autosomal dominant centronuclear myopathy

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
autosomal dominant centronuclear myopathy
DNM2 Causal — ClinGen
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with autosomal dominant centronuclear myopathy.
5 View disease cluster →
X-linked centronuclear myopathy 1 shared geneDNM2 Related via 1 shared gene including DNM2. Congenital deformity of clavicle 1 shared geneDNM2 Related via 1 shared gene including DNM2. Congenital deformity of elbow 1 shared geneDNM2 Related via 1 shared gene including DNM2. Congenital deformity of forearm 1 shared geneDNM2 Related via 1 shared gene including DNM2. Congenital deformity of scapula 1 shared geneDNM2 Related via 1 shared gene including DNM2.