[
  {
    "phenotype_id": "PH3957",
    "phenotype_version_id": 9154,
    "name": "has_mnd_ms_myas_or_huntingtons",
    "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\nSNOMED codelist for the `has_mnd_ms_myas_or_huntingtons` group in the QCovid® to develop the\n COVID\\-19 Population Risk Assessment.\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": "2026-01-26T23:41:31.512715Z",
    "author": "QCovid",
    "collections": [
      {
        "name": "OpenCodelist",
        "value": 31
      },
      {
        "name": "Phenotype Library",
        "value": 18
      }
    ],
    "tags": null,
    "organisation": {
      "id": 1,
      "slug": "opensafely",
      "name": "OpenSAFELY"
    },
    "world_access": 1,
    "updated": "2026-01-26T23:41:31.502622Z",
    "references": [
      {
        "url": "https://digital.nhs.uk/coronavirus/risk-assessment/population/code-list-used-for-population-risk-assessment",
        "title": "NHSD QCovid codelists"
      }
    ],
    "signed_off": [],
    "methodology": "",
    "coding_system": [
      {
        "name": "SNOMED  CT codes",
        "value": 9
      }
    ],
    "open_codelist_id": "qcovid/has_mnd_ms_myas_or_huntingtons",
    "source_reference": "https://www.opencodelists.org/codelist/qcovid/has_mnd_ms_myas_or_huntingtons/4b70c3f1",
    "concept_information": [
      {
        "concept_id": 9331,
        "concept_version_id": 16816,
        "concept_name": "qcovid/has_mnd_ms_myas_or_huntingtons/4b70c3f1",
        "coding_system": {
          "id": 9,
          "name": "SNOMED  CT codes",
          "description": "SNOMED CT codes"
        },
        "phenotype_id": "PH3957",
        "phenotype_version_id": 9154,
        "phenotype_name": "has_mnd_ms_myas_or_huntingtons",
        "code_attribute_header": [],
        "codes": [
          {
            "code": "128212001",
            "description": "Spinal muscular atrophy, type II (disorder)",
            "attributes": null
          },
          {
            "code": "193206003",
            "description": "Persistent neonatal myasthenia gravis (disorder)",
            "attributes": null
          },
          {
            "code": "193207007",
            "description": "Juvenile or adult myasthenia gravis (disorder)",
            "attributes": null
          },
          {
            "code": "193216006",
            "description": "Congenital and developmental myasthenia (disorder)",
            "attributes": null
          },
          {
            "code": "230246005",
            "description": "Progressive bulbar palsy of childhood (disorder)",
            "attributes": null
          },
          {
            "code": "230247001",
            "description": "Distal spinal muscular atrophy (disorder)",
            "attributes": null
          },
          {
            "code": "230248006",
            "description": "Scapuloperoneal spinal muscular atrophy (disorder)",
            "attributes": null
          },
          {
            "code": "230249003",
            "description": "Facioscapulohumeral spinal muscular atrophy (disorder)",
            "attributes": null
          },
          {
            "code": "230250003",
            "description": "Facioscapulohumeral spinal muscular atrophy with sensory loss (disorder)",
            "attributes": null
          },
          {
            "code": "230251004",
            "description": "Scapulohumeral spinal muscular atrophy (disorder)",
            "attributes": null
          },
          {
            "code": "230252006",
            "description": "Oculopharyngeal spinal muscular atrophy (disorder)",
            "attributes": null
          },
          {
            "code": "230253001",
            "description": "Bulbospinal neuronopathy (disorder)",
            "attributes": null
          },
          {
            "code": "230257000",
            "description": "Paraneoplastic motor neurone disease (disorder)",
            "attributes": null
          },
          {
            "code": "230258005",
            "description": "Amyotrophic lateral sclerosis with dementia (disorder)",
            "attributes": null
          },
          {
            "code": "230669004",
            "description": "Genetically determined myasthenia (disorder)",
            "attributes": null
          },
          {
            "code": "230671004",
            "description": "Acetylcholine resynthesis deficiency (disorder)",
            "attributes": null
          },
          {
            "code": "230672006",
            "description": "Congenital myasthenia (disorder)",
            "attributes": null
          },
          {
            "code": "230673001",
            "description": "Congenital end-plate acetylcholine receptor deficiency (disorder)",
            "attributes": null
          },
          {
            "code": "230674007",
            "description": "Pseudomyopathic myasthenia (disorder)",
            "attributes": null
          },
          {
            "code": "230676009",
            "description": "Putative defect in acetylcholine synthesis or packaging (disorder)",
            "attributes": null
          },
          {
            "code": "230677000",
            "description": "Congenital end-plate acetylcholinesterase deficiency (disorder)",
            "attributes": null
          },
          {
            "code": "230678005",
            "description": "Decrease of motor end-plate potential amplitude without acetylcholine receptor deficiency (disorder)",
            "attributes": null
          },
          {
            "code": "230679002",
            "description": "Abnormality of synaptic vesicles (disorder)",
            "attributes": null
          },
          {
            "code": "230685009",
            "description": "Myasthenia gravis associated with thymoma (disorder)",
            "attributes": null
          },
          {
            "code": "230686005",
            "description": "Generalized myasthenia (disorder)",
            "attributes": null
          },
          {
            "code": "230784003",
            "description": "Congenital pseudobulbar palsy (disorder)",
            "attributes": null
          },
          {
            "code": "249892007",
            "description": "Progressive pseudobulbar palsy (disorder)",
            "attributes": null
          },
          {
            "code": "305719002",
            "description": "Neuromyotonia (disorder)",
            "attributes": null
          },
          {
            "code": "31097004",
            "description": "Post poliomyelitis syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "37340000",
            "description": "Motor neuron disease (disorder)",
            "attributes": null
          },
          {
            "code": "5262007",
            "description": "Spinal muscular atrophy (disorder)",
            "attributes": null
          },
          {
            "code": "54280009",
            "description": "Kugelberg-Welander disease (disorder)",
            "attributes": null
          },
          {
            "code": "54304004",
            "description": "Progressive bulbar palsy (disorder)",
            "attributes": null
          },
          {
            "code": "58756001",
            "description": "Huntington's chorea (disorder)",
            "attributes": null
          },
          {
            "code": "64383006",
            "description": "Werdnig-Hoffmann disease (disorder)",
            "attributes": null
          },
          {
            "code": "7379000",
            "description": "Pseudobulbar palsy (disorder)",
            "attributes": null
          },
          {
            "code": "81211007",
            "description": "Primary lateral sclerosis (disorder)",
            "attributes": null
          },
          {
            "code": "85505000",
            "description": "Adult spinal muscular atrophy (disorder)",
            "attributes": null
          },
          {
            "code": "85672005",
            "description": "Anterior horn cell disease (disorder)",
            "attributes": null
          },
          {
            "code": "86044005",
            "description": "Amyotrophic lateral sclerosis (disorder)",
            "attributes": null
          },
          {
            "code": "864471000000106",
            "description": "Anterior opercular syndrome (disorder)",
            "attributes": null
          },
          {
            "code": "88923002",
            "description": "Progressive muscular atrophy (disorder)",
            "attributes": null
          },
          {
            "code": "91637004",
            "description": "Myasthenia gravis (disorder)",
            "attributes": null
          }
        ]
      }
    ],
    "coding_system_release": "",
    "open_codelist_version_id": "4b70c3f1",
    "open_codelist_version_tag": "",
    "status": 1,
    "doi": "https://doi.org/10.48533/yn9s-4m63",
    "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": 9154,
        "version_name": "has_mnd_ms_myas_or_huntingtons",
        "version_date": "2026-01-26T23:41:31.525288Z",
        "is_published": true,
        "is_latest": true
      }
    ]
  }
]