{
    "@context": "http://id.who.int/icd/contexts/contextForICD10Entity.json",
    "@id": "http://id.who.int/icd/release/10/2019/D68.0",
    "parent": [
        "http://id.who.int/icd/release/10/2019/D68"
    ],
    "browserUrl": "http://apps.who.int/classifications/icd10/browse/2019/en#/D68.0",
    "code": "D68.0",
    "title": {
        "@language": "en",
        "@value": "Von Willebrand disease"
    },
    "inclusion": [
        {
            "label": {
                "@language": "en",
                "@value": "Angiohaemophilia"
            }
        },
        {
            "label": {
                "@language": "en",
                "@value": "Factor VIII deficiency with vascular defect"
            }
        },
        {
            "label": {
                "@language": "en",
                "@value": "Vascular haemophilia"
            }
        }
    ],
    "exclusion": [
        {
            "label": {
                "@language": "en",
                "@value": "capillary fragility (hereditary)"
            }
        },
        {
            "label": {
                "@language": "en",
                "@value": "factor VIII deficiency: NOS"
            }
        },
        {
            "label": {
                "@language": "en",
                "@value": "factor VIII deficiency: with functional defect"
            }
        }
    ],
    "classKind": "category"
}