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Disease Myasthenic syndrome, congenital, type Id

Name Myasthenic syndrome, congenital, type Id
Synonyms CMS1D, FORMERLY | CMS4C | CMS Id, FORMERLY | FIM1, FORMERLY | MYASTHENIA, FAMILIAL INFANTILE, 1, FORMERLY | MYASTHENIC SYNDROME, CONGENITAL, 4C, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY | Myasthenic Syndrome, Congenital, Associated With Acetylcholine Receptor Deficiency | Myasthenic Syndrome, Congenital, Postsynaptic, Associated With Acetylcholine Receptor Deficiency | MYASTHENIC SYNDROME, CONGENITAL, TYPE Id
Categories Genetic disease (inborn) | Nervous system disease
MeSH® ID C536090
OMIM® ID 608931

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, type Id 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, type Id Has associated chemicals Has associated genes

Top ↑ Descendants

None.