Search results for Triglycerides Group B

371 hits were found for Triglycerides Group B

# Family MCID Name MIFTS Score
1
c HPT021 Hepatitis 74 0.766
2
P HPT016 Hepatitis B 70 0.659
3
c LVR013 Liver Disease 77 0.378
4
c DBT026 Diabetes Mellitus, Noninsulin-Dependent 92 0.328
5
c DBT009 Diabetes Mellitus 67 0.315
6
c HRT032 Heart Disease 76 0.296
7
c HPT023 Hepatocellular Carcinoma 97 0.280
8
P HPT001 Hepatitis C 69 0.263
9
c BRS047 Breast Cancer 100 0.260
10
c ART022 Arthritis 78 0.253
11
c MYC007 Myocardial Infarction 78 0.244
12
c CRN018 Coronary Artery Anomaly 74 0.238
13
ACQ007 Acquired Immunodeficiency Syndrome 66 0.235
14
ART140 Arteries, Anomalies of 67 0.234
15
LYM019 Lymphosarcoma 59 0.232
16
HMN014 Human Immunodeficiency Virus Infectious Disease 62 0.230
17
LPD008 Lipid Metabolism Disorder 65 0.227
18
c CRN300 Coronary Heart Disease 1 62 0.221
19
VRL011 Viral Infectious Disease 69 0.214
20
ISC004 Ischemia 67 0.213
21
c PNC044 Pancreatitis 62 0.208
22
FTT001 Fatty Liver Disease 66 0.208
23
c LNG032 Lung Cancer 99 0.204
24
P HPT073 Hepatitis C Virus 73 0.196
25
c HYP750 Hypertriglyceridemia, Familial 58 0.188
26
c RHM011 Rheumatoid Arthritis 82 0.188
28
c ALZ034 Alzheimer Disease 88 0.185
29
P HYP555 Hypertriglyceridemia, Transient Infantile 43 0.184
30
c KDN018 Kidney Disease 71 0.184
31
DPR016 Depression 73 0.182
32
c PRS040 Prostate Cancer 93 0.180
33
ISC006 Ischemic Heart Disease 72 0.177
34
c LPS004 Lupus Erythematosus 69 0.177
35
c NNL004 Nonalcoholic Fatty Liver Disease 56 0.177
36
ATM095 Autoimmune Disease 68 0.177
37
c ADN016 Adenocarcinoma 71 0.175
38
P SYS001 Systemic Lupus Erythematosus 88 0.173
39
c ENC018 Encephalopathy 65 0.170
40
LVR012 Liver Cirrhosis 67 0.169
41
VSC007 Vascular Disease 72 0.169
42
P VRL010 Viral Hepatitis 60 0.166
43
P BDY007 Body Mass Index Quantitative Trait Locus 1 48 0.166
44
HMN044 Human Immunodeficiency Virus Type 1 75 0.164
45
c CRD246 Cardiovascular System Disease 57 0.164
46
P PRS136 Prostate Cancer, Hereditary, 6 40 0.164
47
P PRS130 Prostate Cancer, Hereditary, 8 37 0.164
48
ANX010 Anxiety 73 0.163
49
PRT037 Pertussis 71 0.161
50
P FTT008 Fatty Liver Disease, Nonalcoholic 1 61 0.159
51
DMN002 Dementia 69 0.159
52
DRM006 Dermatitis 69 0.157
53
P ACT027 Acute Pancreatitis 59 0.157
54
c MLT020 Multiple Sclerosis 76 0.156
55
ABT001 Abetalipoproteinemia 67 0.153
56
IMM136 Immune System Disease 57 0.153
57
GLC008 Glucose Metabolism Disease 54 0.149
58
c NRP001 Neuropathy 63 0.149
59
THR024 Thrombosis 64 0.147
60
c SCH015 Schizophrenia 73 0.146
61
OCL033 Oculocerebral Syndrome with Hypopigmentation 46 0.144
62
c DRR001 Diarrhea 58 0.143
63
HYP060 Hyperinsulinism 57 0.142
64
c HYP607 Hypercholesterolemia, Familial 82 0.141
65
P CNT035 Central Nervous System Disease 65 0.139
66
RPD005 Rapidly Involuting Congenital Hemangioma 24 0.139
67
CNG034 Congestive Heart Failure 71 0.139
68
HYP266 Hypoxia 63 0.138
69
BNG081 Benign Childhood Occipital Epilepsy, Panayiotopoulos Type 25 0.136
70
MNT002 Mental Depression 65 0.135
71
CYS001 Cystic Fibrosis 83 0.134
72
c ART021 Arteriosclerosis 61 0.133
73
GLC003 Glucose Intolerance 59 0.133
74
AGN016 Aging 63 0.133
75
ALL026 Allergic Hypersensitivity Disease 68 0.133
76
P ACT075 Acute Myocardial Infarction 57 0.132
77
P CHR089 Chronic Kidney Failure 73 0.130
78
c PSR002 Psoriasis 67 0.130
79
GST033 Gestational Diabetes 63 0.129
80
SPS003 Spastic Diplegia 49 0.128
81
c NRB001 Neuroblastoma 73 0.127
82
c MYP004 Myopathy 65 0.126
83
LSH001 Leishmaniasis 72 0.125
84
END057 Endometrial Cancer 69 0.124
85
GST050 Gastrointestinal System Disease 67 0.123
86
c TRC086 Trichohepatoenteric Syndrome 1 61 0.122
87
P TRC078 Trichohepatoenteric Syndrome 2 35 0.122
88
ATH013 Atherosclerosis Susceptibility 61 0.120
89
NNL002 Nonalcoholic Steatohepatitis 55 0.119
90
HYP066 Hyperglycemia 65 0.119
91
SKN016 Skin Disease 68 0.118
92
CRB039 Cerebrovascular Disease 70 0.118
93
P HYP595 Hypertension, Essential 77 0.118
94
BRR014 Barrett Esophagus 71 0.116
95
c PRD008 Periodontitis 66 0.116
96
c HYP086 Hypothyroidism 66 0.116
97
PSY004 Psychotic Disorder 74 0.115
98
c INF037 Inflammatory Bowel Disease 56 0.115
99
c EPL164 Epilepsy 73 0.115
100
CLT003 Colitis 65 0.114
101
c CND004 Candidiasis 63 0.114
102
P MCR113 Microvascular Complications of Diabetes 3 58 0.111
103
P MCR120 Microvascular Complications of Diabetes 7 46 0.111
104
P MCR130 Microvascular Complications of Diabetes 6 43 0.111
105
P MCR133 Microvascular Complications of Diabetes 4 43 0.111
106
P ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 60 0.111
107
NTR005 Nutritional Deficiency Disease 60 0.111
108
DST081 Distal Trisomy 11q 20 0.110
109
P SCL052 Scleroderma, Familial Progressive 68 0.109
110
c THR014 Thrombocytopenia 65 0.109
111
OST012 Osteoarthritis 81 0.108
112
c INF032 Infertility 60 0.107
113
PRD007 Periodontal Disease 66 0.107
114
c NRV007 Nervous System Disease 72 0.107
115
c ART153 Arthrochalasia Ehlers-Danlos Syndrome 22 0.106
116
c OST002 Osteoporosis 74 0.106
117
CRH001 Crohn's Disease 79 0.104
118
c AMY004 Amyloidosis 69 0.104
119
c INT068 Intestinal Disease 62 0.104
120
c RTN024 Retinoblastoma 73 0.104
121
FSH001 Fish-Eye Disease 51 0.103
122
CYT017 Cytophagic Histiocytic Panniculitis 26 0.103
123
ANG054 Angina Pectoris 70 0.103
124
GST045 Gastroenteritis 65 0.103
125
CHN055 Chanarin-Dorfman Syndrome 56 0.102
126
CNT047 Contact Dermatitis 64 0.102
127
URN009 Urinary System Disease 59 0.101
128
ANR007 Anorexia Nervosa 68 0.101
129
THR013 Thoracic Outlet Syndrome 57 0.101
130
VSC003 Visceral Leishmaniasis 61 0.100
131
c NMN002 Niemann-Pick Disease 50 0.100
132
c DBT085 Diabetes Mellitus, Insulin-Dependent 73 0.099
133
c CLC063 Celiac Disease 1 72 0.097
134
STR067 Stroke, Ischemic 84 0.096
135
c THL005 Thalassemia 65 0.096
136
CHL123 Chlamydia 66 0.095
137
PSR001 Psoriatic Arthritis 68 0.095
138
c ATR011 Atrial Fibrillation 69 0.095
139
NRM005 Neuromuscular Disease 61 0.095
140
P PRC016 Pre-Eclampsia 61 0.094
141
P THR001 Thrombocytopenia Due to Platelet Alloimmunization 61 0.093
142
END030 End Stage Renal Failure 60 0.091
143
ADN018 Adenoma 65 0.091
144
c CTR002 Cataract 58 0.091
145
DNT012 Dental Caries 52 0.089
146
HYP056 Hypoglycemia 64 0.089
147
LPD009 Lipid Storage Disease 53 0.089
148
THR100 Thrombocytopenic Purpura, Autoimmune 68 0.089
149
c PRP019 Peripheral Nervous System Disease 66 0.089
150
BRN071 Brain Injury 54 0.088
151
SPN186 Spinal Cord Injury 66 0.088
152
c ABD014 Abdominal Obesity-Metabolic Syndrome 1 58 0.088
153
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 29 0.087
154
FRN020 Frontal Fibrosing Alopecia 32 0.086
155
c ECL001 Eclampsia 59 0.086
156
DFC004 Deficiency Anemia 65 0.085
157
c BPL003 Bipolar Disorder 61 0.085
158
MDD011 Mood Disorder 65 0.085
159
PRT036 Peritonitis 67 0.084
160
PRM236 Primary Biliary Cholangitis 63 0.084
161
c NRF023 Neurofibromatosis, Type Ii 76 0.084
162
c PLY011 Polycystic Ovary Syndrome 64 0.083
163
CYT002 Cytokine Deficiency 39 0.083
164
c PRM006 Primary Biliary Cirrhosis 54 0.082
165
DRL001 Dural Sinus Malformation 23 0.082
166
P BLR024 Biliary Cirrhosis, Primary, 1 39 0.082
167
THY030 Thyroid Gland Disease 51 0.081
168
CRN167 Caronte 19 0.081
169
ART016 Aortic Aneurysm 71 0.081
170
TRN018 Transitional Cell Carcinoma 63 0.081
171
GT001 Gout 62 0.081
172
c MJR001 Major Depressive Disorder 67 0.080
173
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 35 0.080
174
c MCR115 Microvascular Complications of Diabetes 5 71 0.080
175
P PRD040 Periodontitis, Chronic 60 0.079
176
URM002 Uremia 53 0.079
177
HPR003 Heparin-Induced Thrombocytopenia 49 0.078
178
OVR063 Overnutrition 53 0.077
179
DBT010 Diabetic Neuropathy 60 0.076
180
END040 Endogenous Depression 59 0.076
181
IMP005 Impotence 58 0.076
182
GST092 Gastroesophageal Reflux 66 0.075
183
c SLP006 Sleep Apnea 70 0.075
184
c PTY003 Pityriasis Rubra Pilaris 52 0.075
185
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.075
186
PRP027 Peripheral Vascular Disease 72 0.075
187
c DDN001 Duodenal Ulcer 52 0.074
188
c SZR006 Seizure Disorder 61 0.074
189
DMY004 Demyelinating Disease 60 0.073
190
P PLM164 Pulmonary Hypertension, Primary, 1 71 0.072
191
c ICH004 Ichthyosis 57 0.072
192
c MSC033 Muscle Disorders 56 0.072
193
HYP080 Hypogonadism 53 0.072
194
PRP080 Peripheral Artery Disease 56 0.071
195
P BTT014 Beta-Thalassemia 73 0.071
196
c GLY013 Glycogen Storage Disease 62 0.071
197
TRN015 Transient Cerebral Ischemia 59 0.071
198
P BLD140 Blood Group, I System 26 0.071
199
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 65 0.070
200
CLR108 Colorectal Adenoma 64 0.070
201
IRN002 Iron Metabolism Disease 60 0.069
202
ILT001 Ileitis 59 0.069
203
LPD013 Lipidosis with Triglycerid Storage Disease 5 0.069
204
c TRM003 Tremor 56 0.069
205
c DLT002 Dilated Cardiomyopathy 74 0.069
206
RTN018 Retinal Disease 58 0.069
207
c BDY004 Body Mass Index Quantitative Trait Locus 11 74 0.069
208
P BDY020 Body Mass Index Quantitative Trait Locus 19 43 0.069
209
P BDY019 Body Mass Index Quantitative Trait Locus 18 43 0.069
210
P BDY017 Body Mass Index Quantitative Trait Locus 14 41 0.069
211
P BDY011 Body Mass Index Quantitative Trait Locus 10 41 0.069
212
PNC041 Pancreatic Ductal Adenocarcinoma 54 0.068
213
SCK003 Sickle Cell Anemia 75 0.068
214
P MTR002 Mitral Valve Insufficiency 50 0.068
215
RYS001 Reye Syndrome 41 0.068
216
c LCT001 Lactic Acidosis 53 0.068
217
MSC004 Muscle Tissue Disease 39 0.068
218
CHL068 Cholestasis 60 0.067
219
c MSC007 Muscle Hypertrophy 64 0.067
220
P INS002 in Situ Carcinoma 60 0.067
221
P ART138 Aortic Aneurysm, Familial Abdominal, 1 66 0.066
222
MSC190 Muscular Disease 55 0.066
223
INS024 Insulin-Like Growth Factor I 83 0.066
224
KWS001 Kwashiorkor 46 0.065
225
c VSC018 Visceral Steatosis 38 0.065
226
PRP016 Paraplegia 55 0.065
227
HPT019 Hepatic Encephalopathy 60 0.065
228
HDN002 Head Injury 52 0.065
229
BLM002 Bulimia Nervosa 61 0.065
230
MRB003 Morbid Obesity 62 0.065
231
MYC088 Mycobacterium Avium Complex Infections 34 0.065
232
LWC002 Lowe Oculocerebrorenal Syndrome 67 0.064
233
KWS002 Kawasaki Disease 72 0.064
234
AND005 Androgen Insensitivity Syndrome, Mild 19 0.064
235
INT002 Intermittent Claudication 64 0.064
236
P ATR087 Atrial Standstill 1 69 0.064
237
c OPN001 Open-Angle Glaucoma 53 0.063
238
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 37 0.063
239
c HYP069 Hyperparathyroidism 59 0.063
240
PRD004 Prediabetes Syndrome 51 0.063
241
HMZ003 Homozygous Familial Hypercholesterolemia 49 0.063
242
SXL003 Sexual Disorder 53 0.062
243
c CRD132 Cardiac Conduction Defect 64 0.062
244
BLR001 Biliary Atresia 57 0.062
245
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 48 0.062
246
GND003 Gonadal Disease 49 0.061
247
ALC009 Alcoholic Liver Cirrhosis 52 0.061
248
RTN017 Retinal Detachment 62 0.061
249
HPT004 Hepatic Coma 45 0.061
250
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 46 0.061
251
P BNM022 Bone Mineral Density Quantitative Trait Locus 8 40 0.061
252
P PSR017 Psoriasis 2 54 0.060
253
P PNC106 Pancreatic Agenesis 1 52 0.060
254
P TYP024 Type Ii Mixed Cryoglobulinemia 40 0.060
255
CHL045 Choline Deficiency Disease 40 0.060
256
PNC034 Pancreas Disease 60 0.060
257
P HNT004 Huntington Disease-Like 2 48 0.060
258
c HYP014 Hyperuricemia 56 0.060
259
NTR027 Neutrophil Actin Dysfunction 32 0.060
260
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 44 0.059
261
OST003 Osteonecrosis 67 0.059
262
CHL067 Cholecystitis 59 0.059
263
INS001 Insulinoma 66 0.059
264
CHL004 Cholelithiasis 52 0.058
265
STT004 Steatorrhea 43 0.058
266
CRH005 Crohn's Colitis 61 0.057
267
c HYP061 Hypertrophic Cardiomyopathy 59 0.057
268
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 60 0.057
269
P INF071 Inflammatory Bowel Disease 1 57 0.057
270
CRC034 Carcinoma Showing Thymus-Like Differentiation 29 0.057
271
P PSR028 Psoriasis 7 43 0.057
272
P PSR032 Psoriasis 11 43 0.057
273
P PSR018 Psoriasis 13 42 0.057
274
c HYP076 Hyperthyroidism 56 0.056
275
PLM017 Pulmonary Alveolar Microlithiasis 52 0.056
276
BRN056 Bronchopulmonary Dysplasia 61 0.056
277
FXF002 Fox-Fordyce Disease 41 0.056
278
OBS082 Obstructive Nephropathy 52 0.055
279
GRW007 Growth Hormone Deficiency 53 0.055
280
WRN001 Werner Syndrome 74 0.055
281
ALL010 Allergic Contact Dermatitis 61 0.055
282
HYP730 Hypogonadotropic Hypogonadism 58 0.054
283
HYP064 Hypogonadotropism 42 0.054
284
SPN021 Spinal Meningioma 50 0.054
285
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.054
286
BRN080 Brain Ischemia 43 0.054
287
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 36 0.053
288
c CMP008 Compartment Syndrome 52 0.053
289
MTB007 Metabolic Encephalomyopathic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 53 0.053
290
c SLL003 Salla Disease 53 0.053
291
LPT001 Leptospirosis 62 0.052
292
DRM009 Dermatomycosis 36 0.052
293
SCH012 Schizoaffective Disorder 54 0.052
294
WTH001 Withdrawal Disorder 51 0.052
295
KRT009 Keratosis 55 0.052
296
SMT008 Smith-Magenis Syndrome 58 0.052
297
c LYM124 Lymphangiectasia, Intestinal 34 0.051
298
P PRM158 Primary Intestinal Lymphangiectasia 32 0.051
299
HMS001 Hemosiderosis 52 0.051
300
c SHR029 Short Syndrome 57 0.051
301
ADR007 Adrenoleukodystrophy 72 0.051
302
P MNN043 Meningioma, Familial 63 0.051
303
c MLG056 Malignant Hyperthermia 60 0.051
304
CRC021 Carcinosarcoma 62 0.050
305
BLR008 Bilirubin Metabolic Disorder 53 0.050
306
c LYM025 Lymphedema 55 0.050
307
P GLL024 Gallbladder Disease 1 45 0.050
308
PHT003 Phototoxic Dermatitis 44 0.050
309
P HNT011 Huntington Disease-Like 3 40 0.050
310
TRP004 Tropical Sprue 36 0.049
311
BLR006 Biliary Tract Disease 53 0.049
312
c PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 70 0.048
313
P CNG006 Congenital Hypothyroidism 64 0.048
314
SCR001 Secretory Meningioma 40 0.048
315
ACT088 Acute Insulin Response 50 0.048
316
P CNG012 Congenital Generalized Lipodystrophy 52 0.048
317
RCK004 Rickets 66 0.048
318
c FML018 Familial Mediterranean Fever 74 0.047
319
PYR016 Pyridoxine Deficiency 39 0.047
320
CHR177 Chromophobe Renal Cell Carcinoma 54 0.046
321
CRN030 Coronary Stenosis 52 0.046
322
c MYT002 Myotonic Dystrophy 52 0.046
323
CRB009 Cerebritis 39 0.046
324
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 56 0.045
325
IRN001 Iron Deficiency Anemia 54 0.045
326
c CRB088 Cerebral Atrophy 42 0.045
327
AYM001 Ayme-Gripp Syndrome 39 0.045
328
MYT026 Myotonia Atrophica 29 0.045
329
NNT019 Neonatal Hypothyroidism 42 0.044
330
c ANL018 Analbuminemia 48 0.044
331
INT007 Intermediate Coronary Syndrome 50 0.044
332
DSM006 Desmoplastic Infantile Ganglioglioma 28 0.044
333
DBT084 Diabetes Mellitus, Ketosis-Prone 62 0.044
334
CHL147 Chlamydia Pneumonia 42 0.044
335
LNG073 Long-Chain 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 60 0.044
336
KRT002 Keratomalacia 51 0.044
337
P SCN007 Secondary Hyperparathyroidism 56 0.044
338
TXC020 Toxic Oil Syndrome 37 0.043
339
DBT008 Diabetic Angiopathy 48 0.043
340
ONC002 Onchocerciasis 54 0.043
341
c GLL020 Gallbladder Disease 64 0.042
342
c SHR001 Short Bowel Syndrome 52 0.042
343
P NMN015 Niemann-Pick Disease, Type C1 68 0.042
344
c ZLL001 Zellweger Syndrome 57 0.042
345
MTR003 Mitral Valve Stenosis 51 0.042
346
KRT008 Keratopathy 47 0.042
347
c ACT008 Actinic Keratosis 55 0.041
348
c MTC069 Mitochondrial Disorders 51 0.041
349
ATN004 Autonomic Neuropathy 46 0.040
350
MNS002 Mini Stroke 25 0.040
351
OCL069 Ocular Motor Apraxia 51 0.040
352
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 48 0.039
353
FRZ001 Frozen Shoulder 53 0.039
354
NTR046 Neutrophil Migration 56 0.038
355
LPD004 Lipoid Nephrosis 51 0.038
356
SBL008 Sea-Blue Histiocyte Disease 49 0.038
357
ACT236 Acute Motor and Sensory Axonal Neuropathy 23 0.038
358
ADL030 Adult-Onset Still's Disease 66 0.037
359
P HRD010 Hereditary Spastic Paraplegia 69 0.037
360
CRY035 Cryptorchidism, Unilateral or Bilateral 61 0.037
361
PRP017 Periapical Periodontitis 48 0.036
362
LPP002 Lipoprotein Glomerulopathy 47 0.036
363
MTC005 Mitochondrial Metabolism Disease 46 0.036
364
PRT019 Protein-Losing Enteropathy 41 0.036
365
HYP190 Hypoalphalipoproteinemia, Primary 59 0.035
366
P BRN108 Branchiootic Syndrome 1 48 0.035
367
MNN034 Mannose-Binding Lectin Deficiency 44 0.034
368
HYP264 Hypertonia 37 0.034
369
CRN239 Carnitine Deficiency, Systemic Primary 54 0.032
370
BLP005 Blepharitis 45 0.032
371
FTL021 Fetal Macrosomia 47 0.030
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