[
  {
    "phenotype_id": "PH3170",
    "phenotype_version_id": 8153,
    "name": "Neurological disorders (not including epilepsy)",
    "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": "2026-01-26T23:05:40.077939Z",
    "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": "2026-01-26T23:05:40.070825Z",
    "references": [],
    "signed_off": [],
    "methodology": "",
    "coding_system": [
      {
        "name": "Read codes v3",
        "value": 6
      }
    ],
    "open_codelist_id": "ons/neurological-disorders-not-including-epilepsy",
    "source_reference": "https://www.opencodelists.org/codelist/ons/neurological-disorders-not-including-epilepsy/22dbd4f7",
    "concept_information": [
      {
        "concept_id": 8330,
        "concept_version_id": 15815,
        "concept_name": "ons/neurological-disorders-not-including-epilepsy/22dbd4f7",
        "coding_system": {
          "id": 6,
          "name": "Read codes v3",
          "description": "Read codes v3"
        },
        "phenotype_id": "PH3170",
        "phenotype_version_id": 8153,
        "phenotype_name": "Neurological disorders (not including epilepsy)",
        "code_attribute_header": [],
        "codes": [
          {
            "code": "A411.",
            "description": "Creutzfeldt-Jakob disease",
            "attributes": null
          },
          {
            "code": "A413.",
            "description": "Progressive multifocal leucoencephalopathy",
            "attributes": null
          },
          {
            "code": "Eu022",
            "description": "[X]Dementia in Huntington's disease",
            "attributes": null
          },
          {
            "code": "Eu023",
            "description": "[X]Dementia in Parkinson's disease",
            "attributes": null
          },
          {
            "code": "F0301",
            "description": "Subacute sclerosing panencephalitis",
            "attributes": null
          },
          {
            "code": "F11x7",
            "description": "Cerebral degeneration due to Creutzfeldt-Jakob disease",
            "attributes": null
          },
          {
            "code": "F11x8",
            "description": "Cerebral degeneration due to multifocal leucoencephalopathy",
            "attributes": null
          },
          {
            "code": "F12..",
            "description": "Parkinson's disease",
            "attributes": null
          },
          {
            "code": "F12z.",
            "description": "Parkinson's disease NOS",
            "attributes": null
          },
          {
            "code": "F1304",
            "description": "Progressive supranuclear palsy",
            "attributes": null
          },
          {
            "code": "F134.",
            "description": "Huntington's disease",
            "attributes": null
          },
          {
            "code": "F140.",
            "description": "Friedreich ataxia",
            "attributes": null
          },
          {
            "code": "F142.",
            "description": "Primary cerebellar degeneration",
            "attributes": null
          },
          {
            "code": "F142z",
            "description": "Primary cerebellar degeneration NOS",
            "attributes": null
          },
          {
            "code": "F1440",
            "description": "Alcoholic cerebellar degeneration",
            "attributes": null
          },
          {
            "code": "F152.",
            "description": "Motor neurone disease",
            "attributes": null
          },
          {
            "code": "F1522",
            "description": "Progressive bulbar palsy",
            "attributes": null
          },
          {
            "code": "F1524",
            "description": "Primary lateral sclerosis",
            "attributes": null
          },
          {
            "code": "F152z",
            "description": "Motor neurone disease NOS",
            "attributes": null
          },
          {
            "code": "F20..",
            "description": "Multiple sclerosis",
            "attributes": null
          },
          {
            "code": "F200.",
            "description": "Multiple sclerosis of the brainstem",
            "attributes": null
          },
          {
            "code": "F201.",
            "description": "Multiple sclerosis of the spinal cord",
            "attributes": null
          },
          {
            "code": "F202.",
            "description": "Generalised multiple sclerosis",
            "attributes": null
          },
          {
            "code": "F203.",
            "description": "Exacerbation of multiple sclerosis",
            "attributes": null
          },
          {
            "code": "F20z.",
            "description": "Multiple sclerosis NOS",
            "attributes": null
          },
          {
            "code": "F210.",
            "description": "Optic neuromyelitis",
            "attributes": null
          },
          {
            "code": "F211.",
            "description": "(Schilder's disease) or (Balo's concentric sclerosis)",
            "attributes": null
          },
          {
            "code": "F22..",
            "description": "(Hemiplegia) or (hemiparesis)",
            "attributes": null
          },
          {
            "code": "F220.",
            "description": "Flaccid hemiplegia",
            "attributes": null
          },
          {
            "code": "F221.",
            "description": "(Spastic hemiplegia) or (spastic foot)",
            "attributes": null
          },
          {
            "code": "F222.",
            "description": "Left: [hemiplegia] or [sided weakness]",
            "attributes": null
          },
          {
            "code": "F223.",
            "description": "Right: [hemiplegia] or [sided weakness]",
            "attributes": null
          },
          {
            "code": "F22z.",
            "description": "Hemiplegia NOS",
            "attributes": null
          },
          {
            "code": "F23..",
            "description": "Congenital cerebral palsy (& spastic)",
            "attributes": null
          },
          {
            "code": "F231.",
            "description": "Infantile hemiplegia",
            "attributes": null
          },
          {
            "code": "F234.",
            "description": "Infantile hemiplegia NOS",
            "attributes": null
          },
          {
            "code": "F23y.",
            "description": "Other congenital cerebral palsy",
            "attributes": null
          },
          {
            "code": "F23y0",
            "description": "Ataxic infantile cerebral palsy",
            "attributes": null
          },
          {
            "code": "F23y1",
            "description": "Hypotonic cerebral palsy",
            "attributes": null
          },
          {
            "code": "F23yz",
            "description": "Other infantile cerebral palsy NOS",
            "attributes": null
          },
          {
            "code": "F23z.",
            "description": "Congenital cerebral palsy NOS",
            "attributes": null
          },
          {
            "code": "F240.",
            "description": "Quadriplegia",
            "attributes": null
          },
          {
            "code": "F380.",
            "description": "Myasthenia gravis",
            "attributes": null
          },
          {
            "code": "F3800",
            "description": "Persistent neonatal myasthenia gravis",
            "attributes": null
          },
          {
            "code": "F3801",
            "description": "Juvenile or adult myasthenia gravis",
            "attributes": null
          },
          {
            "code": "F380z",
            "description": "Myasthenia gravis NOS",
            "attributes": null
          },
          {
            "code": "F381.",
            "description": "Myasthenic syndrome due to disease EC",
            "attributes": null
          },
          {
            "code": "F3810",
            "description": "Eaton Lambert myasthenic syndrome",
            "attributes": null
          },
          {
            "code": "F3813",
            "description": "(Myasth syndr due to diab amyotroph) or (diab amyotroph)",
            "attributes": null
          },
          {
            "code": "F383.",
            "description": "Congenital and developmental myasthenia",
            "attributes": null
          },
          {
            "code": "F390.",
            "description": "Congenital hereditary muscular dystrophy",
            "attributes": null
          },
          {
            "code": "F390z",
            "description": "Congenital hereditary muscular dystrophy NOS",
            "attributes": null
          },
          {
            "code": "F391.",
            "description": "Hereditary progressive muscular dystrophy",
            "attributes": null
          },
          {
            "code": "F3910",
            "description": "Duchenne muscular dystrophy",
            "attributes": null
          },
          {
            "code": "F3911",
            "description": "Erb's muscular dystrophy",
            "attributes": null
          },
          {
            "code": "F3912",
            "description": "Pelvic muscular dystrophy",
            "attributes": null
          },
          {
            "code": "F3913",
            "description": "Other limb girdle muscular dystrophy",
            "attributes": null
          },
          {
            "code": "F3914",
            "description": "Facioscapulohumeral muscular dystrophy",
            "attributes": null
          },
          {
            "code": "F3915",
            "description": "Distal muscular dystrophy with juvenile onset",
            "attributes": null
          },
          {
            "code": "F3916",
            "description": "Ocular muscular dystrophy",
            "attributes": null
          },
          {
            "code": "F3917",
            "description": "Oculopharyngeal muscular dystrophy",
            "attributes": null
          },
          {
            "code": "F3918",
            "description": "Becker muscular dystrophy",
            "attributes": null
          },
          {
            "code": "F391y",
            "description": "(Oth specif hered progress musc dystrophy) or (distal dystr)",
            "attributes": null
          },
          {
            "code": "F391z",
            "description": "Hereditary progressive muscular dystrophy NOS",
            "attributes": null
          },
          {
            "code": "F39B.",
            "description": "Muscular dystrophy",
            "attributes": null
          },
          {
            "code": "Fyu84",
            "description": "[X]Other myasthenic syndromes in neoplastic disease CE",
            "attributes": null
          },
          {
            "code": "Fyu85",
            "description": "[X]Myasthenic syndromes/other diseases classified elsewhere",
            "attributes": null
          },
          {
            "code": "Fyu90",
            "description": "[X]Other infantile cerebral palsy",
            "attributes": null
          },
          {
            "code": "G669.",
            "description": "Cerebral palsy, not congenital or infantile, acute",
            "attributes": null
          },
          {
            "code": "X002i",
            "description": "Western Pacific motor neurone disease",
            "attributes": null
          },
          {
            "code": "X002j",
            "description": "Madras-type motor neurone disease",
            "attributes": null
          },
          {
            "code": "X002l",
            "description": "Paraneoplastic motor neurone disease",
            "attributes": null
          },
          {
            "code": "X002R",
            "description": "Prog spinocerebellar ataxia with retained tendon reflexes",
            "attributes": null
          },
          {
            "code": "X002U",
            "description": "Secondary cerebellar degeneration",
            "attributes": null
          },
          {
            "code": "X003a",
            "description": "Juvenile Parkinson's disease",
            "attributes": null
          },
          {
            "code": "X003p",
            "description": "Juvenile onset Huntington's disease",
            "attributes": null
          },
          {
            "code": "X003q",
            "description": "Late onset Huntington's disease",
            "attributes": null
          },
          {
            "code": "X003r",
            "description": "Akinetic-rigid form of Huntington's disease",
            "attributes": null
          },
          {
            "code": "X005c",
            "description": "Acute relapsing multiple sclerosis",
            "attributes": null
          },
          {
            "code": "X005d",
            "description": "Chronic progressive multiple sclerosis",
            "attributes": null
          },
          {
            "code": "X005e",
            "description": "Remittent-progressive multiple sclerosis",
            "attributes": null
          },
          {
            "code": "X005l",
            "description": "Balo concentric sclerosis",
            "attributes": null
          },
          {
            "code": "X005Q",
            "description": "Neuraxonal leucodystrophy",
            "attributes": null
          },
          {
            "code": "X007Q",
            "description": "Alternating hemiplegia of childhood",
            "attributes": null
          },
          {
            "code": "X00AX",
            "description": "Chr inflamm demyelinat polyradiculoneuropathy with cns demye",
            "attributes": null
          },
          {
            "code": "X00Cb",
            "description": "Genetically determined myasthenia",
            "attributes": null
          },
          {
            "code": "X00Ce",
            "description": "Congenital myasthenia",
            "attributes": null
          },
          {
            "code": "X00Cu",
            "description": "Myasthenia gravis associated with thymoma",
            "attributes": null
          },
          {
            "code": "X00Cv",
            "description": "Generalised myasthenia",
            "attributes": null
          },
          {
            "code": "X00Cw",
            "description": "Myopathy in myasthenia gravis",
            "attributes": null
          },
          {
            "code": "X00DE",
            "description": "Lacunar ataxic hemiparesis",
            "attributes": null
          },
          {
            "code": "X00Em",
            "description": "Infantile cerebral palsy",
            "attributes": null
          },
          {
            "code": "X00En",
            "description": "Spastic cerebral palsy",
            "attributes": null
          },
          {
            "code": "X00Eo",
            "description": "Cerebral palsy with spastic tetraparesis",
            "attributes": null
          },
          {
            "code": "X00Eq",
            "description": "Cerebral palsy with spastic/ataxic diplegia",
            "attributes": null
          },
          {
            "code": "X00Er",
            "description": "Monoplegic cerebral palsy affecting upper limb",
            "attributes": null
          },
          {
            "code": "X00Es",
            "description": "Monoplegic cerebral palsy affecting lower limb",
            "attributes": null
          },
          {
            "code": "X00Eu",
            "description": "Dyskinetic cerebral palsy",
            "attributes": null
          },
          {
            "code": "X00Ew",
            "description": "Dystonic/rigid cerebral palsy",
            "attributes": null
          },
          {
            "code": "X40VL",
            "description": "Late infantile metachromatic leucodystrophy",
            "attributes": null
          },
          {
            "code": "X40VM",
            "description": "Juvenile metachromatic leucodystrophy",
            "attributes": null
          },
          {
            "code": "X40VN",
            "description": "Adult metachromatic leucodystrophy",
            "attributes": null
          },
          {
            "code": "X708b",
            "description": "Hutterite type of muscular dystrophy",
            "attributes": null
          },
          {
            "code": "X708d",
            "description": "Autosomal domin muscular dystrophy with limb girdle distrib",
            "attributes": null
          },
          {
            "code": "X708e",
            "description": "Autosomal domin muscular dystrophy with gene located at 5q31",
            "attributes": null
          },
          {
            "code": "X708f",
            "description": "Late onset proximal muscular dystrophy with dysarthria",
            "attributes": null
          },
          {
            "code": "X708g",
            "description": "Muscular dystrophy not predom limb girdle in distribution",
            "attributes": null
          },
          {
            "code": "X708h",
            "description": "X-linked muscular dystrophy not predominantly limb girdle",
            "attributes": null
          },
          {
            "code": "X708H",
            "description": "Muscular dystrophy with predom proximl limb girdle distribut",
            "attributes": null
          },
          {
            "code": "X708i",
            "description": "Emery-Dreifuss muscular dystrophy",
            "attributes": null
          },
          {
            "code": "X708I",
            "description": "X-linked muscular dystrophy with limb girdle distribution",
            "attributes": null
          },
          {
            "code": "X708J",
            "description": "X-linked muscular dystrophy with abnormal dystrophin",
            "attributes": null
          },
          {
            "code": "X708k",
            "description": "Autosom recessive muscular dystrophy not predom limb girdle",
            "attributes": null
          },
          {
            "code": "X708K",
            "description": "Intermediate X-linked muscular dystrophy",
            "attributes": null
          },
          {
            "code": "X708l",
            "description": "Scapulohumeral muscular dystrophy",
            "attributes": null
          },
          {
            "code": "X708L",
            "description": "Manifesting female carrier of X-linked muscular dystrophy",
            "attributes": null
          },
          {
            "code": "X708m",
            "description": "Distal muscular dystrophy",
            "attributes": null
          },
          {
            "code": "X708M",
            "description": "X-linked limb girdle muscul dystrophy with normal dystrophin",
            "attributes": null
          },
          {
            "code": "X708n",
            "description": "Autosomal dominant muscular dystrophy not predom limb girdle",
            "attributes": null
          },
          {
            "code": "X708N",
            "description": "Ji muscular dystrophy",
            "attributes": null
          },
          {
            "code": "X708o",
            "description": "Benign scapuloperoneal muscular dystrophy",
            "attributes": null
          },
          {
            "code": "X708P",
            "description": "Autosomal recess muscular dystrophy with limb girdle distrib",
            "attributes": null
          },
          {
            "code": "X708q",
            "description": "Benign congen muscular dystrophy wth finger flex contracture",
            "attributes": null
          },
          {
            "code": "X708r",
            "description": "Distal muscular dystrophy with adult onset",
            "attributes": null
          },
          {
            "code": "X708S",
            "description": "Fukuyama muscular dystrophy",
            "attributes": null
          },
          {
            "code": "X708T",
            "description": "Autosomal recess muscular dystrophy with gene located at 15q",
            "attributes": null
          },
          {
            "code": "X708U",
            "description": "Reunion-Indiana Amish type muscular dystrophy",
            "attributes": null
          },
          {
            "code": "X708V",
            "description": "Congenital muscular dystrophy",
            "attributes": null
          },
          {
            "code": "X708W",
            "description": "Western type of congenital muscular dystrophy",
            "attributes": null
          },
          {
            "code": "X708Y",
            "description": "Ullrich congenital muscular dystrophy",
            "attributes": null
          },
          {
            "code": "X708Z",
            "description": "Eichsfeld type congenital muscular dystrophy",
            "attributes": null
          },
          {
            "code": "X76je",
            "description": "Spastic quadriplegia",
            "attributes": null
          },
          {
            "code": "X76n9",
            "description": "Hemiparesis",
            "attributes": null
          },
          {
            "code": "Xa0fr",
            "description": "Right hemiplegia",
            "attributes": null
          },
          {
            "code": "Xa0fs",
            "description": "Left hemiplegia",
            "attributes": null
          },
          {
            "code": "Xa0ft",
            "description": "Right hemiparesis",
            "attributes": null
          },
          {
            "code": "Xa0fu",
            "description": "Left hemiparesis",
            "attributes": null
          },
          {
            "code": "Xa0lL",
            "description": "Muscular dystrophy",
            "attributes": null
          },
          {
            "code": "Xa0lM",
            "description": "Ataxic cerebral palsy",
            "attributes": null
          },
          {
            "code": "Xa0ON",
            "description": "Severe childhood autosomal recessive muscular dystrophy",
            "attributes": null
          },
          {
            "code": "Xa0ZY",
            "description": "Cerebro-oculo-dysgenesis-muscular dystrophy syndrome",
            "attributes": null
          },
          {
            "code": "XaA1S",
            "description": "New variant of Creutzfeldt-Jakob disease",
            "attributes": null
          },
          {
            "code": "XaadE",
            "description": "Choreoathetoid cerebral palsy",
            "attributes": null
          },
          {
            "code": "XaaRV",
            "description": "Referral to community Parkinson's service",
            "attributes": null
          },
          {
            "code": "XaaVG",
            "description": "Gross Motor Function Classification System Cerebral Palsy",
            "attributes": null
          },
          {
            "code": "Xab3R",
            "description": "Bilateral spastic cerebral palsy",
            "attributes": null
          },
          {
            "code": "XaB4V",
            "description": "Leucodystrophy without a known biochemical basis",
            "attributes": null
          },
          {
            "code": "Xab7w",
            "description": "Seen by Parkinson's disease service",
            "attributes": null
          },
          {
            "code": "XabbC",
            "description": "Referral to community Parkinson disease clin nurse spcialist",
            "attributes": null
          },
          {
            "code": "XaBE2",
            "description": "Cerebral palsy, not congenital or infantile, acute",
            "attributes": null
          },
          {
            "code": "XabVp",
            "description": "Sporadic Creutzfeldt-Jakob disease",
            "attributes": null
          },
          {
            "code": "XaELO",
            "description": "Residual hemiplegia",
            "attributes": null
          },
          {
            "code": "XaeUM",
            "description": "Multiple system atrophy, cerebellar variant",
            "attributes": null
          },
          {
            "code": "XaeUN",
            "description": "Multiple system atrophy, Parkinson variant",
            "attributes": null
          },
          {
            "code": "XaKA8",
            "description": "Specialised services for pts with multiple sclerosis ESA",
            "attributes": null
          },
          {
            "code": "XaKvm",
            "description": "Multiple sclerosis review",
            "attributes": null
          },
          {
            "code": "XaKvn",
            "description": "Multiple sclerosis multidisciplinary review",
            "attributes": null
          },
          {
            "code": "XaKzg",
            "description": "Multiple sclerosis care plan agreed",
            "attributes": null
          },
          {
            "code": "XaL3N",
            "description": "Hemiparesis NOS",
            "attributes": null
          },
          {
            "code": "XaOfZ",
            "description": "Cerebral degeneration in Parkinson's disease",
            "attributes": null
          },
          {
            "code": "XaOzZ",
            "description": "Benign multiple sclerosis",
            "attributes": null
          },
          {
            "code": "XaP0r",
            "description": "Primary progressive multiple sclerosis",
            "attributes": null
          },
          {
            "code": "XaP0X",
            "description": "Malignant multiple sclerosis",
            "attributes": null
          },
          {
            "code": "XaP1B",
            "description": "Relapsing and remitting multiple sclerosis",
            "attributes": null
          },
          {
            "code": "XaP1V",
            "description": "Secondary progressive multiple sclerosis",
            "attributes": null
          },
          {
            "code": "XaPSa",
            "description": "Management of multiple sclerosis in stable disability phase",
            "attributes": null
          },
          {
            "code": "XaPSb",
            "description": "Management of MS in progressive disability phase",
            "attributes": null
          },
          {
            "code": "XaPSc",
            "description": "Management of multiple sclerosis in palliative phase",
            "attributes": null
          },
          {
            "code": "XaPSY",
            "description": "Management of multiple sclerosis in onset phase",
            "attributes": null
          },
          {
            "code": "XaPSZ",
            "description": "Management of multiple sclerosis in early disease phase",
            "attributes": null
          },
          {
            "code": "XaQwf",
            "description": "History of Parkinson's disease",
            "attributes": null
          },
          {
            "code": "XaX9A",
            "description": "Multiple sclerosis monitoring administration",
            "attributes": null
          },
          {
            "code": "XaX9F",
            "description": "Multiple sclerosis monitoring first letter",
            "attributes": null
          },
          {
            "code": "XaX9H",
            "description": "Multiple sclerosis monitoring second letter",
            "attributes": null
          },
          {
            "code": "XaX9J",
            "description": "Multiple sclerosis monitoring telephone invitation",
            "attributes": null
          },
          {
            "code": "XaX9L",
            "description": "Multiple sclerosis monitoring third letter",
            "attributes": null
          },
          {
            "code": "XaXGu",
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