myofibrillar myopathy Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Myofibrillar structural changes characterized by abnormal intracellular accumulation of the intermediate filament desmin and other proteins. (Human Phenotype Ontology, HP_0003715)
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5 genes associated with the myofibrillar myopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
BAG3 BCL2-associated athanogene 3
FHL1 four and a half LIM domains 1
FLNC filamin C, gamma
LDB3 LIM domain binding 3
MYOT myotilin