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Disease Phosphoribosylpyrophosphate synthetase deficiency

Name Phosphoribosylpyrophosphate synthetase deficiency
Categories Genetic disease (inborn) | Metabolic disease
MeSH® ID C537897

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 Purine-Pyrimidine Metabolism, Inborn Errors Has associated chemicals Has associated genes Phosphoribosylpyrophosphate synthetase deficiency
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 Purine-Pyrimidine Metabolism, Inborn Errors Has associated chemicals Has associated genes Phosphoribosylpyrophosphate synthetase deficiency

Top ↑ Descendants

None.