drug metabolism, poor, CYP2C19-Related

Preferred Label : drug metabolism, poor, CYP2C19-Related;

MeSH note : mutation in CYP2C19;

Origin ID

C563703;

UMLS CUI

C1836023;

Automatic exact mappings (from CISMeF team)
- Drug metabolism, poor, cyp2c19-related [OMIM Phenotype]
MeSH term(s) associated for indexing
- metabolism, inborn errors [MeSH Descriptor]
Record concept(s)
- drug metabolism, poor, CYP2C19-Related [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Drug metabolism, poor, cyp2c19-related [OMIM Phenotype]