Oculopharyngeal muscular dystrophy

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
OCULOPHARYNGEAL MUSCULAR DYSTROPHY
270MONDO:0008116
PABPN1 Causal
20301305
GenCC, Orphanet
OCULOPHARYNGEAL MUSCULAR DYSTROPHY 1
164300MONDO:0958176
PABPN1 Causal
34225694 36847015 16648376 21742497
ClinVar, HPO
OCULOPHARYNGEAL MUSCULAR DYSTROPHY 2
620460C5830682MONDO:0958195
HNRNPA2B1 Causal
35484142
ClinVar, Disgenet, GWAS catalog, HPO
All2 Causal2 Unknown0
Related Diseases Diseases that share the most curated genes with Oculopharyngeal muscular dystrophy.
5 View disease cluster →
inclusion body myopathy with early-onset paget disease with or without frontotemporal dementia 2 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.