Deafness, Autosomal Dominant 7 (DFNA7)

Alias:

Dfna7

Autosomal Dominant Nonsyndromic Deafness 7

Autosomal Dominant Nonsyndromic Hearing Loss 7

Deafness, Autosomal Dominant, Type 7

Deafness, Autosomal Dominant, 7

Autosomal Dominant Deafness 7

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Deafness, Autosomal Dominant 7, also known as dfna7, is related to deafness, autosomal dominant 16 and deafness, autosomal dominant 21. An important gene associated with Deafness, Autosomal Dominant 7 is LMX1A (LIM Homeobox Transcription Factor 1 Alpha), and among its related pathways/superpathways are RhoGDI Pathway and Cytoskeleton remodeling_RalA regulation pathway. Affiliated tissues include brain, and related phenotypes are nervous system and hearing/vestibular/ear

Related ID：

MALACARDS：DFN163

OMIM：601412

MESH：D006319