Search results for "[genes] VWF"

101 hits were found for '[genes] VWF'

# Family MCID Name MIFTS Score
1
VNW001 Von Willebrand's Disease 63 19.841
2
VNW005 Von Willebrand Disease, Type 1 41 16.600
3
PRP027 Peripheral Vascular Disease 62 14.030
4
P CRN211 Coronary Artery Disease 68 12.549
5
STR067 Stroke, Ischemic 68 12.549
6
VSC007 Vascular Disease 55 12.549
7
P THR015 Thrombophilia 52 12.549
8
c ACT075 Acute Myocardial Infarction 50 12.549
9
VSC011 Vasculitis 50 12.549
10
INT002 Intermittent Claudication 48 12.549
11
ANG020 Angiosarcoma 46 12.549
12
URM002 Uremia 44 12.549
13
P HML001 Hemolytic-Uremic Syndrome 44 12.549
14
HLL004 Hellp Syndrome 42 12.549
15
ANG011 Angiodysplasia 39 12.549
16
BLD053 Blood Platelet Disease 32 12.549
17
VNW003 Von Willibrand Disease, Type 3 28 12.549
18
TYP017 Type 2n Von Willebrand Disease 26 12.549
19
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 84 10.867
20
P MYC007 Myocardial Infarction 76 10.867
21
P HRD008 Hereditary Hemorrhagic Telangiectasia 74 10.867
22
MLR004 Malaria 72 10.867
23
c HYP595 Hypertension, Essential 68 10.867
24
GLN010 Glanzmann Thrombasthenia 65 10.867
25
c HMP029 Hemophilia a 64 10.867
26
P ESS003 Essential Thrombocythemia 63 10.867
27
TKY001 Takayasu's Arteritis 57 10.867
28
BRN082 Bernard-Soulier Syndrome, Type C 51 10.867
29
P THR014 Thrombocytopenia 50 10.867
30
SPT005 Spotted Fever 49 10.867
31
c THR092 Thrombophilia Due to Thrombin Defect 49 10.867
32
P THR005 Thrombotic Thrombocytopenic Purpura 48 10.867
33
PRP030 Purpura 47 10.867
34
EVN001 Evans' Syndrome 46 10.867
35
P VNS003 Venous Insufficiency 44 10.867
36
FCT013 Factor V Leiden Thrombophilia 43 10.867
37
FCT001 Factor Viii Deficiency 42 10.867
38
CRN017 Coronary Thrombosis 42 10.867
39
VSC006 Vascular Cancer 40 10.867
40
HPT009 Hepatopulmonary Syndrome 39 10.867
41
HMR002 Hemarthrosis 39 10.867
42
DBT008 Diabetic Angiopathy 38 10.867
43
ESN011 Eisenmenger Syndrome 38 10.867
44
LMB062 Limb Ischemia 38 10.867
45
RYN001 Raynaud Disease 36 10.867
46
TYP015 Type 2b Von Willebrand Disease 33 10.867
47
VNW006 Von Willebrand Disease, Types 2a, 2b, 2m, and 2n 32 10.867
48
P BLD051 Blood Coagulation Disease 30 10.867
49
QLT001 Qualitative Platelet Defect 30 10.867
50
INT078 Intracranial Thrombosis 29 10.867
51
c INH004 Inherited Blood Coagulation Disease 25 10.867
52
TYP016 Type 2m Von Willebrand Disease 24 10.867
53
TYP014 Type 2a Von Willebrand Disease 24 10.867
54
BHC002 Behcet's Disease 63 8.873
55
WGN006 Wegener Granulomatosis 59 8.873
56
CRB039 Cerebrovascular Disease 58 8.873
57
FCT003 Factor X Deficiency 58 8.873
58
FCT006 Factor V Deficiency 54 8.873
59
GRY002 Gray Platelet Syndrome 53 8.873
60
P HMP007 Hemophilia 51 8.873
61
c THR082 Thrombophilia Due to Activated Protein C Resistance 50 8.873
62
ART111 Artery Disease 48 8.873
63
c AFB002 Afibrinogenemia, Congenital 46 8.873
64
c ART101 Aortic Valve Disease 2 46 8.873
65
c ALM001 Al Amyloidosis 45 8.873
66
INT007 Intermediate Coronary Syndrome 45 8.873
67
CRT049 Critical Limb Ischemia 44 8.873
68
CLS007 Classic Kaposi Sarcoma 44 8.873
69
P CLL015 Collagen Disease 43 8.873
70
c ART115 Aortic Valve Disease 1 43 8.873
71
P HYD002 Hydronephrosis 42 8.873
72
LYM008 Lymphangiosarcoma 41 8.873
73
P AFB001 Afibrinogenemia 41 8.873
74
ANG054 Angina Pectoris 41 8.873
75
HRT012 Heart Valve Disease 40 8.873
76
VLV044 Vulvar Intraepithelial Neoplasia 40 8.873
77
CRD144 Cardiovascular Disease Risk Factor ) 39 8.873
78
BWN001 Bowen-Conradi Syndrome 39 8.873
79
KPS002 Kaposiform Hemangioendothelioma 37 8.873
80
MDT001 Mediterranean Spotted Fever 36 8.873
81
c THR044 Thrombotic Thrombocytopenic Purpura, Acquired 36 8.873
82
INT013 Intramuscular Hemangioma 35 8.873
83
MYX007 Myxosarcoma 34 8.873
84
LVR002 Liver Angiosarcoma 33 8.873
85
OST008 Osteosclerotic Myeloma 33 8.873
86
ACQ017 Acquired Von Willebrand Syndrome 33 8.873
87
VNW004 Von Willebrand Disease, Platelet-Type 30 8.873
88
HYP008 Hypertensive Retinopathy 29 8.873
89
SKL005 Skull Base Meningioma 28 8.873
90
INF011 Infiltrating Angiolipoma 27 8.873
91
FNT004 Fainting 27 8.873
92
MNC004 Monoclonal Paraproteinemia 24 8.873
93
P MLD013 Mild Hemophilia a 24 8.873
94
SPL011 Spleen Cancer 23 8.873
95
HMN011 Hemangioma of Intra-Abdominal Structure 23 8.873
96
KHR001 Kahrizi Syndrome 23 8.873
97
DPN002 Deep Angioma 23 8.873
98
UNL013 Unilateral Absence of a Pulmonary Artery 20 8.873
99
SPL001 Spleen Angiosarcoma 18 8.873
100
PLC002 Plica Syndrome 18 8.873
101
SPH003 Sphenoorbital Meningioma 15 8.873