Search results for "[genes] APOA1"

57 hits were found for '[genes] APOA1'

# Family MCID Name MIFTS Score
1
P AMY082 Amyloidosis, Familial Visceral 45 18.009
2
P CRN211 Coronary Artery Disease 74 16.673
3
TNG002 Tangier Disease 61 16.673
4
HYP121 Hypoalphalipoproteinemia 61 16.673
5
P HYP117 Hypertriglyceridemia 65 16.673
6
P AMY004 Amyloidosis 63 16.673
7
ART111 Artery Disease 56 15.221
8
P DBT085 Diabetes Mellitus, Insulin-Dependent 80 13.614
9
P HYP607 Hypercholesterolemia, Familial 77 13.614
10
ABT001 Abetalipoproteinemia 60 13.614
11
NRM003 Norum Disease 53 13.614
12
P NPH012 Nephrotic Syndrome 55 13.614
13
P PLY019 Polyneuropathy 53 13.614
14
P MYC007 Myocardial Infarction 80 11.790
15
P ALG002 Alagille Syndrome 70 11.790
16
c AMY087 Amyloidosis, Hereditary, Transthyretin-Related 46 11.790
17
P HYP614 Hyperlipidemia, Familial Combined 50 11.790
18
FSH001 Fish-Eye Disease 44 11.790
19
PRP027 Peripheral Vascular Disease 69 11.790
20
P HYP090 Hyperalphalipoproteinemia 45 11.790
21
CRT016 Carotid Artery Disease 54 11.790
22
ART021 Arteriosclerosis 59 11.790
23
CRN030 Coronary Stenosis 50 11.790
24
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 81 9.626
25
c HYP595 Hypertension, Essential 69 9.626
26
P OBS005 Obesity 91 9.626
27
CHY002 Chylomicron Retention Disease 54 9.626
28
CRB039 Cerebrovascular Disease 49 9.626
29
LPP001 Lipoprotein Lipase Deficiency 63 9.626
30
HPT025 Hepatic Lipase Deficiency 45 9.626
31
c HYP163 Hyperlipidemia Type 3 52 9.626
32
VSC007 Vascular Disease 51 9.626
33
LPD008 Lipid Metabolism Disorder 42 9.626
34
P GLL020 Gallbladder Disease 59 9.626
35
ATH003 Atherosclerosis 63 9.626
36
c HRD039 Hereditary Amyloidosis 43 9.626
37
P AVS004 Avascular Necrosis of the Femoral Head 55 9.626
38
P FML035 Familial Hyperlipidemia 49 9.626
39
c HYP032 Hyperlipoproteinemia Type Iv 36 9.626
40
HYP081 Hypolipoproteinemia 42 9.626
41
TST018 Testicular Yolk Sac Tumor 40 9.626
42
ISC006 Ischemic Heart Disease 54 9.626
43
ARC001 Arcus Senilis 36 9.626
44
P TRN034 Transverse Myelitis 43 9.626
45
DYS013 Dysbaric Osteonecrosis 33 9.626
46
MYL001 Myelitis 35 9.626
47
c ACT159 Acute Transverse Myelitis 27 9.626
48
HMZ003 Homozygous Familial Hypercholesterolemia 43 9.626
49
FTL021 Fetal Macrosomia 38 9.626
50
APD001 Apo a-I Deficiency 18 9.626
51
c MTB001 Metabolic Syndrome X 61 6.807
52
c INH020 Inherited Metabolic Disorder 49 6.807
53
APM002 Aapoai Amyloidosis 11 6.807
54
DSS024 Disease of Anatomical Entity 40 6.807
55
P ACQ009 Acquired Metabolic Disease 42 6.807
56
AP1001 Apoa1-Associated Familial High Density Lipoprotein Deficiency 3 6.807
57
c AP1002 Apoa1-Related Familial Visceral Amyloidosis 5 6.807