Deafness, Autosomal Dominant 15 (DFNA15)

Alias:

Dfna15

Autosomal Dominant Nonsyndromic Deafness 15

Autosomal Dominant Nonsyndromic Hearing Loss 15

Deafness, Autosomal Dominant, Type 15

Deafness, Autosomal Dominant, 15

Autosomal Dominant Deafness 15

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Deafness, Autosomal Dominant 15, also known as dfna15, is related to deafness, autosomal dominant 11 and nonsyndromic hearing loss. An important gene associated with Deafness, Autosomal Dominant 15 is POU4F3 (POU Class 4 Homeobox 3). Related phenotypes are hearing impairment and nervous system

Related ID：

MALACARDS：DFN117

OMIM：602459

MESH：D006319