| Panel | Mode of inheritance | Details |
|---|---|---|
1 panel | ||
Green in Fetal anomaliesR-numbers: R21, R412 Signed-off version 7.0 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Joubert syndrome, Bardet-Biedl syndrome, retinitis pigmentosa, complex neurodevelopmental disorder MONDO:0100038 |