generalized limb muscle atrophy Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Generalized (unlocalized) atrophy affecting muscles of the limbs in both proximal and distal locations. (Human Phenotype Ontology, HP_0009055)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0009055
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Genes

2 genes associated with the generalized limb muscle atrophy 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
PUS1 pseudouridylate synthase 1