handgrip myotonia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Difficulty releasing one's grip associated with prolonged first handgrip relaxation times. (Human Phenotype Ontology, HP_0012899)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0012899
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Genes

2 genes associated with the handgrip myotonia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

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