Search results for hyperlipoproteinemia

147 hits were found for hyperlipoproteinemia

# Family MCID Name MIFTS Score
1
c HYP740 Hyperlipoproteinemia, Type V 48 8.436
2
P HYP724 Hyperlipoproteinemia, Type Iii 59 8.227
3
P HYP607 Hypercholesterolemia, Familial 81 6.800
4
c HYP739 Hyperlipoproteinemia, Type Iv 51 6.515
5
c HYP768 Hyperlipoproteinemia, Type I 44 5.841
6
FML026 Familial Lipoprotein Lipase Deficiency 46 5.817
7
P FML035 Familial Hyperlipidemia 48 5.480
8
c HYP819 Hyperlipoproteinemia, Type Id 19 4.614
9
APL017 Apolipoprotein C-Ii Deficiency 36 4.113
10
c HYP163 Hyperlipidemia Type 3 18 3.649
11
P HYP614 Hyperlipidemia, Familial Combined 57 2.991
12
c HYP734 Hypercholesterolemia, Autosomal Dominant, Type B 44 2.909
13
HYP738 Hyperlipoproteinemia, Type Ii, and Deafness 11 2.115
14
CHY007 Chylomicronemia, Familial, Due to Circulating Inhibitor of Lipoprotein Lipase 10 2.088
15
c BLD140 Blood Group, I System 37 0.211
16
P HYP750 Hypertriglyceridemia, Familial 55 0.157
17
P PNC044 Pancreatitis 64 0.140
18
XNT003 Xanthomatosis 53 0.140
19
ISC006 Ischemic Heart Disease 73 0.131
20
LPD008 Lipid Metabolism Disorder 59 0.131
21
P DBT009 Diabetes Mellitus 72 0.122
22
P GLL020 Gallbladder Disease 64 0.122
23
HYP732 Hyperalphalipoproteinemia 1 52 0.122
24
c HYP555 Hypertriglyceridemia, Transient Infantile 34 0.122
25
P HRT032 Heart Disease 80 0.111
26
c HYP805 Hypercholesterolemia, Autosomal Dominant, 3 47 0.111
27
LPP002 Lipoprotein Glomerulopathy 44 0.111
28
c RCR022 Recurrent Acute Pancreatitis 43 0.111
29
c ACT027 Acute Pancreatitis 61 0.099
30
BDY004 Body Mass Index Quantitative Trait Locus 11 75 0.086
31
P CRN018 Coronary Artery Anomaly 69 0.086
32
TNG002 Tangier Disease 65 0.086
33
ABT001 Abetalipoproteinemia 64 0.086
34
LCT022 Lecithin:cholesterol Acyltransferase Deficiency 61 0.086
35
ATH013 Atherosclerosis Susceptibility 59 0.086
36
P CRN300 Coronary Heart Disease 1 57 0.086
37
HMZ003 Homozygous Familial Hypercholesterolemia 54 0.086
38
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 54 0.086
39
INN002 Inner Ear Disease 52 0.086
40
BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.086
41
HYP081 Hypolipoproteinemia 49 0.086
42
BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.086
43
HPT025 Hepatic Lipase Deficiency 48 0.086
44
BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.086
45
BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.086
46
BDY010 Body Mass Index Quantitative Trait Locus 4 45 0.086
47
BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.086
48
ADT003 Auditory System Disease 44 0.086
49
BDY006 Body Mass Index Quantitative Trait Locus 8 42 0.086
50
BDY012 Body Mass Index Quantitative Trait Locus 7 42 0.086
51
c HNT011 Huntington Disease-Like 3 35 0.086
52
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 21 0.086
53
P MYC007 Myocardial Infarction 81 0.070
54
P HPT021 Hepatitis 75 0.070
55
PRP027 Peripheral Vascular Disease 71 0.070
56
VSC007 Vascular Disease 71 0.070
57
P ANR048 Aniridia 1 68 0.070
58
CRB039 Cerebrovascular Disease 68 0.070
59
ISC004 Ischemia 66 0.070
60
P ART021 Arteriosclerosis 62 0.070
61
HYP190 Hypoalphalipoproteinemia, Primary 61 0.070
62
P GLY013 Glycogen Storage Disease 61 0.070
63
P NPH012 Nephrotic Syndrome 60 0.070
64
P HST010 Histiocytosis 60 0.070
65
ACN002 Acanthosis Nigricans 60 0.070
66
URT039 Urticaria 59 0.070
67
CRT016 Carotid Artery Disease 58 0.070
68
HYP060 Hyperinsulinism 56 0.070
69
P HYP818 Hypobetalipoproteinemia, Familial, 1 54 0.070
70
CHY002 Chylomicron Retention Disease 54 0.070
71
VTM028 Vitamin E, Familial Isolated Deficiency of 52 0.070
72
CRN030 Coronary Stenosis 52 0.070
73
ART140 Arteries, Anomalies of 51 0.070
74
c LKD015 Leukodystrophy, Hypomyelinating, 3 44 0.070
75
SCH076 Schnyder Corneal Dystrophy 44 0.070
76
SBL008 Sea-Blue Histiocyte Disease 43 0.070
77
CRB008 Cerebral Atherosclerosis 42 0.070
78
ARC023 Arcus Corneae 40 0.070
79
XNT009 Xanthoma Disseminatum 38 0.070
80
FML330 Familial Lcat Deficiency 37 0.070
81
DYS013 Dysbaric Osteonecrosis 35 0.070
82
DFC001 Defective Apolipoprotein B-100 31 0.070
83
LPS020 Lipase Deficiency, Combined 31 0.070
84
HYP160 Hyperkeratosis Lenticularis Perstans 28 0.070
85
LRY026 Laryngeal Cleft 25 0.070
86
GRW032 Growth Factors, Combined Defect of 22 0.070
87
ANR038 Anorexia Nervosa 1 21 0.070
88
BLD137 Blood Group--Ahonen 17 0.070
89
P ALZ034 Alzheimer Disease 95 0.050
90
MYL069 Myeloma, Multiple 86 0.050
91
MLR004 Malaria 86 0.050
92
P LKM002 Leukemia 75 0.050
93
SMT004 Smith-Lemli-Opitz Syndrome 70 0.050
94
P KDN018 Kidney Disease 69 0.050
95
PRT036 Peritonitis 67 0.050
96
P LYM026 Lymphoblastic Leukemia 66 0.050
97
P THR014 Thrombocytopenia 65 0.050
98
AGN016 Aging 65 0.050
99
c ACT075 Acute Myocardial Infarction 64 0.050
100
CRB011 Cerebrotendinous Xanthomatosis 64 0.050
101
P SPN046 Spinal Muscular Atrophy 63 0.050
102
P ALC004 Alcohol Abuse 63 0.050
103
P HYP086 Hypothyroidism 62 0.050
104
MRB003 Morbid Obesity 61 0.050
105
ANR040 Aneurysm 61 0.050
106
c PNC108 Pancreatitis, Hereditary 60 0.050
107
P INF032 Infertility 59 0.050
108
STS003 Sitosterolemia 58 0.050
109
GLC003 Glucose Intolerance 58 0.050
110
P SJG008 Sjogren Syndrome 58 0.050
111
c GLY060 Glycogen Storage Disease Ia 57 0.050
112
HMR039 Hemorrhage, Intracerebral 57 0.050
113
IMM158 Immune Suppression 57 0.050
114
BTN003 Biotinidase Deficiency 56 0.050
115
P THY032 Thyroiditis 56 0.050
116
P MSC003 Muscular Atrophy 55 0.050
117
P SYP003 Syphilis 55 0.050
118
ANG054 Angina Pectoris 53 0.050
119
c BLM008 Bulimia Nervosa 2 53 0.050
120
GRW007 Growth Hormone Deficiency 52 0.050
121
URM002 Uremia 52 0.050
122
LMB062 Limb Ischemia 52 0.050
123
ADR056 Adrenal Insufficiency, Congenital, with 46,xy Sex Reversal, Partial or Complete 52 0.050
124
c NGH026 Night Blindness, Congenital Stationary, Type 1a 51 0.050
125
FCL012 Facial Paralysis 50 0.050
126
PNC001 Pancytopenia 50 0.050
127
CTN014 Cutaneous Mastocytosis 50 0.050
128
RNL024 Renal Glucosuria 50 0.050
129
c AMY009 Amyloidosis Aa 48 0.050
130
ART004 Aortic Atherosclerosis 48 0.050
131
AMY082 Amyloidosis, Familial Visceral 47 0.050
132
c BRN108 Branchiootic Syndrome 1 47 0.050
133
c HRD039 Hereditary Amyloidosis 47 0.050
134
END072 Endotheliitis 46 0.050
135
c NRP053 Neuropathy, Hereditary Sensory and Autonomic, Type Iia 45 0.050
136
FSH001 Fish-Eye Disease 45 0.050
137
PRX014 Proximal Spinal Muscular Atrophy 42 0.050
138
STT004 Steatorrhea 41 0.050
139
LTH045 Lutheran Suppressor, X-Linked 41 0.050
140
c CNG033 Congenital Syphilis 40 0.050
141
CHL050 Cholesterol Ester Storage Disease 38 0.050
142
CRN274 Corneal Dystrophy, Posterior Amorphous 33 0.050
143
PLM156 Palmoplantar Carcinoma, Multiple Self-Healing 33 0.050
144
ALR002 Al-Raqad Syndrome 30 0.050
145
LGP003 Logopenic Progressive Aphasia 23 0.050
146
LPD028 Lipodystrophy Due to Peptidic Growth Factors Deficiency 19 0.050
147
c HYP804 Hyperlipidemia, Combined, 1 18 0.050
Content
Loading form....