[
  {
    "phenotype_id": "PH2207",
    "phenotype_version_id": 5078,
    "name": "Amyloidosis 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 `AMYLOID_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": "2026-01-26T21:55:05.103672Z",
    "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": "2026-01-26T21:55:08.652990Z",
    "references": [],
    "signed_off": [],
    "methodology": "",
    "coding_system": [
      {
        "name": "SNOMED  CT codes",
        "value": 9
      }
    ],
    "open_codelist_id": "nhsd-primary-care-domain-refsets/amyloid_cod",
    "source_reference": "https://www.opencodelists.org/codelist/nhsd-primary-care-domain-refsets/amyloid_cod/20250912",
    "concept_information": [
      {
        "concept_id": 5255,
        "concept_version_id": 12740,
        "concept_name": "nhsd-primary-care-domain-refsets/amyloid_cod/20250912",
        "coding_system": {
          "id": 9,
          "name": "SNOMED  CT codes",
          "description": "SNOMED CT codes"
        },
        "phenotype_id": "PH2207",
        "phenotype_version_id": 5078,
        "phenotype_name": "Amyloidosis codes",
        "code_attribute_header": [],
        "codes": [
          {
            "code": "111032003",
            "description": "Macular cutaneous amyloidosis",
            "attributes": null
          },
          {
            "code": "111390002",
            "description": "Dominant primary localized cutaneous amyloidosis",
            "attributes": null
          },
          {
            "code": "111391003",
            "description": "Other localized amyloid deposit",
            "attributes": null
          },
          {
            "code": "111392005",
            "description": "Localized amyloid deposit",
            "attributes": null
          },
          {
            "code": "11426004",
            "description": "Gingival amyloidosis",
            "attributes": null
          },
          {
            "code": "1148862002",
            "description": "Deficiency of factor X due to systemic amyloidosis",
            "attributes": null
          },
          {
            "code": "1156789004",
            "description": "Autosomal dominant Alzheimer disease due to mutation of amyloid precursor protein",
            "attributes": null
          },
          {
            "code": "1187126002",
            "description": "Integral membrane protein 2B related amyloidosis",
            "attributes": null
          },
          {
            "code": "1187147003",
            "description": "Familial non-neuropathic amyloidosis of heart",
            "attributes": null
          },
          {
            "code": "1187149000",
            "description": "Localized hereditary amyloidosis of heart",
            "attributes": null
          },
          {
            "code": "1187538003",
            "description": "Secondary systemic amyloid angiopathy of cerebrum",
            "attributes": null
          },
          {
            "code": "1187539006",
            "description": "Non-neuropathic heredofamilial amyloidosis angiopathy of cerebrum",
            "attributes": null
          },
          {
            "code": "1187540008",
            "description": "Secondary systemic amyloidosis of heart",
            "attributes": null
          },
          {
            "code": "1187553006",
            "description": "Disorder of glomerulus due to secondary systemic amyloidosis",
            "attributes": null
          },
          {
            "code": "1187554000",
            "description": "Disorder of glomerulus due to familial amyloid polyneuropathy",
            "attributes": null
          },
          {
            "code": "1187555004",
            "description": "Disorder of glomerulus due to organ-limited amyloidosis",
            "attributes": null
          },
          {
            "code": "1187557007",
            "description": "Disorder of glomerulus due to amyloidosis",
            "attributes": null
          },
          {
            "code": "1192004",
            "description": "Familial amyloid neuropathy, Finnish type",
            "attributes": null
          },
          {
            "code": "1228881003",
            "description": "Leukocyte chemotactic factor-2 amyloidosis",
            "attributes": null
          },
          {
            "code": "1231149005",
            "description": "AH amyloidosis",
            "attributes": null
          },
          {
            "code": "1259488005",
            "description": "Dementia due to cerebral amyloid angiopathy",
            "attributes": null
          },
          {
            "code": "129592008",
            "description": "Amyloid polyneuropathy",
            "attributes": null
          },
          {
            "code": "129593003",
            "description": "Entrapment syndrome due to amyloid",
            "attributes": null
          },
          {
            "code": "15123008",
            "description": "Familial amyloid nephropathy with urticaria AND deafness",
            "attributes": null
          },
          {
            "code": "154769007",
            "description": "Amyloidosis",
            "attributes": null
          },
          {
            "code": "16573007",
            "description": "Senile cardiac amyloidosis",
            "attributes": null
          },
          {
            "code": "1671000",
            "description": "Sago spleen",
            "attributes": null
          },
          {
            "code": "17602002",
            "description": "Amyloidosis",
            "attributes": null
          },
          {
            "code": "190923000",
            "description": "Sporadic primary amyloidosis",
            "attributes": null
          },
          {
            "code": "190925007",
            "description": "Secondary amyloidosis",
            "attributes": null
          },
          {
            "code": "190927004",
            "description": "Primary amyloidosis NEC",
            "attributes": null
          },
          {
            "code": "190928009",
            "description": "Localised non-hereditary amyloidosis",
            "attributes": null
          },
          {
            "code": "190929001",
            "description": "[X]Heredofamilial amyloidosis, unspecified",
            "attributes": null
          },
          {
            "code": "190930006",
            "description": "Other specified amyloidosis",
            "attributes": null
          },
          {
            "code": "190931005",
            "description": "Amyloidosis NOS",
            "attributes": null
          },
          {
            "code": "191113004",
            "description": "[X]Other amyloidosis",
            "attributes": null
          },
          {
            "code": "191121005",
            "description": "[X]Heredofamilial amyloidosis, unspecified",
            "attributes": null
          },
          {
            "code": "192918007",
            "description": "Autonomic neuropathy due to amyloidosis",
            "attributes": null
          },
          {
            "code": "193187004",
            "description": "Polyneuropathy due to amyloidosis",
            "attributes": null
          },
          {
            "code": "193247000",
            "description": "Amyloid myopathy",
            "attributes": null
          },
          {
            "code": "195228000",
            "description": "Cerebral amyloid angiopathy",
            "attributes": null
          },
          {
            "code": "196135008",
            "description": "Pulmonary amyloidosis",
            "attributes": null
          },
          {
            "code": "197604006",
            "description": "Nephrotic syndrome in amyloidosis",
            "attributes": null
          },
          {
            "code": "201337008",
            "description": "Amyloidosis of skin",
            "attributes": null
          },
          {
            "code": "201725009",
            "description": "Arthritis secondary to amyloidosis",
            "attributes": null
          },
          {
            "code": "209962000",
            "description": "Myeloma-associated amyloidosis",
            "attributes": null
          },
          {
            "code": "230359004",
            "description": "Secondary amyloid encephalopathy",
            "attributes": null
          },
          {
            "code": "230724001",
            "description": "Cerebral amyloid angiopathy",
            "attributes": null
          },
          {
            "code": "230725000",
            "description": "Sporadic cerebral amyloid angiopathy",
            "attributes": null
          },
          {
            "code": "230726004",
            "description": "Icelandic type amyloidosis",
            "attributes": null
          },
          {
            "code": "23132008",
            "description": "Amyloid light-chain amyloidosis",
            "attributes": null
          },
          {
            "code": "231928002",
            "description": "Amyloid of cornea",
            "attributes": null
          },
          {
            "code": "232076001",
            "description": "Amyloid of vitreous",
            "attributes": null
          },
          {
            "code": "232459006",
            "description": "Laryngeal amyloidosis",
            "attributes": null
          },
          {
            "code": "234510005",
            "description": "Amyloidosis of spleen",
            "attributes": null
          },
          {
            "code": "237864008",
            "description": "AL amyloidosis",
            "attributes": null
          },
          {
            "code": "237865009",
            "description": "Primary amyloidosis of light chain type",
            "attributes": null
          },
          {
            "code": "237866005",
            "description": "Amyloid polyneuropathy type I",
            "attributes": null
          },
          {
            "code": "237867001",
            "description": "Hereditary cerebrovascular amyloidosis",
            "attributes": null
          },
          {
            "code": "237868006",
            "description": "Familial non-neuropathic amyloidosis",
            "attributes": null
          },
          {
            "code": "237869003",
            "description": "Localized hereditary amyloidosis",
            "attributes": null
          },
          {
            "code": "237870002",
            "description": "Familial lichen amyloidosis",
            "attributes": null
          },
          {
            "code": "237871003",
            "description": "Papular cutaneous amyloid",
            "attributes": null
          },
          {
            "code": "237872005",
            "description": "Poikilodermal cutaneous amyloid",
            "attributes": null
          },
          {
            "code": "237873000",
            "description": "Primary familial amyloid myopathy",
            "attributes": null
          },
          {
            "code": "237874006",
            "description": "Primary sporadic amyloid myopathy",
            "attributes": null
          },
          {
            "code": "237875007",
            "description": "Localized non-hereditary amyloidosis",
            "attributes": null
          },
          {
            "code": "237876008",
            "description": "Arthritis secondary to amyloidosis",
            "attributes": null
          },
          {
            "code": "237877004",
            "description": "Wild type ATTR amyloidosis",
            "attributes": null
          },
          {
            "code": "27097002",
            "description": "Danish type familial amyloid cardiomyopathy",
            "attributes": null
          },
          {
            "code": "274545008",
            "description": "[EDTA] Amyloid associated with renal failure",
            "attributes": null
          },
          {
            "code": "274945004",
            "description": "Amyloid A amyloidosis",
            "attributes": null
          },
          {
            "code": "278899001",
            "description": "Amyloid of urinary bladder",
            "attributes": null
          },
          {
            "code": "281034005",
            "description": "Reactive systemic amyloidosis",
            "attributes": null
          },
          {
            "code": "281882003",
            "description": "AD type amyloidosis",
            "attributes": null
          },
          {
            "code": "282354001",
            "description": "Amyloid of prostate",
            "attributes": null
          },
          {
            "code": "282355000",
            "description": "Amyloid of testes",
            "attributes": null
          },
          {
            "code": "282357008",
            "description": "Amyloid of ureter",
            "attributes": null
          },
          {
            "code": "282834007",
            "description": "Cutaneous amyloidosis",
            "attributes": null
          },
          {
            "code": "302871005",
            "description": "Primary amyloidosis",
            "attributes": null
          },
          {
            "code": "302887008",
            "description": "Neuropathy in secondary amyloidosis",
            "attributes": null
          },
          {
            "code": "311495006",
            "description": "Amyloid disease of the urethra",
            "attributes": null
          },
          {
            "code": "32599008",
            "description": "Hemodialysis-associated amyloidosis",
            "attributes": null
          },
          {
            "code": "35080000",
            "description": "Amyloidosis, type I",
            "attributes": null
          },
          {
            "code": "361199007",
            "description": "Lattice corneal dystrophy",
            "attributes": null
          },
          {
            "code": "367528006",
            "description": "Amyloidosis due to familial Mediterranean fever",
            "attributes": null
          },
          {
            "code": "367601000119103",
            "description": "Hereditary amyloidosis",
            "attributes": null
          },
          {
            "code": "38606009",
            "description": "Bullous cutaneous amyloidosis",
            "attributes": null
          },
          {
            "code": "39502009",
            "description": "Isolated atrial amyloid",
            "attributes": null
          },
          {
            "code": "397883002",
            "description": "Swedish type amyloid polyneuropathy",
            "attributes": null
          },
          {
            "code": "397906009",
            "description": "Portuguese type amyloid polyneuropathy",
            "attributes": null
          },
          {
            "code": "397960001",
            "description": "Andrade type amyloid polyneuropathy",
            "attributes": null
          },
          {
            "code": "398163002",
            "description": "Japanese type amyloid polyneuropathy",
            "attributes": null
          },
          {
            "code": "398229007",
            "description": "Amyloid polyneuropathy type I",
            "attributes": null
          },
          {
            "code": "398247001",
            "description": "Jewish type amyloid polyneuropathy",
            "attributes": null
          },
          {
            "code": "402452001",
            "description": "Primary systemic (AL fibril type) amyloidosis",
            "attributes": null
          },
          {
            "code": "402453006",
            "description": "Amyloid light chain amyloidosis due to multiple myeloma",
            "attributes": null
          },
          {
            "code": "402454000",
            "description": "Primary systemic amyloidosis due to occult plasma cell dyscrasia",
            "attributes": null
          },
          {
            "code": "402455004",
            "description": "Macroglossia due to amyloidosis",
            "attributes": null
          },
          {
            "code": "402456003",
            "description": "Pseudoscleroderma due to amyloid light-chain amyloidosis",
            "attributes": null
          },
          {
            "code": "402457007",
            "description": "Secondary systemic amyloidosis affecting skin (AA fibril type)",
            "attributes": null
          },
          {
            "code": "402458002",
            "description": "Hemodialysis-associated secondary amyloidosis of skin",
            "attributes": null
          },
          {
            "code": "402459005",
            "description": "Heredofamilial systemic amyloidosis affecting skin",
            "attributes": null
          },
          {
            "code": "402460000",
            "description": "Familial amyloid polyneuropathy with cutaneous amyloidosis",
            "attributes": null
          },
          {
            "code": "402461001",
            "description": "Maculopapular amyloidosis",
            "attributes": null
          },
          {
            "code": "402462008",
            "description": "Nodular amyloidosis",
            "attributes": null
          },
          {
            "code": "402463003",
            "description": "Familial localized cutaneous amyloidosis",
            "attributes": null
          },
          {
            "code": "402464009",
            "description": "Secondary localized cutaneous amyloidosis",
            "attributes": null
          },
          {
            "code": "402719006",
            "description": "Systemic amyloidosis affecting skin",
            "attributes": null
          },
          {
            "code": "402720000",
            "description": "Amyloidosis limited to skin",
            "attributes": null
          },
          {
            "code": "40933005",
            "description": "Isolated corneal amyloidosis",
            "attributes": null
          },
          {
            "code": "413011000000101",
            "description": "[X]Heredofamilial amyloidosis, unspecified",
            "attributes": null
          },
          {
            "code": "415061000000103",
            "description": "[X]Heredofamilial amyloidosis, unspecified",
            "attributes": null
          },
          {
            "code": "41590007",
            "description": "Familial amyloid polyneuropathy, Jewish type",
            "attributes": null
          },
          {
            "code": "417939004",
            "description": "Amyloid corneal degeneration",
            "attributes": null
          },
          {
            "code": "418946006",
            "description": "Lattice corneal dystrophy Type III",
            "attributes": null
          },
          {
            "code": "419051009",
            "description": "Polymorphic amyloid degeneration of cornea",
            "attributes": null
          },
          {
            "code": "419087002",
            "description": "Lattice corneal dystrophy Type II",
            "attributes": null
          },
          {
            "code": "419197009",
            "description": "Lattice corneal dystrophy Type I",
            "attributes": null
          },
          {
            "code": "419398009",
            "description": "Meretoja syndrome",
            "attributes": null
          },
          {
            "code": "419900000",
            "description": "Gelatinous droplike corneal dystrophy",
            "attributes": null
          },
          {
            "code": "42295001",
            "description": "Familial amyloid polyneuropathy",
            "attributes": null
          },
          {
            "code": "425879009",
            "description": "Amyloid A nephropathy",
            "attributes": null
          },
          {
            "code": "426598005",
            "description": "Amyloid light-chain nephropathy",
            "attributes": null
          },
          {
            "code": "430081000000106",
            "description": "Amyloid associated with renal failure - European Dialysis and Transplant Association",
            "attributes": null
          },
          {
            "code": "43532007",
            "description": "Hereditary oculoleptomeningeal amyloid angiopathy",
            "attributes": null
          },
          {
            "code": "442012008",
            "description": "Amyloidogenic transthyretin amyloidosis",
            "attributes": null
          },
          {
            "code": "444231000000105",
            "description": "[X]Other amyloidosis",
            "attributes": null
          },
          {
            "code": "4463009",
            "description": "Familial amyloid polyneuropathy, type II",
            "attributes": null
          },
          {
            "code": "45502001",
            "description": "Cerebrovascular amyloidosis",
            "attributes": null
          },
          {
            "code": "45639009",
            "description": "Hereditary cerebral amyloid angiopathy, Icelandic type",
            "attributes": null
          },
          {
            "code": "4645000",
            "description": "Senile brain amyloidosis",
            "attributes": null
          },
          {
            "code": "48713002",
            "description": "Amyloid nephropathy",
            "attributes": null
          },
          {
            "code": "510351000000103",
            "description": "AL amyloidosis",
            "attributes": null
          },
          {
            "code": "5134006",
            "description": "Familial amyloid polyneuropathy, type VI",
            "attributes": null
          },
          {
            "code": "56453003",
            "description": "Hereditary cerebral amyloid angiopathy, Dutch type",
            "attributes": null
          },
          {
            "code": "56871000",
            "description": "Localized amyloidosis",
            "attributes": null
          },
          {
            "code": "57174000",
            "description": "Focal amyloid",
            "attributes": null
          },
          {
            "code": "58629009",
            "description": "Dilated cardiomyopathy due to amyloidosis",
            "attributes": null
          },
          {
            "code": "59017008",
            "description": "Conjunctival amyloidosis",
            "attributes": null
          },
          {
            "code": "598371000000106",
            "description": "Amyloidosis NOS",
            "attributes": null
          },
          {
            "code": "60733007",
            "description": "Hypothyroidism due to amyloidosis",
            "attributes": null
          },
          {
            "code": "61985005",
            "description": "Primary localized cutaneous amyloidosis",
            "attributes": null
          },
          {
            "code": "620101000000101",
            "description": "Primary amyloidosis NEC",
            "attributes": null
          },
          {
            "code": "633241000000101",
            "description": "Other specified amyloidosis",
            "attributes": null
          },
          {
            "code": "66451004",
            "description": "Familial visceral amyloidosis, Ostertag type",
            "attributes": null
          },
          {
            "code": "69078007",
            "description": "Age-related amyloidosis",
            "attributes": null
          },
          {
            "code": "700323004",
            "description": "Amyloid pterygium",
            "attributes": null
          },
          {
            "code": "703220002",
            "description": "Hereditary cystatin C amyloid angiopathy",
            "attributes": null
          },
          {
            "code": "703313007",
            "description": "Cerebral amyloid angiopathy associated with systemic amyloidosis",
            "attributes": null
          },
          {
            "code": "707090004",
            "description": "Spondyloarthropathy due to hemodialysis-associated amyloidosis",
            "attributes": null
          },
          {
            "code": "71041007",
            "description": "Lattice corneal dystrophy",
            "attributes": null
          },
          {
            "code": "715655000",
            "description": "Transthyretin related familial amyloid cardiomyopathy",
            "attributes": null
          },
          {
            "code": "716704007",
            "description": "Primary localized cutaneous nodular amyloidosis",
            "attributes": null
          },
          {
            "code": "718105008",
            "description": "Lichen amyloidosis",
            "attributes": null
          },
          {
            "code": "721661009",
            "description": "Amyloidosis of small intestine",
            "attributes": null
          },
          {
            "code": "722292000",
            "description": "Autosomal dominant beta2-microglobulinic amyloidosis",
            "attributes": null
          },
          {
            "code": "722948009",
            "description": "Glomerular disorder due to non-neuropathic heredofamilial amyloidosis",
            "attributes": null
          },
          {
            "code": "724357007",
            "description": "Hereditary cerebral hemorrhage with amyloidosis",
            "attributes": null
          },
          {
            "code": "733422008",
            "description": "Prion protein systemic amyloidosis",
            "attributes": null
          },
          {
            "code": "733729003",
            "description": "Primary localized cutaneous amyloidosis",
            "attributes": null
          },
          {
            "code": "764849002",
            "description": "Amyloidosis cutis dyschromia",
            "attributes": null
          },
          {
            "code": "783160006",
            "description": "Hereditary gelsolin amyloidosis",
            "attributes": null
          },
          {
            "code": "783161005",
            "description": "Familial dementia British type",
            "attributes": null
          },
          {
            "code": "783258000",
            "description": "Familial dementia Danish type",
            "attributes": null
          },
          {
            "code": "790731321000119100",
            "description": "Lattice dystrophy of substantia propria of cornea of bilateral eyes",
            "attributes": null
          },
          {
            "code": "79754008",
            "description": "Restrictive cardiomyopathy secondary to amyloidosis",
            "attributes": null
          },
          {
            "code": "8231007",
            "description": "Ocular amyloid deposit",
            "attributes": null
          },
          {
            "code": "84137001",
            "description": "AA amyloidosis",
            "attributes": null
          },
          {
            "code": "841951000000103",
            "description": "Senile cardiac amyloidosis",
            "attributes": null
          },
          {
            "code": "847041000000109",
            "description": "Amyloid cardiomyopathy",
            "attributes": null
          },
          {
            "code": "847051000000107",
            "description": "Amyloid cardiomyopathy",
            "attributes": null
          },
          {
            "code": "847141000000105",
            "description": "Amyloidosis of stomach",
            "attributes": null
          },
          {
            "code": "847151000000108",
            "description": "Amyloid of stomach",
            "attributes": null
          },
          {
            "code": "854071000000105",
            "description": "Amyloidosis of intestine",
            "attributes": null
          },
          {
            "code": "854081000000107",
            "description": "Amyloidosis of intestine",
            "attributes": null
          },
          {
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