autosomal recessive limb-girdle muscular dystrophy

Log in to bookmark this disease

Bookmark This Disease

Download as CSV Download as PDF
Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
autosomal recessive limb-girdle muscular dystrophy
HMGCR Unknown — ClinGen
JAG2 Unknown — ClinGen
POGLUT1 Unknown — ClinGen
POPDC3 Unknown — ClinGen
TCAP Unknown — ClinGen
All14 Causal9 Unknown5
Related Diseases Diseases that share the most curated genes with autosomal recessive limb-girdle muscular dystrophy.
5 View disease cluster →
Limb girdle muscular dystrophy 14 shared genesSGCA, HMGCR, TRAPPC11, ANO5, SGCD, DYSF, SGCG, TCAP, POPDC3, CAPN3, JAG2, POGLUT1 +2 more Related via 14 shared genes including SGCA, HMGCR, TRAPPC11. Muscular dystrophy 13 shared genesSGCA, HMGCR, TRAPPC11, ANO5, SGCD, DYSF, SGCG, TCAP, POPDC3, CAPN3, JAG2, SGCB +1 more Related via 13 shared genes including SGCA, HMGCR, TRAPPC11. Sarcoglycanopathies 2 shared genesSGCA, SGCG Related via 2 shared genes including SGCA, SGCG. Intellectual developmental disorder movement cerebellar 1 shared geneTRAPPC11 Related via 1 shared gene including TRAPPC11. Asymptomatic hyperckemia-myalgia-rhabdomyolysis syndrome 1 shared geneANO5 Related via 1 shared gene including ANO5.