Search results for "[genes] VWF"

97 hits were found for '[genes] VWF'

# Family MCID Name MIFTS Score
1
VNW001 Von Willebrand's Disease 61 18.955
2
VNW005 Von Willebrand Disease, Type 1 42 16.717
3
P MYC007 Myocardial Infarction 77 12.637
4
P CRN211 Coronary Artery Disease 69 12.637
5
STR067 Stroke, Ischemic 66 12.637
6
PRP027 Peripheral Vascular Disease 59 12.637
7
VSC007 Vascular Disease 55 12.637
8
P THR015 Thrombophilia 54 12.637
9
P THR014 Thrombocytopenia 54 12.637
10
c ACT075 Acute Myocardial Infarction 51 12.637
11
DSS009 Disseminated Intravascular Coagulation 49 12.637
12
ANG020 Angiosarcoma 48 12.637
13
INT002 Intermittent Claudication 47 12.637
14
P HML001 Hemolytic-Uremic Syndrome 47 12.637
15
PRP030 Purpura 47 12.637
16
URM002 Uremia 46 12.637
17
LMB062 Limb Ischemia 43 12.637
18
ANG011 Angiodysplasia 39 12.637
19
BLD053 Blood Platelet Disease 35 12.637
20
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 76 10.944
21
MLR004 Malaria 75 10.944
22
P HRD008 Hereditary Hemorrhagic Telangiectasia 71 10.944
23
P ESS003 Essential Thrombocythemia 65 10.944
24
P CSH001 Cushing's Syndrome 64 10.944
25
CNG034 Congestive Heart Failure 64 10.944
26
GLN010 Glanzmann Thrombasthenia 62 10.944
27
c HMP029 Hemophilia a 58 10.944
28
BRN082 Bernard-Soulier Syndrome, Type C 51 10.944
29
c THR092 Thrombophilia Due to Thrombin Defect 51 10.944
30
c AFB002 Afibrinogenemia, Congenital 49 10.944
31
P THR005 Thrombotic Thrombocytopenic Purpura 49 10.944
32
FCT004 Factor Xii Deficiency 49 10.944
33
CRN017 Coronary Thrombosis 45 10.944
34
P CLL015 Collagen Disease 44 10.944
35
HPT009 Hepatopulmonary Syndrome 44 10.944
36
VSC006 Vascular Cancer 42 10.944
37
DBT008 Diabetic Angiopathy 40 10.944
38
HMR002 Hemarthrosis 40 10.944
39
FCT001 Factor Viii Deficiency 40 10.944
40
TYP015 Type 2b Von Willebrand Disease 34 10.944
41
QLT001 Qualitative Platelet Defect 34 10.944
42
RYN001 Raynaud Disease 33 10.944
43
VNW006 Von Willebrand Disease, Types 2a, 2b, 2m, and 2n 29 10.944
44
FCT013 Factor V Leiden Thrombophilia 26 10.944
45
VNW003 Von Willibrand Disease, Type 3 26 10.944
46
TYP017 Type 2n Von Willebrand Disease 26 10.944
47
TYP014 Type 2a Von Willebrand Disease 25 10.944
48
TYP016 Type 2m Von Willebrand Disease 23 10.944
49
c HYP595 Hypertension, Essential 62 8.936
50
BHC002 Behcet's Disease 60 8.936
51
WGN006 Wegener Granulomatosis 57 8.936
52
CRB039 Cerebrovascular Disease 55 8.936
53
FCT006 Factor V Deficiency 54 8.936
54
P HMP007 Hemophilia 50 8.936
55
ART111 Artery Disease 49 8.936
56
c THR082 Thrombophilia Due to Activated Protein C Resistance 48 8.936
57
c ART115 Aortic Valve Disease 1 47 8.936
58
LYM008 Lymphangiosarcoma 46 8.936
59
c ALM001 Al Amyloidosis 46 8.936
60
CRT049 Critical Limb Ischemia 45 8.936
61
c ART101 Aortic Valve Disease 2 45 8.936
62
INT007 Intermediate Coronary Syndrome 44 8.936
63
HMR001 Hemorrhagic Thrombocythemia 44 8.936
64
ANG054 Angina Pectoris 42 8.936
65
P HYD002 Hydronephrosis 42 8.936
66
ESN011 Eisenmenger Syndrome 41 8.936
67
PLC005 Placental Insufficiency 41 8.936
68
VLV044 Vulvar Intraepithelial Neoplasia 40 8.936
69
HRT012 Heart Valve Disease 39 8.936
70
P AFB001 Afibrinogenemia 39 8.936
71
BWN001 Bowen-Conradi Syndrome 39 8.936
72
OST008 Osteosclerotic Myeloma 38 8.936
73
LVR002 Liver Angiosarcoma 38 8.936
74
KRN001 Korean Hemorrhagic Fever 37 8.936
75
CHL028 Childhood Type Dermatomyositis 37 8.936
76
MYX007 Myxosarcoma 37 8.936
77
P BLD051 Blood Coagulation Disease 37 8.936
78
INT013 Intramuscular Hemangioma 36 8.936
79
GNR003 Generalized Atherosclerosis 35 8.936
80
FNT004 Fainting 33 8.936
81
c INH004 Inherited Blood Coagulation Disease 33 8.936
82
ACQ017 Acquired Von Willebrand Syndrome 32 8.936
83
c PRM225 Primary Thrombocytopenia 32 8.936
84
VNW004 Von Willebrand Disease, Platelet-Type 29 8.936
85
MNC004 Monoclonal Paraproteinemia 29 8.936
86
INF011 Infiltrating Angiolipoma 28 8.936
87
SKL005 Skull Base Meningioma 26 8.936
88
SPL011 Spleen Cancer 26 8.936
89
P MLD013 Mild Hemophilia a 26 8.936
90
HYP008 Hypertensive Retinopathy 26 8.936
91
PLC002 Plica Syndrome 22 8.936
92
KHR001 Kahrizi Syndrome 22 8.936
93
c THR044 Thrombotic Thrombocytopenic Purpura, Acquired 20 8.936
94
DPN002 Deep Angioma 19 8.936
95
SPL001 Spleen Angiosarcoma 16 8.936
96
SPH003 Sphenoorbital Meningioma 16 8.936
97
DSS024 Disease of Anatomical Entity 34 6.318