Myotonia congenita Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_2106)
External Link http://www.ncbi.nlm.nih.gov/medgen/?term=C0027127
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Genes

1 genes associated with the Myotonia congenita phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
CLCN1 chloride channel, voltage-sensitive 1