Panel | Mode of inheritance | Details |
---|---|---|
4 panels | ||
Green in ArthrogryposisR-numbers: R83 Signed-off version 6.3 | BOTH monoallelic and biallelic, autosomal or pseudoautosomal | Phenotypes Ullrich congenital muscular dystrophy 2, bethlem myopathy 2 |
Component of the following Super Panels:
R-numbers: R432 Signed-off version 1.0 | BOTH monoallelic and biallelic, autosomal or pseudoautosomal | Phenotypes Ullrich congenital muscular dystrophy 2, OMIM:616470, Bethlem myopathy 2, OMIM:616471 |
R-numbers: R101 Signed-off version 3.0 | BOTH monoallelic and biallelic, autosomal or pseudoautosomal | Phenotypes Bethlem myopathy 2, OMIM:616471 |
Green in Fetal anomaliesR-numbers: R21, R412 Signed-off version 4.0 | BOTH monoallelic and biallelic, autosomal or pseudoautosomal | Phenotypes Bethlem myopathy 2, 616471, ?Ullrich congenital muscular dystrophy 2, 616470 |