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Disease Myasthenic syndrome, congenital, postsynaptic slow-channel

Name Myasthenic syndrome, congenital, postsynaptic slow-channel
Synonyms CMS1A | CMS2A, FORMERLY | CMS IIa, FORMERLY | MYASTHENIC SYNDROME, CONGENITAL, 1A, SLOW-CHANNEL | Myasthenic syndrome, congenital, type IIa | MYASTHENIC SYNDROME, CONGENITAL, TYPE IIa, FORMERLY
Categories Genetic disease (inborn) | Nervous system disease
MeSH® ID C536091
OMIM® ID 601462

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, congenital, postsynaptic slow-channel Has associated chemicals Has associated genes
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, congenital, postsynaptic slow-channel Has associated chemicals Has associated genes

Top ↑ Descendants

None.