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 Date: 2012-08-28 15:52:15Medical genetics Hyperammonemia Glutaric aciduria type 1 Isovaleric acidemia Medium-chain acyl-coenzyme A dehydrogenase deficiency Methylmalonic acidemia Propionic acidemia Fatty-acid metabolism disorder Carnitine-acylcarnitine translocase deficiency Health Rare diseases Genetic genealogy |
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Microsoft Word[removed]Condition list.doc | Int. J. BiosciInternational Journal of Biosciences (IJB) ISSN: PrintOnline) Vol. 1, No. 6, p, 2011DocID: 17AqU - View Document |
| Medium chain acyl-CoA Dehydrogenase Deficiency (MCADD)DocID: HZG0 - View Document |
| Carnitine/Acylcarnitine Translocase Deficiency (CACT) A fatty acid oxidation disorder What is it? Carnitine/Acylcarnitine Translocase Deficiency (also known as CACT) is an inherited fatty acid oxidation disorder. PatientDocID: HuOH - View Document |
| Microsoft Word - mso31.docDocID: HkpM - View Document |
| Microsoft Word - FAOD.docDocID: HahR - View Document |