NCOA3

nuclear receptor coactivator 3
OMIM: 601937, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red NCOA3 in Monogenic hearing loss


Level 2: Audiology
Version 6.13
Latest signed off version: v6.0 (6 May 2026)

Component of the following Super Panels:

  • Paediatric disorders
  • review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Literature
    Phenotypes
    • non-syndromic hearing loss