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Disease Peroxisome Biogenesis Disorder, Complementation Group 13

Name Peroxisome Biogenesis Disorder, Complementation Group 13
Categories Genetic disease (inborn) | Metabolic disease
MeSH® ID C566625

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 Peroxisomal Disorders Has associated chemicals Has associated genes Peroxisome Biogenesis Disorder, Complementation Group 13
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 Peroxisomal Disorders Has associated chemicals Has associated genes Peroxisome Biogenesis Disorder, Complementation Group 13

Top ↑ Descendants

None.