Search results for "hypoalphalipoproteinemias"

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

81 hits were found for 'hypoalphalipoproteinemias'

# Family MCID Name MIFTS Score
1
FML164 Familial Hdl Deficiency 52 6.440
2
HYP121 Hypoalphalipoproteinemia 52 5.354
3
TNG002 Tangier Disease 71 4.629
4
P HYP117 Hypertriglyceridemia 67 0.142
5
c HYP095 Hypercholesterolemia 73 0.116
6
ART111 Artery Disease 62 0.116
7
ATH003 Atherosclerosis 69 0.101
8
c HPT021 Hepatitis 64 0.101
9
EYD002 Eye Disease 59 0.101
10
FSH001 Fish-Eye Disease 56 0.101
11
P OBS005 Obesity 91 0.082
12
P HYP075 Hypertension 87 0.082
13
P FML021 Familial Hypercholesterolemia 86 0.082
14
P NMN002 Niemann-Pick Disease 80 0.082
15
P SRC013 Sarcoidosis 75 0.082
16
P AMY004 Amyloidosis 68 0.082
17
P HYP090 Hyperalphalipoproteinemia 56 0.082
18
HYP037 Hyperhomocysteinemia 53 0.082
19
END072 Endotheliitis 51 0.082
20
HPT025 Hepatic Lipase Deficiency 47 0.082
21
SMT004 Smith-Lemli-Opitz Syndrome 84 0.058
22
P ALG002 Alagille Syndrome 81 0.058
23
AND002 Androgen Insensitivity Syndrome 80 0.058
24
ANK002 Ankylosing Spondylitis 77 0.058
25
CRB011 Cerebrotendinous Xanthomatosis 76 0.058
26
P ANG001 Angelman Syndrome 70 0.058
27
VSC007 Vascular Disease 70 0.058
28
P CNG401 Congenital Heart Disease 69 0.058
29
ART021 Arteriosclerosis 68 0.058
30
PRP027 Peripheral Vascular Disease 68 0.058
31
c AXN002 Axenfeld-Rieger Syndrome 67 0.058
32
P FML020 Familial Combined Hyperlipidemia 66 0.058
33
ART019 Aortic Valve Stenosis 64 0.058
34
c GLL020 Gallbladder Disease 64 0.058
35
CRN018 Coronary Artery Anomaly 63 0.058
36
ACN002 Acanthosis Nigricans 63 0.058
37
ACR008 Acrocallosal Syndrome 60 0.058
38
P AVS004 Avascular Necrosis of the Femoral Head 59 0.058
39
ISC006 Ischemic Heart Disease 58 0.058
40
c FML035 Familial Hyperlipidemia 56 0.058
41
P SPR013 Spiradenoma 56 0.058
42
c BNG049 Benign Recurrent Intrahepatic Cholestasis 55 0.058
43
c FML016 Familial Hypertriglyceridemia 54 0.058
44
NM001 Noma 53 0.058
45
THR013 Thoracic Outlet Syndrome 52 0.058
46
AMY053 Amyloidosis, Secondary 52 0.058
47
MNN014 Mononeuritis 51 0.058
48
CRN020 Coronary Restenosis 51 0.058
49
P HYP027 Hypobetalipoproteinemia 51 0.058
50
c HYP011 Hyperlipoproteinemia Type Iii 50 0.058
51
P HYP031 Hyperlipoproteinemia Type V 50 0.058
52
CHY002 Chylomicron Retention Disease 49 0.058
53
ALC010 Alcoholic Cardiomyopathy 49 0.058
54
ACN014 Acanthocytosis 49 0.058
55
LPD008 Lipid Metabolism Disorder 48 0.058
56
LPP002 Lipoprotein Glomerulopathy 48 0.058
57
c HRD039 Hereditary Amyloidosis 48 0.058
58
P HRD092 Hereditary Diffuse Leukoencephalopathy with Spheroids 47 0.058
59
FTT003 Fatty Acid Oxidation Disorders 47 0.058
60
CRB008 Cerebral Atherosclerosis 47 0.058
61
c AML002 Amelogenesis Imperfecta 47 0.058
62
P CRT018 Carotid Intimal Medial Thickness 47 0.058
63
SPL018 Splenomegaly 47 0.058
64
NRM003 Norum Disease 45 0.058
65
CHL074 Cholesteryl Ester Storage Disease 45 0.058
66
P ATX010 Ataxia Neuropathy Spectrum 43 0.058
67
DFC001 Defective Apolipoprotein B-100 43 0.058
68
HYP574 Hypercholesterolemia, Familial, Modifier of 40 0.058
69
HYP456 Hyperapobetalipoproteinemia 40 0.058
70
ADL086 Adolescent Idiopathic Scoliosis 39 0.058
71
CRN127 Coronary Artery Disease in Familial Hypercholesterolemia, Protection Against 38 0.058
72
ALN001 Aland Island Eye Disease 38 0.058
73
c HYP296 Hypercholesterolemia, Familial, Due to Ldlr Defect, Modifier of 37 0.058
74
c SRC025 Sarcoidosis 1 36 0.058
75
LDL001 Ldl Cholesterol Level Qtl2 36 0.058
76
SYN053 Syndromic Diarrhea 34 0.058
77
ATM021 Autoimmune Inner Ear Disease 34 0.058
78
c HYP164 Hyperlipoproteinemia Type 2 32 0.058
79
TFT003 Tufting Enteropathy 28 0.058
80
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 28 0.058
81
LGP003 Logopenic Progressive Aphasia 23 0.058