Panel | Mode of inheritance | Details |
---|---|---|
2 panels | ||
Green in ArthrogryposisR-numbers: R83 Signed-off version 8.0 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Arthrogryposis multiplex congenita 2, neurogenic type, OMIM:208100 |
Green in Fetal anomaliesR-numbers: R21, R412 Signed-off version 5.0 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Arthrogryposis multiplex congenita 2, neurogenic type, OMIM:208100 |