Panel | Mode of inheritance | Details |
---|---|---|
4 panels | ||
R-numbers: R57 Signed-off version 4.3 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Hyperphenylalaninemia, mild, non-BH4-deficient, 617384 |
Green in DDG2PComponent of the following Super Panels:
Signed-off version 4.3 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Hyperphenylalaninemia, Dystonia, and Intellectual Disability |
Green in Intellectual disabilityComponent of the following Super Panels:
R-numbers: R29 Signed-off version 6.13 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Hyperphenylalaninemia, mild, non-BH4-deficient, 617384, Hyperphenylalaninemia, Dystonia, and Intellectual Disability |
Green in Likely inborn error of metabolismComponent of the following Super Panels:
R-numbers: R98 Signed-off version 5.6 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Hyperphenylalaninemia, mild, non-BH4-deficient, 617384 |