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:0019587MONDO_0019587
ABCC1 Unknown — ClinGen
ACTG1 Unknown
16950128 12519370 6865942 22366783 14684684 8941379 19477959 5654493 10524632 3737401 3351890 11474115 13680526 12388543 2837653 20847274 3472224 16773128
Open Targets
ATP-dependent chromatin remodeling Rap1 signaling pathway Phagosome +51 more
ATP11A Unknown — ClinGen
CD164 Unknown — ClinGen
COL11A1 Unknown — ClinGen
LMX1A Unknown — ClinGen —
PSMC3 Unknown
32500975 37256937
Open Targets
Proteasome Alzheimer disease Parkinson disease +58 more
RIPOR2 Unknown — ClinGen —
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.