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GENATLAS PHENOTYPE

last update : 18-01-2012

Symbol	DFNB3
Location	17p11.2
Name	neurosensory deafness 3
Corresponding gene	MYO15A
related resource	Genetics hearing impairment
Main clinical features	non syndromic, prelingual, profund, stable, putative homolog of mouse shaker 2 (Bengkala, Bali, India kindreds)
Genetic determination	autosomal recessive
Prevalence	10 p100 of all DFNB (PMID: 21117948)
Function/system disorder	ear
Type	disease

Gene product

Name	unconventional myosin (MYO15)

Remark(s)