ELMOD3

ELMO domain containing 3
OMIM: 615427, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Amber ELMOD3 in Monogenic hearing loss


Level 2: Audiology
Version 6.22
Latest signed off version: v6.0 (6 May 2026)

Component of the following Super Panels:

  • Paediatric disorders
  • review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
    Sources
    • Expert Review Amber
    • Expert
    • Radboud University Medical Center, Nijmegen
    Phenotypes
    • ?Deafness, autosomal recessive 88, 615429
    • Deafness, autosomal dominant