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

99 hits were found for 'hypoalphalipoproteinemias'

# ++ Fam MCID Name MIFTS Score
1
FML164 Familial Hdl Deficiency 43 6.411
2
HYP121 Hypoalphalipoproteinemia 44 5.957
3
TNG002 Tangier Disease 64 4.582
4
END072 Endotheliitis 51 0.313
5
P HYP117 Hypertriglyceridemia 63 0.231
6
ACN014 Acanthocytosis 43 0.211
7
P AVS004 Avascular Necrosis of the Femoral Head 40 0.211
8
c RNG028 Ring Chromosome Y 17 0.211
9
P HYP090 Hyperalphalipoproteinemia 43 0.196
10
FML235 Familial Combined Hyperlipoproteinemia 26 0.196
11
PCK001 Pick's Disease 68 0.163
12
MTH028 Mthfr Thermolabile Variant 17 0.154
13
c BNG049 Benign Recurrent Intrahepatic Cholestasis 45 0.133
14
HPT025 Hepatic Lipase Deficiency 38 0.133
15
ANK002 Ankylosing Spondylitis 75 0.122
16
CRN030 Coronary Stenosis 47 0.122
17
HMC014 Homocysteinemia 46 0.122
18
HRD039 Hereditary Amyloidosis 42 0.122
19
P SRC025 Sarcoidosis 1 30 0.122
20
TFT003 Tufting Enteropathy 26 0.122
21
VSC007 Vascular Disease 69 0.109
22
CRN211 Coronary Artery Disease, 68 0.109
23
c HYP095 Hypercholesterolemia 65 0.109
24
ART004 Aortic Atherosclerosis 51 0.109
25
ATH003 Atherosclerosis 69 0.094
26
P CRN157 Coronary Heart Disease 59 0.094
27
THR013 Thoracic Outlet Syndrome 53 0.094
28
EYD002 Eye Disease 50 0.094
29
P AML002 Amelogenesis Imperfecta 47 0.094
30
TRN007 Transsexualism 47 0.094
31
MNN014 Mononeuritis 40 0.094
32
ENT001 Enterocele 39 0.094
33
c ERL004 Early Yaws 29 0.094
34
LPD027 Lip Disease 23 0.094
35
LPS005 Lipase Deficiency Combined 22 0.094
36
P OBS005 Obesity 79 0.077
37
P HYP075 Hypertension 76 0.077
38
P FML021 Familial Hypercholesterolemia 76 0.077
39
P NMN002 Niemann-Pick Disease 72 0.077
40
BRN024 Bronchitis 71 0.077
41
ACN002 Acanthosis Nigricans 70 0.077
42
P AMY004 Amyloidosis 65 0.077
43
ABT001 Abetalipoproteinemia 64 0.077
44
c SRC013 Sarcoidosis 60 0.077
45
HYP037 Hyperhomocysteinemia 55 0.077
46
SPL018 Splenomegaly 50 0.077
47
CHY002 Chylomicron Retention Disease 46 0.077
48
CRD053 Cardiovascular Disease Risk Factor 42 0.077
49
HYP456 Hyperapobetalipoproteinemia 35 0.077
50
CHL074 Cholesteryl Ester Storage Disease 34 0.077
51
ARC001 Arcus Senilis 34 0.077
52
DFC001 Defective Apolipoprotein B-100 30 0.077
53
NMN003 Niemann–pick Disease 29 0.077
54
NNS006 Non-Suppurative Otitis Media 24 0.077
55
P DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 23 0.077
56
LGP003 Logopenic Progressive Aphasia 22 0.077
57
IDP013 Idiopathic Adolescent Scoliosis 20 0.077
58
AND002 Androgen Insensitivity Syndrome 75 0.054
59
PRP027 Peripheral Vascular Disease 71 0.054
60
P ALG002 Alagille Syndrome 68 0.054
61
P CHR089 Chronic Kidney Failure 68 0.054
62
P ANG001 Angelman Syndrome 67 0.054
63
CRB011 Cerebrotendinous Xanthomatosis 66 0.054
64
P CNG026 Congenital Heart Defect 65 0.054
65
c HPT021 Hepatitis 65 0.054
66
ART019 Aortic Valve Stenosis 64 0.054
67
WST001 West Syndrome 64 0.054
68
ART021 Arteriosclerosis 63 0.054
69
ISC006 Ischemic Heart Disease 62 0.054
70
P HMC002 Homocystinuria 61 0.054
71
P FML020 Familial Combined Hyperlipidemia 59 0.054
72
MLT074 Multiple Endocrine Neoplasia 58 0.054
73
c HRD002 Hereditary Angioedema 58 0.054
74
c AXN002 Axenfeld-Rieger Syndrome 57 0.054
75
P XNT003 Xanthomatosis 54 0.054
76
c FML035 Familial Hyperlipidemia 53 0.054
77
ACR008 Acrocallosal Syndrome 53 0.054
78
P GLL020 Gallbladder Disease 52 0.054
79
P HYP027 Hypobetalipoproteinemia 51 0.054
80
LPP001 Lipoprotein Lipase Deficiency 50 0.054
81
AMY053 Amyloidosis, Secondary 50 0.054
82
CRT016 Carotid Artery Disease 49 0.054
83
CRN024 Corneal Disease 48 0.054
84
c FML016 Familial Hypertriglyceridemia 48 0.054
85
CRN029 Coronary Arteriosclerosis 45 0.054
86
FSH001 Fish-Eye Disease 41 0.054
87
LPD008 Lipid Metabolism Disorder 41 0.054
88
c CRT018 Carotid Intimal Medial Thickness 39 0.054
89
LPP002 Lipoprotein Glomerulopathy 39 0.054
90
NRM003 Norum Disease 39 0.054
91
c HYP011 Hyperlipoproteinemia Type Iii 34 0.054
92
c ATX010 Ataxia Neuropathy Spectrum 33 0.054
93
P SLP004 Salpingo-Oophoritis 30 0.054
94
HRD092 Hereditary Diffuse Leukoencephalopathy with Spheroids 29 0.054
95
HMG020 Hmg Coa Lyase Deficiency 28 0.054
96
ALN001 Aland Island Eye Disease 27 0.054
97
c NMN006 Niemann-Pick Disease Type D 22 0.054
98
ATM021 Autoimmune Inner Ear Disease 20 0.054
99
P ISC010 Isochromosome Yp 14 0.054