Search results for Adenosine

3231 hits were found for Adenosine

# Family MCID Name MIFTS Score
1
ADN001 Adenosine Deaminase Deficiency 59 56.389
2
SVR095 Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Negative, Nk Cell-Negative, Due to Adenosine Deaminase Deficiency 47 47.164
3
HYP241 Hypermethioninemia Due to Adenosine Kinase Deficiency 37 30.329
4
VSC058 Vasculitis, Autoinflammation, Immunodeficiency, and Hematologic Defects Syndrome 49 27.649
5
MYP071 Myopathy Due to Myoadenylate Deaminase Deficiency 43 24.371
6
PRT037 Pertussis 65 23.437
7
ADN039 Adenosine Triphosphate, Elevated, of Erythrocytes 19 23.072
8
SVR004 Severe Combined Immunodeficiency 72 19.835
9
LPP008 Lipoprotein Quantitative Trait Locus 65 18.461
10
CMB007 Combined Immunodeficiency 57 17.401
11
ART140 Arteries, Anomalies of 53 17.257
12
ISC004 Ischemia 61 16.869
13
ADN079 Adenosine Triphosphatase Deficiency, Anemia Due to 8 16.114
14
ADN084 Adenosine Deaminase, Elevated, Hemolytic Anemia Due to 11 16.005
15
ATR057 Atrioventricular Block 54 15.405
16
CHL014 Cholera 62 15.168
17
CRN030 Coronary Stenosis 50 15.145
18
HYP266 Hypoxia 57 15.112
19
SVR066 Severe Combined Immunodeficiency, X-Linked 66 12.026
20
P ATR011 Atrial Fibrillation 66 11.533
21
ANX004 Anoxia 40 11.036
22
ANG054 Angina Pectoris 66 10.935
23
P NRB001 Neuroblastoma 66 10.817
24
P SZR006 Seizure Disorder 70 10.636
25
P MYC007 Myocardial Infarction 70 10.258
26
c ACT075 Acute Myocardial Infarction 56 10.066
27
ERY039 Erythrocyte Amp Deaminase Deficiency 22 10.040
28
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 9.523
29
CYT002 Cytokine Deficiency 43 9.434
30
P CRN300 Coronary Heart Disease 1 73 9.424
31
IMM167 Immune Deficiency Disease 78 9.391
32
c HML041 Hemolytic Anemia Due to Erythrocyte Adenosine Deaminase Overproduction 6 9.390
33
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 80 9.182
34
P CRD119 Cardiac Arrest 67 8.757
35
48X005 48,xyyy 39 8.722
36
MYC005 Myocardial Stunning 46 8.683
37
SYN036 Syncope 45 8.551
38
GLM045 Glioma 63 8.436
39
GLL048 Glial Tumor 52 8.386
40
P HNT016 Huntington Disease 73 8.357
41
PLM129 Pulmonary Disease, Chronic Obstructive 74 8.310
42
P PHC003 Pheochromocytoma 69 8.234
43
ADR040 Adrenal Gland Pheochromocytoma 46 8.227
44
P PLM037 Pulmonary Hypertension 72 8.222
45
P LKM071 Leukemia, Chronic Lymphocytic 75 8.071
46
c ATR087 Atrial Standstill 1 74 8.048
47
HYP066 Hyperglycemia 61 7.962
48
PLR008 Pleurisy 50 7.960
49
P HRT032 Heart Disease 81 7.898
50
ALL029 Allergic Disease 59 7.874
51
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 7.833
52
CYS001 Cystic Fibrosis 78 7.827
53
c PRC016 Pre-Eclampsia 65 7.772
54
CRB004 Cerebral Artery Occlusion 45 7.695
55
PLR001 Pleural Tuberculosis 49 7.672
56
SPN186 Spinal Cord Injury 61 7.611
57
P EPL164 Epilepsy 68 7.607
58
P PRK057 Parkinson Disease, Late-Onset 80 7.580
59
P AST005 Asthma 76 7.509
60
CNG034 Congestive Heart Failure 69 7.490
61
P VSC007 Vascular Disease 63 7.469
62
c ACT071 Acute Kidney Failure 60 7.466
63
LNG099 Lung Disease 62 7.410
64
ALL006 Allergic Asthma 56 7.393
65
P CHR345 Chronic Pain 50 7.391
66
P LKM002 Leukemia 67 7.351
67
c HYP595 Hypertension, Essential 85 7.329
68
P OVR042 Ovarian Cancer 88 7.311
69
PRT036 Peritonitis 65 7.180
70
BRN071 Brain Injury 50 7.149
71
P GLM040 Glioma Susceptibility 1 71 7.107
72
MLG169 Malignant Astrocytoma 57 7.055
73
WLF001 Wolff-Parkinson-White Syndrome 65 7.025
74
ATH013 Atherosclerosis Susceptibility 63 7.013
75
TRM010 Traumatic Brain Injury 51 6.890
76
P DBT009 Diabetes Mellitus 67 6.858
77
HLX001 Helix Syndrome 48 6.853
78
P PRK039 Parkinsonism 55 6.800
79
NNL005 Non-Alcoholic Fatty Liver Disease 63 6.781
80
PNG002 Pain Agnosia 51 6.709
81
P HYP086 Hypothyroidism 69 6.701
82
P MNN013 Meningitis 65 6.701
83
PLM010 Pulmonary Edema 55 6.622
84
FTT001 Fatty Liver Disease 62 6.604
85
P SCK005 Sickle Cell Disease 56 6.600
86
c TYP009 Type 2 Diabetes Mellitus 92 6.588
87
GLB002 Glioblastoma 67 6.578
88
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 6.562
89
LYM027 Lymphopenia 56 6.469
90
c MGR028 Migraine with or Without Aura 1 64 6.445
91
P TRM003 Tremor 48 6.414
92
P ART022 Arthritis 71 6.331
93
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 6.329
94
BNR002 Bone Resorption Disease 47 6.314
95
HYP056 Hypoglycemia 65 6.300
96
c DLT002 Dilated Cardiomyopathy 78 6.279
97
CLT003 Colitis 63 6.254
98
P KDN018 Kidney Disease 72 6.254
99
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 6.243
100
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 6.243
101
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 6.231
102
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 6.231
103
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 6.231
104
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 6.231
105
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 6.231
106
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 6.231
107
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 6.231
108
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 6.231
109
c MCR130 Microvascular Complications of Diabetes 6 41 6.202
110
c MCR120 Microvascular Complications of Diabetes 7 47 6.202
111
c MCR113 Microvascular Complications of Diabetes 3 52 6.202
112
c MCR133 Microvascular Complications of Diabetes 4 41 6.202
113
P RHM011 Rheumatoid Arthritis 82 6.162
114
INT007 Intermediate Coronary Syndrome 54 6.159
115
c HYP836 Hypercholesterolemia, Familial, 1 73 6.158
116
AGN016 Aging 54 6.145
117
P HML002 Hemolytic Anemia 62 6.130
118
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 6.082
119
IMP005 Impotence 52 6.068
120
P MYC084 Mycobacterium Tuberculosis 1 68 6.048
121
P ADL010 Adult Respiratory Distress Syndrome 71 6.047
122
c PRG042 Progressive Familial Heart Block, Type Ia 66 6.024
123
P BCL017 B-Cell Lymphoma 59 6.017
124
TXC005 Toxic Shock Syndrome 62 6.009
125
STT001 Status Epilepticus 59 5.940
126
P RHN004 Rhinitis 57 5.905
127
TBR011 Tuberculous Meningitis 48 5.901
128
P ALZ034 Alzheimer Disease 87 5.883
129
P HYP076 Hyperthyroidism 53 5.848
130
RPD005 Rapidly Involuting Congenital Hemangioma 46 5.728
131
c PLM164 Pulmonary Hypertension, Primary, 1 76 5.636
132
P THR014 Thrombocytopenia 66 5.629
133
DFC004 Deficiency Anemia 74 5.543
134
ALL003 Allergic Rhinitis 67 5.526
135
GST033 Gestational Diabetes 61 5.518
136
c MCR115 Microvascular Complications of Diabetes 5 65 5.473
137
P LTR001 Lateral Sclerosis 58 5.461
138
c AMY091 Amyotrophic Lateral Sclerosis 1 88 5.451
139
HYP060 Hyperinsulinism 54 5.426
140
P LVR013 Liver Disease 69 5.398
141
P BRS047 Breast Cancer 98 5.392
142
PLM001 Pulmonary Tuberculosis 69 5.389
143
ANR040 Aneurysm 61 5.378
144
HMN044 Human Immunodeficiency Virus Type 1 78 5.377
145
P LYM118 Lymphoma 67 5.359
146
P TMP001 Temporal Lobe Epilepsy 49 5.352
147
P PLM036 Pulmonary Fibrosis 66 5.339
148
c HYP724 Hyperlipoproteinemia, Type Iii 67 5.330
149
P SLP005 Sleep Disorder 61 5.308
150
P MLN008 Melanoma 76 5.274
151
OST159 Osteogenic Sarcoma 66 5.241
152
P LKM062 Leukemia, Acute Lymphoblastic 69 5.213
153
LPD008 Lipid Metabolism Disorder 62 5.203
154
PRP027 Peripheral Vascular Disease 71 5.197
155
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 5.174
156
P HYP069 Hyperparathyroidism 62 5.123
157
c CHR684 Chronic Kidney Disease 69 5.112
158
47X002 47,xyy 48 5.107
159
P MSC005 Muscular Dystrophy 67 5.090
160
P HPT023 Hepatocellular Carcinoma 96 5.088
161
c TYP008 Type 1 Diabetes Mellitus 70 5.087
162
LFT001 Left Bundle Branch Hemiblock 47 5.079
163
P DRR001 Diarrhea 55 5.048
164
ATM095 Autoimmune Disease 61 4.997
165
VLK001 Volkmann Contracture 23 4.967
166
ALC007 Alcohol Dependence 66 4.933
167
MYL069 Myeloma, Multiple 77 4.912
168
P VSC011 Vasculitis 61 4.868
169
PRT251 Proteinuria, Chronic Benign 57 4.863
170
c SYS001 Systemic Lupus Erythematosus 87 4.851
171
END086 End Stage Renal Disease 52 4.812
172
RNL077 Renal Fibrosis 46 4.807
173
P PSR002 Psoriasis 63 4.806
174
TBR008 Tuberculous Peritonitis 35 4.802
175
P MYP004 Myopathy 67 4.800
176
MTB004 Metabolic Acidosis 48 4.797
177
P CLR023 Colorectal Cancer 100 4.786
178
SLP001 Sleeping Sickness 56 4.763
179
P HYP098 Hypereosinophilic Syndrome 66 4.763
180
PST011 Pustulosis of Palm and Sole 52 4.763
181
MNT002 Mental Depression 57 4.720
182
P SCH015 Schizophrenia 74 4.713
183
P ENC018 Encephalopathy 62 4.705
184
P HDC001 Headache 57 4.703
185
GSG001 Gas Gangrene 52 4.695
186
P GST053 Gastric Cancer 83 4.693
187
TTN003 Tetanus 65 4.671
188
P PLY017 Polyarteritis Nodosa 60 4.663
189
VCC001 Vaccinia 47 4.650
190
P HYP061 Hypertrophic Cardiomyopathy 69 4.640
191
P MYL006 Myeloid Leukemia 61 4.626
192
THR024 Thrombosis 56 4.620
193
ACQ007 Acquired Immunodeficiency Syndrome 59 4.601
194
P HRP006 Herpes Simplex 65 4.535
195
P DRM053 Dermatitis, Atopic 65 4.530
196
OCL069 Ocular Motor Apraxia 57 4.516
197
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 4.509
198
LVR012 Liver Cirrhosis 63 4.499
199
CHL068 Cholestasis 61 4.499
200
CRT015 Carotid Artery Occlusion 45 4.489
201
P BNG032 Benign Mesothelioma 53 4.459
202
PRN001 Purine Nucleoside Phosphorylase Deficiency 53 4.455
203
DPR016 Depression 65 4.453
204
P LPS004 Lupus Erythematosus 61 4.452
205
P MJR001 Major Depressive Disorder 68 4.436
206
HRY003 Hairy Cell Leukemia 61 4.412
207
P SCK002 Sick Sinus Syndrome 55 4.400
208
P KLZ004 Kala-Azar 1 41 4.399
209
LSH001 Leishmaniasis 64 4.399
210
P PNC025 Panic Disorder 52 4.389
211
c LKM061 Leukemia, Acute Myeloid 83 4.364
212
DBT010 Diabetic Neuropathy 54 4.348
213
CHR074 Choriocarcinoma 46 4.317
214
TRN015 Transient Cerebral Ischemia 63 4.312
215
HYP014 Hyperuricemia 51 4.304
216
INS024 Insulin-Like Growth Factor I 78 4.303
217
P GRF003 Graft-Versus-Host Disease 71 4.291
218
ALL014 Allergic Encephalomyelitis 34 4.274
219
P NTR004 Neutropenia 63 4.266
220
OCL006 Ocular Hypertension 53 4.266
221
RTN003 Retinal Ischemia 49 4.264
222
P PNM007 Pneumonia 67 4.247
223
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 4.233
224
P ECL001 Eclampsia 52 4.230
225
STM007 Stomatitis 54 4.230
226
MDD011 Mood Disorder 62 4.227
227
c ACT027 Acute Pancreatitis 60 4.213
228
CRB086 Cerebral Aneurysms 40 4.213
229
HYP005 Hypokalemia 55 4.209
230
c MJR022 Major Affective Disorder 8 38 4.197
231
c MJR024 Major Affective Disorder 9 41 4.197
232
P BPL003 Bipolar Disorder 56 4.197
233
PRC013 Pericarditis 53 4.180
234
HMC014 Homocysteinemia 52 4.175
235
CRB039 Cerebrovascular Disease 66 4.172
236
P ADN016 Adenocarcinoma 63 4.166
237
P ALC033 Alcohol Use Disorder 61 4.156
238
P RSP003 Respiratory Failure 74 4.147
239
PPL052 Papillomatosis, Confluent and Reticulated 34 4.147
240
P INF037 Inflammatory Bowel Disease 53 4.139
241
RTN020 Retinal Vascular Disease 46 4.136
242
APN006 Apnea of Prematurity 24 4.132
243
P SLP006 Sleep Apnea 69 4.129
244
c LKM005 Leukemia, T-Cell, Chronic 34 4.087
245
LWC001 Low Compliance Bladder 45 4.075
246
ULC004 Ulcerative Colitis 74 4.074
247
WTH001 Withdrawal Disorder 48 4.063
248
P NRP001 Neuropathy 60 4.049
249
INT030 Intracranial Aneurysm 55 4.021
250
STR067 Stroke, Ischemic 80 3.993
251
P MVM001 Movement Disease 61 3.993
252
EXT007 Extracutaneous Mastocytoma 38 3.979
253
MST004 Mast Cell Neoplasm 42 3.979
254
PRP007 Priapism 47 3.957
255
ATS010 Autosomal Recessive Disease 42 3.945
256
P GRV001 Graves' Disease 55 3.938
257
OST012 Osteoarthritis 77 3.928
258
P LNG064 Lung Cancer Susceptibility 3 70 3.921
259
SNT005 Sinoatrial Node Disease 47 3.893
260
IRN002 Iron Metabolism Disease 57 3.890
261
BCT022 Bacterial Infectious Disease 56 3.885
262
ASP030 Aspirin Resistance 40 3.883
263
c ATS007 Autism Spectrum Disorder 72 3.879
264
P ATS364 Autism 69 3.877
265
P UVT001 Uveitis 57 3.848
266
P GST044 Gastritis 55 3.848
267
DYS022 Dyschromatosis Symmetrica Hereditaria 48 3.832
268
P DMN001 Diamond-Blackfan Anemia 71 3.824
269
EXR010 Exercise-Induced Bronchoconstriction 34 3.809
270
P PNC035 Pancreatic Cancer 86 3.808
271
P LNG032 Lung Cancer 98 3.781
272
P SRC025 Sarcoidosis 1 71 3.771
273
CRH001 Crohn's Disease 80 3.760
274
ACT098 Acute Erythroid Leukemia 55 3.748
275
P PLY014 Polycystic Kidney Disease 69 3.746
276
PLR007 Pleural Empyema 51 3.727
277
ADN018 Adenoma 59 3.724
278
ANX010 Anxiety 70 3.721
279
CRD132 Cardiac Conduction Defect 60 3.715
280
P INF032 Infertility 57 3.706
281
c HPT073 Hepatitis C Virus 71 3.688
282
RST023 Resting Heart Rate, Variation in 40 3.688
283
P PRD008 Periodontitis 64 3.683
284
P PRP019 Peripheral Nervous System Disease 58 3.682
285
c PRM005 Primary Hyperparathyroidism 59 3.676
286
c LKM063 Leukemia, Chronic Myeloid 71 3.673
287
MSC157 Muscular Dystrophy, Duchenne Type 79 3.672
288
THY029 Thyroid Carcinoma 51 3.656
289
P SYS005 Systemic Scleroderma 74 3.641
290
GT001 Gout 64 3.631
291
P BLD134 Bladder Cancer 79 3.623
292
P PNC044 Pancreatitis 61 3.619
293
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 3.575
294
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 3.571
295
P MYC008 Myocarditis 59 3.561
296
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 44 3.539
297
c PCH010 Pachyonychia Congenita 3 43 3.539
298
LYM019 Lymphosarcoma 46 3.530
299
P ART005 Arteriovenous Malformation 65 3.523
300
LSC001 Lesch-Nyhan Syndrome 62 3.517
301
TRY001 Trypanosomiasis 50 3.517
302
INT002 Intermittent Claudication 61 3.510
303
P TXP001 Toxoplasmosis 60 3.506
304
P PRS040 Prostate Cancer 95 3.496
305
DPH001 Diphtheria 59 3.489
306
PRS045 Prostatic Hypertrophy 53 3.478
307
c ACT073 Acute Leukemia 58 3.474
308
NNL006 Non-Alcoholic Steatohepatitis 54 3.472
309
PTT037 Pituitary Tumors 44 3.432
310
P PSD015 Pseudohypoparathyroidism 55 3.429
311
P RNV001 Renovascular Hypertension 49 3.429
312
SQM006 Squamous Cell Carcinoma 60 3.421
313
DRM006 Dermatitis 62 3.414
314
SCN049 Second-Degree Atrioventricular Block 33 3.403
315
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 3.400
316
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 3.391
317
SCK003 Sickle Cell Anemia 74 3.387
318
P MLT020 Multiple Sclerosis 79 3.385
319
IGR001 Ige Responsiveness, Atopic 59 3.381
320
PST028 Post-Traumatic Stress Disorder 59 3.369
321
CLN015 Colon Adenocarcinoma 65 3.366
322
P PRC012 Pericardial Effusion 50 3.351
323
P DYS154 Dystonia 64 3.351
324
c SML038 Small Cell Cancer of the Lung 69 3.349
325
CRV035 Cervical Cancer 73 3.349
326
c PRG043 Progressive Familial Heart Block, Type Ib 54 3.343
327
RGH001 Right Bundle Branch Block 47 3.343
328
c BCT007 Bacterial Meningitis 55 3.341
329
HMN014 Human Immunodeficiency Virus Infectious Disease 54 3.336
330
c BRN108 Branchiootic Syndrome 1 62 3.332
331
P HPT021 Hepatitis 69 3.331
332
ESP021 Esophageal Cancer 83 3.324
333
AMN003 Amnestic Disorder 54 3.315
334
P CYS018 Cystitis 59 3.299
335
VSC003 Visceral Leishmaniasis 55 3.297
336
CMP010 Complex Regional Pain Syndrome 60 3.296
337
HYP017 Hypophosphatemia 49 3.296
338
SVR001 Severe Acute Respiratory Syndrome 67 3.290
339
P RST001 Restless Legs Syndrome 52 3.285
340
ART016 Aortic Aneurysm 68 3.285
341
GLC003 Glucose Intolerance 54 3.280
342
c SCL052 Scleroderma, Familial Progressive 61 3.278
343
PPT005 Peptic Ulcer Disease 58 3.278
344
c ACT134 Acute Liver Failure 59 3.268
345
P DBT005 Diabetes Insipidus 54 3.262
346
BRN024 Bronchitis 67 3.260
347
SKN016 Skin Disease 63 3.242
348
BRN004 Brain Edema 54 3.239
349
c CHR688 Chronic Acquired Demyelinating Polyneuropathy 16 3.234
350
CTY001 Cat Eye Syndrome 44 3.220
351
P HYP024 Hypoparathyroidism 55 3.220
352
PRS021 Prostatic Adenoma 43 3.217
353
CRD137 Cardiogenic Shock 56 3.198
354
URM002 Uremia 47 3.182
355
HMP009 Haemophilus Influenzae 41 3.167
356
MLR004 Malaria 80 3.166
357
HPT004 Hepatic Coma 43 3.166
358
P LCT001 Lactic Acidosis 51 3.151
359
INS001 Insulinoma 59 3.148
360
P PLY011 Polycystic Ovary Syndrome 57 3.147
361
CRD223 Cardiac Arrhythmia 63 3.144
362
P THL005 Thalassemia 56 3.141
363
CHL065 Cholangiocarcinoma 58 3.134
364
INT079 Intrahepatic Cholangiocarcinoma 51 3.134
365
PRS129 Prostatic Hyperplasia, Benign 49 3.131
366
P EXN002 Exanthem 58 3.129
367
URT010 Ureteral Obstruction 45 3.125
368
P DNG005 Dengue Virus 56 3.125
369
P ATT013 Attention Deficit-Hyperactivity Disorder 64 3.124
370
P BND020 Bone Disease 59 3.110
371
MRP001 Morphine Dependence 42 3.095
372
P ENC004 Encephalitis 61 3.090
373
HMP001 Hemopericardium 47 3.088
374
c THY107 Thymoma, Familial 42 3.086
375
P THY023 Thymoma 64 3.086
376
BRN002 Bronchiolitis 57 3.084
377
P GLM007 Glomerulonephritis 60 3.083
378
ACT084 Acute Stress Disorder 54 3.079
379
c EXD008 Exudative Vitreoretinopathy 1 71 3.077
380
ADG002 Audiogenic Seizures 25 3.077
381
P MLN007 Male Infertility 56 3.077
382
ACT003 Acute Kidney Tubular Necrosis 46 3.072
383
c ATM099 Autoimmune Uveitis 45 3.072
384
CHC001 Chickenpox 57 3.035
385
P MYS003 Myasthenia Gravis 68 3.030
386
LMB062 Limb Ischemia 55 3.026
387
P CHR012 Chronic Granulomatous Disease 69 3.022
388
PSR001 Psoriatic Arthritis 62 3.014
389
INT323 Intraocular Pressure Quantitative Trait Locus 64 3.014
390
P RTN024 Retinoblastoma 73 3.003
391
CHG001 Chagas Disease 66 3.003
392
END057 Endometrial Cancer 72 3.001
393
DWN001 Down Syndrome 70 2.999
394
MSL001 Measles 61 2.995
395
P MLG056 Malignant Hyperthermia 66 2.991
396
HDN002 Head Injury 44 2.989
397
CLP006 Clopidogrel Resistance 44 2.989
398
c ATS347 Autosomal Dominant Polycystic Kidney Disease 66 2.986
400
P KDN017 Kidney Cancer 61 2.981
401
P OPT006 Optic Nerve Disease 58 2.972
402
PRP016 Paraplegia 52 2.972
403
P THY032 Thyroiditis 57 2.969
404
BRK010 Burkitt Lymphoma 66 2.965
405
P BRS044 Breast Adenocarcinoma 58 2.948
406
PLY150 Polykaryocytosis Inducer 29 2.943
407
c INH020 Inherited Metabolic Disorder 48 2.941
408
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 2.940
409
PLM134 Pulmonary Fibrosis, Idiopathic 76 2.932
410
c DMN023 Diamond-Blackfan Anemia 1 66 2.916
411
P LNG028 Long Qt Syndrome 64 2.903
412
HRT012 Heart Valve Disease 53 2.896
413
c FML001 Familial Atrial Fibrillation 65 2.895
414
P OST002 Osteoporosis 76 2.893
415
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 2.893
416
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 2.893
417
P ALP008 Alopecia 54 2.891
418
HYP003 Hypermethioninemia 51 2.890
419
SRC014 Sarcoma 65 2.875
420
P HYP265 Hypotonia 42 2.871
421
OVR094 Ovarian Epithelial Cancer 39 2.871
422
c ART115 Aortic Valve Disease 1 74 2.848
423
P CRD246 Cardiovascular System Disease 56 2.821
424
CRN019 Coronary Artery Vasospasm 47 2.815
425
STR089 Storage Pool Platelet Disease 47 2.814
426
P SNS001 Sensorineural Hearing Loss 59 2.813
427
P HYP750 Hypertriglyceridemia, Familial 62 2.811
428
RCK004 Rickets 68 2.807
429
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 2.799
430
SPN035 Spindle Cell Sarcoma 54 2.792
431
HPT019 Hepatic Encephalopathy 59 2.782
432
GST023 Gastric Ulcer 52 2.780
433
GTR002 Goiter 53 2.778
434
FCL014 Focal Epilepsy 53 2.778
435
CMM004 Common Variable Immunodeficiency 72 2.755
436
PRC005 Pericardial Tuberculosis 33 2.752
437
P SBS003 Substance Abuse 54 2.750
438
TLN003 Telangiectasis 51 2.748
439
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 60 2.746
440
DSS009 Disseminated Intravascular Coagulation 57 2.744
441
RNL114 Renal Cell Carcinoma, Nonpapillary 80 2.743
442
CRB090 Cerebral Hypoxia 42 2.743
443
CNS004 Constipation 56 2.742
444
THR035 Thrombasthenia 48 2.742
445
P WSK001 Wiskott-Aldrich Syndrome 72 2.742
446
c ESS001 Essential Tremor 57 2.742
447
BRN056 Bronchopulmonary Dysplasia 56 2.722
448
OCL010 Ocular Hypotension 37 2.721
449
c HPT015 Hepatitis D 49 2.716
450
PRT013 Portal Hypertension 59 2.702
451
P INT143 Interstitial Cystitis 60 2.699
452
CRN017 Coronary Thrombosis 46 2.698
453
P ART021 Arteriosclerosis 54 2.695
454
BRK012 Broken Heart Syndrome 42 2.684
455
P NRC002 Narcolepsy 56 2.684
456
c ART138 Aortic Aneurysm, Familial Abdominal, 1 61 2.682
457
c BCT013 Bacterial Pneumonia 48 2.675
458
OPT003 Opiate Dependence 49 2.673
459
P MCR129 Microvascular Complications of Diabetes 1 68 2.656
460
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 45 2.650
461
c HPT016 Hepatitis B 62 2.650
462
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 2.639
463
P EYD002 Eye Disease 57 2.632
464
c HPT001 Hepatitis C 62 2.630
465
P DDN001 Duodenal Ulcer 53 2.630
466
NRR001 Neuroretinitis 42 2.625
467
RTN023 Retinitis 46 2.625
468
P BRL012 Bare Lymphocyte Syndrome, Type Ii 65 2.623
469
ANT039 Antisynthetase Syndrome 55 2.616
470
ARG004 Argyria 26 2.602
471
P FBR017 Fibrosarcoma 56 2.602
472
ATN004 Autonomic Neuropathy 42 2.598
473
P RTN018 Retinal Disease 53 2.598
474
P SKN015 Skin Carcinoma 71 2.583
475
GST050 Gastrointestinal System Disease 55 2.580
476
c ACT135 Acute Graft Versus Host Disease 51 2.578
477
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 2.577
478
NRM005 Neuromuscular Disease 63 2.576
479
P ESP024 Esophagitis 60 2.573
480
P LPR021 Leprosy 3 71 2.568
481
HNS001 Hansen's Disease 32 2.568
482
P END044 Endometriosis 62 2.562
483
P PRP029 Porphyria 60 2.560
484
RHB024 Rhabdomyosarcoma 2 67 2.558
485
ASP003 Aseptic Meningitis 50 2.554
486
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 2.553
487
KWS002 Kawasaki Disease 65 2.549
488
c SPN225 Spondyloarthropathy 1 70 2.547
489
BLD053 Blood Platelet Disease 51 2.543
490
CCN001 Cocaine Dependence 48 2.543
491
PRP030 Purpura 54 2.536
492
DRG003 Drug Dependence 46 2.535
493
PNC001 Pancytopenia 53 2.532
494
INT066 Interstitial Lung Disease 60 2.528
495
P TBR001 Tuberous Sclerosis 69 2.523
496
P ADL017 Adult T-Cell Leukemia 56 2.516
497
P MYP006 Myopia 56 2.513
498
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 57 2.509
499
LYM040 Lymphoblastic Lymphoma 53 2.505
500
P OST001 Osteopetrosis 71 2.505
501
TYP007 Typhoid Fever 64 2.496
502
TRD006 Tardive Dyskinesia 53 2.488
503
ACT119 Acute Promyelocytic Leukemia 62 2.482
504
PRP080 Peripheral Artery Disease 54 2.481
505
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 63 2.469
506
P CHN012 Chondrosarcoma 57 2.468
507
SDD001 Sudden Infant Death Syndrome 60 2.457
508
c PNS012 Paine Syndrome 60 2.450
509
BRC012 Brucellosis 66 2.450
510
HGH043 High Grade Glioma 45 2.439
511
DFF005 Diffuse Large B-Cell Lymphoma 54 2.438
512
PST092 Posttransplant Acute Limbic Encephalitis 28 2.426
513
c VRL010 Viral Hepatitis 53 2.405
514
c TBR025 Tuberous Sclerosis 1 84 2.397
515
c GRV008 Graves Disease 1 54 2.395
516
THR099 Third-Degree Atrioventricular Block 42 2.394
517
THR004 Thrombocytosis 53 2.392
518
c SCN007 Secondary Hyperparathyroidism 51 2.392
519
VSC002 Vascular Dementia 60 2.392
520
ENT004 Enthesopathy 51 2.385
521
P RRH023 Rare Hereditary Hemochromatosis 54 2.383
522
NPH009 Nephrolithiasis 54 2.380
523
P RTN016 Retinal Degeneration 52 2.375
524
P INF038 Influenza 68 2.370
525
PNC129 Pancreatic Adenocarcinoma 65 2.368
526
TRC003 Trichomoniasis 53 2.368
527
LGH007 Leigh Syndrome 70 2.364
528
CHL123 Chlamydia 58 2.357
529
IRR002 Irritable Bowel Syndrome 65 2.357
530
P MTC069 Mitochondrial Disorders 57 2.343
531
HRW001 Hair Whorl 35 2.343
532
c JVN010 Juvenile Rheumatoid Arthritis 66 2.342
533
P NPH012 Nephrotic Syndrome 60 2.333
534
c DNT047 Dentinogenesis Imperfecta Type 2 35 2.331
535
SPL018 Splenomegaly 49 2.328
536
P RHB003 Rhabdomyosarcoma 66 2.326
537
c GLL024 Gallbladder Disease 1 52 2.319
538
c BTT014 Beta-Thalassemia 72 2.319
539
P HMC002 Homocystinuria 53 2.318
540
P FBR031 Febrile Seizures 52 2.318
541
c MCR112 Microvascular Complications of Diabetes 2 42 2.315
542
PLM033 Pulmonary Embolism 58 2.309
543
ADR016 Adrenal Cortical Carcinoma 62 2.309
544
BLR008 Bilirubin Metabolic Disorder 57 2.309
545
BRN012 Bronchiolitis Obliterans 56 2.302
546
c ART101 Aortic Valve Disease 2 66 2.299
547
LYM143 Lymphoma, Non-Hodgkin, Familial 75 2.295
548
P ALP061 Alopecia, Androgenetic, 1 49 2.292
549
AND014 Androgenic Alopecia 47 2.292
550
ART002 Arts Syndrome 66 2.285
551
INF013 Inferior Myocardial Infarction 33 2.285
552
MCR013 Microphthalmia 60 2.284
553
RDC006 Red Cell Aplasia 44 2.277
554
HRN029 Hearing Loss, Noise-Induced 37 2.266
555
P OBS001 Obstructive Jaundice 48 2.266
556
P VNW001 Von Willebrand's Disease 65 2.262
557
ADL002 Adult Syndrome 70 2.251
558
ILT001 Ileitis 48 2.240
559
DMY004 Demyelinating Disease 50 2.240
560
ANT024 Anthrax Disease 58 2.234
561
P HYD006 Hydrocephalus 61 2.234
562
P MNC007 Monocytic Leukemia 47 2.233
563
c HPT003 Hepatitis a 63 2.231
564
c PRG020 Paragangliomas 3 39 2.204
565
P ACT105 Acute Mountain Sickness 52 2.192
566
TCL027 T-Cell Acute Lymphoblastic Leukemia 51 2.189
567
ORL011 Oral Cancer 60 2.185
568
ORL015 Oral Squamous Cell Carcinoma 43 2.183
569
c ATM011 Autoimmune Hepatitis 63 2.183
570
HPT014 Hepatorenal Syndrome 49 2.183
571
CVD001 Covid-19 57 2.171
572
MYC006 Mycosis Fungoides 65 2.165
573
GST092 Gastroesophageal Reflux 61 2.165
574
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 61 2.165
575
MLG079 Malignant Pleural Mesothelioma 42 2.165
576
P NNT058 Neonatal Diabetes 52 2.165
577
LYM133 Lymphoma, Hodgkin, Classic 74 2.163
578
P BRN022 Bronchiectasis 60 2.154
579
ADR054 Adrenocortical Carcinoma, Hereditary 47 2.144
580
ADR004 Adrenal Cortical Adenocarcinoma 38 2.144
581
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 2.139
582
FBR047 Fibromyalgia 58 2.139
583
P DMN002 Dementia 66 2.139
584
NRF007 Neurofibroma 64 2.136
585
END040 Endogenous Depression 55 2.133
586
WLS001 Wilson Disease 70 2.129
587
CMB081 Combined Immunodeficiency, X-Linked 38 2.129
588
URT049 Urate Oxidase, Pseudogene 24 2.128
589
PLC002 Plica Syndrome 35 2.128
590
SYN007 Synovitis 55 2.128
591
PPL022 Papilloma 53 2.128
592
SQM002 Squamous Cell Papilloma 46 2.128
593
WST005 West Nile Virus 57 2.119
594
P PRR002 Pure Red-Cell Aplasia 47 2.117
595
ILS001 Ileus 50 2.114
596
P URT039 Urticaria 58 2.101
597
CHR178 Chromosomal Triplication 34 2.101
598
P OVR082 Overgrowth Syndrome 49 2.099
599
P OPN001 Open-Angle Glaucoma 55 2.087
600
MTB016 Metabolic Myopathy 30 2.085
601
NWC001 Newcastle Disease 47 2.082
602
P INT068 Intestinal Disease 53 2.073
603
P MTR014 Motor Neuron Disease 65 2.073
604
RTN017 Retinal Detachment 60 2.069
605
c MST023 Mesothelioma, Malignant 56 2.068
606
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 39 2.061
607
HRT011 Heart Septal Defect 49 2.061
608
CHR073 Choreatic Disease 54 2.061
609
P RTN008 Retinitis Pigmentosa 80 2.052
610
AGR002 Agoraphobia 45 2.050
611
GST040 Gastric Adenocarcinoma 67 2.045
612
VRL011 Viral Infectious Disease 61 2.041
613
HMG002 Hemoglobinuria 50 2.038
614
YLL002 Yellow Fever 61 2.038
615
MYL009 Myelodysplastic Syndrome 67 2.035
616
CRT013 Carotid Stenosis 51 2.034
617
CRB037 Cerebral Palsy 67 2.034
618
ETN001 Eating Disorder 59 2.033
619
SYS003 Systolic Heart Failure 49 2.031
620
TRT001 Teratocarcinoma 42 2.017
621
MCL006 Macular Retinal Edema 57 2.015
622
HLC007 Helicobacter Pylori Infection 67 2.006
623
P PSD087 Pseudoxanthoma Elasticum 67 2.006
624
PYR041 Pyruvate Kinase Deficiency of Red Cells 57 2.006
626
P MGR001 Migraine Without Aura 49 2.001
627
P PLM006 Pulmonary Alveolar Proteinosis 53 1.992
628
THY030 Thyroid Gland Disease 50 1.990
629
ABD004 Abdominal Tuberculosis 39 1.985
630
HYP020 Hyperprolactinemia 63 1.985
631
P TRN020 Turner Syndrome 67 1.985
632
c VRL012 Viral Meningitis 46 1.982
633
P HRD011 Hereditary Spherocytosis 64 1.982
634
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 42 1.978
635
FRS012 First-Degree Atrioventricular Block 39 1.978
636
HMS001 Hemosiderosis 48 1.978
637
P FTL001 Fetal Alcohol Syndrome 55 1.975
638
BCT004 Bacteriuria 47 1.974
639
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 1.962
640
ERY069 Erythrokeratoderma ''en Cocardes'' 27 1.954
641
P CTR002 Cataract 60 1.954
642
P HRD217 Hereditary Optic Neuropathy 36 1.950
643
P ACN011 Acne 57 1.950
644
XRD010 Xeroderma Pigmentosum, Variant Type 73 1.948
645
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 1.948
646
MDD018 Middle East Respiratory Syndrome 44 1.948
647
DSS032 Disease by Infectious Agent 55 1.930
648
HRP004 Herpes Zoster 61 1.928
649
P ART023 Arthropathy 61 1.923
650
P MCR010 Microcephaly 60 1.921
651
P CMP008 Compartment Syndrome 50 1.921
654
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 60 1.920
655
P RNL015 Renal Hypertension 45 1.920
656
BRN028 Brain Cancer 74 1.905
657
MYL005 Myelofibrosis 71 1.905
658
SPS057 Spasticity 42 1.894
659
CRT072 Creutzfeldt-Jakob Disease 68 1.894
660
c ATM101 Autoimmune Gastritis 40 1.890
661
P ATR005 Atrophic Gastritis 50 1.890
662
P URN019 Urinary Tract Infection 49 1.890
663
P MYT002 Myotonic Dystrophy 51 1.890
664
PTH003 Pathologic Nystagmus 52 1.890
665
P PLY018 Polycythemia 56 1.880
666
P HYP050 Hyperinsulinemic Hypoglycemia 57 1.871
667
P CTN015 Cutaneous T Cell Lymphoma 48 1.866
668
SCR003 Secretory Diarrhea 35 1.866
669
CLR109 Colorectal Adenocarcinoma 50 1.861
670
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 50 1.859
671
P CND004 Candidiasis 58 1.857
672
MSC007 Muscle Hypertrophy 64 1.846
673
c GLC092 Glaucoma, Primary Open Angle 62 1.843
674
HSH003 Hashimoto Thyroiditis 60 1.843
675
OMN001 Omenn Syndrome 63 1.835
676
MCR004 Macroglobulinemia 49 1.835
677
MTC005 Mitochondrial Metabolism Disease 45 1.828
678
P MDL005 Medulloblastoma 75 1.828
679
PNM008 Pneumothorax 54 1.828
680
c EPS039 Episodic Pain Syndrome, Familial, 1 42 1.828
681
P MSC003 Muscular Atrophy 52 1.826
682
c CNT035 Central Nervous System Disease 54 1.825
683
PLS011 Plasmacytoma 56 1.818
684
P FML355 Familial Intrahepatic Cholestasis 42 1.808
685
PRX097 Paroxysmal Dystonia 32 1.808
686
PLS007 Plasmodium Falciparum Malaria 52 1.808
687
c SVR005 Severe Pre-Eclampsia 50 1.808
688
c OPT053 Optic Atrophy 1 62 1.802
689
INT040 Intrinsic Asthma 36 1.797
690
P ART018 Aortic Valve Insufficiency 52 1.796
691
CNN005 Connective Tissue Disease 67 1.796
692
P CYS039 Cystic Kidney Disease 53 1.796
693
PRN011 Pernicious Anemia 53 1.792
694
TRN018 Transitional Cell Carcinoma 56 1.790
695
CHK001 Chikungunya 60 1.788
696
SPN051 Spondylitis 51 1.788
697
INF009 Inflammatory Spondylopathy 30 1.788
698
c CNG027 Congenital Hemolytic Anemia 48 1.785
699
INT075 Intracranial Hypertension 53 1.778
700
P TTR001 Tetralogy of Fallot 69 1.775
701
TNG002 Tangier Disease 64 1.774
702
P FRG001 Fragile X Syndrome 70 1.765
703
VLV047 Volvulus of Midgut 52 1.757
704
P ANR048 Aniridia 1 64 1.752
705
CTN007 Cutaneous Leishmaniasis 62 1.751
706
HYP025 Hyperphosphatemia 48 1.747
707
VSC004 Vasculogenic Impotence 29 1.747
708
P ANT006 Antiphospholipid Syndrome 55 1.747
709
MNN009 Meningoencephalitis 48 1.747
710
P BNC003 Bone Cancer 58 1.747
711
c ALP101 Alpha-Thalassemia 62 1.737
712
P CNR004 Cone-Rod Dystrophy 2 74 1.736
713
c DMN028 Diamond-Blackfan Anemia 12 23 1.733
714
KRT002 Keratomalacia 55 1.732
715
TCL003 T Cell Deficiency 44 1.730
716
GLM044 Glomerular Disease 35 1.728
717
P AGM001 Agammaglobulinemia 68 1.728
718
OPD006 Opioid Addiction 48 1.728
719
c RTN047 Retinitis Pigmentosa 18 46 1.716
720
DBT084 Diabetes Mellitus, Ketosis-Prone 60 1.715
721
ADR022 Adrenomyeloneuropathy 39 1.715
722
ADR007 Adrenoleukodystrophy 73 1.715
723
c HYP326 Hyperinsulinemic Hypoglycemia, Familial, 5 51 1.715
724
c HYP271 Hyperinsulinemic Hypoglycemia, Familial, 4 53 1.715
725
P HRM001 Hermansky-Pudlak Syndrome 65 1.715
726
HYP072 Hypersensitivity Reaction Type Iii Disease 39 1.715
727
c PRG047 Progressive Familial Intrahepatic Cholestasis 64 1.715
728
CNT047 Contact Dermatitis 57 1.715
729
P PTT006 Pituitary Adenoma 55 1.713
730
GNG013 Gingivitis 59 1.707
731
CLR030 Clear Cell Renal Cell Carcinoma 54 1.699
732
P ATX030 Ataxia-Telangiectasia 80 1.694
733
CYN003 Cyanide Poisoning 22 1.693
734
P CRN038 Carney Complex Variant 64 1.693
735
MLD018 Mild Cognitive Impairment 48 1.693
736
P PLM034 Pulmonary Emphysema 58 1.693
737
P FNC004 Fanconi Syndrome 60 1.693
738
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 1.690
739
EXT033 Extrapulmonary Tuberculosis 45 1.690
740
SCH014 Schistosomiasis 56 1.690
741
HYP006 Hypertensive Heart Disease 49 1.690
742
c BLD120 Bleeding Disorder, Platelet-Type, 8 36 1.687
743
c LKM056 Leukemia, Chronic Lymphocytic 2 48 1.684
744
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 64 1.684
745
RFL001 Reflex Sympathetic Dystrophy 51 1.684
746
GST045 Gastroenteritis 58 1.683
747
MMM001 Mammary Paget's Disease 53 1.683
748
THR100 Thrombocytopenic Purpura, Autoimmune 61 1.675
749
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 60 1.674
750
P ESN008 Eosinophilic Pneumonia 50 1.674
751
PLR022 Pleural Disease 45 1.674
752
PLG002 Plague 58 1.673
753
PRV004 Periventricular Leukomalacia 52 1.661
754
c FML021 Familial Hypercholesterolemia 72 1.661
755
P SLM003 Salmonellosis 54 1.656
756
OCL052 Ocular Dominance 40 1.656
757
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 1.656
758
P AMY004 Amyloidosis 70 1.650
759
P NRF002 Neurofibromatosis 57 1.650
760
HPR003 Heparin-Induced Thrombocytopenia 47 1.650
761
P PTN014 Patent Ductus Arteriosus 1 59 1.647
762
BRN032 Brain Glioma 45 1.633
763
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 1.631
764
CYN002 Cyanosis, Transient Neonatal 43 1.631
765
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 1.631
766
P CHL066 Cholangitis 52 1.631
767
APN008 Apnea, Obstructive Sleep 67 1.630
768
PLM031 Poliomyelitis 63 1.618
769
OTT002 Otitis Media 71 1.615
770
P PLY168 Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease 65 1.615
771
c ACT249 Acute Asthma 40 1.615
772
HMN047 Human Cytomegalovirus Infection 57 1.615
773
URL001 Urolithiasis 46 1.615
774
OST011 Osteomalacia 52 1.615
775
P PLY019 Polyneuropathy 52 1.615
776
CRY014 Cryptococcal Meningitis 48 1.605
777
SVR096 Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Positive, Nk Cell-Negative 53 1.605
778
OBS082 Obstructive Nephropathy 41 1.605
779
RYN005 Raynaud Phenomenon 45 1.600
780
P MTC133 Mitochondrial Myopathy 50 1.600
781
c CHR711 Chronic Asthma 41 1.590
782
P GCH001 Gaucher's Disease 70 1.589
783
c DWL002 Dowling-Degos Disease 1 58 1.580
784
c PSD108 Pseudohypoparathyroidism, Type Ia 65 1.580
785
P SPP010 Suppressor of Tumorigenicity 3 51 1.580
786
PSY004 Psychotic Disorder 66 1.580
787
THY111 Thyroid Carcinoma, Familial Medullary 67 1.579
788
MCL003 Macular Holes 44 1.579
789
THY125 Thyroid Gland Medullary Carcinoma 48 1.579
790
PPL002 Papillary Carcinoma 46 1.579
791
WLL004 Wallerian Degeneration 38 1.579
792
P OLG002 Oligodendroglioma 66 1.576
793
PNC041 Pancreatic Ductal Adenocarcinoma 51 1.576
794
MLT131 Multifocal Atrial Tachycardia 17 1.568
795
c THR092 Thrombophilia Due to Thrombin Defect 74 1.568
796
FBR009 Fibrous Dysplasia 48 1.568
797
PLC008 Placenta Disease 49 1.568
798
RSP019 Respiratory Distress Syndrome in Premature Infants 52 1.568
799
NWB001 Newborn Respiratory Distress Syndrome 56 1.568
800
RSP007 Respiratory Distress Syndrome, Infant 40 1.568
801
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 1.549
802
SNG003 Single Ventricular Heart 30 1.543
803
GNT167 Genetic Obesity 30 1.543
804
P GLL022 Guillain-Barre Syndrome 60 1.543
805
CNS002 Constrictive Pericarditis 40 1.543
806
DWR001 Dwarfism 44 1.543
807
P LYM033 Lymphoproliferative Syndrome 59 1.536
808
P STS003 Sitosterolemia 53 1.536
809
P HYP077 Hypertrichosis 46 1.536
810
P VNT002 Ventricular Septal Defect 58 1.536
811
P RNL007 Renal Tubular Acidosis 50 1.536
812
P HMP007 Hemophilia 52 1.536
813
CNG506 Congenital Amyoplasia 27 1.531
814
P ANP001 Anaplastic Large Cell Lymphoma 61 1.531
815
THY122 Thyroid Gland Cancer 59 1.531
816
FDL002 Food Allergy 47 1.530
817
EPD015 Epidemic Typhus 44 1.529
818
NNT012 Neonatal Jaundice 53 1.529
819
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 1.512
820
PLY100 Polyploidy 36 1.505
821
BCT021 Bacterial Sepsis 43 1.505
822
c THY109 Thyroid Cancer, Nonmedullary, 1 55 1.505
823
STT041 Stuttering 52 1.505
824
MST005 Mastitis 53 1.505
825
CHR100 Chronic Ulcer of Skin 57 1.503
826
CHD001 Chediak-Higashi Syndrome 67 1.503
827
PLY001 Polycythemia Vera 69 1.503
828
CHL004 Cholelithiasis 49 1.503
829
HMP005 Hemiplegia 54 1.503
830
ATN005 Autonomic Dysfunction 46 1.503
831
MYX004 Myxedema 43 1.497
832
CLF027 Cleft Palate, Isolated 64 1.495
833
END072 Endotheliitis 36 1.494
834
PRT029 Parathyroid Adenoma 51 1.491
835
SKN019 Skin Melanoma 71 1.489
836
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 1.483
837
PRS047 Prostatitis 58 1.483
838
HMG005 Hemoglobinopathy 56 1.483
839
CCN002 Cocaine Abuse 49 1.478
840
QBC001 Quebec Platelet Disorder 44 1.476
841
ZLL002 Zollinger-Ellison Syndrome 55 1.469
842
KRT019 Keratitis, Hereditary 66 1.469
843
PRS063 Paresthesia 39 1.469
844
P CLS010 Cluster Headache 42 1.469
845
LBR038 Leber Hereditary Optic Neuropathy, Modifier of 62 1.466
846
VRC005 Varicose Veins 60 1.466
847
DYS192 Dystonia, Dopa-Responsive 55 1.466
848
NPH091 Nephrolithiasis, Calcium Oxalate 61 1.466
849
HPT022 Hepatoblastoma 54 1.466
850
P MGR003 Migraine with Aura 52 1.466
851
P PRN023 Prion Disease 60 1.466
852
P MTR003 Mitral Valve Stenosis 53 1.466
853
ACT049 Acute Disseminated Encephalomyelitis 48 1.458
854
KPS004 Kaposi Sarcoma 77 1.449
855
PLT016 Platelet Adenylate Cyclase Activity 16 1.449
856
BSL008 Basal Ganglia Disease 41 1.449
857
DRY001 Dry Eye Syndrome 50 1.449
858
ACR007 Acromegaly 70 1.449
859
PLM035 Pulmonary Eosinophilia 49 1.449
860
P HYP263 Hypersomnia 41 1.449
861
DSR074 Disorder of Purine Metabolism 23 1.446
862
FRC011 Fructose Intolerance, Hereditary 55 1.440
863
P NSP012 Nasopharyngeal Carcinoma 61 1.433
864
P FML018 Familial Mediterranean Fever 73 1.433
865
MCC012 Mccune-Albright Syndrome 70 1.433
866
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 32 1.433
867
ESP023 Esophageal Disease 52 1.433
868
P THR005 Thrombotic Thrombocytopenic Purpura 64 1.433
869
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 66 1.432
870
c WLM013 Wilms Tumor 1 66 1.432
871
c DMN020 Diamond-Blackfan Anemia 8 25 1.431
872
c DMN017 Diamond-Blackfan Anemia 10 35 1.431
873
c DMN019 Diamond-Blackfan Anemia 4 27 1.431
874
c DMN018 Diamond-Blackfan Anemia 5 39 1.431
875
c DMN021 Diamond-Blackfan Anemia 6 37 1.431
876
c DMN024 Diamond-Blackfan Anemia 7 27 1.431
877
c DMN006 Diamond-Blackfan Anemia 3 38 1.431
878
c OVR114 Ovarian Cancer 1 59 1.429
879
LYD001 Leydig Cell Tumor 45 1.425
880
NRT004 Neuritis 53 1.425
881
PRQ002 Paraquat Poisoning 28 1.425
882
P VTR007 Vitreoretinopathy 46 1.425
883
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 1.425
884
SML019 Smallpox 55 1.425
885
P DRM010 Dermatomyositis 61 1.425
886
VRC001 Varicocele 48 1.425
887
IRN001 Iron Deficiency Anemia 58 1.425
888
c RNG015 Ring Chromosome 2 22 1.425
889
TRN030 Transient Erythroblastopenia of Childhood 33 1.402
890
HYP114 Hypertensive Nephropathy 36 1.402
891
INT394 Intermittent Asthma 21 1.402
892
P PRD021 Periodic Paralysis 41 1.402
893
TNS005 Tonsillitis 57 1.402
894
MST020 Mast Cell Activation Syndrome 28 1.402
895
MYT011 Myotonia 39 1.402
896
PYR010 Peyronie's Disease 50 1.397
897
SNS003 Sensory Peripheral Neuropathy 52 1.397
898
P INS002 in Situ Carcinoma 53 1.397
899
P NRV007 Nervous System Disease 67 1.397
900
c HMN021 Human T-Cell Leukemia Virus Type 1 47 1.397
901
TND005 Tendinitis 54 1.391
902
ADN022 Adenylosuccinase Deficiency 44 1.385
903
PRG009 Progressive Multifocal Leukoencephalopathy 58 1.383
904
c ATS204 Autosomal Recessive Non-Syndromic Intellectual Disability 48 1.383
905
OBS002 Obsessive-Compulsive Disorder 68 1.382
906
P MJR007 Major Affective Disorder 1 42 1.382
907
IDP073 Idiopathic Hypercalciuria 40 1.382
908
LNG039 Lung Squamous Cell Carcinoma 57 1.382
909
BLD131 Bladder Urothelial Carcinoma 60 1.382
910
ALC006 Alcoholic Hepatitis 61 1.382
911
P MYG005 Myoglobinuria 40 1.382
912
P PTS002 Ptosis 52 1.382
913
MNN017 Mononeuropathy 41 1.382
914
P TRC031 Trichorhinophalangeal Syndrome 38 1.382
915
ACT200 Acute Monoblastic Leukemia 41 1.382
916
HML018 Homologous Wasting Disease 21 1.377
917
SXL003 Sexual Disorder 49 1.359
918
ENT011 Enterocolitis 55 1.359
919
c PLY170 Polycystic Kidney Disease 4 with or Without Polycystic Liver Disease 63 1.359
920
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 55 1.359
921
c JVN061 Juvenile Arthritis 56 1.359
922
OST003 Osteonecrosis 61 1.359
923
RNL034 Renal Cell Carcinoma 4 15 1.359
924
c ANM038 Anemia, Autoimmune Hemolytic 64 1.351
926
c CHR418 Chronic Leukemia 48 1.351
927
NTR005 Nutritional Deficiency Disease 61 1.342
928
c DRR009 Diarrhea 6 45 1.342
929
c LKM070 Leukemia, Acute Monocytic 56 1.337
930
PSD014 Pseudopseudohypoparathyroidism 54 1.337
931
ATR089 Atrioventricular Dissociation 21 1.337
932
TST044 Testicular Torsion 45 1.337
933
P BRB001 Beriberi 44 1.337
934
GNR004 Generalized Anxiety Disorder 55 1.337
935
P MYC033 Myoclonus 47 1.337
936
EMB004 Embryonal Carcinoma 56 1.336
937
BHC003 Behcet Syndrome 71 1.332
938
SPT004 Septic Arthritis 58 1.332
939
DRM014 Dermatofibrosarcoma Protuberans 65 1.326
940
CRB001 Cerebral Lymphoma 36 1.326
941
P PRM002 Primary Hyperoxaluria 65 1.326
942
LGS001 Legius Syndrome 60 1.319
943
P SDR003 Sideroblastic Anemia 51 1.319
944
INT078 Intracranial Thrombosis 50 1.319
945
RLP002 Relapsing-Remitting Multiple Sclerosis 56 1.319
946
RFL002 Reflex Epilepsy 41 1.319
947
P HMN010 Hemangioma 62 1.319
948
GLC009 Glucosephosphate Dehydrogenase Deficiency 53 1.319
949
c MLG069