Search results for Morphine

1060 hits were found for Morphine

# Family MCID Name MIFTS Score
1
MRP001 Morphine Dependence 41 8.086
2
PNG002 Pain Agnosia 51 1.306
3
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.492
4
c PNS012 Paine Syndrome 61 0.485
5
P CHR345 Chronic Pain 44 0.469
6
WTH001 Withdrawal Disorder 48 0.467
7
OPT003 Opiate Dependence 50 0.369
8
48X005 48,xyyy 39 0.336
9
CNS004 Constipation 58 0.324
10
OPD006 Opioid Addiction 48 0.322
11
DPR016 Depression 63 0.247
12
DRG003 Drug Dependence 47 0.209
13
OPD001 Opioid Abuse 46 0.203
14
PRT037 Pertussis 65 0.194
15
P TRM003 Tremor 54 0.194
16
BCK006 Back Pain 42 0.194
17
P DRR001 Diarrhea 55 0.192
18
P NRB001 Neuroblastoma 72 0.183
19
AMN003 Amnestic Disorder 54 0.183
20
ANX010 Anxiety 73 0.180
21
MNT002 Mental Depression 58 0.177
22
P PTS002 Ptosis 53 0.177
23
P SZR006 Seizure Disorder 56 0.172
24
NNT008 Neonatal Abstinence Syndrome 41 0.172
25
VSL002 Visual Epilepsy 59 0.171
26
ALL026 Allergic Hypersensitivity Disease 62 0.165
27
SBC016 Subacute Delirium 44 0.164
28
P SBS003 Substance Abuse 55 0.160
29
P SCL018 Scoliosis 60 0.157
30
P RSP003 Respiratory Failure 74 0.155
31
ISC004 Ischemia 58 0.155
32
P HDC001 Headache 57 0.155
33
P MYC007 Myocardial Infarction 70 0.152
34
P TRN020 Turner Syndrome 67 0.151
35
CHL067 Cholecystitis 57 0.149
36
c ACT075 Acute Myocardial Infarction 57 0.149
37
P SCK005 Sickle Cell Disease 50 0.146
38
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.141
39
ILS001 Ileus 51 0.141
40
P CNR004 Cone-Rod Dystrophy 2 73 0.136
41
P KDN018 Kidney Disease 72 0.136
42
c RHB024 Rhabdomyosarcoma 2 67 0.136
43
P NRP001 Neuropathy 56 0.136
44
P MYC033 Myoclonus 46 0.134
45
OST012 Osteoarthritis 78 0.133
46
ADL002 Adult Syndrome 70 0.133
47
P SLP006 Sleep Apnea 69 0.131
48
P BNC003 Bone Cancer 58 0.131
49
CHL079 Children's Interstitial Lung Disease 26 0.129
50
SPN186 Spinal Cord Injury 60 0.127
51
MCS002 Mucositis 56 0.127
52
LNG099 Lung Disease 60 0.124
53
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.122
54
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.120
55
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.120
56
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.120
57
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.120
58
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.120
59
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.120
60
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.120
61
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.120
62
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.120
63
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.120
64
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.120
65
IDP070 Idiopathic Scoliosis 42 0.120
66
HYP266 Hypoxia 57 0.118
67
PLM010 Pulmonary Edema 54 0.118
68
CYT002 Cytokine Deficiency 42 0.118
69
ATX019 Ataxia with Vitamin E Deficiency 42 0.118
70
HYP066 Hyperglycemia 61 0.116
71
P AGN002 Agnosia 55 0.114
72
CNG034 Congestive Heart Failure 69 0.112
73
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.110
74
SPS057 Spasticity 45 0.108
75
MNN017 Mononeuropathy 42 0.108
76
P HRT032 Heart Disease 75 0.105
77
c FNC043 Fanconi Anemia, Complementation Group E 62 0.105
78
SCK003 Sickle Cell Anemia 74 0.103
79
HYP056 Hypoglycemia 66 0.103
80
LPP008 Lipoprotein Quantitative Trait Locus 62 0.103
81
P PRP019 Peripheral Nervous System Disease 58 0.103
82
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.099
83
DFC004 Deficiency Anemia 70 0.099
84
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.099
85
P LVR013 Liver Disease 68 0.099
86
ACQ007 Acquired Immunodeficiency Syndrome 60 0.099
87
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.096
88
CHL014 Cholera 59 0.096
89
47X002 47,xyy 49 0.096
90
LPT014 Leptin Deficiency or Dysfunction 74 0.094
91
HMN044 Human Immunodeficiency Virus Type 1 71 0.094
92
APN008 Apnea, Obstructive Sleep 64 0.094
93
P PNC044 Pancreatitis 61 0.094
94
DBT010 Diabetic Neuropathy 54 0.094
95
ALC007 Alcohol Dependence 66 0.091
96
P HRP006 Herpes Simplex 65 0.091
97
PRT036 Peritonitis 64 0.091
98
P GLM045 Glioma 63 0.091
99
NPH091 Nephrolithiasis, Calcium Oxalate 60 0.091
100
c MGR028 Migraine with or Without Aura 1 67 0.089
101
ANG054 Angina Pectoris 66 0.089
102
c MCL013 Mucolipidosis Iv 66 0.089
103
GLL048 Glial Tumor 45 0.089
104
c GZP005 Gaze Palsy, Familial Horizontal, with Progressive Scoliosis 1 44 0.089
105
P BRS047 Breast Cancer 97 0.083
106
TTN003 Tetanus 65 0.083
107
ING001 Inguinal Hernia 60 0.083
108
OCL069 Ocular Motor Apraxia 51 0.083
109
SPR126 Superior Semicircular Canal Dehiscence 40 0.083
110
c HMG029 Hemoglobin Se Disease 39 0.083
111
P CLR023 Colorectal Cancer 99 0.081
112
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.081
113
DWN001 Down Syndrome 70 0.081
114
P PNM007 Pneumonia 68 0.081
115
c ACT027 Acute Pancreatitis 60 0.081
116
PRP016 Paraplegia 52 0.081
117
P LNG032 Lung Cancer 98 0.078
118
c HYP595 Hypertension, Essential 84 0.078
119
IMM167 Immune Deficiency Disease 78 0.078
120
P EXN002 Exanthem 57 0.078
121
INT007 Intermediate Coronary Syndrome 55 0.078
122
P DDN001 Duodenal Ulcer 52 0.078
123
ART140 Arteries, Anomalies of 52 0.078
124
HLX001 Helix Syndrome 47 0.078
125
VRS002 Virus-Associated Trichodysplasia Spinulosa 32 0.078
126
P CRD119 Cardiac Arrest 67 0.075
127
P ENC018 Encephalopathy 61 0.075
128
SYN007 Synovitis 54 0.075
129
PST021 Postpartum Depression 50 0.075
130
PST053 Postherpetic Neuralgia 40 0.075
131
ANX004 Anoxia 40 0.075
132
PLC002 Plica Syndrome 36 0.075
133
P ART022 Arthritis 69 0.071
134
ART016 Aortic Aneurysm 69 0.071
135
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.071
136
PST028 Post-Traumatic Stress Disorder 58 0.071
137
THR024 Thrombosis 57 0.071
138
PNM008 Pneumothorax 56 0.071
139
NPH009 Nephrolithiasis 55 0.071
140
P RST001 Restless Legs Syndrome 54 0.071
141
MCN017 Meconium Ileus 52 0.071
142
ACT084 Acute Stress Disorder 47 0.071
143
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.071
144
BLR004 Biliary Dyskinesia 38 0.071
145
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.071
146
LVR012 Liver Cirrhosis 62 0.068
147
APP008 Appendicitis 61 0.068
148
INT066 Interstitial Lung Disease 60 0.068
149
STT001 Status Epilepticus 60 0.068
150
P INT070 Intestinal Obstruction 58 0.068
151
NWB001 Newborn Respiratory Distress Syndrome 58 0.068
152
MTN003 Motion Sickness 53 0.068
153
BHR001 Behr Syndrome 51 0.068
154
BRN071 Brain Injury 49 0.068
155
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.068
156
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.068
157
BNN005 Bunion 33 0.068
158
INF118 Inflammatory Myopathy with Abundant Macrophages 28 0.068
159
CYT018 Cytochrome P450 2d6 Variant 27 0.068
160
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.065
161
P DMN002 Dementia 66 0.065
162
MDD011 Mood Disorder 62 0.065
163
HRP004 Herpes Zoster 60 0.065
164
PRT058 Pure Autonomic Failure 59 0.065
165
P ALC033 Alcohol Use Disorder 58 0.065
166
P URT039 Urticaria 58 0.065
167
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.065
168
PTH003 Pathologic Nystagmus 52 0.065
169
P ECL001 Eclampsia 50 0.065
170
STM007 Stomatitis 50 0.065
171
DYS073 Dysphagia 50 0.065
172
HDN002 Head Injury 46 0.065
173
URL001 Urolithiasis 45 0.065
174
ENT001 Enterocele 39 0.065
175
MYL069 Myeloma, Multiple 85 0.061
176
P GST053 Gastric Cancer 83 0.061
177
AST005 Asthma 76 0.061
178
GLB015 Glioblastoma Multiforme 75 0.061
179
P LKM002 Leukemia 68 0.061
180
P VSC007 Vascular Disease 63 0.061
181
P CRN300 Coronary Heart Disease 1 63 0.061
182
P MYL006 Myeloid Leukemia 60 0.061
183
FBR047 Fibromyalgia 58 0.061
184
RSP019 Respiratory Distress Syndrome in Premature Infants 58 0.061
185
P CRD246 Cardiovascular System Disease 57 0.061
186
P DBT005 Diabetes Insipidus 55 0.061
187
END040 Endogenous Depression 55 0.061
188
HRT012 Heart Valve Disease 53 0.061
189
c XNT010 Xanthinuria, Type I 53 0.061
190
TRM010 Traumatic Brain Injury 51 0.061
191
ACT017 Acute Chest Syndrome 51 0.061
192
DGN001 Degenerative Disc Disease 48 0.061
193
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.061
194
HRN003 Heroin Dependence 44 0.061
195
ARC002 Arachnoiditis 42 0.061
196
RDN001 Reading Disorder 40 0.061
197
SPN354 Spinal Arachnoiditis 36 0.061
198
c LKM005 Leukemia, T-Cell, Chronic 34 0.061
199
c LKM061 Leukemia, Acute Myeloid 84 0.057
200
c THR092 Thrombophilia Due to Thrombin Defect 73 0.057
201
KHL003 Kohlschutter-Tonz Syndrome 65 0.057
202
c PRC016 Pre-Eclampsia 63 0.057
203
INT146 Intervertebral Disc Disease 63 0.057
204
TXC005 Toxic Shock Syndrome 62 0.057
205
PNM010 Pneumothorax, Primary Spontaneous 60 0.057
206
c ACT071 Acute Kidney Failure 60 0.057
207
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.057
208
ANR040 Aneurysm 59 0.057
209
P BCL017 B-Cell Lymphoma 58 0.057
210
P GLL020 Gallbladder Disease 57 0.057
211
STR081 Stormorken Syndrome 57 0.057
212
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.057
213
AGN016 Aging 56 0.057
214
NRT001 Neurotic Disorder 53 0.057
215
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.057
216
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.057
217
CNT017 Central Nervous System Origin Vertigo 45 0.057
218
ESP021 Esophageal Cancer 90 0.053
219
P PNC035 Pancreatic Cancer 84 0.053
220
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.053
221
c LKM063 Leukemia, Chronic Myeloid 72 0.053
222
CRB037 Cerebral Palsy 69 0.053
223
P LKM062 Leukemia, Acute Lymphoblastic 69 0.053
224
P LYM118 Lymphoma 68 0.053
225
OBS002 Obsessive-Compulsive Disorder 68 0.053
226
P PLM037 Pulmonary Hypertension 67 0.053
227
PPL049 Papillon-Lefevre Syndrome 65 0.053
228
P ADL010 Adult Respiratory Distress Syndrome 65 0.053
229
P DBT009 Diabetes Mellitus 64 0.053
230
LSH001 Leishmaniasis 63 0.053
231
FTT001 Fatty Liver Disease 61 0.053
232
CMP010 Complex Regional Pain Syndrome 58 0.053
233
LYM027 Lymphopenia 58 0.053
234
PLS011 Plasmacytoma 56 0.053
235
RFL001 Reflex Sympathetic Dystrophy 54 0.053
236
PLS009 Plasma Cell Neoplasm 51 0.053
237
LNG031 Lung Benign Neoplasm 51 0.053
238
CHL004 Cholelithiasis 49 0.053
239
LPT006 Leptin Receptor Deficiency 48 0.053
240
P BNG032 Benign Mesothelioma 46 0.053
241
DVR002 Diverticulitis 43 0.053
242
TRP009 Triple X Syndrome 42 0.053
243
GST020 Gastric Antral Vascular Ectasia 41 0.053
244
P KLZ004 Kala-Azar 1 41 0.053
245
P SCL057 Scoliosis, Isolated 1 41 0.053
246
NPH098 Nephrolithiasis, X-Linked Recessive, with Renal Failure 41 0.053
247
CRB079 Cerebrospinal Fluid Leak 35 0.053
248
P HPT023 Hepatocellular Carcinoma 100 0.048
249
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.048
250
CYS001 Cystic Fibrosis 81 0.048
251
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.048
252
P LKM071 Leukemia, Chronic Lymphocytic 79 0.048
253
P OST002 Osteoporosis 74 0.048
254
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.048
255
c HPT073 Hepatitis C Virus 72 0.048
256
OTT002 Otitis Media 72 0.048
257
c EXD008 Exudative Vitreoretinopathy 1 71 0.048
258
P EPL164 Epilepsy 71 0.048
259
P AMY004 Amyloidosis 70 0.048
260
MYL009 Myelodysplastic Syndrome 70 0.048
261
MYL005 Myelofibrosis 70 0.048
262
P TTR001 Tetralogy of Fallot 70 0.048
263
PLY001 Polycythemia Vera 69 0.048
264
LYM133 Lymphoma, Hodgkin, Classic 69 0.048
265
MNT001 Mantle Cell Lymphoma 69 0.048
266
P ESS003 Essential Thrombocythemia 68 0.048
267
BRN024 Bronchitis 68 0.048
268
BRK010 Burkitt Lymphoma 67 0.048
269
CRB039 Cerebrovascular Disease 67 0.048
270
P FLL037 Follicular Lymphoma 67 0.048
271
MYC006 Mycosis Fungoides 66 0.048
272
P MNN013 Meningitis 66 0.048
273
MYL031 Myeloproliferative Neoplasm 66 0.048
274
IRR002 Irritable Bowel Syndrome 65 0.048
275
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.048
276
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.048
277
MSC007 Muscle Hypertrophy 64 0.048
278
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.048
279
ANR007 Anorexia Nervosa 63 0.048
280
P ART023 Arthropathy 62 0.048
281
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.048
282
DRM006 Dermatitis 61 0.048
283
P ENC004 Encephalitis 61 0.048
284
WLD007 Waldenstroem's Macroglobulinemia 61 0.048
285
SZR001 Sezary's Disease 60 0.048
286
CRD223 Cardiac Arrhythmia 60 0.048
287
P CHR285 Chronic Myelomonocytic Leukemia 60 0.048
288
IDP011 Idiopathic Interstitial Pneumonia 59 0.048
289
SPN027 Spinal Stenosis 59 0.048
290
P SLP005 Sleep Disorder 59 0.048
291
PLM033 Pulmonary Embolism 59 0.048
292
P BRS044 Breast Adenocarcinoma 59 0.048
293
P GLL022 Guillain-Barre Syndrome 59 0.048
294
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.048
295
c ACT073 Acute Leukemia 58 0.048
296
P ANP001 Anaplastic Large Cell Lymphoma 58 0.048
297
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.048
298
BRN056 Bronchopulmonary Dysplasia 57 0.048
299
P PLY018 Polycythemia 56 0.048
300
P ADL017 Adult T-Cell Leukemia 56 0.048
301
P GST044 Gastritis 56 0.048
302
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.048
303
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.048
304
HRY003 Hairy Cell Leukemia 55 0.048
305
CRT017 Cartilage Disease 54 0.048
306
LYM040 Lymphoblastic Lymphoma 54 0.048
307
NNL006 Non-Alcoholic Steatohepatitis 54 0.048
308
P CNT005 Central Nervous System Lymphoma 53 0.048
309
FNG017 Fungal Infectious Disease 53 0.048
310
TXC002 Toxic Encephalopathy 53 0.048
311
c GLL024 Gallbladder Disease 1 53 0.048
312
ANG046 Angioimmunoblastic T-Cell Lymphoma 52 0.048
313
MRG003 Marginal Zone B-Cell Lymphoma 52 0.048
314
P RCT021 Rectum Cancer 52 0.048
315
SPL004 Splenic Marginal Zone Lymphoma 51 0.048
316
END086 End Stage Renal Disease 51 0.048
317
c ALM001 Al Amyloidosis 50 0.048
318
c PRM012 Primary Polycythemia 50 0.048
319
RDC002 Radiculopathy 50 0.048
320
HYP080 Hypogonadism 50 0.048
321
TCL002 T-Cell Large Granular Lymphocyte Leukemia 49 0.048
322
c THR090 Thrombocythemia 1 49 0.048
323
PCT003 Pectus Excavatum 49 0.048
324
MCR004 Macroglobulinemia 49 0.048
325
c FLL041 Follicular Lymphoma 1 49 0.048
326
CHR563 Chronic Eosinophilic Leukemia 48 0.048
327
c LKM056 Leukemia, Chronic Lymphocytic 2 48 0.048
328
MNC006 Monoclonal Gammopathy of Uncertain Significance 48 0.048
329
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.048
330
c PRM226 Primary Central Nervous System Lymphoma 48 0.048
331
PRL017 Prolymphocytic Leukemia 47 0.048
332
PLS025 Plasmablastic Lymphoma 47 0.048
333
CRD137 Cardiogenic Shock 47 0.048
334
LYM019 Lymphosarcoma 46 0.048
335
CLN045 Colonic Benign Neoplasm 46 0.048
336
P HMR005 Hemorrhoid 46 0.048
337
EXT010 Extramedullary Plasmacytoma 45 0.048
339
DMP001 Dumping Syndrome 44 0.048
340
c PRM038 Primary Agammaglobulinemia 44 0.048
341
BNM001 Bone Marrow Cancer 43 0.048
342
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.048
343
DRG024 Drug Allergy 42 0.048
344
CHR286 Chronic Neutrophilic Leukemia 42 0.048
345
LRG008 Large Granular Lymphocyte Leukemia 41 0.048
346
c PLM150 Pulmonary Alveolar Proteinosis, Acquired 40 0.048
347
ALG001 Algoneurodystrophy 39 0.048
348
SPS019 Spastic Paraparesis 38 0.048
349
NDL020 Nodal Marginal Zone B-Cell Lymphoma 34 0.048
350
c TCL024 T-Cell Non-Hodgkin Lymphoma 34 0.048
351
c RST012 Restless Legs Syndrome 1 34 0.048
352
RFR002 Refractory Hairy Cell Leukemia 33 0.048
353
LYM048 Lymphoma, Large-Cell, Immunoblastic 29 0.048
354
CLS052 Classic Hairy Cell Leukemia 27 0.048
355
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 27 0.048
356
FTL073 Fetal Anticonvulsant Syndrome 26 0.048
357
ADG002 Audiogenic Seizures 25 0.048
358
P PRS040 Prostate Cancer 97 0.043
359
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.043
360
BRN028 Brain Cancer 74 0.043
361
PRP027 Peripheral Vascular Disease 71 0.043
362
CNT097 Central Hypoventilation Syndrome, Congenital 71 0.043
363
P MYS003 Myasthenia Gravis 68 0.043
364
P MJR001 Major Depressive Disorder 68 0.043
365
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.043
366
P SKN015 Skin Carcinoma 66 0.043
367
P NSP012 Nasopharyngeal Carcinoma 66 0.043
368
P PLM036 Pulmonary Fibrosis 65 0.043
369
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.043
370
P THY023 Thymoma 65 0.043
371
CLF027 Cleft Palate, Isolated 64 0.043
372
P ADN016 Adenocarcinoma 64 0.043
373
P ANR048 Aniridia 1 63 0.043
374
c HPT001 Hepatitis C 62 0.043
375
VRL011 Viral Infectious Disease 61 0.043
376
P KDN017 Kidney Cancer 60 0.043
377
TRG002 Trigeminal Neuralgia 60 0.043
378
SQM006 Squamous Cell Carcinoma 60 0.043
379
P PTN014 Patent Ductus Arteriosus 1 60 0.043
380
ORL011 Oral Cancer 60 0.043
381
P CYS018 Cystitis 59 0.043
382
CNT047 Contact Dermatitis 58 0.043
383
DSS008 Disease of Mental Health 58 0.043
384
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.043
385
HYP005 Hypokalemia 55 0.043
386
NRG002 Neurogenic Bladder 55 0.043
387
P INF037 Inflammatory Bowel Disease 54 0.043
388
PRS045 Prostatic Hypertrophy 53 0.043
389
P LCT002 Lactose Intolerance 53 0.043
390
GST023 Gastric Ulcer 53 0.043
391
EXP004 Exophthalmos 52 0.043
392
c THY107 Thymoma, Familial 52 0.043
393
SPS003 Spastic Diplegia 51 0.043
394
NRM004 Neuroma 51 0.043
395
SPN019 Spondylolisthesis 51 0.043
396
P AST007 Astrocytoma 51 0.043
397
P OVR082 Overgrowth Syndrome 50 0.043
398
c DYS119 Dystonia 9 50 0.043
399
P CMP008 Compartment Syndrome 49 0.043
400
SPL018 Splenomegaly 48 0.043
401
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 47 0.043
402
ATN005 Autonomic Dysfunction 46 0.043
403
HPT004 Hepatic Coma 45 0.043
404
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 45 0.043
405
SPS007 Spastic Cerebral Palsy 45 0.043
406
RTR001 Retrograde Amnesia 44 0.043
407
P BLP003 Blepharospasm 44 0.043
408
URT014 Ureterolithiasis 44 0.043
409
PLY068 Polysubstance Abuse 43 0.043
410
PRS063 Paresthesia 41 0.043
411
ANG049 Angioedema Induced by Ace Inhibitors 40 0.043
412
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.043
414
c PRS136 Prostate Cancer, Hereditary, 6 33 0.043
415
c PRS130 Prostate Cancer, Hereditary, 8 32 0.043
416
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.043
417
STR067 Stroke, Ischemic 81 0.037
418
c HYP836 Hypercholesterolemia, Familial, 1 73 0.037
419
RNL065 Renal Cell Carcinoma, Papillary, 1 73 0.037
420
P PHC003 Pheochromocytoma 71 0.037
421
P OCL013 Oculodentodigital Dysplasia 69 0.037
422
P HYP086 Hypothyroidism 69 0.037
423
MST024 Mastocytosis, Cutaneous 69 0.037
424
P THR014 Thrombocytopenia 67 0.037
425
GST092 Gastroesophageal Reflux 67 0.037
426
GRG001 Greig Cephalopolysyndactyly Syndrome 66 0.037
427
c MCR129 Microvascular Complications of Diabetes 1 66 0.037
428
c SML038 Small Cell Cancer of the Lung 65 0.037
429
P PRS038 Personality Disorder 65 0.037
430
c DBT099 Diabetes Mellitus, Type I 65 0.037
431
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.037
432
P ESP024 Esophagitis 62 0.037
433
NTR005 Nutritional Deficiency Disease 62 0.037
434
P INT143 Interstitial Cystitis 61 0.037
435
P VNT002 Ventricular Septal Defect 60 0.037
436
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.037
437
HYD002 Hydronephrosis 60 0.037
438
ETN001 Eating Disorder 60 0.037
439
P LYM033 Lymphoproliferative Syndrome 59 0.037
440
PPT005 Peptic Ulcer Disease 59 0.037
441
MNR012 Meniere Disease 57 0.037
442
c VSC019 Vesicoureteral Reflux 1 57 0.037
443
c MST023 Mesothelioma, Malignant 57 0.037
444
BLR008 Bilirubin Metabolic Disorder 57 0.037
445
GST050 Gastrointestinal System Disease 56 0.037
446
BRN004 Brain Edema 56 0.037
447
P PLM034 Pulmonary Emphysema 55 0.037
448
CHR100 Chronic Ulcer of Skin 55 0.037
449
CLF004 Cleft Lip/palate 54 0.037
450
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 54 0.037
451
PST046 Post-Transplant Lymphoproliferative Disease 53 0.037
452
P EPD016 Epidermolysis Bullosa 53 0.037
453
CLF001 Cleft Lip 53 0.037
454
INT075 Intracranial Hypertension 53 0.037
455
IMP005 Impotence 52 0.037
456
P NRC002 Narcolepsy 52 0.037
457
FML037 Female Breast Cancer 52 0.037
458
LMY002 Leiomyoma 52 0.037
460
AVD001 Avoidant Personality Disorder 51 0.037
461
IFP001 Ifap Syndrome with or Without Bresheck Syndrome 51 0.037
462
P HYP040 Hypospadias 51 0.037
463
c INF145 Infantile Liver Failure Syndrome 1 50 0.037
464
NTR046 Neutrophil Migration 50 0.037
465
MTB004 Metabolic Acidosis 50 0.037
466
HRT011 Heart Septal Defect 50 0.037
467
ATY042 Atypical Chronic Myeloid Leukemia 49 0.037
468
MYL075 Myelodysplastic/myeloproliferative Neoplasm 49 0.037
469
P MST002 Mast-Cell Leukemia 49 0.037
470
CCN002 Cocaine Abuse 49 0.037
471
ACT029 Acute Interstitial Pneumonia 49 0.037
472
INT054 Intraocular Lymphoma 48 0.037
473
SBS004 Substance Dependence 48 0.037
474
SXL003 Sexual Disorder 47 0.037
475
CRD001 Cardiac Tamponade 47 0.037
476
LYM012 Lymphoplasmacytic Lymphoma 47 0.037
477
GST071 Gastrointestinal Carcinoma 47 0.037
478
CNT033 Central Nervous System Cancer 47 0.037
479
HYD005 Hydrocele 46 0.037
480
ADR040 Adrenal Gland Pheochromocytoma 46 0.037
481
INT253 Intestinal Benign Neoplasm 45 0.037
482
PRL008 Paralytic Ileus 45 0.037
483
LYM051 Lymphomatoid Granulomatosis 45 0.037
484
LTH001 Lethal Midline Granuloma 44 0.037
485
HRT015 Heritable Pulmonary Arterial Hypertension 44 0.037
486
PTT037 Pituitary Tumors 44 0.037
487
P BCL004 B-Cell Non-Hodgkin Lymphoma 44 0.037
488
CRB090 Cerebral Hypoxia 44 0.037
489
P MJR007 Major Affective Disorder 1 43 0.037
490
URM005 Uremic Pruritus 42 0.037
491
P CRN035 Cranial Nerve Palsy 42 0.037
492
49X006 49, Xxxxy Syndrome 41 0.037
493
RFL002 Reflex Epilepsy 40 0.037
494
c CHR682 Chronic Bilirubin Encephalopathy 39 0.037
495
ACT167 Acute Generalized Exanthematous Pustulosis 37 0.037
496
MYL067 Myeloproliferative Disorder, Chronic, with Eosinophilia 37 0.037
497
SYS070 Systemic Epstein-Barr Virus-Positive T-Cell Lymphoma of Childhood 36 0.037
498
HRW001 Hair Whorl 36 0.037
499
ACL001 Acalculous Cholecystitis 35 0.037
500
PPL052 Papillomatosis, Confluent and Reticulated 33 0.037
501
SML008 Small Intestine Lymphoma 33 0.037
502
c RNG008 Ring Chromosome 13 31 0.037
503
SNG003 Single Ventricular Heart 30 0.037
504
DVR001 Diverticulitis of Colon 25 0.037
505
c DMN005 Diamond-Blackfan Anemia 2 25 0.037
506
NNT018 Neonatal Herpes 24 0.037
507
PNS018 Pain Sensitivity Quantitative Trait Locus 1 23 0.037
508
HYP705 Hyperadrenalism 20 0.037
509
P OVR042 Ovarian Cancer 88 0.030
510
P ALZ034 Alzheimer Disease 88 0.030
511
MLR004 Malaria 81 0.030
512
P RHM011 Rheumatoid Arthritis 80 0.030
513
P BLD134 Bladder Cancer 79 0.030
514
INS024 Insulin-Like Growth Factor I 79 0.030
515
CRV035 Cervical Cancer 76 0.030
516
END057 Endometrial Cancer 74 0.030
517
CRH001 Crohn's Disease 74 0.030
518
SVR004 Severe Combined Immunodeficiency 73 0.030
519
c SPN225 Spondyloarthropathy 1 73 0.030
520
P MLT020 Multiple Sclerosis 72 0.030
521
P HNT016 Huntington Disease 72 0.030
522
P FML011 Familial Adenomatous Polyposis 72 0.030
523
P GRF003 Graft-Versus-Host Disease 72 0.030
524
FBR012 Fabry Disease 72 0.030
525
P BRG001 Brugada Syndrome 71 0.030
526
c CHR684 Chronic Kidney Disease 70 0.030
527
P MLN008 Melanoma 69 0.030
528
CHL065 Cholangiocarcinoma 68 0.030
529
CMM004 Common Variable Immunodeficiency 68 0.030
530
SKN019 Skin Melanoma 68 0.030
531
PNC129 Pancreatic Adenocarcinoma 68 0.030
532
c MCL062 Mucolipidosis Ii Alpha/beta 68 0.030
533
P HPT021 Hepatitis 67 0.030
534
c PRD013 Periodic Fever, Familial, Autosomal Dominant 67 0.030
535
PSY004 Psychotic Disorder 67 0.030
536
P MLG056 Malignant Hyperthermia 67 0.030
537
OST159 Osteogenic Sarcoma 66 0.030
538
P DYS154 Dystonia 65 0.030
539
PRP001 Propionic Acidemia 65 0.030
540
ATX029 Ataxia, Early-Onset, with Oculomotor Apraxia and Hypoalbuminemia 65 0.030
541
KWS002 Kawasaki Disease 65 0.030
542
P MST009 Mastocytosis 64 0.030
543
c EPS035 Episodic Ataxia, Type 2 63 0.030
544
c DPH024 Diaphragmatic Hernia, Congenital 63 0.030
545
c ACT068 Acute Cystitis 63 0.030
546
CTN007 Cutaneous Leishmaniasis 62 0.030
547
CRC021 Carcinosarcoma 62 0.030
548
CHL068 Cholestasis 61 0.030
549
DCB001 Decubitus Ulcer 61 0.030
550
c LPM012 Lipomatosis, Multiple 60 0.030
551
P TXP001 Toxoplasmosis 60 0.030
552
HPT019 Hepatic Encephalopathy 60 0.030
553
P ATR010 Atrial Heart Septal Defect 60 0.030
554
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.030
555
P CTR002 Cataract 60 0.030
556
PRT013 Portal Hypertension 59 0.030
557
c PCH015 Pachyonychia Congenita 1 59 0.030
558
IGR001 Ige Responsiveness, Atopic 59 0.030
559
PRN019 Perinatal Necrotizing Enterocolitis 59 0.030
560
CRY035 Cryptorchidism, Unilateral or Bilateral 58 0.030
561
SPR004 Supravalvular Aortic Stenosis 58 0.030
562
P MTR012 Mitral Valve Disease 58 0.030
563
P CND004 Candidiasis 58 0.030
564
P END033 Endocarditis 57 0.030
565
TNS005 Tonsillitis 57 0.030
566
P BPL003 Bipolar Disorder 56 0.030
567
P PYL005 Pyelonephritis 56 0.030
568
P FBR017 Fibrosarcoma 56 0.030
569
HMT008 Hematuria, Benign Familial 56 0.030
570
c INT072 Intestinal Pseudo-Obstruction 56 0.030
571
BCT022 Bacterial Infectious Disease 56 0.030
572
ALL010 Allergic Contact Dermatitis 56 0.030
573
INT030 Intracranial Aneurysm 56 0.030
574
ATR057 Atrioventricular Block 55 0.030
575
c FML035 Familial Hyperlipidemia 55 0.030
576
P MLN007 Male Infertility 55 0.030
577
VSC003 Visceral Leishmaniasis 55 0.030
578
P DYS193 Dystonia 11, Myoclonic 55 0.030
579
P STR020 Strabismus 55 0.030
580
HMP005 Hemiplegia 55 0.030
581
GLC003 Glucose Intolerance 54 0.030
582
P ALP008 Alopecia 54 0.030
583
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 0.030
584
GST037 Gastroparesis 54 0.030
585
PRC013 Pericarditis 54 0.030
586
AMN001 Amenorrhea 54 0.030
587
P LTR001 Lateral Sclerosis 54 0.030
588
MYM001 Myoma 54 0.030
589
SNS003 Sensory Peripheral Neuropathy 54 0.030
590
PTT009 Pituitary Gland Disease 54 0.030
591
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.030
592
BRN038 Bronchial Disease 53 0.030
593
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 53 0.030
594
DNT012 Dental Caries 53 0.030
595
INT051 Intussusception 53 0.030
596
P SPN429 Spinocerebellar Ataxia, Autosomal Recessive, with Axonal Neuropathy 2 52 0.030
597
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.030
598
ACR041 Acromelic Frontonasal Dysostosis 52 0.030
599
NRT004 Neuritis 52 0.030
600
BWN001 Bowen-Conradi Syndrome 52 0.030
601
PPT001 Peptic Esophagitis 52 0.030
602
SPN051 Spondylitis 51 0.030
603
c SCN036 Secondary Progressive Multiple Sclerosis 51 0.030
604
MYL001 Myelitis 51 0.030
605
ENT011 Enterocolitis 51 0.030
606
c PNC106 Pancreatic Agenesis 1 51 0.030
607
HYP781 Hypoascorbemia 51 0.030
608
BRX001 Bruxism 50 0.030
609
STT002 Status Asthmaticus 50 0.030
610
P MYT002 Myotonic Dystrophy 49 0.030
611
VRC001 Varicocele 49 0.030
612
CCN001 Cocaine Dependence 48 0.030
613
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 48 0.030
614
PTC002 Potocki-Lupski Syndrome 48 0.030
615
PNC034 Pancreas Disease 48 0.030
616
PRD004 Prediabetes Syndrome 47 0.030
617
P CLL015 Collagen Disease 47 0.030
618
SRT004 Serotonin Syndrome 47 0.030
619
P OVR046 Ovarian Cyst 47 0.030
620
P BLD051 Blood Coagulation Disease 46 0.030
621
CMP090 Complement Component 3 Deficiency, Autosomal Recessive 45 0.030
622
P TRN034 Transverse Myelitis 45 0.030
623
CYN002 Cyanosis, Transient Neonatal 45 0.030
624
NWC001 Newcastle Disease 45 0.030
625
CRB004 Cerebral Artery Occlusion 45 0.030
626
IMM136 Immune System Disease 45 0.030
627
CRT015 Carotid Artery Occlusion 45 0.030
628
MYF001 Myofibroma 45 0.030
629
BCT021 Bacterial Sepsis 44 0.030
630
LWC001 Low Compliance Bladder 43 0.030
631
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 43 0.030
632
STL007 Steel Syndrome 43 0.030
633
P PRT026 Parotitis 42 0.030
634
MYF002 Myofascial Pain Syndrome 42 0.030
635
MCH006 Mechanical Strabismus 42 0.030
636
DBT002 Diabetic Autonomic Neuropathy 41 0.030
637
c MJR024 Major Affective Disorder 9 41 0.030
638
IMM080 Immunodeficiency 23 40 0.030
639
PLM005 Pleomorphic Lipoma 40 0.030
640
OCL010 Ocular Hypotension 39 0.030
641
PLC009 Placenta Praevia 39 0.030
642
SCR015 Scarlet Fever 39 0.030
643
c ACR088 Aicardi-Goutieres Syndrome 3 39 0.030
644
c PLM022 Pulmonary Valve Insufficiency 39 0.030
645
SPR024 Supratentorial Cancer 39 0.030
646
CDQ001 Cauda Equina Syndrome 38 0.030
647
c MJR022 Major Affective Disorder 8 38 0.030
648
INF039 Infratentorial Cancer 38 0.030
649
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 37 0.030
650
CHL013 Cholecystolithiasis 37 0.030
651
PST030 Postcholecystectomy Syndrome 33 0.030
652
HND015 Hand Skill, Relative 33 0.030
653
SPN031 Supine Hypotensive Syndrome 32 0.030
654
INF009 Inflammatory Spondylopathy 31 0.030
655
CHR281 Chronic Hiccups 31 0.030
656
PLX004 Plexopathy 30 0.030
657
RSP007 Respiratory Distress Syndrome, Infant 30 0.030
658
HTT002 Hutterite Cerebroosteonephrodysplasia Syndrome 26 0.030
659
URT049 Urate Oxidase, Pseudogene 25 0.030
660
HPS001 Hip Subluxation 20 0.030
661
OPD004 Opioid Dependence 1 16 0.030
662
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.022
663
NRL016 Neural Tube Defects 82 0.022
664
P ATX030 Ataxia-Telangiectasia 82 0.022
665
P GLM040 Glioma Susceptibility 1 81 0.022
666
P RTT002 Rett Syndrome 80 0.022
667
P LNG064 Lung Cancer Susceptibility 3 78 0.022
668
P PRK057 Parkinson Disease, Late-Onset 78 0.022
669
PHN003 Phenylketonuria 75 0.022
670
P SCH015 Schizophrenia 74 0.022
671
ULC004 Ulcerative Colitis 73 0.022
672
SCH036 Scheie Syndrome 72 0.022
673
c MLT156 Multiple Endocrine Neoplasia, Type I 72 0.022
674
APR006 Apert Syndrome 70 0.022
675
c PNC108 Pancreatitis, Hereditary 70 0.022
676
P MYP004 Myopathy 70 0.022
677
P RTH006 Rothmund-Thomson Syndrome, Type 2 69 0.022
678
ACR008 Acrocallosal Syndrome 69 0.022
679
P MCP040 Mucopolysaccharidosis-Plus Syndrome 69 0.022
680
c PRG042 Progressive Familial Heart Block, Type Ia 69 0.022
681
EWN003 Ewing Sarcoma 69 0.022
682
P ANG001 Angelman Syndrome 69 0.022
683
P INF038 Influenza 68 0.022
684
RCK004 Rickets 68 0.022
685
FCT007 Factor Vii Deficiency 67 0.022
686
OMN001 Omenn Syndrome 67 0.022
687
P BLD062 Bile Duct Cancer 67 0.022
688
WLF001 Wolff-Parkinson-White Syndrome 66 0.022
689
P CLC063 Celiac Disease 1 66 0.022
690
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.022
691
CHD001 Chediak-Higashi Syndrome 66 0.022
692
P MSC005 Muscular Dystrophy 66 0.022
693
SPN209 Spondyloepiphyseal Dysplasia with Congenital Joint Dislocations 66 0.022
694
ART001 Arterial Tortuosity Syndrome 66 0.022
695
c FML346 Familial Adenomatous Polyposis 1 66 0.022
696
c HRD010 Hereditary Spastic Paraplegia 66 0.022
697
AND002 Androgen Insensitivity Syndrome 66 0.022
698
CHR593 Chromosome 16p13.3 Deletion Syndrome, Proximal 66 0.022
699
P ATR011 Atrial Fibrillation 66 0.022
700
P HYD006 Hydrocephalus 66 0.022
701
P DRM053 Dermatitis, Atopic 66 0.022
702
P NRV007 Nervous System Disease 66 0.022
703
GTL001 Gitelman Syndrome 65 0.022
704
c FML001 Familial Atrial Fibrillation 65 0.022
705
LWC002 Lowe Oculocerebrorenal Syndrome 65 0.022
706
SRC014 Sarcoma 65 0.022
707
ATM096 Autoimmune Polyendocrine Syndrome, Type I, with or Without Reversible Metaphyseal Dysplasia 65 0.022
708
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.022
709
BRR014 Barrett Esophagus 65 0.022
710
c ART101 Aortic Valve Disease 2 65 0.022
711
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 65 0.022
712
TBC004 Tobacco Addiction 64 0.022
713
GT001 Gout 64 0.022
714
DGR001 Digeorge Syndrome 64 0.022
715
PRP083 Porphyria, Acute Intermittent 64 0.022
716
LYM017 Lyme Disease 64 0.022
717
HYP020 Hyperprolactinemia 64 0.022
718
OST017 Osteomyelitis 64 0.022
719
P RHB003 Rhabdomyosarcoma 63 0.022
720
TYP007 Typhoid Fever 63 0.022
721
PLG002 Plague 63 0.022
722
c MLG084 Malignant Fibrous Histiocytoma 63 0.022
723
P CRG003 Crigler-Najjar Syndrome, Type I 63 0.022
724
ACT119 Acute Promyelocytic Leukemia 63 0.022
725
P SHR029 Short Syndrome 63 0.022
726
c SYS004 Systemic Mastocytosis 63 0.022
727
P LMY004 Leiomyosarcoma 63 0.022
728
TRN015 Transient Cerebral Ischemia 63 0.022
729
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.022
730
LPD008 Lipid Metabolism Disorder 62 0.022
731
CLT003 Colitis 62 0.022
732
c HPT003 Hepatitis a 62 0.022
733
P TRC086 Trichohepatoenteric Syndrome 1 62 0.022
734
P ORT004 Orthostatic Intolerance 62 0.022
735
ATM095 Autoimmune Disease 62 0.022
736
P ACR001 Aicardi-Goutieres Syndrome 62 0.022
737
BRS099 Breast Ductal Carcinoma 62 0.022
738
P PRP029 Porphyria 62 0.022
739
ESP020 Esophageal Atresia 62 0.022
740
SPN404 Spinal and Bulbar Muscular Atrophy, X-Linked 1 61 0.022
741
c MCP047 Mucopolysaccharidosis, Type Iva 61 0.022
742
YLL002 Yellow Fever 61 0.022
743
CHR066 Chronic Fatigue Syndrome 61 0.022
744
P SJG008 Sjogren Syndrome 61 0.022
745
SDD001 Sudden Infant Death Syndrome 61 0.022
746
P ART067 Aortic Aneurysm, Familial Thoracic 1 61 0.022
747
P NPH012 Nephrotic Syndrome 60 0.022
748
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.022
749
DPH001 Diphtheria 60 0.022
750
P BNG030 Benign Ependymoma 60 0.022
751
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.022
752
ACN002 Acanthosis Nigricans 60 0.022
753
P ALP009 Alopecia Areata 60 0.022
754
P SNS001 Sensorineural Hearing Loss 60 0.022
755
VRC005 Varicose Veins 60 0.022
756
INS001 Insulinoma 60 0.022
757
P THL005 Thalassemia 60 0.022
758
P MYC008 Myocarditis 59 0.022
759
P AXN002 Axenfeld-Rieger Syndrome 59 0.022
760
P BND020 Bone Disease 59 0.022
761
GRD007 Grade Iii Astrocytoma 59 0.022
762
IRN001 Iron Deficiency Anemia 59 0.022
763
ADN018 Adenoma 59 0.022
764
P SYP003 Syphilis 58 0.022
765
GLB001 Gilbert Syndrome 58 0.022
766
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 58 0.022
767
RBS001 Rabies 58 0.022
768
SPT004 Septic Arthritis 58 0.022
769
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.022
770
EYD002 Eye Disease 58 0.022
771
c MCP004 Mucopolysaccharidosis Iv 57 0.022
772
P GLL018 Gallbladder Cancer 57 0.022
773
P INF032 Infertility 57 0.022
774
P UVT001 Uveitis 57 0.022
775
BLM002 Bulimia Nervosa 57 0.022
776
c CHL119 Cholangitis, Primary Sclerosing 57 0.022
777
IRN002 Iron Metabolism Disease 57 0.022
778
P RHN004 Rhinitis 57 0.022
779
DSS009 Disseminated Intravascular Coagulation 57 0.022
780
THY022 Thymic Carcinoma 57 0.022
781
c LKM070 Leukemia, Acute Monocytic 57 0.022
782
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 57 0.022
783
AYM001 Ayme-Gripp Syndrome 57 0.022
784
PPL058 Papilloma of Choroid Plexus 56 0.022
785
P CHN012 Chondrosarcoma 56 0.022
786
CMR002 Coumarin Resistance 56 0.022
787
LST001 Listeriosis 56 0.022
788
P MLT074 Multiple Endocrine Neoplasia 56 0.022
789
ALL006 Allergic Asthma 56 0.022
790
LMY014 Leiomyoma, Uterine 56 0.022
791
ADN027 Adenomyosis 56 0.022
792
SFT003 Soft Tissue Sarcoma 56 0.022
793
SCH003 Schizophreniform Disorder 56 0.022
794
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.022
795
P PLY019 Polyneuropathy 56 0.022
796
c THY109 Thyroid Cancer, Nonmedullary, 1 56 0.022
797
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.022
798
P ATR001 Atrioventricular Septal Defect 55 0.022
799
LMB062 Limb Ischemia 55 0.022
800
P PTT006 Pituitary Adenoma 55 0.022
801
TRC109 Tracheoesophageal Fistula with or Without Esophageal Atresia 55 0.022
802
ACT058 Active Peptic Ulcer Disease 55 0.022
803
P HYP076 Hyperthyroidism 55 0.022
804
P ALP106 Alport Syndrome 1, X-Linked 55 0.022
805
BRN045 Brunner Syndrome 55 0.022
806
P VNS003 Venous Insufficiency 55 0.022
807
P FNG006 Feingold Syndrome 1 55 0.022
808
P LRY044 Larynx Cancer 55 0.022
809
PRP030 Purpura 54 0.022
810
TRD006 Tardive Dyskinesia 54 0.022
811
PYD001 Pyoderma Gangrenosum 54 0.022
812
GLS001 Gliosarcoma 54 0.022
813
SCH071 Schaaf-Yang Syndrome 54 0.022
814
P EPS030 Episodic Kinesigenic Dyskinesia 1 54 0.022
815
P DXT004 Dextro-Looped Transposition of the Great Arteries 54 0.022
816
RLP001 Relapsing Polychondritis 54 0.022
817
FCL014 Focal Epilepsy 54 0.022
818
MWT001 Mowat-Wilson Syndrome 54 0.022
819
VLC001 Velocardiofacial Syndrome 54 0.022
820
CLL010 Cellular Ependymoma 54 0.022
821
THR013 Thoracic Outlet Syndrome 54 0.022
822
ANL018 Analbuminemia 54 0.022
823
HMS001 Hemosiderosis 54 0.022
824
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 54 0.022
825
CLL003 Cellulitis 54 0.022
826
CLR030 Clear Cell Renal Cell Carcinoma 53 0.022
827
P LCH002 Lichen Planus 53 0.022
828
FRZ001 Frozen Shoulder 53 0.022
829
KRT006 Keratoconjunctivitis 53 0.022
830
P MNC007 Monocytic Leukemia 53 0.022
831
P EMB005 Embryonal Rhabdomyosarcoma 53 0.022
832
BRD004 Borderline Personality Disorder 53 0.022
833
P SHR001 Short Bowel Syndrome 53 0.022
834
P GRS003 Griscelli Syndrome 53 0.022
835
KNS001 Kniest Dysplasia 53 0.022
836
SPN035 Spindle Cell Sarcoma 53 0.022
837
ALC009 Alcoholic Liver Cirrhosis 53 0.022
838
c CNT035 Central Nervous System Disease 52 0.022
839
DMY004 Demyelinating Disease 52 0.022
840
LYS002 Lysosomal Storage Disease 52 0.022
841
HRP009 Herpes Simplex Encephalitis 52 0.022
842
c ACR116 Aicardi-Goutieres Syndrome 1 52 0.022
843
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.022
844
P NRD007 Neurodegeneration with Brain Iron Accumulation 52 0.022
845
ACT200 Acute Monoblastic Leukemia 52 0.022
846
ART074 Aortic Dissection 52 0.022
847
PRV004 Periventricular Leukomalacia 52 0.022
848
CLR109 Colorectal Adenocarcinoma 51 0.022
849
P LCT001 Lactic Acidosis 51 0.022
850
c PRM108 Primary Progressive Multiple Sclerosis 51 0.022
851
INT079 Intrahepatic Cholangiocarcinoma 51 0.022
852
PLS006 Plasmodium Vivax Malaria 51 0.022
853
ASP003 Aseptic Meningitis 51 0.022
854
c VRL007 Viral Encephalitis 51 0.022
855
P CHL066 Cholangitis 51 0.022
856
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.022
857
CHR005 Chorioamnionitis 51 0.022
858
GNT002 Giant Cell Glioblastoma 50 0.022
859
SCH012 Schizoaffective Disorder 50 0.022
860
RTN003 Retinal Ischemia 50 0.022
861
BLP005 Blepharitis 50 0.022
862
c SVR005 Severe Pre-Eclampsia 50 0.022
863
P MTR003 Mitral Valve Stenosis 50 0.022
864
FSC004 Fasciitis 50 0.022
865
PYD002 Pyoderma 50 0.022
866
P TMP001 Temporal Lobe Epilepsy 50 0.022
867
BLR001 Biliary Atresia 50 0.022
868
DBT004 Diabetic Polyneuropathy 49 0.022
869
RBF001 Riboflavin Deficiency 49 0.022
870
ENT004 Enthesopathy 49 0.022
871
KRT001 Keratoconjunctivitis Sicca 49 0.022
872
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 49 0.022
873
c NRB010 Neuroblastoma 1 49 0.022
874
LFT001 Left Bundle Branch Hemiblock 49 0.022
875
HDR003 Hidradenitis 49 0.022
876
GST049 Gastrointestinal System Cancer 49 0.022
877
P MGR001 Migraine Without Aura 49 0.022
878
PTH002 Pathological Gambling 49 0.022
879
URM002 Uremia 49 0.022
880
HST010 Histiocytosis 48 0.022
881
QDR001 Quadriplegia 48 0.022
882
c BCT013 Bacterial Pneumonia 48 0.022
883
c DSB006 Desbuquois Dysplasia 1 48 0.022
884
NCR007 Necrotizing Fasciitis 48 0.022
885
P SCL009 Sclerosing Cholangitis 48 0.022
886
VTM033 Vitamin K Deficiency Bleeding 48 0.022
887
P PRN026 Porencephaly 48 0.022
888
GLC106 Glucocorticoid Resistance, Generalized 48 0.022
889
BLY001 B-Lymphoblastic Leukemia/lymphoma 48 0.022
890
c MTR002 Mitral Valve Insufficiency 48 0.022
891
HPR003 Heparin-Induced Thrombocytopenia 48 0.022
892
PRP007 Priapism 47 0.022
893
CRY008 Cryopyrin-Associated Periodic Syndrome 47 0.022
894
DRY001 Dry Eye Syndrome 47 0.022
895
P CRN028 Corneal Ulcer 47 0.022
896
P RNL015 Renal Hypertension 47 0.022
897
P ERY008 Erythromelalgia 47 0.022
898
KRT002 Keratomalacia 47 0.022
899
ANT011 Antisocial Personality Disorder 47 0.022
900
P ENC008 Encephalocele 47 0.022
901
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 47 0.022
902
TST044 Testicular Torsion 47 0.022
903
P PRC019 Precocious Puberty 46 0.022
904
c CNT075 Central Precocious Puberty 46 0.022
905
ASP004 Asphyxia Neonatorum 46 0.022
906
TST014 Testicular Cancer 46 0.022
907
SMT001 Somatization Disorder 46 0.022
908
MTS001 Mutism 46 0.022
909
SPN020 Spondylosis 46 0.022
910
KRT013 Keratolytic Winter Erythema 46 0.022
911
UMB002 Umbilical Hernia 46 0.022
912
P PLL002 Pellagra 46 0.022
913
OBS003 Obsessive-Compulsive Personality Disorder 46 0.022
914
c DRR009 Diarrhea 6 46 0.022
915
c MLG068 Malignant Glioma 46 0.022
916
BNS007 Bone Sarcoma 45 0.022
917
MXD026 Mixed Glioma 45 0.022
918
PST048 Postural Orthostatic Tachycardia Syndrome 45 0.022
919
CNV002 Conversion Disorder 45 0.022
920
URT010 Ureteral Obstruction 45 0.022
921
NRS003 Neurosyphilis 45 0.022
922
ORL013 Oral Lichen Planus 45 0.022
923
STS002 Situs Inversus 45 0.022
924
c SPN097 Spinocerebellar Ataxia 23 45 0.022
925
INT304 Interstitial Pneumonitis, Desquamative, Familial 45 0.022
926
NNS002 Nonspecific Interstitial Pneumonia 45 0.022
927
OVR112 Ovarian Germ Cell Cancer 45 0.022
928
ASP008 Aspiration Pneumonitis 45 0.022
929
c CLR017 Clear Cell Sarcoma 45 0.022
930
GRN017 Granulocytopenia 44 0.022
931
P SMK004 Smoking As a Quantitative Trait Locus 3 44 0.022
932
OVR063 Overnutrition 44 0.022
933
VNC001 Von Economo's Disease 44 0.022
934
THR012 Thoracic Cancer 44 0.022
935
c SPR086 Spermatogenic Failure 3 44 0.022
936
CHL109 Childhood Apraxia of Speech 44 0.022
937
c RHB023 Rhabdomyosarcoma, Embryonal, 1 43 0.022
938
PST020 Postpoliomyelitis Syndrome 43 0.022
939
ORL015 Oral Squamous Cell Carcinoma 43 0.022
940
P HYP265 Hypotonia 43 0.022
941
P STR092 Striatal Degeneration, Autosomal Dominant 2 42 0.022
942
P VND001 Vein Disease 42 0.022
943
TRC097 Tracheomalacia 42 0.022
944
P CLS010 Cluster Headache 42 0.022
945
ORB013 Orbital Disease 42 0.022
946
GLC096 Galactorrhea 42 0.022
947
CTS005 Catastrophic Antiphospholipid Syndrome 42 0.022
948
RST023 Resting Heart Rate, Variation in 41 0.022
949
P RRH023 Rare Hereditary Hemochromatosis 41 0.022
950
PLY021 Polyradiculopathy 41 0.022
951
PCD001 Pica Disease 41 0.022
952
ACT088 Acute Insulin Response 41 0.022
953
SPN362 Spondylometaphyseal Dysplasia, Sedaghatian Type 41 0.022
954
ASY002 Asymptomatic Neurosyphilis 41 0.022
955
P MLG074 Malignant Mesenchymoma 40 0.022
956
KDN007 Kidney Clear Cell Sarcoma 40 0.022
957
HYP030 Hypoactive Sexual Desire Disorder 40 0.022
958
P TRC031 Trichorhinophalangeal Syndrome 40 0.022
959
UTR043 Uterine Sarcoma 39 0.022
960
P INT260 Intracranial Berry Aneurysm 39 0.022
961
P ARC016 Auriculocondylar Syndrome 1 39 0.022
962
LKP003 Leukoplakia 39 0.022
963
c ACT004 Acute Diarrhea 39 0.022
964
FML039 Female Reproductive System Disease 39 0.022
965
PRM127 Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type 38 0.022
966
ANT019 Anterograde Amnesia 38 0.022
967
CHL039 Choledocholithiasis 38 0.022
968
ANG016 Angiokeratoma 38 0.022
969
HYP264 Hypertonia 38 0.022
970
c ACT159 Acute Transverse Myelitis 38 0.022
971
OVR094 Ovarian Epithelial Cancer 38 0.022
972
SCR039 Scorpion Envenomation 38 0.022
973
SWL001 Swallowing Disorders 38 0.022
974
MCP033 Mucopolysaccharidoses 38 0.022
975
CRB009 Cerebritis 37 0.022
976
AKN002 Akinetic Mutism 37 0.022
977
DDN027 Duodenum Disease 37 0.022
978
P MRQ003 Morquio Syndrome 37 0.022
979
GLM044 Glomerular Disease 37 0.022
980
c HTR021 Heterotaxy, Visceral, 5, Autosomal 37 0.022
981
GRS001 Gerstmann Syndrome 36 0.022
982
CMP006 Complex Partial Epilepsy 36 0.022
983
PRT009 Parotid Gland Cancer 36 0.022
984
TRG003 Trigeminal Nerve Disease 36 0.022
985
ABD010 Abdominal Wall Defect 36 0.022
986
CRY036 Cryptogenic Cirrhosis 36 0.022
987
ESP029 Esophageal Atresia/tracheoesophageal Fistula 36 0.022
988
MDN008 Median Arcuate Ligament Syndrome 35 0.022
989
EPD005 Epidural Abscess 35 0.022
990
PLN026 Pilonidal Sinus 35 0.022
991
TLS001 Tolosa-Hunt Syndrome 35 0.022
992
PRG080 Progressive Non-Infectious Anterior Vertebral Fusion 35 0.022
993
c MJR008 Major Affective Disorder 2 35 0.022
994
ATX010 Ataxia Neuropathy Spectrum 34 0.022
995
FBR002 Fibrosarcoma of Bone 34 0.022
996
SPN043 Spinal Cord Glioma 34 0.022
997
GRM010 Germ Cells Tumors 34 0.022
998
BWN003 Bowenoid Papulosis 34 0.022
999
c EPL125 Epileptic Encephalopathy, Early Infantile, 24 34 0.022
1000
GLC024 Glucose Transporter Type 1 Deficiency Syndrome 34 0.022
1001
BRN041 Bornholm Eye Disease 34 0.022
1002
c MJR023 Major Affective Disorder 7 33 0.022
1003
c CHR064 Chronic Monocytic Leukemia 33 0.022
1004
ALR002 Al-Raqad Syndrome 33 0.022
1005
PRS064 Persistent Vegetative State 33 0.022
1006
DDN004 Duodenogastric Reflux 33 0.022
1007
ACT064 Acute Necrotizing Encephalitis 33 0.022
1008
c MJR003 Major Affective Disorder 6 33 0.022
1009
c MJR006 Major Affective Disorder 5 33 0.022
1010
DYS140 Dyskinesia, Familial, with Facial Myokymia 33 0.022
1011
AMN014 Aminopterin Syndrome Sine Aminopterin 33 0.022
1012
SBV001 Subvalvular Aortic Stenosis 33 0.022
1013
INF013 Inferior Myocardial Infarction 33 0.022
1014
c BLD140 Blood Group, I System 32 0.022
1015
FMR018 Femoral-Facial Syndrome 32 0.022
1016
NRN002 Neuronitis 32 0.022
1017
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 32 0.022
1018
PRX097 Paroxysmal Dystonia 32 0.022
1019
RHS001 Rh Isoimmunization 32 0.022
1020
SPC003 Specific Developmental Disorder 31 0.022
1021
EXN003 Exencephaly 31 0.022
1022
FMR003 Femoral Neuropathy 31 0.022
1023
NRG001 Neurogenic Bowel 31 0.022
1024
ASP036 Aspirin Allergy 30 0.022
1025
FNT004 Fainting 30 0.022
1026
MTY003 Mutyh Polyposis 30 0.022
1027
ACT228 Acute Radiation Syndrome 29 0.022
1028
ANT013 Anterior Spinal Artery Syndrome 29 0.022
1029
CRD220 Cardiac Valvular Defect, Developmental 29 0.022
1030
DSC004 Discitis 29 0.022
1031
c MJR004 Major Affective Disorder 4 28 0.022
1032
TMP019 Temporomandibular Joint Anomaly 28 0.022
1033
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 28 0.022
1034
SPN185 Spinal Cord Infarction 28 0.022
1035
ARG004 Argyria 27 0.022
1036
BRB003 Barbiturate Abuse 27 0.022
1037
MDR006 Moderate and Severe Traumatic Brain Injury 27 0.022
1038
RHH001 Rohhad 27 0.022
1039
c RNG015 Ring Chromosome 2 26 0.022
1040
c ACQ029 Acquired Porencephaly 26 0.022
1041
ETH012 Ethylene Glycol Poisoning 26 0.022
1042
MLG164 Malignant Epithelial Tumor of Ovary 26 0.022
1043
c FRN037 Frontal Encephalocele 26 0.022
1044
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.022
1045
c TRN053 Transient Pseudohypoaldosteronism 25 0.022
1046
CPG001 Capgras Syndrome 24 0.022
1047
OGL001 Ogilvie Syndrome 24 0.022
1048
CNG092 Congenital Extrahepatic Portosystemic Shunt 23 0.022
1049
BLD165 Blood Group, Colton System 20 0.022
1050
LNP001 Loin Pain Hematuria Syndrome 18 0.022
1051
IDP022 Idiopathic Spinal Cord Herniation 17 0.022
1052
PNT023 Pontine Hemorrhage 17 0.022
1053
PLY028 Polycystic Bone Disease 17 0.022
1054
BLD137 Blood Group--Ahonen 16 0.022
1055
MTR086 Motor Stereotypies 16 0.022
1056
ADS006 Aids - Neurological Complications 15 0.022
1057
c ADL020 Adult Malignant Mesenchymoma 11 0.022
1058
ERL051 Early Response to Neural Induction Gene 10 0.022
1059
CHL016 Childhood Malignant Mesenchymoma 8 0.022
1060
ACT171 Acute Opioid Poisoning 6 0.022
Content
Loading form....