anemia, nonspherocytic hemolytic, due to G6pd deficiency

Preferred Label : anemia, nonspherocytic hemolytic, due to G6pd deficiency;

Origin ID

C567533;

UMLS CUI

C2720289;

Automatic exact mappings (from CISMeF team)
- Anemia, nonspherocytic hemolytic, due to g6pd deficiency [OMIM Phenotype]
MeSH term(s) associated for indexing
- genetic diseases, X-linked [MeSH Descriptor]
- glucosephosphate dehydrogenase deficiency [MeSH Descriptor]
Record concept(s)
- anemia, nonspherocytic hemolytic, due to G6pd deficiency [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Anemia, nonspherocytic hemolytic, due to g6pd deficiency [OMIM Phenotype]