anemia, nonspherocytic hemolytic, possibly due to defect in porphyrin metabolism

Preferred Label : anemia, nonspherocytic hemolytic, possibly due to defect in porphyrin metabolism;

Origin ID

C565952;

UMLS CUI

C1859785;

Automatic exact mappings (from CISMeF team)
- Anemia, nonspherocytic hemolytic, possibly due to defect in porphyrin metabolism [OMIM Phenotype]
MeSH term(s) associated for indexing
- anemia, hemolytic, congenital nonspherocytic [MeSH Descriptor]
Record concept(s)
- anemia, nonspherocytic hemolytic, possibly due to defect in porphyrin metabolism [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Anemia, nonspherocytic hemolytic, possibly due to defect in porphyrin metabolism [OMIM Phenotype]