Search results for "hyperlipoproteinemia"

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

73 hits were found for 'hyperlipoproteinemia'

# Family MCID Name MIFTS Score
1
FML026 Familial Lipoprotein Lipase Deficiency 44 7.009
2
HYP286 Hyperchylomicronemia, Late-Onset 33 6.925
3
c HYP032 Hyperlipoproteinemia Type Iv 28 6.371
4
c HYP163 Hyperlipidemia Type 3 23 5.706
5
P HYP607 Hypercholesterolemia, Familial 81 5.547
6
c HYP011 Hyperlipoproteinemia Type Iii 42 5.289
7
LPP001 Lipoprotein Lipase Deficiency 61 3.772
8
P HYP289 Hyperlipoproteinemia, Type Ib 21 3.649
9
c HYP592 Hyperlipoproteinemia, Type 1d 12 3.649
10
P FML035 Familial Hyperlipidemia 48 3.025
11
P HYP614 Hyperlipidemia, Familial Combined 41 2.953
12
P HYP117 Hypertriglyceridemia 61 2.333
13
P PNC044 Pancreatitis 59 0.137
14
ATH003 Atherosclerosis 56 0.137
15
XNT003 Xanthomatosis 41 0.137
16
P GLL020 Gallbladder Disease 56 0.106
17
ISC006 Ischemic Heart Disease 51 0.106
18
LPP002 Lipoprotein Glomerulopathy 46 0.106
19
INN002 Inner Ear Disease 33 0.106
20
P OBS005 Obesity 94 0.087
21
P NPH012 Nephrotic Syndrome 60 0.087
22
ACN002 Acanthosis Nigricans 55 0.087
23
P HST010 Histiocytosis 55 0.087
24
c ACT027 Acute Pancreatitis 55 0.087
25
P HYP090 Hyperalphalipoproteinemia 50 0.087
26
P HYP060 Hyperinsulinism 47 0.087
27
c RCR022 Recurrent Acute Pancreatitis 41 0.087
28
P TRC086 Trichohepatoenteric Syndrome 1 39 0.087
29
P MYC007 Myocardial Infarction 81 0.061
30
c MLT019 Multiple Myeloma 75 0.061
31
CRB011 Cerebrotendinous Xanthomatosis 66 0.061
32
P ANG001 Angelman Syndrome 66 0.061
33
TNG002 Tangier Disease 63 0.061
34
ANR007 Anorexia Nervosa 62 0.061
35
PRT036 Peritonitis 61 0.061
36
P HYP086 Hypothyroidism 59 0.061
37
VSC007 Vascular Disease 59 0.061
38
c MTB001 Metabolic Syndrome X 58 0.061
39
P SPN046 Spinal Muscular Atrophy 57 0.061
40
P THY032 Thyroiditis 56 0.061
41
URT039 Urticaria 55 0.061
42
P HPT021 Hepatitis 55 0.061
43
CLT003 Colitis 54 0.061
44
MNR002 Meniere's Disease 53 0.061
45
ISC004 Ischemia 53 0.061
46
P MYL007 Myeloma 53 0.061
47
ICH002 Ichthyosis Bullosa of Siemens 52 0.061
48
P GLY013 Glycogen Storage Disease 51 0.061
49
P SYP003 Syphilis 48 0.061
50
c SPN225 Spondyloarthropathy 1 48 0.061
51
P BLN003 Blindness 47 0.061
52
SCH016 Schimke Immunoosseous Dysplasia 46 0.061
53
GRW007 Growth Hormone Deficiency 46 0.061
54
HYP037 Hyperhomocysteinemia 45 0.061
55
THR013 Thoracic Outlet Syndrome 45 0.061
56
P MSC003 Muscular Atrophy 44 0.061
57
ADR042 Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency 45 0.061
58
C2D001 C2 Deficiency 44 0.061
59
P SJG001 Sjogren's Syndrome 42 0.061
60
SPL018 Splenomegaly 40 0.061
61
KRT012 Keratoderma 39 0.061
62
ANG054 Angina Pectoris 43 0.061
63
LMB062 Limb Ischemia 38 0.061
64
ANM028 Anemia, Sideroblastic, Pyridoxine-Refractory, Autosomal Recessive 38 0.061
65
TTR016 Tetra-Amelia Syndrome 36 0.061
66
NPH017 Nephrosis 36 0.061
67
FCL012 Facial Paralysis 35 0.061
68
c CNG033 Congenital Syphilis 34 0.061
69
c ART101 Aortic Valve Disease 2 32 0.061
70
NTR005 Nutritional Deficiency Disease 28 0.061
71
TFT003 Tufting Enteropathy 26 0.061
72
LGP003 Logopenic Progressive Aphasia 20 0.061
73
c FML073 Familial Hypothyroidism 13 0.061