Search results for hyperlipoproteinemia

195 hits were found for hyperlipoproteinemia

# Family MCID Name MIFTS Score
1
HYP286 Hyperchylomicronemia, Late-Onset 45 7.780
2
FML026 Familial Lipoprotein Lipase Deficiency 44 6.059
3
c HYP163 Hyperlipidemia Type 3 36 6.059
4
P HYP032 Hyperlipoproteinemia Type Iv 34 5.790
5
P HYP607 Hypercholesterolemia, Familial 76 5.689
6
c HYP011 Hyperlipoproteinemia Type Iii 42 5.440
7
LPP001 Lipoprotein Lipase Deficiency 63 4.608
8
P FML035 Familial Hyperlipidemia 48 4.596
9
c HYP592 Hyperlipoproteinemia, Type 1d 17 4.569
10
c HYP289 Hyperlipoproteinemia, Type Ib 23 4.070
11
P HYP614 Hyperlipidemia, Familial Combined 50 2.865
12
c LDL002 Ldlr-Related Familial Hypercholesterolemia, Autosomal Dominant 7 2.837
13
CRD144 Cardiovascular Disease Risk Factor ) 40 2.043
14
c HYP288 Hypercholesterolemia, Due to Ligand-Defective Apo B 37 2.006
15
P HYP117 Hypertriglyceridemia 61 0.149
16
P PNC044 Pancreatitis 61 0.110
17
ATH003 Atherosclerosis 65 0.101
18
XNT003 Xanthomatosis 46 0.101
19
ISC006 Ischemic Heart Disease 68 0.090
20
LPD008 Lipid Metabolism Disorder 58 0.090
21
P HRT032 Heart Disease 75 0.078
22
P GLL020 Gallbladder Disease 59 0.078
23
P HYP060 Hyperinsulinism 58 0.078
24
PNC034 Pancreas Disease 58 0.078
25
c ACT027 Acute Pancreatitis 57 0.078
26
INN002 Inner Ear Disease 49 0.078
27
P HYP090 Hyperalphalipoproteinemia 48 0.078
28
LPP002 Lipoprotein Glomerulopathy 46 0.078
29
c RCR022 Recurrent Acute Pancreatitis 41 0.078
30
P OBS005 Obesity 92 0.064
31
VSC007 Vascular Disease 67 0.064
32
PRT036 Peritonitis 63 0.064
33
ISC004 Ischemia 61 0.064
34
P NPH012 Nephrotic Syndrome 59 0.064
35
P HST010 Histiocytosis 58 0.064
36
ACN002 Acanthosis Nigricans 57 0.064
37
P LPD010 Lipodystrophy 55 0.064
38
c INH020 Inherited Metabolic Disorder 49 0.064
39
END038 Endocrine Pancreas Disease 41 0.064
40
c HYP555 Hypertriglyceridemia, Transient Infantile 29 0.064
41
P MLT019 Multiple Myeloma 83 0.045
42
P DBT085 Diabetes Mellitus, Insulin-Dependent 80 0.045
43
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 80 0.045
44
P MYC007 Myocardial Infarction 79 0.045
45
P LVR013 Liver Disease 75 0.045
46
P CRN211 Coronary Artery Disease 74 0.045
47
P LKM002 Leukemia 71 0.045
48
KWS002 Kawasaki Disease 70 0.045
49
P HPT021 Hepatitis 69 0.045
50
PRP027 Peripheral Vascular Disease 68 0.045
51
P MNN013 Meningitis 67 0.045
52
OBS061 Obstructive Sleep Apnea 66 0.045
53
c CHR089 Chronic Kidney Failure 66 0.045
54
ACR007 Acromegaly 66 0.045
55
P SPN046 Spinal Muscular Atrophy 65 0.045
56
P ORT004 Orthostatic Intolerance 64 0.045
57
P HYP086 Hypothyroidism 64 0.045
58
P LYM026 Lymphoblastic Leukemia 62 0.045
59
TNG002 Tangier Disease 62 0.045
60
P SLP006 Sleep Apnea 61 0.045
61
HYP056 Hypoglycemia 61 0.045
62
CRB011 Cerebrotendinous Xanthomatosis 61 0.045
63
HYP066 Hyperglycemia 61 0.045
64
TYP007 Typhoid Fever 61 0.045
65
P ANR007 Anorexia Nervosa 61 0.045
66
APP008 Appendicitis 60 0.045
67
P GLY013 Glycogen Storage Disease 60 0.045
68
ALC006 Alcoholic Hepatitis 59 0.045
69
GST045 Gastroenteritis 59 0.045
70
FTT001 Fatty Liver Disease 59 0.045
71
P INF032 Infertility 59 0.045
72
MRB003 Morbid Obesity 58 0.045
73
ART021 Arteriosclerosis 58 0.045
74
ETN001 Eating Disorder 58 0.045
75
RSP006 Respiratory System Disease 58 0.045
76
HMR004 Hemorrhagic Fever with Renal Syndrome 58 0.045
77
URT039 Urticaria 57 0.045
78
CRT016 Carotid Artery Disease 57 0.045
79
GST033 Gestational Diabetes 57 0.045
80
c PRC016 Pre-Eclampsia 56 0.045
81
INT002 Intermittent Claudication 56 0.045
82
STF001 Stiff-Person Syndrome 56 0.045
83
PRP019 Peripheral Nervous System Disease 55 0.045
84
GLC003 Glucose Intolerance 55 0.045
85
END030 End Stage Renal Failure 55 0.045
86
P HYP083 Hypopituitarism 54 0.045
87
P THY032 Thyroiditis 54 0.045
88
P END033 Endocarditis 54 0.045
89
P SYP003 Syphilis 53 0.045
90
P DBT005 Diabetes Insipidus 53 0.045
91
c ABD014 Abdominal Obesity-Metabolic Syndrome 1 52 0.045
92
BRN106 Burns 52 0.045
93
P FML012 Familial Partial Lipodystrophy 52 0.045
94
P PYL005 Pyelonephritis 52 0.045
95
c LPD037 Lipodystrophy, Familial Partial, 2 52 0.045
96
ADR044 Adrenal Insufficiency, Congenital, with 46xy Sex Reversal, Partial or Complete 52 0.045
97
CRN030 Coronary Stenosis 51 0.045
98
STM006 Stomach Disease 50 0.045
99
c ART115 Aortic Valve Disease 1 50 0.045
100
GRW007 Growth Hormone Deficiency 50 0.045
101
FCL012 Facial Paralysis 50 0.045
102
RLP001 Relapsing Polychondritis 50 0.045
103
P MSC003 Muscular Atrophy 50 0.045
104
P SJG001 Sjogren's Syndrome 50 0.045
105
c ACT068 Acute Cystitis 50 0.045
106
NNL002 Nonalcoholic Steatohepatitis 50 0.045
107
URN009 Urinary System Disease 50 0.045
108
HYP037 Hyperhomocysteinemia 50 0.045
109
OVR063 Overnutrition 50 0.045
110
ANG054 Angina Pectoris 50 0.045
111
c SVR005 Severe Pre-Eclampsia 49 0.045
112
PRT038 Protein-Energy Malnutrition 49 0.045
113
LMB062 Limb Ischemia 48 0.045
114
MNR002 Meniere's Disease 48 0.045
115
URM002 Uremia 48 0.045
116
THY030 Thyroid Gland Disease 48 0.045
117
DBT084 Diabetes Mellitus, Ketosis-Prone 47 0.045
118
PTT009 Pituitary Gland Disease 47 0.045
119
IMM104 Immunodeficiency with Hyper-Igm, Type 2 47 0.045
120
HYP043 Hyperandrogenism 47 0.045
121
OPS006 Opsoclonus-Myoclonus Syndrome 46 0.045
122
CLC001 Calciphylaxis 46 0.045
123
CRD137 Cardiogenic Shock 46 0.045
124
PTT004 Pituitary Apoplexy 46 0.045
125
ICH002 Ichthyosis Bullosa of Siemens 45 0.045
126
c NGH019 Night Blindness, Congenital Stationary , 1a, X-Linked 45 0.045
127
c ACT042 Acute Pyelonephritis 45 0.045
128
C2D001 C2 Deficiency 45 0.045
129
SHH001 Sheehan Syndrome 44 0.045
130
CLD007 Cold Agglutinin Disease 44 0.045
131
PLR005 Pleuropneumonia 43 0.045
132
PRD004 Prediabetes Syndrome 43 0.045
133
IDP033 Idiopathic Edema 42 0.045
134
GLC008 Glucose Metabolism Disease 42 0.045
135
NTR018 Neutrophilia, Hereditary 42 0.045
136
DDN006 Duodenitis 42 0.045
137
c VRL005 Viral Pneumonia 42 0.045
138
P CHL066 Cholangitis 42 0.045
139
P ACQ022 Acquired Generalized Lipodystrophy 42 0.045
140
RBF001 Riboflavin Deficiency 42 0.045
141
P ABD016 Abdominal Obesity-Metabolic Syndrome 41 0.045
142
DCB001 Decubitus Ulcer 41 0.045
143
P CPL003 Capillary Leak Syndrome 41 0.045
144
CST005 Castleman Disease 41 0.045
145
MDS022 Mediastinitis 41 0.045
146
FTL021 Fetal Macrosomia 41 0.045
147
CHR034 Chromophobe Adenoma 40 0.045
148
NPH004 Nephropathia Epidemica 40 0.045
149
EMP001 Empty Sella Syndrome 40 0.045
150
MNC019 Monocarboxylate Transporter 1 Deficiency 40 0.045
151
c SBC007 Subacute Thyroiditis 40 0.045
152
PTT003 Pituitary-Dependent Cushing's Disease 39 0.045
153
SPN369 Spinal Disease 39 0.045
154
c ATM092 Autoimmune Polyendocrine Syndrome, Type Ii 39 0.045
155
GND003 Gonadal Disease 39 0.045
156
c CNG033 Congenital Syphilis 39 0.045
157
ACT088 Acute Insulin Response 39 0.045
158
ADR009 Adrenal Cortex Disease 39 0.045
159
c CLL012 Cell Type Benign Neoplasm 39 0.045
160
MNR003 Mineral Metabolism Disease 38 0.045
161
HYP070 Hyperpituitarism 38 0.045
162
P ACQ009 Acquired Metabolic Disease 38 0.045
163
SXD001 Sex Differentiation Disease 38 0.045
164
c PNC106 Pancreatic Agenesis 1 37 0.045
165
c MCR120 Microvascular Complications of Diabetes 7 37 0.045
166
ETH004 Euthyroid Sick Syndrome 36 0.045
167
MLT002 Multiple Symmetrical Lipomatosis 36 0.045
168
PRX014 Proximal Spinal Muscular Atrophy 36 0.045
169
ARC001 Arcus Senilis 35 0.045
170
HRP002 Herpes Gestationis 34 0.045
171
BCK003 Background Diabetic Retinopathy 34 0.045
172
c ACT036 Acute Cholangitis 34 0.045
173
CRY008 Cryopyrin-Associated Periodic Syndrome 34 0.045
174
FTL004 Fetal Erythroblastosis 33 0.045
175
END036 Endocrine Organ Benign Neoplasm 33 0.045
176
ACD004 Acdc 33 0.045
177
CLC003 Cloacogenic Carcinoma 32 0.045
178
SCL022 Scleredema 32 0.045
179
PYR004 Pyuria 32 0.045
180
c DRR007 Diarrhea 7 31 0.045
181
IDP041 Idiopathic Recurrent Pericarditis 30 0.045
182
MCN011 Mucinoses 29 0.045
183
NNS003 Non-Secretory Myeloma 28 0.045
184
SCL002 Scleredema Adultorum 27 0.045
185
THY001 Thyroid Crisis 27 0.045
186
PNC048 Pancreatic Lipase Deficiency 27 0.045
187
c MLG042 Malignant Otitis Externa 26 0.045
188
PST014 Postsurgical Hypothyroidism 23 0.045
189
GRW032 Growth Factors, Combined Defect of 22 0.045
190
c HNT011 Huntington Disease-Like 3 22 0.045
191
LGP003 Logopenic Progressive Aphasia 22 0.045
192
c SBC010 Subacute Glomerulonephritis 19 0.045
193
c HYP333 Hyperlipidemia, Combined, 2 15 0.045
194
LPD028 Lipodystrophy Due to Peptidic Growth Factors Deficiency 14 0.045
195
CMP036 Complement Component C2 Deficiency 8 0.045
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