Search results for Triglycerides Group D

343 hits were found for Triglycerides Group D

# Family MCID Name MIFTS Score
1
c DBT026 Diabetes Mellitus, Noninsulin-Dependent 92 0.394
2
c DBT009 Diabetes Mellitus 67 0.393
3
c HPT021 Hepatitis 74 0.349
4
c HRT032 Heart Disease 76 0.324
5
c BRS047 Breast Cancer 100 0.311
6
c LVR013 Liver Disease 77 0.294
7
RCK004 Rickets 66 0.287
8
c MYC007 Myocardial Infarction 78 0.258
9
c CRN018 Coronary Artery Anomaly 74 0.256
10
NTR005 Nutritional Deficiency Disease 60 0.255
11
DPR016 Depression 73 0.254
12
c KDN018 Kidney Disease 71 0.254
13
c ART022 Arthritis 78 0.254
14
ART140 Arteries, Anomalies of 67 0.249
15
LPD008 Lipid Metabolism Disorder 65 0.242
16
c CRN300 Coronary Heart Disease 1 62 0.241
17
FTT001 Fatty Liver Disease 66 0.228
18
c PRS040 Prostate Cancer 93 0.225
19
ISC004 Ischemia 67 0.224
20
c OST002 Osteoporosis 74 0.219
21
c CRD246 Cardiovascular System Disease 57 0.217
22
c SCH015 Schizophrenia 73 0.215
23
c ALZ034 Alzheimer Disease 88 0.213
24
P PRS136 Prostate Cancer, Hereditary, 6 40 0.209
25
P PRS130 Prostate Cancer, Hereditary, 8 37 0.209
26
ANX010 Anxiety 73 0.208
27
c PNC044 Pancreatitis 62 0.202
28
c HYP069 Hyperparathyroidism 59 0.202
29
P BDY007 Body Mass Index Quantitative Trait Locus 1 48 0.201
30
c NNL004 Nonalcoholic Fatty Liver Disease 56 0.201
31
c LNG032 Lung Cancer 99 0.201
32
ISC006 Ischemic Heart Disease 72 0.200
33
GLC008 Glucose Metabolism Disease 54 0.194
34
P HPT001 Hepatitis C 69 0.194
35
P CHR089 Chronic Kidney Failure 73 0.193
36
VSC007 Vascular Disease 72 0.190
37
THR024 Thrombosis 64 0.189
38
ACQ007 Acquired Immunodeficiency Syndrome 66 0.189
39
HYP060 Hyperinsulinism 57 0.189
40
MNT002 Mental Depression 65 0.188
41
c MLT020 Multiple Sclerosis 76 0.188
42
GST033 Gestational Diabetes 63 0.187
43
c RHM011 Rheumatoid Arthritis 82 0.186
44
HMN014 Human Immunodeficiency Virus Infectious Disease 62 0.184
45
P HPT016 Hepatitis B 70 0.181
46
PSY004 Psychotic Disorder 74 0.179
48
DRM006 Dermatitis 69 0.176
49
DMN002 Dementia 69 0.175
50
c ENC018 Encephalopathy 65 0.174
51
OCL033 Oculocerebral Syndrome with Hypopigmentation 46 0.173
52
AGN016 Aging 63 0.171
53
c ADN016 Adenocarcinoma 71 0.169
54
ATM095 Autoimmune Disease 68 0.167
55
c DRR001 Diarrhea 58 0.162
56
GLC003 Glucose Intolerance 59 0.159
57
c LPS004 Lupus Erythematosus 69 0.158
58
c NRP001 Neuropathy 63 0.157
59
c ART021 Arteriosclerosis 61 0.156
60
P ACT027 Acute Pancreatitis 59 0.155
61
CYS001 Cystic Fibrosis 83 0.155
62
CNG034 Congestive Heart Failure 71 0.155
63
P FTT008 Fatty Liver Disease, Nonalcoholic 1 61 0.152
64
c HPT023 Hepatocellular Carcinoma 97 0.150
65
P MCR113 Microvascular Complications of Diabetes 3 58 0.149
66
P MCR120 Microvascular Complications of Diabetes 7 46 0.149
67
P MCR130 Microvascular Complications of Diabetes 6 43 0.149
68
P MCR133 Microvascular Complications of Diabetes 4 43 0.149
69
P SYS001 Systemic Lupus Erythematosus 88 0.149
70
c PLY011 Polycystic Ovary Syndrome 64 0.148
71
P SCN007 Secondary Hyperparathyroidism 56 0.148
72
c INF037 Inflammatory Bowel Disease 56 0.148
73
URN009 Urinary System Disease 59 0.146
74
c MYP004 Myopathy 65 0.145
75
P CNT035 Central Nervous System Disease 65 0.144
76
GST050 Gastrointestinal System Disease 67 0.144
77
P HPT073 Hepatitis C Virus 73 0.142
78
c INT068 Intestinal Disease 62 0.142
79
c PRD008 Periodontitis 66 0.141
80
RPD005 Rapidly Involuting Congenital Hemangioma 24 0.140
81
P ACT075 Acute Myocardial Infarction 57 0.140
82
ALL026 Allergic Hypersensitivity Disease 68 0.139
83
P PRC016 Pre-Eclampsia 61 0.138
84
P HYP595 Hypertension, Essential 77 0.138
85
SPS003 Spastic Diplegia 49 0.137
86
HYP066 Hyperglycemia 65 0.136
87
c PSR002 Psoriasis 67 0.136
88
HMN044 Human Immunodeficiency Virus Type 1 75 0.133
89
OST012 Osteoarthritis 81 0.132
90
CRH001 Crohn's Disease 79 0.132
91
SKN016 Skin Disease 68 0.130
92
c HYP086 Hypothyroidism 66 0.130
93
PRD007 Periodontal Disease 66 0.130
94
VRL011 Viral Infectious Disease 69 0.129
95
c DBT085 Diabetes Mellitus, Insulin-Dependent 73 0.128
96
c EPL164 Epilepsy 73 0.128
97
c RTN024 Retinoblastoma 73 0.128
98
CRB039 Cerebrovascular Disease 70 0.126
99
ATH013 Atherosclerosis Susceptibility 61 0.126
100
END057 Endometrial Cancer 69 0.125
101
c HYP607 Hypercholesterolemia, Familial 82 0.125
102
c MJR001 Major Depressive Disorder 67 0.125
103
c NRV007 Nervous System Disease 72 0.122
104
HYP266 Hypoxia 63 0.122
105
NNL002 Nonalcoholic Steatohepatitis 55 0.122
106
c NRB001 Neuroblastoma 73 0.121
107
P TRC078 Trichohepatoenteric Syndrome 2 35 0.120
108
ADN018 Adenoma 65 0.120
109
CYT017 Cytophagic Histiocytic Panniculitis 26 0.120
110
GST045 Gastroenteritis 65 0.119
111
MDD011 Mood Disorder 65 0.119
112
c INF032 Infertility 60 0.119
113
CLT003 Colitis 65 0.119
114
FSH001 Fish-Eye Disease 51 0.118
115
DST081 Distal Trisomy 11q 20 0.118
116
IMM136 Immune System Disease 57 0.116
117
c TRC086 Trichohepatoenteric Syndrome 1 61 0.115
118
P ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 60 0.115
119
LVR012 Liver Cirrhosis 67 0.115
120
c ABD014 Abdominal Obesity-Metabolic Syndrome 1 58 0.113
121
END030 End Stage Renal Failure 60 0.110
122
ANG054 Angina Pectoris 70 0.110
123
P SCL052 Scleroderma, Familial Progressive 68 0.109
124
BRN071 Brain Injury 54 0.109
125
c ECL001 Eclampsia 59 0.109
126
P BNM022 Bone Mineral Density Quantitative Trait Locus 8 40 0.108
127
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 46 0.108
128
STR067 Stroke, Ischemic 84 0.106
129
SPN186 Spinal Cord Injury 66 0.106
130
c CTR002 Cataract 58 0.104
131
c BPL003 Bipolar Disorder 61 0.104
132
CNT047 Contact Dermatitis 64 0.104
133
DNT012 Dental Caries 52 0.103
134
c CND004 Candidiasis 63 0.103
135
c THR014 Thrombocytopenia 65 0.103
136
NRM005 Neuromuscular Disease 61 0.102
137
c PRP019 Peripheral Nervous System Disease 66 0.102
138
c THL005 Thalassemia 65 0.101
139
P PRD040 Periodontitis, Chronic 60 0.101
140
c ATR011 Atrial Fibrillation 69 0.101
141
ANR007 Anorexia Nervosa 68 0.101
142
URM002 Uremia 53 0.101
143
THR100 Thrombocytopenic Purpura, Autoimmune 68 0.099
144
END040 Endogenous Depression 59 0.099
145
c CLC063 Celiac Disease 1 72 0.098
146
c MSC033 Muscle Disorders 56 0.098
147
IMP005 Impotence 58 0.096
148
PRM236 Primary Biliary Cholangitis 63 0.096
149
CLR108 Colorectal Adenoma 64 0.096
150
c PRM006 Primary Biliary Cirrhosis 54 0.096
151
P BLR024 Biliary Cirrhosis, Primary, 1 39 0.096
152
LPD009 Lipid Storage Disease 53 0.095
153
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 35 0.095
154
P VRL010 Viral Hepatitis 60 0.095
155
LYM019 Lymphosarcoma 59 0.094
156
DRL001 Dural Sinus Malformation 23 0.094
157
c AMY004 Amyloidosis 69 0.094
158
OVR063 Overnutrition 53 0.094
159
c ART153 Arthrochalasia Ehlers-Danlos Syndrome 22 0.094
160
c NRF023 Neurofibromatosis, Type Ii 76 0.093
161
HYP056 Hypoglycemia 64 0.093
162
THR013 Thoracic Outlet Syndrome 57 0.092
163
P THR001 Thrombocytopenia Due to Platelet Alloimmunization 61 0.092
164
ILT001 Ileitis 59 0.092
165
BRR014 Barrett Esophagus 71 0.092
166
c SLP006 Sleep Apnea 70 0.091
167
DFC004 Deficiency Anemia 65 0.091
168
THY030 Thyroid Gland Disease 51 0.090
169
c LCT001 Lactic Acidosis 53 0.089
170
PSR001 Psoriatic Arthritis 68 0.089
171
c MCR115 Microvascular Complications of Diabetes 5 71 0.089
172
MSC190 Muscular Disease 55 0.089
173
MSC004 Muscle Tissue Disease 39 0.089
174
CHL123 Chlamydia 66 0.088
175
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 37 0.088
176
PRD004 Prediabetes Syndrome 51 0.088
177
FRN020 Frontal Fibrosing Alopecia 32 0.087
178
c BDY004 Body Mass Index Quantitative Trait Locus 11 74 0.086
179
P BDY020 Body Mass Index Quantitative Trait Locus 19 43 0.086
180
P BDY019 Body Mass Index Quantitative Trait Locus 18 43 0.086
181
P BDY017 Body Mass Index Quantitative Trait Locus 14 41 0.086
182
P BDY011 Body Mass Index Quantitative Trait Locus 10 41 0.086
183
HYP080 Hypogonadism 53 0.086
184
PRP080 Peripheral Artery Disease 56 0.086
185
DMY004 Demyelinating Disease 60 0.086
186
BNG081 Benign Childhood Occipital Epilepsy, Panayiotopoulos Type 25 0.086
187
c SZR006 Seizure Disorder 61 0.085
188
PRT036 Peritonitis 67 0.085
189
CRH005 Crohn's Colitis 61 0.084
190
GND003 Gonadal Disease 49 0.083
191
ART016 Aortic Aneurysm 71 0.082
192
c TRM003 Tremor 56 0.082
193
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 65 0.082
194
c ICH004 Ichthyosis 57 0.082
195
IRN002 Iron Metabolism Disease 60 0.082
196
GT001 Gout 62 0.081
197
CHL068 Cholestasis 60 0.081
198
PRT037 Pertussis 71 0.081
199
DBT010 Diabetic Neuropathy 60 0.081
200
c CRD132 Cardiac Conduction Defect 64 0.081
201
INS024 Insulin-Like Growth Factor I 83 0.080
202
PRP027 Peripheral Vascular Disease 72 0.079
203
c DDN001 Duodenal Ulcer 52 0.079
204
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.079
205
c SHR001 Short Bowel Syndrome 52 0.078
206
HDN002 Head Injury 52 0.078
207
MRB003 Morbid Obesity 62 0.078
208
KWS001 Kwashiorkor 46 0.078
209
c VSC018 Visceral Steatosis 38 0.078
210
INT002 Intermittent Claudication 64 0.077
211
SCH012 Schizoaffective Disorder 54 0.077
212
P INF071 Inflammatory Bowel Disease 1 57 0.077
213
NTR027 Neutrophil Actin Dysfunction 32 0.076
214
P PNC106 Pancreatic Agenesis 1 52 0.076
215
TRN018 Transitional Cell Carcinoma 63 0.075
216
c OPN001 Open-Angle Glaucoma 53 0.075
217
PNC034 Pancreas Disease 60 0.075
218
SCK003 Sickle Cell Anemia 75 0.075
219
SXL003 Sexual Disorder 53 0.074
220
RTN018 Retinal Disease 58 0.073
221
P BTT014 Beta-Thalassemia 73 0.073
222
c FML018 Familial Mediterranean Fever 74 0.073
223
GRW007 Growth Hormone Deficiency 53 0.073
224
TRN015 Transient Cerebral Ischemia 59 0.072
225
BLR001 Biliary Atresia 57 0.072
226
BRN056 Bronchopulmonary Dysplasia 61 0.071
227
P ART138 Aortic Aneurysm, Familial Abdominal, 1 66 0.071
228
c GLY013 Glycogen Storage Disease 62 0.071
229
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 29 0.070
230
HYP064 Hypogonadotropism 42 0.070
231
BLM002 Bulimia Nervosa 61 0.070
232
GST092 Gastroesophageal Reflux 66 0.070
233
P INS002 in Situ Carcinoma 60 0.070
234
c DLT002 Dilated Cardiomyopathy 74 0.069
235
CYT002 Cytokine Deficiency 39 0.069
236
c MSC007 Muscle Hypertrophy 64 0.069
237
P MTR002 Mitral Valve Insufficiency 50 0.068
238
OST003 Osteonecrosis 67 0.066
239
c NMN002 Niemann-Pick Disease 50 0.066
240
P PLM164 Pulmonary Hypertension, Primary, 1 71 0.066
241
c HYP076 Hyperthyroidism 56 0.065
242
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 36 0.065
243
ADR007 Adrenoleukodystrophy 72 0.064
244
KWS002 Kawasaki Disease 72 0.064
245
P NMN015 Niemann-Pick Disease, Type C1 68 0.064
246
P PSR017 Psoriasis 2 54 0.063
247
PLM017 Pulmonary Alveolar Microlithiasis 52 0.063
248
STT004 Steatorrhea 43 0.063
249
c SLL003 Salla Disease 53 0.063
250
c HYP014 Hyperuricemia 56 0.062
251
CHL004 Cholelithiasis 52 0.062
252
LWC002 Lowe Oculocerebrorenal Syndrome 67 0.062
253
HPR003 Heparin-Induced Thrombocytopenia 49 0.062
254
P BLD140 Blood Group, I System 26 0.061
255
CRC021 Carcinosarcoma 62 0.060
256
ALL010 Allergic Contact Dermatitis 61 0.060
257
BRN080 Brain Ischemia 43 0.060
258
TRP004 Tropical Sprue 36 0.058
259
P ATR087 Atrial Standstill 1 69 0.058
260
IRN001 Iron Deficiency Anemia 54 0.057
261
c PTY003 Pityriasis Rubra Pilaris 52 0.057
262
KRT009 Keratosis 55 0.057
263
OBS082 Obstructive Nephropathy 52 0.056
264
PNC041 Pancreatic Ductal Adenocarcinoma 54 0.056
265
BLR008 Bilirubin Metabolic Disorder 53 0.056
266
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.056
267
HYP730 Hypogonadotropic Hypogonadism 58 0.056
268
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 60 0.056
269
P PSR028 Psoriasis 7 43 0.055
270
P PSR032 Psoriasis 11 43 0.055
271
P PSR018 Psoriasis 13 42 0.055
272
WRN001 Werner Syndrome 74 0.055
273
HPT019 Hepatic Encephalopathy 60 0.055
274
WTH001 Withdrawal Disorder 51 0.054
275
ALC009 Alcoholic Liver Cirrhosis 52 0.054
276
CRC034 Carcinoma Showing Thymus-Like Differentiation 29 0.054
277
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 48 0.052
278
RTN017 Retinal Detachment 62 0.052
279
c ZLL001 Zellweger Syndrome 57 0.052
280
LSH001 Leishmaniasis 72 0.052
281
c SHR029 Short Syndrome 57 0.052
282
c MYT002 Myotonic Dystrophy 52 0.052
283
ACT088 Acute Insulin Response 50 0.052
284
BLR006 Biliary Tract Disease 53 0.051
285
MYC088 Mycobacterium Avium Complex Infections 34 0.051
286
MYT026 Myotonia Atrophica 29 0.051
287
CRN167 Caronte 19 0.051
288
PRP016 Paraplegia 55 0.051
289
DBT084 Diabetes Mellitus, Ketosis-Prone 62 0.050
290
HPT004 Hepatic Coma 45 0.050
291
INS001 Insulinoma 66 0.050
292
P CNG006 Congenital Hypothyroidism 64 0.050
293
AND005 Androgen Insensitivity Syndrome, Mild 19 0.050
294
c ACT008 Actinic Keratosis 55 0.050
295
KRT002 Keratomalacia 51 0.050
296
CRN030 Coronary Stenosis 52 0.049
297
c LYM025 Lymphedema 55 0.049
298
c CMP008 Compartment Syndrome 52 0.049
299
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 44 0.049
300
PHT003 Phototoxic Dermatitis 44 0.049
301
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 56 0.048
302
NNT019 Neonatal Hypothyroidism 42 0.048
303
HMS001 Hemosiderosis 52 0.048
304
MNS002 Mini Stroke 25 0.047
305
P TYP024 Type Ii Mixed Cryoglobulinemia 40 0.047
306
c CRB088 Cerebral Atrophy 42 0.047
307
INT007 Intermediate Coronary Syndrome 50 0.047
308
P GLL024 Gallbladder Disease 1 45 0.046
309
LNG073 Long-Chain 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 60 0.046
310
MTR003 Mitral Valve Stenosis 51 0.046
311
FXF002 Fox-Fordyce Disease 41 0.046
312
c HYP061 Hypertrophic Cardiomyopathy 59 0.046
313
DSM006 Desmoplastic Infantile Ganglioglioma 28 0.045
314
ACT236 Acute Motor and Sensory Axonal Neuropathy 23 0.045
315
ATN004 Autonomic Neuropathy 46 0.045
316
c PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 70 0.044
317
CRY035 Cryptorchidism, Unilateral or Bilateral 61 0.044
318
MTB007 Metabolic Encephalomyopathic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 53 0.044
319
DBT008 Diabetic Angiopathy 48 0.044
320
CHR177 Chromophobe Renal Cell Carcinoma 54 0.043
321
OCL069 Ocular Motor Apraxia 51 0.043
322
FTL021 Fetal Macrosomia 47 0.042
323
CHL147 Chlamydia Pneumonia 42 0.041
324
PRT019 Protein-Losing Enteropathy 41 0.041
325
c MTC069 Mitochondrial Disorders 51 0.041
326
CHL013 Cholecystolithiasis 37 0.041
327
SPN021 Spinal Meningioma 50 0.041
328
SCR001 Secretory Meningioma 40 0.041
329
DRM009 Dermatomycosis 36 0.041
330
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 48 0.040
331
c ANL018 Analbuminemia 48 0.040
332
CHL067 Cholecystitis 59 0.040
333
LPD004 Lipoid Nephrosis 51 0.039
334
KRT008 Keratopathy 47 0.039
335
MTC005 Mitochondrial Metabolism Disease 46 0.039
336
VSC003 Visceral Leishmaniasis 61 0.039
337
P MNN043 Meningioma, Familial 63 0.038
338
c GLL020 Gallbladder Disease 64 0.036
339
PYR016 Pyridoxine Deficiency 39 0.036
340
HYP264 Hypertonia 37 0.035
341
NTR046 Neutrophil Migration 56 0.034
342
BLP005 Blepharitis 45 0.034
343
P BRN108 Branchiootic Syndrome 1 48 0.032
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