1. Genes and Genomic Entities
  2. DFNB59

DFNB59

pejvakin
OMIM: 610219, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Green DFNB59 in Auditory Neuropathy Spectrum Disorde

Level 3: Non-syndromic hearing loss
Level 2: Hearing and ear disorders
Version 1.10

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Expert Review
Phenotypes
  • 610219
Tags
  • new-gene-name
Green DFNB59 in Monogenic hearing loss


Level 2: Audiology
Version 5.57
Latest signed off version: v5.0 (30 Apr 2025)

Component of the following Super Panels:

  • Paediatric disorders

    		•  review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Expert
    • Radboud University Medical Center, Nijmegen
    • Illumina TruGenome Clinical Sequencing Services
    • Emory Genetics Laboratory
    • UKGTN
    Phenotypes
    • hearing loss
    • Deafness, autosomal recessive 59, 610220
    • Nonsyndromic Hearing Loss, Recessive
    Tags
    • new-gene-name