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GENATLAS PHENOTYPE

last update : 21-01-2014

Symbol	DFNB86
Location	16p13.3
Name	deafness, autosomal recessive 86
Corresponding gene	TBC1D24
Main clinical features	prelingual onset of profound hearing loss affecting all frequencies
Genetic determination	autosomal recessive
Function/system disorder	ear
Type	disease

Remark(s)