bn:01835305n
Noun Concept
Categories: Rare diseases, Autosomal recessive disorders, Amino acid metabolism disorders
EN
glutaric aciduria type 1  glutaric acidemia I  glutaric aciduria 1  glutaryl-CoA dehydrogenase deficiency  glutaryl-coenzyme A dehydrogenase deficiency
EN
Glutaric acidemia type 1 is an inherited disorder in which the body is unable to completely break down the amino acids lysine, hydroxylysine and tryptophan. Wikipedia
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