Cerebral Amyloid Angiopathy

Disease • C0085220

Definition

A disorder characterized by the deposition of amyloid in the wall of the vessels in the brain.

Synonyms

Cerebral Amyloid Angiopathy • Cerebral Amyloid Angiopathies • Amyloid Angiopathy, Cerebral • Angiopathy, Cerebral Amyloid • Congophilic Angiopathy • Congophilic Angiopathies • Angiopathy, Congophilic • Cerebral Amyloid Angiopathy [Disease/Finding]

Linked items?Related concepts, ordered by their global importance in the network.

APP gene    APOE gene    Alzheimer's Disease    Amyloidosis    Cerebral hemisphere hemorrhage    Dementia, familial Danish    Cerebral Arterial Diseases    Dementia, familial British    Familial Cerebral Amyloid Angiopathy    C1854045   

Related concepts

# Concept name Type Relation Support Score
1 C1854045 Other Known Explain 48.14244
2 Cerebral hemisphere hemorrhage Disease Known Explain 38.52795
3 Familial Cerebral Amyloid Angiopathy Disease Known Explain 29.87711
4 Cerebral Arterial Diseases Disease Known Explain 27.69647
5 Amyloidosis Disease Known Explain 26.19218
6 Dementia, familial Danish Disease Known Explain 19.18783
7 Dementia, familial British Disease Known Explain 18.53636
8 Amyloidosis, Familial Disease Inferred Explain 5.33668
9 Alzheimer's Disease Disease Known Explain 2.57289
10 APOE gene Gene Known Explain 2.27610
11 Cerebral Infarction Disease Inferred Explain 2.27125
12 Infarction, Middle Cerebral Artery Disease Inferred Explain 2.01721
13 Infarction, Anterior Cerebral Artery Disease Inferred Explain 2.01721
14 Infarction, Posterior Cerebral Artery Disease Inferred Explain 2.01721
15 Intracranial Arterial Diseases Disease Inferred Explain 1.70188
16 Basal Ganglia Hemorrhage Disease Inferred Explain 1.58524
17 Moyamoya Disease Disease Inferred Explain 1.47985
18 CADASIL Syndrome Disease Inferred Explain 1.46853
19 Traumatic cerebral hemorrhage Other Inferred Explain 1.43368
20 Amyloid Neuropathies Disease Inferred Explain 1.35997
21 APP gene Gene Known Explain 1.29016
22 Intracranial Hemorrhages Disease Inferred Explain 0.96697
23 Hereditary oculoleptomeningeal amyloid angiopathy Disease Inferred Explain 0.90300
24 Brain Diseases, Metabolic, Inborn Disease Inferred Explain 0.78154
25 phenylmethylpyrazolone Compound Inferred Explain 0.56632
26 Amyloid Neuropathies, Familial Disease Inferred Explain 0.54898
27 Basal Ganglia Cerebrovascular Disease Disease Inferred Explain 0.52837
28 AMYLOIDOSIS, PRIMARY CUTANEOUS Disease Inferred Explain 0.50032
29 Brain Hemorrhage, Traumatic Other Inferred Explain 0.47639
30 CST3 gene Gene Inferred Explain 0.46873
31 VAD protocol Other Inferred Explain 0.43711
32 Amyloidosis, familial visceral Disease Inferred Explain 0.42427
33 Proteostasis Deficiencies Disease Inferred Explain 0.41725
34 Meretoja syndrome Disease Inferred Explain 0.40842
35 ITM2B gene Gene Inferred Explain 0.37662
36 AMYLOIDOSIS OF GINGIVA AND CONJUNCTIVA, WITH MENTAL RETARDATION Disease Inferred Explain 0.36227
37 Presenile dementia Disease Inferred Explain 0.33667
38 Presenile dementia, uncomplicated Disease Inferred Explain 0.33667
39 C1629045 Other Inferred Explain 0.32238
40 Aminophylline Compound Inferred Explain 0.30466
41 Dementia, Vascular Disease Inferred Explain 0.29298
42 Warfarin Compound Inferred Explain 0.28110
43 Dementia Disease Inferred Explain 0.24289
44 Cerebrovascular Disorders Disease Inferred Explain 0.24182
45 SPASTIC ATAXIA Disease Inferred Explain 0.23724
46 PLAT gene Gene Inferred Explain 0.19792
47 Gerstmann-Straussler-Scheinker Disease Disease Inferred Explain 0.19439
48 Intracranial Arteriosclerosis Disease Inferred Explain 0.17984
49 ZDHHC13 gene Gene Inferred Explain 0.17636
50 Carotid Artery Diseases Disease Inferred Explain 0.16121
51 Intracranial Aneurysm Disease Inferred Explain 0.15362
52 Traumatic intracranial hemorrhage Other Inferred Explain 0.15348
53 Intracranial Arteriovenous Malformation Disease Inferred Explain 0.14883
54 Arterial Occlusive Diseases Disease Inferred Explain 0.11611
55 Presenile dementia, Kraepelin type Disease Inferred Explain 0.10841
56 Finnish type amyloidosis Disease Inferred Explain 0.09991
57 KWD-2019 Compound Inferred Explain 0.09403
58 GSN gene Gene Inferred Explain 0.08499
59 POLYCYSTIC LIPOMEMBRANOUS OSTEODYSPLASIA WITH SCLEROSING LEUKOENCEPHALOPATHY Disease Inferred Explain 0.08445
60 MMP9 gene Gene Inferred Explain 0.08328
61 ATAXIA WITH MYOCLONIC EPILEPSY AND PRESENILE DEMENTIA Disease Inferred Explain 0.08205
62 Frontotemporal dementia Disease Inferred Explain 0.08106
63 Hematoma, Subdural Disease Inferred Explain 0.07843
64 Cranial Epidural Hematomas Other Inferred Explain 0.07843
65 Multi-infarct dementia Disease Inferred Explain 0.06362
66 Inborn Errors of Metabolism Disease Inferred Explain 0.05648
67 HMOX1 gene Gene Inferred Explain 0.05628
68 Pituitary Apoplexy Disease Inferred Explain 0.05617
69 NOTCH3 gene Gene Inferred Explain 0.05266
70 Subarachnoid Hemorrhage Disease Inferred Explain 0.05082
71 OSMR gene Gene Inferred Explain 0.05075
72 Cerebellar Ataxia Disease Inferred Explain 0.04308
73 Hematoma Disease Inferred Explain 0.04027
74 Corneal dystrophy Disease Inferred Explain 0.03579
75 Brain Infarction Disease Inferred Explain 0.03535
76 Genetic Diseases, Inborn Disease Inferred Explain 0.02710
77 Diethylstilbestrol Compound Inferred Explain 0.02710
78 Heredodegenerative Disorders, Nervous System Disease Inferred Explain 0.02681
79 Capillary Leak Syndrome Disease Inferred Explain 0.02550
80 Aneurysm Disease Inferred Explain 0.02530
81 Gingiva Other Inferred Explain 0.02471
82 Nephrotic Syndrome Disease Inferred Explain 0.02439
83 Hemorrhage Disease Inferred Explain 0.02298
84 Theophylline Compound Inferred Explain 0.02057
85 Cataract Adverse Event Disease Inferred Explain 0.01928
86 Peripheral Neuropathy Disease Inferred Explain 0.01866
87 Arteriosclerosis Disease Inferred Explain 0.01860
88 Congenital arteriovenous malformation Other Inferred Explain 0.01792
89 TDP-43 Proteinopathies Disease Inferred Explain 0.01563
90 Ethylenediamines Compound Inferred Explain 0.01528
91 Brain Injuries Other Inferred Explain 0.01523
92 Subarachnoid Hemorrhage, Traumatic Other Inferred Explain 0.01405
93 Bradycardia Disease Inferred Explain 0.01371
94 Central Nervous System Vascular Malformations Other Inferred Explain 0.01366
95 Multiple Myeloma Disease Inferred Explain 0.01236
96 Metabolic Diseases Disease Inferred Explain 0.01230
97 Pituitary Diseases Disease Inferred Explain 0.01181
98 Deafness Disease Inferred Explain 0.01136
99 Complete Hearing Loss Disease Inferred Explain 0.01133
100 SPASTIC ATAXIA, CHARLEVOIX-SAGUENAY TYPE Disease Inferred Explain 0.01088