Search results for Omeprazole

920 hits were found for Omeprazole

# Family MCID Name MIFTS Score
1
P DDN001 Duodenal Ulcer 53 33.102
2
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 30.211
3
PPT005 Peptic Ulcer Disease 58 29.751
4
GST092 Gastroesophageal Reflux 61 28.446
5
P ESP024 Esophagitis 60 25.520
6
HLC007 Helicobacter Pylori Infection 67 25.222
7
GST023 Gastric Ulcer 52 23.733
8
P GST044 Gastritis 55 21.288
9
PPT001 Peptic Esophagitis 52 17.846
10
ZLL002 Zollinger-Ellison Syndrome 55 15.803
12
DYS073 Dysphagia 53 9.700
13
ACT058 Active Peptic Ulcer Disease 56 8.759
14
BRR014 Barrett Esophagus 66 8.736
15
P DRR001 Diarrhea 55 8.299
16
P ATR005 Atrophic Gastritis 50 8.297
17
DDN006 Duodenitis 50 7.391
18
P LRY019 Laryngitis 53 7.055
19
P OVR082 Overgrowth Syndrome 49 6.798
20
LPP008 Lipoprotein Quantitative Trait Locus 65 6.610
21
ART140 Arteries, Anomalies of 53 6.359
22
P EXN002 Exanthem 58 6.254
23
CNS004 Constipation 56 6.171
24
GST030 Gastrinoma 45 6.128
25
INT067 Interstitial Nephritis 46 5.931
26
P URT039 Urticaria 58 5.456
27
c SCL052 Scleroderma, Familial Progressive 61 5.424
28
ESP020 Esophageal Atresia 60 4.999
29
IRN002 Iron Metabolism Disease 57 4.983
30
GST050 Gastrointestinal System Disease 55 4.918
31
ISC004 Ischemia 61 4.704
32
48X005 48,xyyy 39 4.655
33
47X002 47,xyy 48 4.625
34
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 72 4.502
35
CYS001 Cystic Fibrosis 78 4.466
36
P ART022 Arthritis 71 4.465
37
PRP027 Peripheral Vascular Disease 71 4.438
38
P HYP098 Hypereosinophilic Syndrome 66 4.428
39
HRN026 Hernia, Hiatus 47 4.422
40
P ESP035 Esophagitis, Eosinophilic, 1 58 4.394
41
P MLT074 Multiple Endocrine Neoplasia 59 4.379
42
VRC005 Varicose Veins 60 4.370
43
ALL029 Allergic Disease 59 4.274
44
P CRN300 Coronary Heart Disease 1 73 4.116
45
P ANR048 Aniridia 1 64 4.109
46
OST012 Osteoarthritis 77 4.096
47
CYT018 Cytochrome P450 2d6 Variant 26 4.080
48
DDN004 Duodenogastric Reflux 31 4.072
49
P PNC044 Pancreatitis 61 4.052
50
ENT011 Enterocolitis 55 4.041
51
P RHM011 Rheumatoid Arthritis 82 4.034
52
CLT003 Colitis 63 4.012
53
LVR012 Liver Cirrhosis 63 3.967
54
DFC004 Deficiency Anemia 74 3.951
55
P HPT021 Hepatitis 69 3.893
56
GST039 Gastroduodenitis 37 3.880
57
P SYS005 Systemic Scleroderma 74 3.864
58
THY029 Thyroid Carcinoma 51 3.827
59
P ANG015 Angioedema 56 3.822
60
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 3.793
61
P CND004 Candidiasis 58 3.783
62
P MYC007 Myocardial Infarction 70 3.773
63
c ACT071 Acute Kidney Failure 60 3.756
64
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 3.742
65
c MLT156 Multiple Endocrine Neoplasia, Type I 72 3.739
66
P INF037 Inflammatory Bowel Disease 53 3.723
67
c HPT001 Hepatitis C 62 3.720
68
THY111 Thyroid Carcinoma, Familial Medullary 67 3.666
69
CRH001 Crohn's Disease 80 3.656
70
HYP005 Hypokalemia 55 3.639
71
DRM006 Dermatitis 62 3.623
72
P NTR004 Neutropenia 63 3.554
73
GST037 Gastroparesis 52 3.514
74
P AST005 Asthma 76 3.512
75
IRN001 Iron Deficiency Anemia 58 3.511
76
P GST053 Gastric Cancer 83 3.484
77
ASP008 Aspiration Pneumonitis 42 3.478
78
P HRT032 Heart Disease 81 3.417
79
P BLD124 Bleeding Disorder, Platelet-Type, 11 67 3.404
80
VTM033 Vitamin K Deficiency Bleeding 48 3.399
81
c TYP009 Type 2 Diabetes Mellitus 92 3.351
82
VTM002 Vitamin B12 Deficiency 48 3.299
83
BNR002 Bone Resorption Disease 47 3.289
84
c SPN225 Spondyloarthropathy 1 70 3.275
85
BLR002 Bile Reflux 38 3.262
86
P PNC035 Pancreatic Cancer 86 3.251
87
ADL002 Adult Syndrome 70 3.226
88
MCS002 Mucositis 56 3.216
89
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 3.192
90
CRB037 Cerebral Palsy 67 3.131
91
ATM095 Autoimmune Disease 61 3.127
92
c DPH024 Diaphragmatic Hernia, Congenital 64 3.121
93
ASP007 Aspiration Pneumonia 49 3.077
94
GST027 Gastric Lymphoma 46 3.053
95
c ACT027 Acute Pancreatitis 60 3.053
96
P VSC011 Vasculitis 61 3.049
97
c CHR684 Chronic Kidney Disease 69 2.955
98
STM007 Stomatitis 54 2.943
99
DSS032 Disease by Infectious Agent 55 2.931
100
GT001 Gout 64 2.931
101
PNC085 Penicillin Allergy 43 2.916
102
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 2.913
103
GRD001 Giardiasis 46 2.913
104
P KDN018 Kidney Disease 72 2.902
105
P LYM118 Lymphoma 67 2.902
106
P TRN020 Turner Syndrome 67 2.897
107
ULC004 Ulcerative Colitis 74 2.890
108
P ALP008 Alopecia 54 2.872
109
P LVR013 Liver Disease 69 2.870
110
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 50 2.845
111
ANG054 Angina Pectoris 66 2.842
112
P HYP069 Hyperparathyroidism 62 2.836
113
ALC007 Alcohol Dependence 66 2.827
114
CRC006 Carcinoid Syndrome 55 2.824
115
AGN016 Aging 54 2.814
116
P MYP004 Myopathy 67 2.794
117
PRT013 Portal Hypertension 59 2.776
118
PLM134 Pulmonary Fibrosis, Idiopathic 76 2.760
119
P PLM036 Pulmonary Fibrosis 66 2.760
120
HYP266 Hypoxia 57 2.753
121
CNT047 Contact Dermatitis 57 2.738
122
FDL002 Food Allergy 47 2.722
123
SPN051 Spondylitis 51 2.690
124
INF009 Inflammatory Spondylopathy 30 2.690
125
ESP021 Esophageal Cancer 83 2.689
126
P INT068 Intestinal Disease 53 2.672
127
BRN014 Bronchopneumonia 53 2.666
128
PRP080 Peripheral Artery Disease 54 2.662
129
P PSR002 Psoriasis 63 2.638
130
PST011 Pustulosis of Palm and Sole 52 2.638
131
GRN017 Granulocytopenia 42 2.630
132
CLS016 Clostridium Difficile Colitis 49 2.619
133
PRP030 Purpura 54 2.600
134
PRN019 Perinatal Necrotizing Enterocolitis 60 2.575
135
P BCL017 B-Cell Lymphoma 59 2.561
136
PRT251 Proteinuria, Chronic Benign 57 2.541
137
BRN056 Bronchopulmonary Dysplasia 56 2.539
138
IRR002 Irritable Bowel Syndrome 65 2.528
139
c HPT003 Hepatitis a 63 2.502
140
FTT001 Fatty Liver Disease 62 2.498
141
HMN044 Human Immunodeficiency Virus Type 1 78 2.491
142
c HPT073 Hepatitis C Virus 71 2.480
143
PYL006 Pyloric Stenosis 48 2.480
144
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 2.462
145
CSY001 C Syndrome 61 2.447
146
HMN014 Human Immunodeficiency Virus Infectious Disease 54 2.447
147
P KLZ004 Kala-Azar 1 41 2.432
148
SYR010 Syringomyelia, Noncommunicating Isolated 36 2.432
149
HYP025 Hyperphosphatemia 48 2.432
150
LSH001 Leishmaniasis 64 2.432
151
P HYD006 Hydrocephalus 61 2.432
152
P SYR001 Syringomyelia 47 2.432
153
THY125 Thyroid Gland Medullary Carcinoma 48 2.430
154
TRN015 Transient Cerebral Ischemia 63 2.375
155
NNL005 Non-Alcoholic Fatty Liver Disease 63 2.372
156
RHB024 Rhabdomyosarcoma 2 67 2.338
157
c SBC035 Subacute Cutaneous Lupus Erythematosus 34 2.307
158
P CTN003 Cutaneous Lupus Erythematosus 52 2.307
159
MNT001 Mantle Cell Lymphoma 67 2.300
160
c DWL002 Dowling-Degos Disease 1 58 2.280
161
c ACT075 Acute Myocardial Infarction 56 2.271
162
ERY003 Erythema Multiforme 56 2.271
163
P ASP006 Aspergillosis 72 2.271
164
P ENC018 Encephalopathy 62 2.271
165
P PRS040 Prostate Cancer 95 2.242
166
c HYP724 Hyperlipoproteinemia, Type Iii 67 2.231
167
MLC004 Mulchandani-Bhoj-Conlin Syndrome 51 2.221
168
P RRH023 Rare Hereditary Hemochromatosis 54 2.221
169
HMS001 Hemosiderosis 48 2.221
170
LYM019 Lymphosarcoma 46 2.217
171
P INF038 Influenza 68 2.211
172
P HML002 Hemolytic Anemia 62 2.191
173
INV001 Invasive Aspergillosis 49 2.170
174
PLM129 Pulmonary Disease, Chronic Obstructive 74 2.163
175
P DBT009 Diabetes Mellitus 67 2.159
176
CMM005 Common Cold 56 2.157
177
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 2.157
178
CLL021 Collagenous Colitis 42 2.156
179
SYN036 Syncope 45 2.156
180
PYR004 Pyuria 36 2.156
181
P CLC063 Celiac Disease 1 66 2.139
182
MYL069 Myeloma, Multiple 77 2.139
183
AMD002 Amed Syndrome, Digenic 37 2.138
184
KRT002 Keratomalacia 55 2.138
185
P ALZ034 Alzheimer Disease 87 2.128
186
LYM015 Lymphocytic Gastritis 32 2.123
187
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 2.118
188
INT007 Intermediate Coronary Syndrome 54 2.117
189
P THR014 Thrombocytopenia 66 2.117
190
PRT036 Peritonitis 65 2.117
191
c CHR057 Chronic Laryngitis 35 2.117
192
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 46 2.111
193
P CRD119 Cardiac Arrest 67 2.094
194
ESP002 Esophageal Varix 51 2.094
195
SBC016 Subacute Delirium 43 2.094
196
GYN001 Gynecomastia 47 2.060
197
INF021 Infant Gynecomastia 30 2.060
198
CLP006 Clopidogrel Resistance 44 2.038
199
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 31 2.030
200
PRN011 Pernicious Anemia 53 2.030
201
CHL068 Cholestasis 61 2.030
202
NRN004 Neuroendocrine Tumor 59 2.030
203
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 2.005
204
TRM010 Traumatic Brain Injury 51 2.005
205
BRN071 Brain Injury 50 2.005
206
c EPS039 Episodic Pain Syndrome, Familial, 1 42 1.992
207
ESN005 Eosinophilic Gastroenteritis 55 1.986
208
ESP018 Esophageal Candidiasis 48 1.976
209
P FNG006 Feingold Syndrome 1 62 1.963
210
P OST002 Osteoporosis 76 1.957
211
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 1.957
212
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 1.957
213
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 80 1.956
214
c VRL010 Viral Hepatitis 53 1.947
215
SVR004 Severe Combined Immunodeficiency 72 1.947
216
GST045 Gastroenteritis 58 1.947
217
CYT002 Cytokine Deficiency 43 1.947
218
P CHR345 Chronic Pain 50 1.937
219
c TYP008 Type 1 Diabetes Mellitus 70 1.923
220
ANT039 Antisynthetase Syndrome 55 1.908
221
P PLY041 Polymyositis 59 1.891
222
FXD003 Fixed Drug Eruption 34 1.891
223
SXL003 Sexual Disorder 49 1.885
224
IMM167 Immune Deficiency Disease 78 1.885
225
HPT004 Hepatic Coma 43 1.885
226
INF118 Inflammatory Myopathy with Abundant Macrophages 27 1.885
227
GST040 Gastric Adenocarcinoma 67 1.885
228
HPT019 Hepatic Encephalopathy 59 1.885
229
P HYP086 Hypothyroidism 69 1.885
230
CYS010 Cystinosis 62 1.885
231
P PNM007 Pneumonia 67 1.876
232
EXC002 Exocrine Pancreatic Insufficiency 42 1.867
233
P LKM002 Leukemia 67 1.866
234
DFF003 Diffuse Scleroderma 41 1.843
235
c SML038 Small Cell Cancer of the Lung 69 1.821
236
LNG031 Lung Benign Neoplasm 51 1.821
237
CRC014 Carcinoid Tumors, Intestinal 46 1.821
238
P ADL010 Adult Respiratory Distress Syndrome 71 1.821
239
ATX019 Ataxia with Vitamin E Deficiency 44 1.816
240
ACT149 Acetaminophen Metabolism 35 1.815
241
CTN007 Cutaneous Leishmaniasis 62 1.815
242
P CHL066 Cholangitis 52 1.815
243
c SCN007 Secondary Hyperparathyroidism 51 1.815
244
ORL005 Oral Candidiasis 56 1.815
245
LYM143 Lymphoma, Non-Hodgkin, Familial 75 1.813
246
INS024 Insulin-Like Growth Factor I 78 1.753
247
MTB004 Metabolic Acidosis 48 1.753
248
P HYP750 Hypertriglyceridemia, Familial 62 1.753
249
c ACT068 Acute Cystitis 61 1.753
250
ALL014 Allergic Encephalomyelitis 34 1.753
251
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 1.734
252
GLS007 Glossitis 47 1.734
253
SCH014 Schistosomiasis 56 1.734
254
NTR005 Nutritional Deficiency Disease 61 1.712
255
CTS005 Catastrophic Antiphospholipid Syndrome 43 1.712
256
CRY008 Cryopyrin-Associated Periodic Syndrome 48 1.712
257
P MTC069 Mitochondrial Disorders 57 1.697
258
DWN001 Down Syndrome 70 1.682
259
P ALP061 Alopecia, Androgenetic, 1 49 1.682
260
AND014 Androgenic Alopecia 47 1.682
261
P HRP006 Herpes Simplex 65 1.682
262
ADN018 Adenoma 59 1.682
263
PRP016 Paraplegia 52 1.682
264
P ADN016 Adenocarcinoma 63 1.682
265
CNG034 Congestive Heart Failure 69 1.682
266
P OST001 Osteopetrosis 71 1.682
267
P OVR042 Ovarian Cancer 88 1.679
268
P INF032 Infertility 57 1.679
269
P DRM053 Dermatitis, Atopic 65 1.657
270
LYM133 Lymphoma, Hodgkin, Classic 74 1.652
271
INT323 Intraocular Pressure Quantitative Trait Locus 64 1.652
272
TRC109 Tracheoesophageal Fistula with or Without Esophageal Atresia 54 1.652
273
P THY032 Thyroiditis 57 1.652
274
IMP005 Impotence 52 1.652
275
SQM006 Squamous Cell Carcinoma 60 1.649
276
THR100 Thrombocytopenic Purpura, Autoimmune 61 1.645
277
CHR280 Chronic Erosive Gastritis 27 1.645
278
HRP004 Herpes Zoster 61 1.634
279
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 1.626
280
P RCT021 Rectum Cancer 54 1.611
281
P ALC033 Alcohol Use Disorder 61 1.607
282
P URN019 Urinary Tract Infection 49 1.606
283
IGR001 Ige Responsiveness, Atopic 59 1.606
284
ANT078 Antipyrine Metabolism 23 1.606
285
SCH012 Schizoaffective Disorder 50 1.606
286
GLB002 Glioblastoma 67 1.606
287
P BND020 Bone Disease 59 1.606
288
P SLP006 Sleep Apnea 69 1.567
289
P MYC084 Mycobacterium Tuberculosis 1 68 1.562
290
OCL069 Ocular Motor Apraxia 57 1.557
291
P DRM010 Dermatomyositis 61 1.547
292
EXF003 Exfoliative Dermatitis 22 1.547
293
P PLM037 Pulmonary Hypertension 72 1.524
294
SVR097 Severe Cutaneous Adverse Reaction 69 1.524
295
MYL005 Myelofibrosis 71 1.524
296
CHL065 Cholangiocarcinoma 58 1.524
297
ERY066 Erythema Multiforme Major 29 1.524
298
VSC003 Visceral Leishmaniasis 55 1.524
299
P PMP001 Pemphigus 55 1.524
300
CLL003 Cellulitis 53 1.524
301
OVR059 Ovary Adenocarcinoma 49 1.524
302
P RNL007 Renal Tubular Acidosis 50 1.524
303
P SHR001 Short Bowel Syndrome 53 1.524
304
INT079 Intrahepatic Cholangiocarcinoma 51 1.524
305
PNC041 Pancreatic Ductal Adenocarcinoma 51 1.524
306
MGS001 Megaesophagus 44 1.524
307
P BRS047 Breast Cancer 98 1.521
308
OST062 Osteoarthritis with Mild Chondrodysplasia 47 1.521
309
c PRS136 Prostate Cancer, Hereditary, 6 33 1.521
310
CMR002 Coumarin Resistance 59 1.521
311
c PRS130 Prostate Cancer, Hereditary, 8 32 1.521
312
PRS047 Prostatitis 58 1.521
313
SKN016 Skin Disease 63 1.500
314
P RHN004 Rhinitis 57 1.500
315
P MLT020 Multiple Sclerosis 79 1.496
316
c ANM043 Anemia, Congenital Dyserythropoietic, Type Ia 52 1.496
317
P CNG003 Congenital Dyserythropoietic Anemia 48 1.496
318
GST013 Gastrojejunal Ulcer 41 1.496
319
P ATR011 Atrial Fibrillation 66 1.479
320
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 1.457
321
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 1.457
322
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 1.457
323
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 1.457
324
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 1.457
325
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 1.457
326
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 1.457
327
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 1.457
328
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 1.457
329
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 1.457
330
NDL024 Nodal Marginal Zone Lymphoma 37 1.436
331
P ERY036 Erythema Nodosum 49 1.436
332
MCR191 Microscopic Colitis 46 1.436
333
OST159 Osteogenic Sarcoma 66 1.436
334
ARG004 Argyria 26 1.436
335
INT040 Intrinsic Asthma 36 1.436
336
P INT070 Intestinal Obstruction 57 1.436
337
LYM017 Lyme Disease 62 1.436
338
P HYP024 Hypoparathyroidism 55 1.436
339
LPD008 Lipid Metabolism Disorder 62 1.436
340
P HMN038 Human Coronavirus Sensitivity 30 1.427
341
BCT022 Bacterial Infectious Disease 56 1.405
342
STM006 Stomach Disease 47 1.405
343
PHR003 Pharyngitis 58 1.405
344
PPL049 Papillon-Lefevre Syndrome 66 1.397
345
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 63 1.397
346
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 1.397
347
CRB009 Cerebritis 43 1.397
348
SPS003 Spastic Diplegia 53 1.397
349
NNL006 Non-Alcoholic Steatohepatitis 54 1.383
350
c CHR708 Chronic Urticaria 42 1.380
351
HYP056 Hypoglycemia 65 1.380
352
P PRK039 Parkinsonism 55 1.364
353
BCK006 Back Pain 47 1.353
354
MTH086 Methotrexate Toxicity 32 1.337
355
P MYS005 Myositis 56 1.337
356
ATR057 Atrioventricular Block 54 1.337
357
c ATM101 Autoimmune Gastritis 40 1.337
358
P LKM062 Leukemia, Acute Lymphoblastic 69 1.337
359
WLF001 Wolff-Parkinson-White Syndrome 65 1.337
360
TST044 Testicular Torsion 45 1.337
361
URM002 Uremia 47 1.337
362
ACT162 Acute Sensory Ataxic Neuropathy 24 1.337
363
P MST009 Mastocytosis 64 1.337
364
ESN004 Eosinophilic Gastritis 34 1.337
365
P MLN007 Male Infertility 56 1.337
366
HYD002 Hydronephrosis 58 1.337
367
P SLP005 Sleep Disorder 61 1.337
368
PRN035 Perniosis 27 1.337
369
c PNS012 Paine Syndrome 60 1.332
370
END086 End Stage Renal Disease 52 1.316
371
PRS045 Prostatic Hypertrophy 53 1.316
372
NRT001 Neurotic Disorder 56 1.307
373
P FBR017 Fibrosarcoma 56 1.303
374
c LKM061 Leukemia, Acute Myeloid 83 1.262
375
SWL001 Swallowing Disorders 38 1.262
376
MNT002 Mental Depression 57 1.257
377
DPR016 Depression 65 1.257
378
P DMN002 Dementia 66 1.248
379
PSR001 Psoriatic Arthritis 62 1.236
380
THR024 Thrombosis 56 1.236
381
ATM052 Autoimmune Disease 1 36 1.236
382
SCH038 Schopf-Schulz-Passarge Syndrome 51 1.236
383
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 1.236
384
P HNT016 Huntington Disease 73 1.236
385
ACT029 Acute Interstitial Pneumonia 59 1.236
386
THY122 Thyroid Gland Cancer 59 1.236
387
IDP011 Idiopathic Interstitial Pneumonia 59 1.236
388
ENT001 Enterocele 42 1.236
389
ACT167 Acute Generalized Exanthematous Pustulosis 38 1.226
390
c ACT134 Acute Liver Failure 59 1.226
391
INT146 Intervertebral Disc Disease 63 1.226
392
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 1.226
393
DGN001 Degenerative Disc Disease 49 1.226
394
SYS004 Systemic Mastocytosis 63 1.226
395
P SCL009 Sclerosing Cholangitis 48 1.226
396
NCR015 Necrotizing Autoimmune Myopathy 27 1.226
397
P GRF003 Graft-Versus-Host Disease 71 1.218
398
c PSR028 Psoriasis 7 43 1.203
399
c PSR017 Psoriasis 2 53 1.203
400
c PSR018 Psoriasis 13 52 1.203
401
c PSR023 Psoriasis 1 52 1.203
402
c PSR032 Psoriasis 11 47 1.203
403
CRH005 Crohn's Colitis 53 1.195
404
P CLR023 Colorectal Cancer 100 1.191
405
P PRK057 Parkinson Disease, Late-Onset 80 1.191
406
DFF005 Diffuse Large B-Cell Lymphoma 54 1.191
407
SKN019 Skin Melanoma 71 1.191
408
PPT002 Peptic Ulcer Perforation 34 1.191
409
CRB039 Cerebrovascular Disease 66 1.191
410
CNT060 Central Serous Chorioretinopathy 38 1.191
411
PRS129 Prostatic Hyperplasia, Benign 49 1.177
412
OTT002 Otitis Media 71 1.177
413
LPT014 Leptin Deficiency or Dysfunction 78 1.177
414
DRG024 Drug Allergy 40 1.177
415
ACH005 Achalasia 55 1.177
416
NRN001 Neuroendocrine Carcinoma 47 1.177
417
PRS021 Prostatic Adenoma 43 1.177
418
P CNJ013 Conjunctivitis 66 1.139
419
P SLM003 Salmonellosis 54 1.131
420
P NRP001 Neuropathy 60 1.106
421
MLR004 Malaria 80 1.101
422
GST019 Gastrointestinal Stromal Tumor 78 1.101
423
P AMY004 Amyloidosis 70 1.101
424
RSC001 Rosacea 55 1.101
425
PLY131 Polyposis, Skin Pigmentation, Alopecia, and Fingernail Changes 44 1.094
426
PRT019 Protein-Losing Enteropathy 45 1.094
427
P HYP077 Hypertrichosis 46 1.094
428
DDN027 Duodenum Disease 34 1.094
429
P ACN011 Acne 57 1.094
430
P UVT001 Uveitis 57 1.094
431
PRM236 Primary Biliary Cholangitis 60 1.094
432
P AGM001 Agammaglobulinemia 68 1.094
433
RYN005 Raynaud Phenomenon 45 1.094
434
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 1.041
435
LYM042 Lymphocytic Colitis 41 1.019
436
c ALB016 Albinism, Oculocutaneous, Type Vii 38 1.019
437
PST092 Posttransplant Acute Limbic Encephalitis 28 1.019
438
ALL007 Allergic Urticaria 28 1.019
439
P HDC001 Headache 57 1.019
440
c BLD140 Blood Group, I System 46 1.012
441
P SZR006 Seizure Disorder 70 0.978
442
c DRM054 Dermatitis, Atopic, 2 46 0.937
443
GLS018 Glass Syndrome 61 0.937
444
HNT002 Hantavirus Pulmonary Syndrome 55 0.937
445
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 0.937
446
LCH014 Lichen Amyloidosis 28 0.930
447
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 0.930
448
ALL003 Allergic Rhinitis 67 0.930
449
P PHC003 Pheochromocytoma 69 0.930
450
P FML011 Familial Adenomatous Polyposis 71 0.930
451
CHR710 Chronic Spontaneous Urticaria 45 0.930
452
c MLT160 Multiple Endocrine Neoplasia, Type Iia 67 0.930
453
c HYP836 Hypercholesterolemia, Familial, 1 73 0.930
454
ADR040 Adrenal Gland Pheochromocytoma 46 0.930
455
SVR001 Severe Acute Respiratory Syndrome 67 0.930
456
TRC005 Tracheal Stenosis 43 0.930
457
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.930
458
PLS006 Plasmodium Vivax Malaria 51 0.930
459
OVR094 Ovarian Epithelial Cancer 39 0.930
460
OST115 Osteonecrosis of the Jaw 41 0.921
461
c RTN047 Retinitis Pigmentosa 18 46 0.921
462
RYN001 Raynaud Disease 50 0.921
463
P RTN024 Retinoblastoma 73 0.921
465
PTY001 Pityriasis Rosea 44 0.921
466
ALL006 Allergic Asthma 56 0.921
467
ALL010 Allergic Contact Dermatitis 56 0.921
468
P LCT001 Lactic Acidosis 51 0.921
469
OST003 Osteonecrosis 61 0.921
470
c ATM011 Autoimmune Hepatitis 63 0.921
471
P INT099 Intrahepatic Cholestasis of Pregnancy 62 0.921
472
DRG026 Drug Reaction with Eosinophilia and Systemic Symptoms 45 0.921
473
c INF071 Inflammatory Bowel Disease 1 65 0.871
474
P LRY029 Laryngomalacia 48 0.850
475
c DRR009 Diarrhea 6 45 0.850
476
ANG049 Angioedema Induced by Ace Inhibitors 40 0.846
477
c OVR114 Ovarian Cancer 1 59 0.846
478
PRP083 Porphyria, Acute Intermittent 65 0.846
479
PRP082 Porphyria, Congenital Erythropoietic 56 0.846
480
CPR004 Coproporphyria, Hereditary 57 0.846
481
P MYL006 Myeloid Leukemia 61 0.846
482
ACT078 Acute Porphyria 49 0.846
483
P PRP029 Porphyria 60 0.846
484
CTN011 Cutaneous Porphyria 45 0.846
485
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.846
486
c CHR064 Chronic Monocytic Leukemia 36 0.846
487
GLC096 Galactorrhea 40 0.832
488
P THL005 Thalassemia 56 0.832
489
P FML018 Familial Mediterranean Fever 73 0.832
490
c BTT014 Beta-Thalassemia 72 0.832
491
DDN011 Duodenal Atresia 48 0.832
492
c PNC106 Pancreatic Agenesis 1 51 0.832
493
ACT003 Acute Kidney Tubular Necrosis 46 0.832
494
RPD005 Rapidly Involuting Congenital Hemangioma 46 0.832
495
BRR002 Barrett's Adenocarcinoma 37 0.832
496
DYS011 Dyskinesia of Esophagus 40 0.832
497
ANR004 Anuria 44 0.832
498
INS001 Insulinoma 59 0.832
499
NPH009 Nephrolithiasis 54 0.832
500
ESP023 Esophageal Disease 52 0.832
501
MLK006 Milk Allergy 47 0.832
502
MCR011 Microinvasive Gastric Cancer 41 0.832
503
CHL147 Chlamydia Pneumonia 47 0.832
504
GTR002 Goiter 53 0.832
505
CLN015 Colon Adenocarcinoma 65 0.832
506
BRC012 Brucellosis 66 0.832
507
CHL123 Chlamydia 58 0.832
508
PNC034 Pancreas Disease 50 0.832
509
VSC002 Vascular Dementia 60 0.832
510
GLC036 Glucagonoma 46 0.832
511
APN008 Apnea, Obstructive Sleep 67 0.806
512
CRD132 Cardiac Conduction Defect 60 0.802
513
SCK003 Sickle Cell Anemia 74 0.802
514
c HYP595 Hypertension, Essential 85 0.802
515
PLM001 Pulmonary Tuberculosis 69 0.802
516
c HRD002 Hereditary Angioedema 62 0.802
517
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.775
518
VLV044 Vulvar Intraepithelial Neoplasia 43 0.775
519
MTC005 Mitochondrial Metabolism Disease 45 0.775
520
CHR682 Chronic Bilirubin Encephalopathy 37 0.775
521
c EHL080 Ehlers-Danlos Syndrome, Musculocontractural Type, 1 52 0.775
522
c PNC108 Pancreatitis, Hereditary 69 0.775
523
HYP781 Hypoascorbemia 52 0.775
524
CVD001 Covid-19 57 0.775
525
MST019 Mastoiditis 41 0.775
526
TNS007 Taeniasis 46 0.775
527
ANL018 Analbuminemia 53 0.775
528
ATN011 Autoinflammation with Infantile Enterocolitis 45 0.775
529
BLC012 Bile Acid Malabsorption, Primary 44 0.775
530
BHR001 Behr Syndrome 51 0.775
531
SCP002 Scapuloperoneal Spinal Muscular Atrophy 55 0.775
532
CRN241 Corneal Dystrophy, Congenital Stromal 49 0.775
533
c FML363 Familial Adult Myoclonic Epilepsy 45 0.775
534
P MSC003 Muscular Atrophy 52 0.775
535
DRM011 Dermatophytosis 52 0.775
536
CRV002 Cervix Uteri Carcinoma in Situ 47 0.775
537
CRV038 Cervical Squamous Cell Carcinoma 58 0.775
538
ACT055 Actinomycosis 55 0.775
539
RCK004 Rickets 68 0.775
540
CYS005 Cysticercosis 60 0.775
541
CRN017 Coronary Thrombosis 46 0.775
542
P SPN046 Spinal Muscular Atrophy 63 0.775
543
TNP001 Tinea Pedis 48 0.775
544
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.775
545
P MLN008 Melanoma 76 0.775
546
DDN009 Duodenal Obstruction 34 0.775
547
P CRV039 Cervicitis 52 0.775
548
TNC001 Tinea Cruris 34 0.775
549
P INS002 in Situ Carcinoma 53 0.775
550
RTC005 Reticulosarcoma 48 0.775
551
CRV045 Cervical Intraepithelial Neoplasia 39 0.775
552
SRT004 Serotonin Syndrome 54 0.721
553
ACR008 Acrocallosal Syndrome 70 0.721
554
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.721
555
P ANP001 Anaplastic Large Cell Lymphoma 61 0.721
556
MYL009 Myelodysplastic Syndrome 67 0.721
557
HMN047 Human Cytomegalovirus Infection 57 0.721
558
CLR108 Colorectal Adenoma 64 0.721
559
c PRG020 Paragangliomas 3 39 0.721
560
P HPT023 Hepatocellular Carcinoma 96 0.721
561
CLR109 Colorectal Adenocarcinoma 50 0.721
562
P NRB001 Neuroblastoma 66 0.721
563
VPM001 Vipoma 49 0.721
564
P LCH002 Lichen Planus 54 0.721
565
P RNV001 Renovascular Hypertension 49 0.721
566
TRC003 Trichomoniasis 53 0.721
567
LNG099 Lung Disease 62 0.721
568
CHL004 Cholelithiasis 49 0.721
569
c PRC016 Pre-Eclampsia 65 0.721
570
TLN003 Telangiectasis 51 0.721
571
BRN012 Bronchiolitis Obliterans 56 0.721
572
P NPH012 Nephrotic Syndrome 60 0.721
573
KRT009 Keratosis 53 0.721
574
P RSP003 Respiratory Failure 74 0.721
575
BRN024 Bronchitis 67 0.721
576
P PRP019 Peripheral Nervous System Disease 58 0.721
577
TNS001 Tenosynovial Giant Cell Tumor 40 0.721
578
BRN002 Bronchiolitis 57 0.721
579
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 60 0.721
580
P HYP009 Hypertrophic Pyloric Stenosis 41 0.721
581
GNR004 Generalized Anxiety Disorder 55 0.721
582
ENT004 Enthesopathy 51 0.721
583
PRS063 Paresthesia 39 0.721
584
c DNT047 Dentinogenesis Imperfecta Type 2 35 0.721
585
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 0.714
586
PMP014 Pemphigoid 51 0.714
587
BLL006 Bullous Pemphigoid 61 0.714
588
SQM013 Squamous Cell Carcinoma, Head and Neck 73 0.675
589
ANX004 Anoxia 40 0.588
590
PRQ002 Paraquat Poisoning 28 0.588
591
SDD008 Sudden Sensorineural Hearing Loss 41 0.588
592
PPL052 Papillomatosis, Confluent and Reticulated 34 0.588
593
PLY150 Polykaryocytosis Inducer 29 0.588
594
THR032 Thoracolaryngopelvic Dysplasia 26 0.588
595
c THR092 Thrombophilia Due to Thrombin Defect 74 0.588
596
P MLT008 Multinodular Goiter 42 0.588
597
P RST001 Restless Legs Syndrome 52 0.588
598
MRG003 Marginal Zone B-Cell Lymphoma 52 0.588
599
LNN001 Lennox-Gastaut Syndrome 61 0.588
600
HRT040 Hirata Disease 38 0.588
601
FSH003 Fish Allergy 30 0.588
602
EXR010 Exercise-Induced Bronchoconstriction 34 0.588
603
KRT019 Keratitis, Hereditary 66 0.588
604
BLD063 Bile Duct Cysts 42 0.588
605
ABN011 Abnormal Hair, Joint Laxity, and Developmental Delay 50 0.588
606
NPH091 Nephrolithiasis, Calcium Oxalate 61 0.588
607
HRW001 Hair Whorl 35 0.588
608
HYP020 Hyperprolactinemia 63 0.588
609
P FLL037 Follicular Lymphoma 74 0.588
610
NRR001 Neuroretinitis 42 0.588
611
P LCT002 Lactose Intolerance 52 0.588
612
ADN067 Adenoid Hypertrophy 39 0.588
613
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 0.588
614
P EMB005 Embryonal Rhabdomyosarcoma 53 0.588
615
P RHB003 Rhabdomyosarcoma 66 0.588
616
RTN023 Retinitis 46 0.588
617
P ACT008 Actinic Keratosis 54 0.588
618
P HMR005 Hemorrhoid 49 0.588
619
P SKN015 Skin Carcinoma 71 0.588
620
P SYP003 Syphilis 59 0.588
621
P ART023 Arthropathy 61 0.588
622
ACQ007 Acquired Immunodeficiency Syndrome 59 0.588
623
ILS001 Ileus 50 0.588
624
NRM005 Neuromuscular Disease 63 0.588
625
CMB007 Combined Immunodeficiency 57 0.588
626
P SNS001 Sensorineural Hearing Loss 59 0.588
627
NSP002 Nasopharyngitis 45 0.588
628
BRN028 Brain Cancer 74 0.588
629
DNG003 Dengue Disease 65 0.588
630
PNC001 Pancytopenia 53 0.588
631
CNN003 Conn's Syndrome 79 0.588
632
TXC005 Toxic Shock Syndrome 62 0.588
633
c BSL007 Basal Cell Carcinoma 68 0.588
634
DMP001 Dumping Syndrome 43 0.588
635
RYS001 Reye Syndrome 49 0.588
636
OPT003 Opiate Dependence 49 0.588
637
CYT005 Cytomegalovirus Retinitis 50 0.588
638
HMP005 Hemiplegia 54 0.588
639
c PRM005 Primary Hyperparathyroidism 59 0.588
640
P CHN059 Chondrocalcinosis 52 0.588
641
ERL001 Early Myoclonic Encephalopathy 62 0.588
642
INT066 Interstitial Lung Disease 60 0.588
643
MDD011 Mood Disorder 62 0.588
644
P GLM007 Glomerulonephritis 60 0.588
645
KLB003 Klebsiella Pneumonia 50 0.588
646
AMN003 Amnestic Disorder 54 0.588
647
ISL001 Islet Cell Tumor 56 0.588
648
P LMY004 Leiomyosarcoma 62 0.588
649
HYP057 Hypervitaminosis D 37 0.588
650
SFT003 Soft Tissue Sarcoma 57 0.588
651
SPL018 Splenomegaly 49 0.588
652
BWN006 Bowen's Disease 32 0.588
653
ACT011 Acute Contagious Conjunctivitis 42 0.551
654
AND005 Androgen Insensitivity Syndrome, Mild 21 0.551
655
c PRM038 Primary Agammaglobulinemia 47 0.551
656
c ANM038 Anemia, Autoimmune Hemolytic 64 0.505
657
DFF010 Diffuse Alopecia Areata 25 0.505
658
DFF036 Differentiated Thyroid Carcinoma 51 0.505
659
P OBS001 Obstructive Jaundice 48 0.505
660
c INT064 Intermediate Uveitis 54 0.505
661
PCH007 Pouchitis 42 0.416
662
P DBT005 Diabetes Insipidus 54 0.416
663
SND005 Sandifer Syndrome 25 0.416
664
DSC009 Discoid Lupus Erythematosus 43 0.416
665
SVR055 Severe Immune-Mediated Enteropathy 22 0.416
666
STN013 Stenotrophomonas Maltophilia Infection 26 0.416
667
SPS057 Spasticity 42 0.416
668
P BLD134 Bladder Cancer 79 0.416
669
PTT048 Pituitary Adenoma, Prolactin-Secreting 64 0.416
670
c GLL024 Gallbladder Disease 1 52 0.416
671
CRD223 Cardiac Arrhythmia 63 0.416
672
P LPR021 Leprosy 3 71 0.416
673
LPD012 Lipoid Congenital Adrenal Hyperplasia 70 0.416
674
CYC008 Cyclic Vomiting Syndrome 46 0.416
675
c DRM040 Dermatitis Herpetiformis, Familial 35 0.416
676
ANX010 Anxiety 70 0.416
677
END057 Endometrial Cancer 72 0.416
678
P SCH015 Schizophrenia 74 0.416
679
LPM012 Lipomatosis, Multiple 60 0.416
680
OBS002 Obsessive-Compulsive Disorder 68 0.416
681
CRT072 Creutzfeldt-Jakob Disease 68 0.416
682
c ATR087 Atrial Standstill 1 74 0.416
683
BLR027 Blue Rubber Bleb Nevus 40 0.416
684
c PRG042 Progressive Familial Heart Block, Type Ia 66 0.416
685
c ART138 Aortic Aneurysm, Familial Abdominal, 1 61 0.416
686
ANS021 Anisocoria 25 0.416
687
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.416
688
VLV047 Volvulus of Midgut 52 0.416
689
MNR012 Meniere Disease 56 0.416
690
P HML033 Hemolytic Uremic Syndrome, Atypical 1 69 0.416
691
CNG064 Congenital Chloride Diarrhea 34 0.416
692
EPD015 Epidemic Typhus 44 0.416
693
P OCL002 Oculocutaneous Albinism 59 0.416
694
HYP017 Hypophosphatemia 49 0.416
695
ATS010 Autosomal Recessive Disease 42 0.416
696
c MJR022 Major Affective Disorder 8 38 0.416
697
DSR012 Disordered Steroidogenesis Due to Cytochrome P450 Oxidoreductase Deficiency 39 0.416
698
TTH002 Tooth Agenesis 61 0.416
699
ART074 Aortic Dissection 53 0.416
700
WTH001 Withdrawal Disorder 48 0.416
701
P CTN015 Cutaneous T Cell Lymphoma 48 0.416
702
CGN006 Cogan Syndrome 49 0.416
703
CRS005 Crest Syndrome 36 0.416
704
P LYM033 Lymphoproliferative Syndrome 59 0.416
705
EXT033 Extrapulmonary Tuberculosis 45 0.416
706
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.416
707
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 32 0.416
708
c PRG043 Progressive Familial Heart Block, Type Ib 54 0.416
709
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.416
710
EWN003 Ewing Sarcoma 70 0.416
711
c MJR024 Major Affective Disorder 9 41 0.416
712
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.416
713
EMN001 Emanuel Syndrome 34 0.416
714
c PRD040 Periodontitis, Chronic 52 0.416
715
c TLN006 Telangiectasia, Hereditary Hemorrhagic, Type 1 55 0.416
716
c THY102 Thyroid Cancer, Nonmedullary, 2 55 0.416
717
c PYL018 Pyloric Stenosis, Infantile Hypertrophic, 1 35 0.416
718
P ATT013 Attention Deficit-Hyperactivity Disorder 64 0.416
719
P HYP726 Hypercalcemia, Infantile, 1 58 0.416
720
INT051 Intussusception 52 0.416
721
P GLM040 Glioma Susceptibility 1 71 0.416
722
MLD001 Melioidosis 67 0.416
723
MNN043 Meningioma, Familial 79 0.416
724
VLL006 Villous Adenoma 41 0.416
725
ORL015 Oral Squamous Cell Carcinoma 43 0.416
726
GST071 Gastrointestinal Carcinoma 46 0.416
727
OPT010 Optic Papillitis 38 0.416
728
OST017 Osteomyelitis 63 0.416
729
CRD137 Cardiogenic Shock 56 0.416
730
FML063 Familial Glucocorticoid Deficiency 58 0.416
731
PRT037 Pertussis 65 0.416
732
P HML001 Hemolytic-Uremic Syndrome 52 0.416
733
NPH003 Nephrocalcinosis 49 0.416
734
ACS001 Acoustic Neuroma 56 0.416
735
P OPN001 Open-Angle Glaucoma 55 0.416
736
PNC028 Pancreatic Steatorrhea 26 0.416
737
FCL090 Facial Cleft 30 0.416
738
FSC002 Fascioliasis 44 0.416
739
P LPS004 Lupus Erythematosus 61 0.416
740
MCR004 Macroglobulinemia 49 0.416
741
DVR002 Diverticulitis 46 0.416
742
c LRG001 Large Cell Carcinoma 48 0.416
743
SMT003 Somatostatinoma 52 0.416
744
AVN001 Avian Influenza 61 0.416
745
CLC001 Calciphylaxis 51 0.416
746
P RPD001 Rapidly Progressive Glomerulonephritis 44 0.416
747
SCR011 Scrapie 39 0.416
748
MCR020 Microsporidiosis 49 0.416
749
NRM001 Neuromyelitis Optica 61 0.416
750
CHR078 Chorioretinitis 51 0.416
751
MCC002 Mucocutaneous Leishmaniasis 47 0.416
752
EXP004 Exophthalmos 51 0.416
753
CHC001 Chickenpox 57 0.416
754
CHR074 Choriocarcinoma 46 0.416
755
TXC002 Toxic Encephalopathy 52 0.416
756
P SBR004 Seborrheic Dermatitis 44 0.416
757
P BCL004 B-Cell Non-Hodgkin Lymphoma 42 0.416
758
P TRM003 Tremor 48 0.416
759
P CYS018 Cystitis 59 0.416
760
INT002 Intermittent Claudication 61 0.416
761
c ACT076 Acute Myocarditis 47 0.416
762
LNT001 Linitis Plastica 29 0.416
763
PNC129 Pancreatic Adenocarcinoma 65 0.416
764
PRC013 Pericarditis 53 0.416
765
P EPL164 Epilepsy 68 0.416
766
P OPT006 Optic Nerve Disease 58 0.416
767
CHL067 Cholecystitis 60 0.416
768
P BPL003 Bipolar Disorder 56 0.416
769
PPL021 Papilledema 49 0.416
770
PNM008 Pneumothorax 54 0.416
771
P HRM001 Hermansky-Pudlak Syndrome 65 0.416
772
ART016 Aortic Aneurysm 68 0.416
773
GRN011 Granulomatous Gastritis 25 0.416
774
HRT012 Heart Valve Disease 53 0.416
775
BLR004 Biliary Dyskinesia 37 0.416
776
SPN035 Spindle Cell Sarcoma 54 0.416
777
P PNC025 Panic Disorder 52 0.416
778
SPN011 Spongiotic Dermatitis 31 0.416
779
SCR001 Secretory Meningioma 40 0.416
780
LYM002 Lymphoplasmacyte-Rich Meningioma 35 0.416
781
EBL001 Ebola Hemorrhagic Fever 56 0.416
782
BRN009 Burning Mouth Syndrome 51 0.416
783
INT071 Intestinal Perforation 49 0.416
784
P PRD008 Periodontitis 64 0.416
785
MCR141 Mucormycosis 59 0.416
786
P DRM007 Dermatitis Herpetiformis 54 0.416
787
PLM005 Pleomorphic Lipoma 40 0.416
788
P LNG064 Lung Cancer Susceptibility 3 70 0.416
789
ADN002 Adenoiditis 36 0.416
790
PLR008 Pleurisy 50 0.416
791
c DLT002 Dilated Cardiomyopathy 78 0.416
792
P PNV001 Panuveitis 49 0.416
793
CRN019 Coronary Artery Vasospasm 47 0.416
794
LWC001 Low Compliance Bladder 45 0.416
795
CGH001 Cough Variant Asthma 34 0.416
796
THY001 Thyroid Crisis 30 0.416
797
ACR007 Acromegaly 70 0.416
798
ADT003 Auditory System Disease 49 0.416
799
BRX001 Bruxism 51 0.416
800
SCR008 Scrub Typhus 57 0.416
801
BLR001 Biliary Atresia 55 0.416
802
FLL027 Fallopian Tube Carcinoma 67 0.416
803
GST020 Gastric Antral Vascular Ectasia 40 0.416
804
ANG011 Angiodysplasia 42 0.416
805
ENM002 Enamel Erosion 25 0.416
806
DRG002 Drug-Induced Hepatitis 42 0.416
807
CHL014 Cholera 62 0.416
808
FNG017 Fungal Infectious Disease 54 0.416
809
P HMR003 Hemorrhagic Disease 59 0.416
810
P GRN010 Granular Cell Tumor 41 0.416
811
MLG169 Malignant Astrocytoma 57 0.416
812
SCL002 Scleredema Adultorum 45 0.416
813
P ECL001 Eclampsia 52 0.416
814
P END044 Endometriosis 62 0.416
815
DPH001 Diphtheria 59 0.416
816
CHR008 Choroiditis 48 0.416
817
RTN001 Retinal Vasculitis 46 0.416
818
P THR005 Thrombotic Thrombocytopenic Purpura 64 0.416
819
SRC014 Sarcoma 65 0.416
820
P HYP040 Hypospadias 51 0.416
821
P MCR010 Microcephaly 60 0.416
822
CRD001 Cardiac Tamponade 43 0.416
823
DSS009 Disseminated Intravascular Coagulation 57 0.416
824
TTN003 Tetanus 65 0.416
825
P PRN023 Prion Disease 60 0.416
826
GST025 Gastric Body Carcinoma 9 0.416
827
P BRT004 Bartter Disease 58 0.416
828
MDD010 Middle Ear Disease 46 0.416
829
GST036 Gastric Leiomyosarcoma 31 0.416
830
PNC027 Pancreatic Gastrinoma 30 0.416
831
P HYP076 Hyperthyroidism 53 0.416
832
RDT001 Radiation Cystitis 31 0.416
833
P LPS002 Liposarcoma 64 0.416
834
WRN003 Wernicke Encephalopathy 46 0.416
835
SGN002 Signet Ring Cell Adenocarcinoma 46 0.416
836
TYP007 Typhoid Fever 64 0.416
837
ISC001 Ischemic Neuropathy 27 0.416
838
P HYP050 Hyperinsulinemic Hypoglycemia 57 0.416
839
P SCL015 Scleritis 48 0.416
840
OPS001 Opisthorchiasis 41 0.416
841
BNG018 Benign Paroxysmal Positional Nystagmus 41 0.416
842
PLS007 Plasmodium Falciparum Malaria 52 0.416
843
LST001 Listeriosis 59 0.416
844
SPN021 Spinal Meningioma 50 0.416
845
RGH001 Right Bundle Branch Block 47 0.416
846
PNM003 Pneumatosis Cystoides Intestinalis 32 0.416
847
HYP014 Hyperuricemia 51 0.416
848
NRM004 Neuroma 49 0.416
849
FNG003 Fungal Esophagitis 21 0.416
850
ALB002 Albinism 47 0.416
851
ANS003 Anisakiasis 38 0.416
852
c ACT135 Acute Graft Versus Host Disease 51 0.416
853
CYT014 Cytochrome P450 Oxidoreductase Deficiency 34 0.416
854
P MYC008 Myocarditis 59 0.416
855
PTH003 Pathologic Nystagmus 52 0.416
856
HNS001 Hansen's Disease 32 0.416
857
THR035 Thrombasthenia 48 0.416
858
CRB089 Cerebral Beriberi 19 0.416
859
PST053 Postherpetic Neuralgia 40 0.416
860
P MYC033 Myoclonus 47 0.416
861
P ATM020 Autoimmune Enteropathy 34 0.416
862
HMP009 Haemophilus Influenzae 41 0.416
863
LKP003 Leukoplakia 39 0.416
864
BRN055 Bronchogenic Cyst 26 0.416
865
P CHR342 Chiari Malformation 41 0.416
866
CLL026 Collagenous Gastritis 13 0.416
867
DPS001 Dipsogenic Diabetes Insipidus 22 0.416
868
ATM060 Autoimmune Atrophic Gastritis 19 0.416
869
c CHR417 Chronic Graft Versus Host Disease 55 0.416
870
CHR281 Chronic Hiccups 28 0.416
871
LCH008 Lichen Planus Pigmentosus 23 0.416
872
ORL013 Oral Lichen Planus 46 0.416
873
P PST059 Pustular Psoriasis 38 0.416
874
FRN020 Frontal Fibrosing Alopecia 48 0.416
875
SPC030 Specific Language Disorder 25 0.390
876
VSL002 Visual Epilepsy 39 0.390
877
P VSC018 Visceral Steatosis 32 0.390
878
P ATS364 Autism 69 0.386
879
P LNG032 Lung Cancer 98 0.386
880
VLV042 Vulvar Vestibulitis Syndrome 37 0.386
881
c LKM056 Leukemia, Chronic Lymphocytic 2 48 0.386
882
c CRD186 Ceroid Lipofuscinosis, Neuronal, 3 63 0.386
883
STR067 Stroke, Ischemic 80 0.386
884
P LKM071 Leukemia, Chronic Lymphocytic 75 0.386
885
c ANG068 Angioedema, Hereditary, Type I 57 0.386
886
NRN005 Neuronal Ceroid-Lipofuscinoses 61 0.386
887
c ATS007 Autism Spectrum Disorder 72 0.386
888
c BNG023 Benign Familial Infantile Epilepsy 57 0.386
889
C1N001 C1 Inhibitor Deficiency 43 0.386
890
GBM001 Gaba Aminotransferase Deficiency 29 0.386
891
c FML001 Familial Atrial Fibrillation 65 0.386
892
P TRC086 Trichohepatoenteric Syndrome 1 59 0.386
893
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 35 0.386
894
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 63 0.386
895
P MJR001 Major Depressive Disorder 68 0.386
896
P NJM001 Nijmegen Breakage Syndrome 76 0.386
897
GTL001 Gitelman Syndrome 65 0.386
898
RNL114 Renal Cell Carcinoma, Nonpapillary 80 0.386
899
CMP040 Complement Component 4, Partial Deficiency of 34 0.386
900
PNG002 Pain Agnosia 51 0.386
901
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 36 0.386
902
SPR126 Superior Semicircular Canal Dehiscence 41 0.386
903
ORB013 Orbital Disease 42 0.386
904
ORB008 Orbital Plasma Cell Granuloma 31 0.386
905
P ALP009 Alopecia Areata 59 0.386
906
END040 Endogenous Depression 55 0.386
907
SNS003 Sensory Peripheral Neuropathy 52 0.386
908
P NRN021 Neuronal Ceroid Lipofuscinosis 65 0.386
909
BRN038 Bronchial Disease 51 0.386
910
HNC001 Henoch-Schoenlein Purpura 54 0.386
911
PLS009 Plasma Cell Neoplasm 64 0.386
912
MDS022 Mediastinitis 47 0.386
913
PLC008 Placenta Disease 49 0.386
914
LRY017 Laryngeal Disease 45 0.386
915
NRN002 Neuronitis 31 0.386
916
P SPN052 Spondyloarthropathy 55 0.386
917
P SCK005 Sickle Cell Disease 56 0.386
918
c HMG029 Hemoglobin Se Disease 40 0.386
919
CHL079 Children's Interstitial Lung Disease 26 0.386
920
P NRV007 Nervous System Disease 67 0.386
Content
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