{
    "@context": "http://id.who.int/icd/contexts/contextForICD10Entity.json",
    "@id": "http://id.who.int/icd/release/10/2008/F02.1",
    "parent": [
        "http://id.who.int/icd/release/10/2008/F02"
    ],
    "browserUrl": "http://apps.who.int/classifications/icd10/browse/2008/en#/F02.1",
    "code": "F02.1",
    "title": {
        "@language": "en",
        "@value": "Dementia in Creutzfeldt-Jakob disease"
    },
    "definition": {
        "@language": "en",
        "@value": "A progressive dementia with extensive neurological signs, due to specific neuropathological changes that are presumed to be caused by a transmissible agent. Onset is usually in middle or later life, but may be at any adult age. The course is subacute, leading to death within one to two years."
    },
    "usage": "aster",
    "classKind": "category"
}