The MalaCard for "hypoalphalipoproteinemias" has been retired.
Searching MalaCards for entries containing "hypoalphalipoproteinemias"

67 hits were found for 'hypoalphalipoproteinemias'

# Family MCID Name MIFTS Score
1
FML164 Familial Hdl Deficiency 53 6.446
2
HYP121 Hypoalphalipoproteinemia 41 5.254
3
TNG002 Tangier Disease 78 4.613
4
P AVS004 Avascular Necrosis of the Femoral Head 49 0.253
5
P HYP090 Hyperalphalipoproteinemia 47 0.237
6
ACN014 Acanthocytosis 32 0.237
7
P HYP117 Hypertriglyceridemia 54 0.229
8
FML235 Familial Combined Hyperlipoproteinemia 26 0.221
9
PCK001 Pick's Disease 74 0.184
10
HPT025 Hepatic Lipase Deficiency 38 0.150
11
EYD002 Eye Disease 60 0.137
12
c BNG049 Benign Recurrent Intrahepatic Cholestasis 48 0.137
13
VSC007 Vascular Disease 72 0.123
14
CRN211 Coronary Artery Disease 72 0.123
15
ART004 Aortic Atherosclerosis 54 0.123
16
CRN030 Coronary Stenosis 53 0.123
17
HRD039 Hereditary Amyloidosis 35 0.123
18
TRN007 Transsexualism 53 0.106
19
LPS005 Lipase Deficiency Combined 26 0.106
20
P FML021 Familial Hypercholesterolemia 87 0.087
21
P NMN002 Niemann-Pick Disease 87 0.087
22
c HPT021 Hepatitis 75 0.087
23
ACN002 Acanthosis Nigricans 73 0.087
24
ABT001 Abetalipoproteinemia 73 0.087
25
ATH003 Atherosclerosis 71 0.087
26
P AMY004 Amyloidosis 65 0.087
27
c HYP095 Hypercholesterolemia 56 0.087
28
CHY002 Chylomicron Retention Disease 49 0.087
29
SPL018 Splenomegaly 37 0.087
30
ARC001 Arcus Senilis 37 0.087
31
CRD053 Cardiovascular Disease Risk Factor 34 0.087
32
CHL074 Cholesteryl Ester Storage Disease 33 0.087
33
HYP456 Hyperapobetalipoproteinemia 32 0.087
34
LGP003 Logopenic Progressive Aphasia 18 0.087
35
P OBS005 Obesity 93 0.061
36
P HYP075 Hypertension 86 0.061
37
P ALG002 Alagille Syndrome 83 0.061
38
CRB011 Cerebrotendinous Xanthomatosis 77 0.061
39
P CHR089 Chronic Kidney Failure 76 0.061
40
PRP027 Peripheral Vascular Disease 75 0.061
41
c SRC013 Sarcoidosis 69 0.061
42
ISC006 Ischemic Heart Disease 69 0.061
43
ART021 Arteriosclerosis 65 0.061
44
WST001 West Syndrome 64 0.061
45
P FML020 Familial Combined Hyperlipidemia 63 0.061
46
ACR008 Acrocallosal Syndrome 59 0.061
47
c HRD002 Hereditary Angioedema 59 0.061
48
c GLL020 Gallbladder Disease 59 0.061
49
c FML035 Familial Hyperlipidemia 59 0.061
50
CRT016 Carotid Artery Disease 58 0.061
51
HYP037 Hyperhomocysteinemia 55 0.061
52
XNT003 Xanthomatosis 55 0.061
53
FSH001 Fish-Eye Disease 54 0.061
54
LPP001 Lipoprotein Lipase Deficiency 53 0.061
55
P HYP027 Hypobetalipoproteinemia 53 0.061
56
CRN029 Coronary Arteriosclerosis 53 0.061
57
CRN024 Corneal Disease 52 0.061
58
c FML016 Familial Hypertriglyceridemia 51 0.061
59
LPD008 Lipid Metabolism Disorder 50 0.061
60
c HYP011 Hyperlipoproteinemia Type Iii 47 0.061
61
NRM003 Norum Disease 46 0.061
62
P ATX010 Ataxia Neuropathy Spectrum 44 0.061
63
P CRN157 Coronary Heart Disease 43 0.061
64
AMY053 Amyloidosis, Secondary 43 0.061
65
LPP002 Lipoprotein Glomerulopathy 40 0.061
66
c CRT018 Carotid Intimal Medial Thickness 37 0.061
67
DFC001 Defective Apolipoprotein B-100 32 0.061