nonsyndromic genetic hearing loss

Log in to bookmark this disease

Bookmark This Disease

This page as CSV This page as PDF All 58 genes as CSV All 58 genes as PDF
Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
nonsyndromic genetic hearing loss
SMPX Unknown — ClinGen —
TBC1D24 Unknown — ClinGen
TJP2 Unknown — ClinGen
TMIE Unknown — ClinGen —
TNC Unknown — ClinGen
TPRN Unknown — ClinGen —
USH1C Unknown — ClinGen —
WHRN Unknown — ClinGen —
All82 Causal24 Unknown58
Related Diseases Diseases that share the most curated genes with nonsyndromic genetic hearing loss.
5 View disease cluster →
Isolated sensorineural deafness 78 shared genesCEACAM16, ESRRB, EYA4, GIPC3, GRAP, MYO15A, NARS2, OTOF, OTOGL, PCDH15, MCM2, OTOG +66 more Related via 78 shared genes including CEACAM16, ESRRB, EYA4. Nonsyndromic hearing loss 72 shared genesCEACAM16, ESRRB, EYA4, GIPC3, MYO15A, OTOF, OTOGL, PCDH15, MCM2, OTOG, TMC1, HGF +60 more Related via 72 shared genes including CEACAM16, ESRRB, EYA4. Deafness 79 shared genesCEACAM16, ESRRB, EYA4, GIPC3, GRAP, MYO15A, NARS2, OTOF, OTOGL, PCDH15, MCM2, OTOG +67 more Related via 79 shared genes including CEACAM16, ESRRB, EYA4. Hereditary hearing loss 39 shared genesESRRB, EYA4, MYO15A, OTOF, PCDH15, TMC1, HGF, RDX, GSDME, COL11A2, MYO6, CDH23 +27 more Related via 39 shared genes including ESRRB, EYA4, MYO15A. Congenital ear anomaly 19 shared genesCEACAM16, MYO15A, OTOF, PCDH15, TMC1, COL11A2, MYO6, CDH23, MYO7A, GJB2, TECTA, CDC14A +7 more Related via 19 shared genes including CEACAM16, MYO15A, OTOF.