FBXO7

PanelMode of inheritanceDetails
3 panels
R-numbers: R56
Signed-off version 1.121
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Parkinson disease 15, autosomal recessive, OMIM:260300
R-numbers: R57
Signed-off version 1.137
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Parkinson disease 15, autosomal recessive, 260300, juvenile parkinsonism, Dystonia
R-numbers: R58
Signed-off version 2.178
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Dystonia, Parkinson disease 15, autosomal recessive, OMIM:260300