119104",
          "description": "Myelomeningocele without hydrocephalus (disorder)"
        },
        {
          "id": 519149,
          "code": "410060009",
          "description": "Hydrencephalomeningocele (disorder)"
        },
        {
          "id": 519150,
          "code": "413808003",
          "description": "Cerebral ventriculomegaly (disorder)"
        },
        {
          "id": 519151,
          "code": "414667000",
          "description": "Meningomyelocele (disorder)"
        },
        {
          "id": 519152,
          "code": "415713009",
          "description": "Thoracic hydromeningocele (disorder)"
        },
        {
          "id": 519153,
          "code": "417658006",
          "description": "Holoanencephaly (disorder)"
        },
        {
          "id": 519154,
          "code": "422474003",
          "description": "Partial absence of septum pellucidum (disorder)"
        },
        {
          "id": 519155,
          "code": "42376006",
          "description": "Occipital encephalocele (disorder)"
        },
        {
          "id": 519156,
          "code": "425687007",
          "description": "Spina bifida aperta of cervical spine (disorder)"
        },
        {
          "id": 519157,
          "code": "427216002",
          "description": "Spina bifida aperta of thoracic spine (disorder)"
        },
        {
          "id": 519158,
          "code": "428190001",
          "description": "Neurogenic bladder due to spina bifida (disorder)"
        },
        {
          "id": 519159,
          "code": "428241007",
          "description": "Ventricular hemorrhage of fetus (disorder)"
        },
        {
          "id": 519160,
          "code": "429466000",
          "description": "Spina bifida aperta of lumbar spine (disorder)"
        },
        {
          "id": 519161,
          "code": "431265009",
          "description": "Fetal microcephaly (disorder)"
        },
        {
          "id": 519162,
          "code": "43427008",
          "description": "Ectopic glial tissue (disorder)"
        },
        {
          "id": 519163,
          "code": "43602006",
          "description": "Subdural intracranial hemorrhage in fetus or newborn (disorder)"
        },
        {
          "id": 519164,
          "code": "438583008",
          "description": "Congenital bilateral perisylvian syndrome (disorder)"
        },
        {
          "id": 519165,
          "code": "442300000",
          "description": "Rhombencephalosynapsis (disorder)"
        },
        {
          "id": 519166,
          "code": "444860006",
          "description": "Meningomyelocele of lumbosacral spine (disorder)"
        },
        {
          "id": 519167,
          "code": "444978000",
          "description": "Meningocele of vertex (disorder)"
        },
        {
          "id": 519168,
          "code": "445116003",
          "description": "Encephalocele of vertex (disorder)"
        },
        {
          "id": 519169,
          "code": "445307009",
          "description": "Spina bifida of sacral region (disorder)"
        },
        {
          "id": 519170,
          "code": "445308004",
          "description": "Split spinal cord malformation (disorder)"
        },
        {
          "id": 519171,
          "code": "445468002",
          "description": "Occipital meningocele (disorder)"
        },
        {
          "id": 519172,
          "code": "448227009",
          "description": "X-linked periventricular heterotopia (disorder)"
        },
        {
          "id": 519173,
          "code": "45163000",
          "description": "Congenital pontocerebellar hypoplasia (disorder)"
        },
        {
          "id": 519174,
          "code": "462165005",
          "description": "Fetal choroid plexus cyst (disorder)"
        },
        {
          "id": 519175,
          "code": "46829007",
          "description": "Developmental displacement of brachial plexus (disorder)"
        },
        {
          "id": 519176,
          "code": "47032000",
          "description": "Congenital hydrocephalus (disorder)"
        },
        {
          "id": 519177,
          "code": "48376004",
          "description": "Congenital pseudoporencephaly (disorder)"
        },
        {
          "id": 519178,
          "code": "4945003",
          "description": "Microgyria (disorder)"
        },
        {
          "id": 519179,
          "code": "49946005",
          "description": "Podencephalus (disorder)"
        },
        {
          "id": 519180,
          "code": "50143004",
          "description": "Kernicterus of newborn (disorder)"
        },
        {
          "id": 519181,
          "code": "50429003",
          "description": "Congenital stenosis of aqueduct of Sylvius (disorder)"
        },
        {
          "id": 519182,
          "code": "50751005",
          "description": "Sinus pericranii (disorder)"
        },
        {
          "id": 519183,
          "code": "5102002",
          "description": "Agenesis of corpus callosum (disorder)"
        },
        {
          "id": 519184,
          "code": "52330001",
          "description": "Meningoencephalocele (disorder)"
        },
        {
          "id": 519185,
          "code": "52713000",
          "description": "Infantile neuroaxonal dystrophy (disorder)"
        },
        {
          "id": 519186,
          "code": "53318002",
          "description": "Spina bifida with hydrocephalus (disorder)"
        },
        {
          "id": 519187,
          "code": "53776005",
          "description": "Encephalocystocele (disorder)"
        },
        {
          "id": 519188,
          "code": "54794009",
          "description": "Ectopic gray matter in centrum ovale (disorder)"
        },
        {
          "id": 519189,
          "code": "55999004",
          "description": "Encephalocele (disorder)"
        },
        {
          "id": 519190,
          "code": "56155002",
          "description": "Hemispheric cerebral agenesis (disorder)"
        },
        {
          "id": 519191,
          "code": "56531003",
          "description": "Ulegyria (disorder)"
        },
        {
          "id": 519192,
          "code": "57148006",
          "description": "Congenital anomaly of brain (disorder)"
        },
        {
          "id": 519193,
          "code": "57284007",
          "description": "Severe birth asphyxia (disorder)"
        },
        {
          "id": 519194,
          "code": "57544002",
          "description": "Multiple malformation syndrome due to non-infectious environmental agents (disorder)"
        },
        {
          "id": 519195,
          "code": "5842009",
          "description": "Spinal cord dysplasia (disorder)"
        },
        {
          "id": 519196,
          "code": "58557008",
          "description": "Spina bifida aperta (disorder)"
        },
        {
          "id": 519197,
          "code": "609417004",
          "description": "Fetal anencephaly (disorder)"
        },
        {
          "id": 519198,
          "code": "609437000",
          "description": "Fetal Alcohol Spectrum Disorder (disorder)"
        },
        {
          "id": 519199,
          "code": "609528003",
          "description": "Posterior fossa arachnoid cyst (disorder)"
        },
        {
          "id": 519200,
          "code": "609529006",
          "description": "Persistent Blake's pouch cyst (disorder)"
        },
        {
          "id": 519201,
          "code": "61819007",
          "description": "Rachischisis (disorder)"
        },
        {
          "id": 519202,
          "code": "62110005",
          "description": "Fetal methyl mercury syndrome (disorder)"
        },
        {
          "id": 519203,
          "code": "62158001",
          "description": "Status marmoratus (disorder)"
        },
        {
          "id": 519204,
          "code": "65144005",
          "description": "Congenital spinal meningocele (disorder)"
        },
        {
          "id": 519205,
          "code": "65455002",
          "description": "Nasal encephalocele (disorder)"
        },
        {
          "id": 519206,
          "code": "65986000",
          "description": "Fetal aminopterin syndrome (disorder)"
        },
        {
          "id": 519207,
          "code": "66038001",
          "description": "Miller syndrome (disorder)"
        },
        {
          "id": 519208,
          "code": "66351003",
          "description": "Fetal trimethadione syndrome (disorder)"
        },
        {
          "id": 519209,
          "code": "67531005",
          "description": "Spina bifida (disorder)"
        },
        {
          "id": 519210,
          "code": "67876003",
          "description": "Congenital obstruction of aqueduct of Sylvius (disorder)"
        },
        {
          "id": 519211,
          "code": "67944007",
          "description": "Lhermitte-Duclos disease (disorder)"
        },
        {
          "id": 519212,
          "code": "697924002",
          "description": "Pulmonary hypertension in neurofibromatosis (disorder)"
        },
        {
          "id": 519213,
          "code": "698999002",
          "description": "Congenital atresia of aqueduct of Sylvius (disorder)"
        },
        {
          "id": 519214,
          "code": "699812002",
          "description": "Subependymal nodular heterotopia (disorder)"
        },
        {
          "id": 519215,
          "code": "70065001",
          "description": "Fetal hydantoin syndrome (disorder)"
        },
        {
          "id": 519216,
          "code": "702361006",
          "description": "Crouzon syndrome with acanthosis nigricans (disorder)"
        },
        {
          "id": 519217,
          "code": "702410002",
          "description": "Iris coloboma with ptosis, hypertelorism, and mental retardation (disorder)"
        },
        {
          "id": 519218,
          "code": "702437000",
          "description": "Amish lethal microcephaly (disorder)"
        },
        {
          "id": 519219,
          "code": "702450004",
          "description": "FOXG1 syndrome (disorder)"
        },
        {
          "id": 519220,
          "code": "702611008",
          "description": "Congenital brain aplasia (disorder)"
        },
        {
          "id": 519221,
          "code": "702628006",
          "description": "Congenital anomaly of cerebrum (disorder)"
        },
        {
          "id": 519222,
          "code": "703389002",
          "description": "Calcium/calmodulin-dependent serine protein kinase related intellectual disability (disorder)"
        },
        {
          "id": 519223,
          "code": "70534000",
          "description": "Occult spinal dysraphism sequence (disorder)"
        },
        {
          "id": 519224,
          "code": "70611002",
          "description": "Perinatal intraventricular hemorrhage (disorder)"
        },
        {
          "id": 519225,
          "code": "707433009",
          "description": "Lymphangioleiomyomatosis due to tuberous sclerosis syndrome (disorder)"
        },
        {
          "id": 519226,
          "code": "711153001",
          "description": "Bowen-Conradi syndrome (disorder)"
        },
        {
          "id": 519227,
          "code": "71178008",
          "description": "Congenital spinal hydromeningocele (disorder)"
        },
        {
          "id": 519228,
          "code": "715344006",
          "description": "Neurofibromatosis Noonan syndrome (disorder)"
        },
        {
          "id": 519229,
          "code": "715406003",
          "description": "Isolated lissencephaly type 1 without known genetic defect (disorder)"
        },
        {
          "id": 519230,
          "code": "715422002",
          "description": "Craniotelencephalic dysplasia (disorder)"
        },
        {
          "id": 519231,
          "code": "715430001",
          "description": "Embryofetopathy caused by indomethacin (disorder)"
        },
        {
          "id": 519232,
          "code": "715431002",
          "description": "Embryopathy caused by phenobarbital (disorder)"
        },
        {
          "id": 519233,
          "code": "715434005",
          "description": "Holoprosencephaly craniosynostosis syndrome (disorder)"
        },
        {
          "id": 519234,
          "code": "715436007",
          "description": "Congenital cerebellar hypoplasia co-occurrent with tapetoretinal degeneration (disorder)"
        },
        {
          "id": 519235,
          "code": "715462003",
          "description": "Microcephalus co-occurrent with cervical spine fusion anomaly (disorder)"
        },
        {
          "id": 519236,
          "code": "715463008",
          "description": "Congenital pontocerebellar hypoplasia type 2 (disorder)"
        },
        {
          "id": 519237,
          "code": "715780008",
          "description": "Lissencephaly type 1 due to doublecortin gene mutation (disorder)"
        },
        {
          "id": 519238,
          "code": "715817007",
          "description": "Lissencephaly co-occurrent with congenital cerebellar hypoplasia (disorder)"
        },
        {
          "id": 519239,
          "code": "715819005",
          "description": "Lissencephaly co-occurrent with congenital cerebellar hypoplasia type B (disorder)"
        },
        {
          "id": 519240,
          "code": "715820004",
          "description": "Lissencephaly co-occurrent with congenital cerebellar hypoplasia type C (disorder)"
        },
        {
          "id": 519241,
          "code": "715821000",
          "description": "Lissencephaly co-occurrent with congenital cerebellar hypoplasia type D (disorder)"
        },
        {
          "id": 519242,
          "code": "715822007",
          "description": "Lissencephaly co-occurrent with congenital cerebellar hypoplasia type F (disorder)"
        },
        {
          "id": 519243,
          "code": "715905006",
          "description": "Unilateral polymicrogyria (disorder)"
        },
        {
          "id": 519244,
          "code": "715981004",
          "description": "Autosomal recessive primary microcephaly (disorder)"
        },
        {
          "id": 519245,
          "code": "715990006",
          "description": "Agenesis of cerebellum and hydrocephalus syndrome (disorder)"
        },
        {
          "id": 519246,
          "code": "716005004",
          "description": "Fetal diethylstilbestrol syndrome (disorder)"
        },
        {
          "id": 519247,
          "code": "716996008",
          "description": "Hypoplasia of corpus callosum and mental retardation with adducted thumbs and spasticity and hydrocephalus syndrome (disorder)"
        },
        {
          "id": 519248,
          "code": "716997004",
          "description": "Joubert syndrome (disorder)"
        },
        {
          "id": 519249,
          "code": "716998009",
          "description": "Joubert syndrome with ocular defect (disorder)"
        },
        {
          "id": 519250,
          "code": "716999001",
          "description": "Joubert syndrome with renal defect (disorder)"
        },
        {
          "id": 519251,
          "code": "717632002",
          "description": "X-linked lissencephaly with agenesis of corpus callosum and genital anomaly syndrome (disorder)"
        },
        {
          "id": 519252,
          "code": "71779008",
          "description": "X-linked hydrocephalus syndrome (disorder)"
        },
        {
          "id": 519253,
          "code": "717939009",
          "description": "Anencephaly without rachischisis (disorder)"
        },
        {
          "id": 519254,
          "code": "717977003",
          "description": "Lissencephaly syndrome Norman Roberts type (disorder)"
        },
        {
          "id": 519255,
          "code": "718228001",
          "description": "Fetal iodine syndrome (disorder)"
        },
        {
          "id": 519256,
          "code": "718573009",
          "description": "Achalasia microcephaly syndrome (disorder)"
        },
        {
          "id": 519257,
          "code": "718605009",
          "description": "Congenital pontocerebellar hypoplasia type 7 (disorder)"
        },
        {
          "id": 519258,
          "code": "718606005",
          "description": "Congenital pontocerebellar hypoplasia type 6 (disorder)"
        },
        {
          "id": 519259,
          "code": "718607001",
          "description": "Congenital pontocerebellar hypoplasia type 5 (disorder)"
        },
        {
          "id": 519260,
          "code": "718608006",
          "description": "Congenital pontocerebellar hypoplasia type 4 (disorder)"
        },
        {
          "id": 519261,
          "code": "718609003",
          "description": "Congenital pontocerebellar hypoplasia type 3 (disorder)"
        },
        {
          "id": 519262,
          "code": "718610008",
          "description": "Congenital pontocerebellar hypoplasia type 1 (disorder)"
        },
        {
          "id": 519263,
          "code": "718611007",
          "description": "Congenital pontocerebellar hypoplasia type 8 (disorder)"
        },
        {
          "id": 519264,
          "code": "718719001",
          "description": "Lissencephaly type 3 familial fetal akinesia sequence syndrome (disorder)"
        },
        {
          "id": 519265,
          "code": "718720007",
          "description": "Lissencephaly type 3 metacarpal bone dysplasia syndrome (disorder)"
        },
        {
          "id": 519266,
          "code": "718759003",
          "description": "Lissencephaly due to tubulin alpha 1A mutation (disorder)"
        },
        {
          "id": 519267,
          "code": "719136005",
          "description": "X-linked intellectual disability with cerebellar hypoplasia syndrome (disorder)"
        },
        {
          "id": 519268,
          "code": "719139003",
          "description": "X-linked Dandy-Walker malformation with intellectual disability, basal ganglia disease and seizure syndrome (disorder)"
        },
        {
          "id": 519269,
          "code": "719162001",
          "description": "Radioulnar synostosis with microcephaly and scoliosis syndrome (disorder)"
        },
        {
          "id": 519270,
          "code": "719377004",
          "description": "Microcephalus with albinism and digital anomaly syndrome (disorder)"
        },
        {
          "id": 519271,
          "code": "719813003",
          "description": "X-linked mandibulofacial dysostosis (disorder)"
        },
        {
          "id": 519272,
          "code": "7199000",
          "description": "Tuberous sclerosis syndrome (disorder)"
        },
        {
          "id": 519273,
          "code": "720408003",
          "description": "Acrofrontofacionasal dysostosis (disorder)"
        },
        {
          "id": 519274,
          "code": "720518006",
          "description": "Athabaskan brainstem dysgenesis syndrome (disorder)"
        },
        {
          "id": 519275,
          "code": "720632004",
          "description": "Central bilateral macrogyria (disorder)"
        },
        {
          "id": 519276,
          "code": "720813007",
          "description": "Craniosynostosis with Dandy-Walker malformation and hydrocephalus syndrome (disorder)"
        },
        {
          "id": 519277,
          "code": "721231007",
          "description": "Hydrocephalus with obesity and hypogonadism syndrome (disorder)"
        },
        {
          "id": 519278,
          "code": "721297008",
          "description": "Galloway Mowat syndrome (disorder)"
        },
        {
          "id": 519279,
          "code": "721845005",
          "description": "Hypomandibular faciocranial dysostosis (disorder)"
        },
        {
          "id": 519280,
          "code": "721847002",
          "description": "Joubert syndrome with congenital hepatic fibrosis (disorder)"
        },
        {
          "id": 519281,
          "code": "721862000",
          "description": "Joubert syndrome with oculorenal defect (disorder)"
        },
        {
          "id": 519282,
          "code": "721873007",
          "description": "Joubert syndrome with orofaciodigital defect (disorder)"
        },
        {
          "id": 519283,
          "code": "722036008",
          "description": "Megalencephaly, polymicrogyria, postaxial polydactyly, hydrocephalus syndrome (disorder)"
        },
        {
          "id": 519284,
          "code": "722385008",
          "description": "Cerebral dysgenesis, neuropathy, ichthyosis, palmoplantar keratoderma syndrome (disorder)"
        },
        {
          "id": 519285,
          "code": "722451006",
          "description": "Gomez Lopez Hernandez syndrome (disorder)"
        },
        {
          "id": 519286,
          "code": "722575008",
          "description": "Traumatic hemorrhage of cerebellum due to birth trauma (disorder)"
        },
        {
          "id": 519287,
          "code": "722576009",
          "description": "Injury of brain stem due to birth trauma (disorder)"
        },
        {
          "id": 519288,
          "code": "722580004",
          "description": "Fetal or neonatal intraventricular non-traumatic hemorrhage grade 4 (disorder)"
        },
        {
          "id": 519289,
          "code": "722581000",
          "description": "Fetal or neonatal non-traumatic intraventricular hemorrhage (disorder)"
        },
        {
          "id": 519290,
          "code": "722583002",
          "description": "Fetal or neonatal non-traumatic hemorrhage of subarachnoid space of brain (disorder)"
        },
        {
          "id": 519291,
          "code": "722584008",
          "description": "Fetal or neonatal non-traumatic hemorrhage of subdural space of brain (disorder)"
        },
        {
          "id": 519292,
          "code": "722905003",
          "description": "Intracranial laceration due to birth trauma (disorder)"
        },
        {
          "id": 519293,
          "code": "722906002",
          "description": "Intracranial hemorrhage due to birth trauma (disorder)"
        },
        {
          "id": 519294,
          "code": "722909009",
          "description": "Traumatic hemorrhage of intracranial epidural space due to birth trauma (disorder)"
        },
        {
          "id": 519295,
          "code": "722989007",
          "description": "Aplasia of optic nerve (disorder)"
        },
        {
          "id": 519296,
          "code": "722990003",
          "description": "Congenital atrophy of optic nerve (disorder)"
        },
        {
          "id": 519297,
          "code": "722992006",
          "description": "Communicating hydrocephalus co-occurrent and due to congenital agenesis of arachnoid villi (disorder)"
        },
        {
          "id": 519298,
          "code": "722996009",
          "description": "Congenital malformation of autonomic nervous system (disorder)"
        },
        {
          "id": 519299,
          "code": "723405001",
          "description": "Microlissencephaly micromelia syndrome (disorder)"
        },
        {
          "id": 519300,
          "code": "723406000",
          "description": "Embryopathy caused by mycophenolate mofetil (disorder)"
        },
        {
          "id": 519301,
          "code": "723612001",
          "description": "Spinal muscular atrophy, Dandy-Walker malformation, cataract syndrome (disorder)"
        },
        {
          "id": 519302,
          "code": "724067006",
          "description": "Permanent neonatal diabetes mellitus with cerebellar agenesis syndrome (disorder)"
        },
        {
          "id": 519303,
          "code": "724144006",
          "description": "Embryofetopathy caused by methimazole (disorder)"
        },
        {
          "id": 519304,
          "code": "724999003",
          "description": "Isolated optic nerve hypoplasia (disorder)"
        },
        {
          "id": 519305,
          "code": "725287006",
          "description": "Embryopathy caused by retinoid (disorder)"
        },
        {
          "id": 519306,
          "code": "726031001",
          "description": "Cerebellar ataxia, intellectual disability, optic atrophy, skin abnormalities syndrome (disorder)"
        },
        {
          "id": 519307,
          "code": "726704006",
          "description": "Cataract, congenital heart disease, neural tube defect syndrome (disorder)"
        },
        {
          "id": 519308,
          "code": "733049004",
          "description": "Encephalopathy, intracerebral calcification, retinal degeneration syndrome (disorder)"
        },
        {
          "id": 519309,
          "code": "733068001",
          "description": "Absent tibia, polydactyly, arachnoid cyst syndrome (disorder)"
        },
        {
          "id": 519310,
          "code": "733072002",
          "description": "Alaninuria, microcephaly, dwarfism, enamel hypoplasia, diabetes mellitus syndrome (disorder)"
        },
        {
          "id": 519311,
          "code": "733092009",
          "description": "Microcephalus, hypergonadotropic hypogonadism, short stature syndrome (disorder)"
        },
        {
          "id": 519312,
          "code": "73331006",
          "description": "Hemimyelia (disorder)"
        },
        {
          "id": 519313,
          "code": "733418003",
          "description": "Joubert syndrome with Jeune asphyxiating thoracic dystrophy (disorder)"
        },
        {
          "id": 519314,
          "code": "735749005",
          "description": "Myelomeningocele co-occurrent with hydrocephalus (disorder)"
        },
        {
          "id": 519315,
          "code": "75076004",
          "description": "Amyelencephalus (disorder)"
        },
        {
          "id": 519316,
          "code": "7611002",
          "description": "Septo-optic dysplasia sequence (disorder)"
        },
        {
          "id": 519317,
          "code": "762295002",
          "description": "Congenital obstructive hydrocephalus (disorder)"
        },
        {
          "id": 519318,
          "code": "763350002",
          "description": "Intellectual disability, obesity, brain malformation, facial dysmorphism syndrome (disorder)"
        },
        {
          "id": 519319,
          "code": "763366000",
          "description": "Leukoencephalopathy, thalamus and brainstem anomalies, high lactate syndrome (disorder)"
        },
        {
          "id": 519320,
          "code": "763717004",
          "description": "Sporadic fetal brain disruption sequence (disorder)"
        },
        {
          "id": 519321,
          "code": "763830009",
          "description": "Oculomaxillofacial dysostosis (disorder)"
        },
        {
          "id": 519322,
          "code": "763861000",
          "description": "Pachygyria, intellectual disability, epilepsy syndrome (disorder)"
        },
        {
          "id": 519323,
          "code": "763889002",
          "description": "Spina bifida and hypospadias syndrome (disorder)"
        },
        {
          "id": 519324,
          "code": "76481000119102",
          "description": "Pressure ulcer due to spina bifida (disorder)"
        },
        {
          "id": 519325,
          "code": "765089003",
          "description": "Focal epilepsy, intellectual disability, cerebro-cerebellar malformation syndrome (disorder)"
        },
        {
          "id": 519326,
          "code": "765331004",
          "description": "Autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis (disorder)"
        },
        {
          "id": 519327,
          "code": "765757003",
          "description": "Bilateral polymicrogyria (disorder)"
        },
        {
          "id": 519328,
          "code": "766709000",
          "description": "Isolated hypoplasia of cerebellar vermis (disorder)"
        },
        {
          "id": 519329,
          "code": "766710005",
          "description": "Isolated focal cortical dysplasia (disorder)"
        },
        {
          "id": 519330,
          "code": "766871009",
          "description": "Diencephalic mesencephalic junction dysplasia (disorder)"
        },
        {
          "id": 519331,
          "code": "766934006",
          "description": "Isolated unilateral hemispheric cerebellar hypoplasia (disorder)"
        },
        {
          "id": 519332,
          "code": "768939009",
          "description": "Primary tethered cord syndrome (disorder)"
        },
        {
          "id": 519333,
          "code": "770408001",
          "description": "Congenital stenosis of cervical spinal canal (disorder)"
        },
        {
          "id": 519334,
          "code": "770560008",
          "description": "Lissencephaly due to LIS1 mutation (disorder)"
        },
        {
          "id": 519335,
          "code": "770725000",
          "description": "Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly (disorder)"
        },
        {
          "id": 519336,
          "code": "771076003",
          "description": "Leptomyelolipoma (disorder)"
        },
        {
          "id": 519337,
          "code": "771142009",
          "description": "Cortical dysplasia with focal epilepsy syndrome (disorder)"
        },
        {
          "id": 519338,
          "code": "771146007",
          "description": "Holoprosencephaly with caudal dysgenesis syndrome (disorder)"
        },
        {
          "id": 519339,
          "code": "771147003",
          "description": "Isolated arhinencephaly (disorder)"
        },
        {
          "id": 519340,
          "code": "771234002",
          "description": "Isolated bilateral hemispheric cerebellar hypoplasia (disorder)"
        },
        {
          "id": 519341,
          "code": "771303004",
          "description": "Severe neonatal onset encephalopathy with microcephaly (disorder)"
        },
        {
          "id": 519342,
          "code": "771336003",
          "description": "Polymicrogyria with optic nerve hypoplasia (disorder)"
        },
        {
          "id": 519343,
          "code": "77224008",
          "description": "Spina bifida of lumbar region (disorder)"
        },
        {
          "id": 519344,
          "code": "773305003",
          "description": "Microcephaly, polymicrogyria, corpus callosum agenesis syndrome (disorder)"
        },
        {
          "id": 519345,
          "code": "773394007",
          "description": "Autosomal recessive frontotemporal pachygyria (disorder)"
        },
        {
          "id": 519346,
          "code": "773497001",
          "description": "Partial corpus callosum agenesis, cerebellar vermis hypoplasia with posterior fossa cysts syndrome (disorder)"
        },
        {
          "id": 519347,
          "code": "773610007",
          "description": "Chudley McCullough syndrome (disorder)"
        },
        {
          "id": 519348,
          "code": "773627004",
          "description": "Porencephaly, microcephaly, bilateral congenital cataract syndrome (disorder)"
        },
        {
          "id": 519349,
          "code": "775907000",
          "description": "Congenital pontocerebellar hypoplasia type 9 (disorder)"
        },
        {
          "id": 519350,
          "code": "778070003",
          "description": "Autosomal dominant primary microcephaly (disorder)"
        },
        {
          "id": 519351,
          "code": "77817004",
          "description": "Neu-Laxova syndrome (disorder)"
        },
        {
          "id": 519352,
          "code": "78071008",
          "description": "Hydromicrocephaly (disorder)"
        },
        {
          "id": 519353,
          "code": "781641005",
          "description": "Schwannomatosis (disorder)"
        },
        {
          "id": 519354,
          "code": "782720005",
          "description": "Congenital pontocerebellar hypoplasia type 10 (disorder)"
        },
        {
          "id": 519355,
          "code": "782879004",
          "description": "Occipital pachygyria and polymicrogyria (disorder)"
        },
        {
          "id": 519356,
          "code": "782884005",
          "description": "Pontine tegmental cap dysplasia (disorder)"
        },
        {
          "id": 519357,
          "code": "783724009",
          "description": "Fetal spina bifida (disorder)"
        },
        {
          "id": 519358,
          "code": "783726006",
          "description": "Fetal hydrocephalus (disorder)"
        },
        {
          "id": 519359,
          "code": "784344009",
          "description": "Cortical dysgenesis with pontocerebellar hypoplasia due to tubulin beta 3 class III mutation (disorder)"
        },
        {
          "id": 519360,
          "code": "785299009",
          "description": "Cobblestone lissencephaly without muscular or ocular involvement (disorder)"
        },
        {
          "id": 519361,
          "code": "785306007",
          "description": "Lissencephaly co-occurrent with congenital cerebellar hypoplasia type E (disorder)"
        },
        {
          "id": 519362,
          "code": "785307003",
          "description": "Lissencephaly co-occurrent with congenital cerebellar hypoplasia type A (disorder)"
        },
        {
          "id": 519363,
          "code": "78693004",
          "description": "Congenital hypoplasia of part of brain (disorder)"
        },
        {
          "id": 519364,
          "code": "78784005",
          "description": "Amyelia (disorder)"
        },
        {
          "id": 519365,
          "code": "789120001",
          "description": "Neurenteric cyst (disorder)"
        },
        {
          "id": 519366,
          "code": "80651009",
          "description": "Aicardi's syndrome (disorder)"
        },
        {
          "id": 519367,
          "code": "81042008",
          "description": "Congenital anomaly of spinal cord (disorder)"
        },
        {
          "id": 519368,
          "code": "81526008",
          "description": "Hydromeningomyelocele (disorder)"
        },
        {
          "id": 519369,
          "code": "816068000",
          "description": "Periventricular nodular heterotopia (disorder)"
        },
        {
          "id": 519370,
          "code": "82058009",
          "description": "Myelocele (disorder)"
        },
        {
          "id": 519371,
          "code": "82203000",
          "description": "Treacher Collins syndrome (disorder)"
        },
        {
          "id": 519372,
          "code": "838339009",
          "description": "Basal encephalocele (disorder)"
        },
        {
          "id": 519373,
          "code": "840471002",
          "description": "Hydrocephalus due to Dandy-Walker malformation (disorder)"
        },
        {
          "id": 519374,
          "code": "840487004",
          "description": "Congenital stenosis of spinal canal (disorder)"
        },
        {
          "id": 519375,
          "code": "84873005",
          "description": "Dural arteriovenous malformation (disorder)"
        },
        {
          "id": 519376,
          "code": "85641006",
          "description": "Hemianencephaly (disorder)"
        },
        {
          "id": 519377,
          "code": "860951008",
          "description": "Congenital anomaly of cauda equina (disorder)"
        },
        {
          "id": 519378,
          "code": "8611000119100",
          "description": "Complex craniosynostosis (disorder)"
        },
        {
          "id": 519379,
          "code": "866053004",
          "description": "Middle interhemispheric variant of holoprosencephaly (disorder)"
        },
        {
          "id": 519380,
          "code": "88425004",
          "description": "Congenital anomaly of nervous system (disorder)"
        },
        {
          "id": 519381,
          "code": "89369001",
          "description": "Anencephalus (disorder)"
        },
        {
          "id": 519382,
          "code": "91848009",
          "description": "Acephaly (disorder)"
        },
        {
          "id": 519383,
          "code": "91849001",
          "description": "Acephalostomia (disorder)"
        },
        {
          "id": 519384,
          "code": "92503002",
          "description": "Neurofibromatosis type 2 (disorder)"
        },
        {
          "id": 519385,
          "code": "92824003",
          "description": "Neurofibromatosis type 1 (disorder)"
        },
        {
          "id": 519386,
          "code": "92904001",
          "description": "Congenital abnormal shape of cerebellum (disorder)"
        },
        {
          "id": 519387,
          "code": "92905000",
          "description": "Congenital abnormal shape of cerebrum (disorder)"
        },
        {
          "id": 519388,
          "code": "93249003",
          "description": "Congenital hypoplasia of cerebrum (disorder)"
        },
        {
          "id": 519389,
          "code": "93557001",
          "description": "Holorachischisis (disorder)"
        },
        {
          "id": 519390,
          "code": "95477007",
          "description": "Congenital degeneration of nervous system (disorder)"
        },
        {
          "id": 519391,
          "code": "95478002",
          "description": "Congenital sacral meningocele (disorder)"
        },
        {
          "id": 519392,
          "code": "95499004",
          "description": "Hypoplasia of the optic nerve (disorder)"
        },
        {
          "id": 519393,
          "code": "95502000",
          "description": "Congenital anomaly of optic nerve (disorder)"
        },
        {
          "id": 519394,
          "code": "95610008",
          "description": "Congenital brain damage (disorder)"
        },
        {
          "id": 519395,
          "code": "95659007",
          "description": "Hindbrain hernia headache (disorder)"
        },
        {
          "id": 519396,
          "code": "9721000119107",
          "description": "Malformation of central nervous system of fetus (disorder)"
        },
        {
          "id": 519397,
          "code": "9740002",
          "description": "Macroencephaly (disorder)"
        }
      ]
    }
  ],
  "version_history": [
    {
      "version_id": 11481,
      "version_name": "Other neurological - congenital neurological condition (SNOMED-CT)",
      "version_date": "2025-01-18T20:07:14.248123Z",
      "is_published": true,
      "is_latest": true
    }
  ]
}