Search results for "hypoalphalipoproteinemias"

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

126 hits were found for 'hypoalphalipoproteinemias'

# Family MCID Name MIFTS Score
1
HYP121 Hypoalphalipoproteinemia 57 8.016
2
TNG002 Tangier Disease 60 4.592
3
APL025 Apolipoprotein a-I Deficiency 33 2.640
4
P HYP117 Hypertriglyceridemia 56 0.124
5
P CRN211 Coronary Artery Disease 68 0.101
6
ART111 Artery Disease 48 0.101
7
FSH001 Fish-Eye Disease 44 0.101
8
P HPT021 Hepatitis 58 0.088
9
EYD002 Eye Disease 54 0.088
10
ATH003 Atherosclerosis 50 0.088
11
P OBS005 Obesity 89 0.072
12
P AMY004 Amyloidosis 60 0.072
13
NRM003 Norum Disease 52 0.072
14
HPT025 Hepatic Lipase Deficiency 45 0.072
15
P HYP090 Hyperalphalipoproteinemia 44 0.072
16
HYP037 Hyperhomocysteinemia 40 0.072
17
END072 Endotheliitis 39 0.072
18
HYP286 Hyperchylomicronemia, Late-Onset 35 0.072
19
HYP081 Hypolipoproteinemia 33 0.072
20
P HYP607 Hypercholesterolemia, Familial 79 0.051
21
HV1006 Hiv-1 77 0.051
22
P ATX030 Ataxia-Telangiectasia 76 0.051
23
ANR002 Aniridia 72 0.051
24
c HYP595 Hypertension, Essential 68 0.051
25
P CNG401 Congenital Heart Disease 68 0.051
26
SMT004 Smith-Lemli-Opitz Syndrome 67 0.051
27
c SPN225 Spondyloarthropathy 1 66 0.051
28
P ALG002 Alagille Syndrome 66 0.051
29
P ANG001 Angelman Syndrome 66 0.051
30
AND015 Androgen Insensitivity 65 0.051
31
P HRM001 Hermansky-Pudlak Syndrome 62 0.051
32
PRP027 Peripheral Vascular Disease 62 0.051
33
P AXN010 Axenfeld-Rieger Syndrome, Type 3 60 0.051
34
c SRC025 Sarcoidosis 1 60 0.051
35
c PNC108 Pancreatitis, Hereditary 59 0.051
36
P HMP002 Hemophagocytic Lymphohistiocytosis 59 0.051
37
P NMN002 Niemann-Pick Disease 59 0.051
38
ART001 Arterial Tortuosity Syndrome 59 0.051
39
P AND016 Andersen Syndrome 58 0.051
40
CRB039 Cerebrovascular Disease 58 0.051
41
ABT001 Abetalipoproteinemia 57 0.051
42
ISC006 Ischemic Heart Disease 56 0.051
43
ACQ007 Acquired Immunodeficiency Syndrome 55 0.051
44
VSC007 Vascular Disease 55 0.051
45
P ACR001 Aicardi-Goutieres Syndrome 53 0.051
46
ACN002 Acanthosis Nigricans 53 0.051
47
LPP001 Lipoprotein Lipase Deficiency 53 0.051
48
DFC004 Deficiency Anemia 52 0.051
49
HNT002 Hantavirus Pulmonary Syndrome 52 0.051
50
c MTB001 Metabolic Syndrome X 52 0.051
51
ART021 Arteriosclerosis 51 0.051
52
ALS001 Alstrom Syndrome 51 0.051
53
P SHR029 Short Syndrome 49 0.051
54
P AVS004 Avascular Necrosis of the Femoral Head 49 0.051
55
c LPD037 Lipodystrophy, Familial Partial, 2 49 0.051
56
LPM004 Lipoma 48 0.051
57
P GLL020 Gallbladder Disease 48 0.051
58
FML026 Familial Lipoprotein Lipase Deficiency 47 0.051
59
THR013 Thoracic Outlet Syndrome 47 0.051
60
ISC004 Ischemia 47 0.051
61
P HYP027 Hypobetalipoproteinemia 47 0.051
62
P SPR013 Spiradenoma 46 0.051
63
P FML035 Familial Hyperlipidemia 46 0.051
64
c ART101 Aortic Valve Disease 2 46 0.051
65
MYC002 Mycobacterium Avium Complex Disease 46 0.051
66
BRR013 Barrett Esophagus/esophageal Adenocarcinoma 46 0.051
67
LPD008 Lipid Metabolism Disorder 45 0.051
68
P AML002 Amelogenesis Imperfecta 45 0.051
69
c NMN016 Niemann-Pick Disease, Type B 44 0.051
70
c HYP163 Hyperlipidemia Type 3 44 0.051
71
LPP002 Lipoprotein Glomerulopathy 43 0.051
72
P AMY082 Amyloidosis, Familial Visceral 43 0.051
73
HMP005 Hemiplegia 43 0.051
74
CRT016 Carotid Artery Disease 42 0.051
75
P HYP614 Hyperlipidemia, Familial Combined 42 0.051
76
P TRC086 Trichohepatoenteric Syndrome 1 42 0.051
77
CRN030 Coronary Stenosis 40 0.051
78
XNT003 Xanthomatosis 39 0.051
79
CRD144 Cardiovascular Disease Risk Factor ) 39 0.051
80
ART004 Aortic Atherosclerosis 39 0.051
81
MNN014 Mononeuritis 39 0.051
82
c RCR022 Recurrent Acute Pancreatitis 38 0.051
83
c HYP288 Hypercholesterolemia, Due to Ligand-Defective Apo B 38 0.051
84
CRB009 Cerebritis 37 0.051
85
ALN001 Aland Island Eye Disease 37 0.051
86
P LKN019 Leukoencephalopathy, Diffuse Hereditary, with Spheroids 37 0.051
87
c HRD039 Hereditary Amyloidosis 36 0.051
88
SDD007 Sudden Cardiac Death 36 0.051
89
SBL008 Sea-Blue Histiocyte Disease 36 0.051
90
PLM005 Pleomorphic Lipoma 36 0.051
91
c AMY009 Amyloidosis Aa 35 0.051
92
HMZ003 Homozygous Familial Hypercholesterolemia 35 0.051
93
ARC001 Arcus Senilis 34 0.051
94
ADS002 Adie Syndrome 34 0.051
95
XNT009 Xanthoma Disseminatum 34 0.051
96
SPL018 Splenomegaly 34 0.051
97
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 34 0.051
98
CRB008 Cerebral Atherosclerosis 33 0.051
99
FTT003 Fatty Acid Oxidation Disorders 33 0.051
100
c LPD021 Lipodystrophy, Familial Partial, Type 3 33 0.051
101
CHL050 Cholesterol Ester Storage Disease 33 0.051
102
ADL086 Adolescent Idiopathic Scoliosis 32 0.051
103
FTL021 Fetal Macrosomia 31 0.051
104
AMS002 Amish Infantile Epilepsy Syndrome 31 0.051
105
P ATX010 Ataxia Neuropathy Spectrum 31 0.051
106
c HYP011 Hyperlipoproteinemia Type Iii 30 0.051
107
HPT074 Hepatic Adenoma, Somatic 30 0.051
108
c JVN024 Juvenile Hereditary Hemochromatosis 30 0.051
109
P CRD132 Cardiac Conduction Defect 29 0.051
110
LPS020 Lipase Deficiency, Combined 28 0.051
111
DFC001 Defective Apolipoprotein B-100 27 0.051
112
TFT003 Tufting Enteropathy 27 0.051
113
HNM002 Hinman Syndrome 27 0.051
114
P CTR077 Citrullinemia, Type Ii, Neonatal-Onset 27 0.051
115
c SRC023 Sarcoidosis 2 27 0.051
116
c HMP022 Hemophagocytic Lymphohistiocytosis, Familial, 1 25 0.051
117
ALR002 Al-Raqad Syndrome 23 0.051
118
MTH028 Mthfr Thermolabile Variant 23 0.051
119
ALG001 Algoneurodystrophy 23 0.051
120
ADL087 Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia 21 0.051
121
c BNG076 Benign Exophthalmos Syndrome 21 0.051
122
ATM021 Autoimmune Inner Ear Disease 21 0.051
123
AND005 Androgen Insensitivity Syndrome, Mild 19 0.051
124
MRB006 Morbid Obesity and Spermatogenic Failure 16 0.051
125
APP012 Apoe P.leu167del-Related Lipid Disorders 14 0.051
126
APD001 Apo a-I Deficiency 13 0.051