Panel | Mode of inheritance | Details |
---|---|---|
3 panels | ||
Green in DDG2PComponent of the following Super Panels:
Signed-off version 4.15 | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | Phenotypes Congenital Hemangioma |
Green in Early onset or syndromic epilepsyComponent of the following Super Panels:
R-numbers: R59 Signed-off version 6.9 | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | Phenotypes Sturge-Weber syndrome, somatic, mosaic, OMIM:185300 |
R-numbers: R327 Signed-off version 2.0 | MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | Phenotypes Phakomatosis pigmentovascularis, Extensive dermal melanocytosis, Sturge-Weber syndrome, somatic, mosaic, OMIM:185300 |