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_0012193MONDO_0015151MONDO_0029133
CAPN3 Unknown
9150160 27259757 28881388 31937337 32342993 32557990 32896923 32994280
ClinGen, Open Targets
  • muscular dystrophy, limb-girdle, autosomal dominant
MONDO_0012193MONDO_0015151MONDO_0029133
DNAJB6 Unknown
22334415 22366786
ClinGen, Open Targets
  • muscular dystrophy, limb-girdle, autosomal dominant
MONDO_0012193MONDO_0015151MONDO_0029133
HNRNPDL Unknown
24647604
ClinGen, Open Targets
All4 Causal1 Unknown3
Related Diseases Diseases that share the most curated genes with Muscular dystrophy, limb-girdle, autosomal dominant.
5 View disease cluster →
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.