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Disease Peroxisome Biogenesis Disorder, Complementation Group 12

Name Peroxisome Biogenesis Disorder, Complementation Group 12
Categories Genetic disease (inborn) | Metabolic disease
MeSH® ID C566405

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 12
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 12

Top ↑ Descendants

None.