[
  {
    "phenotype_id": "PH3136",
    "phenotype_version_id": 8119,
    "name": "Motor Neurone Disease (SNOMED CT)",
    "definition": "This codelist was taken from [OpenCodelists](https://www.opencodelists.org/), created by [OpenSAFELY](https://www.opensafely.org/). We recommend viewing this Phenotype on the OpenCodelist website to view the most recent version.\n\n\nTaken from the Motor Neurone Disease tab of the Population Risk COVID\\-19 Treatments code list v1\\.3, published by NHS Digital, 2021\\-12\\-13\\.\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": "2026-01-26T23:04:48.768942Z",
    "author": "NHS Digital",
    "collections": [
      {
        "name": "OpenCodelist",
        "value": 31
      },
      {
        "name": "Phenotype Library",
        "value": 18
      }
    ],
    "tags": null,
    "organisation": {
      "id": 1,
      "slug": "opensafely",
      "name": "OpenSAFELY"
    },
    "world_access": 1,
    "updated": "2026-01-26T23:04:48.764040Z",
    "references": [
      {
        "url": "https://digital.nhs.uk/coronavirus/treatments/methodology/coding-classifications-used",
        "title": "NHSD Population Risk COVID-19 Treatments"
      }
    ],
    "signed_off": [],
    "methodology": "",
    "coding_system": [
      {
        "name": "SNOMED  CT codes",
        "value": 9
      }
    ],
    "open_codelist_id": "nhsd/motor-neurone-disease-snomed-ct",
    "source_reference": "https://www.opencodelists.org/codelist/nhsd/motor-neurone-disease-snomed-ct/5a2739f8",
    "concept_information": [
      {
        "concept_id": 8296,
        "concept_version_id": 15781,
        "concept_name": "nhsd/motor-neurone-disease-snomed-ct/5a2739f8",
        "coding_system": {
          "id": 9,
          "name": "SNOMED  CT codes",
          "description": "SNOMED CT codes"
        },
        "phenotype_id": "PH3136",
        "phenotype_version_id": 8119,
        "phenotype_name": "Motor Neurone Disease (SNOMED CT)",
        "code_attribute_header": [],
        "codes": [
          {
            "code": "230246005",
            "description": "Progressive bulbar palsy of childhood",
            "attributes": null
          },
          {
            "code": "230253001",
            "description": "Bulbospinal neuronopathy",
            "attributes": null
          },
          {
            "code": "230254007",
            "description": "Western Pacific motor neurone disease",
            "attributes": null
          },
          {
            "code": "230255008",
            "description": "Madras-type motor neurone disease",
            "attributes": null
          },
          {
            "code": "230257000",
            "description": "Paraneoplastic motor neurone disease",
            "attributes": null
          },
          {
            "code": "230258005",
            "description": "Amyotrophic lateral sclerosis with dementia",
            "attributes": null
          },
          {
            "code": "230274000",
            "description": "Frontal lobe degeneration with motor neurone disease",
            "attributes": null
          },
          {
            "code": "230784003",
            "description": "Congenital pseudobulbar palsy",
            "attributes": null
          },
          {
            "code": "249892007",
            "description": "Progressive pseudobulbar palsy",
            "attributes": null
          },
          {
            "code": "37340000",
            "description": "Motor neuron disease",
            "attributes": null
          },
          {
            "code": "398432008",
            "description": "Bulbar weakness",
            "attributes": null
          },
          {
            "code": "46251005",
            "description": "Corticospinal motor disease",
            "attributes": null
          },
          {
            "code": "49793008",
            "description": "Hereditary motor neuron disease",
            "attributes": null
          },
          {
            "code": "54304004",
            "description": "Progressive bulbar palsy",
            "attributes": null
          },
          {
            "code": "583151000000109",
            "description": "Other anterior horn cell disease",
            "attributes": null
          },
          {
            "code": "630471000000103",
            "description": "Anterior horn cell disease NOS",
            "attributes": null
          },
          {
            "code": "646201000000105",
            "description": "Motor neurone disease NOS",
            "attributes": null
          },
          {
            "code": "699866005",
            "description": "Progressive bulbar palsy with sensorineural deafness",
            "attributes": null
          },
          {
            "code": "715565004",
            "description": "Lethal arthrogryposis co-occurrent with anterior horn cell disease",
            "attributes": null
          },
          {
            "code": "717964007",
            "description": "Juvenile primary lateral sclerosis",
            "attributes": null
          },
          {
            "code": "718555006",
            "description": "Juvenile amyotrophic lateral sclerosis",
            "attributes": null
          },
          {
            "code": "722987009",
            "description": "Amyotrophic lateral sclerosis plus syndrome",
            "attributes": null
          },
          {
            "code": "7379000",
            "description": "Pseudobulbar palsy",
            "attributes": null
          },
          {
            "code": "771302009",
            "description": "Autosomal recessive lower motor neuron disease with childhood onset",
            "attributes": null
          },
          {
            "code": "783618006",
            "description": "Lower motor neuron syndrome with late-adult onset",
            "attributes": null
          },
          {
            "code": "784341001",
            "description": "Amyotrophic lateral sclerosis type 4",
            "attributes": null
          },
          {
            "code": "81211007",
            "description": "Primary lateral sclerosis",
            "attributes": null
          },
          {
            "code": "838276009",
            "description": "Amyotrophic lateral sclerosis, parkinsonism, dementia complex",
            "attributes": null
          },
          {
            "code": "84590007",
            "description": "Lower motor neuron disease",
            "attributes": null
          },
          {
            "code": "85672005",
            "description": "Anterior horn cell disease",
            "attributes": null
          },
          {
            "code": "86044005",
            "description": "Amyotrophic lateral sclerosis",
            "attributes": null
          },
          {
            "code": "88923002",
            "description": "Progressive muscular atrophy",
            "attributes": null
          }
        ]
      }
    ],
    "coding_system_release": "",
    "open_codelist_version_id": "5a2739f8",
    "open_codelist_version_tag": "",
    "status": 1,
    "doi": "https://doi.org/10.48533/jpeh-en91",
    "is_deleted": false,
    "publish_status": 2,
    "owner": "ieuan.scanlon",
    "template": {
      "id": 3,
      "name": "OpenCodelists Phenotype",
      "description": "OpenSafely's OpenCodelist Phenotype, visit https://www.opencodelists.org/ to learn more",
      "version_id": 1
    },
    "versions": [
      {
        "version_id": 8119,
        "version_name": "Motor Neurone Disease (SNOMED CT)",
        "version_date": "2026-01-26T23:04:48.775883Z",
        "is_published": true,
        "is_latest": true
      }
    ]
  }
]