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Disease Combined Oxidative Phosphorylation Deficiency 5

Name Combined Oxidative Phosphorylation Deficiency 5
Synonym COXPD5
Categories Genetic disease (inborn) | Metabolic disease
MeSH® ID C567126
OMIM® ID 611719

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 Combined Oxidative Phosphorylation Deficiency 5 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 Combined Oxidative Phosphorylation Deficiency 5 Has associated chemicals Has associated genes
3. 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 Mitochondrial Diseases Has associated chemicals Has associated genes Combined Oxidative Phosphorylation Deficiency 5 Has associated chemicals Has associated genes

Top ↑ Descendants

None.