Search results for hypoalphalipoproteinemias

79 hits were found for hypoalphalipoproteinemias

# Family MCID Name MIFTS Score
1
HYP190 Hypoalphalipoproteinemia, Primary 61 11.967
2
TNG002 Tangier Disease 65 4.827
3
P HYP750 Hypertriglyceridemia, Familial 55 0.129
4
FSH001 Fish-Eye Disease 45 0.129
5
P CRN018 Coronary Artery Anomaly 69 0.116
6
ART140 Arteries, Anomalies of 51 0.116
7
c HYP805 Hypercholesterolemia, Autosomal Dominant, 3 47 0.116
8
c HYP555 Hypertriglyceridemia, Transient Infantile 34 0.116
9
P HRT032 Heart Disease 80 0.100
10
P HPT021 Hepatitis 75 0.100
11
P CRN300 Coronary Heart Disease 1 57 0.100
12
P HYP607 Hypercholesterolemia, Familial 81 0.082
13
BDY004 Body Mass Index Quantitative Trait Locus 11 75 0.082
14
P AMY004 Amyloidosis 69 0.082
15
P HYP724 Hyperlipoproteinemia, Type Iii 59 0.082
16
HYP732 Hyperalphalipoproteinemia 1 52 0.082
17
BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.082
18
HYP081 Hypolipoproteinemia 49 0.082
19
BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.082
20
HPT025 Hepatic Lipase Deficiency 48 0.082
21
BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.082
22
BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.082
23
END072 Endotheliitis 46 0.082
24
BDY010 Body Mass Index Quantitative Trait Locus 4 45 0.082
25
BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.082
26
BDY006 Body Mass Index Quantitative Trait Locus 8 42 0.082
27
BDY012 Body Mass Index Quantitative Trait Locus 7 42 0.082
28
ALP046 Alport Syndrome, X-Linked 74 0.058
29
ISC006 Ischemic Heart Disease 73 0.058
30
SMT004 Smith-Lemli-Opitz Syndrome 70 0.058
31
P ANR048 Aniridia 1 68 0.058
32
AGN016 Aging 65 0.058
33
P GLL020 Gallbladder Disease 64 0.058
34
ABT001 Abetalipoproteinemia 64 0.058
35
LWC002 Lowe Oculocerebrorenal Syndrome 62 0.058
36
LCT022 Lecithin:cholesterol Acyltransferase Deficiency 61 0.058
37
ATH013 Atherosclerosis Susceptibility 59 0.058
38
LPD008 Lipid Metabolism Disorder 59 0.058
39
P HYP614 Hyperlipidemia, Familial Combined 57 0.058
40
HMZ003 Homozygous Familial Hypercholesterolemia 54 0.058
41
P HYP818 Hypobetalipoproteinemia, Familial, 1 54 0.058
42
CHY002 Chylomicron Retention Disease 54 0.058
43
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 54 0.058
44
XNT003 Xanthomatosis 53 0.058
45
VTM028 Vitamin E, Familial Isolated Deficiency of 52 0.058
46
CRN030 Coronary Stenosis 52 0.058
47
PRX028 Peroxisomal Acyl-Coa Oxidase Deficiency 52 0.058
48
HPT082 Hepatic Adenomas, Familial 52 0.058
49
c HYP739 Hyperlipoproteinemia, Type Iv 51 0.058
50
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 51 0.058
51
P FML035 Familial Hyperlipidemia 48 0.058
52
c AMY009 Amyloidosis Aa 48 0.058
53
ART004 Aortic Atherosclerosis 48 0.058
54
c HRD039 Hereditary Amyloidosis 47 0.058
55
FML026 Familial Lipoprotein Lipase Deficiency 46 0.058
56
FTL021 Fetal Macrosomia 46 0.058
57
c LKD015 Leukodystrophy, Hypomyelinating, 3 44 0.058
58
SCH076 Schnyder Corneal Dystrophy 44 0.058
59
c HYP734 Hypercholesterolemia, Autosomal Dominant, Type B 44 0.058
60
LPP002 Lipoprotein Glomerulopathy 44 0.058
61
ADP007 Adie Pupil 41 0.058
62
ARC023 Arcus Corneae 40 0.058
63
ALN001 Aland Island Eye Disease 39 0.058
64
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 37 0.058
65
SLT014 Salt and Pepper Developmental Regression Syndrome 37 0.058
66
FML330 Familial Lcat Deficiency 37 0.058
67
DYS013 Dysbaric Osteonecrosis 35 0.058
68
DFC001 Defective Apolipoprotein B-100 31 0.058
69
LPS020 Lipase Deficiency, Combined 31 0.058
70
ALR002 Al-Raqad Syndrome 30 0.058
71
c SRC023 Sarcoidosis 2 30 0.058
72
P RNG031 Ring Chromosome Y Syndrome 29 0.058
73
ANR038 Anorexia Nervosa 1 21 0.058
74
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 21 0.058
75
c HYP290 Hypobetalipoproteinemia, Familial, 2 18 0.058
76
ATS285 Autosomal Semi-Dominant Severe Lipodystrophic Laminopathy 17 0.058
77
BLD137 Blood Group--Ahonen 17 0.058
78
APD001 Apo a-I Deficiency 15 0.058
79
c HGH032 High Density Lipoprotein Cholesterol Level Quantitative Trait Locus 14 8 0.058
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