late-onset proximal muscle weakness Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Lack of strength of the proximal musculature occuring late in the clinical course. (Human Phenotype Ontology, HP_0003694)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0003694
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Genes

2 genes associated with the late-onset proximal muscle weakness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CRYAB crystallin, alpha B
DES desmin