Autosomal Dominant Nonsyndromic Deafness 77

Autosomal Dominant Nonsyndromic Deafness 77, also known as dfna77, is related to deafness, autosomal dominant 77 and charcot-marie-tooth disease, axonal, type 2o. An important gene associated with Autosomal Dominant Nonsyndromic Deafness 77 is PRR12 (Proline Rich 12), and among its related pathways/superpathways are Class I MHC mediated antigen processing and presentation and Cellular responses to stimuli. Related phenotype is Increased shRNA abundance (Z-score > 2).