Search results for Triglycerides Group B

660 hits were found for Triglycerides Group B

# Family MCID Name MIFTS Score
1
c HPT016 Hepatitis B 63 0.968
2
P HPT021 Hepatitis 69 0.579
3
P LYM031 Lymphocytic Leukemia 56 0.576
4
P HYP750 Hypertriglyceridemia, Familial 62 0.571
5
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.571
6
P LVR013 Liver Disease 71 0.461
7
P CRN300 Coronary Heart Disease 1 59 0.426
8
LPD008 Lipid Metabolism Disorder 64 0.406
9
FTT001 Fatty Liver Disease 63 0.403
10
48X005 48,xyyy 37 0.402
11
P LKM062 Leukemia, Acute Lymphoblastic 68 0.400
12
LVR012 Liver Cirrhosis 67 0.368
13
c HYP836 Hypercholesterolemia, Familial, 1 74 0.359
14
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 91 0.348
15
P CRN018 Coronary Artery Anomaly 67 0.342
16
P NTR004 Neutropenia 64 0.338
17
P HRT032 Heart Disease 78 0.334
18
P HYP724 Hyperlipoproteinemia, Type Iii 74 0.333
19
c VRL010 Viral Hepatitis 56 0.329
20
P DBT009 Diabetes Mellitus 66 0.329
21
LYM133 Lymphoma, Hodgkin, Classic 70 0.329
22
c HPT073 Hepatitis C Virus 74 0.325
23
ATH013 Atherosclerosis Susceptibility 68 0.324
24
P HPT023 Hepatocellular Carcinoma 99 0.320
25
ART140 Arteries, Anomalies of 60 0.313
26
ATM095 Autoimmune Disease 62 0.312
27
HMN044 Human Immunodeficiency Virus Type 1 73 0.304
28
c HPT003 Hepatitis a 60 0.296
29
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.295
30
LYM143 Lymphoma, Non-Hodgkin, Familial 74 0.295
31
P KDN018 Kidney Disease 73 0.292
32
P FTT008 Fatty Liver Disease, Nonalcoholic 1 58 0.292
33
c HPT001 Hepatitis C 62 0.290
34
c BDY007 Body Mass Index Quantitative Trait Locus 1 43 0.281
35
P VSC007 Vascular Disease 65 0.272
36
P BDY004 Body Mass Index Quantitative Trait Locus 11 78 0.271
37
P DRR001 Diarrhea 55 0.265
38
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 67 0.262
39
IMM167 Immune Deficiency Disease 79 0.256
40
ISC004 Ischemia 62 0.250
41
LYM019 Lymphosarcoma 48 0.247
42
DWN001 Down Syndrome 70 0.244
43
ACQ007 Acquired Immunodeficiency Syndrome 61 0.242
44
c SYS001 Systemic Lupus Erythematosus 88 0.241
45
PRT037 Pertussis 66 0.240
46
HYP066 Hyperglycemia 63 0.239
47
CNG034 Congestive Heart Failure 69 0.239
48
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 82 0.238
49
TXC005 Toxic Shock Syndrome 63 0.235
50
HYP060 Hyperinsulinism 55 0.235
51
c HYP595 Hypertension, Essential 87 0.232
52
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.232
53
c BDY021 Body Mass Index Quantitative Trait Locus 20 50 0.232
54
c BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.232
55
c BDY010 Body Mass Index Quantitative Trait Locus 4 48 0.232
56
c BDY015 Body Mass Index Quantitative Trait Locus 12 48 0.232
57
c BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.232
58
c BDY011 Body Mass Index Quantitative Trait Locus 10 47 0.232
59
c BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.232
60
c BDY006 Body Mass Index Quantitative Trait Locus 8 45 0.232
61
c BDY012 Body Mass Index Quantitative Trait Locus 7 45 0.232
62
P MYC007 Myocardial Infarction 74 0.224
63
ADL002 Adult Syndrome 62 0.223
64
CHL014 Cholera 58 0.222
65
DPH001 Diphtheria 61 0.220
66
CRB039 Cerebrovascular Disease 71 0.219
67
47X002 47,xyy 49 0.218
68
c CHR684 Chronic Kidney Disease 68 0.216
69
HYP056 Hypoglycemia 68 0.216
70
CYT002 Cytokine Deficiency 46 0.214
71
P LNG032 Lung Cancer 99 0.214
72
P LPS004 Lupus Erythematosus 62 0.212
73
P CLR023 Colorectal Cancer 100 0.212
74
P PSR002 Psoriasis 63 0.211
75
P ALZ034 Alzheimer Disease 90 0.211
76
PST011 Pustulosis of Palm and Sole 51 0.211
77
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 61 0.209
78
ALL026 Allergic Hypersensitivity Disease 65 0.209
79
P DBT085 Diabetes Mellitus, Insulin-Dependent 68 0.207
80
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 0.205
81
P BRS047 Breast Cancer 99 0.204
82
HLX001 Helix Syndrome 46 0.203
83
DPR016 Depression 64 0.203
84
P ENC004 Encephalitis 64 0.203
85
END030 End Stage Renal Failure 60 0.202
86
c ACT027 Acute Pancreatitis 60 0.202
87
P RHM011 Rheumatoid Arthritis 82 0.200
88
c ACT075 Acute Myocardial Infarction 59 0.199
89
P TRN020 Turner Syndrome 66 0.196
90
P NRP001 Neuropathy 57 0.196
91
HMN014 Human Immunodeficiency Virus Infectious Disease 56 0.196
92
P OVR042 Ovarian Cancer 89 0.196
93
CYS001 Cystic Fibrosis 84 0.195
94
c RHB024 Rhabdomyosarcoma 2 64 0.194
95
HMT018 Hematopoietic Stem Cell Transplantation 54 0.194
96
P GRF003 Graft-Versus-Host Disease 71 0.193
97
GLC003 Glucose Intolerance 55 0.191
98
P HYP086 Hypothyroidism 70 0.190
99
P THR014 Thrombocytopenia 67 0.189
100
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.189
101
P PNC044 Pancreatitis 61 0.189
102
c FML021 Familial Hypercholesterolemia 67 0.187
103
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.187
104
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 0.186
105
DRM006 Dermatitis 63 0.185
106
NNL006 Non-Alcoholic Steatohepatitis 53 0.184
107
MNT002 Mental Depression 60 0.184
108
P ADN016 Adenocarcinoma 65 0.182
109
P NRB010 Neuroblastoma 1 66 0.181
110
P ART022 Arthritis 71 0.181
111
P MLT020 Multiple Sclerosis 73 0.181
112
P PRS040 Prostate Cancer 97 0.181
113
ANG054 Angina Pectoris 66 0.180
114
P MYP004 Myopathy 63 0.180
115
ANX010 Anxiety 75 0.179
116
BCT022 Bacterial Infectious Disease 57 0.177
117
DFC004 Deficiency Anemia 77 0.175
118
CRH001 Crohn's Disease 75 0.175
119
SPL018 Splenomegaly 48 0.173
120
P INF037 Inflammatory Bowel Disease 57 0.173
121
HYP081 Hypolipoproteinemia 51 0.172
122
ABT001 Abetalipoproteinemia 68 0.171
123
P END033 Endocarditis 58 0.170
124
ALC007 Alcohol Dependence 68 0.170
125
c PRC016 Pre-Eclampsia 63 0.170
126
STR067 Stroke, Ischemic 82 0.169
127
P PRD008 Periodontitis 66 0.169
128
INT007 Intermediate Coronary Syndrome 58 0.169
129
P RSP003 Respiratory Failure 75 0.168
130
P CND004 Candidiasis 61 0.168
131
c HNT004 Huntington Disease-Like 2 48 0.167
132
P NPH012 Nephrotic Syndrome 65 0.165
133
GST033 Gestational Diabetes 58 0.162
134
P BLD134 Bladder Cancer 79 0.161
135
P SCH015 Schizophrenia 76 0.160
136
PLM017 Pulmonary Alveolar Microlithiasis 54 0.160
137
LSH001 Leishmaniasis 64 0.160
138
P KLZ004 Kala-Azar 1 43 0.160
139
P ART021 Arteriosclerosis 56 0.159
140
P SZR006 Seizure Disorder 59 0.158
141
P GST053 Gastric Cancer 85 0.158
142
SRC014 Sarcoma 67 0.158
143
c FML035 Familial Hyperlipidemia 56 0.158
144
PRT036 Peritonitis 66 0.157
145
SPN035 Spindle Cell Sarcoma 57 0.157
146
c HNT011 Huntington Disease-Like 3 37 0.157
147
P RHN004 Rhinitis 59 0.157
148
OST012 Osteoarthritis 80 0.156
149
P NRF023 Neurofibromatosis, Type Ii 77 0.154
150
P OST002 Osteoporosis 79 0.154
151
ATX019 Ataxia with Vitamin E Deficiency 46 0.153
152
P PNM007 Pneumonia 71 0.153
153
ADN018 Adenoma 60 0.152
154
GST045 Gastroenteritis 60 0.152
155
c SPN225 Spondyloarthropathy 1 74 0.150
156
P EPL164 Epilepsy 73 0.150
157
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 51 0.150
158
P PRP019 Peripheral Nervous System Disease 64 0.150
159
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 43 0.150
160
P MCR115 Microvascular Complications of Diabetes 5 67 0.149
161
P ASP006 Aspergillosis 67 0.149
162
SKN016 Skin Disease 64 0.149
163
c ATR087 Atrial Standstill 1 76 0.148
164
P PRS038 Personality Disorder 66 0.148
165
c MCR113 Microvascular Complications of Diabetes 3 55 0.148
166
CHL123 Chlamydia 60 0.148
167
c MCR120 Microvascular Complications of Diabetes 7 48 0.147
168
P ALC033 Alcohol Use Disorder 58 0.147
169
P SKN015 Skin Carcinoma 67 0.147
170
c ACT071 Acute Kidney Failure 60 0.147
171
CHL068 Cholestasis 61 0.147
172
GLB002 Glioblastoma 74 0.147
173
c HYP555 Hypertriglyceridemia, Transient Infantile 38 0.147
174
P ENC018 Encephalopathy 64 0.147
175
PRP027 Peripheral Vascular Disease 72 0.147
176
c MCR130 Microvascular Complications of Diabetes 6 42 0.146
177
c MCR133 Microvascular Complications of Diabetes 4 42 0.146
178
GLB015 Glioblastoma Multiforme 60 0.146
179
END057 Endometrial Cancer 74 0.146
180
VSL002 Visual Epilepsy 58 0.145
181
P MJR001 Major Depressive Disorder 69 0.145
182
HYP266 Hypoxia 58 0.145
183
AGN016 Aging 58 0.145
184
LYM027 Lymphopenia 58 0.144
185
P ALP008 Alopecia 58 0.143
186
TRD008 Triiodothyronine Receptor Auxiliary Protein 35 0.143
187
P DRM053 Dermatitis, Atopic 68 0.143
188
CLT003 Colitis 63 0.143
189
NTR005 Nutritional Deficiency Disease 61 0.143
190
PRP030 Purpura 56 0.142
191
ULC004 Ulcerative Colitis 75 0.142
192
c ACT210 Acute Respiratory Distress Syndrome 59 0.142
193
c SCL052 Scleroderma, Familial Progressive 62 0.140
194
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.140
195
P THL005 Thalassemia 62 0.138
196
CNS004 Constipation 59 0.138
197
ATS010 Autosomal Recessive Disease 49 0.138
198
P HYP838 Hyperlipidemia, Familial Combined, 3 54 0.137
199
OCL069 Ocular Motor Apraxia 53 0.136
200
P INF032 Infertility 60 0.134
201
CHL079 Children's Interstitial Lung Disease 27 0.134
202
P GST044 Gastritis 58 0.134
203
P BPL003 Bipolar Disorder 59 0.133
204
c ACT068 Acute Cystitis 63 0.133
205
SPN051 Spondylitis 53 0.133
206
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.133
207
P DMN002 Dementia 68 0.133
208
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 62 0.133
209
OST017 Osteomyelitis 65 0.132
210
THY029 Thyroid Carcinoma 62 0.132
211
INF009 Inflammatory Spondylopathy 29 0.132
212
c MJR024 Major Affective Disorder 9 42 0.132
213
c MJR022 Major Affective Disorder 8 39 0.132
214
P AGM001 Agammaglobulinemia 66 0.131
215
IRN002 Iron Metabolism Disease 58 0.129
216
ANR007 Anorexia Nervosa 64 0.129
217
c HYP272 Hypercholesterolemia, Familial, 3 44 0.129
218
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 65 0.128
219
BRN071 Brain Injury 51 0.128
220
P CTR002 Cataract 62 0.127
221
END040 Endogenous Depression 55 0.127
222
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.127
223
c THR092 Thrombophilia Due to Thrombin Defect 74 0.126
224
P CLC063 Celiac Disease 1 66 0.125
225
PLM001 Pulmonary Tuberculosis 72 0.125
226
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 62 0.125
227
VSC003 Visceral Leishmaniasis 55 0.124
228
THR024 Thrombosis 58 0.124
229
c AMY091 Amyotrophic Lateral Sclerosis 1 88 0.123
230
BNR002 Bone Resorption Disease 51 0.121
231
P PLY011 Polycystic Ovary Syndrome 58 0.121
232
c DLT002 Dilated Cardiomyopathy 81 0.121
233
HPT022 Hepatoblastoma 58 0.121
234
SPN186 Spinal Cord Injury 63 0.120
235
P ESP024 Esophagitis 62 0.120
236
ART016 Aortic Aneurysm 71 0.120
237
INS024 Insulin-Like Growth Factor I 79 0.120
238
RLP002 Relapsing-Remitting Multiple Sclerosis 57 0.120
239
P CRD119 Cardiac Arrest 71 0.118
240
IDP011 Idiopathic Interstitial Pneumonia 65 0.118
241
P PLM036 Pulmonary Fibrosis 66 0.118
242
CNT047 Contact Dermatitis 58 0.117
243
P HYP076 Hyperthyroidism 55 0.117
244
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 41 0.116
245
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 48 0.116
246
ANR040 Aneurysm 60 0.115
247
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.115
249
P SLP006 Sleep Apnea 71 0.115
250
PLM033 Pulmonary Embolism 60 0.114
251
URM002 Uremia 50 0.114
252
ETN001 Eating Disorder 61 0.114
253
TRM010 Traumatic Brain Injury 54 0.114
254
P AST007 Astrocytoma 52 0.114
255
DNT012 Dental Caries 52 0.114
256
P SYS005 Systemic Scleroderma 68 0.113
257
P NMN002 Niemann-Pick Disease 60 0.113
258
HMC014 Homocysteinemia 54 0.112
259
HYP014 Hyperuricemia 52 0.112
260
P RCT021 Rectum Cancer 54 0.112
261
P DDN001 Duodenal Ulcer 50 0.112
262
P APL001 Aplastic Anemia 76 0.111
263
INT323 Intraocular Pressure Quantitative Trait Locus 64 0.111
264
HRW001 Hair Whorl 36 0.111
265
ESP021 Esophageal Cancer 90 0.111
266
PSR001 Psoriatic Arthritis 63 0.110
267
STT004 Steatorrhea 39 0.110
268
P INS002 in Situ Carcinoma 55 0.110
269
MST005 Mastitis 55 0.109
270
P LTR001 Lateral Sclerosis 56 0.109
271
DYS073 Dysphagia 52 0.109
272
PPT005 Peptic Ulcer Disease 60 0.109
273
PRP016 Paraplegia 54 0.108
274
PRM236 Primary Biliary Cholangitis 57 0.107
275
c GLL024 Gallbladder Disease 1 53 0.107
276
GST092 Gastroesophageal Reflux 68 0.107
277
MDD011 Mood Disorder 62 0.107
278
PSY004 Psychotic Disorder 68 0.106
279
P THY023 Thymoma 64 0.106
280
c THY107 Thymoma, Familial 55 0.106
281
P ATR011 Atrial Fibrillation 67 0.105
282
ACN002 Acanthosis Nigricans 62 0.105
283
P PRM006 Primary Biliary Cirrhosis 54 0.105
284
P ATT013 Attention Deficit-Hyperactivity Disorder 66 0.105
286
P AMY004 Amyloidosis 71 0.104
287
P PLY019 Polyneuropathy 55 0.104
288
CHL004 Cholelithiasis 50 0.103
289
GT001 Gout 63 0.103
290
TRN015 Transient Cerebral Ischemia 62 0.103
291
P TRC086 Trichohepatoenteric Syndrome 1 57 0.103
292
CYT008 Cytomegalovirus Infection 58 0.103
293
P ECL001 Eclampsia 53 0.103
294
c INV001 Invasive Aspergillosis 48 0.101
295
CHL065 Cholangiocarcinoma 68 0.101
296
THR013 Thoracic Outlet Syndrome 49 0.101
297
HYP080 Hypogonadism 51 0.100
298
CRN030 Coronary Stenosis 49 0.100
299
P CRD132 Cardiac Conduction Defect 61 0.100
300
HYP064 Hypogonadotropism 40 0.100
301
c BRN108 Branchiootic Syndrome 1 62 0.100
302
IMP005 Impotence 53 0.100
303
DBT010 Diabetic Neuropathy 56 0.099
304
HPT004 Hepatic Coma 42 0.099
305
INT079 Intrahepatic Cholangiocarcinoma 54 0.099
306
VRC005 Varicose Veins 61 0.098
307
RTN017 Retinal Detachment 62 0.098
308
P THY032 Thyroiditis 52 0.098
309
P MYS005 Myositis 54 0.098
310
P SCK005 Sickle Cell Disease 53 0.098
311
DYS015 Dysentery 45 0.098
312
P URT039 Urticaria 61 0.098
313
CRY005 Cryptococcosis 51 0.097
314
PST092 Posttransplant Acute Limbic Encephalitis 29 0.097
315
c PLM164 Pulmonary Hypertension, Primary, 1 79 0.097
316
c ATM011 Autoimmune Hepatitis 63 0.097
317
HMZ003 Homozygous Familial Hypercholesterolemia 48 0.097
318
RHM028 Rheumatic Heart Disease 54 0.096
319
ACT119 Acute Promyelocytic Leukemia 63 0.096
320
c MCR129 Microvascular Complications of Diabetes 1 67 0.096
321
HPT019 Hepatic Encephalopathy 60 0.096
322
HMS001 Hemosiderosis 54 0.096
323
c ART138 Aortic Aneurysm, Familial Abdominal, 1 62 0.095
324
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 63 0.095
325
EYD002 Eye Disease 59 0.094
326
ORL005 Oral Candidiasis 56 0.094
327
TRN018 Transitional Cell Carcinoma 57 0.094
328
PRT013 Portal Hypertension 61 0.094
329
P KDN017 Kidney Cancer 60 0.094
330
LPD009 Lipid Storage Disease 49 0.094
331
P NRV007 Nervous System Disease 68 0.094
332
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 56 0.093
333
INS001 Insulinoma 60 0.093
334
P TRM003 Tremor 55 0.093
335
P LCT001 Lactic Acidosis 52 0.093
336
RCK004 Rickets 70 0.093
337
BLR008 Bilirubin Metabolic Disorder 58 0.093
338
PLY150 Polykaryocytosis Inducer 31 0.093
339
CRT013 Carotid Stenosis 50 0.093
340
DYS014 Dyspepsia 51 0.093
341
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 54 0.093
342
P LNG064 Lung Cancer Susceptibility 3 79 0.093
343
P HYD006 Hydrocephalus 68 0.092
344
EXC002 Exocrine Pancreatic Insufficiency 41 0.092
345
P OPN001 Open-Angle Glaucoma 50 0.092
346
c CNG216 Congenital Hydrocephalus 55 0.092
347
LPT014 Leptin Deficiency or Dysfunction 72 0.092
348
CLN015 Colon Adenocarcinoma 65 0.092
349
IMM064 Immunodeficiency, Common Variable, 10 51 0.091
350
ENT011 Enterocolitis 51 0.091
351
P RRH023 Rare Hereditary Hemochromatosis 41 0.091
353
GST040 Gastric Adenocarcinoma 67 0.090
354
BND020 Bone Disease 60 0.090
355
P HYP061 Hypertrophic Cardiomyopathy 68 0.090
356
c INH020 Inherited Metabolic Disorder 51 0.090
357
c INF071 Inflammatory Bowel Disease 1 66 0.089
358
IRR002 Irritable Bowel Syndrome 65 0.088
359
GNG013 Gingivitis 60 0.088
360
PRP080 Peripheral Artery Disease 51 0.088
361
c BTT014 Beta-Thalassemia 73 0.088
362
c PRD040 Periodontitis, Chronic 56 0.088
363
P GLL022 Guillain-Barre Syndrome 56 0.087
364
PPL022 Papilloma 56 0.087
365
P ICH004 Ichthyosis 55 0.087
366
CHL067 Cholecystitis 60 0.087
367
P BLD124 Bleeding Disorder, Platelet-Type, 11 66 0.086
368
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.086
369
P SLP005 Sleep Disorder 58 0.086
370
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 65 0.086
371
MYL005 Myelofibrosis 69 0.085
372
PNC129 Pancreatic Adenocarcinoma 69 0.084
373
c SVR001 Severe Acute Respiratory Syndrome 56 0.084
374
SCK003 Sickle Cell Anemia 74 0.084
375
CLR108 Colorectal Adenoma 64 0.084
376
SQM002 Squamous Cell Papilloma 49 0.084
377
SCH012 Schizoaffective Disorder 50 0.084
378
SPS057 Spasticity 38 0.083
379
KRT009 Keratosis 52 0.083
380
HDN002 Head Injury 47 0.082
381
P LMY004 Leiomyosarcoma 63 0.082
382
OVR082 Overgrowth Syndrome 51 0.082
383
BRD004 Borderline Personality Disorder 51 0.082
384
P DRM010 Dermatomyositis 62 0.081
385
BRR014 Barrett Esophagus 67 0.081
386
ALL010 Allergic Contact Dermatitis 56 0.079
387
MTB004 Metabolic Acidosis 48 0.079
388
CRH005 Crohn's Colitis 56 0.079
389
P GLY013 Glycogen Storage Disease 59 0.079
390
PRM127 Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type 38 0.078
391
FDL002 Food Allergy 52 0.078
392
P HYP069 Hyperparathyroidism 64 0.078
393
ARG004 Argyria 28 0.077
394
c MCR112 Microvascular Complications of Diabetes 2 42 0.077
395
c HYP768 Hyperlipoproteinemia, Type I 50 0.077
396
KRT006 Keratoconjunctivitis 53 0.077
397
P PLY018 Polycythemia 56 0.077
398
CLR109 Colorectal Adenocarcinoma 51 0.076
399
PLY001 Polycythemia Vera 70 0.076
400
ART002 Arts Syndrome 63 0.076
401
AZS001 Azoospermia 51 0.076
402
IMP004 Impetigo 47 0.076
403
KHL003 Kohlschutter-Tonz Syndrome 63 0.076
404
MNN042 Meningioma, Radiation-Induced 64 0.076
405
KRT002 Keratomalacia 47 0.075
406
BRN056 Bronchopulmonary Dysplasia 57 0.075
407
SXL003 Sexual Disorder 49 0.075
408
c MNN043 Meningioma, Familial 74 0.075
409
SPN021 Spinal Meningioma 40 0.075
410
RFR010 Refractory Anemia 50 0.075
411
P INT068 Intestinal Disease 56 0.075
412
VSC002 Vascular Dementia 57 0.074
413
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.074
414
INT002 Intermittent Claudication 60 0.074
415
P HYP730 Hypogonadotropic Hypogonadism 54 0.073
416
GRW007 Growth Hormone Deficiency 48 0.073
417
MSC007 Muscle Hypertrophy 65 0.073
418
P ADL010 Adult Respiratory Distress Syndrome 61 0.073
419
P MSC003 Muscular Atrophy 52 0.073
420
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 36 0.073
421
GST050 Gastrointestinal System Disease 57 0.073
422
GST020 Gastric Antral Vascular Ectasia 42 0.073
423
LYM002 Lymphoplasmacyte-Rich Meningioma 40 0.073
424
BLM002 Bulimia Nervosa 56 0.072
425
SCR001 Secretory Meningioma 38 0.072
426
PRN019 Perinatal Necrotizing Enterocolitis 55 0.072
427
P SHR001 Short Bowel Syndrome 50 0.072
428
RYS001 Reye Syndrome 49 0.072
429
THY030 Thyroid Gland Disease 53 0.072
430
c DNT047 Dentinogenesis Imperfecta Type 2 34 0.072
431
PLC008 Placenta Disease 51 0.071
432
c BLD140 Blood Group, I System 29 0.071
433
c NMN016 Niemann-Pick Disease, Type B 61 0.070
434
OST003 Osteonecrosis 62 0.070
435
KWS002 Kawasaki Disease 65 0.070
436
ALC006 Alcoholic Hepatitis 60 0.070
437
P MLN007 Male Infertility 57 0.069
438
HYP017 Hypophosphatemia 48 0.069
439
CMM005 Common Cold 57 0.069
440
LPT001 Leptospirosis 60 0.069
441
P HMP002 Hemophagocytic Lymphohistiocytosis 68 0.068
442
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 57 0.068
443
FCL014 Focal Epilepsy 56 0.067
444
P MCR010 Microcephaly 56 0.067
445
HYP732 Hyperalphalipoproteinemia 1 55 0.067
446
P PLY014 Polycystic Kidney Disease 61 0.066
447
SDD001 Sudden Infant Death Syndrome 61 0.066
448
PRD004 Prediabetes Syndrome 49 0.066
449
P HYP121 Hypoalphalipoproteinemia 49 0.066
450
ANX004 Anoxia 44 0.066
451
BRS051 Breast Disease 59 0.065
452
P BRS044 Breast Adenocarcinoma 59 0.065
453
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 29 0.065
454
CRD223 Cardiac Arrhythmia 61 0.065
455
OBS529 Obsolete: Combined Hyperlipidemia 22 0.065
456
IRN001 Iron Deficiency Anemia 59 0.065
457
LWC002 Lowe Oculocerebrorenal Syndrome 63 0.065
458
STT001 Status Epilepticus 61 0.064
459
OBS524 Obsolete: Benign Exophthalmos Syndrome 13 0.064
460
P RTN008 Retinitis Pigmentosa 77 0.064
461
CRY035 Cryptorchidism, Unilateral or Bilateral 61 0.064
462
MYC088 Mycobacterium Avium Complex Infections 30 0.063
463
TRP009 Triple X Syndrome 42 0.063
464
CHL147 Chlamydia Pneumonia 39 0.063
465
BLR001 Biliary Atresia 51 0.063
466
ADR007 Adrenoleukodystrophy 72 0.062
467
P ANT006 Antiphospholipid Syndrome 56 0.062
468
DRG003 Drug Dependence 48 0.062
469
CRC021 Carcinosarcoma 62 0.062
470
LYM035 Lymphangiectasis 33 0.061
471
CHL045 Choline Deficiency Disease 39 0.061
472
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.061
473
NPH091 Nephrolithiasis, Calcium Oxalate 66 0.061
474
TNG002 Tangier Disease 64 0.061
475
P HYP265 Hypotonia 43 0.060
476
P LYM025 Lymphedema 54 0.060
477
LPD004 Lipoid Nephrosis 48 0.060
478
c FML001 Familial Atrial Fibrillation 67 0.060
479
AND005 Androgen Insensitivity Syndrome, Mild 20 0.060
480
LYS012 Lysosomal Acid Lipase Deficiency 63 0.059
481
P LPS002 Liposarcoma 62 0.059
482
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 48 0.059
483
RST023 Resting Heart Rate, Variation in 43 0.059
484
c PNC108 Pancreatitis, Hereditary 70 0.059
485
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 55 0.058
486
ASC009 Ascites, Chylous 37 0.058
487
KWS001 Kwashiorkor 46 0.058
488
FRC011 Fructose Intolerance, Hereditary 52 0.058
489
WTH001 Withdrawal Disorder 47 0.058
490
CLR030 Clear Cell Renal Cell Carcinoma 54 0.058
491
P RTN016 Retinal Degeneration 56 0.058
492
c VRL007 Viral Encephalitis 49 0.058
493
P PRP029 Porphyria 58 0.057
494
GLL018 Gallbladder Cancer 57 0.057
495
ACT088 Acute Insulin Response 42 0.057
496
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 56 0.057
497
P VSC018 Visceral Steatosis 34 0.057
498
P ANL018 Analbuminemia 51 0.056
499
P MTR003 Mitral Valve Stenosis 54 0.056
500
WLF001 Wolff-Parkinson-White Syndrome 65 0.056
501
P FML011 Familial Adenomatous Polyposis 73 0.056
502
VTM033 Vitamin K Deficiency Bleeding 47 0.056
503
P RTN022 Retinal Vein Occlusion 50 0.055
504
LPD013 Lipidosis with Triglycerid Storage Disease 4 0.055
505
c GRV008 Graves Disease 1 55 0.055
506
PTH003 Pathologic Nystagmus 53 0.054
507
CYN002 Cyanosis, Transient Neonatal 45 0.054
508
P FML018 Familial Mediterranean Fever 70 0.054
509
P GLM044 Glomerular Disease 42 0.054
510
c HYP839 Hyperlipidemia, Familial Combined, 1 28 0.054
511
HYP043 Hyperandrogenism 48 0.054
512
P OBS001 Obstructive Jaundice 49 0.054
513
ILT001 Ileitis 50 0.054
514
c NMN015 Niemann-Pick Disease, Type C1 67 0.054
515
P RTN018 Retinal Disease 53 0.054
516
P CMP008 Compartment Syndrome 45 0.054
517
ART004 Aortic Atherosclerosis 47 0.053
518
P HYP083 Hypopituitarism 53 0.053
519
ATN005 Autonomic Dysfunction 48 0.052
520
c ART101 Aortic Valve Disease 2 67 0.052
521
c HYP740 Hyperlipoproteinemia, Type V 53 0.052
522
MSN001 Mesangial Proliferative Glomerulonephritis 45 0.051
523
INT052 Intestinal Volvulus 44 0.051
524
P MTR012 Mitral Valve Disease 59 0.051
525
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 44 0.051
526
LPT006 Leptin Receptor Deficiency 47 0.051
527
ADR022 Adrenomyeloneuropathy 39 0.051
528
P ZLL001 Zellweger Syndrome 56 0.051
529
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 65 0.051
530
c CNG012 Congenital Generalized Lipodystrophy 53 0.050
531
MSC190 Muscular Disease 54 0.050
532
ASP026 Asplenia, Isolated Congenital 45 0.050
533
P MLG056 Malignant Hyperthermia 60 0.050
534
PRT038 Protein-Energy Malnutrition 56 0.050
535
ONC002 Onchocerciasis 50 0.050
536
c SPR086 Spermatogenic Failure 3 41 0.049
537
CRT084 Creatinine Clearance Quantitative Trait Locus 26 0.049
538
c SCN007 Secondary Hyperparathyroidism 52 0.049
539
NTR046 Neutrophil Migration 49 0.049
540
c ATM075 Autoimmune Encephalitis 39 0.049
541
PHN003 Phenylketonuria 73 0.049
542
PRT019 Protein-Losing Enteropathy 41 0.048
543
ATN004 Autonomic Neuropathy 43 0.048
544
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 56 0.048
545
c CNG006 Congenital Hypothyroidism 65 0.048
546
RTN020 Retinal Vascular Disease 49 0.048
547
MNC019 Monocarboxylate Transporter 1 Deficiency 47 0.048
548
P SBR004 Seborrheic Dermatitis 41 0.048
549
P SHR029 Short Syndrome 56 0.048
550
FRZ001 Frozen Shoulder 53 0.048
551
ASP007 Aspiration Pneumonia 46 0.047
552
MMM001 Mammary Paget's Disease 53 0.047
553
CTS005 Catastrophic Antiphospholipid Syndrome 44 0.047
554
DVR002 Diverticulitis 44 0.047
555
CHY002 Chylomicron Retention Disease 63 0.047
556
P GLL020 Gallbladder Disease 60 0.047
557
P PLY006 Polydactyly 58 0.047
558
ERL001 Early Myoclonic Encephalopathy 60 0.047
559
P MYT002 Myotonic Dystrophy 52 0.046
560
SCT005 Scott Syndrome 48 0.046
561
CRY008 Cryopyrin-Associated Periodic Syndrome 48 0.046
562
P HYP024 Hypoparathyroidism 56 0.046
563
PYR016 Pyridoxine Deficiency 31 0.045
564
CRB009 Cerebritis 31 0.045
565
GNT167 Genetic Obesity 35 0.045
566
c SVR005 Severe Pre-Eclampsia 50 0.045
567
P MTC069 Mitochondrial Disorders 57 0.045
568
CRT016 Carotid Artery Disease 53 0.045
569
MYT026 Myotonia Atrophica 25 0.045
570
c HRD010 Hereditary Spastic Paraplegia 67 0.044
571
c HYP841 Hypoalphalipoproteinemia, Primary, 1 53 0.044
572
PTT048 Pituitary Adenoma, Prolactin-Secreting 61 0.044
573
HMR004 Hemorrhagic Fever with Renal Syndrome 54 0.044
574
c PRM158 Primary Intestinal Lymphangiectasia 30 0.044
575
TRG002 Trigeminal Neuralgia 58 0.044
576
KRN001 Korean Hemorrhagic Fever 42 0.044
577
TXC020 Toxic Oil Syndrome 34 0.044
578
FML235 Familial Combined Hyperlipoproteinemia 29 0.044
579
FLL008 Folliculitis 46 0.043
580
TRP004 Tropical Sprue 41 0.043
581
P PRP003 Porphyria Cutanea Tarda 66 0.043
582
ACR041 Acromelic Frontonasal Dysostosis 50 0.043
583
ATN011 Autoinflammation with Infantile Enterocolitis 45 0.043
584
HYP006 Hypertensive Heart Disease 49 0.043
585
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 61 0.043
586
CHD004 Chudley-Mccullough Syndrome 44 0.042
587
TBR011 Tuberculous Meningitis 50 0.042
588
c VRL012 Viral Meningitis 47 0.042
589
HTC003 Hutchinson-Gilford Progeria Syndrome 64 0.041
590
ACT162 Acute Sensory Ataxic Neuropathy 27 0.041
591
FTL021 Fetal Macrosomia 43 0.041
592
P LCT002 Lactose Intolerance 51 0.041
593
XNT003 Xanthomatosis 48 0.041
594
CRN017 Coronary Thrombosis 45 0.041
595
CHR177 Chromophobe Renal Cell Carcinoma 58 0.040
596
SCH038 Schopf-Schulz-Passarge Syndrome 48 0.040
597
P MTR004 Maturity-Onset Diabetes of the Young 66 0.040
598
OVR063 Overnutrition 47 0.040
599
CHL013 Cholecystolithiasis 37 0.039
600
ADL030 Adult-Onset Still's Disease 59 0.039
601
PRX001 Peroxisomal Disease 45 0.039
602
P HYP535 Hypogonadotropic Hypogonadism 7 with or Without Anosmia 59 0.039
603
WRN001 Werner Syndrome 68 0.039
604
P TRC031 Trichorhinophalangeal Syndrome 41 0.039
605
LYM007 Lymphangioleiomyomatosis 67 0.039
606
BLP005 Blepharitis 48 0.038
607
HTT002 Hutterite Cerebroosteonephrodysplasia Syndrome 26 0.038
608
c LPD015 Lipodystrophy, Familial Partial, Type 2 60 0.038
609
P PLY188 Polyendocrinopathy 35 0.037
610
P PTY003 Pityriasis Rubra Pilaris 53 0.037
611
PYL006 Pyloric Stenosis 47 0.037
612
DRM009 Dermatomycosis 38 0.037
613
ACT017 Acute Chest Syndrome 47 0.036
614
LNN001 Lennox-Gastaut Syndrome 56 0.036
615
LYM022 Lymphangioma 52 0.036
616
PLC005 Placental Insufficiency 55 0.035
617
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 64 0.035
618
P RTN014 Retinal Artery Occlusion 46 0.035
619
P TRC005 Tracheal Stenosis 39 0.035
620
CRB025 Carbohydrate Metabolic Disorder 45 0.035
621
c RRL003 Rare Lymphatic Malformation 32 0.035
622
GLC008 Glucose Metabolism Disease 47 0.034
623
c ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 36 0.034
624
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 62 0.034
625
MTC005 Mitochondrial Metabolism Disease 50 0.034
626
c RCR022 Recurrent Acute Pancreatitis 46 0.034
627
BRN026 Branch Retinal Artery Occlusion 41 0.034
628
P LPM005 Lipomatosis 49 0.033
629
c HMP022 Hemophagocytic Lymphohistiocytosis, Familial, 1 50 0.033
630
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 43 0.033
631
c FTL070 Fetal Akinesia Deformation Sequence 2 33 0.033
632
SBL008 Sea-Blue Histiocyte Disease 46 0.033
633
MCR225 Macrophage Activation Syndrome 46 0.033
634
c DBT093 Diabetes Mellitus, Noninsulin-Dependent, 1 26 0.033
635
EXF003 Exfoliative Dermatitis 28 0.032
636
P FML187 Familial Hypertension 35 0.032
637
URT049 Urate Oxidase, Pseudogene 26 0.032
638
c EXS019 Exostoses, Multiple, Type I 51 0.032
639
MNN034 Mannose-Binding Lectin Deficiency 46 0.032
640
MYC005 Myocardial Stunning 45 0.032
641
RTR012 Retroperitoneal Liposarcoma 24 0.032
642
ADR041 Adrenal Cortical Adenoma 44 0.031
643
ARC023 Arcus Corneae 40 0.031
644
P HYP078 Hypertrophy of Breast 35 0.031
645
MYC019 Mycobacterium Marinum 31 0.031
646
ESN017 Eosinophilic Granuloma 38 0.029
647
MRS001 Marasmus 39 0.029
648
CRN239 Carnitine Deficiency, Systemic Primary 56 0.029
649
c NMN014 Niemann-Pick Disease, Type C2 53 0.029
650
ORG002 Organic Acidemia 43 0.027
651
P FML012 Familial Partial Lipodystrophy 54 0.027
652
HMC040 Homocystinuria Due to Cystathionine Beta-Synthase Deficiency 48 0.027
653
MLT118 Multiple Acyl-Coa Dehydrogenase Deficiency 64 0.027
654
BRR012 Berardinelli-Seip Congenital Lipodystrophy 46 0.027
655
P HYP058 Hypervitaminosis a 45 0.027
656
ABD017 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 44 0.027
657
VLL006 Villous Adenoma 37 0.027
658
LGS001 Legius Syndrome 57 0.025
659
FLT006 Floating-Harbor Syndrome 46 0.025
660
RTN021 Retinal Vascular Occlusion 42 0.025
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