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 64 9.252
2
TNG002 Tangier Disease 63 4.802
3
P HYP117 Hypertriglyceridemia 61 0.129
4
P CRN211 Coronary Artery Disease 73 0.105
5
ART111 Artery Disease 55 0.105
6
FSH001 Fish-Eye Disease 47 0.105
7
ATH003 Atherosclerosis 56 0.091
8
P HPT021 Hepatitis 55 0.091
9
EYD002 Eye Disease 54 0.091
10
P OBS005 Obesity 94 0.074
11
P AMY004 Amyloidosis 63 0.074
12
P HYP090 Hyperalphalipoproteinemia 50 0.074
13
NRM003 Norum Disease 48 0.074
14
HYP037 Hyperhomocysteinemia 45 0.074
15
END072 Endotheliitis 44 0.074
16
HPT025 Hepatic Lipase Deficiency 44 0.074
17
P HYP607 Hypercholesterolemia, Familial 81 0.053
18
P ATX030 Ataxia-Telangiectasia 76 0.053
19
GLC006 Galactosemia 75 0.053
20
SMT004 Smith-Lemli-Opitz Syndrome 74 0.053
21
P ALG002 Alagille Syndrome 73 0.053
22
CNG034 Congestive Heart Failure 69 0.053
23
AND015 Androgen Insensitivity 69 0.053
24
CRB011 Cerebrotendinous Xanthomatosis 66 0.053
25
P ANG001 Angelman Syndrome 66 0.053
26
ABT001 Abetalipoproteinemia 63 0.053
27
P NMN002 Niemann-Pick Disease 63 0.053
28
P CNG401 Congenital Heart Disease 62 0.053
29
c HYP595 Hypertension, Essential 66 0.053
30
P LVR013 Liver Disease 62 0.053
31
LPP001 Lipoprotein Lipase Deficiency 61 0.053
32
PRP027 Peripheral Vascular Disease 60 0.053
33
VSC007 Vascular Disease 59 0.053
34
c MTB001 Metabolic Syndrome X 58 0.053
35
ALS001 Alstrom Syndrome 58 0.053
36
ART021 Arteriosclerosis 58 0.053
37
P GLL020 Gallbladder Disease 56 0.053
38
LPM004 Lipoma 56 0.053
39
ACN002 Acanthosis Nigricans 55 0.053
40
ACR008 Acrocallosal Syndrome 55 0.053
41
P AVS004 Avascular Necrosis of the Femoral Head 54 0.053
42
DFC004 Deficiency Anemia 54 0.053
43
P ACR001 Aicardi-Goutieres Syndrome 54 0.053
44
ISC004 Ischemia 53 0.053
45
P AND016 Andersen Syndrome 54 0.053
46
P PLY019 Polyneuropathy 52 0.053
47
ISC006 Ischemic Heart Disease 51 0.053
48
MYC002 Mycobacterium Avium Complex Disease 51 0.053
49
CHL068 Cholestasis 50 0.053
50
P AXN010 Axenfeld-Rieger Syndrome, Type 3 50 0.053
51
ART001 Arterial Tortuosity Syndrome 48 0.053
52
CHY002 Chylomicron Retention Disease 48 0.053
53
P FML035 Familial Hyperlipidemia 48 0.053
54
c SPN225 Spondyloarthropathy 1 48 0.053
55
P SPR013 Spiradenoma 47 0.053
56
P HYP027 Hypobetalipoproteinemia 47 0.053
57
LPP002 Lipoprotein Glomerulopathy 46 0.053
58
SCH016 Schimke Immunoosseous Dysplasia 46 0.053
59
P AML002 Amelogenesis Imperfecta 45 0.053
60
THR013 Thoracic Outlet Syndrome 45 0.053
61
PPT005 Peptic Ulcer Disease 45 0.053
62
NM001 Noma 44 0.053
63
c SRC025 Sarcoidosis 1 44 0.053
64
HMP005 Hemiplegia 44 0.053
65
HMZ003 Homozygous Familial Hypercholesterolemia 44 0.053
66
MNN014 Mononeuritis 43 0.053
67
CRN020 Coronary Restenosis 42 0.053
68
c HYP011 Hyperlipoproteinemia Type Iii 42 0.053
69
P AMY082 Amyloidosis, Familial Visceral 43 0.053
70
LPD008 Lipid Metabolism Disorder 41 0.053
71
ALC010 Alcoholic Cardiomyopathy 41 0.053
72
c HRD039 Hereditary Amyloidosis 41 0.053
73
P HYP614 Hyperlipidemia, Familial Combined 41 0.053
74
SPL018 Splenomegaly 40 0.053
75
FTT003 Fatty Acid Oxidation Disorders 39 0.053
76
CRB008 Cerebral Atherosclerosis 39 0.053
77
P TRC086 Trichohepatoenteric Syndrome 1 39 0.053
78
ANM028 Anemia, Sideroblastic, Pyridoxine-Refractory, Autosomal Recessive 38 0.053
79
c LPD037 Lipodystrophy, Familial Partial, 2 37 0.053
80
TTR016 Tetra-Amelia Syndrome 36 0.053
81
DFC001 Defective Apolipoprotein B-100 34 0.053
82
ALN001 Aland Island Eye Disease 34 0.053
83
c NMN016 Niemann-Pick Disease, Type B 34 0.053
84
c LPD021 Lipodystrophy, Familial Partial, Type 3 33 0.053
85
CRB009 Cerebritis 33 0.053
86
P LKN019 Leukoencephalopathy, Diffuse Hereditary, with Spheroids 33 0.053
87
c ART101 Aortic Valve Disease 2 32 0.053
88
HYP286 Hyperchylomicronemia, Late-Onset 33 0.053
89
PSL001 Pasli Disease 30 0.053
90
ADS002 Adie Syndrome 30 0.053
91
LPS020 Lipase Deficiency, Combined 30 0.053
92
P ATX010 Ataxia Neuropathy Spectrum 29 0.053
93
ATM021 Autoimmune Inner Ear Disease 29 0.053
94
NTR005 Nutritional Deficiency Disease 28 0.053
95
TFT003 Tufting Enteropathy 26 0.053
96
HNM002 Hinman Syndrome 26 0.053
97
c JVN024 Juvenile Hereditary Hemochromatosis 25 0.053
98
CTR077 Citrullinemia, Type Ii, Neonatal-Onset 24 0.053
99
c HMP022 Hemophagocytic Lymphohistiocytosis, Familial, 1 23 0.053
100
LGP003 Logopenic Progressive Aphasia 20 0.053
101
c SCL030 Scoliosis, Idiopathic 1 20 0.053
102
c BNG076 Benign Exophthalmos Syndrome 19 0.053
103
AND005 Androgen Insensitivity Syndrome, Mild 17 0.053
104
HYP081 Hypolipoproteinemia 16 0.053
105
OTP003 Oto-Palatal-Digital Syndrome 14 0.053