Panel | Mode of inheritance | Details |
---|---|---|
8 panels | ||
R-numbers: R31 Signed-off version 4.14 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes 3-methylglutaconic aciduria, type VIII 617248 |
R-numbers: R57 Signed-off version 4.3 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes 3-methylglutaconic aciduria, type VIII 617248 |
Green in Early onset or syndromic epilepsyComponent of the following Super Panels:
R-numbers: R59 Signed-off version 5.10 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes 3-methylglutaconic aciduria, type VIII |
Green in Intellectual disabilityComponent of the following Super Panels:
R-numbers: R29 Signed-off version 6.13 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes 3-methylglutaconic aciduria, type VIII 617248 |
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 3-methylglutaconic aciduria, type VIII 617248 |
Green in Mitochondrial disordersComponent of the following Super Panels:
Signed-off version 6.4 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes 3-methylglutaconic aciduria, type VIII 617248 |
R-numbers: R63 Signed-off version 3.105 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes 3-methylglutaconic aciduria, type VIII, 617248 |
R-numbers: R15 Signed-off version 5.3 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes 3-methylglutaconic aciduria, type VIII, 617248, early onset neurological syndrome, neutropenia |