[
  {
    "phenotype_id": "PH3169",
    "phenotype_version_id": 8152,
    "name": "Neurological disorders",
    "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\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": "2026-01-26T23:05:38.529628Z",
    "author": "Office for National Statistics",
    "collections": [
      {
        "name": "OpenCodelist",
        "value": 31
      },
      {
        "name": "Phenotype Library",
        "value": 18
      }
    ],
    "tags": null,
    "organisation": {
      "id": 1,
      "slug": "opensafely",
      "name": "OpenSAFELY"
    },
    "world_access": 1,
    "updated": "2026-01-26T23:05:38.524903Z",
    "references": [],
    "signed_off": [],
    "methodology": "",
    "coding_system": [
      {
        "name": "SNOMED  CT codes",
        "value": 9
      }
    ],
    "open_codelist_id": "ons/neurological-disorders",
    "source_reference": "https://www.opencodelists.org/codelist/ons/neurological-disorders/54fabb61",
    "concept_information": [
      {
        "concept_id": 8329,
        "concept_version_id": 15814,
        "concept_name": "ons/neurological-disorders/54fabb61",
        "coding_system": {
          "id": 9,
          "name": "SNOMED  CT codes",
          "description": "SNOMED CT codes"
        },
        "phenotype_id": "PH3169",
        "phenotype_version_id": 8152,
        "phenotype_name": "Neurological disorders",
        "code_attribute_header": [],
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            "description": "Deficiency of enoyl-coenzyme A hydratase",
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            "description": "Anterior choroidal artery syndrome",
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            "description": "Late-infantile neuronal ceroid lipofuscinosis",
            "attributes": null
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            "description": "Cerebrovascular accident due to occlusion of right middle cerebral artery",
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            "description": "Cerebrovascular accident due to occlusion of left middle cerebral artery",
            "attributes": null
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            "description": "Cerebrovascular accident due to thrombus of right middle cerebral artery",
            "attributes": null
          },
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            "description": "Cerebrovascular accident due to thrombus of left middle cerebral artery",
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            "description": "Musicogenic seizure",
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            "description": "External capsule hemorrhage",
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            "description": "Intracerebral hemorrhage, multiple localized",
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            "description": "Cerebral infarct due to thrombosis of precerebral arteries",
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            "code": "57981008",
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            "code": "58756001",
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            "code": "62009002",
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            "code": "63135006",
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            "code": "68618008",
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            "code": "702383005",
            "description": "Distal myopathy 2",
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            "code": "7033004",
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            "code": "711406009",
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            "code": "713275003",
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            "code": "71444005",
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            "code": "716278005",
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            "code": "716722005",
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            "code": "716723000",
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            "code": "717964007",
            "description": "Juvenile primary lateral sclerosis",
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            "code": "718177001",
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            "code": "71831005",
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            "code": "718555006",
            "description": "Juvenile amyotrophic lateral sclerosis",
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            "code": "718572004",
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            "code": "719836007",
            "description": "X-linked distal arthrogryposis multiplex congenita",
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            "code": "722987009",
            "description": "Amyotrophic lateral sclerosis plus syndrome",
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            "code": "723308003",
            "description": "Epidermolysis bullosa simplex with muscular dystrophy",
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            "code": "723612001",
            "description": "Spinal muscular atrophy, Dandy-Walker malformation, cataract syndrome",
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            "description": "Stroke co-occurrent with migraine",
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            "code": "725046003",
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            "code": "725420009",
            "description": "Congenital muscular dystrophy Paradas type",
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            "code": "726021008",
            "description": "Long chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency",
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            "description": "Embolus of right middle cerebral artery",
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            "description": "Occlusion of left middle cerebral artery by embolus",
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            "description": "Autosomal dominant congenital benign spinal muscular atrophy",
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            "description": "Autosomal recessive myogenic arthrogryposis multiplex congenita",
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