| Panel | Mode of inheritance | Details |
|---|---|---|
6 panels | ||
Green in CleftingComponent of the following Super Panels:
Signed-off version 3.1 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes ROBINOW SYNDROME, AUTOSOMAL RECESSIVE, RRS |
Green in DDG2PComponent of the following Super Panels:
Signed-off version 3.1 | BOTH monoallelic and biallelic, autosomal or pseudoautosomal | Phenotypes ROBINOW SYNDROME, AUTOSOMAL DOMINANT 180700, BRACHYDACTYLY, TYPE B1 113000, ROR2-RELATED DISORDERS AR 268310 |
Green in Fetal anomaliesR-numbers: R21, R412 Signed-off version 2.1 | BOTH monoallelic and biallelic, autosomal or pseudoautosomal | Phenotypes ROR2-RELATED DISORDERS AR, BRACHYDACTYLY, TYPE B1, ROBINOW SYNDROME, AUTOSOMAL DOMINANT |
Green in Intellectual disabilityComponent of the following Super Panels:
R-numbers: R29 Signed-off version 4.4 | BOTH monoallelic and biallelic, autosomal or pseudoautosomal | Phenotypes BRACHYDACTYLY, TYPE B1 |
Green in Limb disordersComponent of the following Super Panels:
Signed-off version 3.1 | BOTH monoallelic and biallelic, autosomal or pseudoautosomal | Phenotypes Brachydactyly, type B1 113000, Robinow syndrome, autosomal recessive 268310 |
Green in Skeletal dysplasiaComponent of the following Super Panels:
R-numbers: R104 Signed-off version 3.1 | BOTH monoallelic and biallelic, autosomal or pseudoautosomal | Phenotypes Brachydactyly, type B1 113000, Robinow syndrome, autosomal recessive 268310 |