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GENATLAS PHENOTYPE

last update : 11-09-2019

Symbol	DFNA65
Location	16p13.3
Name	deafness, autosomal dominant 65
Corresponding gene	TBC1D24
Main clinical features	characterized by postlingual onset of slowly progressive hearing loss in the third decade initially affecting the high frequencies, the hearing loss eventually affects all frequencies and results in severe to profound deafness in the seventh decade
Genetic determination	autosomal dominant
Function/system disorder	ear
Type	disease

Remark(s)