myotonia congenita Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_2106)
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Genes

2 genes associated with the disease myotonia congenita in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
CLCN1 chloride channel, voltage-sensitive 1
SCN4A sodium channel, voltage gated, type IV alpha subunit