MYASTHENIC SYNDROME, CONGENITAL, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link http://ctdbase.org/detail.go?type=disease&acc=OMIM:608931
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Genes

4 genes/proteins associated with the disease MYASTHENIC SYNDROME, CONGENITAL, ASSOCIATED WITH ACETYLCHOLINE RECEPTOR DEFICIENCY from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
CHRNB1 cholinergic receptor, nicotinic, beta 1 (muscle) 2.88009
RAPSN receptor-associated protein of the synapse 2.88009
MUSK muscle, skeletal, receptor tyrosine kinase 2.88009
CHRNE cholinergic receptor, nicotinic, epsilon (muscle) 2.88009