| Panel | Mode of inheritance | Details |
|---|---|---|
1 panel | ||
Green in Fetal anomaliesR-numbers: R21, R412 Signed-off version 6.0 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Arthrogryposis multiplex congenita 4, neurogenic, with agenesis of the corpus callosum, OMIM:618766 |