Genomics England
GMS Panels
Panels
Genes and Entities

CRYGD

crystallin gamma D
OMIM: 123690
PanelMode of inheritanceDetails
3 panels
Green
in Bilateral congenital or childhood onset cataracts
R-numbers: R31
Signed-off version 6.6
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Cataracts, Cataract 4, multiple types, 115700, CATARACT CONGENITAL CERULEAN TYPE 3, CATARACT AUTOSOMAL DOMINANT
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 5.48
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
CRYGD-related cataract, OMIM:115700
Green
in Fetal anomalies
R-numbers: R21, R412
Signed-off version 5.80
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
CATARACT AUTOSOMAL DOMINANT, CATARACT CONGENITAL CERULEAN TYPE 3