Deafness, Autosomal Recessive 110 (DFNB110)

Alias:

Dfnb110

Autosomal Recessive Nonsyndromic Deafness 110

Hearing Loss, Autosomal Recessive 110

Deafness, Autosomal Recessive, 110

Autosomal Recessive Deafness 110

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Deafness, Autosomal Recessive 110, also known as dfnb110, is related to deafness, autosomal dominant 4b and labyrinthitis. An important gene associated with Deafness, Autosomal Recessive 110 is COCH (Cochlin). Affiliated tissues include brain, and related phenotypes are sensorineural hearing impairment and abnormal vestibular function

Related ID：

MALACARDS：DFN367

OMIM：618094

MESH：D006319