Deafness, Autosomal Dominant 12 (DFNA12)

Alias:

Dfna12

Dfna8

Autosomal Dominant Nonsyndromic Deafness 12

Deafness, Autosomal Dominant 8/12

Non-Syndromic Sensorineural Deafness Autosomal Dominant Type 12

Autosomal Dominant Nonsyndromic Hearing Loss 12

Deafness, Autosomal Dominant, Type 12

Deafness, Autosomal Dominant, 12

Deafness, Autosomal Dominant 8

Autosomal Dominant Deafness 12

Autosomal Dominant Deafness 8

Deafness Autosomal Dominant 8

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Deafness, Autosomal Dominant 12, also known as dfna12, is related to rare genetic deafness and non-syndromic genetic deafness. An important gene associated with Deafness, Autosomal Dominant 12 is TECTA (Tectorin Alpha), and among its related pathways/superpathways are G-protein signaling G-Protein alpha-i signaling cascades and Myometrial relaxation and contraction pathways. Affiliated tissues include brain.

Related ID：

MALACARDS：DFN353

OMIM：601543

MESH：D006319