mild hereditary spherocytosis due to combined deficiency of spectrin and ankyrin

Preferred Label : mild hereditary spherocytosis due to combined deficiency of spectrin and ankyrin;

Origin ID

DC-15132;

UMLS CUI

C0272036;

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