| Panel | Mode of inheritance | Details |
|---|---|---|
2 panels | ||
Green in DDG2PComponent of the following Super Panels:
Signed-off version 7.0 | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | Phenotypes TCP1-related neurodevelopmental disorder with polymicrogyria |
Green in Fetal anomaliesR-numbers: R21, R412 Signed-off version 7.0 | MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | Phenotypes Intellectual developmental disorder with polymicrogyria and seizures, OMIM:621021 |