Vacuolar myopathy

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
VACUOLAR MYOPATHY
C2931230
CASQ1 Unknown — Disgenet
GNE Unknown — Disgenet
HNRNPA2B1 Unknown — Disgenet
HSPB8 Unknown — Disgenet
STIM1 Unknown — Disgenet
VACUOLAR MYOPATHY WITH SARCOPLASMIC RETICULUM PROTEIN AGGREGATES
88635
CASQ1 Unknown
25116801
Orphanet
All5 Causal0 Unknown5
Related Diseases Diseases that share the most curated genes with Vacuolar myopathy.
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Tubular aggregate myopathy 2 shared genesSTIM1, CASQ1 Related via 2 shared genes including STIM1, CASQ1. inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2 1 shared geneHNRNPA2B1 Related via 1 shared gene including HNRNPA2B1. combined immunodeficiency due to STIM1 deficiency 1 shared geneSTIM1 Related via 1 shared gene including STIM1. Distal axonal motor neuropathy-myofibrillar myopathy syndrome 1 shared geneHSPB8 Related via 1 shared gene including HSPB8. neuronopathy, distal hereditary motor, autosomal dominant 1 shared geneHSPB8 Related via 1 shared gene including HSPB8.