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Disease Hyperprolinemia type 2

Name Hyperprolinemia type 2
Synonyms 1 alpha pyrroline-5-carboxylate dehydrogenase deficiency | 1-Pyrroline-5-Carboxylate Dehydrogenase Deficiency | HPII | Hyperprolinemia, Type II | HYRPRO2 | Pyrroline-5-Carboxylate Dehydrogenase Deficiency | Pyrroline Carboxylate Dehydrogenase Deficiency | Type 2 hyperprolinemia
Categories Genetic disease (inborn) | Metabolic disease
MeSH® ID C538385
OMIM® ID 239510

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 Hyperprolinemia type 2 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 Hyperprolinemia type 2 Has associated chemicals Has associated genes

Top ↑ Descendants

None.