| 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 |
| Similar Terms | |
| 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.
| Symbol | Name |
|---|---|
| TRPV4 | transient receptor potential cation channel, subfamily V, member 4 |
