{
    "@context": "http://id.who.int/icd/contexts/contextForICD10Entity.json",
    "@id": "http://id.who.int/icd/release/10/2010/D72.0",
    "parent": [
        "http://id.who.int/icd/release/10/2010/D72"
    ],
    "browserUrl": "http://apps.who.int/classifications/icd10/browse/2010/en#/D72.0",
    "code": "D72.0",
    "title": {
        "@language": "en",
        "@value": "Genetic anomalies of leukocytes"
    },
    "inclusion": [
        {
            "label": {
                "@language": "en",
                "@value": "Anomaly (granulation)(granulocyte) or syndrome: Alder"
            }
        },
        {
            "label": {
                "@language": "en",
                "@value": "Anomaly (granulation)(granulocyte) or syndrome: May-Hegglin"
            }
        },
        {
            "label": {
                "@language": "en",
                "@value": "Anomaly (granulation)(granulocyte) or syndrome: Pelger-Hu\u00ebt"
            }
        },
        {
            "label": {
                "@language": "en",
                "@value": "Hereditary: leukocytic: hypersegmentation"
            }
        },
        {
            "label": {
                "@language": "en",
                "@value": "Hereditary: leukocytic: hyposegmentation"
            }
        },
        {
            "label": {
                "@language": "en",
                "@value": "Hereditary: leukomelanopathy"
            }
        }
    ],
    "exclusion": [
        {
            "label": {
                "@language": "en",
                "@value": "Chediak(-Steinbrinck)-Higashi syndrome"
            }
        }
    ],
    "classKind": "category"
}