| Panel | Mode of inheritance | Details |
|---|---|---|
2 panels | ||
Green in Fetal anomaliesR-numbers: R21, R412 Signed-off version 7.0 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Meier-Gorlin syndrome, Meier-Gorlin syndrome 9, OMIM:621512 |
Green in Severe microcephalyR-numbers: R88 Signed-off version 9.0 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Meier-Gorlin syndrome like, Meier-Gorlin syndrome, MONDO:0016817, Meier-Gorlin syndrome 9, OMIM:621512 |