e/3-hydroxy-3-methylglutaryl-CoA lyase deficiency

Information
has gloss	eng: 3-hydroxy-3-methylglutaryl-CoA lyase deficiency also referred to as HMG-CoA lyase deficiency or Hydroxymethylglutaric aciduria, is an uncommon inherited disorder in which the body cannot properly process the amino acid leucine. Additionally, the disorder prevents the body from making ketones, which are used for energy during fasting.
lexicalization	eng: 3-hydroxy 3-methyl glutaryl-coa lyase deficiency
lexicalization	eng: 3-hydroxy-3-methylglutaryl-CoA lyase deficiency
instance of	(noun) an impairment of health or a condition of abnormal functioning disease