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