Panel | Mode of inheritance | Details |
---|---|---|
5 panels | ||
Green in CleftingComponent of the following Super Panels:
Signed-off version 6.0 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Robinow syndrome, autosomal recessive, OMIM:268310 |
Green in DDG2PComponent of the following Super Panels:
Signed-off version 4.6 | BOTH monoallelic and biallelic, autosomal or pseudoautosomal | Phenotypes Brachydactyly, type B1, OMIM:113000 (AD), Robinow syndrome, autosomal recessive, OMIM:268310 (AR) |
Green in Fetal anomaliesR-numbers: R21, R412 Signed-off version 4.0 | BOTH monoallelic and biallelic, autosomal or pseudoautosomal | Phenotypes Brachydactyly, type B1, OMIM:113000 (AD), Robinow syndrome, autosomal recessive, OMIM:268310 (AR) |
Green in Limb disordersComponent of the following Super Panels:
Signed-off version 6.0 | BOTH monoallelic and biallelic, autosomal or pseudoautosomal | Phenotypes Brachydactyly, type B1, OMIM:113000 (AD), Robinow syndrome, autosomal recessive, OMIM:268310 (AR) |
Green in Skeletal dysplasiaComponent of the following Super Panels:
R-numbers: R104 Signed-off version 6.0 | BOTH monoallelic and biallelic, autosomal or pseudoautosomal | Phenotypes Brachydactyly, type B1, OMIM:113000 (AD), Robinow syndrome, autosomal recessive, OMIM:268310 (AR) |