| Panel | Mode of inheritance | Details |
|---|---|---|
4 panels | ||
Component of the following Super Panels:
Signed-off version 6.7 | MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | Phenotypes Dystonia 30, OMIM:619291, Dystonia Associated with Lysosomal Abnormalities |
R-numbers: R57 Signed-off version 8.13 | MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | Phenotypes Dystonia 30, OMIM:619291, Dystonia Associated with Lysosomal Abnormalities |
Green in Likely inborn error of metabolismComponent of the following Super Panels:
R-numbers: R98 Signed-off version 9.29 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Mucopolysaccharidosis-like syndrome (biallelic), Dystonia Associated with Lysosomal Abnormalities (monoallelic), Dystonia 30, OMIM:619291 |
Green in Lysosomal storage disorderR-numbers: R276 Signed-off version 3.10 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Mucopolysaccharidosis-like syndrome (biallelic), Dystonia Associated with Lysosomal Abnormalities (monoallelic), Dystonia 30, OMIM:619291 |