{
    "@context": "http://id.who.int/icd/contexts/contextForICD10Entity.json",
    "@id": "http://id.who.int/icd/release/10/2010/F02.2",
    "parent": [
        "http://id.who.int/icd/release/10/2010/F02"
    ],
    "browserUrl": "http://apps.who.int/classifications/icd10/browse/2010/en#/F02.2",
    "code": "F02.2",
    "title": {
        "@language": "en",
        "@value": "Dementia in Huntington disease"
    },
    "definition": {
        "@language": "en",
        "@value": "A dementia occurring as part of a widespread degeneration of the brain. The disorder is transmitted by a single autosomal dominant gene. Symptoms typically emerge in the third and fourth decade. Progression is slow, leading to death usually within 10 to 15 years."
    },
    "inclusion": [
        {
            "label": {
                "@language": "en",
                "@value": "Dementia in Huntington chorea"
            }
        }
    ],
    "usage": "aster",
    "classKind": "category"
}