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

120 hits were found for 'hyperlipoproteinemia'

# Family MCID Name MIFTS Score
1
FML026 Familial Lipoprotein Lipase Deficiency 52 6.292
2
c HYP032 Hyperlipoproteinemia Type Iv 20 6.173
3
P HYP031 Hyperlipoproteinemia Type V 45 6.127
4
P HYP163 Hyperlipidemia Type 3 27 5.433
5
c HYP011 Hyperlipoproteinemia Type Iii 47 5.044
6
c HYP289 Hyperlipoproteinemia, Type Ib 28 3.988
7
P FML021 Familial Hypercholesterolemia 87 3.530
8
c HYP164 Hyperlipoproteinemia Type 2 10 3.482
9
P HYP117 Hypertriglyceridemia 54 3.359
10
c FML035 Familial Hyperlipidemia 59 2.951
11
P FML020 Familial Combined Hyperlipidemia 63 2.907
12
FML235 Familial Combined Hyperlipoproteinemia 26 2.820
13
LPP001 Lipoprotein Lipase Deficiency 53 2.100
14
c FML016 Familial Hypertriglyceridemia 51 2.072
15
HYP456 Hyperapobetalipoproteinemia 32 2.072
16
RPD005 Rapidly Involuting Congenital Hemangioma 16 0.225
17
ICH002 Ichthyosis Bullosa of Siemens 50 0.213
18
GLL008 Gilles De La Tourette Syndrome 73 0.199
19
IDP042 Idiopathic Recurrent Stupor 15 0.199
20
VND002 Van Der Woude Syndrome 43 0.150
21
P TYP009 Type 2 Diabetes Mellitus 93 0.141
22
c DBT009 Diabetes Mellitus 80 0.141
23
ACN002 Acanthosis Nigricans 73 0.141
24
MSC006 Muscle Glycogenosis 36 0.141
25
P MLR006 Male Reproductive Organ Cancer 23 0.141
26
XNT003 Xanthomatosis 55 0.130
27
TRN012 Transient Global Amnesia 42 0.130
28
HPT025 Hepatic Lipase Deficiency 38 0.130
29
P JVN024 Juvenile Hereditary Hemochromatosis 35 0.130
30
ANK002 Ankylosing Spondylitis 75 0.119
31
ATH003 Atherosclerosis 71 0.119
32
c PNC044 Pancreatitis 67 0.119
33
c HYP095 Hypercholesterolemia 56 0.119
34
FNC040 Fanconi Bickel Syndrome 54 0.119
35
PHS016 Phosphorylase Kinase Deficiency of Liver and Muscle, Autosomal Recessive 26 0.119
36
TFT003 Tufting Enteropathy 21 0.119
37
APL017 Apolipoprotein C-Ii Deficiency 11 0.119
38
P ATX002 Ataxia Telangiectasia 93 0.106
39
21H001 21-Hydroxylase Deficiency 87 0.106
40
c LCL006 Localized Scleroderma 68 0.106
41
WST001 West Syndrome 64 0.106
42
ART004 Aortic Atherosclerosis 54 0.106
43
SYN053 Syndromic Diarrhea 42 0.106
44
c GLY026 Glycogen Storage Disease Type 13 31 0.106
45
c GLY025 Glycogen Storage Disease Type 12 29 0.106
46
GLY054 Glycogen Storage Disease Due to Phosphorylase Kinase Deficiency 23 0.106
47
c FML139 Familial Myeloma 18 0.106
48
c TYP008 Type 1 Diabetes Mellitus 77 0.092
49
P ACT074 Acute Lymphocytic Leukemia 77 0.092
50
P TYP020 Type 1 Diabetes 69 0.092
51
ISC006 Ischemic Heart Disease 69 0.092
52
c GLL020 Gallbladder Disease 59 0.092
53
c HYP060 Hyperinsulinism 56 0.092
54
THR013 Thoracic Outlet Syndrome 54 0.092
55
c GLY023 Glycogen Storage Disease Type 0 43 0.092
56
INN002 Inner Ear Disease 38 0.092
57
ERL004 Early Yaws 33 0.092
58
KRT012 Keratoderma 31 0.092
59
P OBS005 Obesity 93 0.075
60
P MLT019 Multiple Myeloma 89 0.075
61
GLN003 Glanzmann's Thrombasthenia 80 0.075
62
TNG002 Tangier Disease 78 0.075
63
ABT001 Abetalipoproteinemia 73 0.075
64
P HST010 Histiocytosis 71 0.075
65
RLP001 Relapsing Polychondritis 69 0.075
66
P MTB001 Metabolic Syndrome X 67 0.075
67
c NPH012 Nephrotic Syndrome 66 0.075
68
c ACT027 Acute Pancreatitis 63 0.075
69
c MYL007 Myeloma 59 0.075
70
MYC002 Mycobacterium Avium Complex Disease 57 0.075
71
c GLY013 Glycogen Storage Disease 55 0.075
72
ANG054 Angina Pectoris 52 0.075
73
STT004 Steatorrhea 50 0.075
74
P HYP141 Hyperphenylalaninemia 49 0.075
75
P ATX010 Ataxia Neuropathy Spectrum 44 0.075
76
TRN044 Transposition of the Great Arteries 36 0.075
77
c HNT004 Huntington Disease-Like 2 30 0.075
78
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 28 0.075
79
NTR005 Nutritional Deficiency Disease 28 0.075
80
LGP003 Logopenic Progressive Aphasia 18 0.075
81
P ALZ001 Alzheimer's Disease 103 0.053
82
P MYC007 Myocardial Infarction 88 0.053
83
P HYP075 Hypertension 86 0.053
84
PRT036 Peritonitis 78 0.053
85
CRB011 Cerebrotendinous Xanthomatosis 77 0.053
86
P CHR089 Chronic Kidney Failure 76 0.053
87
c HPT021 Hepatitis 75 0.053
88
P GLY008 Glycogen Storage Disease Ii 73 0.053
89
VSC007 Vascular Disease 72 0.053
90
P ANG001 Angelman Syndrome 70 0.053
91
ART019 Aortic Valve Stenosis 68 0.053
92
c HYP086 Hypothyroidism 68 0.053
93
P ANR007 Anorexia Nervosa 67 0.053
94
c THY032 Thyroiditis 67 0.053
95
c GLY028 Glycogen Storage Disease Type 1a 65 0.053
96
ISC004 Ischemia 64 0.053
97
c GLY007 Glycogen Storage Disease Iv 64 0.053
98
c SPN046 Spinal Muscular Atrophy 63 0.053
99
ART001 Arterial Tortuosity Syndrome 62 0.053
100
URT039 Urticaria 61 0.053
101
P SYP003 Syphilis 56 0.053
102
HYP037 Hyperhomocysteinemia 55 0.053
103
LPC002 Lip Cancer 55 0.053
104
P HYP027 Hypobetalipoproteinemia 53 0.053
105
MNR002 Meniere's Disease 52 0.053
106
SJG001 Sjogren's Syndrome 52 0.053
107
P MSC003 Muscular Atrophy 52 0.053
108
FCL012 Facial Paralysis 49 0.053
109
RCR001 Recurrent Corneal Erosion 44 0.053
110
AND003 Andersen-Tawil Syndrome 43 0.053
111
P CRN157 Coronary Heart Disease 43 0.053
112
LPP002 Lipoprotein Glomerulopathy 40 0.053
113
c CNG033 Congenital Syphilis 40 0.053
114
c ADL016 Adult Spinal Muscular Atrophy 39 0.053
115
c GLY003 Glycogen Storage Disease Iii 33 0.053
116
c GLY009 Glycogen Storage Disease Xv 26 0.053
117
AND005 Androgen Insensitivity Syndrome, Mild 18 0.053
118
P ISC010 Isochromosome Yp 14 0.053
119
c HNT011 Huntington Disease-Like 3 13 0.053
120
OTP003 Oto-Palatal-Digital Syndrome 13 0.053