Search results for "hyperlipoproteinemia"

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

248 hits were found for 'hyperlipoproteinemia'

# Family MCID Name MIFTS Score
1
FML026 Familial Lipoprotein Lipase Deficiency 47 7.306
2
HYP286 Hyperchylomicronemia, Late-Onset 35 7.248
3
c HYP163 Hyperlipidemia Type 3 44 6.134
4
c HYP032 Hyperlipoproteinemia Type Iv 33 5.775
5
P HYP607 Hypercholesterolemia, Familial 79 5.732
6
c HYP011 Hyperlipoproteinemia Type Iii 30 5.424
7
P FML035 Familial Hyperlipidemia 46 4.117
8
P HYP289 Hyperlipoproteinemia, Type Ib 24 4.061
9
LPP001 Lipoprotein Lipase Deficiency 53 3.602
10
c HYP592 Hyperlipoproteinemia, Type 1d 17 3.562
11
P HYP614 Hyperlipidemia, Familial Combined 42 2.834
12
P HYP117 Hypertriglyceridemia 56 2.183
13
CRD144 Cardiovascular Disease Risk Factor ) 39 2.004
14
c LDL002 Ldlr-Related Familial Hypercholesterolemia, Autosomal Dominant 8 2.004
15
ATH003 Atherosclerosis 50 0.102
16
P PNC044 Pancreatitis 51 0.093
17
XNT003 Xanthomatosis 39 0.093
18
ISC006 Ischemic Heart Disease 56 0.083
19
P OBS005 Obesity 89 0.072
20
P HRM001 Hermansky-Pudlak Syndrome 62 0.072
21
c PNC108 Pancreatitis, Hereditary 59 0.072
22
P HMP002 Hemophagocytic Lymphohistiocytosis 59 0.072
23
ACN002 Acanthosis Nigricans 53 0.072
24
HNT002 Hantavirus Pulmonary Syndrome 52 0.072
25
P GLL020 Gallbladder Disease 48 0.072
26
THR013 Thoracic Outlet Syndrome 47 0.072
27
LPP002 Lipoprotein Glomerulopathy 43 0.072
28
LMB062 Limb Ischemia 38 0.072
29
INN002 Inner Ear Disease 38 0.072
30
P HPT021 Hepatitis 58 0.059
31
SCH016 Schimke Immunoosseous Dysplasia 51 0.059
32
P HST010 Histiocytosis 51 0.059
33
c ACT027 Acute Pancreatitis 47 0.059
34
P HYP060 Hyperinsulinism 44 0.059
35
P HYP090 Hyperalphalipoproteinemia 44 0.059
36
P TRC086 Trichohepatoenteric Syndrome 1 42 0.059
37
RTN003 Retinal Ischemia 40 0.059
38
TTR016 Tetra-Amelia Syndrome 38 0.059
39
c RCR022 Recurrent Acute Pancreatitis 38 0.059
40
HMZ003 Homozygous Familial Hypercholesterolemia 35 0.059
41
P RNL014 Renal Cell Carcinoma 81 0.041
42
c MLT019 Multiple Myeloma 77 0.041
43
P MYC007 Myocardial Infarction 76 0.041
44
ANR002 Aniridia 72 0.041
45
VNH007 Von Hippel-Lindau Syndrome 68 0.041
46
c SPN225 Spondyloarthropathy 1 66 0.041
47
P ANG001 Angelman Syndrome 66 0.041
48
AND015 Androgen Insensitivity 65 0.041
49
P RNL101 Renal Cell Carcinoma, Papillary 65 0.041
50
PRP027 Peripheral Vascular Disease 62 0.041
51
P KDN017 Kidney Cancer 60 0.041
52
P AXN010 Axenfeld-Rieger Syndrome, Type 3 60 0.041
53
THR006 Thromboangiitis Obliterans 60 0.041
54
TNG002 Tangier Disease 60 0.041
55
TYP007 Typhoid Fever 59 0.041
56
PRT036 Peritonitis 58 0.041
57
P SPN046 Spinal Muscular Atrophy 58 0.041
58
CRB011 Cerebrotendinous Xanthomatosis 58 0.041
59
P ADN016 Adenocarcinoma 56 0.041
60
LPT001 Leptospirosis 55 0.041
61
VSC007 Vascular Disease 55 0.041
62
CHR072 Chordoma 55 0.041
63
P HMN010 Hemangioma 54 0.041
64
P SJG001 Sjogren's Syndrome 54 0.041
65
P MYL007 Myeloma 54 0.041
66
ALC006 Alcoholic Hepatitis 53 0.041
67
PST028 Post-Traumatic Stress Disorder 53 0.041
68
DBT010 Diabetic Neuropathy 53 0.041
69
P HYP086 Hypothyroidism 52 0.041
70
P NPH012 Nephrotic Syndrome 52 0.041
71
P ANR007 Anorexia Nervosa 52 0.041
72
c MTB001 Metabolic Syndrome X 52 0.041
73
ICH002 Ichthyosis Bullosa of Siemens 51 0.041
74
OST003 Osteonecrosis 50 0.041
75
URT039 Urticaria 50 0.041
76
ADR042 Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency 49 0.041
77
P GLY013 Glycogen Storage Disease 49 0.041
78
HPT022 Hepatoblastoma 49 0.041
79
P THY032 Thyroiditis 48 0.041
80
THR004 Thrombocytosis 48 0.041
81
INT002 Intermittent Claudication 48 0.041
82
CLT003 Colitis 47 0.041
83
ISC004 Ischemia 47 0.041
84
CRN014 Cronkhite-Canada Syndrome 46 0.041
85
PSD007 Pseudomyxoma Peritonei 46 0.041
86
c ART101 Aortic Valve Disease 2 46 0.041
87
DBT004 Diabetic Polyneuropathy 46 0.041
88
P ACT105 Acute Mountain Sickness 46 0.041
89
ANG020 Angiosarcoma 46 0.041
90
LPD008 Lipid Metabolism Disorder 45 0.041
91
FLT006 Floating-Harbor Syndrome 45 0.041
92
P PRT013 Portal Hypertension 45 0.041
93
c RNL003 Renal Clear Cell Carcinoma 45 0.041
94
P RTN022 Retinal Vein Occlusion 45 0.041
95
P MSC003 Muscular Atrophy 45 0.041
96
P VNS003 Venous Insufficiency 44 0.041
97
ESP023 Esophageal Disease 44 0.041
98
c MLG002 Malignant Peritoneal Mesothelioma 44 0.041
99
P SYP003 Syphilis 44 0.041
100
HMN009 Hemangioblastoma 43 0.041
101
ADR016 Adrenal Cortical Carcinoma 43 0.041
102
c MLG079 Malignant Pleural Mesothelioma 43 0.041
103
c PND001 Pain Disorder 43 0.041
104
PLC005 Placental Insufficiency 43 0.041
105
FCL012 Facial Paralysis 43 0.041
106
ELS001 Eales Disease 43 0.041
107
P CLR030 Clear Cell Renal Cell Carcinoma 43 0.041
108
HYP266 Hypoxia 42 0.041
109
INF034 Infective Endocarditis 42 0.041
110
SYR002 Syringocystadenoma Papilliferum 42 0.041
111
PRC012 Pericardial Effusion 41 0.041
112
NTR005 Nutritional Deficiency Disease 41 0.041
113
SPN035 Spindle Cell Sarcoma 41 0.041
114
ANG054 Angina Pectoris 41 0.041
115
OPT003 Opiate Dependence 41 0.041
116
HRT012 Heart Valve Disease 40 0.041
117
BRD005 Borderline Leprosy 40 0.041
118
HYP037 Hyperhomocysteinemia 40 0.041
119
CYS014 Cystadenocarcinoma 40 0.041
120
c CNT016 Central Retinal Vein Occlusion 40 0.041
121
CHR177 Chromophobe Renal Cell Carcinoma 40 0.041
122
CYS009 Cystadenoma 40 0.041
123
DRR008 Diarrhea 1, Secretory Chloride, Congenital 40 0.041
124
C2D001 C2 Deficiency 39 0.041
125
MNR002 Meniere's Disease 39 0.041
126
EPT010 Epithelial-Myoepithelial Carcinoma 39 0.041
127
MNN014 Mononeuritis 39 0.041
128
P CHL066 Cholangitis 39 0.041
129
PRP080 Peripheral Artery Disease 39 0.041
130
GRW007 Growth Hormone Deficiency 38 0.041
131
HTS001 Hiatus Hernia 38 0.041
132
CLL002 Collecting Duct Carcinoma 38 0.041
133
RTN021 Retinal Vascular Occlusion 38 0.041
134
SRC027 Sarcoma, Synovial 37 0.041
135
KPS002 Kaposiform Hemangioendothelioma 37 0.041
136
MYX001 Myxopapillary Ependymoma 37 0.041
137
P PRX014 Proximal Spinal Muscular Atrophy 37 0.041
138
ASP007 Aspiration Pneumonia 37 0.041
139
SPR007 Superior Mesenteric Artery Syndrome 37 0.041
140
MYP100 Myopathy, X-Linked, with Excessive Autophagy 36 0.041
141
ESP025 Esophagus Adenocarcinoma 36 0.041
142
PLS002 Peliosis Hepatis 36 0.041
143
STM006 Stomach Disease 36 0.041
144
c CNG033 Congenital Syphilis 35 0.041
145
MCN008 Mucinous Cystadenocarcinoma 35 0.041
146
OVR012 Ovarian Serous Cystadenocarcinoma 35 0.041
147
PRC010 Pericardial Mesothelioma 35 0.041
148
PRV003 Perivascular Epithelioid Cell Tumor 34 0.041
149
SPL007 Splenic Abscess 34 0.041
150
JJN008 Jejunoileitis 34 0.041
151
HDR004 Hidradenoma 34 0.041
152
SPL018 Splenomegaly 34 0.041
153
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 34 0.041
154
APP003 Appendiceal Neoplasm 34 0.041
155
CRB004 Cerebral Artery Occlusion 33 0.041
156
c FML156 Familial Hyperaldosteronism 33 0.041
157
BRN026 Branch Retinal Artery Occlusion 33 0.041
158
HYP016 Hypochondriasis 33 0.041
159
P SRT002 Sertoli Cell Tumor 33 0.041
160
ABD004 Abdominal Tuberculosis 33 0.041
161
ESN004 Eosinophilic Gastritis 33 0.041
162
MRN001 Marantic Endocarditis 33 0.041
163
HPT004 Hepatic Coma 32 0.041
164
ECC004 Eccrine Porocarcinoma 32 0.041
165
PNM003 Pneumatosis Cystoides Intestinalis 32 0.041
166
PNC002 Pancreatic Mucinous Cystadenoma 32 0.041
167
HMC014 Homocysteinemia 32 0.041
168
INT104 Intravascular Papillary Endothelial Hyperplasia 32 0.041
169
EXH001 Exhibitionism 31 0.041
170
c HNT004 Huntington Disease-Like 2 31 0.041
171
P MSN005 Mesenchymal Chondrosarcoma 31 0.041
172
BLT003 Blue Toe Syndrome 31 0.041
173
P ADN017 Adenofibroma 31 0.041
174
P ATX010 Ataxia Neuropathy Spectrum 31 0.041
175
TRN051 Translocation Renal Cell Carcinoma 31 0.041
176
BLD033 Bile Duct Adenoma 31 0.041
177
PRP028 Peripheral Vertigo 31 0.041
178
RTN013 Retinal Hemangioblastoma 31 0.041
179
CYS015 Cystadenofibroma 30 0.041
180
MLG098 Malignant Mixed Mullerian Tumor 30 0.041
181
RDT001 Radiation Cystitis 30 0.041
182
PRM014 Periampullary Adenocarcinoma 30 0.041
183
c ACT072 Acute Laryngitis 30 0.041
184
PPT002 Peptic Ulcer Perforation 30 0.041
185
ART110 Arteritic Anterior Ischemic Optic Neuropathy 30 0.041
186
SRC001 Sarcomatoid Mesothelioma 29 0.041
187
PNC028 Pancreatic Steatorrhea 29 0.041
188
NPH006 Nephrogenic Adenofibroma 29 0.041
189
MCN016 Mucinous Tubular and Spindle Cell Carcinoma 29 0.041
190
PHT004 Photoallergic Dermatitis 29 0.041
191
GST090 Gastroduodenal Crohn's Disease 28 0.041
192
ANG007 Angiokeratoma Circumscriptum 28 0.041
193
NNT005 Neonatal Candidiasis 28 0.041
194
FMR011 Fumarate Hydratase Deficiency 28 0.041
195
ISC005 Ischemic Bone Disease 28 0.041
196
c KDN016 Kidney Benign Neoplasm 28 0.041
197
MTN001 Metanephric Adenoma 28 0.041
198
GRN011 Granulomatous Gastritis 28 0.041
199
PLM007 Pulmonary Aspergilloma 28 0.041
200
RNL018 Renal Pelvis Carcinoma 28 0.041
201
c CHR057 Chronic Laryngitis 28 0.041
202
LRY007 Laryngeal Tuberculosis 28 0.041
203
ISC001 Ischemic Neuropathy 28 0.041
204
SCR001 Secretory Meningioma 28 0.041
205
CHR055 Chordoid Meningioma 27 0.041
206
P GST047 Gastrointestinal Neuroendocrine Tumor 27 0.041
207
TFT003 Tufting Enteropathy 27 0.041
208
FML029 Familial Renal Papillary Carcinoma 27 0.041
209
CHR083 Chromophobe Adenocarcinoma 27 0.041
210
PRC011 Parachordoma 27 0.041
211
OSS002 Ossifying Fibromyxoid Tumor 27 0.041
212
BPH002 Biphasic Synovial Sarcoma 27 0.041
213
FNC002 Functional Diarrhea 26 0.041
214
BLD041 Bladder Calculus 26 0.041
215
CLR112 Clear Cell Papillary Renal Cell Carcinoma 26 0.041
216
NDL010 Nodular Hidradenoma 26 0.041
217
END001 Endometrial Mucinous Adenocarcinoma 25 0.041
218
CTR009 Cataract Congenital Dominant Non Nuclear 25 0.041
219
MNP001 Monophasic Synovial Sarcoma 25 0.041
220
MCR014 Microcystic Adenoma 25 0.041
221
ANS018 Anismus 25 0.041
222
P BNG013 Benign Breast Phyllodes Tumor 25 0.041
223
CLR018 Clear Cell Meningioma 24 0.041
224
ADR040 Adrenal Gland Pheochromocytoma 24 0.041
225
END074 Endocardium Disease 24 0.041
226
RMN001 Rumination Disorder 24 0.041
227
FBR001 Fibrous Meningioma 24 0.041
228
END051 Endolymphatic Sac Tumor 24 0.041
229
TBL016 Tubulocystic Carcinoma 24 0.041
230
CHR067 Chronic Intestinal Vascular Insufficiency 24 0.041
231
ALR002 Al-Raqad Syndrome 23 0.041
232
c MLG042 Malignant Otitis Externa 23 0.041
233
SQM005 Squamous Papillomatosis 23 0.041
234
ABR002 Abrikosov's Tumor 23 0.041
235
BLD005 Bile Duct Mucoepidermoid Carcinoma 22 0.041
236
FNC006 Functional Gastric Disease 22 0.041
237
ACT058 Active Peptic Ulcer Disease 22 0.041
238
LWR004 Lower Urinary Tract Calculus 22 0.041
239
FNG003 Fungal Esophagitis 21 0.041
240
THY104 Thyroid Carcinoma Somatic 21 0.041
241
INT049 Intrahepatic Bile Duct Adenoma 20 0.041
242
TRN002 Transitional Meningioma 20 0.041
243
CRV014 Cervical Adenoma Malignum 18 0.041
244
c HNT011 Huntington Disease-Like 3 17 0.041
245
c LRG016 Large Intestine Adenocarcinoma 16 0.041
246
CRV037 Cervical Mucinous Adenocarcinoma 14 0.041
247
CMP036 Complement Component C2 Deficiency 10 0.041
248
c HYP333 Hyperlipidemia, Combined, 2 8 0.041