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bn:01835305n
Noun Concept
Categories: Autosomal recessive disorders, Amino acid metabolism disorders, Rare diseases
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
Definitions
Relations
Sources
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
IS A
disease
rare disease
organic acidemia
neurometabolic disease
autosomal recessive disease
GENETIC ASSOCIATION
glutaryl-CoA dehydrogenase
HEALTH SPECIALTY
endocrinology
Wikipedia
EN
glutaric aciduria type 1
Wikidata
EN
glutaric aciduria type 1
Wikipedia Redirections
EN
Glutari aciduria, glutaric acidemia, Glutaric acidemia I, glutaric acidemia type 1, glutaric acidemia type I, glutaric aciduria, Glutaric aciduria I, Glutaryl-CoA dehydrogenase deficiency
Wikidata Alias
EN
GA1, Ga 1, GCDHD, glutaric academia type 1, glutaric acidemia I, GLUTARIC ACIDEMIA I, glutaric acidemia type 1, Glutaric Aciduria, Type 1, glutaric aciduria 1, Glutaric Aciduria 1, Glutaric aciduria type 1, glutaric aciduria type I, glutaryl-CoA dehydrogenase deficiency, glutaryl-coA dehydrogenase deficiency, glutaryl-coenzyme A dehydrogenase deficiency, Glutaryl-coenzyme A dehydrogenase deficiency

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