Search results for Triglycerides Group B

214 hits were found for Triglycerides Group B

# Family MCID Name MIFTS Score
1
P HPT021 Hepatitis 76 0.798
2
c HPT016 Hepatitis B 67 0.555
3
P LVR013 Liver Disease 75 0.336
4
AGN016 Aging 64 0.329
5
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 91 0.311
6
P DBT009 Diabetes Mellitus 64 0.299
7
P PNC044 Pancreatitis 64 0.288
8
END072 Endotheliitis 45 0.270
9
P BRS047 Breast Cancer 100 0.253
10
VRL011 Viral Infectious Disease 63 0.252
11
P HRT032 Heart Disease 74 0.252
12
ACQ007 Acquired Immunodeficiency Syndrome 63 0.237
13
c HPT001 Hepatitis C 71 0.235
14
P CRN018 Coronary Artery Anomaly 68 0.233
15
LYM019 Lymphosarcoma 55 0.233
16
TYP041 Type I 56 0.233
17
ART140 Arteries, Anomalies of 65 0.229
18
P ART022 Arthritis 76 0.222
19
LPD008 Lipid Metabolism Disorder 58 0.221
20
P LNG032 Lung Cancer 98 0.221
21
c CRN300 Coronary Heart Disease 1 64 0.211
22
P MYC007 Myocardial Infarction 79 0.203
23
ISC004 Ischemia 65 0.198
24
c HPT073 Hepatitis C Virus 72 0.186
25
IMM136 Immune System Disease 56 0.183
26
P RHM011 Rheumatoid Arthritis 80 0.181
27
P ENC018 Encephalopathy 62 0.180
28
P ALZ034 Alzheimer Disease 87 0.179
29
DPR016 Depression 72 0.174
30
GLC008 Glucose Metabolism Disease 52 0.173
31
P KDN018 Kidney Disease 68 0.171
32
P ADN016 Adenocarcinoma 70 0.167
33
ANX010 Anxiety 72 0.166
34
c CNT035 Central Nervous System Disease 63 0.165
35
P LPS004 Lupus Erythematosus 68 0.162
36
c SYS001 Systemic Lupus Erythematosus 86 0.158
37
ISC006 Ischemic Heart Disease 72 0.156
38
DMN002 Dementia 68 0.156
39
OCL033 Oculocerebral Syndrome with Hypopigmentation 45 0.155
40
FTT001 Fatty Liver Disease 60 0.155
41
VSC007 Vascular Disease 68 0.153
42
ATM095 Autoimmune Disease 64 0.153
43
P THY032 Thyroiditis 55 0.153
44
P SCH015 Schizophrenia 69 0.146
45
CYS001 Cystic Fibrosis 84 0.144
46
NRN002 Neuronitis 41 0.142
47
P MYP004 Myopathy 68 0.139
48
P MLT020 Multiple Sclerosis 78 0.137
49
SPS003 Spastic Diplegia 54 0.135
50
THR024 Thrombosis 61 0.135
51
GST050 Gastrointestinal System Disease 64 0.134
52
HMN044 Human Immunodeficiency Virus Type 1 70 0.134
53
P NRP001 Neuropathy 63 0.134
54
P ART021 Arteriosclerosis 60 0.133
55
MNT002 Mental Depression 57 0.132
56
P HYP607 Hypercholesterolemia, Familial 79 0.132
57
c TRC078 Trichohepatoenteric Syndrome 2 34 0.132
58
P PNM007 Pneumonia 69 0.131
59
c CHR089 Chronic Kidney Failure 72 0.131
60
HYP266 Hypoxia 61 0.130
61
PSY004 Psychotic Disorder 71 0.129
62
P DRR001 Diarrhea 56 0.127
63
CNG034 Congestive Heart Failure 72 0.126
64
RTN023 Retinitis 50 0.126
65
P ESP024 Esophagitis 63 0.121
66
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 59 0.121
67
CRB009 Cerebritis 41 0.121
68
P NRV007 Nervous System Disease 73 0.119
69
URN009 Urinary System Disease 55 0.117
70
P NNL004 Nonalcoholic Fatty Liver Disease 51 0.116
71
ANR040 Aneurysm 60 0.115
72
c FTT008 Fatty Liver Disease, Nonalcoholic 1 39 0.113
73
P INF032 Infertility 59 0.111
74
HYP060 Hyperinsulinism 56 0.111
75
P INT068 Intestinal Disease 64 0.109
76
P PRD008 Periodontitis 66 0.108
77
c ACT027 Acute Pancreatitis 60 0.108
78
OST012 Osteoarthritis 82 0.108
79
P NMN002 Niemann-Pick Disease 60 0.107
80
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 21 0.106
81
CLT003 Colitis 62 0.105
82
LPD009 Lipid Storage Disease 51 0.105
83
P OST002 Osteoporosis 76 0.105
84
HYP066 Hyperglycemia 63 0.104
85
P HYP086 Hypothyroidism 64 0.104
86
GLC003 Glucose Intolerance 56 0.102
87
c HYP595 Hypertension, Essential 76 0.102
88
NRM005 Neuromuscular Disease 60 0.100
89
P EPL164 Epilepsy 69 0.100
90
BDY007 Body Mass Index Quantitative Trait Locus 1 26 0.099
91
P INF037 Inflammatory Bowel Disease 53 0.099
92
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 59 0.099
93
CRH001 Crohn's Disease 78 0.097
94
P ATR011 Atrial Fibrillation 68 0.093
95
NNL002 Nonalcoholic Steatohepatitis 50 0.092
96
CRB039 Cerebrovascular Disease 67 0.092
97
P AMY004 Amyloidosis 68 0.090
98
GST045 Gastroenteritis 64 0.089
99
GST033 Gestational Diabetes 60 0.088
100
ADN018 Adenoma 63 0.087
101
END030 End Stage Renal Failure 56 0.084
102
P CLC063 Celiac Disease 1 71 0.084
103
P DBT085 Diabetes Mellitus, Insulin-Dependent 65 0.084
104
c SCL052 Scleroderma, Familial Progressive 64 0.083
105
c MCR113 Microvascular Complications of Diabetes 3 52 0.083
106
c MCR130 Microvascular Complications of Diabetes 6 40 0.083
107
c MCR120 Microvascular Complications of Diabetes 7 37 0.083
108
c MCR133 Microvascular Complications of Diabetes 4 35 0.083
109
STR067 Stroke, Ischemic 82 0.083
110
BRN106 Burns 56 0.083
111
ANG054 Angina Pectoris 66 0.082
112
OVR063 Overnutrition 53 0.082
113
THY030 Thyroid Gland Disease 51 0.081
114
BRN071 Brain Injury 53 0.078
115
PLC008 Placenta Disease 61 0.077
116
PRM236 Primary Biliary Cholangitis 55 0.077
117
P PRM006 Primary Biliary Cirrhosis 53 0.077
118
HYP056 Hypoglycemia 62 0.076
119
P CTR002 Cataract 60 0.076
120
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 55 0.076
121
c BLR024 Biliary Cirrhosis, Primary, 1 36 0.076
122
GT001 Gout 57 0.076
123
MSC004 Muscle Tissue Disease 39 0.075
124
LPD013 Lipidosis with Triglycerid Storage Disease 4 0.075
125
DDN006 Duodenitis 48 0.074
126
ART016 Aortic Aneurysm 69 0.074
127
P MSC033 Muscle Disorders 52 0.074
128
DNT012 Dental Caries 51 0.073
129
PRP080 Peripheral Artery Disease 53 0.072
130
SPS057 Spasticity 41 0.072
131
DMY004 Demyelinating Disease 57 0.071
132
P TRM003 Tremor 54 0.071
133
THR100 Thrombocytopenic Purpura, Autoimmune 62 0.071
134
PRD004 Prediabetes Syndrome 45 0.071
135
INS024 Insulin-Like Growth Factor I 82 0.071
136
BRC012 Brucellosis 70 0.071
137
c BLD140 Blood Group, I System 23 0.070
138
DBT010 Diabetic Neuropathy 59 0.070
139
PNC041 Pancreatic Ductal Adenocarcinoma 52 0.070
140
CHL068 Cholestasis 60 0.069
141
KWS001 Kwashiorkor 42 0.069
142
P VSC018 Visceral Steatosis 37 0.068
143
P ICH004 Ichthyosis 54 0.068
144
PNC034 Pancreas Disease 57 0.067
145
ILT001 Ileitis 56 0.066
146
P SZR006 Seizure Disorder 56 0.066
147
GND003 Gonadal Disease 46 0.066
148
PRP027 Peripheral Vascular Disease 70 0.066
149
STT004 Steatorrhea 41 0.066
150
CHL123 Chlamydia 64 0.066
151
PSR001 Psoriatic Arthritis 65 0.066
152
HYP080 Hypogonadism 51 0.064
153
P DLT002 Dilated Cardiomyopathy 76 0.064
154
PRD007 Periodontal Disease 64 0.064
155
P GLY013 Glycogen Storage Disease 61 0.064
156
CLR108 Colorectal Adenoma 60 0.063
157
c ART138 Aortic Aneurysm, Familial Abdominal, 1 64 0.062
158
P PLY011 Polycystic Ovary Syndrome 63 0.061
159
BRN080 Brain Ischemia 44 0.061
160
ABD017 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 48 0.061
161
SCK003 Sickle Cell Anemia 72 0.061
162
SCH012 Schizoaffective Disorder 54 0.060
163
P LYM124 Lymphangiectasia, Intestinal 34 0.059
164
c PRM158 Primary Intestinal Lymphangiectasia 31 0.059
165
PRP016 Paraplegia 53 0.058
166
TRN015 Transient Cerebral Ischemia 56 0.058
167
ADR007 Adrenoleukodystrophy 71 0.057
168
HDN002 Head Injury 47 0.057
169
URM002 Uremia 52 0.056
170
TRP004 Tropical Sprue 37 0.056
171
HYP064 Hypogonadotropism 40 0.056
172
c INF071 Inflammatory Bowel Disease 1 53 0.055
173
CHR177 Chromophobe Renal Cell Carcinoma 55 0.055
174
HYP730 Hypogonadotropic Hypogonadism 56 0.054
175
HMS001 Hemosiderosis 51 0.053
176
IMP005 Impotence 55 0.052
177
CHL067 Cholecystitis 57 0.052
178
c MTR002 Mitral Valve Insufficiency 46 0.052
179
P INT001 Intrahepatic Cholestasis 60 0.052
180
DBT008 Diabetic Angiopathy 47 0.051
181
P DDN001 Duodenal Ulcer 52 0.051
182
P CRB088 Cerebral Atrophy 39 0.051
183
P HYP076 Hyperthyroidism 56 0.051
184
BLR006 Biliary Tract Disease 54 0.051
185
KRT009 Keratosis 53 0.050
186
P HYP061 Hypertrophic Cardiomyopathy 64 0.050
187
P CRD132 Cardiac Conduction Defect 59 0.050
188
WRN001 Werner Syndrome 69 0.049
189
INT007 Intermediate Coronary Syndrome 52 0.049
190
TXC020 Toxic Oil Syndrome 36 0.049
191
P HYP014 Hyperuricemia 55 0.049
192
GNG011 Gingival Disease 49 0.049
193
P ZLL001 Zellweger Syndrome 56 0.048
194
CHL004 Cholelithiasis 50 0.047
195
P GLL020 Gallbladder Disease 64 0.046
196
P PTY003 Pityriasis Rubra Pilaris 50 0.046
197
RYS001 Reye Syndrome 49 0.046
198
c NMN015 Niemann-Pick Disease, Type C1 68 0.044
199
P FML018 Familial Mediterranean Fever 73 0.044
200
CRC034 Carcinoma Showing Thymus-Like Differentiation 23 0.044
201
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 59 0.043
202
P ACT008 Actinic Keratosis 54 0.043
203
INT002 Intermittent Claudication 61 0.043
204
MNS002 Mini Stroke 23 0.043
205
LPT001 Leptospirosis 64 0.042
206
ADL030 Adult-Onset Still's Disease 64 0.041
207
ONC002 Onchocerciasis 52 0.041
208
ATN004 Autonomic Neuropathy 46 0.038
209
BLP005 Blepharitis 43 0.037
210
HYP190 Hypoalphalipoproteinemia, Primary 58 0.036
211
SBL008 Sea-Blue Histiocyte Disease 41 0.036
212
END040 Endogenous Depression 50 0.034
213
FTL021 Fetal Macrosomia 46 0.034
214
RTN021 Retinal Vascular Occlusion 43 0.034
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