Welander distal myopathy

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
WELANDER DISTAL MYOPATHY
604454C0221054
TIA1 Causal — ClinVar, Disgenet, HPO
SQSTM1 Unknown — Disgenet
WELANDER DISTAL MYOPATHY, SWEDISH TYPE
C2931290MESH:C536690
TIA1 Unknown
23348830 23401021
CTD, Disgenet
All2 Causal1 Unknown2
Related Diseases Diseases that share the most curated genes with Welander distal myopathy.
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frontotemporal dementia and/or amyotrophic lateral sclerosis 3 1 shared geneSQSTM1 Related via 1 shared gene including SQSTM1. amyotrophic lateral sclerosis 26 with or without frontotemporal dementia 1 shared geneTIA1 Related via 1 shared gene including TIA1. Paget disease 1 shared geneSQSTM1 Related via 1 shared gene including SQSTM1. Distal myopathy 2 shared genesSQSTM1, TIA1 Related via 2 shared genes including SQSTM1, TIA1. Frontotemporal dementia with motor neuron disease 1 shared geneSQSTM1 Related via 1 shared gene including SQSTM1.