muscular dystrophy, limb-girdle, autosomal dominant

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
muscular dystrophy, limb-girdle, autosomal dominant
TNPO3 Causal — ClinGen
CAPN3 Unknown — ClinGen
DNAJB6 Unknown — ClinGen
HNRNPDL Unknown — ClinGen
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.