bn:03434730n
Noun Concept
Categories: Autosomal recessive disorders, Amino acid metabolism disorders
EN
isobutyryl-coenzyme A dehydrogenase deficiency  Acad8 Deficiency  Acyl-Coa Dehydrogenase Family, Member 8, Deficiency of  Acyl-CoaA dehydrogenase family, member 8, deficiency of  Ibd Deficiency
EN
Isobutyryl-coenzyme A dehydrogenase deficiency is a rare metabolic disorder in which the body is unable to process certain amino acids properly. Wikipedia
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