nonprogressive muscular atrophy Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Muscular atrophy that does not display a progression in severity with time. (Human Phenotype Ontology, HP_0008964)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0008964
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Genes

1 genes associated with the nonprogressive muscular atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
TRPV4 transient receptor potential cation channel, subfamily V, member 4