Deafness, Autosomal Dominant 10 (DFNA10)

Alias:

Dfna10

Autosomal Dominant Nonsyndromic Deafness 10

Non-Syndromic Sensorineural Deafness Autosomal Dominant Type 10

Non-Syndromic Neurosensory Deafness Autosomal Dominant Type 10

Autosomal Dominant Nonsyndromic Hearing Loss 10

Deafness, Autosomal Dominant, Type 10

Deafness, Autosomal Dominant, 10

Autosomal Dominant Deafness 10

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Deafness, Autosomal Dominant 10, also known as dfna10, is related to cardiomyopathy, dilated, 1j and deafness, autosomal dominant 12. An important gene associated with Deafness, Autosomal Dominant 10 is EYA4 (EYA Transcriptional Coactivator And Phosphatase 4), and among its related pathways/superpathways are DNA Double Strand Break Response and Sensory processing of sound. Affiliated tissues include brain, and related phenotypes are Increased Nanog expression and nervous system

Related ID：

MALACARDS：DFN107

OMIM：601316

MESH：D006319