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- 3-hydroxy-3-methylglutaryl-CoA_lyase_deficiency abstract "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.".
- 3-hydroxy-3-methylglutaryl-CoA_lyase_deficiency diseasesdb "29826".
- 3-hydroxy-3-methylglutaryl-CoA_lyase_deficiency meshId "C538324".
- 3-hydroxy-3-methylglutaryl-CoA_lyase_deficiency omim "246450".
- 3-hydroxy-3-methylglutaryl-CoA_lyase_deficiency thumbnail HMG_coenzyme_A.svg?width=300.
- 3-hydroxy-3-methylglutaryl-CoA_lyase_deficiency wikiPageExternalLink ghr.nlm.nih.gov.
- 3-hydroxy-3-methylglutaryl-CoA_lyase_deficiency wikiPageExternalLink condition=3hydroxy3methylglutarylcoenzymealyasedeficiency;jsessionid=3329E3ED085B1A6E5BE651FC9159D676.
- 3-hydroxy-3-methylglutaryl-CoA_lyase_deficiency wikiPageExternalLink HMGCoA.html.
- 3-hydroxy-3-methylglutaryl-CoA_lyase_deficiency wikiPageExternalLink www.oaanews.org.
- 3-hydroxy-3-methylglutaryl-CoA_lyase_deficiency wikiPageID "1972009".
- 3-hydroxy-3-methylglutaryl-CoA_lyase_deficiency wikiPageRevisionID "538061532".
- 3-hydroxy-3-methylglutaryl-CoA_lyase_deficiency caption HMG-CoA.
- 3-hydroxy-3-methylglutaryl-CoA_lyase_deficiency diseasesdb "29826".
- 3-hydroxy-3-methylglutaryl-CoA_lyase_deficiency hasPhotoCollection 3-hydroxy-3-methylglutaryl-CoA_lyase_deficiency.
- 3-hydroxy-3-methylglutaryl-CoA_lyase_deficiency meshid "538324.0".
- 3-hydroxy-3-methylglutaryl-CoA_lyase_deficiency name "3".
- 3-hydroxy-3-methylglutaryl-CoA_lyase_deficiency omim "246450".
- 3-hydroxy-3-methylglutaryl-CoA_lyase_deficiency wordnet_type synset-disease-noun-1.
- 3-hydroxy-3-methylglutaryl-CoA_lyase_deficiency subject Category:Amino_acid_metabolism_disorders.
- 3-hydroxy-3-methylglutaryl-CoA_lyase_deficiency subject Category:Cholesterol_and_steroid_metabolism_disorders.
- 3-hydroxy-3-methylglutaryl-CoA_lyase_deficiency type Disease.
- 3-hydroxy-3-methylglutaryl-CoA_lyase_deficiency type AilmentCondition.
- 3-hydroxy-3-methylglutaryl-CoA_lyase_deficiency type Situation.
- 3-hydroxy-3-methylglutaryl-CoA_lyase_deficiency comment "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.".
- 3-hydroxy-3-methylglutaryl-CoA_lyase_deficiency label "3-hydroxy-3-methylglutaryl-CoA lyase deficiency".
- 3-hydroxy-3-methylglutaryl-CoA_lyase_deficiency sameAs m.06b076.
- 3-hydroxy-3-methylglutaryl-CoA_lyase_deficiency sameAs Q4634217.
- 3-hydroxy-3-methylglutaryl-CoA_lyase_deficiency sameAs Q4634217.
- 3-hydroxy-3-methylglutaryl-CoA_lyase_deficiency sameAs 2621.
- 3-hydroxy-3-methylglutaryl-CoA_lyase_deficiency wasDerivedFrom 3-hydroxy-3-methylglutaryl-CoA_lyase_deficiency?oldid=538061532.
- 3-hydroxy-3-methylglutaryl-CoA_lyase_deficiency depiction HMG_coenzyme_A.svg.
- 3-hydroxy-3-methylglutaryl-CoA_lyase_deficiency isPrimaryTopicOf 3-hydroxy-3-methylglutaryl-CoA_lyase_deficiency.
- 3-hydroxy-3-methylglutaryl-CoA_lyase_deficiency name "3-hydroxy-3-methylglutaryl-CoA lyase deficiency".