Autosomal recessive limb-girdle muscular dystrophy

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Subtype of: Limb-girdle muscular dystrophy
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
autosomal recessive limb-girdle muscular dystrophy
MONDO_0014142MONDO_0957270MONDO_0030456MONDO_0029136MONDO_0012652MONDO_0013390MONDO_0014474MONDO_0014782MONDO_0030014MONDO_0971171MONDO_0011170MONDO_0014900MONDO_0012127
GMPPB Unknown
27874200 28456886 25681410 26133662 23768512 27147698 26503795 25529582 24896178
Open Targets
HMGCR Unknown
36745799 37167966
ClinGen, Open Targets
JAG2 Unknown
33861953 39121631 39649397
ClinGen, Open Targets
LAMA2 Unknown
21953594 24957499
Open Targets
LOC102723370 Unknown
20096397 22499103 25864073 25891276 25929793 32925086 33496727
Open Targets —
PLEC Unknown
21109228 20624679 28447722 22144912 21263134 31509265 28824526 27234031 25556389
Open Targets
POGLUT1 Unknown
27807076 29034878 31897643 33861953
ClinGen, Open Targets
POPDC1 Unknown
26642364
Open Targets —
POPDC3 Unknown
31610034 35075722 35842834 37104941
ClinGen, Open Targets
SNUPN Unknown
38366623 38413582
Open Targets
TCAP Unknown
10655062 15582318 18948002 20186049 21530252 23479141 25055047 27532257 29797799 29935994 32761539 36463458 37216648 39015008
ClinGen, Open Targets
TOR1AIP1 Unknown
32055997 24856141 27342937 30723199 31299614 25425325 33215087 34164833
Open Targets —
TTN Unknown
27532257 20186049 22335739 27869827 29238064 25589632 26777568 12145747
Open Targets
All22 Causal9 Unknown13
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.