Drug metabolism, poor, cyp2c19-related

Preferred Label : Drug metabolism, poor, cyp2c19-related;

Type : Phenotype, molecular basis known;

Included titles and symbols : Mephenytoin, poor metabolism of; Omeprazole, poor metabolism of; Proguanil, poor metabolism of; Clopidogrel, poor metabolism of;

Inheritance : Autosomal recessive;

Molecular basis : Caused by mutation in the cytochrome P450, subfamily IIC (mephenytoin 4'-hydroxylase) gene (CYP2C, 124020.0001);

Prefixed ID : #609535;

Details

Origin ID

609535;

UMLS CUI

C1836023;

Automatic exact mappings (from CISMeF team)
- Prediction of resistance to clopidogrel [ORDO Disease]
- drug metabolism, poor, CYP2C19-Related [MeSH concept]
- drug metabolism, poor, CYP2C19-Related [MeSH Supplementary Concept]
- proguanil, poor metabolism of [MeSH concept]
- proguanil, poor metabolism of [MeSH Supplementary Concept]
Genes related to phenotype
- Cytochrome p450, subfamily iic, polypeptide 19 [OMIM gene]
ORDO concept(s)
- Prediction of resistance to clopidogrel [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- drug metabolism, poor, CYP2C19-Related [MeSH Supplementary Concept]
- drug metabolism, poor, CYP2C19-Related [MeSH concept]

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