spherocytosis, type 4

Preferred Label : spherocytosis, type 4;

MeSH note : aka SPH4 or HS4; mutations in SLC4A1;

MeSH synonym : spherocytosis, hereditary, 4;

Origin ID

C567208;

UMLS CUI

C2675212;

Automatic exact mappings (from CISMeF team)
- hereditary spherocytosis type 4 [DO Concept]
Currated CISMeF NLP mapping
- Spherocytosis, type 4 [OMIM Phenotype]
MeSH term(s) associated for indexing
- spherocytosis, hereditary [MeSH Descriptor]
Record concept(s)
- spherocytosis, type 4 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Spherocytosis, type 4 [OMIM Phenotype]