rippling muscle disease Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A muscle tissue disease characterized by muscles unusually sensitive to movement or pressure; the proximal muscles are most affected, especially the thighs. (Human Disease Ontology, DOID_0060255)
External Link http://www.omim.org/entry/606072
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Genes

1 genes associated with the rippling muscle disease phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
CAV3 caveolin 3