Literature summary for 4.1.3.4 extracted from

Reimao, S.; Morgado, C.; Almeida, I.T.; Silva, M.; Real, H.C.; Campos, J.
3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiency: Initial presentation in a young adult (2009), J. Inherit. Metab. Dis., 32, S49-52.

Application

Application	Comment	Organism
medicine	3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiency is a rare inborn error affecting leucine catabolism and ketogenesis, usually presenting in the neonatal period	Homo sapiens

Organism	UniProt	Comment	Textmining
Homo sapiens	-	-	-

Synonyms	Comment	Organism
3-hydroxy-3-methylglutaryl-coenzyme A lyase	-	Homo sapiens
HMG-CoA lyase	-	Homo sapiens

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Release 2023.1 (January 2023)