Search results for "[genes] VWF"

92 hits were found for '[genes] VWF'

# Family MCID Name MIFTS Score
1
VNW005 Von Willebrand Disease, Type 1 48 17.917
2
VNW007 Von Willebrand Disease 57 16.760
3
VNW006 Von Willebrand Disease, Types 2a, 2b, 2m, and 2n 35 14.165
4
STR067 Stroke, Ischemic 74 12.669
5
VNW004 Von Willebrand Disease, Platelet-Type 40 12.669
6
P MYC007 Myocardial Infarction 80 10.972
7
MLR004 Malaria 80 10.972
8
BRN082 Bernard-Soulier Syndrome, Type C 51 10.972
9
P HRD008 Hereditary Hemorrhagic Telangiectasia 72 10.972
10
P PLM037 Pulmonary Hypertension 78 10.972
11
c THR092 Thrombophilia Due to Thrombin Defect 56 10.972
12
GLN010 Glanzmann Thrombasthenia 64 10.972
13
PLM033 Pulmonary Embolism 59 10.972
14
c HMP029 Hemophilia a 61 10.972
15
CRB039 Cerebrovascular Disease 49 10.972
16
PRP027 Peripheral Vascular Disease 69 10.972
17
TKY002 Takayasu Arteritis 60 10.972
18
VNW003 Von Willibrand Disease, Type 3 29 10.972
19
PRP030 Purpura 60 10.972
20
SPT005 Spotted Fever 56 10.972
21
P HML001 Hemolytic-Uremic Syndrome 50 10.972
22
P THR015 Thrombophilia 59 10.972
23
P VNS003 Venous Insufficiency 53 10.972
24
DSS009 Disseminated Intravascular Coagulation 52 10.972
25
INT002 Intermittent Claudication 56 10.972
26
P THR005 Thrombotic Thrombocytopenic Purpura 55 10.972
27
FCT001 Factor Viii Deficiency 41 10.972
28
URM002 Uremia 36 10.972
29
ANG011 Angiodysplasia 44 10.972
30
DBT008 Diabetic Angiopathy 30 10.972
31
ANG020 Angiosarcoma 53 10.972
32
HPT009 Hepatopulmonary Syndrome 48 10.972
33
TYP017 Type 2n Von Willebrand Disease 19 10.972
34
LMB062 Limb Ischemia 48 10.972
35
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 81 8.959
36
c HYP595 Hypertension, Essential 69 8.959
37
P ESS003 Essential Thrombocythemia 66 8.959
38
c ART101 Aortic Valve Disease 2 56 8.959
39
c AFB002 Afibrinogenemia, Congenital 51 8.959
40
WGN006 Wegener Granulomatosis 63 8.959
41
FCT003 Factor X Deficiency 62 8.959
42
FCT006 Factor V Deficiency 62 8.959
43
c ART115 Aortic Valve Disease 1 53 8.959
44
c THR082 Thrombophilia Due to Activated Protein C Resistance 57 8.959
45
GRY002 Gray Platelet Syndrome 55 8.959
46
INT007 Intermediate Coronary Syndrome 52 8.959
47
RYN001 Raynaud Disease 41 8.959
48
BWN001 Bowen-Conradi Syndrome 51 8.959
49
VSC007 Vascular Disease 51 8.959
50
P HMP007 Hemophilia 55 8.959
51
KHR001 Kahrizi Syndrome 21 8.959
52
c ALM001 Al Amyloidosis 45 8.959
53
LYM008 Lymphangiosarcoma 48 8.959
54
ACT058 Active Peptic Ulcer Disease 44 8.959
55
SPL011 Spleen Cancer 38 8.959
56
CHL028 Childhood Type Dermatomyositis 40 8.959
57
HYD002 Hydronephrosis 48 8.959
58
KPS002 Kaposiform Hemangioendothelioma 41 8.959
59
KRN001 Korean Hemorrhagic Fever 39 8.959
60
PLC002 Plica Syndrome 25 8.959
61
LVR002 Liver Angiosarcoma 44 8.959
62
BLD053 Blood Platelet Disease 44 8.959
63
ACQ017 Acquired Von Willebrand Syndrome 35 8.959
64
HYP008 Hypertensive Retinopathy 33 8.959
65
QLT001 Qualitative Platelet Defect 30 8.959
66
c ACT075 Acute Myocardial Infarction 61 8.959
67
UNL013 Unilateral Absence of a Pulmonary Artery 22 8.959
68
ART111 Artery Disease 56 8.959
69
VLV044 Vulvar Intraepithelial Neoplasia 44 8.959
70
INT013 Intramuscular Hemangioma 34 8.959
71
P BLD051 Blood Coagulation Disease 44 8.959
72
SKL005 Skull Base Meningioma 29 8.959
73
SPL001 Spleen Angiosarcoma 19 8.959
74
ESN011 Eisenmenger Syndrome 45 8.959
75
c INH004 Inherited Blood Coagulation Disease 38 8.959
76
P MLD013 Mild Hemophilia a 28 8.959
77
SPH003 Sphenoorbital Meningioma 9 8.959
78
CNT046 Central Nervous System Vasculitis 44 8.959
79
MNC004 Monoclonal Paraproteinemia 35 8.959
80
MYX007 Myxosarcoma 38 8.959
81
DPN002 Deep Angioma 20 8.959
82
INF011 Infiltrating Angiolipoma 29 8.959
83
CRD144 Cardiovascular Disease Risk Factor ) 42 8.959
84
c PRM225 Primary Thrombocytopenia 42 8.959
85
ANG054 Angina Pectoris 48 8.959
86
FNT004 Fainting 33 8.959
87
ATM012 Autoimmune Disease of Blood 36 8.959
88
OST008 Osteosclerotic Myeloma 37 8.959
89
TYP014 Type 2a Von Willebrand Disease 17 8.959
90
TYP015 Type 2b Von Willebrand Disease 29 8.959
91
TYP016 Type 2m Von Willebrand Disease 18 8.959
92
DSS024 Disease of Anatomical Entity 40 6.335