Congenital sensorineural hearing loss

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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
CONGENITAL SENSORINEURAL HEARING LOSS
C1865866
ILDR1 Unknown — Disgenet —
KARS1 Unknown — Disgenet
MITF Unknown — Disgenet
MYO15A Unknown — Disgenet
POU4F3 Unknown — Disgenet —
TBCEL-TECTA Unknown — Disgenet —
TECTA Unknown — Disgenet
USH2A Unknown — Disgenet —
All8 Causal0 Unknown8
Related Diseases Diseases that share the most curated genes with Congenital sensorineural hearing loss.
5 View disease cluster →
Congenital ear anomaly 5 shared genesMYO15A, USH2A, TBCEL-TECTA, MITF, TECTA Related via 5 shared genes including MYO15A, USH2A, TBCEL-TECTA. Waardenburg syndrome type 2 1 shared geneMITF Related via 1 shared gene including MITF. Deafness with congenital and adult-onset progressive leukodystrophy 1 shared geneKARS1 Related via 1 shared gene including KARS1. Early onset progressive leukoencephalopathy-central nervous system calcification-hearing loss-visual impairment syndrome 1 shared geneKARS1 Related via 1 shared gene including KARS1. Early-onset progressive leukoencephalopathy-central nervous system calcification-deafness-visual impairment syndrome 1 shared geneKARS1 Related via 1 shared gene including KARS1.