myopathy, proximal, and ophthalmoplegia

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
myopathy, proximal, and ophthalmoplegia
MYH2 Causal
23489661 15548556 23388406 24193343 11114175 20418530
ClinGen
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with myopathy, proximal, and ophthalmoplegia.
5 View disease cluster →
Childhood-onset autosomal recessive myopathy with external ophthalmoplegia 1 shared geneMYH2 Related via 1 shared gene including MYH2. Congenital myopathy 1 shared geneMYH2 Related via 1 shared gene including MYH2. Muscular dystrophy 1 shared geneMYH2 Related via 1 shared gene including MYH2. Myositis 1 shared geneMYH2 Related via 1 shared gene including MYH2. Myopathy 1 shared geneMYH2 Related via 1 shared gene including MYH2.