Search results for "[genes] APOA1"

61 hits were found for '[genes] APOA1'

# Family MCID Name MIFTS Score
1
P CRN211 Coronary Artery Disease 74 19.166
2
P AMY004 Amyloidosis 68 17.928
3
P AMY082 Amyloidosis, Familial Visceral 48 17.928
4
TNG002 Tangier Disease 63 16.598
5
P HYP117 Hypertriglyceridemia 65 15.152
6
ART111 Artery Disease 61 15.152
7
HYP121 Hypoalphalipoproteinemia 60 15.152
8
P NPH012 Nephrotic Syndrome 56 15.152
9
CRN030 Coronary Stenosis 53 15.152
10
P OBS005 Obesity 91 13.553
11
P DBT085 Diabetes Mellitus, Insulin-Dependent 80 13.553
12
P HYP607 Hypercholesterolemia, Familial 77 13.553
13
VSC007 Vascular Disease 70 13.553
14
CRB039 Cerebrovascular Disease 67 13.553
15
ABT001 Abetalipoproteinemia 63 13.553
16
ART021 Arteriosclerosis 61 13.553
17
P PRP023 Peripheral Neuropathy 56 13.553
18
P PLY019 Polyneuropathy 55 13.553
19
HPT022 Hepatoblastoma 55 13.553
20
NRM003 Norum Disease 54 13.553
21
P HYP614 Hyperlipidemia, Familial Combined 54 13.553
22
P FML035 Familial Hyperlipidemia 53 13.553
23
P HYP090 Hyperalphalipoproteinemia 52 13.553
24
c HRD039 Hereditary Amyloidosis 49 13.553
25
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 80 11.737
26
P MYC007 Myocardial Infarction 80 11.737
27
ATH003 Atherosclerosis 65 11.737
28
LPD008 Lipid Metabolism Disorder 56 11.737
29
CRT016 Carotid Artery Disease 51 11.737
30
SLP001 Sleeping Sickness 51 11.737
31
c AMY087 Amyloidosis, Hereditary, Transthyretin-Related 49 11.737
32
CRB008 Cerebral Atherosclerosis 46 11.737
33
APL025 Apolipoprotein a-I Deficiency 41 11.737
34
ARC001 Arcus Senilis 39 11.737
35
ISC006 Ischemic Heart Disease 73 9.583
36
c HYP595 Hypertension, Essential 68 9.583
37
P GLL020 Gallbladder Disease 61 9.583
38
LPP001 Lipoprotein Lipase Deficiency 59 9.583
39
P AVS004 Avascular Necrosis of the Femoral Head 56 9.583
40
c HYP163 Hyperlipidemia Type 3 53 9.583
41
P BDD001 Budd-Chiari Syndrome 52 9.583
42
CHY002 Chylomicron Retention Disease 52 9.583
43
MYL001 Myelitis 46 9.583
44
HYP081 Hypolipoproteinemia 46 9.583
45
HPT025 Hepatic Lipase Deficiency 44 9.583
46
FSH001 Fish-Eye Disease 44 9.583
47
FTL021 Fetal Macrosomia 41 9.583
48
P TRN034 Transverse Myelitis 41 9.583
49
TST018 Testicular Yolk Sac Tumor 40 9.583
50
c AMY009 Amyloidosis Aa 39 9.583
51
c HYP032 Hyperlipoproteinemia Type Iv 39 9.583
52
DYS013 Dysbaric Osteonecrosis 38 9.583
53
AMY005 Amyloid Neuropathy 33 9.583
54
c ACT159 Acute Transverse Myelitis 32 9.583
55
APD001 Apo a-I Deficiency 12 9.583
56
c INH020 Inherited Metabolic Disorder 51 6.776
57
GLC008 Glucose Metabolism Disease 47 6.776
58
P ACQ009 Acquired Metabolic Disease 43 6.776
59
APM002 Aapoai Amyloidosis 12 6.776
60
c AP1002 Apoa1-Related Familial Visceral Amyloidosis 6 6.776
61
AP1001 Apoa1-Associated Familial High Density Lipoprotein Deficiency 4 6.776