Search results for "hypoalphalipoproteinemias"

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

87 hits were found for 'hypoalphalipoproteinemias'

# Family MCID Name MIFTS Score
1
FML164 Familial Hdl Deficiency 53 6.452
2
HYP121 Hypoalphalipoproteinemia 54 5.332
3
TNG002 Tangier Disease 73 4.622
4
P HYP117 Hypertriglyceridemia 67 0.139
5
c HYP095 Hypercholesterolemia 72 0.114
6
ART111 Artery Disease 63 0.114
7
FSH001 Fish-Eye Disease 56 0.114
8
ATH003 Atherosclerosis 68 0.098
9
c HPT021 Hepatitis 63 0.098
10
EYD002 Eye Disease 58 0.098
11
P OBS005 Obesity 89 0.080
12
P HYP075 Hypertension 85 0.080
13
P FML021 Familial Hypercholesterolemia 85 0.080
14
P NMN002 Niemann-Pick Disease 83 0.080
15
P SRC013 Sarcoidosis 73 0.080
16
P AMY004 Amyloidosis 73 0.080
17
P HYP090 Hyperalphalipoproteinemia 56 0.080
18
HYP037 Hyperhomocysteinemia 52 0.080
19
END072 Endotheliitis 50 0.080
20
HPT025 Hepatic Lipase Deficiency 47 0.080
21
SMT004 Smith-Lemli-Opitz Syndrome 84 0.057
22
P ALG002 Alagille Syndrome 81 0.057
23
AND002 Androgen Insensitivity Syndrome 80 0.057
24
CRB011 Cerebrotendinous Xanthomatosis 76 0.057
25
ANK002 Ankylosing Spondylitis 76 0.057
26
P ANG001 Angelman Syndrome 71 0.057
27
c AXN002 Axenfeld-Rieger Syndrome 69 0.057
28
VSC007 Vascular Disease 69 0.057
29
P CNG401 Congenital Heart Disease 69 0.057
30
ART021 Arteriosclerosis 67 0.057
31
ALS001 Alstrom Syndrome 67 0.057
32
PRP027 Peripheral Vascular Disease 67 0.057
33
P FML020 Familial Combined Hyperlipidemia 66 0.057
34
P CRN018 Coronary Artery Anomaly 65 0.057
35
ACN002 Acanthosis Nigricans 64 0.057
36
ART019 Aortic Valve Stenosis 63 0.057
37
c GLL020 Gallbladder Disease 63 0.057
38
ACR008 Acrocallosal Syndrome 61 0.057
39
P AVS004 Avascular Necrosis of the Femoral Head 60 0.057
40
ISC006 Ischemic Heart Disease 58 0.057
41
c FML035 Familial Hyperlipidemia 55 0.057
42
P SPR013 Spiradenoma 55 0.057
43
c BNG049 Benign Recurrent Intrahepatic Cholestasis 55 0.057
44
c FML016 Familial Hypertriglyceridemia 53 0.057
45
P HYP027 Hypobetalipoproteinemia 52 0.057
46
THR013 Thoracic Outlet Syndrome 52 0.057
47
CHY002 Chylomicron Retention Disease 52 0.057
48
NM001 Noma 52 0.057
49
AMY053 Amyloidosis, Secondary 51 0.057
50
P HYP031 Hyperlipoproteinemia Type V 51 0.057
51
MNN014 Mononeuritis 51 0.057
52
CRN020 Coronary Restenosis 50 0.057
53
P HRD092 Hereditary Diffuse Leukoencephalopathy with Spheroids 50 0.057
54
LPP002 Lipoprotein Glomerulopathy 50 0.057
55
c HYP011 Hyperlipoproteinemia Type Iii 49 0.057
56
ALC010 Alcoholic Cardiomyopathy 49 0.057
57
ACN014 Acanthocytosis 48 0.057
58
LPD008 Lipid Metabolism Disorder 47 0.057
59
NNT020 Neonatal Intrahepatic Cholestasis Caused by Citrin Deficiency 47 0.057
60
c HRD039 Hereditary Amyloidosis 47 0.057
61
P ATX010 Ataxia Neuropathy Spectrum 47 0.057
62
FTT003 Fatty Acid Oxidation Disorders 47 0.057
63
CRB008 Cerebral Atherosclerosis 46 0.057
64
c AML002 Amelogenesis Imperfecta 46 0.057
65
P CRT018 Carotid Intimal Medial Thickness 46 0.057
66
SPL018 Splenomegaly 46 0.057
67
NRM003 Norum Disease 44 0.057
68
CHL074 Cholesteryl Ester Storage Disease 44 0.057
69
DFC001 Defective Apolipoprotein B-100 42 0.057
70
P HMP014 Hemophagocytic Lymphohistiocytosis, Familial, 4 42 0.057
71
HYP574 Hypercholesterolemia, Familial, Modifier of 40 0.057
72
P LPD015 Lipodystrophy, Familial Partial, Type 2 40 0.057
73
ADL086 Adolescent Idiopathic Scoliosis 40 0.057
74
ALN001 Aland Island Eye Disease 39 0.057
75
HYP456 Hyperapobetalipoproteinemia 39 0.057
76
c SRC025 Sarcoidosis 1 39 0.057
77
CRN127 Coronary Artery Disease in Familial Hypercholesterolemia, Protection Against 38 0.057
78
c HYP164 Hyperlipoproteinemia Type 2 37 0.057
79
c HYP296 Hypercholesterolemia, Familial, Due to Ldlr Defect, Modifier of 36 0.057
80
LDL001 Ldl Cholesterol Level Qtl2 35 0.057
81
SYN053 Syndromic Diarrhea 34 0.057
82
ATM021 Autoimmune Inner Ear Disease 33 0.057
83
INS013 Insulin Resistance, Severe, Digenic 31 0.057
84
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 29 0.057
85
TFT003 Tufting Enteropathy 28 0.057
86
CMP061 Complete Lcat Deficiency 27 0.057
87
LGP003 Logopenic Progressive Aphasia 24 0.057