Search results for "[genes] SERPINE1"

83 hits were found for '[genes] SERPINE1'

# Family MCID Name MIFTS Score
1
PLS029 Plasminogen Activator Inhibitor-1 Deficiency 31 17.125
2
P CRN211 Coronary Artery Disease 69 15.855
3
P BRS047 Breast Cancer 100 14.473
4
P MYC007 Myocardial Infarction 77 14.473
5
P THR015 Thrombophilia 54 14.473
6
P FBR017 Fibrosarcoma 51 14.473
7
DSS009 Disseminated Intravascular Coagulation 49 14.473
8
P FML035 Familial Hyperlipidemia 47 14.473
9
P OBS005 Obesity 87 12.945
10
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 76 12.945
11
STR067 Stroke, Ischemic 66 12.945
12
PRP027 Peripheral Vascular Disease 59 12.945
13
P HYP117 Hypertriglyceridemia 58 12.945
14
VSC007 Vascular Disease 55 12.945
15
ART021 Arteriosclerosis 53 12.945
16
c MTB001 Metabolic Syndrome X 53 12.945
17
c ACT075 Acute Myocardial Infarction 51 12.945
18
P HYP060 Hyperinsulinism 49 12.945
19
PRT011 Protein C Deficiency 45 12.945
20
HYP037 Hyperhomocysteinemia 44 12.945
21
HLL004 Hellp Syndrome 42 12.945
22
RNL077 Renal Fibrosis 40 12.945
23
P DBT085 Diabetes Mellitus, Insulin-Dependent 77 11.211
24
P LVR013 Liver Disease 60 11.211
25
PRT036 Peritonitis 59 11.211
26
c MCR115 Microvascular Complications of Diabetes 5 57 11.211
27
LGG001 Legg-Calve-Perthes Disease 56 11.211
28
ATH003 Atherosclerosis 56 11.211
29
PLM033 Pulmonary Embolism 51 11.211
30
c THR092 Thrombophilia Due to Thrombin Defect 51 11.211
31
OST003 Osteonecrosis 51 11.211
32
PSD002 Pseudotumor Cerebri 49 11.211
33
INT002 Intermittent Claudication 47 11.211
34
LPD008 Lipid Metabolism Disorder 47 11.211
35
IDP011 Idiopathic Interstitial Pneumonia 46 11.211
36
CRN017 Coronary Thrombosis 45 11.211
37
P RTN022 Retinal Vein Occlusion 44 11.211
38
PST095 Post-Thrombotic Syndrome 42 11.211
39
c SVR005 Severe Pre-Eclampsia 42 11.211
40
PRT018 Portal Vein Thrombosis 41 11.211
41
CRN030 Coronary Stenosis 41 11.211
42
HPT046 Hepatic Veno-Occlusive Disease 40 11.211
43
FCT005 Factor Xiii Deficiency 40 11.211
44
P VNS003 Venous Insufficiency 38 11.211
45
HPT002 Hepatic Vein Thrombosis 35 11.211
46
c CHR431 Chronic Venous Insufficiency 35 11.211
47
CRT004 Carotid Artery Thrombosis 33 11.211
48
c HYP595 Hypertension, Essential 62 9.154
49
BHC002 Behcet's Disease 60 9.154
50
CRB039 Cerebrovascular Disease 55 9.154
51
DSM004 Desmoid Tumor 54 9.154
52
APP008 Appendicitis 54 9.154
53
P PRC031 Preeclampsia/eclampsia 1 49 9.154
54
ART111 Artery Disease 49 9.154
55
c PRC016 Pre-Eclampsia 48 9.154
56
c THR082 Thrombophilia Due to Activated Protein C Resistance 48 9.154
57
INT007 Intermediate Coronary Syndrome 44 9.154
58
PNM013 Pneumococcal Meningitis 43 9.154
59
LMR001 Lemierre's Syndrome 43 9.154
60
OVR063 Overnutrition 41 9.154
61
SHW001 Shwartzman Phenomenon 38 9.154
62
PRN021 Paranasal Sinus Disease 38 9.154
63
CRD144 Cardiovascular Disease Risk Factor ) 37 9.154
64
DYS013 Dysbaric Osteonecrosis 36 9.154
65
TBR009 Tuberculous Empyema 35 9.154
66
MNN021 Meningococcemia 34 9.154
67
LVD002 Livedoid Vasculopathy 33 9.154
68
CNT060 Central Serous Chorioretinopathy 33 9.154
69
BLT003 Blue Toe Syndrome 33 9.154
70
CTS005 Catastrophic Antiphospholipid Syndrome 32 9.154
71
SBN001 Subendocardial Myocardial Infarction 31 9.154
72
MCK002 Meckel's Diverticulum 31 9.154
73
ISC005 Ischemic Bone Disease 31 9.154
74
NNT024 Neonatal Stroke 29 9.154
75
ACT056 Acute Cor Pulmonale 28 9.154
76
INF133 Inferior Vena Cava Interruption 25 9.154
77
P ACT080 Acute Pulmonary Heart Disease 22 9.154
78
c THR044 Thrombotic Thrombocytopenic Purpura, Acquired 20 9.154
79
HPR003 Heparin-Induced Thrombocytopenia 44 6.473
80
GLC008 Glucose Metabolism Disease 35 6.473
81
DSS024 Disease of Anatomical Entity 34 6.473
82
P ACQ009 Acquired Metabolic Disease 33 6.473
83
CNG460 Congenital Plasminogen Activator Inhibitor Type 1 Deficiency 5 6.473