EPHA10

EPH receptor A10
OMIM: 611123, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red EPHA10 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 MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Literature
    Phenotypes
    • postlingual non-syndromic genetic hearing loss, MONDO:0016298