Search results for "[genes] APOA1"

62 hits were found for '[genes] APOA1'

# Family MCID Name MIFTS Score
1
P CRN211 Coronary Artery Disease 74 19.057
2
TNG002 Tangier Disease 62 19.057
3
P AMY082 Amyloidosis, Familial Visceral 45 19.057
4
P AMY004 Amyloidosis 65 17.826
5
HYP121 Hypoalphalipoproteinemia 61 17.826
6
CRN030 Coronary Stenosis 51 16.504
7
P DBT085 Diabetes Mellitus, Insulin-Dependent 80 15.066
8
P HYP607 Hypercholesterolemia, Familial 76 15.066
9
PRP027 Peripheral Vascular Disease 69 15.066
10
VSC007 Vascular Disease 67 15.066
11
P HYP117 Hypertriglyceridemia 61 15.066
12
ABT001 Abetalipoproteinemia 60 15.066
13
ART021 Arteriosclerosis 58 15.066
14
ART111 Artery Disease 55 15.066
15
HPT022 Hepatoblastoma 55 15.066
16
NRM003 Norum Disease 51 15.066
17
P HYP614 Hyperlipidemia, Familial Combined 50 15.066
18
P HYP090 Hyperalphalipoproteinemia 48 15.066
19
P FML035 Familial Hyperlipidemia 48 15.066
20
c HRD039 Hereditary Amyloidosis 46 15.066
21
P OBS005 Obesity 92 13.475
22
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 80 13.475
23
P MYC007 Myocardial Infarction 79 13.475
24
P ALG002 Alagille Syndrome 72 13.475
25
ATH003 Atherosclerosis 65 13.475
26
CRB039 Cerebrovascular Disease 63 13.475
27
P GLL020 Gallbladder Disease 59 13.475
28
LPD008 Lipid Metabolism Disorder 58 13.475
29
CRT016 Carotid Artery Disease 57 13.475
30
SLP001 Sleeping Sickness 48 13.475
31
c AMY087 Amyloidosis, Hereditary, Transthyretin-Related 46 13.475
32
FSH001 Fish-Eye Disease 43 13.475
33
CRB008 Cerebral Atherosclerosis 43 13.475
34
ARC001 Arcus Senilis 35 13.475
35
c HYP595 Hypertension, Essential 69 11.670
36
ISC006 Ischemic Heart Disease 68 11.670
37
LPP001 Lipoprotein Lipase Deficiency 63 11.670
38
EYD002 Eye Disease 61 11.670
39
CHY002 Chylomicron Retention Disease 57 11.670
40
P AVS004 Avascular Necrosis of the Femoral Head 56 11.670
41
P TRN034 Transverse Myelitis 49 11.670
42
HPT025 Hepatic Lipase Deficiency 48 11.670
43
P PLL002 Pellagra 45 11.670
44
c ACT159 Acute Transverse Myelitis 42 11.670
45
HYP081 Hypolipoproteinemia 42 11.670
46
c HYP011 Hyperlipoproteinemia Type Iii 42 11.670
47
FTL021 Fetal Macrosomia 41 11.670
48
TST018 Testicular Yolk Sac Tumor 40 11.670
49
c AMY009 Amyloidosis Aa 39 11.670
50
FML330 Familial Lcat Deficiency 34 11.670
51
P HYP032 Hyperlipoproteinemia Type Iv 34 11.670
52
AMY005 Amyloid Neuropathy 33 11.670
53
DYS013 Dysbaric Osteonecrosis 32 11.670
54
APD001 Apo a-I Deficiency 20 11.670
55
APM002 Aapoai Amyloidosis 11 11.670
56
c AP1002 Apoa1-Related Familial Visceral Amyloidosis 5 11.670
57
AP1001 Apoa1-Associated Familial High Density Lipoprotein Deficiency 3 11.670
58
c INH020 Inherited Metabolic Disorder 49 9.528
59
LKC005 Leukocyte Adhesion Deficiency, Type Iii 47 9.528
60
c LKD015 Leukodystrophy, Hypomyelinating, 3 42 9.528
61
P ACQ009 Acquired Metabolic Disease 38 9.528
62
c AML020 Amelogenesis Imperfecta, Type Iv 33 9.528