Sickle-cell disorders

Preferred Label : Sickle-cell disorders;

Origin ID

D57;

Automatic exact mappings (from CISMeF team)
- Hereditary haemolytic anaemia [ICPC-3 diagnosis]
- Sickle cell anemia [LOINC component]
- Sickle cell disorders [MedDRA LLT]
- anemia, sickle cell [MeSH Descriptor]
Exclusion CIM-10
- Beta thalassaemia [ICD-10 Sub-category (who)]
- Hereditary elliptocytosis [ICD-10 Sub-category (who)]
- Hereditary haemolytic anaemia, unspecified [ICD-10 Sub-category (who)]
- Hereditary spherocytosis [ICD-10 Sub-category (who)]
- Other haemoglobinopathies [ICD-10 Sub-category (who)]
- Other specified hereditary haemolytic anaemias [ICD-10 Sub-category (who)]
Exclusion(s) CIM-10
- Haemorrhagic and haematological disorders of fetus and newborn [ICD-10 Block (who)]
HRDO close match(es)
- Sickle cell anemia [ORDO Disease]
Metaterm(s)
- hematology [CISMeF Metaterm]
- pediatrics [CISMeF Metaterm]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]