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References OMIM Gene GeneReviews HGMD HGNC
last update : 31-01-2020
Symbol DFNA67
Location 20q13.33
Name deafness, autosomal dominant 67
Corresponding gene OSBPL2
Main clinical features nonsyndromic sensorineural hearing loss; age at onset of hearing loss ranged from 5 to 32 years and was accompanied by high frequency tinnitus
Genetic determination autosomal dominant
Function/system disorder ear
Type disease