Search results for "[genes] VWF"

105 hits were found for '[genes] VWF'

# Family MCID Name MIFTS Score
1
VNW001 Von Willebrand's Disease 61 18.652
2
VNW005 Von Willebrand Disease, Type 1 49 16.449
3
PRP027 Peripheral Vascular Disease 69 15.229
4
VNW006 Von Willebrand Disease, Types 2a, 2b, 2m, and 2n 42 15.229
5
VNW003 Von Willibrand Disease, Type 3 30 15.229
6
STR067 Stroke, Ischemic 75 13.902
7
P CRN211 Coronary Artery Disease 74 13.902
8
P ESS003 Essential Thrombocythemia 70 13.902
9
VSC007 Vascular Disease 67 13.902
10
c HMP029 Hemophilia a 63 13.902
11
VSC011 Vasculitis 62 13.902
12
c ACT075 Acute Myocardial Infarction 60 13.902
13
P THR015 Thrombophilia 59 13.902
14
P HMR003 Hemorrhagic Disease 57 13.902
15
INT002 Intermittent Claudication 56 13.902
16
ANG020 Angiosarcoma 53 13.902
17
P HML001 Hemolytic-Uremic Syndrome 51 13.902
18
HLL004 Hellp Syndrome 50 13.902
19
URM002 Uremia 48 13.902
20
BLD053 Blood Platelet Disease 46 13.902
21
ANG011 Angiodysplasia 44 13.902
22
MLR004 Malaria 83 12.435
23
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 80 12.435
24
P PLM037 Pulmonary Hypertension 79 12.435
25
P MYC007 Myocardial Infarction 79 12.435
26
P HRD008 Hereditary Hemorrhagic Telangiectasia 72 12.435
27
P THR014 Thrombocytopenia 64 12.435
28
GLN010 Glanzmann Thrombasthenia 63 12.435
29
TKY002 Takayasu Arteritis 61 12.435
30
P PRT013 Portal Hypertension 60 12.435
31
PRP030 Purpura 58 12.435
32
THR024 Thrombosis 57 12.435
33
P THR005 Thrombotic Thrombocytopenic Purpura 55 12.435
34
c THR092 Thrombophilia Due to Thrombin Defect 54 12.435
35
c AFB002 Afibrinogenemia, Congenital 54 12.435
36
P VNS003 Venous Insufficiency 54 12.435
37
SPT005 Spotted Fever 53 12.435
38
VSC006 Vascular Cancer 51 12.435
39
P CLL015 Collagen Disease 50 12.435
40
BRN082 Bernard-Soulier Syndrome, Type C 50 12.435
41
LMB062 Limb Ischemia 48 12.435
42
CRN017 Coronary Thrombosis 48 12.435
43
HMR002 Hemarthrosis 48 12.435
44
HPT009 Hepatopulmonary Syndrome 48 12.435
45
ESN011 Eisenmenger Syndrome 45 12.435
46
DBT008 Diabetic Angiopathy 44 12.435
47
RYN001 Raynaud Disease 43 12.435
48
QLT001 Qualitative Platelet Defect 32 12.435
49
c HYP595 Hypertension, Essential 69 10.769
50
WGN006 Wegener Granulomatosis 63 10.769
51
FCT003 Factor X Deficiency 61 10.769
52
P HMP007 Hemophilia 57 10.769
53
ART111 Artery Disease 55 10.769
54
GRY002 Gray Platelet Syndrome 55 10.769
55
c THR082 Thrombophilia Due to Activated Protein C Resistance 54 10.769
56
c ART101 Aortic Valve Disease 2 53 10.769
57
FCT022 Factor Xi Deficiency, Autosomal Recessive 53 10.769
58
CRT049 Critical Limb Ischemia 51 10.769
59
IMM136 Immune System Disease 51 10.769
60
c ART115 Aortic Valve Disease 1 50 10.769
61
INT007 Intermediate Coronary Syndrome 50 10.769
62
ANG054 Angina Pectoris 50 10.769
63
P AFB001 Afibrinogenemia 48 10.769
64
LYM008 Lymphangiosarcoma 47 10.769
65
VLV044 Vulvar Intraepithelial Neoplasia 47 10.769
66
HDN002 Head Injury 45 10.769
67
LVR002 Liver Angiosarcoma 43 10.769
68
ACT058 Active Peptic Ulcer Disease 43 10.769
69
CHL028 Childhood Type Dermatomyositis 42 10.769
70
c THR044 Thrombotic Thrombocytopenic Purpura, Acquired 42 10.769
71
P BLD051 Blood Coagulation Disease 42 10.769
72
KPS002 Kaposiform Hemangioendothelioma 41 10.769
73
CRD144 Cardiovascular Disease Risk Factor ) 40 10.769
74
HYP008 Hypertensive Retinopathy 40 10.769
75
KRN001 Korean Hemorrhagic Fever 39 10.769
76
c PRM225 Primary Thrombocytopenia 39 10.769
77
MYX007 Myxosarcoma 38 10.769
78
ACQ017 Acquired Von Willebrand Syndrome 37 10.769
79
c INH004 Inherited Blood Coagulation Disease 36 10.769
80
OST008 Osteosclerotic Myeloma 36 10.769
81
INT078 Intracranial Thrombosis 36 10.769
82
ATM012 Autoimmune Disease of Blood 35 10.769
83
MNC004 Monoclonal Paraproteinemia 34 10.769
84
FNT004 Fainting 33 10.769
85
INT013 Intramuscular Hemangioma 33 10.769
86
INF011 Infiltrating Angiolipoma 32 10.769
87
VNW004 Von Willebrand Disease, Platelet-Type 31 10.769
88
TYP015 Type 2b Von Willebrand Disease 30 10.769
89
SKL005 Skull Base Meningioma 29 10.769
90
P MLD013 Mild Hemophilia a 29 10.769
91
DPN002 Deep Angioma 21 10.769
92
PLC002 Plica Syndrome 21 10.769
93
UNL013 Unilateral Absence of a Pulmonary Artery 21 10.769
94
KHR001 Kahrizi Syndrome 21 10.769
95
TYP014 Type 2a Von Willebrand Disease 20 10.769
96
TYP017 Type 2n Von Willebrand Disease 19 10.769
97
TYP016 Type 2m Von Willebrand Disease 18 10.769
98
SPL001 Spleen Angiosarcoma 17 10.769
99
SPH003 Sphenoorbital Meningioma 9 10.769
100
CRB039 Cerebrovascular Disease 63 8.793
101
c HMP013 Hemophagocytic Lymphohistiocytosis, Familial, 3 37 8.793
102
c DFN130 Deafness, Autosomal Recessive 21 34 8.793
103
c DBT051 Diabetes Mellitus, Insulin-Dependent, 17 29 8.793
104
ANM031 Anomalous Left Coronary Artery from the Pulmonary Artery 24 8.793
105
c ALZ041 Alzheimer's Disease 13 23 8.793