Panel | Mode of inheritance | Details |
---|---|---|
4 panels | ||
Green in ArthrogryposisR-numbers: R83 Signed-off version 7.7 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes presynaptic CMS, Congenital myasthenic syndrome |
R-numbers: R57 Signed-off version 5.4 | BOTH monoallelic and biallelic, autosomal or pseudoautosomal | Phenotypes Spastic ataxia 1, autosomal dominant, 108600 |
Green in Congenital myaesthenic syndromeComponent of the following Super Panels:
R-numbers: R80 Signed-off version 4.8 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Myasthenic syndrome, congenital, 25, OMIM:618323 |
Green in Fetal anomaliesR-numbers: R21, R412 Signed-off version 4.195 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Myasthenic syndrome, congenital, 25 |