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von Willebrand Disease
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Disease • C0042974
Definition
Hereditary or acquired coagulation disorder characterized by a qualitative or quantitative deficiency of the von Willebrand factor. The latter plays an important role in platelet adhesion. Signs and symptoms include bruises, nose bleeding, gum bleeding fo
Synonyms
von Willebrand Disease • von Willebrand Diseases • von Willebrand's Disease • von Willebrand's Diseases • von Willebrands Disease • von Willebrands Diseases • Angiohemophilia • Hemophilia, Vascular • Vascular hemophilia • Vascular Hemophilias • PSEUDOHEMOPHILIA • WILLEBRAND-JUERGENS DISEASE • Pseudohemophilia type B • Constitutional thrombopathy • Factor VIII deficiency with vascular defect • Angiohemophilias • Angiohemophilia, A • Angiohemophilia, B • Vascular pseudohemophilia • von Willebrand's-Jurgens' disease • von Willebrand • VON WILLEBRAND DIS • VON WILLEBRANDS DIS • von Willebrand Diseases [Disease/Finding]
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VWF gene
Hemorrhagic Disorders
Blood Coagulation Disorders, Inherited
Coagulation Protein Disorders
Blood Platelet Disorders
von Willebrand Disease, Recessive Form
Von Willebrand disease, platelet type
VON WILLEBRAND DISEASE, X-LINKED FORM
von Willebrand Disease, Type 3
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Related concepts
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#
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Concept name
|
Type
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Relation
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Support
|
Score
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|
1
|
von Willebrand Disease, Type 3
|
Disease
|
Known
|
Explain
|
52.57362
|
|
2
|
VON WILLEBRAND DISEASE, X-LINKED FORM
|
Disease
|
Known
|
Explain
|
52.57362
|
|
3
|
Von Willebrand disease, platelet type
|
Disease
|
Known
|
Explain
|
49.00145
|
|
4
|
von Willebrand Disease, Recessive Form
|
Disease
|
Known
|
Explain
|
47.28204
|
|
5
|
VWF gene
|
Gene
|
Known
|
Explain
|
45.76899
|
|
6
|
Coagulation Protein Disorders
|
Disease
|
Known
|
Explain
|
39.12110
|
|
7
|
Blood Coagulation Disorders, Inherited
|
Disease
|
Known
|
Explain
|
34.87238
|
|
8
|
Hemorrhagic Disorders
|
Disease
|
Known
|
Explain
|
30.28635
|
|
9
|
Blood Platelet Disorders
|
Disease
|
Known
|
Explain
|
27.86182
|
|
10
|
Hypoprothrombinemias
|
Disease
|
Inferred
|
Explain
|
3.02237
|
|
11
|
Factor VII Deficiency
|
Disease
|
Inferred
|
Explain
|
3.01670
|
|
12
|
Factor V Deficiency
|
Disease
|
Inferred
|
Explain
|
3.00573
|
|
13
|
Factor X Deficiency
|
Disease
|
Inferred
|
Explain
|
2.98356
|
|
14
|
Factor XI Deficiency
|
Disease
|
Inferred
|
Explain
|
2.98068
|
|
15
|
Factor XII Deficiency
|
Disease
|
Inferred
|
Explain
|
2.93361
|
|
16
|
Factor XIII Deficiency
|
Disease
|
Inferred
|
Explain
|
2.76995
|
|
17
|
GP1BA gene
|
Gene
|
Inferred
|
Explain
|
2.73725
|
|
18
|
Hemophilia B
|
Disease
|
Inferred
|
Explain
|
2.66140
|
|
19
|
Afibrinogenemia
|
Disease
|
Inferred
|
Explain
|
2.61130
|
|
20
|
Thrombasthenia
|
Disease
|
Inferred
|
Explain
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2.43626
|
|
21
|
Hemophilia A
|
Disease
|
Inferred
|
Explain
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2.33067
|
|
22
|
VWF wt Allele
|
Gene
|
Inferred
|
Explain
|
2.11590
|
|
23
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Bernard-Soulier Syndrome
|
Disease
|
Inferred
|
Explain
|
2.04398
|
|
24
|
Gray Platelet Syndrome
|
Disease
|
Inferred
|
Explain
|
1.87202
|
|
25
|
Activated Protein C Resistance
|
Disease
|
Inferred
|
Explain
|
1.86466
|
|
26
|
Platelet Storage Pool Deficiency
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Disease
|
Inferred
|
Explain
|
1.70730
|
|
27
|
Blood Coagulation Disorders
|
Disease
|
Inferred
|
Explain
|
1.30660
|
|
28
|
Hermanski-Pudlak Syndrome
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Disease
|
Inferred
|
Explain
|
1.01800
|
|
29
|
Wiskott-Aldrich Syndrome
|
Disease
|
Inferred
|
Explain
|
0.78891
|
|
30
|
Thrombocytosis
|
Disease
|
Inferred
|
Explain
|
0.76830
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|
31
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PLATELET DISORDER, FAMILIAL, WITH ASSOCIATED MYELOID MALIGNANCY
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Disease
|
Inferred
|
Explain
|
0.69554
|
|
32
|
STORMORKEN SYNDROME
|
Disease
|
Inferred
|
Explain
|
0.59778
|
|
33
|
Thrombocythemia, Essential
|
Disease
|
Inferred
|
Explain
|
0.52641
|
|
34
|
Hematological Disease
|
Disease
|
Inferred
|
Explain
|
0.48229
|
|
35
|
Disseminated Intravascular Coagulation
|
Disease
|
Inferred
|
Explain
|
0.33345
|
|
36
|
Antithrombin III Deficiency
|
Disease
|
Inferred
|
Explain
|
0.29493
|
|
37
|
Thrombocytopenia
|
Disease
|
Inferred
|
Explain
|
0.29250
|
|
38
|
Protein C Deficiency
|
Disease
|
Inferred
|
Explain
|
0.27641
|
|
39
|
Vitamin K Deficiency
|
Disease
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Inferred
|
Explain
|
0.27042
|
|
40
|
Thrombophilia
|
Disease
|
Inferred
|
Explain
|
0.26639
|
|
41
|
Waterhouse-Friderichsen Syndrome
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Disease
|
Inferred
|
Explain
|
0.20898
|
|
42
|
F7 gene
|
Gene
|
Inferred
|
Explain
|
0.20179
|
|
43
|
F11 gene
|
Gene
|
Inferred
|
Explain
|
0.18733
|
|
44
|
Purpura, Thrombocytopenic, Idiopathic
|
Disease
|
Inferred
|
Explain
|
0.18578
|
|
45
|
F13B gene
|
Gene
|
Inferred
|
Explain
|
0.14596
|
|
46
|
F9 gene
|
Gene
|
Inferred
|
Explain
|
0.14116
|
|
47
|
Hereditary factor I deficiency disease
|
Disease
|
Inferred
|
Explain
|
0.13683
|
|
48
|
ITGA2 gene
|
Gene
|
Inferred
|
Explain
|
0.12603
|
|
49
|
F12 gene
|
Gene
|
Inferred
|
Explain
|
0.10927
|
|
50
|
F5 gene
|
Gene
|
Inferred
|
Explain
|
0.10268
|
|
51
|
GIANT PLATELET SYNDROME WITH THROMBOCYTOPENIA
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Disease
|
Inferred
|
Explain
|
0.10249
|
|
52
|
GP9 gene
|
Gene
|
Inferred
|
Explain
|
0.09820
|
|
53
|
Pupil constriction
|
Function
|
Inferred
|
Explain
|
0.09557
|
|
54
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Pupil constriction observed
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Disease
|
Inferred
|
Explain
|
0.09557
|
|
55
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Genetic Diseases, X-Linked
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Disease
|
Inferred
|
Explain
|
0.09349
|
|
56
|
Vascular Hemostatic Disorders
|
Disease
|
Inferred
|
Explain
|
0.09048
|
|
57
|
Miosis disorder
|
Disease
|
Inferred
|
Explain
|
0.08334
|
|
58
|
Malnutrition
|
Disease
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Inferred
|
Explain
|
0.08302
|
|
59
|
FGA gene
|
Gene
|
Inferred
|
Explain
|
0.07417
|
|
60
|
F13A1 gene
|
Gene
|
Inferred
|
Explain
|
0.07283
|
|
61
|
F10 gene
|
Gene
|
Inferred
|
Explain
|
0.07225
|
|
62
|
FGB gene
|
Gene
|
Inferred
|
Explain
|
0.06938
|
|
63
|
Blood Platelets
|
Other
|
Inferred
|
Explain
|
0.06768
|
|
64
|
F2 gene
|
Gene
|
Inferred
|
Explain
|
0.06504
|
|
65
|
ITGA2B gene
|
Gene
|
Inferred
|
Explain
|
0.06191
|
|
66
|
CFI gene
|
Gene
|
Inferred
|
Explain
|
0.06112
|
|
67
|
Asplenia
|
Other
|
Inferred
|
Explain
|
0.05804
|
|
68
|
GP1BB gene
|
Gene
|
Inferred
|
Explain
|
0.05717
|
|
69
|
ATAXIA, SPASTIC, WITH CONGENITAL MIOSIS
|
Disease
|
Inferred
|
Explain
|
0.05702
|
|
70
|
PLA2G4A gene
|
Gene
|
Inferred
|
Explain
|
0.05645
|
|
71
|
Microcoria, congenital
|
Other
|
Inferred
|
Explain
|
0.05478
|
|
72
|
P2RX1 gene
|
Gene
|
Inferred
|
Explain
|
0.05390
|
|
73
|
blood coagulation, intrinsic pathway
|
Function
|
Inferred
|
Explain
|
0.05042
|
|
74
|
OPHTHALMOPLEGIA TOTALIS WITH PTOSIS AND MIOSIS
|
Disease
|
Inferred
|
Explain
|
0.04598
|
|
75
|
Myeloproliferative disease
|
Disease
|
Inferred
|
Explain
|
0.04463
|
|
76
|
Lymphopenia
|
Disease
|
Inferred
|
Explain
|
0.04422
|
|
77
|
Blood Protein Disorders
|
Disease
|
Inferred
|
Explain
|
0.04320
|
|
78
|
Genetic Diseases, Inborn
|
Disease
|
Inferred
|
Explain
|
0.03731
|
|
79
|
F8 gene
|
Gene
|
Inferred
|
Explain
|
0.03662
|
|
80
|
MTHFR gene
|
Gene
|
Inferred
|
Explain
|
0.03480
|
|
81
|
PROC gene
|
Gene
|
Inferred
|
Explain
|
0.03061
|
|
82
|
Protein S Deficiency
|
Disease
|
Inferred
|
Explain
|
0.02883
|
|
83
|
ITGB3 gene
|
Gene
|
Inferred
|
Explain
|
0.02594
|
|
84
|
HEMOPHILIA A WITH VASCULAR ABNORMALITY
|
Disease
|
Inferred
|
Explain
|
0.02585
|
|
85
|
Ivemark syndrome
|
Other
|
Inferred
|
Explain
|
0.02130
|
|
86
|
Purpura
|
Disease
|
Inferred
|
Explain
|
0.02031
|
|
87
|
Gestodene
|
Compound
|
Inferred
|
Explain
|
0.01929
|
|
88
|
Immunologic Deficiency Syndromes
|
Disease
|
Inferred
|
Explain
|
0.01720
|
|
89
|
nilestriol
|
Compound
|
Inferred
|
Explain
|
0.01685
|
|
90
|
Anti-Retroviral Agents
|
Compound
|
Inferred
|
Explain
|
0.01598
|
|
91
|
Mercilon
|
Compound
|
Inferred
|
Explain
|
0.01546
|
|
92
|
von Willebrand factor
|
Domain
|
Inferred
|
Explain
|
0.01517
|
|
93
|
Weibel-Palade Bodies
|
Component
|
Inferred
|
Explain
|
0.01349
|
|
94
|
Go 6983
|
Compound
|
Inferred
|
Explain
|
0.01289
|
|
95
|
propylene dichloride
|
Compound
|
Inferred
|
Explain
|
0.01247
|
|
96
|
cell-substrate adhesion
|
Function
|
Inferred
|
Explain
|
0.01245
|
|
97
|
JAK2 gene
|
Gene
|
Inferred
|
Explain
|
0.01209
|
|
98
|
platelet alpha granule
|
Component
|
Inferred
|
Explain
|
0.01204
|
|
99
|
ECM-receptor interaction - Homo sapiens (human)
|
Pathway
|
Inferred
|
Explain
|
0.01167
|
|
100
|
GP5 gene
|
Gene
|
Inferred
|
Explain
|
0.01125
|
|