Search results for "VWF"

63 hits were found for 'VWF'

# Family MCID Name MIFTS Score
1
VNW006 Von Willebrand Disease, Types 2a, 2b, 2m, and 2n 23 14.375
2
VNW003 Von Willibrand Disease, Type 3 19 6.258
3
VNW001 Von Willebrand's Disease 67 6.159
4
VNW005 Von Willebrand Disease, Type 1 39 6.159
5
PRP030 Purpura 54 3.573
6
c HMP029 Hemophilia a 66 3.386
7
P HMP007 Hemophilia 59 3.386
8
CRN017 Coronary Thrombosis 50 3.327
9
ANG011 Angiodysplasia 48 3.327
10
INT002 Intermittent Claudication 47 3.327
11
ESN011 Eisenmenger Syndrome 40 3.327
12
TYP014 Type 2a Von Willebrand Disease 29 3.001
13
TYP015 Type 2b Von Willebrand Disease 39 2.975
14
TYP017 Type 2n Von Willebrand Disease 30 2.881
15
TYP016 Type 2m Von Willebrand Disease 29 2.881
16
P THR005 Thrombotic Thrombocytopenic Purpura 53 2.622
17
P MYC007 Myocardial Infarction 81 2.461
18
c CNT016 Central Retinal Vein Occlusion 49 2.394
19
ACQ017 Acquired Von Willebrand Syndrome 41 2.394
20
VNW004 Von Willebrand Disease, Platelet-Type 31 2.394
21
P PLM037 Pulmonary Hypertension 85 2.352
22
P TMP003 Temporal Arteritis 62 2.352
23
FCT004 Factor Xii Deficiency 58 2.352
24
c ALM001 Al Amyloidosis 56 2.352
25
P AFB001 Afibrinogenemia 55 2.352
26
c MLG069 Malignant Hypertension 54 2.352
27
FCT001 Factor Viii Deficiency 51 2.352
28
VLV044 Vulvar Intraepithelial Neoplasia 48 2.352
29
DBT008 Diabetic Angiopathy 47 2.352
30
ULL001 Ullrich Congenital Muscular Dystrophy 46 2.352
31
c SVR056 Severe Hemophilia a 43 2.352
32
HMR002 Hemarthrosis 43 2.352
33
AFR002 African Tick-Bite Fever 42 2.352
34
FNT004 Fainting 33 2.352
35
P MLD013 Mild Hemophilia a 30 2.352
36
c ATM061 Autoimmune Polyglandular Syndrome Type 3 30 2.352
37
QLT001 Qualitative Platelet Defect 16 2.352
38
END072 Endotheliitis 44 0.302
39
P CSH001 Cushing's Syndrome 76 0.093
40
ISC004 Ischemia 53 0.093
41
P HML001 Hemolytic-Uremic Syndrome 43 0.093
42
P ESS003 Essential Thrombocythemia 66 0.066
43
P HYP086 Hypothyroidism 59 0.066
44
P GLM007 Glomerulonephritis 59 0.066
45
VSC007 Vascular Disease 59 0.066
46
c PRC016 Pre-Eclampsia 58 0.066
47
P THR014 Thrombocytopenia 56 0.066
48
MLN008 Melanoma 55 0.066
49
P HYP076 Hyperthyroidism 54 0.066
50
P ECL001 Eclampsia 53 0.066
51
P GLY013 Glycogen Storage Disease 51 0.066
52
P RNL101 Renal Cell Carcinoma, Papillary 59 0.066
53
HYP266 Hypoxia 49 0.066
54
P RTN022 Retinal Vein Occlusion 48 0.066
55
CTN007 Cutaneous Leishmaniasis 57 0.066
56
P HYP083 Hypopituitarism 47 0.066
57
PPT005 Peptic Ulcer Disease 45 0.066
58
RTN023 Retinitis 44 0.066
59
P CLL015 Collagen Disease 43 0.066
60
CRT049 Critical Limb Ischemia 43 0.066
61
BRN082 Bernard-Soulier Syndrome, Type C 42 0.066
62
LMB062 Limb Ischemia 38 0.066
63
c THR054 Thrombotic Thrombocytopenic Purpura, Familial 35 0.066