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GENATLAS PHENOTYPE

last update : 28-11-2012

Symbol	DFNB18B
Location	11p15.1
Name	deafness, autosomal recessive 18B
Corresponding gene	OTOG
Main clinical features	moderate nonsyndromic hearing loss nonsyndromic deafness, who all had flat to shallow U-shaped audiograms prelingual onset of the hearing impairment, and delayed motor development, suggestive of vestibular problems at a young age
Genetic determination	autosomal recessive
	autosomal dominant
Function/system disorder	ear
Type	disease

Remark(s)