Search results for DAPT

101 hits were found for DAPT

# Family MCID Name MIFTS Score
1
ISC004 Ischemia 58 0.420
2
LPP008 Lipoprotein Quantitative Trait Locus 62 0.393
3
ART140 Arteries, Anomalies of 52 0.374
4
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.367
5
P CRN300 Coronary Heart Disease 1 63 0.367
6
P MYC007 Myocardial Infarction 70 0.318
7
THR024 Thrombosis 57 0.299
8
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.280
9
STR067 Stroke, Ischemic 81 0.225
10
CRB039 Cerebrovascular Disease 67 0.218
11
ANG054 Angina Pectoris 66 0.159
12
INT007 Intermediate Coronary Syndrome 55 0.150
13
CRN030 Coronary Stenosis 50 0.140
14
P HRT032 Heart Disease 75 0.130
15
PRP027 Peripheral Vascular Disease 71 0.130
16
ATH013 Atherosclerosis Susceptibility 65 0.130
17
P VSC007 Vascular Disease 63 0.130
18
c ACT075 Acute Myocardial Infarction 57 0.130
19
48X005 48,xyyy 39 0.130
20
P ATR011 Atrial Fibrillation 66 0.118
21
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.106
22
P CRD246 Cardiovascular System Disease 57 0.106
23
P ART021 Arteriosclerosis 54 0.106
24
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.106
25
P OVR042 Ovarian Cancer 88 0.092
26
P GST053 Gastric Cancer 83 0.092
27
GLB015 Glioblastoma Multiforme 75 0.092
28
OST159 Osteogenic Sarcoma 66 0.092
29
c FML001 Familial Atrial Fibrillation 65 0.092
30
PRP080 Peripheral Artery Disease 53 0.092
31
CRN020 Coronary Restenosis 39 0.092
32
P CRN133 Coronary Artery Disease, Autosomal Dominant, 1 32 0.092
33
CRV035 Cervical Cancer 76 0.075
34
CNG034 Congestive Heart Failure 69 0.075
35
P THR014 Thrombocytopenia 67 0.075
36
c ART101 Aortic Valve Disease 2 65 0.075
37
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.075
38
LPD008 Lipid Metabolism Disorder 62 0.075
39
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.075
40
TNG007 Tongue Carcinoma 51 0.075
41
P BLD051 Blood Coagulation Disease 46 0.075
42
CRB004 Cerebral Artery Occlusion 45 0.075
43
P ALZ034 Alzheimer Disease 88 0.053
44
MYL069 Myeloma, Multiple 85 0.053
45
P PNC035 Pancreatic Cancer 84 0.053
46
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.053
47
END057 Endometrial Cancer 74 0.053
48
P KDN018 Kidney Disease 72 0.053
49
HMN044 Human Immunodeficiency Virus Type 1 71 0.053
50
c EXD008 Exudative Vitreoretinopathy 1 71 0.053
51
P ATS364 Autism 70 0.053
52
c CHR684 Chronic Kidney Disease 70 0.053
53
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.053
54
ART016 Aortic Aneurysm 69 0.053
55
c BSL007 Basal Cell Carcinoma 68 0.053
56
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.053
57
P TRN020 Turner Syndrome 67 0.053
58
c ATS007 Autism Spectrum Disorder 67 0.053
59
c RHB024 Rhabdomyosarcoma 2 67 0.053
60
TTN003 Tetanus 65 0.053
61
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.053
62
PRT037 Pertussis 65 0.053
63
CLN015 Colon Adenocarcinoma 65 0.053
64
PLM031 Poliomyelitis 64 0.053
65
P GLM045 Glioma 63 0.053
66
TRN015 Transient Cerebral Ischemia 63 0.053
67
ALL026 Allergic Hypersensitivity Disease 62 0.053
68
P ENC018 Encephalopathy 61 0.053
69
DPH001 Diphtheria 60 0.053
70
ACQ007 Acquired Immunodeficiency Syndrome 60 0.053
71
SQM006 Squamous Cell Carcinoma 60 0.053
72
ORL011 Oral Cancer 60 0.053
73
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.053
74
VSL002 Visual Epilepsy 59 0.053
75
ADN018 Adenoma 59 0.053
76
ANR040 Aneurysm 59 0.053
77
P BCL017 B-Cell Lymphoma 58 0.053
78
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.053
79
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.053
80
EYD002 Eye Disease 58 0.053
81
P UVT001 Uveitis 57 0.053
82
P SZR006 Seizure Disorder 56 0.053
83
BRN004 Brain Edema 56 0.053
84
ATR057 Atrioventricular Block 55 0.053
85
PRS045 Prostatic Hypertrophy 53 0.053
86
GSG001 Gas Gangrene 53 0.053
87
PRS021 Prostatic Adenoma 51 0.053
88
TRM010 Traumatic Brain Injury 51 0.053
89
P PRC012 Pericardial Effusion 51 0.053
90
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 51 0.053
91
PRS129 Prostatic Hyperplasia, Benign 49 0.053
92
P CRV031 Cervical Adenocarcinoma 49 0.053
93
HMP001 Hemopericardium 48 0.053
94
HLX001 Helix Syndrome 47 0.053
95
CRN017 Coronary Thrombosis 47 0.053
96
GLL048 Glial Tumor 45 0.053
97
THR099 Third-Degree Atrioventricular Block 45 0.053
98
c ATM099 Autoimmune Uveitis 45 0.053
99
SBC016 Subacute Delirium 44 0.053
100
TNG009 Tongue Squamous Cell Carcinoma 44 0.053
101
PRL045 Proline-Negative Auxotroph of Hamster, Complementation of 18 0.053
Content
Loading form....