|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||Muscular atrophy that does not display a progression in severity with time. (Human Phenotype Ontology, HP_0008964)|
|Downloads & Tools|
1 genes associated with the nonprogressive muscular atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
|TRPV4||transient receptor potential cation channel, subfamily V, member 4|