Search results for "hypoalphalipoproteinemias"

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

72 hits were found for 'hypoalphalipoproteinemias'

# Family MCID Name MIFTS Score
1
FML164 Familial Hdl Deficiency 51 6.446
2
HYP121 Hypoalphalipoproteinemia 52 6.047
3
TNG002 Tangier Disease 70 4.612
4
P HYP117 Hypertriglyceridemia 65 0.147
5
CRN211 Coronary Artery Disease 84 0.120
6
c HYP095 Hypercholesterolemia 70 0.120
7
ART111 Artery Disease 60 0.120
8
ATH003 Atherosclerosis 68 0.104
9
c HPT021 Hepatitis 64 0.104
10
EYD002 Eye Disease 60 0.104
11
FSH001 Fish-Eye Disease 55 0.104
12
P OBS005 Obesity 89 0.085
13
P HYP075 Hypertension 85 0.085
14
P FML021 Familial Hypercholesterolemia 85 0.085
15
c SRC013 Sarcoidosis 68 0.085
16
P AMY004 Amyloidosis 67 0.085
17
HYP037 Hyperhomocysteinemia 51 0.085
18
END072 Endotheliitis 50 0.085
19
HPT025 Hepatic Lipase Deficiency 46 0.085
20
P SMT004 Smith-Lemli-Opitz Syndrome 82 0.060
21
P NMN002 Niemann-Pick Disease 81 0.060
22
AND002 Androgen Insensitivity Syndrome 80 0.060
23
P ALG002 Alagille Syndrome 80 0.060
24
CRB011 Cerebrotendinous Xanthomatosis 75 0.060
25
ANK002 Ankylosing Spondylitis 74 0.060
26
P ANG001 Angelman Syndrome 70 0.060
27
VSC007 Vascular Disease 70 0.060
28
ACN002 Acanthosis Nigricans 69 0.060
29
PRP027 Peripheral Vascular Disease 67 0.060
30
ART021 Arteriosclerosis 67 0.060
31
c AXN002 Axenfeld-Rieger Syndrome 66 0.060
32
ART019 Aortic Valve Stenosis 64 0.060
33
P FML020 Familial Combined Hyperlipidemia 63 0.060
34
c GLL020 Gallbladder Disease 63 0.060
35
ACR008 Acrocallosal Syndrome 59 0.060
36
P AVS004 Avascular Necrosis of the Femoral Head 59 0.060
37
P CNG401 Congenital Heart Disease 58 0.060
38
c FML035 Familial Hyperlipidemia 55 0.060
39
P HYP090 Hyperalphalipoproteinemia 55 0.060
40
P BNG049 Benign Recurrent Intrahepatic Cholestasis 54 0.060
41
c FML016 Familial Hypertriglyceridemia 52 0.060
42
AMY053 Amyloidosis, Secondary 52 0.060
43
NM001 Noma 52 0.060
44
THR013 Thoracic Outlet Syndrome 52 0.060
45
MNN014 Mononeuritis 51 0.060
46
CRN020 Coronary Restenosis 50 0.060
47
P HYP027 Hypobetalipoproteinemia 49 0.060
48
c HYP011 Hyperlipoproteinemia Type Iii 49 0.060
49
ALC010 Alcoholic Cardiomyopathy 48 0.060
50
CHY002 Chylomicron Retention Disease 48 0.060
51
ACN014 Acanthocytosis 48 0.060
52
LPP002 Lipoprotein Glomerulopathy 47 0.060
53
c HRD039 Hereditary Amyloidosis 47 0.060
54
FTT003 Fatty Acid Oxidation Disorders 47 0.060
55
CRB008 Cerebral Atherosclerosis 47 0.060
56
SPL018 Splenomegaly 46 0.060
57
P HRD092 Hereditary Diffuse Leukoencephalopathy with Spheroids 46 0.060
58
P CRT018 Carotid Intimal Medial Thickness 45 0.060
59
LPD008 Lipid Metabolism Disorder 45 0.060
60
NRM003 Norum Disease 44 0.060
61
DFC001 Defective Apolipoprotein B-100 42 0.060
62
CHL074 Cholesteryl Ester Storage Disease 42 0.060
63
P ATX010 Ataxia Neuropathy Spectrum 41 0.060
64
HYP456 Hyperapobetalipoproteinemia 39 0.060
65
P SRC025 Sarcoidosis 1 36 0.060
66
FML235 Familial Combined Hyperlipoproteinemia 33 0.060
67
HYP574 Hypercholesterolemia, Familial, Modifier of 32 0.060
68
SYN053 Syndromic Diarrhea 32 0.060
69
CRN127 Coronary Artery Disease in Familial Hypercholesterolemia, Protection Against 29 0.060
70
TFT003 Tufting Enteropathy 28 0.060
71
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 28 0.060
72
LGP003 Logopenic Progressive Aphasia 22 0.060