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Results 1 - 10 of 490 for Formation
  1. Surfactant dysfunction 
    ... addition, SP-B plays a role in the formation of lamellar bodies.Mutations in the SFTPB gene ... protein also appears to be involved in the formation of lamellar bodies.ABCA3 gene mutations, which cause ...
    https://medlineplus.gov/genetics/condition/surfactant-dysfunction - Genetics
  2. Clopidogrel resistance 
    ... drug is typically given to prevent blood clot formation in individuals with a history of stroke; heart ... attack or stroke caused by abnormal blood clot formation; those with stents can develop blood clots (thromboses) ...
    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. 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
  10. SOST-related sclerosing bone dysplasia 
    ... disorder of bone development characterized by excessive bone formation (hyperostosis). As a result of hyperostosis, bones throughout ... increases pressure on the brain. The excessive bone formation seen in this condition seems to occur throughout ...
    https://medlineplus.gov/.../sost-related-sclerosing-bone-dysplasia - Genetics
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