Symptom Information: Sort according to HPO 

1
 (HPO:0001288) Gait disturbance Very frequent [Orphanet] 318 / 7739
2
 (HPO:0100022) Abnormality of movement Very frequent [Orphanet] 129 / 7739
3
 (HPO:0000006) Autosomal dominant inheritance 2518 / 7739
4
 (HPO:0000739) Anxiety 67 / 7739
5
 (HPO:0001260) Dysarthria Occasional [HPO:probinson] 329 / 7739
6
 (HPO:0001270) Motor delay 322 / 7739
7
 (HPO:0002072) Chorea 53 / 7739
8
 (HPO:0003621) Juvenile onset 105 / 7739
9
 (HPO:0003812) Phenotypic variability 129 / 7739