Search results for "hypoalphalipoproteinemias"

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

105 hits were found for 'hypoalphalipoproteinemias'

# Family MCID Name MIFTS Score
1
HYP121 Hypoalphalipoproteinemia 73 8.817
2
TNG002 Tangier Disease 72 4.803
3
P HYP117 Hypertriglyceridemia 71 0.129
4
P CRN211 Coronary Artery Disease 77 0.105
5
ART111 Artery Disease 62 0.105
6
FSH001 Fish-Eye Disease 54 0.105
7
ATH003 Atherosclerosis 65 0.091
8
P HPT021 Hepatitis 63 0.091
9
EYD002 Eye Disease 61 0.091
10
P OBS005 Obesity 98 0.074
11
P AMY004 Amyloidosis 73 0.074
12
P HYP090 Hyperalphalipoproteinemia 57 0.074
13
NRM003 Norum Disease 55 0.074
14
END072 Endotheliitis 51 0.074
15
HYP037 Hyperhomocysteinemia 51 0.074
16
HPT025 Hepatic Lipase Deficiency 51 0.074
17
P ATX030 Ataxia-Telangiectasia 86 0.053
18
GLC006 Galactosemia 85 0.053
19
SMT004 Smith-Lemli-Opitz Syndrome 85 0.053
20
P ALG002 Alagille Syndrome 84 0.053
21
P HYP607 Hypercholesterolemia, Familial 80 0.053
22
AND015 Androgen Insensitivity 78 0.053
23
CNG034 Congestive Heart Failure 77 0.053
24
CRB011 Cerebrotendinous Xanthomatosis 76 0.053
25
P ANG001 Angelman Syndrome 76 0.053
26
ABT001 Abetalipoproteinemia 72 0.053
27
P NMN002 Niemann-Pick Disease 72 0.053
28
P LVR013 Liver Disease 71 0.053
29
P CNG401 Congenital Heart Disease 70 0.053
30
LPP001 Lipoprotein Lipase Deficiency 69 0.053
31
VSC007 Vascular Disease 67 0.053
32
c MTB001 Metabolic Syndrome X 67 0.053
33
ALS001 Alstrom Syndrome 67 0.053
34
ART021 Arteriosclerosis 66 0.053
35
PRP027 Peripheral Vascular Disease 66 0.053
36
P GLL020 Gallbladder Disease 64 0.053
37
LPM004 Lipoma 64 0.053
38
ACN002 Acanthosis Nigricans 63 0.053
39
ACR008 Acrocallosal Syndrome 63 0.053
40
P ACR001 Aicardi-Goutieres Syndrome 62 0.053
41
c HYP595 Hypertension, Essential 62 0.053
42
P AVS004 Avascular Necrosis of the Femoral Head 62 0.053
43
ISC004 Ischemia 61 0.053
44
DFC004 Deficiency Anemia 61 0.053
45
P AND016 Andersen Syndrome 61 0.053
46
P PLY019 Polyneuropathy 60 0.053
47
ISC006 Ischemic Heart Disease 59 0.053
48
MYC002 Mycobacterium Avium Complex Disease 59 0.053
49
CHL068 Cholestasis 58 0.053
50
P AXN010 Axenfeld-Rieger Syndrome, Type 3 57 0.053
51
ART001 Arterial Tortuosity Syndrome 56 0.053
52
P FML035 Familial Hyperlipidemia 55 0.053
53
P SPR013 Spiradenoma 54 0.053
54
P HYP027 Hypobetalipoproteinemia 54 0.053
55
CHY002 Chylomicron Retention Disease 54 0.053
56
LPP002 Lipoprotein Glomerulopathy 54 0.053
57
SCH016 Schimke Immunoosseous Dysplasia 53 0.053
58
P AML002 Amelogenesis Imperfecta 52 0.053
59
PPT005 Peptic Ulcer Disease 52 0.053
60
c SPN225 Spondyloarthropathy 1 52 0.053
61
THR013 Thoracic Outlet Syndrome 52 0.053
62
NM001 Noma 52 0.053
63
HMP005 Hemiplegia 51 0.053
64
HMZ003 Homozygous Familial Hypercholesterolemia 50 0.053
65
c HYP011 Hyperlipoproteinemia Type Iii 49 0.053
66
MNN014 Mononeuritis 49 0.053
67
CRN020 Coronary Restenosis 49 0.053
68
P AMY082 Amyloidosis, Familial Visceral 48 0.053
69
ALC010 Alcoholic Cardiomyopathy 48 0.053
70
LPD008 Lipid Metabolism Disorder 47 0.053
71
c HRD039 Hereditary Amyloidosis 47 0.053
72
P HYP614 Hyperlipidemia, Familial Combined 46 0.053
73
SPL018 Splenomegaly 46 0.053
74
FTT003 Fatty Acid Oxidation Disorders 46 0.053
75
CRB008 Cerebral Atherosclerosis 45 0.053
76
P TRC086 Trichohepatoenteric Syndrome 1 45 0.053
77
c SRC025 Sarcoidosis 1 43 0.053
78
ANM028 Anemia, Sideroblastic, Pyridoxine-Refractory, Autosomal Recessive 42 0.053
79
DFC001 Defective Apolipoprotein B-100 42 0.053
80
TTR016 Tetra-Amelia Syndrome 42 0.053
81
c LPD037 Lipodystrophy, Familial Partial, 2 42 0.053
82
ALN001 Aland Island Eye Disease 39 0.053
83
c JVN024 Juvenile Hereditary Hemochromatosis 38 0.053
84
c NMN016 Niemann-Pick Disease, Type B 38 0.053
85
c LPD021 Lipodystrophy, Familial Partial, Type 3 38 0.053
86
CRB009 Cerebritis 37 0.053
87
P LKN019 Leukoencephalopathy, Diffuse Hereditary, with Spheroids 37 0.053
88
c ART101 Aortic Valve Disease 2 37 0.053
89
HYP286 Hyperchylomicronemia, Late-Onset 37 0.053
90
PSL001 Pasli Disease 35 0.053
91
ADS002 Adie Syndrome 34 0.053
92
LPS020 Lipase Deficiency, Combined 34 0.053
93
ATM021 Autoimmune Inner Ear Disease 33 0.053
94
NTR005 Nutritional Deficiency Disease 31 0.053
95
TFT003 Tufting Enteropathy 31 0.053
96
HNM002 Hinman Syndrome 29 0.053
97
P ATX010 Ataxia Neuropathy Spectrum 29 0.053
98
CTR077 Citrullinemia, Type Ii, Neonatal-Onset 26 0.053
99
c HMP022 Hemophagocytic Lymphohistiocytosis, Familial, 1 25 0.053
100
LGP003 Logopenic Progressive Aphasia 25 0.053
101
c SCL030 Scoliosis, Idiopathic 1 22 0.053
102
c BNG076 Benign Exophthalmos Syndrome 21 0.053
103
AND005 Androgen Insensitivity Syndrome, Mild 19 0.053
104
HYP081 Hypolipoproteinemia 18 0.053
105
OTP003 Oto-Palatal-Digital Syndrome 17 0.053