neuromuscular disease, congenital, with uniform type 1 fiber Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.omim.org/entry/117000
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Genes

1 genes associated with the neuromuscular disease, congenital, with uniform type 1 fiber phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
RYR1 ryanodine receptor 1 (skeletal)