Search results for "hyperlipoproteinemia"

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

92 hits were found for 'hyperlipoproteinemia'

# Family MCID Name MIFTS Score
1
HYP286 Hyperchylomicronemia, Late-Onset 46 7.862
2
LPP001 Lipoprotein Lipase Deficiency 65 7.691
3
c HYP163 Hyperlipidemia Type 3 34 6.261
4
c HYP032 Hyperlipoproteinemia Type Iv 27 5.866
5
P HYP607 Hypercholesterolemia, Familial 77 5.787
6
c HYP011 Hyperlipoproteinemia Type Iii 41 5.531
7
P FML035 Familial Hyperlipidemia 50 4.655
8
c HYP592 Hyperlipoproteinemia, Type 1d 16 4.168
9
P HYP289 Hyperlipoproteinemia, Type Ib 23 4.127
10
P HYP614 Hyperlipidemia, Familial Combined 51 2.866
11
c LDL002 Ldlr-Related Familial Hypercholesterolemia, Autosomal Dominant 7 2.866
12
P HYP117 Hypertriglyceridemia 65 2.275
13
CRD144 Cardiovascular Disease Risk Factor ) 40 2.026
14
c HYP288 Hypercholesterolemia, Due to Ligand-Defective Apo B 36 2.026
15
P PNC044 Pancreatitis 60 0.141
16
ATH003 Atherosclerosis 62 0.129
17
XNT003 Xanthomatosis 47 0.129
18
P HRT032 Heart Disease 76 0.100
19
ISC006 Ischemic Heart Disease 68 0.100
20
P HYP060 Hyperinsulinism 59 0.100
21
P GLL020 Gallbladder Disease 59 0.100
22
c ACT027 Acute Pancreatitis 56 0.100
23
INN002 Inner Ear Disease 50 0.100
24
LPP002 Lipoprotein Glomerulopathy 46 0.100
25
c RCR022 Recurrent Acute Pancreatitis 41 0.100
26
P OBS005 Obesity 93 0.081
27
LPD008 Lipid Metabolism Disorder 58 0.081
28
ACN002 Acanthosis Nigricans 57 0.081
29
P HST010 Histiocytosis 55 0.081
30
P HYP090 Hyperalphalipoproteinemia 46 0.081
31
P MLT019 Multiple Myeloma 80 0.058
32
P MYC007 Myocardial Infarction 79 0.058
33
P HPT021 Hepatitis 70 0.058
34
VSC007 Vascular Disease 67 0.058
35
P HYP086 Hypothyroidism 65 0.058
36
P SPN046 Spinal Muscular Atrophy 63 0.058
37
P ANR007 Anorexia Nervosa 63 0.058
38
PRT036 Peritonitis 62 0.058
39
HYP056 Hypoglycemia 61 0.058
40
TNG002 Tangier Disease 61 0.058
41
HYP066 Hyperglycemia 60 0.058
42
CRB011 Cerebrotendinous Xanthomatosis 60 0.058
43
INS001 Insulinoma 59 0.058
44
ISC004 Ischemia 59 0.058
45
URT039 Urticaria 59 0.058
46
P GLY013 Glycogen Storage Disease 59 0.058
47
P HYP604 Hyperinsulinemic Hypoglycemia, Familial, 2 58 0.058
48
PNC034 Pancreas Disease 57 0.058
49
P MTR004 Maturity-Onset Diabetes of the Young 57 0.058
50
GST033 Gestational Diabetes 56 0.058
51
PRL032 Perlman Syndrome 55 0.058
52
P THY032 Thyroiditis 54 0.058
53
ADR044 Adrenal Insufficiency, Congenital, with 46xy Sex Reversal, Partial or Complete 53 0.058
54
P SYP003 Syphilis 53 0.058
55
P SJG001 Sjogren's Syndrome 53 0.058
56
P DBT083 Diabetes Mellitus, Permanent Neonatal 53 0.058
57
P NNT009 Neonatal Diabetes Mellitus 52 0.058
58
P MSC003 Muscular Atrophy 51 0.058
59
ANG054 Angina Pectoris 51 0.058
60
FNC009 Fanconi-Bickel Syndrome 51 0.058
61
STM006 Stomach Disease 50 0.058
62
MNR002 Meniere's Disease 50 0.058
63
FCL012 Facial Paralysis 50 0.058
64
HYP037 Hyperhomocysteinemia 50 0.058
65
c INH020 Inherited Metabolic Disorder 49 0.058
66
GRW007 Growth Hormone Deficiency 48 0.058
67
LMB062 Limb Ischemia 48 0.058
68
c DBT064 Diabetes Mellitus, Transient Neonatal, 1 44 0.058
69
C2D001 C2 Deficiency 44 0.058
70
P PNC045 Pancreatic Agenesis 44 0.058
71
ICH002 Ichthyosis Bullosa of Siemens 43 0.058
72
EXC002 Exocrine Pancreatic Insufficiency 43 0.058
73
END038 Endocrine Pancreas Disease 43 0.058
74
FCT008 Factitious Disorder 43 0.058
75
INT060 Intestinal Atresia 40 0.058
76
c PNC106 Pancreatic Agenesis 1 40 0.058
77
ACT088 Acute Insulin Response 39 0.058
78
HMH002 Hemihypertrophy 39 0.058
79
c CNG033 Congenital Syphilis 39 0.058
80
PRX014 Proximal Spinal Muscular Atrophy 36 0.058
81
MNG006 Monogenic Diabetes 35 0.058
82
c HYP601 Hyperinsulinemic Hypoglycemia, Familial, 3 30 0.058
83
c HYP555 Hypertriglyceridemia, Transient Infantile 29 0.058
84
MNC002 Munchausen by Proxy 28 0.058
85
PNC048 Pancreatic Lipase Deficiency 26 0.058
86
c HNT011 Huntington Disease-Like 3 24 0.058
87
GRW032 Growth Factors, Combined Defect of 23 0.058
88
LGP003 Logopenic Progressive Aphasia 22 0.058
89
c HYP333 Hyperlipidemia, Combined, 2 18 0.058
90
c DBT013 Diabetes Mellitus, 6q24-Related Transient Neonatal 15 0.058
91
c PTR018 Paternal Uniparental Disomy of Chromosome 6 13 0.058
92
CMP036 Complement Component C2 Deficiency 8 0.058