[
  {
    "phenotype_id": "PH2803",
    "phenotype_version_id": 7088,
    "name": "Motor neurone disease codes",
    "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 `MND_COD` refset published by NHSD. Contains public sector information licensed under the UK Open Government Licence v3\\.0 (https://www.nationalarchives.gov.uk/doc/open\\-government\\-licence/version/3/).\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": "2026-01-26T22:44:40.451858Z",
    "author": "NHSD Primary Care Domain Refsets",
    "collections": [
      {
        "name": "OpenCodelist",
        "value": 31
      },
      {
        "name": "Phenotype Library",
        "value": 18
      }
    ],
    "tags": null,
    "organisation": {
      "id": 1,
      "slug": "opensafely",
      "name": "OpenSAFELY"
    },
    "world_access": 1,
    "updated": "2026-01-26T22:44:43.307427Z",
    "references": [],
    "signed_off": [],
    "methodology": "",
    "coding_system": [
      {
        "name": "SNOMED  CT codes",
        "value": 9
      }
    ],
    "open_codelist_id": "nhsd-primary-care-domain-refsets/mnd_cod",
    "source_reference": "https://www.opencodelists.org/codelist/nhsd-primary-care-domain-refsets/mnd_cod/20250912",
    "concept_information": [
      {
        "concept_id": 7265,
        "concept_version_id": 14750,
        "concept_name": "nhsd-primary-care-domain-refsets/mnd_cod/20250912",
        "coding_system": {
          "id": 9,
          "name": "SNOMED  CT codes",
          "description": "SNOMED CT codes"
        },
        "phenotype_id": "PH2803",
        "phenotype_version_id": 7088,
        "phenotype_name": "Motor neurone disease codes",
        "code_attribute_header": [],
        "codes": [
          {
            "code": "103851000119100",
            "description": "Restrictive lung disease due to amyotrophic lateral sclerosis",
            "attributes": null
          },
          {
            "code": "1105051000000102",
            "description": "Subacute combined degeneration of spinal cord due to use of nitrous oxide",
            "attributes": null
          },
          {
            "code": "1172689007",
            "description": "Prenatal-onset spinal muscular atrophy with congenital bone fractures",
            "attributes": null
          },
          {
            "code": "1197152005",
            "description": "Distal hereditary motor neuropathy type 5",
            "attributes": null
          },
          {
            "code": "1197523001",
            "description": "Autosomal dominant amyotrophic lateral sclerosis type 1",
            "attributes": null
          },
          {
            "code": "1197524007",
            "description": "Autosomal recessive amyotrophic lateral sclerosis type 1",
            "attributes": null
          },
          {
            "code": "1201863001",
            "description": "Amyotrophic lateral sclerosis type 1",
            "attributes": null
          },
          {
            "code": "1201947005",
            "description": "Juvenile amyotrophic lateral sclerosis type 2",
            "attributes": null
          },
          {
            "code": "1201950008",
            "description": "Amyotrophic lateral sclerosis type 3",
            "attributes": null
          },
          {
            "code": "1201961000",
            "description": "Juvenile amyotrophic lateral sclerosis type 5",
            "attributes": null
          },
          {
            "code": "1204334005",
            "description": "Amyotrophic lateral sclerosis type 6",
            "attributes": null
          },
          {
            "code": "1204349002",
            "description": "Amyotrophic lateral sclerosis type 7",
            "attributes": null
          },
          {
            "code": "1204350002",
            "description": "Amyotrophic lateral sclerosis type 8",
            "attributes": null
          },
          {
            "code": "1204351003",
            "description": "Amyotrophic lateral sclerosis type 9",
            "attributes": null
          },
          {
            "code": "1208412003",
            "description": "Amyotrophic lateral sclerosis type 10",
            "attributes": null
          },
          {
            "code": "1208615009",
            "description": "Neurogenic scapuloperoneal syndrome Kaeser type",
            "attributes": null
          },
          {
            "code": "1230343006",
            "description": "Distal hereditary motor neuropathy type 2",
            "attributes": null
          },
          {
            "code": "1259121008",
            "description": "Amyotrophic lateral sclerosis, parkinsonism, dementia complex of West New Guinea",
            "attributes": null
          },
          {
            "code": "1259122001",
            "description": "Amyotrophic lateral sclerosis with parkinsonism",
            "attributes": null
          },
          {
            "code": "1259123006",
            "description": "Amyotrophic lateral sclerosis, parkinsonism, dementia complex of Kii Peninsula",
            "attributes": null
          },
          {
            "code": "1259124000",
            "description": "Amyotrophic lateral sclerosis with frontotemporal dementia",
            "attributes": null
          },
          {
            "code": "1259125004",
            "description": "Amyotrophic lateral sclerosis with multiple system atrophy",
            "attributes": null
          },
          {
            "code": "1259126003",
            "description": "Amyotrophic lateral sclerosis with autonomic dysfunction",
            "attributes": null
          },
          {
            "code": "1259127007",
            "description": "Amyotrophic lateral sclerosis with cerebellar dysfunction",
            "attributes": null
          },
          {
            "code": "1259129005",
            "description": "Amyotrophic lateral sclerosis with spinocerebellar ataxia",
            "attributes": null
          },
          {
            "code": "1263497002",
            "description": "Motor neuron disease due to neoplastic disease",
            "attributes": null
          },
          {
            "code": "1263531001",
            "description": "Motor neuron disease due to and following radiotherapy to spinal cord",
            "attributes": null
          },
          {
            "code": "1263534009",
            "description": "Motor neuron disease due to herpes zoster",
            "attributes": null
          },
          {
            "code": "1263535005",
            "description": "Motor neuron disease due to human immunodeficiency virus infection",
            "attributes": null
          },
          {
            "code": "1263536006",
            "description": "Motor neuron disease due to hereditary spastic paraplegia",
            "attributes": null
          },
          {
            "code": "1263538007",
            "description": "Motor neuron disease due to gammopathy",
            "attributes": null
          },
          {
            "code": "128212001",
            "description": "Spinal muscular atrophy, type II",
            "attributes": null
          },
          {
            "code": "1299151005",
            "description": "O'Sullivan McLeod syndrome",
            "attributes": null
          },
          {
            "code": "155014006",
            "description": "(Anterior horn cell disease) or (muscular atrophy)",
            "attributes": null
          },
          {
            "code": "155015007",
            "description": "Motor neurone disease",
            "attributes": null
          },
          {
            "code": "155016008",
            "description": "Other anterior horn cell disease &amp;/or Werdnig-Hoffman disease",
            "attributes": null
          },
          {
            "code": "192884004",
            "description": "Anterior horn cell disease",
            "attributes": null
          },
          {
            "code": "192885003",
            "description": "Unspecified spinal muscular atrophy",
            "attributes": null
          },
          {
            "code": "192887006",
            "description": "Spinal muscular atrophy NOS",
            "attributes": null
          },
          {
            "code": "192888001",
            "description": "Motor neurone disease",
            "attributes": null
          },
          {
            "code": "192889009",
            "description": "Motor neurone disease",
            "attributes": null
          },
          {
            "code": "192890000",
            "description": "Motor neurone disease NOS",
            "attributes": null
          },
          {
            "code": "192891001",
            "description": "Other anterior horn cell disease",
            "attributes": null
          },
          {
            "code": "192892008",
            "description": "Anterior horn cell disease NOS",
            "attributes": null
          },
          {
            "code": "194461001",
            "description": "[X]Other inherited spinal muscular atrophy",
            "attributes": null
          },
          {
            "code": "230246005",
            "description": "Progressive bulbar palsy of childhood",
            "attributes": null
          },
          {
            "code": "230247001",
            "description": "Distal spinal muscular atrophy",
            "attributes": null
          },
          {
            "code": "230248006",
            "description": "Scapuloperoneal spinal muscular atrophy",
            "attributes": null
          },
          {
            "code": "230249003",
            "description": "Facioscapulohumeral spinal muscular atrophy",
            "attributes": null
          },
          {
            "code": "230250003",
            "description": "Facioscapulohumeral spinal muscular atrophy with sensory loss",
            "attributes": null
          },
          {
            "code": "230251004",
            "description": "Scapulohumeral spinal muscular atrophy",
            "attributes": null
          },
          {
            "code": "230252006",
            "description": "Oculopharyngeal spinal muscular atrophy",
            "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": "230264003",
            "description": "Troyer syndrome",
            "attributes": null
          },
          {
            "code": "230274000",
            "description": "Frontal lobe degeneration with motor neurone disease",
            "attributes": null
          },
          {
            "code": "230547002",
            "description": "Bulbar palsy",
            "attributes": null
          },
          {
            "code": "230784003",
            "description": "Congenital pseudobulbar palsy",
            "attributes": null
          },
          {
            "code": "249892007",
            "description": "Progressive pseudobulbar palsy",
            "attributes": null
          },
          {
            "code": "267693003",
            "description": "(Anterior horn cell disease) or (muscular atrophy)",
            "attributes": null
          },
          {
            "code": "267694009",
            "description": "Other anterior horn cell disease &amp;/or Werdnig-Hoffman disease",
            "attributes": null
          },
          {
            "code": "305719002",
            "description": "Neuromyotonia",
            "attributes": null
          },
          {
            "code": "31097004",
            "description": "Post poliomyelitis syndrome",
            "attributes": null
          },
          {
            "code": "367094007",
            "description": "Postpolio syndrome",
            "attributes": null
          },
          {
            "code": "37340000",
            "description": "Motor neuron disease",
            "attributes": null
          },
          {
            "code": "398432008",
            "description": "Bulbar weakness",
            "attributes": null
          },
          {
            "code": "412291000000109",
            "description": "[X]Other spinal muscular atrophies and related syndromes",
            "attributes": null
          },
          {
            "code": "430031000000107",
            "description": "[X]Other inherited spinal muscular atrophy",
            "attributes": null
          },
          {
            "code": "44395000",
            "description": "Spastic tetraplegia with rigidity syndrome",
            "attributes": null
          },
          {
            "code": "46251005",
            "description": "Corticospinal motor disease",
            "attributes": null
          },
          {
            "code": "49793008",
            "description": "Hereditary motor neuron disease",
            "attributes": null
          },
          {
            "code": "5262007",
            "description": "Spinal muscular atrophy",
            "attributes": null
          },
          {
            "code": "54280009",
            "description": "Kugelberg-Welander disease",
            "attributes": null
          },
          {
            "code": "54304004",
            "description": "Progressive bulbar palsy",
            "attributes": null
          },
          {
            "code": "583151000000109",
            "description": "Other anterior horn cell disease",
            "attributes": null
          },
          {
            "code": "60576007",
            "description": "Subacute combined degeneration of spinal cord",
            "attributes": null
          },
          {
            "code": "630471000000103",
            "description": "Anterior horn cell disease NOS",
            "attributes": null
          },
          {
            "code": "64383006",
            "description": "Werdnig-Hoffmann disease",
            "attributes": null
          },
          {
            "code": "646181000000106",
            "description": "Unspecified spinal muscular atrophy",
            "attributes": null
          },
          {
            "code": "646191000000108",
            "description": "Spinal muscular atrophy NOS",
            "attributes": null
          },
          {
            "code": "646201000000105",
            "description": "Motor neurone disease NOS",
            "attributes": null
          },
          {
            "code": "699866005",
            "description": "Progressive bulbar palsy with sensorineural deafness",
            "attributes": null
          },
          {
            "code": "703524005",
            "description": "Spinal muscular atrophy with progressive myoclonic epilepsy",
            "attributes": null
          },
          {
            "code": "703544004",
            "description": "Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia",
            "attributes": null
          },
          {
            "code": "711406009",
            "description": "Autosomal recessive axonal neuropathy with neuromyotonia",
            "attributes": null
          },
          {
            "code": "711483003",
            "description": "Spinal muscular atrophy with respiratory distress type 1",
            "attributes": null
          },
          {
            "code": "715565004",
            "description": "Lethal arthrogryposis co-occurrent with anterior horn cell disease",
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          },
          {
            "code": "717964007",
            "description": "Juvenile primary lateral sclerosis",
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          },
          {
            "code": "718555006",
            "description": "Juvenile amyotrophic lateral sclerosis",
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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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          },
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            "code": "723612001",
            "description": "Spinal muscular atrophy, Dandy-Walker malformation, cataract syndrome",
            "attributes": null
          },
          {
            "code": "7379000",
            "description": "Pseudobulbar palsy",
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          },
          {
            "code": "757061000000109",
            "description": "Neuromyotonia",
            "attributes": null
          },
          {
            "code": "763067000",
            "description": "Autosomal dominant congenital benign spinal muscular atrophy",
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          },
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            "code": "763533003",
            "description": "Distal hereditary motor neuropathy Jerash type",
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          },
          {
            "code": "766764008",
            "description": "X-linked distal spinal muscular atrophy type 3",
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          },
          {
            "code": "770430000",
            "description": "Autosomal recessive distal spinal muscular atrophy type 3",
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          },
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          },
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            "code": "771081007",
            "description": "Distal hereditary motor neuropathy type 7",
            "attributes": null
          },
          {
            "code": "771238004",
            "description": "Spinal atrophy, ophthalmoplegia, pyramidal syndrome",
            "attributes": null
          },
          {
            "code": "771302009",
            "description": "Autosomal recessive lower motor neuron disease with childhood onset",
            "attributes": null
          },
          {
            "code": "771475006",
            "description": "Young adult-onset distal hereditary motor neuropathy",
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          },
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          },
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            "description": "Postpolio syndrome",
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          },
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            "description": "Lower motor neuron syndrome with late-adult onset",
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          },
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            "description": "Autosomal dominant adult-onset proximal spinal muscular atrophy",
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            "description": "Primary lateral sclerosis",
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            "code": "838276009",
            "description": "Amyotrophic lateral sclerosis, parkinsonism, dementia complex",
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            "description": "Lower motor neuron disease",
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            "code": "86044005",
            "description": "Amyotrophic lateral sclerosis",
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            "description": "Anterior opercular syndrome",
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            "description": "Progressive muscular atrophy",
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            "code": "95647008",
            "description": "Upper motor neuron disease",
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      }
    ],
    "coding_system_release": "",
    "open_codelist_version_id": "34d45f63",
    "open_codelist_version_tag": "20250912",
    "status": 1,
    "doi": "https://doi.org/10.48533/y6pe-5e23",
    "is_deleted": false,
    "publish_status": 2,
    "owner": "ieuan.scanlon",
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    "versions": [
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]