Search results for hyperlipoproteinemia

215 hits were found for hyperlipoproteinemia

# Family MCID Name MIFTS Score
1
HYP286 Hyperchylomicronemia, Late-Onset 43 7.527
2
P HYP724 Hyperlipoproteinemia, Type Iii 56 7.353
3
FML026 Familial Lipoprotein Lipase Deficiency 48 6.058
4
c HYP032 Hyperlipoproteinemia Type Iv 33 5.775
5
P HYP607 Hypercholesterolemia, Familial 75 5.338
6
c HYP592 Hyperlipoproteinemia, Type 1d 23 4.579
7
P FML035 Familial Hyperlipidemia 47 4.521
8
c HYP289 Hyperlipoproteinemia, Type Ib 24 4.068
9
LPP001 Lipoprotein Lipase Deficiency 59 3.599
10
c HYP163 Hyperlipidemia Type 3 16 3.518
11
P HYP614 Hyperlipidemia, Familial Combined 50 2.864
12
c HYP288 Hypercholesterolemia, Due to Ligand-Defective Apo B 40 2.837
13
c LDL002 Ldlr-Related Familial Hypercholesterolemia, Autosomal Dominant 7 2.837
14
CRD144 Cardiovascular Disease Risk Factor ) 40 2.042
15
P HYP117 Hypertriglyceridemia 61 0.145
16
P PNC044 Pancreatitis 60 0.107
17
XNT003 Xanthomatosis 46 0.107
18
ATH003 Atherosclerosis 65 0.097
19
LPD008 Lipid Metabolism Disorder 57 0.097
20
P OBS005 Obesity 91 0.087
21
P HRT032 Heart Disease 75 0.087
22
P HYP060 Hyperinsulinism 57 0.087
23
P GLL020 Gallbladder Disease 58 0.075
24
ACN002 Acanthosis Nigricans 56 0.075
25
c ACT027 Acute Pancreatitis 56 0.075
26
ISC006 Ischemic Heart Disease 53 0.075
27
P HYP090 Hyperalphalipoproteinemia 49 0.075
28
INN002 Inner Ear Disease 48 0.075
29
LPP002 Lipoprotein Glomerulopathy 45 0.075
30
c RCR022 Recurrent Acute Pancreatitis 40 0.075
31
P DBT085 Diabetes Mellitus, Insulin-Dependent 79 0.062
32
P MYC007 Myocardial Infarction 77 0.062
33
P CRN211 Coronary Artery Disease 73 0.062
34
VSC007 Vascular Disease 65 0.062
35
PRT036 Peritonitis 60 0.062
36
ISC004 Ischemia 59 0.062
37
HYP066 Hyperglycemia 59 0.062
38
P NPH012 Nephrotic Syndrome 59 0.062
39
GLC003 Glucose Intolerance 54 0.062
40
P HST010 Histiocytosis 54 0.062
41
ANG054 Angina Pectoris 49 0.062
42
GRW007 Growth Hormone Deficiency 48 0.062
43
ANV001 Anovulation 44 0.062
44
FTL021 Fetal Macrosomia 41 0.062
45
c HYP555 Hypertriglyceridemia, Transient Infantile 30 0.062
46
GRW032 Growth Factors, Combined Defect of 23 0.062
47
MLR004 Malaria 82 0.044
48
P MLT019 Multiple Myeloma 82 0.044
49
INS024 Insulin-Like Growth Factor I 75 0.044
50
P LVR013 Liver Disease 72 0.044
51
P LKM002 Leukemia 72 0.044
52
P HPT021 Hepatitis 68 0.044
53
KWS002 Kawasaki Disease 67 0.044
54
ACR007 Acromegaly 66 0.044
55
P MNN013 Meningitis 65 0.044
56
P TRN020 Turner Syndrome 65 0.044
57
PRP027 Peripheral Vascular Disease 65 0.044
58
OBS061 Obstructive Sleep Apnea 65 0.044
59
c CHR089 Chronic Kidney Failure 65 0.044
60
P PLY011 Polycystic Ovary Syndrome 63 0.044
61
P SPN046 Spinal Muscular Atrophy 63 0.044
62
CRB011 Cerebrotendinous Xanthomatosis 62 0.044
63
TNG002 Tangier Disease 62 0.044
64
TYP007 Typhoid Fever 61 0.044
65
P LYM026 Lymphoblastic Leukemia 60 0.044
66
P SLP006 Sleep Apnea 60 0.044
67
DFC004 Deficiency Anemia 60 0.044
68
P HYP086 Hypothyroidism 60 0.044
69
LPR018 Leprechaunism 60 0.044
70
RSP006 Respiratory System Disease 60 0.044
71
P ANR007 Anorexia Nervosa 60 0.044
72
c ACT075 Acute Myocardial Infarction 59 0.044
73
P GLY013 Glycogen Storage Disease 59 0.044
74
LRN004 Laron Dwarfism 59 0.044
75
CRN036 Craniopharyngioma 59 0.044
76
APP008 Appendicitis 59 0.044
77
FTT001 Fatty Liver Disease 59 0.044
78
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 58 0.044
79
MRB003 Morbid Obesity 58 0.044
80
GST045 Gastroenteritis 57 0.044
81
P INF032 Infertility 57 0.044
82
ART021 Arteriosclerosis 57 0.044
83
RBS003 Rabson-Mendenhall Syndrome 57 0.044
84
ARM001 Aromatase Deficiency 57 0.044
85
STF001 Stiff-Person Syndrome 56 0.044
86
CRT016 Carotid Artery Disease 56 0.044
87
P SLV001 Silver-Russell Syndrome 56 0.044
88
ETN001 Eating Disorder 56 0.044
89
HMR004 Hemorrhagic Fever with Renal Syndrome 56 0.044
90
URT039 Urticaria 56 0.044
91
PNC034 Pancreas Disease 55 0.044
92
GST033 Gestational Diabetes 55 0.044
93
ART111 Artery Disease 55 0.044
94
ALS001 Alstrom Syndrome 55 0.044
95
INT002 Intermittent Claudication 55 0.044
96
P HYP050 Hyperinsulinemic Hypoglycemia 55 0.044
97
P AVS004 Avascular Necrosis of the Femoral Head 54 0.044
98
P HYP083 Hypopituitarism 54 0.044
99
P THY032 Thyroiditis 53 0.044
100
P LPD010 Lipodystrophy 53 0.044
101
P END033 Endocarditis 53 0.044
102
THL018 Thalassemia Major 52 0.044
103
BRN106 Burns 52 0.044
104
P PYL005 Pyelonephritis 52 0.044
105
END030 End Stage Renal Failure 51 0.044
106
RLP001 Relapsing Polychondritis 51 0.044
107
P FML012 Familial Partial Lipodystrophy 51 0.044
108
P SYP003 Syphilis 51 0.044
109
c LPD015 Lipodystrophy, Familial Partial, Type 2 51 0.044
110
P PLY017 Polyarteritis Nodosa 51 0.044
111
NNL002 Nonalcoholic Steatohepatitis 50 0.044
112
P HYP014 Hyperuricemia 50 0.044
113
P MSC003 Muscular Atrophy 49 0.044
114
P SJG001 Sjogren's Syndrome 49 0.044
115
ADR044 Adrenal Insufficiency, Congenital, with 46xy Sex Reversal, Partial or Complete 49 0.044
116
FCL012 Facial Paralysis 49 0.044
117
HYP037 Hyperhomocysteinemia 49 0.044
118
CRN030 Coronary Stenosis 49 0.044
119
DBT084 Diabetes Mellitus, Ketosis-Prone 49 0.044
120
IDP002 Idiopathic Juvenile Osteoporosis 48 0.044
121
MNR002 Meniere's Disease 48 0.044
122
PRT038 Protein-Energy Malnutrition 48 0.044
123
c ABD014 Abdominal Obesity-Metabolic Syndrome 1 48 0.044
124
c SVR005 Severe Pre-Eclampsia 48 0.044
125
P PTT050 Pituitary Adenoma, Growth Hormone-Secreting 48 0.044
126
P CHL066 Cholangitis 48 0.044
127
OVR063 Overnutrition 48 0.044
128
URM002 Uremia 48 0.044
129
LMB062 Limb Ischemia 47 0.044
130
CTN014 Cutaneous Mastocytosis 47 0.044
131
NTR005 Nutritional Deficiency Disease 47 0.044
132
AML029 Ameloblastoma 47 0.044
133
C2D001 C2 Deficiency 46 0.044
134
HYP043 Hyperandrogenism 46 0.044
135
CLD007 Cold Agglutinin Disease 46 0.044
136
PTT009 Pituitary Gland Disease 46 0.044
137
DNT012 Dental Caries 46 0.044
138
c ACT068 Acute Cystitis 45 0.044
139
INT067 Interstitial Nephritis 45 0.044
140
c INH020 Inherited Metabolic Disorder 45 0.044
141
ICH002 Ichthyosis Bullosa of Siemens 45 0.044
142
c NGH019 Night Blindness, Congenital Stationary , 1a, X-Linked 45 0.044
143
GLC008 Glucose Metabolism Disease 44 0.044
144
c ACT042 Acute Pyelonephritis 44 0.044
145
c MCR113 Microvascular Complications of Diabetes 3 44 0.044
146
SHH001 Sheehan Syndrome 44 0.044
147
P AML002 Amelogenesis Imperfecta 44 0.044
148
RBF001 Riboflavin Deficiency 44 0.044
149
P ATM019 Autoimmune Polyendocrine Syndrome 43 0.044
150
SYS003 Systolic Heart Failure 43 0.044
151
PRD004 Prediabetes Syndrome 43 0.044
152
LYM020 Lymph Node Cancer 42 0.044
153
MNN006 Meninges Hemangiopericytoma 42 0.044
154
END038 Endocrine Pancreas Disease 42 0.044
155
DCB001 Decubitus Ulcer 42 0.044
156
c ATM092 Autoimmune Polyendocrine Syndrome, Type Ii 42 0.044
157
P ACQ022 Acquired Generalized Lipodystrophy 42 0.044
158
ART008 Arteriosclerosis Obliterans 42 0.044
159
c VRL005 Viral Pneumonia 42 0.044
160
IDP033 Idiopathic Edema 42 0.044
161
INS006 Insulin Autoimmune Syndrome 41 0.044
162
GRW016 Growth Hormone Deficiency, Isolated, Type Ib 41 0.044
163
P CPL003 Capillary Leak Syndrome 41 0.044
164
P ABD016 Abdominal Obesity-Metabolic Syndrome 41 0.044
165
ASP007 Aspiration Pneumonia 40 0.044
166
P ACQ009 Acquired Metabolic Disease 40 0.044
167
DNT001 Dental Fluorosis 40 0.044
168
MDS022 Mediastinitis 40 0.044
169
HYP070 Hyperpituitarism 40 0.044
170
CST005 Castleman Disease 39 0.044
171
c SBC007 Subacute Thyroiditis 39 0.044
172
PRX014 Proximal Spinal Muscular Atrophy 39 0.044
173
FST010 Fasting Hypoglycemia 39 0.044
174
LCL004 Localized Osteosarcoma 39 0.044
175
URM005 Uremic Pruritus 38 0.044
176
SPN369 Spinal Disease 38 0.044
177
DFF006 Diffuse Idiopathic Skeletal Hyperostosis 38 0.044
178
NTR018 Neutrophilia, Hereditary 38 0.044
179
SPN036 Spinal Chordoma 38 0.044
180
ACT088 Acute Insulin Response 38 0.044
181
CHL050 Cholesterol Ester Storage Disease 37 0.044
182
ACD009 Acid-Labile Subunit, Deficiency of 37 0.044
183
c SCN052 Secondary Adrenal Insufficiency 37 0.044
184
c CNG033 Congenital Syphilis 37 0.044
185
ETH004 Euthyroid Sick Syndrome 36 0.044
186
NPH004 Nephropathia Epidemica 36 0.044
187
BCK003 Background Diabetic Retinopathy 35 0.044
188
ARC001 Arcus Senilis 35 0.044
189
ACD004 Acdc 35 0.044
190
MLT002 Multiple Symmetrical Lipomatosis 34 0.044
191
c AML017 Amelogenesis Imperfecta, Type Ib 34 0.044
192
MNC019 Monocarboxylate Transporter 1 Deficiency 34 0.044
193
CRY008 Cryopyrin-Associated Periodic Syndrome 33 0.044
194
SLP010 Slipped Capital Femoral Epiphysis 33 0.044
195
CHR100 Chronic Ulcer of Skin 32 0.044
196
c ACT036 Acute Cholangitis 32 0.044
197
PYR004 Pyuria 31 0.044
198
CCL002 Cecal Disease 30 0.044
199
IDP041 Idiopathic Recurrent Pericarditis 30 0.044
200
PNC048 Pancreatic Lipase Deficiency 30 0.044
201
c AML057 Amelogenesis Imperfecta, Type Iiia 29 0.044
202
P BRC003 Brachyolmia 27 0.044
203
DNT006 Dental Pulp Necrosis 27 0.044
204
P HYP658 Hypoplastic Amelogenesis Imperfecta 26 0.044
205
c HNT011 Huntington Disease-Like 3 26 0.044
206
TTH005 Teeth Hard Tissue Disease 26 0.044
207
c MLG042 Malignant Otitis Externa 25 0.044
208
HYP160 Hyperkeratosis Lenticularis Perstans 24 0.044
209
HYP644 Hypocalcified Amelogenesis Imperfecta 22 0.044
210
LGP003 Logopenic Progressive Aphasia 22 0.044
211
XLN218 X-Linked Amelogenesis Imperfecta Hypoplastic/hypomaturation 2 19 0.044
212
AML005 Amelogenesis Imperfecta Hypomaturation Type 18 0.044
213
c HYP333 Hyperlipidemia, Combined, 2 17 0.044
214
LPD028 Lipodystrophy Due to Peptidic Growth Factors Deficiency 17 0.044
215
CMP036 Complement Component C2 Deficiency 8 0.044
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