myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.omim.org/entry/608931
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Genes

4 genes associated with the myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
CHRNB1 cholinergic receptor, nicotinic, beta 1 (muscle)
CHRNE cholinergic receptor, nicotinic, epsilon (muscle)
MUSK muscle, skeletal, receptor tyrosine kinase
RAPSN receptor-associated protein of the synapse