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GENATLAS PHENOTYPE

last update : 11-04-2022

Symbol	DFNB97
Location	7q13.2
Name	deafness, autosomal recessive 97
Corresponding gene	MET
Main clinical features	delay in development of speech with hearing loss found at or before 2 years of age audiometry revealed a severe degree of sensorineural hearing loss, with intrafamilial variation in thresholds, and intact vestibular function
Genetic determination	autosomal recessive
Function/system disorder	ear
Type	disease

Remark(s)