GRHL2

grainyhead like transcription factor 2
OMIM: 608576
PanelMode of inheritanceDetails
2 panels
R-numbers: R262
Signed-off version 2.1
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Corneal dystrophy, posterior polymorphous, 4 618031
R-numbers: R67
Signed-off version 3.3
BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Phenotypes
hearing loss, Deafness, autosomal dominant 28, 608641, #616029: Ectodermal dysplasia/short stature syndrome