Search results for "[genes] VWF"

97 hits were found for '[genes] VWF'

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