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nonsyndromic genetic deafness

Disease Summary
Associated Targets (249)
Tbio

185

Tchem

30

Tdark

23

Tclin

11


Explore Associated Targets
Mondo Description A disease characterized by hearing loss that is not part of a larger syndrome.
Disease Ontology Description An auditory system disease that is associated with permanent hearing loss caused by damage to structures in the inner ear and/or the middle ear, which is not associated with other signs and symptoms.
Mondo Term and Equivalent IDs
MONDO:0019497:  nonsyndromic genetic deafness
EFO:0009076: 
GARD:0006410: 
MESH:C580334: 
Orphanet:87884: 
UMLS:CN043648: 
GWAS Targets (0)
No GWAS traits found
Target Novelty (Tin-x)