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Disease Oculopharyngodistal Myopathy

Name Oculopharyngodistal Myopathy
Categories Genetic disease (inborn) | Musculoskeletal disease | Nervous system disease
MeSH® ID C563508

Top ↑ Ancestors

1. DiseasesMusculoskeletal Diseases Has associated chemicals Has associated genes Has associated exposure references Muscular Diseases Has associated chemicals Has associated genes Muscular Disorders, Atrophic Has associated chemicals Has associated genes Muscular Dystrophies Has associated chemicals Has associated genes Oculopharyngodistal Myopathy
2. DiseasesNervous System Diseases Has associated chemicals Has associated genes Has associated exposure references Neuromuscular Diseases Has associated chemicals Has associated genes Has associated exposure references Muscular Diseases Has associated chemicals Has associated genes Muscular Disorders, Atrophic Has associated chemicals Has associated genes Muscular Dystrophies Has associated chemicals Has associated genes Oculopharyngodistal Myopathy
3. 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 Muscular Dystrophies Has associated chemicals Has associated genes Oculopharyngodistal Myopathy

Top ↑ Descendants

None.