scapuloperoneal amyotrophy Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Muscular atrophy in the distribution of shoulder girdle and peroneal muscles. (Human Phenotype Ontology, HP_0003697)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0003697
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Genes

3 genes associated with the scapuloperoneal amyotrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
MYH7 myosin, heavy chain 7, cardiac muscle, beta
PLEKHG5 pleckstrin homology domain containing, family G (with RhoGef domain) member 5
TRPV4 transient receptor potential cation channel, subfamily V, member 4