Panel | Mode of inheritance | Details |
---|---|---|
3 panels | ||
Green in Early onset or syndromic epilepsyComponent of the following Super Panels:
R-numbers: R59 Signed-off version 4.0 | BOTH monoallelic and biallelic, autosomal or pseudoautosomal | Phenotypes Epileptic encephalopathy, infantile or early childhood, 3 618012, Cutis laxa, autosomal recessive, type IID 617403 |
R-numbers: R101 Signed-off version 3.0 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Cutis laxa, autosomal recessive, type IID, OMIM:617403 |
Component of the following Super Panels:
R-numbers: R29 Signed-off version 5.0 | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | Phenotypes Developmental and epileptic encephalopathy 93, OMIM:618012 |