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Methylmalonyl-CoA mutase deficiency

Methylmalonyl-CoA mutase deficiency
Classification & external resources
OMIM 251000
DiseasesDB 29509

Methylmalonyl-CoA mutase deficiency ("MUT") is an inborn error of organic acid metabolism. It is one of the 29 conditions currently recommended for newborn screening by the American College of Medical Genetics.

It is a form of Methylmalonic acidemia.

See also

  • Methylmalonyl-CoA mutase
This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "Methylmalonyl-CoA_mutase_deficiency". A list of authors is available in Wikipedia.
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