{
"@context": "http://id.who.int/icd/contexts/contextForICD10Entity.json",
"@id": "http://id.who.int/icd/release/10/2016/D58.2",
"parent": [
"http://id.who.int/icd/release/10/2016/D58"
],
"browserUrl": "http://apps.who.int/classifications/icd10/browse/2016/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"
}