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GENATLAS PHENOTYPE

last update : 22-09-2017

Symbol	DFNA4B
Location	19q13.31
Name	Deafness, autosomal dominant 4B
Corresponding gene	CEACAM16
Main clinical features	nonsyndromic progressive sensorineural hearing loss with postlingual onset, sensorineural hearing loss began in the second decade and led to severe to profound impairment by the age of 40 years
Genetic determination	autosomal dominant
Function/system disorder	ear
Type	disease

Remark(s)