GRXCR1

glutaredoxin and cysteine rich domain containing 1
OMIM: 613283
PanelMode of inheritanceDetails
1 panel
Component of the following Super Panels:
  • - Paediatric disorders
R-numbers: R67
Signed-off version 4.42
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Nonsyndromic Hearing Loss, Recessive, Deafness, autosomal recessive 25, 613285, hearing loss