Panel | Mode of inheritance | Details |
---|---|---|
2 panels | ||
R-numbers: R56 Signed-off version 3.12 | 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: R58 Signed-off version 4.41 | 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 |