Paradoxical Myotonia Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A type of myotonia that worsens with repeated muscle contractions. (Human Phenotype Ontology, HP_0011809)
External Link https://www.disgenet.org/browser/0/1/0/C4023179
Similar Terms
Downloads & Tools

Genes

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

Symbol Name
SCN4A sodium channel, voltage gated, type IV alpha subunit