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"3-hydroxy-3-methylglutaryl-coa"
- 3-hydroxy-3-methylglutaryl-CoA lyase deficiency (also known as HMG-CoA lyase deficiency) is an uncommon inherited disorder in which ... not show signs and symptoms of the condition. 3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiency 3-OH 3-CH3 glutaric aciduria ...
- ... Health Condition 3-hydroxy-3-methylglutarate-CoA lyase 3-hydroxy-3-methylglutaryl-Coenzyme A lyase 3-hydroxymethyl-3-methylglutaryl-CoA lyase 3- ... CoA lyase HMGCL_HUMAN Tests of HMGCL PubMed 3-HYDROXY-3-METHYLGLUTARYL-CoA LYASE; HMGCL NCBI Gene ClinVar Al-Sayed M, ...
- Amino Acid Metabolism Disorders (National Library of Medicine)Metabolism is the process your body uses to make energy from the food you eat. Food is made up of proteins, carbohydrates, and fats. Your digestive system breaks ...
- Genetic Brain Disorders (National Library of Medicine)A genetic brain disorder is caused by a variation or a mutation in a gene. A variation is a different form of a gene. A mutation is a change in a gene. ...
- Newborn Screening (National Library of Medicine)Your newborn infant has screening tests before leaving the hospital. There may be different tests depending on the state where you live. They include: Tests ...
- ... called 3-methylglutaconyl-CoA into another molecule called 3-hydroxy-3-methylglutaryl-CoA.3-methylglutaconyl-CoA hydratase also has the ability ...
