Muscular dystrophy, limb-girdle, autosomal dominant

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Subtype of: Muscular dystrophy
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Pathways column key: KEGG Reactome
Disease terms Disease ID Gene Symbol Classification References Source Pathways
  • muscular dystrophy, limb-girdle, autosomal dominant
MONDO_0012034
TNPO3 Causal
23543484 23667635 31071488 31192305 31465518
ClinGen, Open Targets
All4 Causal1 Unknown3
Related Diseases Diseases that share the most curated genes with Muscular dystrophy, limb-girdle, autosomal dominant.
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Paresthesia 1 shared geneCAPN3 Related via 1 shared gene including CAPN3. Limb-girdle muscular dystrophy 4 shared genesTNPO3, CAPN3, DNAJB6, HNRNPDL Related via 4 shared genes including TNPO3, CAPN3, DNAJB6. Muscular dystrophy 4 shared genesTNPO3, CAPN3, DNAJB6, HNRNPDL Related via 4 shared genes including TNPO3, CAPN3, DNAJB6. Autoimmune musculoskeletal system disorder 1 shared geneTNPO3 Related via 1 shared gene including TNPO3. Myofibrillar myopathy 1 shared geneDNAJB6 Related via 1 shared gene including DNAJB6.