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Disease Peroxisome Biogenesis Disorder, Complementation Group 3

Name Peroxisome Biogenesis Disorder, Complementation Group 3
Categories Genetic disease (inborn) | Metabolic disease
MeSH® ID C566633

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 3
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 3

Top ↑ Descendants

None.