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Disease 5-oxoprolinase deficiency

Name 5-oxoprolinase deficiency
Synonyms 5-alpha-oxoprolinase deficiency | OPLAHD | Oxoprolinuria due to 5-oxoprolinase deficiency | Oxoprolinuria Due To Oxoprolinase Deficiency
Categories Genetic disease (inborn) | Metabolic disease
MeSH® ID C535322
OMIM® ID 260005

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 5-oxoprolinase 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 5-oxoprolinase deficiency Has associated chemicals Has associated genes

Top ↑ Descendants

None.