OTOG

otogelin
OMIM: 604487, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Green OTOG in Monogenic hearing loss


Level 2: Audiology
Version 6.10
Latest signed off version: v6.0 (6 May 2026)

Component of the following Super Panels:

  • Paediatric disorders
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Expert
    • Radboud University Medical Center, Nijmegen
    • UKGTN
    Phenotypes
    • Deafness, autosomal recessive 18B, 614945