Search results for "hyperlipoproteinemia"

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

205 hits were found for 'hyperlipoproteinemia'

# Family MCID Name MIFTS Score
1
FML026 Familial Lipoprotein Lipase Deficiency 49 7.201
2
HYP286 Hyperchylomicronemia, Late-Onset 36 7.167
3
c HYP032 Hyperlipoproteinemia Type Iv 33 6.007
4
c HYP163 Hyperlipidemia Type 3 43 5.759
5
c HYP011 Hyperlipoproteinemia Type Iii 32 5.669
6
P HYP607 Hypercholesterolemia, Familial 74 5.656
7
P FML035 Familial Hyperlipidemia 47 4.520
8
c HYP592 Hyperlipoproteinemia, Type 1d 15 4.058
9
P HYP289 Hyperlipoproteinemia, Type Ib 23 4.026
10
LPP001 Lipoprotein Lipase Deficiency 51 3.501
11
P HYP614 Hyperlipidemia, Familial Combined 45 2.806
12
P HYP117 Hypertriglyceridemia 58 2.114
13
CRD144 Cardiovascular Disease Risk Factor ) 37 1.984
14
c HYP288 Hypercholesterolemia, Due to Ligand-Defective Apo B 37 1.984
15
c LDL002 Ldlr-Related Familial Hypercholesterolemia, Autosomal Dominant 7 1.984
16
P HPT021 Hepatitis 63 0.118
17
P LKM002 Leukemia 63 0.109
18
P NRP001 Neuropathy 47 0.077
19
ANR040 Aneurysm 46 0.077
20
CRB009 Cerebritis 44 0.077
21
P BRS047 Breast Cancer 100 0.063
22
P OBS005 Obesity 87 0.063
23
P INF038 Influenza 67 0.063
24
P LVR013 Liver Disease 60 0.063
25
P PNM007 Pneumonia 56 0.063
26
c VRL010 Viral Hepatitis 54 0.063
27
FTT001 Fatty Liver Disease 53 0.063
28
P PNC044 Pancreatitis 53 0.063
29
P RHN004 Rhinitis 52 0.063
30
P OPN001 Open-Angle Glaucoma 48 0.063
31
CHL067 Cholecystitis 47 0.063
32
LPD008 Lipid Metabolism Disorder 47 0.063
33
P ATX004 Ataxia 43 0.063
34
END072 Endotheliitis 41 0.063
35
P CHL066 Cholangitis 40 0.063
36
NRN002 Neuronitis 36 0.063
37
P CLR023 Colorectal Cancer 91 0.045
38
P RHM011 Rheumatoid Arthritis 87 0.045
39
HPT023 Hepatocellular Carcinoma 87 0.045
40
HV1006 Hiv-1 78 0.045
41
P AST005 Asthma 77 0.045
42
P SCH015 Schizophrenia 76 0.045
43
HDG012 Hodgkin Lymphoma 73 0.045
44
P PHC003 Pheochromocytoma 70 0.045
45
P HMC003 Hemochromatosis 69 0.045
46
P CRN211 Coronary Artery Disease 69 0.045
47
MYL009 Myelodysplastic Syndrome 65 0.045
48
c HPT001 Hepatitis C 65 0.045
49
ALL003 Allergic Rhinitis 64 0.045
50
CMM004 Common Variable Immunodeficiency 63 0.045
51
P ART022 Arthritis 63 0.045
52
c HPT073 Hepatitis C Virus 62 0.045
53
P END044 Endometriosis 62 0.045
54
P MYL006 Myeloid Leukemia 61 0.045
55
SRC014 Sarcoma 61 0.045
56
ALC007 Alcohol Dependence 60 0.045
57
ART016 Aortic Aneurysm 60 0.045
58
ORN006 Ornithine Transcarbamylase Deficiency 60 0.045
59
c NRF018 Neurofibromatosis, Type 1 59 0.045
60
P KDN017 Kidney Cancer 59 0.045
61
P NRF002 Neurofibromatosis 59 0.045
62
P LYM118 Lymphoma 57 0.045
63
P DRM010 Dermatomyositis 57 0.045
64
P AST007 Astrocytoma 57 0.045
65
c HMP004 Hemophilia B 57 0.045
66
c ATM011 Autoimmune Hepatitis 56 0.045
67
P GCH001 Gaucher's Disease 56 0.045
68
ATH003 Atherosclerosis 56 0.045
69
P NPH012 Nephrotic Syndrome 55 0.045
70
P MNN013 Meningitis 55 0.045
71
MXD005 Mixed Connective Tissue Disease 54 0.045
72
P MSC005 Muscular Dystrophy 54 0.045
73
P HYP020 Hyperprolactinemia 54 0.045
74
c SYS004 Systemic Mastocytosis 53 0.045
75
P ANT006 Antiphospholipid Syndrome 53 0.045
76
PSD007 Pseudomyxoma Peritonei 53 0.045
77
c ACT027 Acute Pancreatitis 53 0.045
78
HYP066 Hyperglycemia 53 0.045
79
DBN001 Dubin-Johnson Syndrome 53 0.045
80
P CRB042 Cerebellar Ataxia 52 0.045
81
ART001 Arterial Tortuosity Syndrome 52 0.045
82
P CNJ013 Conjunctivitis 52 0.045
83
HRY003 Hairy Cell Leukemia 52 0.045
84
P CTS001 Cutis Laxa 51 0.045
85
HYP056 Hypoglycemia 51 0.045
86
ALV002 Alveolar Echinococcosis 51 0.045
87
P HRD011 Hereditary Spherocytosis 51 0.045
88
DBT010 Diabetic Neuropathy 51 0.045
89
INT066 Interstitial Lung Disease 51 0.045
90
HPT019 Hepatic Encephalopathy 51 0.045
91
LNG099 Lung Disease 50 0.045
92
P LRY019 Laryngitis 50 0.045
93
TRG002 Trigeminal Neuralgia 50 0.045
94
P HMP007 Hemophilia 50 0.045
95
OCL008 Oculopharyngeal Muscular Dystrophy 50 0.045
96
P THY032 Thyroiditis 49 0.045
97
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 49 0.045
98
P DGR001 Digeorge Syndrome 49 0.045
99
SML019 Smallpox 49 0.045
100
P TRT010 Teratoma 49 0.045
101
ECH003 Echinococcosis 49 0.045
102
TRY001 Trypanosomiasis 49 0.045
103
c ACT073 Acute Leukemia 49 0.045
104
ART111 Artery Disease 49 0.045
105
PLM012 Pulmonary Sarcoidosis 48 0.045
106
P MST009 Mastocytosis 48 0.045
107
MRK001 Merkel Cell Carcinoma 48 0.045
108
SPH001 Sapho Syndrome 48 0.045
109
CNN005 Connective Tissue Disease 48 0.045
110
P HML001 Hemolytic-Uremic Syndrome 47 0.045
111
ART031 Aortic Coarctation 47 0.045
112
P MYT002 Myotonic Dystrophy 47 0.045
113
CNS004 Constipation 46 0.045
114
P END033 Endocarditis 46 0.045
115
P FBR031 Febrile Seizures 46 0.045
116
P GLM045 Glioma 46 0.045
117
HYP266 Hypoxia 46 0.045
118
GST037 Gastroparesis 46 0.045
119
P DRR001 Diarrhea 45 0.045
120
TRM010 Traumatic Brain Injury 45 0.045
121
WST005 West Nile Virus 45 0.045
122
SCR002 Scurvy 45 0.045
123
c MLG068 Malignant Glioma 44 0.045
124
P PRG013 Paraganglioma 44 0.045
125
END031 Endometrial Stromal Sarcoma 43 0.045
126
P ENC018 Encephalopathy 43 0.045
127
GNG004 Ganglioglioma 43 0.045
128
BRN071 Brain Injury 43 0.045
129
SYN005 Synostosis 42 0.045
130
RST001 Restless Legs Syndrome 42 0.045
131
P CYS017 Cystic Teratoma 42 0.045
132
SPR099 Supravalvar Aortic Stenosis 42 0.045
133
ANG054 Angina Pectoris 42 0.045
134
MNR002 Meniere's Disease 42 0.045
135
RTN023 Retinitis 42 0.045
136
PRP007 Priapism 42 0.045
137
c INH020 Inherited Metabolic Disorder 41 0.045
138
P INT030 Intracranial Aneurysm 41 0.045
139
INF034 Infective Endocarditis 41 0.045
140
CRB086 Cerebral Aneurysms 41 0.045
141
P CRV039 Cervicitis 41 0.045
142
MYM001 Myoma 41 0.045
143
P PRP023 Peripheral Neuropathy 41 0.045
144
STS002 Situs Inversus 41 0.045
145
DBT006 Diabetic Macular Edema 41 0.045
146
P SCL009 Sclerosing Cholangitis 41 0.045
147
C2D001 C2 Deficiency 40 0.045
148
SRT004 Serotonin Syndrome 40 0.045
149
HMG002 Hemoglobinuria 40 0.045
150
ICH002 Ichthyosis Bullosa of Siemens 40 0.045
151
LYM051 Lymphomatoid Granulomatosis 40 0.045
152
P PSD015 Pseudohypoparathyroidism 40 0.045
153
URT010 Ureteral Obstruction 40 0.045
154
SKL014 Skeletal Dysplasia 40 0.045
155
PNC034 Pancreas Disease 39 0.045
156
CHR008 Choroiditis 39 0.045
157
P BLP003 Blepharospasm 39 0.045
158
GYN001 Gynecomastia 39 0.045
159
PRL017 Prolymphocytic Leukemia 39 0.045
160
P KRT005 Keratoacanthoma 39 0.045
161
NTR005 Nutritional Deficiency Disease 39 0.045
162
SWN001 Swine Influenza 38 0.045
163
SPN021 Spinal Meningioma 37 0.045
164
CHR276 Chronic Active Epstein-Barr Virus Infection 37 0.045
165
SKL017 Skeletal Dysplasias 37 0.045
166
ASP007 Aspiration Pneumonia 37 0.045
167
P CHR345 Chronic Pain 37 0.045
168
PLS002 Peliosis Hepatis 36 0.045
169
SPN119 Spondylarthropathy 36 0.045
170
DYS015 Dysentery 36 0.045
171
RCT011 Rectal Prolapse 35 0.045
172
c CTS030 Cutis Laxa, Autosomal Recessive, Type Ia 34 0.045
173
c RCR022 Recurrent Acute Pancreatitis 34 0.045
174
VLV010 Vulvovaginitis 34 0.045
175
MTR003 Mitral Valve Stenosis 34 0.045
176
STM006 Stomach Disease 33 0.045
177
ACR005 Acrodermatitis 33 0.045
178
c CTS008 Cutis Laxa, Autosomal Dominant 31 0.045
179
c CTS034 Cutis Laxa, Autosomal Recessive Type 1 31 0.045
180
XNT002 Xanthogranulomatous Cholecystitis 31 0.045
181
ACR097 Acrodermatitis Chronica Atrophicans 31 0.045
182
SCR003 Secretory Diarrhea 29 0.045
183
P DYS021 Dysautonomia 29 0.045
184
BCL011 Bacillary Angiomatosis 29 0.045
185
KDN013 Kidney Hypertrophy 29 0.045
186
EMP002 Emphysematous Cholecystitis 28 0.045
187
c ACQ027 Acquired Cutis Laxa 27 0.045
188
ANG037 Angiomatosis 27 0.045
189
PLM058 Pulmonary Atresia with Intact Ventricular Septum 26 0.045
190
MCR095 Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis 26 0.045
191
LYM095 Lymphangiomatosis 25 0.045
192
c CTS019 Cutis Laxa, Ad 25 0.045
193
c PNC106 Pancreatic Agenesis 1 25 0.045
194
DFF031 Diffuse Alveolar Hemorrhage 24 0.045
195
DRR004 Diarrhea 3, Secretory Sodium, Congenital, Syndromic 24 0.045
196
PNC048 Pancreatic Lipase Deficiency 23 0.045
197
LGP003 Logopenic Progressive Aphasia 21 0.045
198
IGG014 Igg4-Related Sclerosing Cholangitis 20 0.045
199
INF021 Infant Gynecomastia 17 0.045
200
PHC002 Phacogenic Glaucoma 17 0.045
201
c FBL003 Fbln5-Related Cutis Laxa 15 0.045
202
c HYP333 Hyperlipidemia, Combined, 2 10 0.045
203
CMP036 Complement Component C2 Deficiency 10 0.045
204
FML285 Familial Apolipoprotein C-Ii Deficiency 9 0.045
205
PNC098 Pancreatic Triacylglycerol Lipase Deficiency 6 0.045