Skip navigation

Disease Molybdenum Cofactor Deficiency, Complementation Group A

Name Molybdenum Cofactor Deficiency, Complementation Group A
Categories Genetic disease (inborn) | Metabolic disease
MeSH® ID C565372

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 Metal Metabolism, Inborn Errors Has associated chemicals Has associated genes Molybdenum Cofactor Deficiency, Complementation Group A
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 Metal Metabolism, Inborn Errors Has associated chemicals Has associated genes Molybdenum Cofactor Deficiency, Complementation Group A

Top ↑ Descendants

None.