Search results for "[genes] SERPINE1"

77 hits were found for '[genes] SERPINE1'

# Family MCID Name MIFTS Score
1
PLS029 Plasminogen Activator Inhibitor-1 Deficiency 38 17.310
2
P CRN211 Coronary Artery Disease 68 16.026
3
P BRS047 Breast Cancer 100 14.630
4
P THR015 Thrombophilia 52 14.630
5
P FBR017 Fibrosarcoma 50 14.630
6
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 84 13.085
7
STR067 Stroke, Ischemic 68 13.085
8
PRP027 Peripheral Vascular Disease 62 13.085
9
P HYP117 Hypertriglyceridemia 56 13.085
10
VSC007 Vascular Disease 55 13.085
11
c MTB001 Metabolic Syndrome X 52 13.085
12
ART021 Arteriosclerosis 51 13.085
13
c ACT075 Acute Myocardial Infarction 50 13.085
14
DSS009 Disseminated Intravascular Coagulation 48 13.085
15
P HYP060 Hyperinsulinism 44 13.085
16
HLL004 Hellp Syndrome 42 13.085
17
HYP037 Hyperhomocysteinemia 40 13.085
18
RNL077 Renal Fibrosis 37 13.085
19
P OBS005 Obesity 89 11.332
20
P DBT085 Diabetes Mellitus, Insulin-Dependent 82 11.332
21
P MYC007 Myocardial Infarction 76 11.332
22
c HYP595 Hypertension, Essential 68 11.332
23
P ADL010 Adult Respiratory Distress Syndrome 55 11.332
24
PLM033 Pulmonary Embolism 53 11.332
25
LGG001 Legg-Calve-Perthes Disease 52 11.332
26
OST003 Osteonecrosis 50 11.332
27
c THR092 Thrombophilia Due to Thrombin Defect 49 11.332
28
INT002 Intermittent Claudication 48 11.332
29
THR016 Thrombophlebitis 48 11.332
30
P MCR115 Microvascular Complications of Diabetes 5 47 11.332
31
INT075 Intracranial Hypertension 46 11.332
32
IDP011 Idiopathic Interstitial Pneumonia 46 11.332
33
P RTN022 Retinal Vein Occlusion 45 11.332
34
P VNS003 Venous Insufficiency 44 11.332
35
CRN017 Coronary Thrombosis 42 11.332
36
INF034 Infective Endocarditis 42 11.332
37
PRT018 Portal Vein Thrombosis 41 11.332
38
CRN030 Coronary Stenosis 40 11.332
39
CRS001 Crescentic Glomerulonephritis 38 11.332
40
PST095 Post-Thrombotic Syndrome 38 11.332
41
PLC001 Placenta Accreta 36 11.332
42
c CHR431 Chronic Venous Insufficiency 35 11.332
43
HPT002 Hepatic Vein Thrombosis 32 11.332
44
CRT004 Carotid Artery Thrombosis 32 11.332
45
CRB039 Cerebrovascular Disease 58 9.253
46
c PRC016 Pre-Eclampsia 51 9.253
47
c THR082 Thrombophilia Due to Activated Protein C Resistance 50 9.253
48
ART111 Artery Disease 48 9.253
49
P PRC031 Preeclampsia/eclampsia 1 47 9.253
50
P ECL001 Eclampsia 47 9.253
51
LPD008 Lipid Metabolism Disorder 45 9.253
52
LMR001 Lemierre's Syndrome 43 9.253
53
P CLR030 Clear Cell Renal Cell Carcinoma 43 9.253
54
QBC001 Quebec Platelet Disorder 39 9.253
55
CRD144 Cardiovascular Disease Risk Factor ) 39 9.253
56
PRN021 Paranasal Sinus Disease 38 9.253
57
P RTN014 Retinal Artery Occlusion 38 9.253
58
MDD003 Middle Cerebral Artery Infarction 36 9.253
59
c THR044 Thrombotic Thrombocytopenic Purpura, Acquired 36 9.253
60
MCK002 Meckel's Diverticulum 35 9.253
61
CHN053 Chondromyxoid Fibroma 35 9.253
62
ARG001 Argentine Hemorrhagic Fever 34 9.253
63
CTS005 Catastrophic Antiphospholipid Syndrome 34 9.253
64
P ART084 Arteriovenous Fistula 34 9.253
65
MNN021 Meningococcemia 33 9.253
66
DYS013 Dysbaric Osteonecrosis 33 9.253
67
LVD002 Livedoid Vasculopathy 32 9.253
68
BLT003 Blue Toe Syndrome 31 9.253
69
NNT024 Neonatal Stroke 31 9.253
70
AMR003 Amaurosis Fugax 30 9.253
71
CNT060 Central Serous Chorioretinopathy 30 9.253
72
SBN001 Subendocardial Myocardial Infarction 28 9.253
73
ACT056 Acute Cor Pulmonale 27 9.253
74
INF133 Inferior Vena Cava Interruption 26 9.253
75
P ACT080 Acute Pulmonary Heart Disease 20 9.253
76
CNG460 Congenital Plasminogen Activator Inhibitor Type 1 Deficiency 6 9.253
77
P ESS003 Essential Thrombocythemia 63 6.543