Cochlear diseases

Log in to bookmark this disease

Bookmark This Disease

Download as CSV Download as PDF
Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
COCHLEAR DISEASES
C0009197MESH:D015834
MPV17 Unknown
18818194
CTD, Disgenet
PCDH15 Unknown
10978835
CTD, Disgenet —
All2 Causal0 Unknown2
Related Diseases Diseases that share the most curated genes with Cochlear diseases.
5 View disease cluster →
Navajo neurohepatopathy 1 shared geneMPV17 Related via 1 shared gene including MPV17. Retinitis pigmentosa-deafness syndrome 1 shared genePCDH15 Related via 1 shared gene including PCDH15. Male reproductive organ cancer 1 shared genePCDH15 Related via 1 shared gene including PCDH15. Mitochondrial dna depletion syndrome 1 shared geneMPV17 Related via 1 shared gene including MPV17. Congenital ear anomaly 1 shared genePCDH15 Related via 1 shared gene including PCDH15.