You are using an outdated browser. Please upgrade your browser to improve your experience.

autosomal dominant nonsyndromic deafness 10

Disease Summary
Associated Targets (1)
Tbio

1


Mondo Description Any autosomal dominant nonsyndromic deafness in which the cause of the disease is a mutation in the EYA4 gene.
Uniprot Description A form of non-syndromic sensorineural hearing loss. Sensorineural deafness results from damage to the neural receptors of the inner ear, the nerve pathways to the brain, or the area of the brain that receives sound information.
Mondo Term and Equivalent IDs
MONDO:0011031:  autosomal dominant nonsyndromic deafness 10
MESH:C563354: 
UMLS:C1832476: