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bn:03434730n
Noun Concept
Categories: Amino acid metabolism disorders, Autosomal recessive 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
Definitions
Relations
Sources
EN
Isobutyryl-coenzyme A dehydrogenase deficiency is a rare metabolic disorder in which the body is unable to process certain amino acids properly. Wikipedia
IS A
disease
rare disease
congenital disorders of amino acid metabolism
dilated cardiomyopathy
GENETIC ASSOCIATION
ACAD8
Wikipedia
EN
isobutyryl-coenzyme A dehydrogenase deficiency
Wikidata
EN
Isobutyryl-coenzyme A dehydrogenase deficiency
Wikipedia Redirections
EN
IBD deficiency, isobutyryl-CoA dehydrogenase deficiency
Wikidata Alias
EN
Acad8 Deficiency, Acyl-Coa Dehydrogenase Family, Member 8, Deficiency of, Acyl-CoaA dehydrogenase family, member 8, deficiency of, Ibd Deficiency, Isobutyric aciduria, Isobutyryl-CoA dehydrogenase deficiency

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