Myotonia Congenita Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_2106)
External Link
Similar Terms
Downloads & Tools


2 genes/proteins associated with the disease Myotonia Congenita from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
CLCN1 chloride channel, voltage-sensitive 1 2.88009
SCN4A sodium channel, voltage gated, type IV alpha subunit 2.88009