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Disease 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency

Name 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency
Synonyms 3-Hydroxy-3-Methylglutaric Aciduria | 3-Hydroxy 3-Methyl Glutaric Aciduria | 3-Hydroxy-3-Methylglutaryl-Coenzyme A Lyase Deficiency | 3-Hydroxyl 3-Methyl Glutaric Aciduria | Deficiency of Hydroxymethylglutaryl-CoA Lyase | HL DEFICIENCY | HMGCLD | HMGCL DEFICIENCY | HMG CoA Lyase Deficiency | HMG-CoA Lyase Deficiency | Hydroxymethylglutaric Aciduria
Categories Genetic disease (inborn) | Metabolic disease
MeSH® ID C538324
OMIM® ID 246450

Top ↑ Ancestors

1. DiseasesCongenital, Hereditary, and Neonatal Diseases and Abnormalities Has associated chemicals Has associated genes Has associated exposure references Genetic Diseases, Inborn Has associated chemicals Has associated genes Has associated exposure references Metabolism, Inborn Errors Has associated chemicals Has associated genes Has associated exposure references Amino Acid Metabolism, Inborn Errors Has associated chemicals Has associated genes Has associated exposure references 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency Has associated chemicals Has associated genes
2. DiseasesNutritional and Metabolic Diseases Has associated chemicals Has associated genes Has associated exposure references Metabolic Diseases Has associated chemicals Has associated genes Has associated exposure references Metabolism, Inborn Errors Has associated chemicals Has associated genes Has associated exposure references Amino Acid Metabolism, Inborn Errors Has associated chemicals Has associated genes Has associated exposure references 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiency Has associated chemicals Has associated genes

Top ↑ Descendants

None.