Search results for "[genes] VWF"

37 hits were found for '[genes] VWF'

# Family MCID Name MIFTS Score
1
VNW006 Von Willebrand Disease, Types 2a, 2b, 2m, and 2n 23 62.001
2
VNW003 Von Willibrand Disease, Type 3 19 26.968
3
VNW001 Von Willebrand's Disease 67 24.967
4
VNW005 Von Willebrand Disease, Type 1 39 24.967
5
c HMP029 Hemophilia a 66 14.415
6
P HMP007 Hemophilia 59 14.415
7
PRP030 Purpura 54 14.415
8
CRN017 Coronary Thrombosis 50 14.415
9
ANG011 Angiodysplasia 48 14.415
10
INT002 Intermittent Claudication 47 14.415
11
ESN011 Eisenmenger Syndrome 40 14.415
12
TYP015 Type 2b Von Willebrand Disease 39 12.484
13
TYP017 Type 2n Von Willebrand Disease 30 12.484
14
TYP014 Type 2a Von Willebrand Disease 29 12.484
15
TYP016 Type 2m Von Willebrand Disease 29 12.484
16
P PLM037 Pulmonary Hypertension 85 10.193
17
P MYC007 Myocardial Infarction 81 10.193
18
P TMP003 Temporal Arteritis 62 10.193
19
FCT004 Factor Xii Deficiency 58 10.193
20
c ALM001 Al Amyloidosis 56 10.193
21
P AFB001 Afibrinogenemia 55 10.193
22
c MLG069 Malignant Hypertension 54 10.193
23
P THR005 Thrombotic Thrombocytopenic Purpura 53 10.193
24
FCT001 Factor Viii Deficiency 51 10.193
25
c CNT016 Central Retinal Vein Occlusion 49 10.193
26
VLV044 Vulvar Intraepithelial Neoplasia 48 10.193
27
DBT008 Diabetic Angiopathy 47 10.193
28
ULL001 Ullrich Congenital Muscular Dystrophy 46 10.193
29
c SVR056 Severe Hemophilia a 43 10.193
30
HMR002 Hemarthrosis 43 10.193
31
AFR002 African Tick-Bite Fever 42 10.193
32
ACQ017 Acquired Von Willebrand Syndrome 41 10.193
33
FNT004 Fainting 33 10.193
34
VNW004 Von Willebrand Disease, Platelet-Type 31 10.193
35
P MLD013 Mild Hemophilia a 30 10.193
36
c ATM061 Autoimmune Polyglandular Syndrome Type 3 30 10.193
37
QLT001 Qualitative Platelet Defect 16 10.193