Search results for CETP

64 hits were found for CETP

# Family MCID Name MIFTS Score
1
HYP732 Hyperalphalipoproteinemia 1 51 19.453
2
c HYP607 Hypercholesterolemia, Familial 82 4.097
3
ABT001 Abetalipoproteinemia 67 3.534
4
TNG002 Tangier Disease 64 3.534
5
CRN030 Coronary Stenosis 52 3.534
6
c FML035 Familial Hyperlipidemia 50 3.534
7
c CRN300 Coronary Heart Disease 1 62 3.333
8
LPD008 Lipid Metabolism Disorder 65 3.254
9
c MYC007 Myocardial Infarction 78 3.232
10
c DBT026 Diabetes Mellitus, Noninsulin-Dependent 92 3.184
11
VSC007 Vascular Disease 72 3.184
12
ATH013 Atherosclerosis Susceptibility 61 3.184
13
ART004 Aortic Atherosclerosis 45 3.097
14
c GLL020 Gallbladder Disease 64 3.060
15
FDL002 Food Allergy 54 3.060
16
CRN020 Coronary Restenosis 39 3.060
17
c CRN018 Coronary Artery Anomaly 74 2.883
19
c CRD246 Cardiovascular System Disease 57 2.542
20
c BDY004 Body Mass Index Quantitative Trait Locus 11 74 2.499
21
LCT022 Lecithin:cholesterol Acyltransferase Deficiency 61 2.499
22
P ALZ049 Alzheimer Disease 2 61 2.499
23
c HYP724 Hyperlipoproteinemia, Type Iii 61 2.499
24
HYP190 Hypoalphalipoproteinemia, Primary 59 2.499
25
c HYP750 Hypertriglyceridemia, Familial 58 2.499
26
P HNT010 Huntington Disease-Like 1 50 2.499
27
ARC023 Arcus Corneae 41 2.499
28
P HYP290 Hypobetalipoproteinemia, Familial, 2 39 2.499
29
FRT005 Fruit Allergy 28 2.499
30
VST003 Vestibular Nystagmus 26 2.499
31
BSL001 Basilar Artery Insufficiency 19 2.499
32
CHR570 Cherry Allergy 14 2.499
33
ART140 Arteries, Anomalies of 67 2.174
34
c HRT032 Heart Disease 76 0.225
35
c ALZ034 Alzheimer Disease 88 0.192
36
c DBT009 Diabetes Mellitus 67 0.166
37
DST081 Distal Trisomy 11q 20 0.136
38
c ATR011 Atrial Fibrillation 69 0.118
39
ISC004 Ischemia 67 0.118
40
CYT017 Cytophagic Histiocytic Panniculitis 26 0.118
41
DPR016 Depression 73 0.096
42
DMN002 Dementia 69 0.096
43
FTT001 Fatty Liver Disease 66 0.096
44
c HYP086 Hypothyroidism 66 0.096
45
c ART021 Arteriosclerosis 61 0.096
46
P CHR020 Chronic Interstitial Cystitis 39 0.096
47
TQP001 Taqi Polymorphism 35 0.096
48
P HYP595 Hypertension, Essential 77 0.068
49
ISC006 Ischemic Heart Disease 72 0.068
50
CNG034 Congestive Heart Failure 71 0.068
51
ART016 Aortic Aneurysm 71 0.068
52
LWC002 Lowe Oculocerebrorenal Syndrome 67 0.068
53
P ART138 Aortic Aneurysm, Familial Abdominal, 1 66 0.068
54
c END044 Endometriosis 65 0.068
55
SCH014 Schistosomiasis 62 0.068
56
HMR039 Hemorrhage, Intracerebral 62 0.068
57
P FTT008 Fatty Liver Disease, Nonalcoholic 1 61 0.068
58
c NPH012 Nephrotic Syndrome 59 0.068
59
VSC002 Vascular Dementia 58 0.068
61
NNL002 Nonalcoholic Steatohepatitis 55 0.068
62
CRB085 Cerebral Hemorrhage 46 0.068
63
DGS002 Degos 'en Cocarde' Erythrokeratoderma 26 0.068
64
RPD005 Rapidly Involuting Congenital Hemangioma 24 0.068
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