Search results for "hyperlipoproteinemia"

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

96 hits were found for 'hyperlipoproteinemia'

# Family MCID Name MIFTS Score
1
HYP286 Hyperchylomicronemia, Late-Onset 45 7.859
2
FML026 Familial Lipoprotein Lipase Deficiency 51 6.809
3
c HYP163 Hyperlipidemia Type 3 52 6.269
4
c HYP032 Hyperlipoproteinemia Type Iv 36 6.218
5
P HYP607 Hypercholesterolemia, Familial 77 5.817
6
c HYP011 Hyperlipoproteinemia Type Iii 34 5.540
7
LPP001 Lipoprotein Lipase Deficiency 63 4.685
8
P FML035 Familial Hyperlipidemia 49 4.183
9
c HYP592 Hyperlipoproteinemia, Type 1d 16 4.165
10
P HYP289 Hyperlipoproteinemia, Type Ib 24 4.124
11
P HYP614 Hyperlipidemia, Familial Combined 50 2.864
12
c LDL002 Ldlr-Related Familial Hypercholesterolemia, Autosomal Dominant 7 2.864
13
P HYP117 Hypertriglyceridemia 65 2.322
14
CRD144 Cardiovascular Disease Risk Factor ) 42 2.025
15
P PNC044 Pancreatitis 62 0.150
16
ATH003 Atherosclerosis 63 0.139
17
XNT003 Xanthomatosis 45 0.127
18
c HYP555 Hypertriglyceridemia, Transient Infantile 26 0.114
19
P HYP060 Hyperinsulinism 58 0.114
20
ACN002 Acanthosis Nigricans 59 0.098
21
P GLL020 Gallbladder Disease 59 0.098
22
PNC034 Pancreas Disease 56 0.098
23
INN002 Inner Ear Disease 48 0.098
24
P HRT032 Heart Disease 64 0.098
25
LPP002 Lipoprotein Glomerulopathy 46 0.098
26
c ACT027 Acute Pancreatitis 59 0.098
27
ISC006 Ischemic Heart Disease 54 0.098
28
c RCR022 Recurrent Acute Pancreatitis 36 0.098
29
P OBS005 Obesity 91 0.080
30
FNC009 Fanconi-Bickel Syndrome 51 0.080
31
P DBT083 Diabetes Mellitus, Permanent Neonatal 51 0.080
32
ICH002 Ichthyosis Bullosa of Siemens 44 0.080
33
c HYP604 Hyperinsulinemic Hypoglycemia, Familial, 2 53 0.080
34
PRL032 Perlman Syndrome 55 0.080
35
c DBT064 Diabetes Mellitus, Transient Neonatal, 1 44 0.080
36
P NPH012 Nephrotic Syndrome 55 0.080
37
HYP066 Hyperglycemia 61 0.080
38
ADR044 Adrenal Insufficiency, Congenital, with 46xy Sex Reversal, Partial or Complete 36 0.080
39
C2D001 C2 Deficiency 45 0.080
40
HYP056 Hypoglycemia 60 0.080
41
LPD008 Lipid Metabolism Disorder 42 0.080
42
P MTR004 Maturity-Onset Diabetes of the Young 58 0.080
43
INS001 Insulinoma 60 0.080
44
P HST010 Histiocytosis 56 0.080
45
P HYP090 Hyperalphalipoproteinemia 45 0.080
46
c DBT044 Diabetes Mellitus, Transient Neonatal, 3 32 0.080
47
P HYP050 Hyperinsulinemic Hypoglycemia 55 0.080
48
c MTR075 Maturity-Onset Diabetes of the Young, Type 13 32 0.080
49
GST033 Gestational Diabetes 54 0.080
50
P NNT009 Neonatal Diabetes Mellitus 50 0.080
51
GLC003 Glucose Intolerance 56 0.080
52
LGP003 Logopenic Progressive Aphasia 21 0.080
53
c HNT011 Huntington Disease-Like 3 23 0.080
54
FCT008 Factitious Disorder 42 0.080
55
EXC002 Exocrine Pancreatic Insufficiency 41 0.080
56
MNC002 Munchausen by Proxy 29 0.080
57
HMH002 Hemihypertrophy 37 0.080
58
P PNC045 Pancreatic Agenesis 44 0.080
59
c DBT013 Diabetes Mellitus, 6q24-Related Transient Neonatal 15 0.080
60
END038 Endocrine Pancreas Disease 42 0.080
61
ACT088 Acute Insulin Response 39 0.080
62
c PTR018 Paternal Uniparental Disomy of Chromosome 6 13 0.080
63
CMP036 Complement Component C2 Deficiency 8 0.080
64
MNG006 Monogenic Diabetes 34 0.080
65
c MLT019 Multiple Myeloma 77 0.057
66
P MYC007 Myocardial Infarction 80 0.057
67
TNG002 Tangier Disease 61 0.057
68
P SPN046 Spinal Muscular Atrophy 62 0.057
69
CRB011 Cerebrotendinous Xanthomatosis 60 0.057
70
URT039 Urticaria 58 0.057
71
P HPT021 Hepatitis 74 0.057
72
P ANR007 Anorexia Nervosa 63 0.057
73
P HYP086 Hypothyroidism 63 0.057
74
P SJG001 Sjogren's Syndrome 55 0.057
75
PRT036 Peritonitis 65 0.057
76
FCL012 Facial Paralysis 50 0.057
77
VSC007 Vascular Disease 51 0.057
78
MNR002 Meniere's Disease 49 0.057
79
PNC048 Pancreatic Lipase Deficiency 25 0.057
80
STM006 Stomach Disease 48 0.057
81
P GLY013 Glycogen Storage Disease 58 0.057
82
P SYP003 Syphilis 51 0.057
83
P MSC003 Muscular Atrophy 51 0.057
84
P THY032 Thyroiditis 57 0.057
85
c PNC106 Pancreatic Agenesis 1 31 0.057
86
GRW032 Growth Factors, Combined Defect of 23 0.057
87
c CNG033 Congenital Syphilis 39 0.057
88
PRX014 Proximal Spinal Muscular Atrophy 34 0.057
89
c INH020 Inherited Metabolic Disorder 49 0.057
90
GRW007 Growth Hormone Deficiency 49 0.057
91
HYP037 Hyperhomocysteinemia 49 0.057
92
P MYL007 Myeloma 52 0.057
93
ISC004 Ischemia 56 0.057
94
c HYP333 Hyperlipidemia, Combined, 2 16 0.057
95
ANG054 Angina Pectoris 48 0.057
96
LMB062 Limb Ischemia 48 0.057