Search results for "[genes] SERPINE1"

87 hits were found for '[genes] SERPINE1'

# Family MCID Name MIFTS Score
1
PLS029 Plasminogen Activator Inhibitor-1 Deficiency 43 18.074
2
P BRS047 Breast Cancer 100 14.288
3
P HYP117 Hypertriglyceridemia 65 14.288
4
STR067 Stroke, Ischemic 74 12.780
5
P MYC007 Myocardial Infarction 80 12.780
6
P THR015 Thrombophilia 59 12.780
7
P FBR017 Fibrosarcoma 55 12.780
8
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 81 11.068
9
P DBT085 Diabetes Mellitus, Insulin-Dependent 80 11.068
10
P CRN211 Coronary Artery Disease 74 11.068
11
LGG001 Legg-Calve-Perthes Disease 58 11.068
12
c THR092 Thrombophilia Due to Thrombin Defect 56 11.068
13
PLM033 Pulmonary Embolism 59 11.068
14
CRB039 Cerebrovascular Disease 49 11.068
15
BRG013 Buerger Disease 54 11.068
16
THR016 Thrombophlebitis 55 11.068
17
PRT036 Peritonitis 65 11.068
18
c MCR115 Microvascular Complications of Diabetes 5 60 11.068
19
VSC007 Vascular Disease 51 11.068
20
P ADL010 Adult Respiratory Distress Syndrome 60 11.068
21
IDP011 Idiopathic Interstitial Pneumonia 57 11.068
22
P ANT006 Antiphospholipid Syndrome 60 11.068
23
KLN001 Klinefelter's Syndrome 52 11.068
24
P ABD003 Abdominal Aortic Aneurysm 43 11.068
25
OST003 Osteonecrosis 45 11.068
26
P VNS003 Venous Insufficiency 53 11.068
27
DSS009 Disseminated Intravascular Coagulation 52 11.068
28
INT002 Intermittent Claudication 56 11.068
29
ART021 Arteriosclerosis 59 11.068
30
INT075 Intracranial Hypertension 52 11.068
31
FCT005 Factor Xiii Deficiency 42 11.068
32
HPT046 Hepatic Veno-Occlusive Disease 46 11.068
33
P HYP060 Hyperinsulinism 58 11.068
34
PST095 Post-Thrombotic Syndrome 48 11.068
35
HLL004 Hellp Syndrome 48 11.068
36
INF034 Infective Endocarditis 50 11.068
37
PRT018 Portal Vein Thrombosis 48 11.068
38
c ACT075 Acute Myocardial Infarction 61 11.068
39
HPT002 Hepatic Vein Thrombosis 38 11.068
40
PLC001 Placenta Accreta 39 11.068
41
CRN030 Coronary Stenosis 50 11.068
42
P RTN022 Retinal Vein Occlusion 36 11.068
43
CRS001 Crescentic Glomerulonephritis 41 11.068
44
c CHR431 Chronic Venous Insufficiency 43 11.068
45
RNL077 Renal Fibrosis 48 11.068
46
c HYP595 Hypertension, Essential 69 9.037
47
P OBS005 Obesity 91 9.037
48
P ESS003 Essential Thrombocythemia 66 9.037
49
P PRC031 Preeclampsia/eclampsia 1 53 9.037
50
c THR082 Thrombophilia Due to Activated Protein C Resistance 57 9.037
51
c MTB001 Metabolic Syndrome X 61 9.037
52
QBC001 Quebec Platelet Disorder 51 9.037
53
APP008 Appendicitis 61 9.037
54
c PRC016 Pre-Eclampsia 57 9.037
55
MCK002 Meckel's Diverticulum 36 9.037
56
ARG001 Argentine Hemorrhagic Fever 35 9.037
57
LMR001 Lemierre's Syndrome 43 9.037
58
DSM004 Desmoid Tumor 55 9.037
59
AMR003 Amaurosis Fugax 38 9.037
60
LVD002 Livedoid Vasculopathy 33 9.037
61
CNT060 Central Serous Chorioretinopathy 42 9.037
62
NNT024 Neonatal Stroke 34 9.037
63
URT031 Ureteral Disease 45 9.037
64
ART111 Artery Disease 56 9.037
65
ISC015 Ischemic Colitis 38 9.037
66
PRN021 Paranasal Sinus Disease 50 9.037
67
CTS005 Catastrophic Antiphospholipid Syndrome 39 9.037
68
DYS013 Dysbaric Osteonecrosis 33 9.037
69
TBR009 Tuberculous Empyema 25 9.037
70
SHW001 Shwartzman Phenomenon 38 9.037
71
CHN053 Chondromyxoid Fibroma 38 9.037
72
INF133 Inferior Vena Cava Interruption 28 9.037
73
c MLG080 Malignant Secondary Hypertension 28 9.037
74
P RTN014 Retinal Artery Occlusion 32 9.037
75
P ACT080 Acute Pulmonary Heart Disease 31 9.037
76
BLT003 Blue Toe Syndrome 33 9.037
77
CRD144 Cardiovascular Disease Risk Factor ) 42 9.037
78
ACT056 Acute Cor Pulmonale 29 9.037
79
ISC005 Ischemic Bone Disease 38 9.037
80
SBN001 Subendocardial Myocardial Infarction 33 9.037
81
c MLG003 Malignant Renovascular Hypertension 20 9.037
82
MNN021 Meningococcemia 35 9.037
83
ATS001 Autistic Disorder 60 6.390
84
GLC008 Glucose Metabolism Disease 44 6.390
85
OVR063 Overnutrition 49 6.390
86
DSS024 Disease of Anatomical Entity 40 6.390
87
P ACQ009 Acquired Metabolic Disease 42 6.390