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Disease Myasthenic Syndrome due to Mutation in SCN4A

Name Myasthenic Syndrome due to Mutation in SCN4A
Categories Genetic disease (inborn) | Nervous system disease
MeSH® ID C565830

Top ↑ Ancestors

1. 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 Neuromuscular Junction Diseases Has associated chemicals Has associated genes Myasthenic Syndromes, Congenital Has associated chemicals Has associated genes Myasthenic Syndrome due to Mutation in SCN4A
2. 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 Myasthenic Syndromes, Congenital Has associated chemicals Has associated genes Myasthenic Syndrome due to Mutation in SCN4A

Top ↑ Descendants

None.