{ "@context": "http://id.who.int/icd/contexts/contextForICD10Entity.json", "@id": "http://id.who.int/icd/release/10/2010/D58.2", "parent": [ "http://id.who.int/icd/release/10/2010/D58" ], "browserUrl": "http://apps.who.int/classifications/icd10/browse/2010/en#/D58.2", "code": "D58.2", "title": { "@language": "en", "@value": "Other haemoglobinopathies" }, "inclusion": [ { "label": { "@language": "en", "@value": "Abnormal haemoglobin NOS" } }, { "label": { "@language": "en", "@value": "Congenital Heinz body anaemia" } }, { "label": { "@language": "en", "@value": "Disease: Hb-C" } }, { "label": { "@language": "en", "@value": "Disease: Hb-D" } }, { "label": { "@language": "en", "@value": "Disease: Hb-E" } }, { "label": { "@language": "en", "@value": "Haemoglobinopathy NOS" } }, { "label": { "@language": "en", "@value": "Unstable haemoglobin haemolytic disease" } } ], "exclusion": [ { "label": { "@language": "en", "@value": "familial polycythaemia" } }, { "label": { "@language": "en", "@value": "Hb-M disease" } }, { "label": { "@language": "en", "@value": "hereditary persistence of fetal haemoglobin [HPFH]" } }, { "label": { "@language": "en", "@value": "high-altitude polycythaemia" } }, { "label": { "@language": "en", "@value": "methaemoglobinaemia" } } ], "classKind": "category" }