Deafness, Autosomal Dominant 80 (DFNA80)

Alias:

Dfna80

Deafness, Autosomal Dominant, Type 80

Hearing Loss, Autosomal Dominant 80

Deafness, Autosomal Dominant, 80

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Basic Information

Medical Symptom

Gene & Mutation

Related Drugs

Disease Model

References Literature

Deafness, Autosomal Dominant 80, also known as dfna80, is related to renal hypodysplasia/aplasia 3. An important gene associated with Deafness, Autosomal Dominant 80 is GREB1L (GREB1 Like Retinoic Acid Receptor Coactivator). Affiliated tissues include brain, and related phenotypes are congenital sensorineural hearing impairment and cochlear aplasia

Related ID：

MALACARDS：DFN390

OMIM：619274

MESH：D006319