inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2

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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 2
HNRNPA2B1 Causal
23455423
ClinGen
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 2.
5 View disease cluster →
Oculopharyngeal muscular dystrophy 1 shared geneHNRNPA2B1 Related via 1 shared gene including HNRNPA2B1. Vacuolar myopathy 1 shared geneHNRNPA2B1 Related via 1 shared gene including HNRNPA2B1. T-cell leukemia-lymphoma 1 shared geneHNRNPA2B1 Related via 1 shared gene including HNRNPA2B1. Frontotemporal dementia 1 shared geneHNRNPA2B1 Related via 1 shared gene including HNRNPA2B1. Amyotrophic lateral sclerosis 1 shared geneHNRNPA2B1 Related via 1 shared gene including HNRNPA2B1.