Deafness, Autosomal Dominant 36 (DFNA36)

Alias:

Dfna36

Autosomal Dominant Nonsyndromic Deafness 36

Non-Syndromic Sensorineural Deafness Autosomal Dominant Type 36

Non-Syndromic Neurosensory Deafness Autosomal Dominant Type 36

Autosomal Dominant Nonsyndromic Hearing Loss 36

Deafness, Autosomal Dominant, Type 36

Deafness, Autosomal Dominant, 36

Autosomal Dominant Deafness 36

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Deafness, Autosomal Dominant 36, also known as dfna36, is related to deafness, autosomal recessive 7 and nonsyndromic hearing loss, and has symptoms including tinnitus An important gene associated with Deafness, Autosomal Dominant 36 is TMC1 (Transmembrane Channel Like 1), and among its related pathways/superpathways are Olfactory Signaling Pathway and Sensory processing of sound. Affiliated tissues include brain, and related phenotypes are sensorineural hearing impairment and tinnitus

Related ID：

MALACARDS：DFN128

OMIM：606705

MESH：D006319