[
  {
    "phenotype_id": "PH4471",
    "phenotype_version_id": 9762,
    "name": "CCU022_1 Hyperlipidemia",
    "definition": "Phecode 272\\.1: Hyperlipidemia\n",
    "implementation": "",
    "publications": [],
    "validation": "",
    "citation_requirements": "",
    "created": "2026-08-17T03:51:39.255116Z",
    "author": "Liu, H., Mizani, M. A., Zhao, Y., Wood, A., Inouye, M., Price, A. L., Jiang, X., on behalf of the CVD-COVID-UK/COVID-IMPACT Consortium",
    "collections": [
      {
        "name": "BHF Data Science Centre",
        "value": 20
      },
      {
        "name": "Phenotype Library",
        "value": 18
      }
    ],
    "tags": null,
    "organisation": null,
    "world_access": 1,
    "updated": "2026-08-17T22:31:29.849863Z",
    "sex": [
      {
        "name": "Both",
        "value": "3"
      }
    ],
    "type": [
      {
        "name": "Disease or syndrome",
        "value": "2"
      }
    ],
    "trials": [],
    "ontology": null,
    "phenoflowid": "",
    "data_sources": null,
    "endorsements": [],
    "project_name": "",
    "coding_system": [
      {
        "name": "SNOMED  CT codes",
        "value": 9
      },
      {
        "name": "ICD10 codes",
        "value": 4
      }
    ],
    "corresp_author": "",
    "event_date_range": "",
    "concept_information": [
      {
        "concept_id": 11558,
        "concept_version_id": 19043,
        "concept_name": "ICD-10",
        "coding_system": {
          "id": 4,
          "name": "ICD10 codes",
          "description": "ICD10 Codes"
        },
        "phenotype_id": "PH4471",
        "phenotype_version_id": 9762,
        "phenotype_name": "CCU022_1 Hyperlipidemia",
        "code_attribute_header": null,
        "codes": [
          {
            "code": "E780",
            "description": "Pure hypercholesterolaemia",
            "attributes": null
          },
          {
            "code": "E781",
            "description": "Pure hyperglyceridaemia",
            "attributes": null
          },
          {
            "code": "E782",
            "description": "Mixed hyperlipidaemia",
            "attributes": null
          },
          {
            "code": "E783",
            "description": "Hyperchylomicronaemia",
            "attributes": null
          },
          {
            "code": "E784",
            "description": "Other hyperlipidaemia",
            "attributes": null
          },
          {
            "code": "E785",
            "description": "Hyperlipidaemia, unspecified",
            "attributes": null
          }
        ]
      },
      {
        "concept_id": 11559,
        "concept_version_id": 19044,
        "concept_name": "SNOMED",
        "coding_system": {
          "id": 9,
          "name": "SNOMED  CT codes",
          "description": "SNOMED CT codes"
        },
        "phenotype_id": "PH4471",
        "phenotype_version_id": 9762,
        "phenotype_name": "CCU022_1 Hyperlipidemia",
        "code_attribute_header": null,
        "codes": [
          {
            "code": "137931000119102",
            "description": "Hyperlipidemia due to type 2 diabetes mellitus (disorder)",
            "attributes": null
          },
          {
            "code": "137941000119106",
            "description": "Hyperlipidemia due to type 1 diabetes mellitus (disorder)",
            "attributes": null
          },
          {
            "code": "1571000119104",
            "description": "Mixed hyperlipidemia due to type 1 diabetes mellitus (disorder)",
            "attributes": null
          },
          {
            "code": "190773008",
            "description": "Hyperbetalipoproteinemia (disorder)",
            "attributes": null
          },
          {
            "code": "190774002",
            "description": "Hyperlipidemia group A (disorder)",
            "attributes": null
          },
          {
            "code": "238038003",
            "description": "Familial hyperlipoproteinemia (disorder)",
            "attributes": null
          },
          {
            "code": "238040008",
            "description": "Familial combined hyperlipidemia (disorder)",
            "attributes": null
          },
          {
            "code": "238076009",
            "description": "Primary hypercholesterolemia (disorder)",
            "attributes": null
          },
          {
            "code": "238077000",
            "description": "Polygenic hypercholesterolemia (disorder)",
            "attributes": null
          },
          {
            "code": "238078005",
            "description": "Familial hypercholesterolemia - homozygous (disorder)",
            "attributes": null
          },
          {
            "code": "238079002",
            "description": "Familial hypercholesterolemia - heterozygous (disorder)",
            "attributes": null
          },
          {
            "code": "238081000",
            "description": "Familial defective apolipoprotein B-100 (disorder)",
            "attributes": null
          },
          {
            "code": "238083002",
            "description": "Primary hypertriglyceridemia (disorder)",
            "attributes": null
          },
          {
            "code": "238086005",
            "description": "Fredrickson type I hyperlipoproteinemia (disorder)",
            "attributes": null
          },
          {
            "code": "238088006",
            "description": "Primary combined hyperlipidemia (disorder)",
            "attributes": null
          },
          {
            "code": "267432004",
            "description": "Pure hypercholesterolemia (disorder)",
            "attributes": null
          },
          {
            "code": "267434003",
            "description": "Mixed hyperlipidemia (disorder)",
            "attributes": null
          },
          {
            "code": "267435002",
            "description": "Familial hyperchylomicronemia (disorder)",
            "attributes": null
          },
          {
            "code": "275598004",
            "description": "Familial hyperlipoproteinemia type I",
            "attributes": null
          },
          {
            "code": "299465007",
            "description": "Familial multiple lipoprotein-type hyperlipidemia (disorder)",
            "attributes": null
          },
          {
            "code": "33513003",
            "description": "Familial apolipoprotein C-II deficiency (disorder)",
            "attributes": null
          },
          {
            "code": "34349009",
            "description": "Familial type 5 hyperlipoproteinemia (disorder)",
            "attributes": null
          },
          {
            "code": "34528009",
            "description": "Familial hypertriglyceridemia (disorder)",
            "attributes": null
          },
          {
            "code": "397915002",
            "description": "Fredrickson type IIa hyperlipoproteinemia (disorder)",
            "attributes": null
          },
          {
            "code": "398036000",
            "description": "Familial hypercholesterolemia (disorder)",
            "attributes": null
          },
          {
            "code": "398796005",
            "description": "Familial hyperbetalipoproteinemia and hyperprebetalipoproteinemia",
            "attributes": null
          },
          {
            "code": "403829002",
            "description": "Familial hypercholesterolemia due to heterozygous low density lipoprotein receptor mutation (disorder)",
            "attributes": null
          },
          {
            "code": "403830007",
            "description": "Familial hypercholesterolemia due to homozygous low density lipoprotein receptor mutation (disorder)",
            "attributes": null
          },
          {
            "code": "403831006",
            "description": "Familial hypercholesterolemia due to genetic defect of apolipoprotein B (disorder)",
            "attributes": null
          },
          {
            "code": "701000119103",
            "description": "Mixed hyperlipidemia due to type 2 diabetes mellitus (disorder)",
            "attributes": null
          },
          {
            "code": "767133009",
            "description": "Compound familial hypercholesterolemia",
            "attributes": null
          },
          {
            "code": "773726000",
            "description": "Hypercholesterolemia due to cholesterol 7alpha-hydroxylase deficiency",
            "attributes": null
          }
        ]
      }
    ],
    "status": 1,
    "doi": "https://doi.org/10.48533/mhy7-5a82",
    "is_deleted": false,
    "publish_status": 2,
    "owner": "Hongjiao.Liu",
    "template": {
      "id": 2,
      "name": "BHF Data Science Centre Phenotype",
      "description": "BHF Data Science Centre Phenotype definitions that describe a list of clinical codes, algorithms using clinical codes, or set of clinical trials. Visit the BHF Data Science Centre website to learn more: https://bhfdatasciencecentre.org",
      "version_id": 1
    },
    "versions": [
      {
        "version_id": 9762,
        "version_name": "CCU022_1 Hyperlipidemia",
        "version_date": "2026-08-17T22:31:29.862114Z",
        "is_published": true,
        "is_latest": true
      }
    ]
  }
]