Autosomal dominant nonsyndromic hearing loss

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Subtype of: Nonsyndromic hearing loss
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Pathways column key: KEGG Reactome
Disease Term Disease ID Gene Symbol Classification References Source Pathways
autosomal dominant nonsyndromic hearing loss
MONDO_0030719MONDO:0019587MONDO_0019587
ATP2B2 Causal
17234811 30535804 33105617 33111345
ClinGen, Open Targets
PDE1C Causal — ClinGen
PLS1 Causal — ClinGen —
WFS1 Causal
28271591 27185633 27217304 40779032 23903355 29207974 33693650 39221226
Open Targets
All12 Causal4 Unknown8
Related Diseases Diseases that share the most curated genes with Autosomal dominant nonsyndromic hearing loss.
5 View disease cluster →
Nonsyndromic hearing loss 9 shared genesCOL11A1, LMX1A, ATP2B2, RIPOR2, PDE1C, ATP11A, ABCC1, CD164, PLS1 Related via 9 shared genes including COL11A1, LMX1A, ATP2B2. Isolated sensorineural deafness 9 shared genesCOL11A1, LMX1A, ATP2B2, RIPOR2, PDE1C, ATP11A, ABCC1, CD164, PLS1 Related via 9 shared genes including COL11A1, LMX1A, ATP2B2. Intervertebral disc displacement 1 shared geneCOL11A1 Related via 1 shared gene including COL11A1. Congenital hearing disorder 1 shared genePLS1 Related via 1 shared gene including PLS1. Machado-joseph disease 1 shared geneATP11A Related via 1 shared gene including ATP11A.