Deafness, Autosomal Recessive 31 (DFNB31)

Alias:

Dfnb31

Autosomal Recessive Nonsyndromic Deafness 31

Non-Syndromic Sensorineural Deafness Autosomal Recessive Type 31

Non-Syndromic Neurosensory Deafness Autosomal Recessive Type 31

Autosomal Recessive Nonsyndromic Hearing Loss 31

Deafness, Autosomal Recessive, Type 31

Deafness, Autosomal Recessive, 31

Autosomal Recessive Deafness 31

Whirler, Mouse, Homolog of

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Deafness, Autosomal Recessive 31, also known as dfnb31, is related to usher syndrome, type iid and retinal degeneration. An important gene associated with Deafness, Autosomal Recessive 31 is WHRN (Whirlin). Affiliated tissues include brain and retina, and related phenotypes are sensorineural hearing impairment and absent vestibular function

Related ID：

MALACARDS：DFN170

OMIM：607084

MESH：D006319