hereditary spherocytosis due to beta spectrin defect

Preferred Label : hereditary spherocytosis due to beta spectrin defect;

Origin ID

DC-15180;

UMLS CUI

C0272039;

Currated CISMeF NLP mapping
- Hereditary spherocytosis due to beta spectrin defect (disorder) [SNOMED CT concept]
ICD-10 exact mapping(s)
- Hereditary spherocytosis [ICD-10 Sub-category (who)]
Metaterm(s)
- hematology [CISMeF Metaterm]
SNOMED CT concept
- Hereditary spherocytosis due to beta spectrin defect (disorder) [SNOMED CT concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Hereditary spherocytosis due to beta spectrin defect (disorder) [SNOMED CT concept]