| Panel | Mode of inheritance | Details |
|---|---|---|
4 panels | ||
Component of the following Super Panels:
Signed-off version 6.7 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Parkinson disease 19b, early-onset, OMIM:615528, Parkinson disease 19a juvenile-onset, OMIM:615528, juvenile onset Parkinson disease 19A, MONDO:0014231 |
R-numbers: R57 Signed-off version 8.13 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Parkinson disease 19b, early-onset, OMIM:615528, Parkinson disease 19a juvenile-onset, OMIM:615528, juvenile onset Parkinson disease 19A, MONDO:0014231 |
Green in Early onset or syndromic epilepsyComponent of the following Super Panels:
Signed-off version 9.56 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Parkinson disease 19b, early-onset, OMIM:615528, Parkinson disease 19a juvenile-onset, OMIM:615528, juvenile onset Parkinson disease 19A, MONDO:0014231 |
Component of the following Super Panels:
Signed-off version 9.4 | BIALLELIC, autosomal or pseudoautosomal | Phenotypes Parkinson disease 19b, early-onset, OMIM:615528, Parkinson disease 19a juvenile-onset, OMIM:615528, juvenile onset Parkinson disease 19A, MONDO:0014231 |