Search results for "APOA1"

51 hits were found for 'APOA1'
Try searching for aoa1

# Family MCID Name MIFTS Score
1
TNG002 Tangier Disease 73 5.589
2
HYP121 Hypoalphalipoproteinemia 54 4.564
3
P AMY004 Amyloidosis 73 4.006
4
ART111 Artery Disease 63 4.006
5
P ALG002 Alagille Syndrome 81 3.227
6
c HYP095 Hypercholesterolemia 72 3.227
7
P HYP117 Hypertriglyceridemia 67 3.227
8
ART021 Arteriosclerosis 67 3.227
9
PRP027 Peripheral Vascular Disease 67 3.227
10
EYD002 Eye Disease 58 3.227
11
FSH001 Fish-Eye Disease 56 3.227
12
P HYP090 Hyperalphalipoproteinemia 56 3.227
13
FML164 Familial Hdl Deficiency 53 3.227
14
TRY001 Trypanosomiasis 49 3.227
15
AMY034 Amyloidosis, 3 or More Types 28 3.227
16
ATH003 Atherosclerosis 68 2.795
17
P FML003 Familial Visceral Amyloidosis 45 2.795
18
P AMY038 Amyloidosis, Renal 35 2.795
19
P MYC007 Myocardial Infarction 92 2.399
20
P FML021 Familial Hypercholesterolemia 85 2.282
21
CRB011 Cerebrotendinous Xanthomatosis 76 2.282
22
P FML020 Familial Combined Hyperlipidemia 66 2.282
23
P INS005 Insulin Resistance 64 2.282
24
c GLL020 Gallbladder Disease 63 2.282
25
P AVS004 Avascular Necrosis of the Femoral Head 60 2.282
26
ISC006 Ischemic Heart Disease 58 2.282
27
c FML035 Familial Hyperlipidemia 55 2.282
28
c FML016 Familial Hypertriglyceridemia 53 2.282
29
CHY002 Chylomicron Retention Disease 52 2.282
30
NM001 Noma 52 2.282
31
RFL001 Reflex Sympathetic Dystrophy 52 2.282
32
AMY053 Amyloidosis, Secondary 51 2.282
33
c HYP011 Hyperlipoproteinemia Type Iii 49 2.282
34
HPT025 Hepatic Lipase Deficiency 47 2.282
35
c HRD039 Hereditary Amyloidosis 47 2.282
36
CRB008 Cerebral Atherosclerosis 46 2.282
37
NRM003 Norum Disease 44 2.282
38
APD001 Apo a-I Deficiency 6 2.282
39
c TYP009 Type 2 Diabetes Mellitus 100 1.613
40
P MLT019 Multiple Myeloma 88 1.613
41
c FML260 Familial Renal Amyloidosis Due to Apolipoprotein Ai Variant 11 1.613
42
c AP1002 Apoa1-Related Familial Visceral Amyloidosis 7 1.613
43
AP1001 Apoa1-Associated Familial High Density Lipoprotein Deficiency 5 1.613
44
APN004 Apoa-I and Apoc-Iii Deficiency, Combined 4 1.613
45
CRN117 Corneal Clouding, Autosomal Recessive 4 1.613
46
P OBS005 Obesity 89 0.071
47
P MLT020 Multiple Sclerosis 84 0.071
48
TRN001 Transthyretin Amyloidosis 65 0.071
49
PYL006 Pyloric Stenosis 49 0.071
50
HYP009 Hypertrophic Pyloric Stenosis 49 0.071
51
OVR105 Ovarian Serous Carcinoma 35 0.071