Search results for "hyperlipoproteinemia"

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

74 hits were found for 'hyperlipoproteinemia'

# Family MCID Name MIFTS Score
1
FML026 Familial Lipoprotein Lipase Deficiency 51 7.725
2
c HYP032 Hyperlipoproteinemia Type Iv 33 7.118
3
HYP286 Hyperchylomicronemia, Late-Onset 37 6.708
4
c HYP163 Hyperlipidemia Type 3 28 6.529
5
c HYP011 Hyperlipoproteinemia Type Iii 49 5.353
6
P HYP607 Hypercholesterolemia, Familial 80 4.769
7
P HYP289 Hyperlipoproteinemia, Type Ib 25 3.674
8
c HYP592 Hyperlipoproteinemia, Type 1d 15 3.674
9
LPP001 Lipoprotein Lipase Deficiency 69 3.172
10
P FML035 Familial Hyperlipidemia 55 3.071
11
P HYP614 Hyperlipidemia, Familial Combined 46 2.121
12
P HYP117 Hypertriglyceridemia 71 0.172
13
P PNC044 Pancreatitis 68 0.136
14
ATH003 Atherosclerosis 65 0.136
15
XNT003 Xanthomatosis 48 0.136
16
P GLL020 Gallbladder Disease 64 0.106
17
ISC006 Ischemic Heart Disease 59 0.106
18
LPP002 Lipoprotein Glomerulopathy 54 0.106
19
INN002 Inner Ear Disease 38 0.106
20
P OBS005 Obesity 98 0.086
21
P NPH012 Nephrotic Syndrome 68 0.086
22
ACN002 Acanthosis Nigricans 63 0.086
23
c ACT027 Acute Pancreatitis 63 0.086
24
P HST010 Histiocytosis 62 0.086
25
P HYP090 Hyperalphalipoproteinemia 57 0.086
26
P HYP060 Hyperinsulinism 55 0.086
27
c RCR022 Recurrent Acute Pancreatitis 47 0.086
28
P TRC086 Trichohepatoenteric Syndrome 1 45 0.086
29
P MYC007 Myocardial Infarction 93 0.061
30
c MLT019 Multiple Myeloma 85 0.061
31
CRB011 Cerebrotendinous Xanthomatosis 76 0.061
32
P ANG001 Angelman Syndrome 76 0.061
33
TNG002 Tangier Disease 72 0.061
34
ANR007 Anorexia Nervosa 71 0.061
35
PRT036 Peritonitis 71 0.061
36
P HYP086 Hypothyroidism 68 0.061
37
VSC007 Vascular Disease 67 0.061
38
c MTB001 Metabolic Syndrome X 67 0.061
39
P SPN046 Spinal Muscular Atrophy 66 0.061
40
P THY032 Thyroiditis 65 0.061
41
URT039 Urticaria 63 0.061
42
P HPT021 Hepatitis 63 0.061
43
CLT003 Colitis 62 0.061
44
MNR002 Meniere's Disease 61 0.061
45
ISC004 Ischemia 61 0.061
46
ICH002 Ichthyosis Bullosa of Siemens 59 0.061
47
P GLY013 Glycogen Storage Disease 59 0.061
48
P MYL007 Myeloma 59 0.061
49
P SYP003 Syphilis 56 0.061
50
P BLN003 Blindness 54 0.061
51
SCH016 Schimke Immunoosseous Dysplasia 53 0.061
52
c SPN225 Spondyloarthropathy 1 52 0.061
53
GRW007 Growth Hormone Deficiency 52 0.061
54
THR013 Thoracic Outlet Syndrome 52 0.061
55
P MSC003 Muscular Atrophy 51 0.061
56
HYP037 Hyperhomocysteinemia 51 0.061
57
C2D001 C2 Deficiency 50 0.061
58
SPL018 Splenomegaly 46 0.061
59
P SJG001 Sjogren's Syndrome 46 0.061
60
KRT012 Keratoderma 45 0.061
61
LMB062 Limb Ischemia 45 0.061
62
ANG054 Angina Pectoris 44 0.061
63
ADR042 Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency 44 0.061
64
ANM028 Anemia, Sideroblastic, Pyridoxine-Refractory, Autosomal Recessive 42 0.061
65
TTR016 Tetra-Amelia Syndrome 42 0.061
66
NPH017 Nephrosis 42 0.061
67
c CNG033 Congenital Syphilis 40 0.061
68
FCL012 Facial Paralysis 38 0.061
69
c ART101 Aortic Valve Disease 2 37 0.061
70
NTR005 Nutritional Deficiency Disease 31 0.061
71
TFT003 Tufting Enteropathy 31 0.061
72
LGP003 Logopenic Progressive Aphasia 25 0.061
73
c FML073 Familial Hypothyroidism 16 0.061
74
FML285 Familial Apolipoprotein C-Ii Deficiency 9 0.061