Search results for "[genes] APOA1"

60 hits were found for '[genes] APOA1'

# Family MCID Name MIFTS Score
1
P CRN211 Coronary Artery Disease 75 19.104
2
P AMY004 Amyloidosis 64 17.870
3
TNG002 Tangier Disease 61 17.870
4
P AMY082 Amyloidosis, Familial Visceral 46 17.870
5
HYP121 Hypoalphalipoproteinemia 61 16.544
6
P HYP117 Hypertriglyceridemia 65 15.103
7
ART111 Artery Disease 57 15.103
8
CRN030 Coronary Stenosis 50 15.103
9
P DBT085 Diabetes Mellitus, Insulin-Dependent 80 13.508
10
P HYP607 Hypercholesterolemia, Familial 77 13.508
11
PRP027 Peripheral Vascular Disease 69 13.508
12
VSC007 Vascular Disease 67 13.508
13
ABT001 Abetalipoproteinemia 60 13.508
14
ART021 Arteriosclerosis 59 13.508
15
P PLY019 Polyneuropathy 54 13.508
16
HPT022 Hepatoblastoma 53 13.508
17
NRM003 Norum Disease 52 13.508
18
P HYP614 Hyperlipidemia, Familial Combined 51 13.508
19
P FML035 Familial Hyperlipidemia 50 13.508
20
P HYP090 Hyperalphalipoproteinemia 46 13.508
21
c HRD039 Hereditary Amyloidosis 44 13.508
22
P OBS005 Obesity 93 11.699
23
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 81 11.699
24
P MYC007 Myocardial Infarction 79 11.699
25
STR067 Stroke, Ischemic 77 11.699
26
P ALG002 Alagille Syndrome 72 11.699
27
LPP001 Lipoprotein Lipase Deficiency 65 11.699
28
ATH003 Atherosclerosis 62 11.699
29
P GLL020 Gallbladder Disease 59 11.699
30
LPD008 Lipid Metabolism Disorder 58 11.699
31
CRT016 Carotid Artery Disease 55 11.699
32
SLP001 Sleeping Sickness 48 11.699
33
c AMY087 Amyloidosis, Hereditary, Transthyretin-Related 46 11.699
34
CRB008 Cerebral Atherosclerosis 43 11.699
35
FSH001 Fish-Eye Disease 43 11.699
36
ARC001 Arcus Senilis 35 11.699
37
c HYP595 Hypertension, Essential 69 9.552
38
ISC006 Ischemic Heart Disease 68 9.552
39
CHY002 Chylomicron Retention Disease 59 9.552
40
P AVS004 Avascular Necrosis of the Femoral Head 56 9.552
41
P TRN034 Transverse Myelitis 48 9.552
42
HPT025 Hepatic Lipase Deficiency 48 9.552
43
P PLL002 Pellagra 45 9.552
44
HMZ003 Homozygous Familial Hypercholesterolemia 44 9.552
45
c ACT159 Acute Transverse Myelitis 42 9.552
46
TST018 Testicular Yolk Sac Tumor 42 9.552
47
HYP081 Hypolipoproteinemia 41 9.552
48
FTL021 Fetal Macrosomia 41 9.552
49
c HYP011 Hyperlipoproteinemia Type Iii 41 9.552
50
c AMY009 Amyloidosis Aa 39 9.552
51
DYS013 Dysbaric Osteonecrosis 33 9.552
52
FML330 Familial Lcat Deficiency 32 9.552
53
AMY005 Amyloid Neuropathy 32 9.552
54
c HYP032 Hyperlipoproteinemia Type Iv 27 9.552
55
APD001 Apo a-I Deficiency 20 9.552
56
c INH020 Inherited Metabolic Disorder 49 6.754
57
P ACQ009 Acquired Metabolic Disease 41 6.754
58
APM002 Aapoai Amyloidosis 11 6.754
59
c AP1002 Apoa1-Related Familial Visceral Amyloidosis 5 6.754
60
AP1001 Apoa1-Associated Familial High Density Lipoprotein Deficiency 3 6.754