Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 3

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
Inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 3
MONDO_0000507
HNRNPA1 Causal
23455423 25616961
Open Targets
All1 Causal1 Unknown0
Related Diseases Diseases that share the most curated genes with Inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 3.
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Distal muscular dystrophy 1 shared geneHNRNPA1 Related via 1 shared gene including HNRNPA1. Distal myopathy 1 shared geneHNRNPA1 Related via 1 shared gene including HNRNPA1. Amyotrophic lateral sclerosis 1 shared geneHNRNPA1 Related via 1 shared gene including HNRNPA1. Multiple sclerosis 1 shared geneHNRNPA1 Related via 1 shared gene including HNRNPA1. Carcinoma 1 shared geneHNRNPA1 Related via 1 shared gene including HNRNPA1.