Rare Genetic Deafness

Rare Genetic Deafness, also known as rare genetic hearing loss, is related to deafness, autosomal recessive 2 and deafness, autosomal dominant 3a. An important gene associated with Rare Genetic Deafness is ADGRV1 (Adhesion G Protein-Coupled Receptor V1), and among its related pathways/superpathways is Aminoglycoside Ototoxicity Pathway, Adverse Drug Reaction. Affiliated tissues include thyroid and bone, and related phenotypes are nervous system and hearing/vestibular/ear