| 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) |
| External Link | http://compbio.charite.de/hpoweb/showterm?id=HP:0009054 |
| Similar Terms | |
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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 |
