Search results for "[genes] VWF"

98 hits were found for '[genes] VWF'

# Family MCID Name MIFTS Score
1
VNW001 Von Willebrand's Disease 61 18.810
2
VNW005 Von Willebrand Disease, Type 1 50 17.734
3
STR067 Stroke, Ischemic 77 14.020
4
PRP027 Peripheral Vascular Disease 69 14.020
5
VNW006 Von Willebrand Disease, Types 2a, 2b, 2m, and 2n 37 14.020
6
VNW003 Von Willibrand Disease, Type 3 29 14.020
7
P CRN211 Coronary Artery Disease 75 12.540
8
P ESS003 Essential Thrombocythemia 68 12.540
9
VSC007 Vascular Disease 67 12.540
10
c HMP029 Hemophilia a 64 12.540
11
VSC011 Vasculitis 62 12.540
12
c ACT075 Acute Myocardial Infarction 60 12.540
13
P THR015 Thrombophilia 59 12.540
14
INT002 Intermittent Claudication 56 12.540
15
ANG020 Angiosarcoma 52 12.540
16
URM002 Uremia 50 12.540
17
P HML001 Hemolytic-Uremic Syndrome 50 12.540
18
HLL004 Hellp Syndrome 49 12.540
19
BLD053 Blood Platelet Disease 46 12.540
20
ANG011 Angiodysplasia 44 12.540
21
TYP014 Type 2a Von Willebrand Disease 19 12.540
22
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 81 10.860
23
MLR004 Malaria 79 10.860
24
P MYC007 Myocardial Infarction 79 10.860
25
P PLM037 Pulmonary Hypertension 79 10.860
26
P HRD008 Hereditary Hemorrhagic Telangiectasia 71 10.860
27
P THR014 Thrombocytopenia 64 10.860
28
GLN010 Glanzmann Thrombasthenia 63 10.860
29
TKY002 Takayasu Arteritis 60 10.860
30
P PRT013 Portal Hypertension 59 10.860
31
PRP030 Purpura 59 10.860
32
P HMR003 Hemorrhagic Disease 57 10.860
33
SPT005 Spotted Fever 56 10.860
34
c THR092 Thrombophilia Due to Thrombin Defect 56 10.860
35
P THR005 Thrombotic Thrombocytopenic Purpura 55 10.860
36
VSC006 Vascular Cancer 54 10.860
37
c AFB002 Afibrinogenemia, Congenital 54 10.860
38
P VNS003 Venous Insufficiency 53 10.860
39
BRN082 Bernard-Soulier Syndrome, Type C 50 10.860
40
P CLL015 Collagen Disease 49 10.860
41
LMB062 Limb Ischemia 48 10.860
42
HPT009 Hepatopulmonary Syndrome 48 10.860
43
HMR002 Hemarthrosis 48 10.860
44
CRN017 Coronary Thrombosis 48 10.860
45
DBT008 Diabetic Angiopathy 45 10.860
46
ESN011 Eisenmenger Syndrome 44 10.860
47
RYN001 Raynaud Disease 44 10.860
48
QLT001 Qualitative Platelet Defect 32 10.860
49
TYP015 Type 2b Von Willebrand Disease 30 10.860
50
TYP017 Type 2n Von Willebrand Disease 18 10.860
51
TYP016 Type 2m Von Willebrand Disease 17 10.860
52
c HYP595 Hypertension, Essential 69 8.867
53
FCT003 Factor X Deficiency 62 8.867
54
WGN006 Wegener Granulomatosis 62 8.867
55
P PRC031 Preeclampsia/eclampsia 1 57 8.867
56
c THR082 Thrombophilia Due to Activated Protein C Resistance 57 8.867
57
ART111 Artery Disease 57 8.867
58
FCT022 Factor Xi Deficiency, Autosomal Recessive 56 8.867
59
P HMP007 Hemophilia 56 8.867
60
c ART101 Aortic Valve Disease 2 55 8.867
61
GRY002 Gray Platelet Syndrome 55 8.867
62
c ART115 Aortic Valve Disease 1 53 8.867
63
INT007 Intermediate Coronary Syndrome 52 8.867
64
ANG054 Angina Pectoris 51 8.867
65
CRT049 Critical Limb Ischemia 51 8.867
66
IMM136 Immune System Disease 50 8.867
67
LYM008 Lymphangiosarcoma 48 8.867
68
ACT058 Active Peptic Ulcer Disease 46 8.867
69
VLV044 Vulvar Intraepithelial Neoplasia 46 8.867
70
P AFB001 Afibrinogenemia 46 8.867
71
P BLD051 Blood Coagulation Disease 45 8.867
72
HDN002 Head Injury 45 8.867
73
LVR002 Liver Angiosarcoma 44 8.867
74
c THR044 Thrombotic Thrombocytopenic Purpura, Acquired 43 8.867
75
c PRM225 Primary Thrombocytopenia 42 8.867
76
KPS002 Kaposiform Hemangioendothelioma 41 8.867
77
CRD144 Cardiovascular Disease Risk Factor ) 40 8.867
78
CHL028 Childhood Type Dermatomyositis 40 8.867
79
KRN001 Korean Hemorrhagic Fever 40 8.867
80
HYP008 Hypertensive Retinopathy 40 8.867
81
c INH004 Inherited Blood Coagulation Disease 39 8.867
82
MYX007 Myxosarcoma 39 8.867
83
ATM012 Autoimmune Disease of Blood 37 8.867
84
MNC004 Monoclonal Paraproteinemia 37 8.867
85
ACQ017 Acquired Von Willebrand Syndrome 36 8.867
86
OST008 Osteosclerotic Myeloma 36 8.867
87
FNT004 Fainting 33 8.867
88
INT013 Intramuscular Hemangioma 33 8.867
89
INF011 Infiltrating Angiolipoma 31 8.867
90
VNW004 Von Willebrand Disease, Platelet-Type 30 8.867
91
SKL005 Skull Base Meningioma 30 8.867
92
P MLD013 Mild Hemophilia a 30 8.867
93
PLC002 Plica Syndrome 25 8.867
94
DPN002 Deep Angioma 21 8.867
95
KHR001 Kahrizi Syndrome 21 8.867
96
UNL013 Unilateral Absence of a Pulmonary Artery 18 8.867
97
SPL001 Spleen Angiosarcoma 17 8.867
98
SPH003 Sphenoorbital Meningioma 9 8.867