Other hereditary haemolytic anaemias

Preferred Label : Other hereditary haemolytic anaemias;

Origin ID

D58;

Automatic exact mappings (from CISMeF team)
- Hereditary haemolytic anaemia [MedDRA Preferred Term]
- Hereditary haemolytic anaemia [ICPC-3 diagnosis]
- Hereditary haemolytic anaemia NOS [MedDRA LLT]
- Hereditary haemolytic anaemias [MedDRA LLT]
- Hereditary hemolytic anemia [MedDRA LLT]
- Hereditary hemolytic anemias [MedDRA LLT]
- anemia, hemolytic, congenital [MeSH concept]
- anemia, hemolytic, congenital [MeSH Descriptor]
- hereditary haemolytic anaemia [ICPC-2 Rubric]
- hereditary hemolytic anemia, nos [SNOMED Notion]
Exclusion(s) CIM-10
- Haemorrhagic and haematological disorders of fetus and newborn [ICD-10 Block (who)]
Metaterm(s)
- hematology [CISMeF Metaterm]
- pediatrics [CISMeF Metaterm]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
Validated automatic mappings to BTNT
- anemia, hemolytic, congenital [MeSH Descriptor]