[
  {
    "phenotype_id": "PH2789",
    "phenotype_version_id": 7052,
    "name": "Mitochondrial 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 `MITOCHOND_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": "2026-01-26T22:44:00.092295Z",
    "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": "2026-01-26T22:44:02.254802Z",
    "references": [],
    "signed_off": [],
    "methodology": "",
    "coding_system": [
      {
        "name": "SNOMED  CT codes",
        "value": 9
      }
    ],
    "open_codelist_id": "nhsd-primary-care-domain-refsets/mitochond_cod",
    "source_reference": "https://www.opencodelists.org/codelist/nhsd-primary-care-domain-refsets/mitochond_cod/20250912",
    "concept_information": [
      {
        "concept_id": 7229,
        "concept_version_id": 14714,
        "concept_name": "nhsd-primary-care-domain-refsets/mitochond_cod/20250912",
        "coding_system": {
          "id": 9,
          "name": "SNOMED  CT codes",
          "description": "SNOMED CT codes"
        },
        "phenotype_id": "PH2789",
        "phenotype_version_id": 7052,
        "phenotype_name": "Mitochondrial disease codes",
        "code_attribute_header": [],
        "codes": [
          {
            "code": "1208937004",
            "description": "Mitochondrial deoxyribonucleic acid depletion syndrome, encephalomyopathic form with variable craniofacial anomalies",
            "attributes": null
          },
          {
            "code": "1231309005",
            "description": "Mitochondrial deoxyribonucleic acid depletion syndrome myopathic form",
            "attributes": null
          },
          {
            "code": "1237514002",
            "description": "Mitochondrial myopathy, cerebellar ataxia, pigmentary retinopathy syndrome",
            "attributes": null
          },
          {
            "code": "1260365000",
            "description": "Dystonia due to mitochondrial disease",
            "attributes": null
          },
          {
            "code": "1263505003",
            "description": "Myoclonic disorder due to mitochondrial disorder",
            "attributes": null
          },
          {
            "code": "1264009006",
            "description": "Isolated cytochrome C oxidase deficiency",
            "attributes": null
          },
          {
            "code": "1279890001",
            "description": "Multiple mitochondrial dysfunctions syndrome type 5",
            "attributes": null
          },
          {
            "code": "1279891002",
            "description": "Multiple mitochondrial dysfunctions syndrome type 6",
            "attributes": null
          },
          {
            "code": "237985009",
            "description": "Pearson's syndrome",
            "attributes": null
          },
          {
            "code": "297231002",
            "description": "3-Methylglutaconic aciduria type 2",
            "attributes": null
          },
          {
            "code": "44423001",
            "description": "Early myoclonic encephalopathy",
            "attributes": null
          },
          {
            "code": "764733009",
            "description": "Progressive external ophthalmoplegia, myopathy, emaciation syndrome",
            "attributes": null
          },
          {
            "code": "783157004",
            "description": "Leigh syndrome with nephrotic syndrome",
            "attributes": null
          },
          {
            "code": "784346006",
            "description": "Navajo neurohepatopathy",
            "attributes": null
          }
        ]
      }
    ],
    "coding_system_release": "",
    "open_codelist_version_id": "2b2eb863",
    "open_codelist_version_tag": "20250912",
    "status": 1,
    "doi": "https://doi.org/10.48533/xx57-1c15",
    "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": 7052,
        "version_name": "Mitochondrial disease codes",
        "version_date": "2026-01-26T22:44:02.270254Z",
        "is_published": true,
        "is_latest": true
      },
      {
        "version_id": 7051,
        "version_name": "Mitochondrial disease codes",
        "version_date": "2026-01-26T22:44:01.196113Z",
        "is_published": true,
        "is_latest": false
      },
      {
        "version_id": 7050,
        "version_name": "Mitochondrial disease codes",
        "version_date": "2026-01-26T22:44:00.104905Z",
        "is_published": true,
        "is_latest": false
      }
    ]
  }
]