|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|Description||A muscular dystrophy which begins at the lower legs and affects the shoulder region earlier and more severely than distal arm. (Human Disease Ontology, DOID_0060253)|
|Downloads & Tools|
1 genes associated with the scapuloperoneal myopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.
|MYH7||myosin, heavy chain 7, cardiac muscle, beta|