scapuloperoneal myopathy Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
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)
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1 genes associated with the scapuloperoneal myopathy 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