Panel | Mode of inheritance | Details |
---|---|---|
2 panels | ||
R-numbers: R135 Signed-off version 2.2 | MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | Phenotypes Noonan syndrome 11, OMIM:618499, Noonan syndrome 11, MONDO:0032786 |
Green in Fetal anomaliesR-numbers: R21, R412 Signed-off version 2.4 | MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | Phenotypes Noonan syndrome 11, OMIM:618499, Noonan syndrome 11, MONDO:0032786 |