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 51 7.235
2
FML026 Familial Lipoprotein Lipase Deficiency 51 6.962
3
P HYP163 Hyperlipidemia Type 3 29 6.688
4
c HYP032 Hyperlipoproteinemia Type Iv 23 6.661
5
c HYP011 Hyperlipoproteinemia Type Iii 49 4.798
6
c HYP289 Hyperlipoproteinemia, Type Ib 43 4.185
7
P FML021 Familial Hypercholesterolemia 85 3.663
8
c HYP164 Hyperlipoproteinemia Type 2 37 3.610
9
P HYP117 Hypertriglyceridemia 67 3.128
10
c FML035 Familial Hyperlipidemia 55 3.044
11
P FML020 Familial Combined Hyperlipidemia 66 2.991
12
c HYP592 Hyperlipoproteinemia, Type 1d 12 2.922
13
c FML016 Familial Hypertriglyceridemia 53 2.115
14
XNT003 Xanthomatosis 50 0.145
15
c PNC044 Pancreatitis 68 0.132
16
c DBT009 Diabetes Mellitus 73 0.118
17
PYR007 Pyridoxine-Refractory Autosomal Recessive Sideroblastic Anemia 43 0.118
18
HYP456 Hyperapobetalipoproteinemia 39 0.118
19
SYN053 Syndromic Diarrhea 34 0.118
20
c HYP095 Hypercholesterolemia 72 0.102
21
ATH003 Atherosclerosis 68 0.102
22
c GLL020 Gallbladder Disease 63 0.102
23
ISC006 Ischemic Heart Disease 58 0.102
24
LPP002 Lipoprotein Glomerulopathy 50 0.102
25
P OBS005 Obesity 89 0.084
26
P MTB001 Metabolic Syndrome X 69 0.084
27
c NPH012 Nephrotic Syndrome 67 0.084
28
P INS005 Insulin Resistance 64 0.084
29
ACN002 Acanthosis Nigricans 64 0.084
30
c ACT027 Acute Pancreatitis 63 0.084
31
P HST010 Histiocytosis 63 0.084
32
c HYP060 Hyperinsulinism 56 0.084
33
P HYP090 Hyperalphalipoproteinemia 56 0.084
34
c RCR022 Recurrent Acute Pancreatitis 46 0.084
35
INN002 Inner Ear Disease 38 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 98 0.059
41
P MYC007 Myocardial Infarction 92 0.059
42
P MLT019 Multiple Myeloma 88 0.059
43
P HYP075 Hypertension 85 0.059
44
CRB011 Cerebrotendinous Xanthomatosis 76 0.059
45
21H001 21-Hydroxylase Deficiency 76 0.059
46
ANK002 Ankylosing Spondylitis 76 0.059
47
TNG002 Tangier Disease 73 0.059
48
P ANG001 Angelman Syndrome 71 0.059
49
PRT036 Peritonitis 71 0.059
50
VSC007 Vascular Disease 69 0.059
51
c HYP086 Hypothyroidism 68 0.059
52
P ANR007 Anorexia Nervosa 65 0.059
53
c THY032 Thyroiditis 65 0.059
54
c SPN046 Spinal Muscular Atrophy 65 0.059
55
ART019 Aortic Valve Stenosis 63 0.059
56
c HPT021 Hepatitis 63 0.059
57
MNR002 Meniere's Disease 63 0.059
58
URT039 Urticaria 63 0.059
59
ART111 Artery Disease 63 0.059
60
ISC004 Ischemia 62 0.059
61
c MYL007 Myeloma 60 0.059
62
c GLY013 Glycogen Storage Disease 59 0.059
63
ICH002 Ichthyosis Bullosa of Siemens 58 0.059
64
P SYP003 Syphilis 57 0.059
65
STT004 Steatorrhea 53 0.059
66
P MSC003 Muscular Atrophy 53 0.059
67
BLN003 Blindness 52 0.059
68
HYP037 Hyperhomocysteinemia 52 0.059
69
GRW007 Growth Hormone Deficiency 52 0.059
70
HPT025 Hepatic Lipase Deficiency 47 0.059
71
SJG001 Sjogren's Syndrome 47 0.059
72
ANG054 Angina Pectoris 46 0.059
73
LMB062 Limb Ischemia 46 0.059
74
KRT012 Keratoderma 45 0.059
75
c JVN024 Juvenile Hereditary Hemochromatosis 44 0.059
76
NPH017 Nephrosis 42 0.059
77
c CNG033 Congenital Syphilis 40 0.059
78
FCL012 Facial Paralysis 40 0.059
79
c PRX014 Proximal Spinal Muscular Atrophy 32 0.059
80
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 29 0.059
81
TFT003 Tufting Enteropathy 28 0.059
82
c HNT004 Huntington Disease-Like 2 27 0.059
83
LGP003 Logopenic Progressive Aphasia 24 0.059
84
c HNT011 Huntington Disease-Like 3 19 0.059
85
OTP003 Oto-Palatal-Digital Syndrome 17 0.059
86
c FML073 Familial Hypothyroidism 15 0.059