Search results for "hyperlipoproteinemia"

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

86 hits were found for 'hyperlipoproteinemia'

# Family MCID Name MIFTS Score
1
P HYP031 Hyperlipoproteinemia Type V 50 7.235
2
FML026 Familial Lipoprotein Lipase Deficiency 48 6.962
3
P HYP163 Hyperlipidemia Type 3 28 6.688
4
c HYP032 Hyperlipoproteinemia Type Iv 24 6.661
5
c HYP011 Hyperlipoproteinemia Type Iii 50 4.798
6
c HYP289 Hyperlipoproteinemia, Type Ib 41 4.160
7
P FML021 Familial Hypercholesterolemia 86 3.663
8
c HYP164 Hyperlipoproteinemia Type 2 32 3.610
9
P HYP117 Hypertriglyceridemia 67 3.128
10
c FML035 Familial Hyperlipidemia 56 3.044
11
P FML020 Familial Combined Hyperlipidemia 66 2.991
12
c HYP592 Hyperlipoproteinemia, Type 1d 10 2.922
13
c FML016 Familial Hypertriglyceridemia 54 2.115
14
XNT003 Xanthomatosis 48 0.145
15
c PNC044 Pancreatitis 69 0.132
16
c DBT009 Diabetes Mellitus 74 0.118
17
PYR007 Pyridoxine-Refractory Autosomal Recessive Sideroblastic Anemia 42 0.118
18
HYP456 Hyperapobetalipoproteinemia 40 0.118
19
SYN053 Syndromic Diarrhea 34 0.118
20
c HYP095 Hypercholesterolemia 73 0.102
21
ATH003 Atherosclerosis 69 0.102
22
c GLL020 Gallbladder Disease 64 0.102
23
ISC006 Ischemic Heart Disease 58 0.102
24
LPP002 Lipoprotein Glomerulopathy 48 0.102
25
P OBS005 Obesity 91 0.084
26
P MTB001 Metabolic Syndrome X 70 0.084
27
c NPH012 Nephrotic Syndrome 67 0.084
28
P INS005 Insulin Resistance 65 0.084
29
c ACT027 Acute Pancreatitis 64 0.084
30
P HST010 Histiocytosis 64 0.084
31
ACN002 Acanthosis Nigricans 63 0.084
32
c HYP060 Hyperinsulinism 57 0.084
33
P HYP090 Hyperalphalipoproteinemia 56 0.084
34
c RCR022 Recurrent Acute Pancreatitis 46 0.084
35
INN002 Inner Ear Disease 39 0.084
36
NTR005 Nutritional Deficiency Disease 33 0.084
37
SBL004 Sea-Blue Histiocytosis 29 0.084
38
APL017 Apolipoprotein C-Ii Deficiency 17 0.084
39
c TYP009 Type 2 Diabetes Mellitus 100 0.059
40
P ALZ001 Alzheimer's Disease 100 0.059
41
P MYC007 Myocardial Infarction 93 0.059
42
P MLT019 Multiple Myeloma 88 0.059
43
P HYP075 Hypertension 87 0.059
44
ANK002 Ankylosing Spondylitis 77 0.059
45
CRB011 Cerebrotendinous Xanthomatosis 76 0.059
46
21H001 21-Hydroxylase Deficiency 74 0.059
47
PRT036 Peritonitis 72 0.059
48
TNG002 Tangier Disease 71 0.059
49
P ANG001 Angelman Syndrome 70 0.059
50
VSC007 Vascular Disease 70 0.059
51
c HYP086 Hypothyroidism 69 0.059
52
P ANR007 Anorexia Nervosa 66 0.059
53
c THY032 Thyroiditis 66 0.059
54
c SPN046 Spinal Muscular Atrophy 66 0.059
55
ART019 Aortic Valve Stenosis 64 0.059
56
c HPT021 Hepatitis 64 0.059
57
URT039 Urticaria 64 0.059
58
ISC004 Ischemia 63 0.059
59
MNR002 Meniere's Disease 63 0.059
60
ART111 Artery Disease 62 0.059
61
c MYL007 Myeloma 61 0.059
62
c GLY013 Glycogen Storage Disease 60 0.059
63
ICH002 Ichthyosis Bullosa of Siemens 58 0.059
64
P SYP003 Syphilis 58 0.059
65
STT004 Steatorrhea 54 0.059
66
P MSC003 Muscular Atrophy 54 0.059
67
BLN003 Blindness 53 0.059
68
HYP037 Hyperhomocysteinemia 53 0.059
69
GRW007 Growth Hormone Deficiency 52 0.059
70
SJG001 Sjogren's Syndrome 48 0.059
71
ANG054 Angina Pectoris 47 0.059
72
HPT025 Hepatic Lipase Deficiency 47 0.059
73
LMB062 Limb Ischemia 46 0.059
74
KRT012 Keratoderma 46 0.059
75
c JVN024 Juvenile Hereditary Hemochromatosis 45 0.059
76
NPH017 Nephrosis 42 0.059
77
c CNG033 Congenital Syphilis 41 0.059
78
FCL012 Facial Paralysis 40 0.059
79
PRX014 Proximal Spinal Muscular Atrophy 32 0.059
80
TFT003 Tufting Enteropathy 28 0.059
81
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 28 0.059
82
c HNT004 Huntington Disease-Like 2 24 0.059
83
LGP003 Logopenic Progressive Aphasia 23 0.059
84
OTP003 Oto-Palatal-Digital Syndrome 17 0.059
85
c HNT011 Huntington Disease-Like 3 16 0.059
86
c FML073 Familial Hypothyroidism 16 0.059