Becker muscular dystrophy

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
BECKER MUSCULAR DYSTROPHY
98895C0917713MONDO:0010311
DMD Causal
10573008
ClinVar, Disgenet, GenCC, Orphanet
PKP2 Unknown — Disgenet
SNTA1 Unknown — Disgenet
All3 Causal1 Unknown2
Related Diseases Diseases that share the most curated genes with Becker muscular dystrophy.
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Benign congenital myopathy 1 shared geneDMD Related via 1 shared gene including DMD. Dystrophinopathy 1 shared geneDMD Related via 1 shared gene including DMD. progressive muscular dystrophy 1 shared geneDMD Related via 1 shared gene including DMD. Leiomyosarcoma 1 shared geneDMD Related via 1 shared gene including DMD. Conduction disorder of the heart 2 shared genesDMD, PKP2 Related via 2 shared genes including DMD, PKP2.