Genomics England
GMS Panels
Panels
Genes and Entities

WHRN

whirlin
OMIM: 607928
PanelMode of inheritanceDetails
2 panels
Green
in Monogenic hearing loss
Component of the following Super Panels:
  • - Paediatric disorders
R-numbers: R67
Signed-off version 4.57
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
#607084:Deafness, autosomal recessive 31, #611383:Usher syndrome, type 2D, hearing loss, Nonsyndromic Hearing Loss, Recessive
Green
in Retinal disorders
R-numbers: R32
Signed-off version 7.0
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Eye Disorders