Panel | Mode of inheritance | Details |
---|---|---|
2 panels | ||
Green in Fetal anomaliesR-numbers: R21, R412 Signed-off version 5.0 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Craniosynostosis, Delayed closure of the fontanelles, cranial defects, clavicular hypoplasia, Anal and Genitourinary malformations, and Skin manifestations, CDAGS syndrome, OMIM:603116 |
R-numbers: R332 Signed-off version 3.0 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes porokeratosis, erythematous cutaneous eruption |