Distal myopathy

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
ADULT-ONSET DISTAL MYOPATHY DUE TO VCP MUTATION
MONDO:0018006
VCP Unknown
21684747
GWAS catalog
ADULT-ONSET FOVEOMACULAR VITELLIFORM DYSTROPHY
MONDO:0011979
BEST1 Unknown
10854112
Disgenet
IMPG1 Unknown
23993198
GWAS catalog —
IMPG2 Unknown
25085631
GWAS catalog —
DISTAL MYOPATHIES
MESH:D049310
MYH7 Unknown — CTD
TTN Unknown
12145747
CTD
DISTAL MYOPATHY 1
C4552004
MYH7 Unknown — Disgenet
DISTAL MYOPATHY WITH VOCAL CORD WEAKNESS
MONDO:0018951
MATR3 Unknown
19344878 24686783 25154462 25185957 25771394 25952333 26199109 26493020 26708275 28029397 29109432 29628183 30015619 30563574 31432357 31475037 32028661 32361838 32731393 33082323 33129345 34659085 35812165 39192891
ClinGen, Disgenet
DISTAL MYOPATHY, NONAKA TYPE
MESH:C536816
GNE Unknown
11916006
CTD
SQSTM1 Unknown — CTD
DISTAL MYOPATHY, WELANDER TYPE
603MONDO:0011466
SQSTM1 Unknown
29457785
Orphanet
TIA1 Unknown
23348830 23401021 251450 28817800 29457785 30348840 9608564
GWAS catalog, Orphanet
All14 Causal4 Unknown10
Related Diseases Diseases that share the most curated genes with Distal myopathy.
5 View disease cluster →
Vitelliform macular dystrophy 4 shared genesBEST1, IMPG1, IMPG2, PRPH2 Related via 4 shared genes including BEST1, IMPG1, IMPG2. Distal muscular dystrophy 3 shared genesMATR3, MYH7, TTN Related via 3 shared genes including MATR3, MYH7, TTN. Welander distal myopathy 2 shared genesSQSTM1, TIA1 Related via 2 shared genes including SQSTM1, TIA1. Multiminicore myopathy 2 shared genesMYH7, TTN Related via 2 shared genes including MYH7, TTN. Bestrophinopathy 2 shared genesBEST1, PRPH2 Related via 2 shared genes including BEST1, PRPH2.