Search results for "[genes] SERPINE1"

83 hits were found for '[genes] SERPINE1'

# Family MCID Name MIFTS Score
1
PLS029 Plasminogen Activator Inhibitor-1 Deficiency 33 17.125
2
P CRN211 Coronary Artery Disease 74 15.855
3
P BRS047 Breast Cancer 100 14.473
4
P MYC007 Myocardial Infarction 80 14.473
5
P FBR017 Fibrosarcoma 60 14.473
6
P THR015 Thrombophilia 57 14.473
7
DSS009 Disseminated Intravascular Coagulation 55 14.473
8
P FML035 Familial Hyperlipidemia 53 14.473
9
P OBS005 Obesity 91 12.945
10
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 80 12.945
11
STR067 Stroke, Ischemic 73 12.945
12
PRP027 Peripheral Vascular Disease 72 12.945
13
VSC007 Vascular Disease 70 12.945
14
P HYP117 Hypertriglyceridemia 65 12.945
15
c MTB001 Metabolic Syndrome X 64 12.945
16
c ACT075 Acute Myocardial Infarction 64 12.945
17
ART021 Arteriosclerosis 61 12.945
18
P HYP060 Hyperinsulinism 58 12.945
19
PRT011 Protein C Deficiency 57 12.945
20
HYP037 Hyperhomocysteinemia 50 12.945
21
RNL077 Renal Fibrosis 50 12.945
22
HLL004 Hellp Syndrome 50 12.945
23
P DBT085 Diabetes Mellitus, Insulin-Dependent 80 11.211
24
P LVR013 Liver Disease 73 11.211
25
PRT036 Peritonitis 68 11.211
26
ATH003 Atherosclerosis 65 11.211
27
OST003 Osteonecrosis 62 11.211
28
c MCR115 Microvascular Complications of Diabetes 5 61 11.211
29
INT002 Intermittent Claudication 59 11.211
30
IDP011 Idiopathic Interstitial Pneumonia 58 11.211
31
LGG001 Legg-Calve-Perthes Disease 57 11.211
32
c THR092 Thrombophilia Due to Thrombin Defect 58 11.211
33
PLM033 Pulmonary Embolism 57 11.211
34
LPD008 Lipid Metabolism Disorder 56 11.211
35
PSD002 Pseudotumor Cerebri 56 11.211
36
c SVR005 Severe Pre-Eclampsia 53 11.211
37
CRN030 Coronary Stenosis 53 11.211
38
P RTN022 Retinal Vein Occlusion 52 11.211
39
PST095 Post-Thrombotic Syndrome 51 11.211
40
CRN017 Coronary Thrombosis 49 11.211
41
PRT018 Portal Vein Thrombosis 49 11.211
42
HPT046 Hepatic Veno-Occlusive Disease 48 11.211
43
P VNS003 Venous Insufficiency 46 11.211
44
HPT002 Hepatic Vein Thrombosis 45 11.211
45
FCT005 Factor Xiii Deficiency 43 11.211
46
c CHR431 Chronic Venous Insufficiency 41 11.211
47
CRT004 Carotid Artery Thrombosis 41 11.211
48
BHC002 Behcet's Disease 69 9.154
49
CRB039 Cerebrovascular Disease 67 9.154
50
c HYP595 Hypertension, Essential 68 9.154
51
DSM004 Desmoid Tumor 65 9.154
52
APP008 Appendicitis 64 9.154
53
ART111 Artery Disease 61 9.154
54
c PRC016 Pre-Eclampsia 60 9.154
55
INT007 Intermediate Coronary Syndrome 56 9.154
56
P PRC031 Preeclampsia/eclampsia 1 54 9.154
57
OVR063 Overnutrition 51 9.154
58
PNM013 Pneumococcal Meningitis 50 9.154
59
c THR082 Thrombophilia Due to Activated Protein C Resistance 50 9.154
60
PRN021 Paranasal Sinus Disease 49 9.154
61
LMR001 Lemierre's Syndrome 47 9.154
62
c THR044 Thrombotic Thrombocytopenic Purpura, Acquired 46 9.154
63
MNN021 Meningococcemia 42 9.154
64
CNT060 Central Serous Chorioretinopathy 41 9.154
65
ISC005 Ischemic Bone Disease 40 9.154
66
SHW001 Shwartzman Phenomenon 39 9.154
67
CRD144 Cardiovascular Disease Risk Factor ) 39 9.154
68
CTS005 Catastrophic Antiphospholipid Syndrome 39 9.154
69
BLT003 Blue Toe Syndrome 38 9.154
70
DYS013 Dysbaric Osteonecrosis 38 9.154
71
TBR009 Tuberculous Empyema 38 9.154
72
SBN001 Subendocardial Myocardial Infarction 38 9.154
73
NNT024 Neonatal Stroke 38 9.154
74
LVD002 Livedoid Vasculopathy 37 9.154
75
ACT056 Acute Cor Pulmonale 33 9.154
76
P ACT080 Acute Pulmonary Heart Disease 33 9.154
77
MCK002 Meckel's Diverticulum 32 9.154
78
INF133 Inferior Vena Cava Interruption 30 9.154
79
HPR003 Heparin-Induced Thrombocytopenia 53 6.473
80
GLC008 Glucose Metabolism Disease 47 6.473
81
P ACQ009 Acquired Metabolic Disease 43 6.473
82
DSS024 Disease of Anatomical Entity 43 6.473
83
CNG460 Congenital Plasminogen Activator Inhibitor Type 1 Deficiency 5 6.473