| Panel | Mode of inheritance | Details |
|---|---|---|
5 panels | ||
Green in CleftingComponent of the following Super Panels:
Signed-off version 5.3 | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | Phenotypes ROBINOW SYNDROME, AUTOSOMAL DOMINANT 1, DRS1 |
Green in DDG2PComponent of the following Super Panels:
Signed-off version 4.3 | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | Phenotypes WNT5A-RELATED ROBINOW SYNDROME, AUTOSOMAL DOMINANT 180700 |
Green in Fetal anomaliesR-numbers: R21, R412 Signed-off version 4.0 | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | Phenotypes WNT5A-RELATED ROBINOW SYNDROME, AUTOSOMAL DOMINANT |
Green in Limb disordersComponent of the following Super Panels:
Signed-off version 5.4 | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | Phenotypes Robinow syndrome, autosomal dominant 1 180700 |
Green in Skeletal dysplasiaComponent of the following Super Panels:
R-numbers: R104 Signed-off version 5.3 | MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | Phenotypes Robinow syndrome, autosomal dominant 1 180700 |