Search results for Fenofibrate

558 hits were found for Fenofibrate

# Family MCID Name MIFTS Score
1
LPD008 Lipid Metabolism Disorder 62 34.487
2
P HYP750 Hypertriglyceridemia, Familial 62 25.627
3
c TYP009 Type 2 Diabetes Mellitus 92 17.688
4
c HYP836 Hypercholesterolemia, Familial, 1 73 17.658
5
c MCR115 Microvascular Complications of Diabetes 5 65 15.731
6
P DBT009 Diabetes Mellitus 67 13.505
7
NNL005 Non-Alcoholic Fatty Liver Disease 63 13.052
8
FTT001 Fatty Liver Disease 62 12.262
9
P CRN300 Coronary Heart Disease 1 73 10.517
10
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 50 10.352
11
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 10.122
12
FML035 Familial Hyperlipidemia 55 10.104
13
c MCR113 Microvascular Complications of Diabetes 3 52 9.770
14
c MCR130 Microvascular Complications of Diabetes 6 41 9.380
15
c MCR120 Microvascular Complications of Diabetes 7 47 9.380
16
c MCR133 Microvascular Complications of Diabetes 4 41 9.380
17
P LVR013 Liver Disease 69 9.052
18
PRM236 Primary Biliary Cholangitis 60 8.556
19
ISC004 Ischemia 61 8.519
20
LPP008 Lipoprotein Quantitative Trait Locus 65 8.370
21
ATH013 Atherosclerosis Susceptibility 63 8.215
22
P MYP004 Myopathy 67 8.109
23
P CRD246 Cardiovascular System Disease 56 7.619
24
LVR012 Liver Cirrhosis 63 7.459
25
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 7.312
26
ART140 Arteries, Anomalies of 53 7.187
27
NNL006 Non-Alcoholic Steatohepatitis 54 7.156
28
c FML021 Familial Hypercholesterolemia 72 7.058
29
P KDN018 Kidney Disease 72 6.926
30
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 63 6.825
31
P HYP838 Hyperlipidemia, Familial Combined, 3 61 6.803
32
P HRT032 Heart Disease 81 6.676
33
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 6.597
34
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 80 6.389
35
MCL006 Macular Retinal Edema 57 6.245
36
GT001 Gout 64 6.197
37
P MCR129 Microvascular Complications of Diabetes 1 68 5.953
38
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 5.944
39
HYP555 Hypertriglyceridemia, Transient Infantile 38 5.922
40
P CHL066 Cholangitis 52 5.712
41
c CHR684 Chronic Kidney Disease 69 5.680
42
HYP066 Hyperglycemia 61 5.651
43
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 5.597
44
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 5.597
45
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 5.597
46
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 5.597
47
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 5.597
48
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 5.597
49
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 5.597
50
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 5.597
51
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 5.597
52
PRT251 Proteinuria, Chronic Benign 57 5.498
53
DBT006 Diabetic Macular Edema 48 5.479
54
c MCR112 Microvascular Complications of Diabetes 2 42 5.295
55
c HYP740 Hyperlipoproteinemia, Type V 53 5.161
56
GLB002 Glioblastoma 67 5.039
57
P VSC007 Vascular Disease 63 5.034
58
c HYP724 Hyperlipoproteinemia, Type Iii 67 5.019
59
CYT002 Cytokine Deficiency 43 4.962
60
ANT039 Antisynthetase Syndrome 55 4.857
61
CHL068 Cholestasis 61 4.786
62
c BLD140 Blood Group, I System 46 4.728
63
HYP060 Hyperinsulinism 54 4.725
64
HMC014 Homocysteinemia 52 4.607
65
P EXN002 Exanthem 58 4.526
66
P ALC033 Alcohol Use Disorder 61 4.502
67
c ACT071 Acute Kidney Failure 60 4.491
68
P SCL009 Sclerosing Cholangitis 48 4.422
69
HYP014 Hyperuricemia 51 4.355
70
P RTN018 Retinal Disease 53 4.189
71
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 66 4.166
72
48X005 48,xyyy 39 4.119
73
HYP056 Hypoglycemia 65 4.047
74
P HYP086 Hypothyroidism 69 4.009
75
RTN020 Retinal Vascular Disease 46 3.996
76
P ART021 Arteriosclerosis 54 3.990
77
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 63 3.983
78
P TRN020 Turner Syndrome 67 3.975
79
ANR040 Aneurysm 61 3.969
80
c TYP008 Type 1 Diabetes Mellitus 70 3.956
81
ART016 Aortic Aneurysm 68 3.930
82
ORL011 Oral Cancer 60 3.924
83
P MYC008 Myocarditis 59 3.859
84
c ART138 Aortic Aneurysm, Familial Abdominal, 1 61 3.809
85
ADL002 Adult Syndrome 70 3.788
86
c HNT011 Huntington Disease-Like 3 34 3.699
87
c GLL024 Gallbladder Disease 1 52 3.676
88
LKS001 Leukostasis 41 3.676
89
SPN186 Spinal Cord Injury 61 3.644
90
c ACT027 Acute Pancreatitis 60 3.638
91
CRB004 Cerebral Artery Occlusion 45 3.619
92
CHL004 Cholelithiasis 49 3.578
93
P PNC044 Pancreatitis 61 3.578
94
GLL048 Glial Tumor 52 3.536
95
HYP266 Hypoxia 57 3.536
97
GLC003 Glucose Intolerance 54 3.518
98
P NRB001 Neuroblastoma 66 3.499
99
P HPT021 Hepatitis 69 3.475
100
P MSC003 Muscular Atrophy 52 3.451
101
BCK003 Background Diabetic Retinopathy 47 3.430
102
P NRP001 Neuropathy 60 3.398
103
P PRS040 Prostate Cancer 95 3.363
104
c CHL119 Cholangitis, Primary Sclerosing 58 3.336
105
P MLN008 Melanoma 76 3.313
106
PLM033 Pulmonary Embolism 58 3.276
107
BLR008 Bilirubin Metabolic Disorder 57 3.247
108
P PLY011 Polycystic Ovary Syndrome 57 3.207
109
c HYP272 Hypercholesterolemia, Familial, 3 45 3.161
110
P SCH015 Schizophrenia 74 3.159
111
P MYC007 Myocardial Infarction 70 3.148
112
RHB024 Rhabdomyosarcoma 2 67 3.124
113
HYP081 Hypolipoproteinemia 49 3.123
114
c HYP839 Hyperlipidemia, Familial Combined, 1 30 3.121
115
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 66 3.121
116
HMN014 Human Immunodeficiency Virus Infectious Disease 54 3.102
117
ALC007 Alcohol Dependence 66 3.085
118
c ATR087 Atrial Standstill 1 74 3.062
119
GLM045 Glioma 63 3.038
120
MYL069 Myeloma, Multiple 77 3.033
121
P MYS005 Myositis 56 3.022
122
P NPH012 Nephrotic Syndrome 60 3.016
123
P RHM011 Rheumatoid Arthritis 82 2.971
124
P PRP019 Peripheral Nervous System Disease 58 2.970
125
RNL077 Renal Fibrosis 46 2.923
126
c HYP595 Hypertension, Essential 85 2.829
127
c ACT075 Acute Myocardial Infarction 56 2.798
128
TRM010 Traumatic Brain Injury 51 2.779
129
CLT003 Colitis 63 2.775
130
P AST005 Asthma 76 2.769
131
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 2.763
132
c HNT004 Huntington Disease-Like 2 52 2.670
133
P RTN024 Retinoblastoma 73 2.670
134
INS001 Insulinoma 59 2.670
135
END086 End Stage Renal Disease 52 2.670
136
PRP027 Peripheral Vascular Disease 71 2.615
137
c DLT002 Dilated Cardiomyopathy 78 2.615
138
ALL029 Allergic Disease 59 2.615
139
P HDC001 Headache 57 2.615
140
P PLY041 Polymyositis 59 2.604
141
CVD001 Covid-19 57 2.570
142
P BLR024 Biliary Cirrhosis, Primary, 1 28 2.562
143
ADR022 Adrenomyeloneuropathy 39 2.559
144
ADR007 Adrenoleukodystrophy 73 2.559
145
STR067 Stroke, Ischemic 80 2.559
146
DST006 Diastolic Heart Failure 45 2.559
147
HMZ003 Homozygous Familial Hypercholesterolemia 60 2.549
148
BRN071 Brain Injury 50 2.501
149
ALL014 Allergic Encephalomyelitis 34 2.457
150
KHN001 Kuhnt-Junius Degeneration 48 2.440
151
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 2.436
152
P HNT016 Huntington Disease 73 2.421
153
RPD005 Rapidly Involuting Congenital Hemangioma 46 2.410
154
c FML116 Familial Cold Autoinflammatory Syndrome 1 55 2.402
155
P EYD002 Eye Disease 57 2.402
156
P VSC018 Visceral Steatosis 32 2.380
157
c ATM022 Autoimmune Myocarditis 36 2.378
158
ALL006 Allergic Asthma 56 2.378
159
CHG001 Chagas Disease 66 2.378
160
SQM006 Squamous Cell Carcinoma 60 2.378
161
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 2.340
162
END072 Endotheliitis 36 2.340
163
GLC008 Glucose Metabolism Disease 40 2.340
164
MTB004 Metabolic Acidosis 48 2.313
165
P LCT001 Lactic Acidosis 51 2.313
166
ATM095 Autoimmune Disease 61 2.287
167
P BCL017 B-Cell Lymphoma 59 2.246
168
ESP021 Esophageal Cancer 83 2.227
169
LNG099 Lung Disease 62 2.175
170
BRN028 Brain Cancer 74 2.175
171
HGH043 High Grade Glioma 45 2.175
172
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 2.165
173
P AMY004 Amyloidosis 70 2.165
174
NTR005 Nutritional Deficiency Disease 61 2.087
175
P HMC002 Homocystinuria 53 2.047
176
AGN016 Aging 54 2.045
177
c HPT003 Hepatitis a 63 2.045
178
P ATS364 Autism 69 2.033
179
P MYC084 Mycobacterium Tuberculosis 1 68 2.033
180
c ATS007 Autism Spectrum Disorder 72 2.033
181
ORL015 Oral Squamous Cell Carcinoma 43 2.033
182
CRH001 Crohn's Disease 80 2.033
183
P EPL164 Epilepsy 68 2.033
184
MCR013 Microphthalmia 60 2.033
185
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 2.023
186
P OVR042 Ovarian Cancer 88 2.023
187
P THR014 Thrombocytopenia 66 2.023
188
ADN018 Adenoma 59 2.023
189
ABD017 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 46 1.964
190
P MLT020 Multiple Sclerosis 79 1.962
191
P ATS011 Autosomal Dominant Nocturnal Frontal Lobe Epilepsy 48 1.962
192
P ART018 Aortic Valve Insufficiency 52 1.962
193
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 1.962
194
P NTR004 Neutropenia 63 1.962
195
HPT067 Hepatocellular Adenoma 43 1.939
196
P RRH023 Rare Hereditary Hemochromatosis 54 1.939
197
CHL147 Chlamydia Pneumonia 47 1.939
198
HMS001 Hemosiderosis 48 1.939
199
IMP005 Impotence 52 1.939
200
CHL123 Chlamydia 58 1.939
201
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 60 1.939
202
P ATR011 Atrial Fibrillation 66 1.888
203
ACT003 Acute Kidney Tubular Necrosis 46 1.888
204
P VSC011 Vasculitis 61 1.888
205
FCL014 Focal Epilepsy 53 1.888
206
P GLY013 Glycogen Storage Disease 60 1.888
207
CNG034 Congestive Heart Failure 69 1.888
208
HMN044 Human Immunodeficiency Virus Type 1 78 1.855
209
THR024 Thrombosis 56 1.855
210
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 60 1.855
211
c THR092 Thrombophilia Due to Thrombin Defect 74 1.831
212
PPL052 Papillomatosis, Confluent and Reticulated 34 1.809
213
c EXD008 Exudative Vitreoretinopathy 1 71 1.809
214
MNT001 Mantle Cell Lymphoma 67 1.809
215
P INF037 Inflammatory Bowel Disease 53 1.809
216
BNR002 Bone Resorption Disease 47 1.809
217
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 1.809
218
c HPT073 Hepatitis C Virus 71 1.809
219
LPP002 Lipoprotein Glomerulopathy 43 1.809
220
URT049 Urate Oxidase, Pseudogene 24 1.809
221
GYN001 Gynecomastia 47 1.809
222
ANG020 Angiosarcoma 64 1.809
223
SNS003 Sensory Peripheral Neuropathy 52 1.809
224
CRN027 Corneal Neovascularization 47 1.809
225
JPN002 Japanese Encephalitis 61 1.809
226
INF021 Infant Gynecomastia 30 1.809
227
CRB039 Cerebrovascular Disease 66 1.809
228
P HYP121 Hypoalphalipoproteinemia 43 1.809
229
P ENC004 Encephalitis 61 1.809
230
c HYP841 Hypoalphalipoproteinemia, Primary, 1 49 1.788
231
P ANR048 Aniridia 1 64 1.788
232
AND005 Androgen Insensitivity Syndrome, Mild 21 1.788
233
ATS010 Autosomal Recessive Disease 42 1.751
234
SLN001 Silent Myocardial Infarction 33 1.751
235
P ALZ034 Alzheimer Disease 87 1.726
236
PLT004 Platelet Glycoprotein Iv Deficiency 56 1.726
237
P PLM037 Pulmonary Hypertension 72 1.726
238
P LKM062 Leukemia, Acute Lymphoblastic 69 1.726
239
P PRK039 Parkinsonism 55 1.726
240
c VRL007 Viral Encephalitis 50 1.726
241
OST012 Osteoarthritis 77 1.726
242
P NRN021 Neuronal Ceroid Lipofuscinosis 65 1.726
243
HYP080 Hypogonadism 50 1.726
244
MYC005 Myocardial Stunning 46 1.726
245
ACT167 Acute Generalized Exanthematous Pustulosis 38 1.636
246
c CRD186 Ceroid Lipofuscinosis, Neuronal, 3 63 1.636
247
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 1.636
248
LMB062 Limb Ischemia 55 1.636
249
47X002 47,xyy 48 1.636
250
P ART022 Arthritis 71 1.636
251
NSP002 Nasopharyngitis 45 1.636
252
OST003 Osteonecrosis 61 1.636
253
CNS004 Constipation 56 1.636
254
c MLG069 Malignant Hypertension 46 1.636
255
CNT060 Central Serous Chorioretinopathy 38 1.636
256
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 1.598
257
SXL003 Sexual Disorder 49 1.587
258
EPT021 Epithelial Recurrent Erosion Dystrophy 46 1.587
259
PLM134 Pulmonary Fibrosis, Idiopathic 76 1.538
260
CYS001 Cystic Fibrosis 78 1.538
261
P PLY014 Polycystic Kidney Disease 69 1.538
262
P PNC035 Pancreatic Cancer 86 1.538
263
HPT025 Hepatic Lipase Deficiency 47 1.538
264
c CRN175 Coronary Heart Disease 4 14 1.538
265
P OTP008 Otopalatodigital Syndrome Spectrum Disorder 25 1.538
266
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 1.538
267
c ATS347 Autosomal Dominant Polycystic Kidney Disease 66 1.538
268
URT010 Ureteral Obstruction 45 1.538
269
HMG002 Hemoglobinuria 50 1.538
270
DBT010 Diabetic Neuropathy 54 1.538
271
P ALP008 Alopecia 54 1.538
272
c HPT001 Hepatitis C 62 1.538
273
P PLM036 Pulmonary Fibrosis 66 1.538
274
HYP006 Hypertensive Heart Disease 49 1.538
275
SYS003 Systolic Heart Failure 49 1.538
276
c AMY009 Amyloidosis Aa 47 1.538
277
P CTN015 Cutaneous T Cell Lymphoma 48 1.518
278
CNT047 Contact Dermatitis 57 1.447
279
END057 Endometrial Cancer 72 1.430
280
PRP080 Peripheral Artery Disease 54 1.430
281
NRN005 Neuronal Ceroid-Lipofuscinoses 61 1.430
282
P LYM118 Lymphoma 67 1.430
283
BRN004 Brain Edema 54 1.430
284
P HYP098 Hypereosinophilic Syndrome 66 1.430
285
CRN036 Craniopharyngioma 64 1.430
286
OVR063 Overnutrition 42 1.430
287
PNC001 Pancytopenia 53 1.430
288
STT001 Status Epilepticus 59 1.430
289
GNT019 Giant Cell Myocarditis 29 1.430
290
CRT084 Creatinine Clearance Quantitative Trait Locus 25 1.398
291
MCL027 Macular Dystrophy, Dominant Cystoid 51 1.398
292
P CNR004 Cone-Rod Dystrophy 2 74 1.398
293
P SLP006 Sleep Apnea 69 1.398
294
PLY105 Polycystic Ovary Syndrome 1 39 1.398
295
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 1.398
296
APN008 Apnea, Obstructive Sleep 67 1.398
297
CRN030 Coronary Stenosis 50 1.398
298
P PRS038 Personality Disorder 65 1.398
299
CNT033 Central Nervous System Cancer 47 1.398
300
PRP016 Paraplegia 52 1.398
301
AMD002 Amed Syndrome, Digenic 37 1.398
302
NNT012 Neonatal Jaundice 53 1.398
303
PLS009 Plasma Cell Neoplasm 64 1.398
304
P NRV006 Nervous System Cancer 48 1.398
305
QDR001 Quadriplegia 50 1.398
306
VRL011 Viral Infectious Disease 61 1.397
307
HPT022 Hepatoblastoma 54 1.373
308
BCT022 Bacterial Infectious Disease 56 1.371
309
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 1.307
310
HYP020 Hyperprolactinemia 63 1.307
311
CLR109 Colorectal Adenocarcinoma 50 1.307
312
P RNV001 Renovascular Hypertension 49 1.307
313
RCK004 Rickets 68 1.307
314
P MDL005 Medulloblastoma 75 1.295
315
c DNT047 Dentinogenesis Imperfecta Type 2 35 1.295
316
c HRM017 Hermansky-Pudlak Syndrome 2 55 1.211
317
c FTL070 Fetal Akinesia Deformation Sequence 2 36 1.211
318
INS024 Insulin-Like Growth Factor I 78 1.162
319
MYC006 Mycosis Fungoides 65 1.162
320
P ATX030 Ataxia-Telangiectasia 80 1.162
321
ANG054 Angina Pectoris 66 1.162
322
HRW001 Hair Whorl 35 1.162
323
P LCH002 Lichen Planus 54 1.162
324
TLN003 Telangiectasis 51 1.162
325
PLG002 Plague 58 1.162
326
P PLY019 Polyneuropathy 52 1.162
327
DRG026 Drug Reaction with Eosinophilia and Systemic Symptoms 45 1.162
328
END062 Endometrial Hyperplasia 48 1.121
329
INT002 Intermittent Claudication 61 1.121
330
PHT004 Photoallergic Dermatitis 28 1.121
331
P OBS001 Obstructive Jaundice 48 1.121
332
P SCK005 Sickle Cell Disease 56 1.121
333
MSC007 Muscle Hypertrophy 64 1.023
334
RNL114 Renal Cell Carcinoma, Nonpapillary 80 1.023
335
P HPT023 Hepatocellular Carcinoma 96 1.023
336
P THY032 Thyroiditis 57 1.023
337
PRT013 Portal Hypertension 59 1.023
338
DRM006 Dermatitis 62 1.023
339
KRT008 Keratopathy 46 1.023
340
PLY100 Polyploidy 36 0.972
341
PRS129 Prostatic Hyperplasia, Benign 49 0.972
342
MLT134 Multiple Pterygium Syndrome, Lethal Type 56 0.972
343
CRG004 Crigler-Najjar Syndrome, Type Ii 46 0.972
344
PLY150 Polykaryocytosis Inducer 29 0.972
345
P CRG003 Crigler-Najjar Syndrome, Type I 63 0.972
347
PRS042 Prostate Disease 42 0.972
348
LYM027 Lymphopenia 56 0.972
349
P LNG064 Lung Cancer Susceptibility 3 70 0.972
350
P MLN007 Male Infertility 56 0.972
351
PRS021 Prostatic Adenoma 43 0.972
352
DRG002 Drug-Induced Hepatitis 42 0.972
353
P ADN016 Adenocarcinoma 63 0.972
354
P END044 Endometriosis 62 0.972
355
PRM013 Premature Menopause 58 0.972
356
PRS045 Prostatic Hypertrophy 53 0.972
357
P INF032 Infertility 57 0.972
358
P LNG032 Lung Cancer 98 0.970
359
RSP019 Respiratory Distress Syndrome in Premature Infants 52 0.939
360
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 49 0.939
361
NWB001 Newborn Respiratory Distress Syndrome 56 0.939
362
P ADL010 Adult Respiratory Distress Syndrome 71 0.939
363
RSP007 Respiratory Distress Syndrome, Infant 40 0.939
364
c AMY091 Amyotrophic Lateral Sclerosis 1 88 0.915
365
TRD006 Tardive Dyskinesia 53 0.915
366
P HYP061 Hypertrophic Cardiomyopathy 69 0.915
367
P GRV001 Graves' Disease 55 0.915
368
CRT013 Carotid Stenosis 51 0.915
369
TRN015 Transient Cerebral Ischemia 63 0.915
370
P LTR001 Lateral Sclerosis 58 0.915
371
TXC005 Toxic Shock Syndrome 62 0.915
372
MCS002 Mucositis 56 0.915
373
CRT015 Carotid Artery Occlusion 45 0.915
374
HYP458 Hyper Ige Syndrome 60 0.913
375
c HYP843 Hypoalphalipoproteinemia, Primary, 2 50 0.913
377
PRD004 Prediabetes Syndrome 52 0.913
378
ATX019 Ataxia with Vitamin E Deficiency 44 0.913
379
c HMC039 Hemochromatosis, Type 1 73 0.793
380
MSC157 Muscular Dystrophy, Duchenne Type 79 0.793
381
P SMK004 Smoking As a Quantitative Trait Locus 3 44 0.793
382
HYP114 Hypertensive Nephropathy 36 0.793
383
TBC004 Tobacco Addiction 63 0.793
384
c SML038 Small Cell Cancer of the Lung 69 0.793
385
P GLM040 Glioma Susceptibility 1 71 0.793
386
OBS082 Obstructive Nephropathy 41 0.793
387
PRX001 Peroxisomal Disease 46 0.793
388
IRD001 Iridocyclitis 53 0.793
389
P MSC005 Muscular Dystrophy 67 0.793
390
IGG001 Iga Glomerulonephritis 50 0.793
391
THR016 Thrombophlebitis 50 0.793
392
P INF038 Influenza 68 0.793
393
NPH009 Nephrolithiasis 54 0.793
394
HLX001 Helix Syndrome 48 0.793
395
CMB007 Combined Immunodeficiency 57 0.793
396
P UVT001 Uveitis 57 0.793
397
CLN015 Colon Adenocarcinoma 65 0.793
398
MLG169 Malignant Astrocytoma 57 0.793
399
P BND020 Bone Disease 59 0.793
400
ART004 Aortic Atherosclerosis 47 0.793
401
SVR004 Severe Combined Immunodeficiency 72 0.793
402
PTT037 Pituitary Tumors 44 0.793
403
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 59 0.793
404
P BLD134 Bladder Cancer 79 0.647
405
P RTN008 Retinitis Pigmentosa 80 0.647
406
RTN017 Retinal Detachment 60 0.647
407
ACT098 Acute Erythroid Leukemia 55 0.647
408
URL001 Urolithiasis 46 0.647
409
P HYP768 Hyperlipoproteinemia, Type I 67 0.647
410
LPT014 Leptin Deficiency or Dysfunction 78 0.647
411
NRR001 Neuroretinitis 42 0.647
412
RTN023 Retinitis 46 0.647
413
P PLY017 Polyarteritis Nodosa 60 0.647
414
P ANT006 Antiphospholipid Syndrome 55 0.647
415
P LPM005 Lipomatosis 47 0.647
416
HST010 Histiocytosis 49 0.647
417
P BRS044 Breast Adenocarcinoma 58 0.647
418
P DRM010 Dermatomyositis 61 0.647
419
P OPT009 Optic Neuritis 57 0.647
420
ALC006 Alcoholic Hepatitis 61 0.647
421
NRT004 Neuritis 53 0.647
422
ATN004 Autonomic Neuropathy 42 0.647
423
c HPT007 Hepatitis E 51 0.647
424
P HYP076 Hyperthyroidism 53 0.647
425
c HPT016 Hepatitis B 62 0.647
426
XNT009 Xanthoma Disseminatum 34 0.647
427
RYN005 Raynaud Phenomenon 45 0.647
428
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.515
429
c NMN016 Niemann-Pick Disease, Type B 56 0.515
430
P NMN002 Niemann-Pick Disease 60 0.515
431
c ATM011 Autoimmune Hepatitis 63 0.515
432
LPD009 Lipid Storage Disease 45 0.484
433
P DBT005 Diabetes Insipidus 54 0.458
434
P SMP003 Simpson-Golabi-Behmel Syndrome 49 0.458
435
MTC005 Mitochondrial Metabolism Disease 45 0.458
436
P HRD217 Hereditary Optic Neuropathy 36 0.458
437
P THL005 Thalassemia 56 0.458
438
c ACT134 Acute Liver Failure 59 0.458
439
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 45 0.458
440
LCT022 Lecithin:cholesterol Acyltransferase Deficiency 58 0.458
441
CRD132 Cardiac Conduction Defect 60 0.458
442
ACY010 Acyl-Coa Dehydrogenase, Very Long-Chain, Deficiency of 64 0.458
443
XNT003 Xanthomatosis 49 0.458
444
CRV035 Cervical Cancer 73 0.458
445
P PHC003 Pheochromocytoma 69 0.458
446
P PRG130 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 1 54 0.458
447
ACN002 Acanthosis Nigricans 56 0.458
448
P BRS047 Breast Cancer 98 0.458
449
c MGR028 Migraine with or Without Aura 1 64 0.458
450
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 57 0.458
451
P FML012 Familial Partial Lipodystrophy 54 0.458
452
c MJR022 Major Affective Disorder 8 38 0.458
453
ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 36 0.458
454
VRL003 Variola Major 43 0.458
455
DFC004 Deficiency Anemia 74 0.458
456
LWG006 Low Grade Glioma 41 0.458
457
P SML001 Small Cell Carcinoma 52 0.458
458
P ACQ022 Acquired Generalized Lipodystrophy 45 0.458
459
KRN002 Kearns-Sayre Syndrome 63 0.458
460
CRN240 Craniometaphyseal Dysplasia, Autosomal Recessive 29 0.458
461
c PRG021 Paragangliomas 4 37 0.458
462
c PRG020 Paragangliomas 3 39 0.458
463
c HNT010 Huntington Disease-Like 1 55 0.458
464
c TYP050 Type 2 Diabetes Mellitus 3 15 0.458
465
LNG108 Langerhans Cell Histiocytosis 58 0.458
466
c NRB014 Neuroblastoma 3 28 0.458
467
P MJR001 Major Depressive Disorder 68 0.458
468
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.458
469
c MJR024 Major Affective Disorder 9 41 0.458
470
MTC027 Mitochondrial Trifunctional Protein Deficiency 57 0.458
471
c PRG038 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 2 49 0.458
472
c NRB010 Neuroblastoma 1 59 0.458
473
THY069 Thyroid Hormone Resistance, Selective Pituitary 36 0.458
474
NPH091 Nephrolithiasis, Calcium Oxalate 61 0.458
475
c GLC092 Glaucoma, Primary Open Angle 62 0.458
476
c PRG040 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 4 53 0.458
477
P EPL116 Epileptic Encephalopathy, Childhood-Onset 43 0.458
478
CHL065 Cholangiocarcinoma 58 0.458
479
DSS032 Disease by Infectious Agent 55 0.458
480
ADR040 Adrenal Gland Pheochromocytoma 46 0.458
481
OST017 Osteomyelitis 63 0.458
482
CNN008 Cinnamon Odor, Pleasantness of 14 0.458
483
NPH003 Nephrocalcinosis 49 0.458
484
c CHR095 Chronic Progressive External Ophthalmoplegia 49 0.458
485
P STS003 Sitosterolemia 53 0.458
486
P OPN001 Open-Angle Glaucoma 55 0.458
487
SVR002 Severe Nonproliferative Diabetic Retinopathy 36 0.458
488
MCL003 Macular Holes 44 0.458
489
P EMB005 Embryonal Rhabdomyosarcoma 53 0.458
490
P RHB003 Rhabdomyosarcoma 66 0.458
491
MLL001 Molluscum Contagiosum 48 0.458
492
MTC004 Mitochondrial Encephalomyopathy 42 0.458
493
APP009 Appendix Adenocarcinoma 45 0.458
494
SML019 Smallpox 55 0.458
495
P MTC133 Mitochondrial Myopathy 50 0.458
496
CLL010 Cellular Ependymoma 57 0.458
497
DRG017 Drug-Induced Vasculitis 16 0.458
498
CNT115 Central Nervous System Embryonal Tumor 21 0.458
499
SVR001 Severe Acute Respiratory Syndrome 67 0.458
500
MCN001 Mucinous Adenocarcinoma 49 0.458
501
P OPT006 Optic Nerve Disease 58 0.458
502
CHL067 Cholecystitis 60 0.458
503
VCC001 Vaccinia 47 0.458
504
P BPL003 Bipolar Disorder 56 0.458
505
MNT002 Mental Depression 57 0.458
506
MLT006 Multidrug-Resistant Tuberculosis 47 0.458
507
P GST044 Gastritis 55 0.458
508
OVR059 Ovary Adenocarcinoma 49 0.458
509
P ART023 Arthropathy 61 0.458
510
ACQ007 Acquired Immunodeficiency Syndrome 59 0.458
511
ANT024 Anthrax Disease 58 0.458
512
P CTR002 Cataract 60 0.458
513
P BNG030 Benign Ependymoma 51 0.458
514
NNL001 Non-Langerhans-Cell Histiocytosis 35 0.458
515
P MMB011 Membranous Nephropathy 50 0.458
516
SPP007 Suppression Amblyopia 38 0.458
517
AMB002 Amblyopia 50 0.458
518
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 0.458
519
c PRC016 Pre-Eclampsia 65 0.458
520
PLC002 Plica Syndrome 35 0.458
521
RTN003 Retinal Ischemia 49 0.458
522
CNN003 Conn's Syndrome 79 0.458
523
P LKM002 Leukemia 67 0.458
524
CHL056 Cheilitis 46 0.458
525
HYP068 Hyperostosis 47 0.458
526
P ECL001 Eclampsia 52 0.458
527
P MYG005 Myoglobinuria 40 0.458
528
P CHN059 Chondrocalcinosis 52 0.458
529
CHL039 Choledocholithiasis 37 0.458
530
c INH020 Inherited Metabolic Disorder 48 0.458
531
DFF006 Diffuse Idiopathic Skeletal Hyperostosis 50 0.458
532
INT079 Intrahepatic Cholangiocarcinoma 51 0.458
533
PLC008 Placenta Disease 49 0.458
534
SPT004 Septic Arthritis 58 0.458
535
ERL001 Early Myoclonic Encephalopathy 62 0.458
536
SYN007 Synovitis 55 0.458
537
MDD011 Mood Disorder 62 0.458
538
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.458
539
LYS002 Lysosomal Storage Disease 51 0.458
540
AMN001 Amenorrhea 54 0.458
541
MLT016 Multicentric Reticulohistiocytosis 39 0.458
542
P URT039 Urticaria 58 0.458
543
GST023 Gastric Ulcer 52 0.458
544
ENT004 Enthesopathy 51 0.458
545
VTR003 Vitreous Detachment 41 0.458
546
P ACT105 Acute Mountain Sickness 52 0.458
547
P BLR006 Biliary Tract Disease 46 0.458
548
DPR016 Depression 65 0.458
549
P ENC018 Encephalopathy 62 0.458
550
HDN002 Head Injury 44 0.458
551
P HYP265 Hypotonia 42 0.458
552
ATN005 Autonomic Dysfunction 46 0.458
553
PRS063 Paresthesia 39 0.458
554
FML330 Familial Lcat Deficiency 33 0.458
555
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 70 0.455
556
P ESP024 Esophagitis 60 0.455
557
CGH001 Cough Variant Asthma 34 0.455
558
BRN024 Bronchitis 67 0.455
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