Panel | Mode of inheritance | Details |
---|---|---|
4 panels | ||
Green in CleftingComponent of the following Super Panels:
Signed-off version 6.0 | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | Phenotypes Frontometaphyseal dysplasia 2, 617137, FMD2, autosomal dominant FMD, AD-FMD |
Green in DDG2PComponent of the following Super Panels:
Signed-off version 4.6 | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | Phenotypes FRONTOMETAPHYSEAL DYSPLASIA 305620, Cardiospondylocarpofacial syndrome |
Green in Fetal anomaliesR-numbers: R21, R412 Signed-off version 4.0 | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | Phenotypes Cardiospondylocarpofacial syndrome, OMIM:157800, Cardiospondylocarpofacial syndrome, MONDO:0008005, Frontometaphyseal dysplasia 2, OMIM:617137, Frontometaphyseal dysplasia 2, MONDO:0014935 |
Green in Skeletal dysplasiaComponent of the following Super Panels:
R-numbers: R104 Signed-off version 6.0 | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | Phenotypes Frontometaphyseal dysplasia 2, 617137 |