GRXCR2

glutaredoxin and cysteine rich domain containing 2
OMIM: 615762, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red GRXCR2 in Monogenic hearing loss

Level 3: Non-syndromic hearing loss
Level 2: Hearing and ear disorders
Version 4.41
Latest signed off version: v4.39 (1 May 2024)

Component of the following Super Panels:

  • Paediatric disorders
  • review Not set
    Sources
    • Expert
    • Radboud University Medical Center, Nijmegen
    Phenotypes
    • ?Deafness, autosomal recessive 101, 615837