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GENATLAS PHENOTYPE

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

Remark(s)