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GENATLAS PHENOTYPE

last update : 29-03-2023

Symbol	DFNB113
Location	19q13.31
Name	deafness, autosomal recessive 113
Corresponding gene	CEACAM16
Main clinical features	postlingual progressive hearing impairment, progressive, mild to moderate sensorineural hearing loss, that started in the second decade of life normal vestibular reflexes, vision, skin, cognitive function, and speech development
Genetic determination	autosomal recessive
Function/system disorder	ear
Type	disease

Remark(s)