Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 10 of 224 for Metabolism
  1. Surfactant dysfunction 
    ... lung disease due to surfactant deficiency Pulmonary surfactant metabolism dysfunction Surfactant metabolism deficiency Genetic Testing Registry: Surfactant ...
    https://medlineplus.gov/genetics/condition/surfactant-dysfunction - Genetics
  2. Clopidogrel resistance 
    ... treated with the drug. CYP2C19-related poor drug metabolism Poor metabolism of clopidogrel Resistance to clopidogrel Genetic Testing Registry: ... Organization for Rare Disorders (NORD) ClinicalTrials.gov DRUG METABOLISM, POOR, CYP2C19-RELATED PubMed Hirota T, Eguchi S, ...
    https://medlineplus.gov/genetics/condition/clopidogrel-resistance - Genetics
  3. MEGDEL syndrome 
    ... J, Morava E, Wevers RA. Inborn errors of metabolism with 3-methylglutaconic aciduria as discriminative feature: proper ...
    https://medlineplus.gov/genetics/condition/megdel-syndrome - Genetics
  4. 3-methylglutaconyl-CoA hydratase deficiency 
    ... J, Morava E, Wevers RA. Inborn errors of metabolism with 3-methylglutaconic aciduria as discriminative feature: proper ...
    https://medlineplus.gov/...methylglutaconyl-coa-hydratase-deficiency - Genetics
  5. Costeff syndrome 
    ... J, Morava E, Wevers RA. Inborn errors of metabolism with 3-methylglutaconic aciduria as discriminative feature: proper ...
    https://medlineplus.gov/genetics/condition/costeff-syndrome - Genetics
  6. Dilated cardiomyopathy with ataxia syndrome 
    ... J, Morava E, Wevers RA. Inborn errors of metabolism with 3-methylglutaconic aciduria as discriminative feature: proper ...
    https://medlineplus.gov/...lated-cardiomyopathy-with-ataxia-syndrome - Genetics
  7. Barth syndrome 
    ... J, Morava E, Wevers RA. Inborn errors of metabolism with 3-methylglutaconic aciduria as discriminative feature: proper ...
    https://medlineplus.gov/genetics/condition/barth-syndrome - Genetics
  8. Methylmalonic acidemia with homocystinuria 
    ... Ronin result in an inborn error of cobalamin metabolism and ribosomopathy. Nat Commun. 2022 Jan 10;13( ... cause a new inborn error of vitamin B12 metabolism. Nat Genet. 2012 Oct;44(10):1152-5. ...
    https://medlineplus.gov/...ethylmalonic-acidemia-with-homocystinuria - Genetics
  9. MMADHC gene 
    ... cblD type MMAD_HUMAN Tests of MMADHC PubMed METABOLISM OF COBALAMIN ASSOCIATED D; MMADHC NCBI Gene ClinVar ... identification for the cblD defect of vitamin B12 metabolism. N Engl J Med. 2008 Apr 3;358( ...
    https://medlineplus.gov/genetics/gene/mmadhc - Genetics
  10. Warfarin resistance 
    ... is unknown. Many genes are involved in the metabolism of warfarin and in determining the drug's ... for 20 percent of the variation in warfarin metabolism due to genetic factors. Polymorphisms in other genes, ...
    https://medlineplus.gov/genetics/condition/warfarin-resistance - Genetics
previous · 1 · 2 · 3 · 4 · 5 · 6 · 7 · 8 · 9 · 10 · next