severe hereditary spherocytosis due to spectrin deficiency

Preferred Label : severe hereditary spherocytosis due to spectrin deficiency;

Origin ID

DC-15114;

UMLS CUI

C0272034;

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