Inclusion body myopathy with Paget disease of bone and frontotemporal dementia

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
inclusion body myopathy with Paget disease of bone and frontotemporal dementia
MONDO_0000507
VCP Causal
15034582 15732117 16247064 16321991 17935506 18341608 20104022 20335036 20512113 21145000 21684747 21822278 21984748 23349634 25125609 25878907 26574898 27209344 27753622 29804830 36980948
ClinGen, Open Targets
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Inclusion body myopathy with Paget disease of bone and frontotemporal dementia.
5 View disease cluster →
Frontotemporal dementia with motor neuron disease 1 shared geneVCP Related via 1 shared gene including VCP. Frontotemporal dementia with or without amyotrophic lateral sclerosis 1 shared geneVCP Related via 1 shared gene including VCP. Distal myopathy 1 shared geneVCP Related via 1 shared gene including VCP. Dejerine-sottas disease 1 shared geneVCP Related via 1 shared gene including VCP. Hypertrophic neuropathy 1 shared geneVCP Related via 1 shared gene including VCP.