myotonia Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An involuntary and painless delay in the relaxation of skeletal muscle following contraction or electrical stimulation. (Human Phenotype Ontology, HP_0002486)
Similar Terms
Downloads & Tools

Genes

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

Symbol Name
CLCN1 chloride channel, voltage-sensitive 1