Search results for "hyperlipoproteinemia"

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

84 hits were found for 'hyperlipoproteinemia'

# Family MCID Name MIFTS Score
1
P HYP031 Hyperlipoproteinemia Type V 49 6.849
2
FML026 Familial Lipoprotein Lipase Deficiency 51 6.538
3
c HYP032 Hyperlipoproteinemia Type Iv 23 6.242
4
P HYP163 Hyperlipidemia Type 3 27 5.927
5
c HYP011 Hyperlipoproteinemia Type Iii 49 4.732
6
c HYP289 Hyperlipoproteinemia, Type Ib 27 4.100
7
P FML021 Familial Hypercholesterolemia 85 3.612
8
c HYP164 Hyperlipoproteinemia Type 2 13 3.558
9
FML235 Familial Combined Hyperlipoproteinemia 33 3.140
10
P HYP117 Hypertriglyceridemia 65 3.087
11
c FML035 Familial Hyperlipidemia 55 3.003
12
P FML020 Familial Combined Hyperlipidemia 63 2.949
13
HYP456 Hyperapobetalipoproteinemia 39 2.155
14
c FML016 Familial Hypertriglyceridemia 52 2.085
15
XNT003 Xanthomatosis 47 0.146
16
c PNC044 Pancreatitis 69 0.133
17
ATH003 Atherosclerosis 68 0.133
18
SYN053 Syndromic Diarrhea 32 0.133
19
c DBT009 Diabetes Mellitus 78 0.119
20
c HYP095 Hypercholesterolemia 70 0.103
21
c GLL020 Gallbladder Disease 63 0.103
22
P MTB001 Metabolic Syndrome X 56 0.103
23
INN002 Inner Ear Disease 39 0.103
24
P OBS005 Obesity 89 0.084
25
ACN002 Acanthosis Nigricans 69 0.084
26
c NPH012 Nephrotic Syndrome 66 0.084
27
P INS005 Insulin Resistance 66 0.084
28
c ACT027 Acute Pancreatitis 63 0.084
29
P HST010 Histiocytosis 62 0.084
30
c HYP060 Hyperinsulinism 55 0.084
31
GRW007 Growth Hormone Deficiency 52 0.084
32
LPP002 Lipoprotein Glomerulopathy 47 0.084
33
c RCR022 Recurrent Acute Pancreatitis 45 0.084
34
SBL004 Sea-Blue Histiocytosis 29 0.084
35
TFT003 Tufting Enteropathy 28 0.084
36
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 28 0.084
37
NTR005 Nutritional Deficiency Disease 25 0.084
38
APL017 Apolipoprotein C-Ii Deficiency 17 0.084
39
P ALZ001 Alzheimer's Disease 97 0.060
40
c TYP009 Type 2 Diabetes Mellitus 95 0.060
41
P MYC007 Myocardial Infarction 92 0.060
42
P HYP075 Hypertension 85 0.060
43
P MLT019 Multiple Myeloma 82 0.060
44
CRB011 Cerebrotendinous Xanthomatosis 75 0.060
45
ANK002 Ankylosing Spondylitis 74 0.060
46
21H001 21-Hydroxylase Deficiency 73 0.060
47
PRT036 Peritonitis 71 0.060
48
P ANG001 Angelman Syndrome 70 0.060
49
VSC007 Vascular Disease 70 0.060
50
TNG002 Tangier Disease 70 0.060
51
c HYP086 Hypothyroidism 69 0.060
52
P ANR007 Anorexia Nervosa 66 0.060
53
c THY032 Thyroiditis 66 0.060
54
c SPN046 Spinal Muscular Atrophy 65 0.060
55
c HPT021 Hepatitis 64 0.060
56
ART019 Aortic Valve Stenosis 64 0.060
57
ISC004 Ischemia 63 0.060
58
MNR002 Meniere's Disease 62 0.060
59
URT039 Urticaria 61 0.060
60
c MYL007 Myeloma 61 0.060
61
ART111 Artery Disease 60 0.060
62
c GLY013 Glycogen Storage Disease 59 0.060
63
ICH002 Ichthyosis Bullosa of Siemens 58 0.060
64
P SYP003 Syphilis 57 0.060
65
P HYP090 Hyperalphalipoproteinemia 55 0.060
66
STT004 Steatorrhea 54 0.060
67
P MSC003 Muscular Atrophy 53 0.060
68
BLN003 Blindness 52 0.060
69
HYP037 Hyperhomocysteinemia 51 0.060
70
ANG054 Angina Pectoris 46 0.060
71
HPT025 Hepatic Lipase Deficiency 46 0.060
72
KRT012 Keratoderma 45 0.060
73
SJG001 Sjogren's Syndrome 44 0.060
74
LMB062 Limb Ischemia 44 0.060
75
NPH017 Nephrosis 42 0.060
76
FCL012 Facial Paralysis 40 0.060
77
c CNG033 Congenital Syphilis 40 0.060
78
c JVN024 Juvenile Hereditary Hemochromatosis 38 0.060
79
PRX014 Proximal Spinal Muscular Atrophy 32 0.060
80
c HNT004 Huntington Disease-Like 2 28 0.060
81
LGP003 Logopenic Progressive Aphasia 22 0.060
82
c HNT011 Huntington Disease-Like 3 16 0.060
83
c FML073 Familial Hypothyroidism 16 0.060
84
OTP003 Oto-Palatal-Digital Syndrome 16 0.060