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GENATLAS PHENOTYPE

last update : 21-09-2011

Symbol	DFNA50
Location	7q32.1-q32.2
HGNC id	18819
Name	neurosensory deafness 50
Corresponding gene	MIR96
Main clinical features	postlingual, progressive, nonsyndromic all-frequency hearing loss hearing loss was initially mild, affecting all frequencies, and progressed to severe or profound in the seventh decade
Genetic determination	autosomal dominant
Function/system disorder	ear
Type	disease

Remark(s)