BabelNet

bn:01240327n

Noun Concept

Categories: Amino acid metabolism disorders, Cholesterol and steroid metabolism disorders, Rare diseases

3-hydroxy-3-methylglutaryl-CoA lyase deficiency 3-HYDROXY-3-METHYLGLUTARYL-CoA LYASE DEFICIENCY; HMGCLD 3-hydroxy 3-methyl glutaryl-coa lyase deficiency Hl Deficiency HMG-CoA lyase deficiency

3-Hydroxy-3-methylglutaryl-CoA lyase deficiency is an uncommon inherited disorder in which the body cannot properly process the amino acid leucine. Wikipedia

Definitions

Relations

Sources

3-Hydroxy-3-methylglutaryl-CoA lyase deficiency is an uncommon inherited disorder in which the body cannot properly process the amino acid leucine. Wikipedia

medical condition Wikidata

IS A

disease

congenital disorders of amino acid metabolism

Wikipedia

3-hydroxy-3-methylglutaryl-CoA lyase deficiency

Wikidata

3-hydroxy-3-methylglutaryl-CoA lyase deficiency

Wikipedia Redirections

3-hydroxy-3-methylglutaryl-CoA lyase deficiency, 3-hydroxy 3-methyl glutaryl-coa lyase deficiency, HMG-CoA lyase deficiency, HMG CoA lyase deficiency, HMG lyase deficiency, Hydroxymethylglutaric aciduria, Hydroxymethylglutaricaciduria, Hydroxymethylglutaryl-CoA lyase deficiency, Hydroxymethylglutaryl lyase deficiency

Wikidata Alias

3-HYDROXY-3-METHYLGLUTARYL-CoA LYASE DEFICIENCY, 3-HYDROXY-3-METHYLGLUTARYL-CoA LYASE DEFICIENCY; HMGCLD, Hl Deficiency, HMG-CoA lyase deficiency, Hmgcl Deficiency, HMGCLD, Hydroxymethylglutaric aciduria