Search results for "[genes] APOA1"

36 hits were found for '[genes] APOA1'

# Family MCID Name MIFTS Score
1
TNG002 Tangier Disease 63 25.060
2
HYP121 Hypoalphalipoproteinemia 64 22.876
3
P AMY082 Amyloidosis, Familial Visceral 43 20.461
4
P CRN211 Coronary Artery Disease 73 17.720
5
P AMY004 Amyloidosis 63 17.720
6
ART111 Artery Disease 55 17.720
7
P ALG002 Alagille Syndrome 73 14.468
8
P HYP117 Hypertriglyceridemia 61 14.468
9
PRP027 Peripheral Vascular Disease 60 14.468
10
ART021 Arteriosclerosis 58 14.468
11
EYD002 Eye Disease 54 14.468
12
P HYP090 Hyperalphalipoproteinemia 50 14.468
13
FSH001 Fish-Eye Disease 47 14.468
14
TRY001 Trypanosomiasis 42 14.468
15
P MYC007 Myocardial Infarction 81 10.231
16
P HYP607 Hypercholesterolemia, Familial 81 10.231
17
CRB011 Cerebrotendinous Xanthomatosis 66 10.231
18
LPP001 Lipoprotein Lipase Deficiency 61 10.231
19
P GLL020 Gallbladder Disease 56 10.231
20
P AVS004 Avascular Necrosis of the Femoral Head 54 10.231
21
ISC006 Ischemic Heart Disease 51 10.231
22
CHY002 Chylomicron Retention Disease 48 10.231
23
P FML035 Familial Hyperlipidemia 48 10.231
24
NRM003 Norum Disease 48 10.231
25
NM001 Noma 44 10.231
26
HPT025 Hepatic Lipase Deficiency 44 10.231
27
HMZ003 Homozygous Familial Hypercholesterolemia 44 10.231
28
RFL001 Reflex Sympathetic Dystrophy 43 10.231
29
c HYP011 Hyperlipoproteinemia Type Iii 42 10.231
30
c HRD039 Hereditary Amyloidosis 41 10.231
31
CRB008 Cerebral Atherosclerosis 39 10.231
32
APD001 Apo a-I Deficiency 4 10.231
33
c ALM001 Al Amyloidosis 56 7.234
34
c FML260 Familial Renal Amyloidosis Due to Apolipoprotein Ai Variant 10 7.234
35
c AP1002 Apoa1-Related Familial Visceral Amyloidosis 6 7.234
36
AP1001 Apoa1-Associated Familial High Density Lipoprotein Deficiency 4 7.234