Deafness, Autosomal Recessive 96 (DFNB96)

Deafness, Autosomal Recessive 96, also known as autosomal recessive nonsyndromic deafness 96, is related to deafness, autosomal recessive and bartter disease. An important gene associated with Deafness, Autosomal Recessive 96 is DFNB96 (Deafness, Autosomal Recessive 96), and among its related pathways/superpathways are Ion channel transport and Diuretics Pathway, Pharmacodynamics. Related phenotype is hearing impairment.