1. Genes and Genomic Entities
  2. OTOA

OTOA

otoancorin
OMIM: 607038, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Green OTOA in Monogenic hearing loss

Level 3: Non-syndromic hearing loss
Level 2: Hearing and ear disorders
Version 4.36
Latest signed off version: v4.0 (22 Mar 2023)

Component of the following Super Panels:

  • Paediatric disorders

    		•  review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Expert
    • Radboud University Medical Center, Nijmegen
    • Emory Genetics Laboratory
    • UKGTN
    Phenotypes
    • hearing loss
    • #607039: Deafness, autosomal recessive 22 [Deafness, sensorineural, severe to profound affecting all frequencies]
    Green OTOA in Severe Paediatric Disorders


    Version 1.184

    		review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Next Generation Children Project
    • Expert Review Green
    • Expert list
    Phenotypes
    • Deafness, autosomal recessive 22, 607039