minicore (multicore) myopathy Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Multiple small zones of sarcomeric disorganization and lack of oxidative activity (known as minicores) in muscle fibers. (Human Phenotype Ontology, HP_0003789)
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3 genes associated with the minicore (multicore) myopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CFL2 cofilin 2 (muscle)
RYR1 ryanodine receptor 1 (skeletal)
SEPN1 selenoprotein N, 1