drug metabolism, poor, CYP2D6-Related

Preferred Label : drug metabolism, poor, CYP2D6-Related;

MeSH note : mutation in CYP2D6;

Origin ID

C563835;

UMLS CUI

C1837154;

Currated CISMeF NLP mapping
- Drug metabolism, poor, cyp2d6-related [OMIM Phenotype]
MeSH term(s) associated for indexing
- cytochrome p-450 cyp2d6 [MeSH Descriptor]
- metabolism, inborn errors [MeSH Descriptor]
Record concept(s)
- drug metabolism, poor, CYP2D6-Related [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Drug metabolism, poor, cyp2d6-related [OMIM Phenotype]