|
1
|
(HPO:0000639)
|
Nystagmus |
|
|
|
|
555 / 7739
|
|
2
|
(HPO:0001251)
|
Ataxia |
|
|
|
|
413 / 7739
|
|
3
|
(HPO:0001260)
|
Dysarthria |
|
|
|
|
329 / 7739
|
|
4
|
(HPO:0001270)
|
Motor delay |
|
|
|
|
322 / 7739
|
|
5
|
(HPO:0001310)
|
Dysmetria |
|
|
|
|
76 / 7739
|
|
6
|
(HPO:0002070)
|
Limb ataxia |
|
|
|
|
41 / 7739
|
|
7
|
(HPO:0002075)
|
Dysdiadochokinesis |
|
|
|
|
40 / 7739
|
|
8
|
(HPO:0002080)
|
Intention tremor |
|
|
|
|
44 / 7739
|
|
9
|
(HPO:0002136)
|
Broad-based gait |
|
|
|
|
30 / 7739
|
|
10
|
(HPO:0002470)
|
Nonprogressive cerebellar ataxia |
|
|
|
|
4 / 7739
|
|
11
|
(HPO:0006855)
|
Cerebellar vermis atrophy |
|
|
|
|
8 / 7739
|
|
12
|
(MedDRA:10053694)
|
Saccadic eye movement |
|
|
|
|
2 / 7739
|
|
13
|
(OMIM)
|
Cognitive impairment, mild |
|
|
|
|
15 / 7739
|
|
14
|
(OMIM)
|
Atrophy of the cerebellar vermis seen on MRI |
|
|
|
|
1 / 7739
|
|
15
|
(HPO:0000006)
|
Autosomal dominant inheritance |
|
|
|
|
2518 / 7739
|
|
16
|
(HPO:0002335)
|
Agenesis of cerebellar vermis |
|
|
|
|
25 / 7739
|
|
17
|
(HPO:0003577)
|
Congenital onset |
|
|
|
|
133 / 7739
|
|
18
|
(HPO:0003812)
|
Phenotypic variability |
|
|
|
|
129 / 7739
|
|
19
|
(HPO:0100543)
|
Cognitive impairment |
|
|
|
|
230 / 7739
|