Symptom Information: Sort according to HPO 

1
(HPO:0001250) Seizures Frequent [Orphanet] 1245 / 7739
2
(HPO:0002315) Headache Very frequent [Orphanet] 175 / 7739
3
(HPO:0002514) Cerebral calcification Frequent [Orphanet] 89 / 7739
4
(HPO:0000708) Behavioral abnormality Very frequent [Orphanet] 212 / 7739
5
(HPO:0000726) Dementia 131 / 7739
6
(HPO:0001297) Stroke 44 / 7739
7
(HPO:0002140) Ischemic stroke Frequent [Orphanet] 70 / 7739
8
(HPO:0002170) Intracranial hemorrhage Very frequent [Orphanet] 40 / 7739
9
(HPO:0002637) Cerebral ischemia 17 / 7739
10
(HPO:0004938) Tortuous cerebral arteries 6 / 7739
11
(HPO:0004968) Recurrent cerebral hemorrhage 1 / 7739
12
(HPO:0011695) Cerebellar hemorrhage 6 / 7739
13
(HPO:0011970) Cerebral amyloid angiopathy 9 / 7739
14
(OMIM) Cerebral artery amyloidosis (amyloid deposition in cerebral arteries) 6 / 7739
15
(OMIM) Recurrent strokes 6 / 7739
16
(MedDRA:10008118) Cerebral infarction 10 / 7739
17
(OMIM) Recurrent cerebral and cerebellar hemorrhage 6 / 7739
18
(OMIM) Microbleeds (less than 5 mm in diameter) occur at the gray-white matter junction in the cerebral hemispheres and cerebellum and do not occur in the thalamus, basal ganglia, or brainstem 6 / 7739
19
(OMIM) Hyaline thickening of cerebral arteries 7 / 7739
20
(OMIM) Dementia, progressive, with onset of disease 6 / 7739
21
(HPO:0001522) Death in infancy Occasional [Orphanet] 275 / 7739
22
(HPO:0100543) Cognitive impairment Very frequent [Orphanet] 230 / 7739
23
(HPO:0000006) Autosomal dominant inheritance 2518 / 7739