spherocytosis, type 3

Preferred Label : spherocytosis, type 3;

MeSH note : aka SPH3 or HS3; mutations in SPTA1;

MeSH synonym : spherocytosis, hereditary, 3;

Origin ID

C567489;

UMLS CUI

C2678338;

Automatic exact mappings (from CISMeF team)
- hereditary spherocytosis type 3 [DO Concept]
Currated CISMeF NLP mapping
- Spherocytosis, type 3 [OMIM Phenotype]
MeSH term(s) associated for indexing
- spectrin [MeSH Descriptor]
- spherocytosis, hereditary [MeSH Descriptor]
Record concept(s)
- spherocytosis, type 3 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Spherocytosis, type 3 [OMIM Phenotype]