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Disease Purine Nucleoside Phosphorylase Deficiency

Name Purine Nucleoside Phosphorylase Deficiency
Synonyms Nucleoside Phosphorylase Deficiency | PNP Deficiency
Categories Genetic disease (inborn) | Metabolic disease
MeSH® ID C562587
OMIM® ID 613179
External Links

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 Purine Nucleoside Phosphorylase 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 Purine-Pyrimidine Metabolism, Inborn Errors Has associated chemicals Has associated genes Purine Nucleoside Phosphorylase Deficiency Has associated chemicals Has associated genes

Top ↑ Descendants

None.