FBXO7

PanelMode of inheritanceDetails
4 panels
R-numbers: R56
Signed-off version 2.1
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Parkinson disease 15, autosomal recessive, OMIM:260300
R-numbers: R57
Signed-off version 2.6
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Parkinson disease 15, autosomal recessive, 260300, juvenile parkinsonism, Dystonia
R-numbers: R60
Signed-off version 2.1
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Parkinson disease 15, autosomal recessive, OMIM:260300
R-numbers: R58
Signed-off version 3.1
BIALLELIC, autosomal or pseudoautosomal
Phenotypes
Dystonia, Parkinson disease 15, autosomal recessive, OMIM:260300