Search results for Adenosine

3282 hits were found for Adenosine

# Family MCID Name MIFTS Score
1
ADN001 Adenosine Deaminase Deficiency 59 57.669
2
SVR095 Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Negative, Nk Cell-Negative, Due to Adenosine Deaminase Deficiency 47 52.934
3
HYP241 Hypermethioninemia Due to Adenosine Kinase Deficiency 38 38.001
4
ADN039 Adenosine Triphosphate, Elevated, of Erythrocytes 19 30.893
5
VSC058 Vasculitis, Autoinflammation, Immunodeficiency, and Hematologic Defects Syndrome 49 25.779
6
MYP071 Myopathy Due to Myoadenylate Deaminase Deficiency 44 24.832
7
ADN079 Adenosine Triphosphatase Deficiency, Anemia Due to 8 24.140
8
ADN084 Adenosine Deaminase, Elevated, Hemolytic Anemia Due to 11 23.094
9
c HML041 Hemolytic Anemia Due to Erythrocyte Adenosine Deaminase Overproduction 5 17.414
10
SVR004 Severe Combined Immunodeficiency 70 13.398
11
LPP008 Lipoprotein Quantitative Trait Locus 65 11.658
12
PRT037 Pertussis 49 11.553
13
CMB007 Combined Immunodeficiency 56 11.109
14
SVR066 Severe Combined Immunodeficiency, X-Linked 65 10.810
15
ART140 Arteries, Anomalies of 52 10.712
16
ISC004 Ischemia 61 10.709
17
ERY039 Erythrocyte Amp Deaminase Deficiency 21 9.682
18
ATR057 Atrioventricular Block 54 8.375
19
CRN030 Coronary Stenosis 50 8.331
20
CHL014 Cholera 62 8.291
21
HYP266 Hypoxia 56 7.513
22
P CRN300 Coronary Heart Disease 1 73 7.300
23
P ATR011 Atrial Fibrillation 66 7.231
24
IMM167 Immune Deficiency Disease 76 6.521
25
ANG054 Angina Pectoris 65 6.394
26
P MYC007 Myocardial Infarction 69 6.244
27
c ACT075 Acute Myocardial Infarction 55 6.055
28
P NRB001 Neuroblastoma 66 5.963
29
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 5.960
30
P SZR006 Seizure Disorder 69 5.546
31
CYT002 Cytokine Deficiency 43 5.518
32
ANX004 Anoxia 40 5.370
33
P AST005 Asthma 75 5.249
34
PLM129 Pulmonary Disease, Chronic Obstructive 74 5.198
35
P HRT032 Heart Disease 84 5.195
36
c HYP724 Hyperlipoproteinemia, Type Iii 66 5.129
37
SYN036 Syncope 44 5.038
38
P LKM071 Leukemia, Chronic Lymphocytic 74 4.938
39
48X005 48,xyyy 39 4.803
40
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 4.792
41
CNG034 Congestive Heart Failure 69 4.756
42
P HNT016 Huntington Disease 73 4.751
43
P PRK057 Parkinson Disease, Late-Onset 79 4.727
44
PLR001 Pleural Tuberculosis 49 4.691
45
c ATR087 Atrial Standstill 1 74 4.638
46
ALL029 Allergic Disease 61 4.603
47
PLR008 Pleurisy 49 4.563
48
P DBT009 Diabetes Mellitus 67 4.543
49
LNG099 Lung Disease 62 4.482
50
MYC005 Myocardial Stunning 45 4.466
51
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 4.451
52
GLL048 Glial Tumor 51 4.409
53
GLM045 Glioma 62 4.404
54
P OVR042 Ovarian Cancer 88 4.366
55
P CRD119 Cardiac Arrest 68 4.360
56
P LKM002 Leukemia 65 4.357
57
P MNN013 Meningitis 65 4.324
58
ATH013 Atherosclerosis Susceptibility 63 4.319
59
P PHC003 Pheochromocytoma 70 4.287
60
ADR040 Adrenal Gland Pheochromocytoma 45 4.285
61
c PRC016 Pre-Eclampsia 64 4.274
62
ALL006 Allergic Asthma 55 4.226
63
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 4.204
64
P CHR345 Chronic Pain 50 4.201
65
CYS001 Cystic Fibrosis 77 4.160
66
P PRK039 Parkinsonism 55 4.137
67
c HYP595 Hypertension, Essential 84 4.133
68
LYM027 Lymphopenia 56 4.122
69
P VSC007 Vascular Disease 62 4.079
70
HYP066 Hyperglycemia 60 4.044
71
WLF001 Wolff-Parkinson-White Syndrome 63 4.021
72
PNG002 Pain Agnosia 51 4.019
73
PRT036 Peritonitis 65 4.004
74
P PLM037 Pulmonary Hypertension 69 3.952
75
P GLM040 Glioma Susceptibility 1 70 3.940
76
MLG169 Malignant Astrocytoma 57 3.909
77
CRB004 Cerebral Artery Occlusion 45 3.898
78
SPN186 Spinal Cord Injury 60 3.874
79
P SCK005 Sickle Cell Disease 56 3.830
80
DFC004 Deficiency Anemia 74 3.813
81
P BDY004 Body Mass Index Quantitative Trait Locus 11 82 3.762
82
P ART022 Arthritis 70 3.754
83
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 3.753
84
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 3.749
85
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 3.749
86
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 3.749
87
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 3.749
88
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 3.749
89
c BDY019 Body Mass Index Quantitative Trait Locus 18 46 3.749
90
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 3.749
91
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 3.749
92
P HYP086 Hypothyroidism 68 3.732
93
c MGR028 Migraine with or Without Aura 1 63 3.731
94
P RHM011 Rheumatoid Arthritis 81 3.729
95
CLT003 Colitis 63 3.713
96
P LYM118 Lymphoma 66 3.700
97
c ACT071 Acute Kidney Failure 60 3.679
98
P HML002 Hemolytic Anemia 62 3.674
99
P ADL010 Adult Respiratory Distress Syndrome 70 3.654
100
TBR011 Tuberculous Meningitis 48 3.643
101
P RHN004 Rhinitis 56 3.641
102
HLX001 Helix Syndrome 47 3.638
103
P ALZ034 Alzheimer Disease 87 3.593
104
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 3.551
105
P EPL164 Epilepsy 70 3.544
106
GLB002 Glioblastoma 67 3.541
107
BRN071 Brain Injury 50 3.532
108
P MYC084 Mycobacterium Tuberculosis 1 68 3.531
109
c TYP009 Type 2 Diabetes Mellitus 91 3.514
110
P TRM003 Tremor 50 3.509
111
ALL003 Allergic Rhinitis 66 3.454
112
PLM001 Pulmonary Tuberculosis 69 3.450
113
P KDN018 Kidney Disease 71 3.423
114
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 3.405
115
AGN016 Aging 53 3.375
116
HMN044 Human Immunodeficiency Virus Type 1 76 3.356
117
TRM010 Traumatic Brain Injury 50 3.349
118
BNR002 Bone Resorption Disease 47 3.320
119
P PLY017 Polyarteritis Nodosa 59 3.316
120
P LVR013 Liver Disease 68 3.297
121
c TYP008 Type 1 Diabetes Mellitus 77 3.261
122
c DLT002 Dilated Cardiomyopathy 79 3.254
123
GSG001 Gas Gangrene 52 3.248
124
PLM010 Pulmonary Edema 54 3.219
125
c MCR133 Microvascular Complications of Diabetes 4 41 3.186
126
c MCR113 Microvascular Complications of Diabetes 3 52 3.186
127
c MCR130 Microvascular Complications of Diabetes 6 41 3.186
128
c MCR120 Microvascular Complications of Diabetes 7 47 3.186
129
HYP056 Hypoglycemia 65 3.147
130
FTT001 Fatty Liver Disease 61 3.136
131
NNL005 Non-Alcoholic Fatty Liver Disease 63 3.120
132
RPD005 Rapidly Involuting Congenital Hemangioma 48 3.119
133
P HYP076 Hyperthyroidism 53 3.093
134
TXC005 Toxic Shock Syndrome 61 3.070
135
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 3.055
136
P DRR001 Diarrhea 55 3.054
137
c PRG042 Progressive Familial Heart Block, Type Ia 65 3.037
138
INT007 Intermediate Coronary Syndrome 53 3.031
139
P HPT023 Hepatocellular Carcinoma 95 2.978
140
OST159 Osteogenic Sarcoma 66 2.977
141
P HYP069 Hyperparathyroidism 62 2.958
142
HYP005 Hypokalemia 55 2.956
143
P BRS047 Breast Cancer 97 2.956
144
STT001 Status Epilepticus 58 2.954
145
P THR014 Thrombocytopenia 66 2.942
146
P MSC005 Muscular Dystrophy 66 2.924
147
P BCL017 B-Cell Lymphoma 57 2.915
148
P VSC011 Vasculitis 61 2.895
149
P DMN001 Diamond-Blackfan Anemia 73 2.886
150
TBR008 Tuberculous Peritonitis 35 2.883
151
ACQ007 Acquired Immunodeficiency Syndrome 58 2.873
152
P HDC001 Headache 56 2.849
153
c HYP836 Hypercholesterolemia, Familial, 1 73 2.836
154
c SYS001 Systemic Lupus Erythematosus 85 2.820
155
ATM095 Autoimmune Disease 61 2.810
156
IMP005 Impotence 52 2.784
157
GST033 Gestational Diabetes 60 2.779
158
P LKM062 Leukemia, Acute Lymphoblastic 69 2.775
159
MNT002 Mental Depression 56 2.772
160
P PNC025 Panic Disorder 52 2.755
161
P HYP098 Hypereosinophilic Syndrome 66 2.751
162
c MCR115 Microvascular Complications of Diabetes 5 65 2.748
163
P PSR002 Psoriasis 63 2.748
164
P MYL006 Myeloid Leukemia 60 2.746
165
END086 End Stage Renal Disease 54 2.741
166
PST011 Pustulosis of Palm and Sole 52 2.740
167
P SLP005 Sleep Disorder 61 2.736
168
RNL077 Renal Fibrosis 46 2.707
169
c FML001 Familial Atrial Fibrillation 65 2.690
170
DPR016 Depression 64 2.682
171
P MLN008 Melanoma 75 2.666
172
P CLR023 Colorectal Cancer 100 2.662
173
P PLM036 Pulmonary Fibrosis 65 2.659
174
c PLM164 Pulmonary Hypertension, Primary, 1 75 2.649
175
P DRM053 Dermatitis, Atopic 65 2.642
176
LPD008 Lipid Metabolism Disorder 61 2.640
177
HYP060 Hyperinsulinism 53 2.632
178
P PNM007 Pneumonia 64 2.632
179
P MJR001 Major Depressive Disorder 68 2.628
180
P BRL012 Bare Lymphocyte Syndrome, Type Ii 65 2.624
181
P TMP001 Temporal Lobe Epilepsy 49 2.609
182
c AMY091 Amyotrophic Lateral Sclerosis 1 87 2.607
183
P LTR001 Lateral Sclerosis 57 2.607
184
MYL069 Myeloma, Multiple 76 2.607
185
ALC007 Alcohol Dependence 65 2.606
186
c CHR684 Chronic Kidney Disease 73 2.580
187
LFT001 Left Bundle Branch Hemiblock 47 2.577
188
P HYP061 Hypertrophic Cardiomyopathy 68 2.575
189
P NTR004 Neutropenia 62 2.572
190
DYS022 Dyschromatosis Symmetrica Hereditaria 49 2.553
191
P ENC018 Encephalopathy 62 2.550
192
P LPS004 Lupus Erythematosus 61 2.548
193
CRH001 Crohn's Disease 80 2.544
194
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 2.539
195
ANR040 Aneurysm 60 2.533
196
P GST053 Gastric Cancer 82 2.522
197
PRN001 Purine Nucleoside Phosphorylase Deficiency 53 2.511
198
ULC004 Ulcerative Colitis 74 2.499
199
P ECL001 Eclampsia 52 2.497
200
PRP027 Peripheral Vascular Disease 71 2.478
201
INS024 Insulin-Like Growth Factor I 77 2.476
202
TTN003 Tetanus 64 2.464
203
P BNG032 Benign Mesothelioma 53 2.462
204
CHR074 Choriocarcinoma 46 2.455
205
47X002 47,xyy 47 2.447
206
LYM019 Lymphosarcoma 46 2.444
207
VLK001 Volkmann Contracture 23 2.437
208
c DMN023 Diamond-Blackfan Anemia 1 68 2.432
209
P HRP006 Herpes Simplex 65 2.430
210
OCL069 Ocular Motor Apraxia 57 2.424
211
HRY003 Hairy Cell Leukemia 53 2.414
212
c LKM061 Leukemia, Acute Myeloid 83 2.413
213
P HPT021 Hepatitis 68 2.408
214
THR024 Thrombosis 56 2.405
215
STM007 Stomatitis 52 2.405
216
ANT039 Antisynthetase Syndrome 55 2.405
217
PRC013 Pericarditis 53 2.404
218
SLP001 Sleeping Sickness 56 2.403
219
MTB004 Metabolic Acidosis 48 2.402
220
VCC001 Vaccinia 49 2.374
221
P SCK002 Sick Sinus Syndrome 55 2.372
222
PRT251 Proteinuria, Chronic Benign 58 2.365
223
OCL006 Ocular Hypertension 53 2.348
224
EXR010 Exercise-Induced Bronchoconstriction 34 2.345
225
RHB024 Rhabdomyosarcoma 2 65 2.344
226
IRN002 Iron Metabolism Disease 56 2.334
227
DBT010 Diabetic Neuropathy 54 2.332
228
ADN018 Adenoma 58 2.315
229
HMN014 Human Immunodeficiency Virus Infectious Disease 54 2.311
230
P SCH015 Schizophrenia 74 2.302
231
P SRC025 Sarcoidosis 1 70 2.291
232
P MVM001 Movement Disease 61 2.280
233
ATS010 Autosomal Recessive Disease 42 2.279
234
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 2.277
235
c PRM005 Primary Hyperparathyroidism 59 2.269
236
STR089 Storage Pool Platelet Disease 46 2.262
237
SCK003 Sickle Cell Anemia 74 2.261
238
P ADN016 Adenocarcinoma 63 2.261
239
ADL002 Adult Syndrome 69 2.259
240
c ATS007 Autism Spectrum Disorder 71 2.255
241
P ALC033 Alcohol Use Disorder 67 2.253
242
P KLZ004 Kala-Azar 1 41 2.252
243
LSH001 Leishmaniasis 63 2.252
244
CMP010 Complex Regional Pain Syndrome 59 2.252
245
CVD001 Covid-19 59 2.252
246
ESP021 Esophageal Cancer 84 2.239
247
ALL014 Allergic Encephalomyelitis 34 2.221
248
P PRD008 Periodontitis 63 2.219
249
MSC157 Muscular Dystrophy, Duchenne Type 78 2.208
250
PLR007 Pleural Empyema 50 2.201
251
P GRV001 Graves' Disease 54 2.201
252
LWC001 Low Compliance Bladder 44 2.192
253
PRC005 Pericardial Tuberculosis 35 2.187
254
P ATS364 Autism 72 2.168
255
CRB039 Cerebrovascular Disease 65 2.164
256
CHL068 Cholestasis 61 2.158
257
P SLP006 Sleep Apnea 69 2.155
258
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 2.148
259
LVR012 Liver Cirrhosis 62 2.148
260
P RSP003 Respiratory Failure 73 2.144
261
STR067 Stroke, Ischemic 79 2.140
262
DRM006 Dermatitis 61 2.138
263
TRN015 Transient Cerebral Ischemia 62 2.136
264
PPL052 Papillomatosis, Confluent and Reticulated 34 2.134
265
OST012 Osteoarthritis 77 2.132
266
MST004 Mast Cell Neoplasm 41 2.117
267
EXT007 Extracutaneous Mastocytoma 38 2.117
268
CRT015 Carotid Artery Occlusion 45 2.114
269
APN006 Apnea of Prematurity 24 2.101
270
c ACT027 Acute Pancreatitis 60 2.077
271
CRB086 Cerebral Aneurysms 40 2.077
272
ANX010 Anxiety 70 2.077
273
P LNG064 Lung Cancer Susceptibility 3 69 2.077
274
c HPT073 Hepatitis C Virus 70 2.073
275
P LNG032 Lung Cancer 98 2.073
276
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 2.068
277
P THY032 Thyroiditis 56 2.063
278
c LKM063 Leukemia, Chronic Myeloid 70 2.061
279
BRK012 Broken Heart Syndrome 42 2.059
280
P PNC035 Pancreatic Cancer 87 2.053
281
c BCT007 Bacterial Meningitis 55 2.049
282
c LKM005 Leukemia, T-Cell, Chronic 33 2.046
283
PTT037 Pituitary Tumors 44 2.042
284
SNT005 Sinoatrial Node Disease 48 2.035
285
c INH020 Inherited Metabolic Disorder 47 2.027
286
P GRF003 Graft-Versus-Host Disease 71 2.025
287
c ACT073 Acute Leukemia 59 2.022
288
RTN003 Retinal Ischemia 48 2.007
289
c BRN108 Branchiootic Syndrome 1 63 2.000
290
P MYP004 Myopathy 67 1.999
291
HYP014 Hyperuricemia 51 1.998
292
ACT098 Acute Erythroid Leukemia 55 1.995
293
P RST001 Restless Legs Syndrome 52 1.995
294
P GST044 Gastritis 55 1.990
295
P TRN020 Turner Syndrome 67 1.989
296
c PNS012 Paine Syndrome 60 1.986
297
P PRP029 Porphyria 60 1.977
298
MDD011 Mood Disorder 61 1.975
299
WTH001 Withdrawal Disorder 47 1.969
300
P UVT001 Uveitis 57 1.967
301
P INF037 Inflammatory Bowel Disease 53 1.962
302
P NRP001 Neuropathy 59 1.962
303
P PRC012 Pericardial Effusion 50 1.961
304
INT030 Intracranial Aneurysm 55 1.958
305
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 1.956
306
PPT005 Peptic Ulcer Disease 58 1.954
307
SRC014 Sarcoma 64 1.935
308
P INF032 Infertility 60 1.935
309
CMB081 Combined Immunodeficiency, X-Linked 39 1.923
310
HMC014 Homocysteinemia 52 1.920
311
RTN020 Retinal Vascular Disease 45 1.910
312
PST028 Post-Traumatic Stress Disorder 58 1.910
313
P BLD134 Bladder Cancer 79 1.906
314
PRP007 Priapism 46 1.905
315
P ART005 Arteriovenous Malformation 64 1.895
316
BCT022 Bacterial Infectious Disease 55 1.887
317
c MJR022 Major Affective Disorder 8 37 1.884
318
c MJR024 Major Affective Disorder 9 40 1.884
319
P BPL003 Bipolar Disorder 56 1.884
320
THY029 Thyroid Carcinoma 55 1.883
321
BRN002 Bronchiolitis 57 1.879
322
SPN035 Spindle Cell Sarcoma 51 1.878
323
IGR001 Ige Responsiveness, Atopic 58 1.870
324
CHC001 Chickenpox 56 1.866
325
P SYS005 Systemic Scleroderma 73 1.864
326
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 1.854
327
P PSD015 Pseudohypoparathyroidism 54 1.852
328
P DBT005 Diabetes Insipidus 54 1.851
329
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 1.846
330
P OST002 Osteoporosis 76 1.846
331
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 1.846
332
DWN001 Down Syndrome 70 1.842
333
RST023 Resting Heart Rate, Variation in 40 1.838
334
CRD132 Cardiac Conduction Defect 59 1.837
335
P HYP024 Hypoparathyroidism 55 1.835
336
c THY107 Thymoma, Familial 42 1.833
337
P THY023 Thymoma 64 1.833
338
c EPS039 Episodic Pain Syndrome, Familial, 1 42 1.831
339
CRD223 Cardiac Arrhythmia 63 1.830
340
CTY001 Cat Eye Syndrome 45 1.830
341
P CRD246 Cardiovascular System Disease 55 1.820
342
P SBS003 Substance Abuse 54 1.816
343
INT002 Intermittent Claudication 61 1.810
344
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 60 1.809
345
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 62 1.808
346
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 1.806
347
P PRP019 Peripheral Nervous System Disease 57 1.801
348
BRK010 Burkitt Lymphoma 65 1.797
349
P PNC044 Pancreatitis 61 1.790
350
SCN049 Second-Degree Atrioventricular Block 34 1.767
351
SQM006 Squamous Cell Carcinoma 59 1.767
352
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 44 1.766
353
c SPN225 Spondyloarthropathy 1 70 1.765
354
AMN003 Amnestic Disorder 53 1.763
355
HMP001 Hemopericardium 47 1.762
356
c PCH010 Pachyonychia Congenita 3 43 1.762
357
P ENC004 Encephalitis 61 1.757
358
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 1.756
359
CRV035 Cervical Cancer 72 1.754
360
P PLY011 Polycystic Ovary Syndrome 57 1.753
361
P TXP001 Toxoplasmosis 59 1.753
362
LYM040 Lymphoblastic Lymphoma 53 1.749
363
P OST001 Osteopetrosis 70 1.749
364
DPH001 Diphtheria 59 1.749
365
NNL006 Non-Alcoholic Steatohepatitis 54 1.749
366
P MYC008 Myocarditis 59 1.742
367
PLY150 Polykaryocytosis Inducer 29 1.741
368
c DMN028 Diamond-Blackfan Anemia 12 23 1.735
369
PSR001 Psoriatic Arthritis 61 1.731
370
ACT084 Acute Stress Disorder 53 1.730
371
P GLM007 Glomerulonephritis 59 1.725
372
HYP003 Hypermethioninemia 51 1.721
373
P DYS154 Dystonia 64 1.719
374
TRY001 Trypanosomiasis 50 1.719
375
ASP030 Aspirin Resistance 41 1.718
376
LSC001 Lesch-Nyhan Syndrome 62 1.715
377
P SNS001 Sensorineural Hearing Loss 60 1.709
378
MYL009 Myelodysplastic Syndrome 67 1.705
379
GT001 Gout 63 1.704
380
MSL001 Measles 61 1.703
381
P MLT020 Multiple Sclerosis 79 1.701
382
VSC003 Visceral Leishmaniasis 54 1.701
383
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 51 1.693
384
BRN024 Bronchitis 67 1.692
385
P EXN002 Exanthem 58 1.688
386
P PLY014 Polycystic Kidney Disease 71 1.687
387
TYP007 Typhoid Fever 63 1.684
388
CLN015 Colon Adenocarcinoma 64 1.678
389
INT323 Intraocular Pressure Quantitative Trait Locus 63 1.674
390
GST050 Gastrointestinal System Disease 55 1.668
391
HYP017 Hypophosphatemia 49 1.665
392
URT010 Ureteral Obstruction 44 1.664
393
SVR001 Severe Acute Respiratory Syndrome 68 1.661
394
P DNG005 Dengue Virus 55 1.659
395
c SCL052 Scleroderma, Familial Progressive 60 1.656
396
SKN016 Skin Disease 63 1.647
397
c PRG043 Progressive Familial Heart Block, Type Ib 54 1.646
398
RGH001 Right Bundle Branch Block 47 1.646
399
P BRS044 Breast Adenocarcinoma 58 1.642
400
P CYS018 Cystitis 58 1.637
401
P THL005 Thalassemia 56 1.633
402
CMM004 Common Variable Immunodeficiency 71 1.632
403
P LNG028 Long Qt Syndrome 63 1.630
404
P PRS040 Prostate Cancer 95 1.630
405
HMP009 Haemophilus Influenzae 41 1.628
406
INS001 Insulinoma 59 1.623
407
SVR096 Severe Combined Immunodeficiency, Autosomal Recessive, T Cell-Negative, B Cell-Positive, Nk Cell-Negative 54 1.619
408
GTR002 Goiter 52 1.618
409
PRS045 Prostatic Hypertrophy 53 1.617
410
P ESP024 Esophagitis 60 1.616
411
P BND020 Bone Disease 60 1.614
412
c VRL010 Viral Hepatitis 52 1.610
413
END057 Endometrial Cancer 76 1.609
414
BLD053 Blood Platelet Disease 51 1.608
415
CCN001 Cocaine Dependence 47 1.608
416
BRN004 Brain Edema 54 1.607
417
MLR004 Malaria 77 1.594
418
P MYS003 Myasthenia Gravis 67 1.594
419
ASP003 Aseptic Meningitis 50 1.593
420
P KDN017 Kidney Cancer 60 1.593
421
TLN003 Telangiectasis 51 1.589
422
HPT004 Hepatic Coma 43 1.585
423
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 1.584
424
c ATM099 Autoimmune Uveitis 44 1.580
425
CHL065 Cholangiocarcinoma 57 1.578
426
INT079 Intrahepatic Cholangiocarcinoma 51 1.578
427
PNC001 Pancytopenia 52 1.570
428
P MCR129 Microvascular Complications of Diabetes 1 67 1.569
429
P RNV001 Renovascular Hypertension 48 1.564
430
c BCT013 Bacterial Pneumonia 47 1.547
431
CRN019 Coronary Artery Vasospasm 47 1.540
432
P ATT013 Attention Deficit-Hyperactivity Disorder 65 1.529
433
ART016 Aortic Aneurysm 68 1.520
434
c ACT134 Acute Liver Failure 57 1.520
435
P LPR021 Leprosy 3 71 1.520
436
HNS001 Hansen's Disease 32 1.520
437
P NRC002 Narcolepsy 55 1.519
438
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 1.514
439
c SML038 Small Cell Cancer of the Lung 68 1.512
440
c CHR688 Chronic Acquired Demyelinating Polyneuropathy 16 1.508
441
END040 Endogenous Depression 54 1.506
442
c HPT016 Hepatitis B 62 1.505
443
PRS021 Prostatic Adenoma 43 1.503
444
P OPT006 Optic Nerve Disease 57 1.501
445
END072 Endotheliitis 36 1.498
446
P MLG056 Malignant Hyperthermia 65 1.496
447
GST023 Gastric Ulcer 52 1.494
448
PRP016 Paraplegia 52 1.491
449
P HYP750 Hypertriglyceridemia, Familial 61 1.488
450
SDD001 Sudden Infant Death Syndrome 60 1.477
451
MRP001 Morphine Dependence 41 1.473
452
P WSK001 Wiskott-Aldrich Syndrome 72 1.472
453
DSS009 Disseminated Intravascular Coagulation 56 1.471
454
OVR094 Ovarian Epithelial Cancer 39 1.471
455
P ALP008 Alopecia 53 1.471
456
c EXD008 Exudative Vitreoretinopathy 1 71 1.469
457
P MLN007 Male Infertility 56 1.469
458
ADG002 Audiogenic Seizures 25 1.469
459
GLC003 Glucose Intolerance 53 1.467
460
OMN001 Omenn Syndrome 63 1.466
461
P HYP265 Hypotonia 42 1.466
462
P MYP006 Myopia 55 1.465
463
P CHR012 Chronic Granulomatous Disease 69 1.464
464
P ANR048 Aniridia 1 66 1.459
465
P RTN024 Retinoblastoma 72 1.459
466
HGH043 High Grade Glioma 46 1.458
467
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 1.454
468
CRD137 Cardiogenic Shock 56 1.451
470
RCK004 Rickets 64 1.450
471
c ART101 Aortic Valve Disease 2 65 1.446
472
P INT143 Interstitial Cystitis 59 1.445
473
BLR008 Bilirubin Metabolic Disorder 57 1.443
474
URM002 Uremia 47 1.442
475
NRR001 Neuroretinitis 42 1.442
476
RTN023 Retinitis 45 1.442
477
P CNR004 Cone-Rod Dystrophy 2 74 1.440
478
P PLM006 Pulmonary Alveolar Proteinosis 53 1.435
479
c ESS001 Essential Tremor 56 1.434
480
c DMN006 Diamond-Blackfan Anemia 3 39 1.433
481
c DMN017 Diamond-Blackfan Anemia 10 36 1.433
482
c DMN019 Diamond-Blackfan Anemia 4 26 1.433
483
c DMN018 Diamond-Blackfan Anemia 5 42 1.433
484
c DMN021 Diamond-Blackfan Anemia 6 38 1.433
485
c DMN024 Diamond-Blackfan Anemia 7 27 1.433
486
c DMN020 Diamond-Blackfan Anemia 8 26 1.433
487
PRS129 Prostatic Hyperplasia, Benign 48 1.430
488
MTB016 Metabolic Myopathy 30 1.424
489
KWS002 Kawasaki Disease 65 1.423
490
P ACT105 Acute Mountain Sickness 52 1.411
491
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 44 1.411
492
P FBR017 Fibrosarcoma 55 1.405
493
LMB062 Limb Ischemia 55 1.404
494
P BRN022 Bronchiectasis 59 1.402
495
HDN002 Head Injury 44 1.399
496
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 1.399
497
ARG004 Argyria 26 1.399
498
RNL114 Renal Cell Carcinoma, Nonpapillary 79 1.396
499
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 65 1.391
500
c LKM056 Leukemia, Chronic Lymphocytic 2 47 1.391
501
RFL001 Reflex Sympathetic Dystrophy 51 1.391
502
CRB090 Cerebral Hypoxia 42 1.385
503
LGH007 Leigh Syndrome 70 1.383
504
INT066 Interstitial Lung Disease 60 1.380
505
OCL010 Ocular Hypotension 37 1.380
506
P RRH023 Rare Hereditary Hemochromatosis 52 1.377
507
VRL011 Viral Infectious Disease 60 1.376
508
BRC012 Brucellosis 66 1.374
509
HRT012 Heart Valve Disease 53 1.371
510
SYS003 Systolic Heart Failure 49 1.371
511
P RHB003 Rhabdomyosarcoma 66 1.367
512
RSP019 Respiratory Distress Syndrome in Premature Infants 52 1.362
513
NWB001 Newborn Respiratory Distress Syndrome 56 1.362
514
RSP007 Respiratory Distress Syndrome, Infant 41 1.362
515
LYM143 Lymphoma, Non-Hodgkin, Familial 74 1.360
516
c ACT135 Acute Graft Versus Host Disease 51 1.359
517
P EYD002 Eye Disease 57 1.358
518
c CNT035 Central Nervous System Disease 53 1.354
519
c HPT003 Hepatitis a 63 1.352
520
c GRV008 Graves Disease 1 54 1.347
521
FCL014 Focal Epilepsy 53 1.347
522
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 1.343
523
c DRR009 Diarrhea 6 46 1.342
524
NTR005 Nutritional Deficiency Disease 60 1.342
525
PLM134 Pulmonary Fibrosis, Idiopathic 76 1.341
526
CHG001 Chagas Disease 65 1.341
527
c ATS347 Autosomal Dominant Polycystic Kidney Disease 64 1.341
528
HSH003 Hashimoto Thyroiditis 60 1.341
529
P END044 Endometriosis 62 1.340
530
c CRD086 Cardiomyopathy, Familial Hypertrophic, 1 69 1.329
531
LYM133 Lymphoma, Hodgkin, Classic 69 1.327
532
c HPT015 Hepatitis D 49 1.326
533
ADR016 Adrenal Cortical Carcinoma 61 1.326
534
c BLD120 Bleeding Disorder, Platelet-Type, 8 35 1.325
535
TRD006 Tardive Dyskinesia 53 1.322
536
P ART021 Arteriosclerosis 53 1.321
537
OPT003 Opiate Dependence 49 1.321
538
PPL022 Papilloma 53 1.318
539
SQM002 Squamous Cell Papilloma 45 1.318
540
DFF005 Diffuse Large B-Cell Lymphoma 55 1.309
541
P DDN001 Duodenal Ulcer 52 1.305
542
ENT004 Enthesopathy 51 1.296
543
ACT003 Acute Kidney Tubular Necrosis 46 1.296
544
P PRR002 Pure Red-Cell Aplasia 46 1.295
545
c GLL024 Gallbladder Disease 1 53 1.295
546
c BTT014 Beta-Thalassemia 72 1.295
547
BHR001 Behr Syndrome 51 1.293
548
c MCL013 Mucolipidosis Iv 64 1.293
549
ACR041 Acromelic Frontonasal Dysostosis 53 1.293
550
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 49 1.293
551
CHR008 Choroiditis 48 1.293
552
CRB009 Cerebritis 43 1.293
553
c PST005 Posterior Uveitis 54 1.293
554
CLL014 Cll/sll 45 1.293
555
GNG013 Gingivitis 59 1.290
556
HPT019 Hepatic Encephalopathy 59 1.286
557
CLP006 Clopidogrel Resistance 44 1.279
558
P ADL017 Adult T-Cell Leukemia 53 1.277
559
CNS004 Constipation 56 1.276
560
THR035 Thrombasthenia 48 1.276
561
BRN012 Bronchiolitis Obliterans 56 1.276
562
BRN056 Bronchopulmonary Dysplasia 57 1.271
563
PRP030 Purpura 54 1.270
564
PRT013 Portal Hypertension 59 1.266
565
IRR002 Irritable Bowel Syndrome 64 1.266
566
P CHN012 Chondrosarcoma 56 1.265
567
HRP004 Herpes Zoster 60 1.264
568
ACT049 Acute Disseminated Encephalomyelitis 53 1.262
569
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 1.261
570
P LCT001 Lactic Acidosis 50 1.259
571
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 1.254
572
NRF007 Neurofibroma 63 1.249
573
THR099 Third-Degree Atrioventricular Block 42 1.246
574
P RTN018 Retinal Disease 53 1.246
575
c HPT001 Hepatitis C 61 1.240
576
ATN004 Autonomic Neuropathy 42 1.240
577
c ART115 Aortic Valve Disease 1 72 1.240
578
NRM005 Neuromuscular Disease 62 1.235
579
c JVN010 Juvenile Rheumatoid Arthritis 52 1.233
580
c MST023 Mesothelioma, Malignant 56 1.232
581
WST005 West Nile Virus 55 1.230
582
THR004 Thrombocytosis 52 1.228
583
c CNG027 Congenital Hemolytic Anemia 49 1.228
584
c MCR112 Microvascular Complications of Diabetes 2 42 1.227
585
PRP080 Peripheral Artery Disease 54 1.226
586
ETN001 Eating Disorder 59 1.223
587
c OVR114 Ovarian Cancer 1 60 1.221
588
KRT002 Keratomalacia 54 1.220
589
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 1.218
590
TCL003 T Cell Deficiency 44 1.214
591
FDL002 Food Allergy 47 1.214
592
P MNC007 Monocytic Leukemia 48 1.206
593
CRN017 Coronary Thrombosis 46 1.203
594
c PRG020 Paragangliomas 3 39 1.199
595
VSC002 Vascular Dementia 59 1.195
596
PLS011 Plasmacytoma 56 1.192
597
PNC129 Pancreatic Adenocarcinoma 64 1.189
598
c SCN007 Secondary Hyperparathyroidism 50 1.189
599
ADR054 Adrenocortical Carcinoma, Hereditary 47 1.184
600
ADR004 Adrenal Cortical Adenocarcinoma 38 1.184
601
OBS082 Obstructive Nephropathy 41 1.183
602
TRC003 Trichomoniasis 53 1.183
603
QBC001 Quebec Platelet Disorder 43 1.181
604
HRW001 Hair Whorl 35 1.177
605
NWC001 Newcastle Disease 47 1.177
606
MCR004 Macroglobulinemia 48 1.174
607
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 1.173
608
P HMC002 Homocystinuria 52 1.171
609
P FBR031 Febrile Seizures 52 1.171
610
CLR109 Colorectal Adenocarcinoma 50 1.166
611
AND014 Androgenic Alopecia 46 1.164
612
P ALP061 Alopecia, Androgenetic, 1 48 1.164
613
P OBS001 Obstructive Jaundice 49 1.164
614
TRN018 Transitional Cell Carcinoma 56 1.163
615
DRG003 Drug Dependence 46 1.162
616
AGR002 Agoraphobia 45 1.161
617
P OPN001 Open-Angle Glaucoma 55 1.160
618
HRN029 Hearing Loss, Noise-Induced 37 1.158
619
TRT001 Teratocarcinoma 41 1.152
620
ILT001 Ileitis 49 1.151
621
DMY004 Demyelinating Disease 50 1.151
622
MYL005 Myelofibrosis 70 1.148
623
c VRL012 Viral Meningitis 46 1.144
624
P HRD011 Hereditary Spherocytosis 63 1.144
625
ORL011 Oral Cancer 60 1.138
626
PST092 Posttransplant Acute Limbic Encephalitis 29 1.135
627
SPR126 Superior Semicircular Canal Dehiscence 41 1.132
628
c HMG029 Hemoglobin Se Disease 41 1.132
629
ATX019 Ataxia with Vitamin E Deficiency 44 1.129
630
P ACR001 Aicardi-Goutieres Syndrome 63 1.128
631
THY030 Thyroid Gland Disease 50 1.128
632
URT049 Urate Oxidase, Pseudogene 24 1.124
633
SYN007 Synovitis 54 1.124
634
PLC002 Plica Syndrome 35 1.124
635
CHL123 Chlamydia 58 1.124
636
NPH009 Nephrolithiasis 54 1.124
637
P OVR082 Overgrowth Syndrome 41 1.116
638
DRM014 Dermatofibrosarcoma Protuberans 64 1.114
639
P PRM002 Primary Hyperoxaluria 65 1.114
640
CRB001 Cerebral Lymphoma 37 1.114
641
c PRM038 Primary Agammaglobulinemia 47 1.112
642
P NPH012 Nephrotic Syndrome 61 1.112
643
PLM033 Pulmonary Embolism 58 1.112
645
RTN017 Retinal Detachment 60 1.109
646
HMG002 Hemoglobinuria 50 1.101
647
YLL002 Yellow Fever 61 1.101
648
PRN011 Pernicious Anemia 52 1.097
649
P HYP050 Hyperinsulinemic Hypoglycemia 56 1.093
650
P TBR001 Tuberous Sclerosis 69 1.093
651
MSC007 Muscle Hypertrophy 64 1.092
652
P HYD006 Hydrocephalus 62 1.087
653
ANT024 Anthrax Disease 57 1.087
654
BCT004 Bacteriuria 48 1.085
655
ACT119 Acute Promyelocytic Leukemia 62 1.083
656
THR100 Thrombocytopenic Purpura, Autoimmune 60 1.083
657
OST015 Osteochondrodysplasia 60 1.082
658
ORL015 Oral Squamous Cell Carcinoma 43 1.074
659
c ATM011 Autoimmune Hepatitis 62 1.074
660
HPT014 Hepatorenal Syndrome 49 1.074
661
P FRG001 Fragile X Syndrome 70 1.072
662
WLS001 Wilson Disease 70 1.068
663
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 1.063
664
CHR178 Chromosomal Triplication 33 1.061
665
c TBR025 Tuberous Sclerosis 1 84 1.057
666
P RTN016 Retinal Degeneration 52 1.057
667
DBT084 Diabetes Mellitus, Ketosis-Prone 59 1.056
668
ATY005 Atypical Teratoid Rhabdoid Tumor 69 1.056
669
P URT039 Urticaria 57 1.054
670
CRY014 Cryptococcal Meningitis 48 1.050
671
P INT068 Intestinal Disease 53 1.047
672
P MTR014 Motor Neuron Disease 65 1.047
673
INT040 Intrinsic Asthma 36 1.041
674
c DNT047 Dentinogenesis Imperfecta Type 2 35 1.040
675
GST040 Gastric Adenocarcinoma 66 1.040
676
APN008 Apnea, Obstructive Sleep 66 1.039
677
MCL006 Macular Retinal Edema 56 1.033
678
VLV047 Volvulus of Midgut 55 1.031
679
c DMN030 Diamond-Blackfan Anemia 13 19 1.031
680
ART002 Arts Syndrome 66 1.029
681
INF013 Inferior Myocardial Infarction 33 1.029
682
HYP020 Hyperprolactinemia 63 1.025
683
ABD004 Abdominal Tuberculosis 39 1.025
684
P VNW001 Von Willebrand's Disease 64 1.023
685
PRT029 Parathyroid Adenoma 51 1.022
686
c RTN047 Retinitis Pigmentosa 18 45 1.021
687
c ATS204 Autosomal Recessive Non-Syndromic Intellectual Disability 47 1.018
688
c TYR012 Tyrosinemia, Type I 61 1.018
689
P EPL140 Epilepsy, Idiopathic Generalized 60 1.018
690
PRG009 Progressive Multifocal Leukoencephalopathy 58 1.018
691
P ART023 Arthropathy 59 1.018
692
ERY069 Erythrokeratoderma ''en Cocardes'' 26 1.018
693
PLG002 Plague 58 1.010
694
NRT004 Neuritis 53 1.005
695
LYD001 Leydig Cell Tumor 45 1.005
696
TCL027 T-Cell Acute Lymphoblastic Leukemia 52 1.005
697
c ATM101 Autoimmune Gastritis 40 1.002
698
P ATR005 Atrophic Gastritis 50 1.002
699
GST092 Gastroesophageal Reflux 59 0.999
700
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 61 0.999
701
MYC006 Mycosis Fungoides 64 0.999
702
P NNT058 Neonatal Diabetes 52 0.999
703
MLG079 Malignant Pleural Mesothelioma 42 0.999
704
INS015 Inosine Triphosphatase Deficiency 22 0.996
705
P CND004 Candidiasis 57 0.993
706
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 0.992
707
FBR047 Fibromyalgia 57 0.992
708
P DMN002 Dementia 65 0.992
709
c GLC092 Glaucoma, Primary Open Angle 60 0.990
710
ILS001 Ileus 49 0.986
711
CHK001 Chikungunya 60 0.976
712
SPN051 Spondylitis 51 0.976
713
INF009 Inflammatory Spondylopathy 30 0.976
714
EPD015 Epidemic Typhus 44 0.975
715
NNT012 Neonatal Jaundice 53 0.975
716
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 40 0.973
717
HRT011 Heart Septal Defect 49 0.973
718
CHR073 Choreatic Disease 53 0.973
719
CCN002 Cocaine Abuse 49 0.968
720
P HMG032 Hemoglobin H Disease 51 0.967
721
FCL010 Focal Epithelial Hyperplasia 36 0.967
722
CTN007 Cutaneous Leishmaniasis 61 0.967
723
P PSD087 Pseudoxanthoma Elasticum 66 0.966
724
CRB037 Cerebral Palsy 66 0.966
725
CRT013 Carotid Stenosis 51 0.966
726
TNG002 Tangier Disease 63 0.964
727
PYR041 Pyruvate Kinase Deficiency of Red Cells 56 0.959
728
IFP003 Ifap Syndrome 2 41 0.959
729
HLC007 Helicobacter Pylori Infection 67 0.959
730
P PTT006 Pituitary Adenoma 55 0.958
731
PLR022 Pleural Disease 45 0.958
732
c OST131 Osteopetrosis, Autosomal Dominant 2 52 0.956
733
c ALP101 Alpha-Thalassemia 62 0.955
734
SPL018 Splenomegaly 47 0.955
735
P HML001 Hemolytic-Uremic Syndrome 52 0.953
736
FRS012 First-Degree Atrioventricular Block 39 0.952
737
HMS001 Hemosiderosis 48 0.952
738
P ACN011 Acne 55 0.952
739
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 42 0.952
740
P HRD217 Hereditary Optic Neuropathy 36 0.952
741
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.948
742
P ESN008 Eosinophilic Pneumonia 50 0.948
743
CLR030 Clear Cell Renal Cell Carcinoma 53 0.946
744
P RNL015 Renal Hypertension 45 0.945
745
ADP007 Adie Pupil 40 0.943
746
HNM002 Hinman Syndrome 29 0.943
747
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 42 0.941
748
RFR010 Refractory Anemia 49 0.941
749
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 59 0.938
750
BRN032 Brain Glioma 45 0.938
751
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.935
752
P URN019 Urinary Tract Infection 48 0.930
753
P MYT002 Myotonic Dystrophy 51 0.930
754
PTH003 Pathologic Nystagmus 52 0.930
755
c CHR711 Chronic Asthma 41 0.927
756
MTB008 Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 42 0.923
757
P SKN015 Skin Carcinoma 71 0.917
758
P OLG002 Oligodendroglioma 66 0.915
759
PNM008 Pneumothorax 54 0.915
760
CNN005 Connective Tissue Disease 66 0.915
761
P AGM001 Agammaglobulinemia 67 0.915
762
P ART018 Aortic Valve Insufficiency 52 0.915
763
P CYS039 Cystic Kidney Disease 52 0.907
764
P ANP001 Anaplastic Large Cell Lymphoma 59 0.904
765
THY122 Thyroid Gland Cancer 59 0.904
766
CNG506 Congenital Amyoplasia 27 0.904
767
MYX004 Myxedema 43 0.904
768
P CRN038 Carney Complex Variant 63 0.899
769
OTT002 Otitis Media 70 0.899
770
HYP458 Hyper Ige Syndrome 60 0.896
771
NRT001 Neurotic Disorder 56 0.896
772
P PRS038 Personality Disorder 65 0.896
773
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.892
774
HMG005 Hemoglobinopathy 55 0.892
775
PRS047 Prostatitis 57 0.892
776
DSR074 Disorder of Purine Metabolism 24 0.891
777
OPD006 Opioid Addiction 48 0.890
778
GLM044 Glomerular Disease 34 0.890
779
FRC011 Fructose Intolerance, Hereditary 55 0.888
780
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 0.887
781
ATM052 Autoimmune Disease 1 36 0.887
782
RDN001 Reading Disorder 40 0.887
783
P RTN008 Retinitis Pigmentosa 79 0.886
784
MLD018 Mild Cognitive Impairment 48 0.881
785
P FNC004 Fanconi Syndrome 60 0.881
786
P PLM034 Pulmonary Emphysema 58 0.881
787
CYN003 Cyanide Poisoning 22 0.881
788
c WLM013 Wilms Tumor 1 65 0.879
789
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 66 0.879
790
CNN003 Conn's Syndrome 77 0.879
791
TND005 Tendinitis 53 0.877
792
ADN022 Adenylosuccinase Deficiency 44 0.874
794
P MGR001 Migraine Without Aura 48 0.874
795
OCL052 Ocular Dominance 40 0.872
796
P SLM003 Salmonellosis 54 0.872
797
TBS010 T-B- Severe Combined Immunodeficiency 25 0.868
798
c CHR064 Chronic Monocytic Leukemia 35 0.867
799
P FTL001 Fetal Alcohol Syndrome 55 0.867
800
HML018 Homologous Wasting Disease 21 0.866
801
PLM031 Poliomyelitis 62 0.863
802
BHC003 Behcet Syndrome 70 0.863
803
SPT004 Septic Arthritis 58 0.863
804
XRD010 Xeroderma Pigmentosum, Variant Type 72 0.861
805
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 0.861
806
MDD018 Middle East Respiratory Syndrome 44 0.861
807
P CMP008 Compartment Syndrome 49 0.861
808
P MCR010 Microcephaly 59 0.854
810
P MTC069 Mitochondrial Disorders 57 0.854
811
THY111 Thyroid Carcinoma, Familial Medullary 67 0.853
812
PPL002 Papillary Carcinoma 46 0.853
813
THY125 Thyroid Gland Medullary Carcinoma 48 0.853
814
MCL003 Macular Holes 44 0.853
815
WLL004 Wallerian Degeneration 38 0.853
816
NSS002 Neisseria Meningitidis Infection 46 0.851
817
CRT072 Creutzfeldt-Jakob Disease 67 0.847
818
SPS057 Spasticity 43 0.847
819
CMB095 Combined T and B Cell Immunodeficiency 28 0.846
820
PFF001 Pfeiffer Syndrome 77 0.846
821
c PRG106 Progressive Muscular Dystrophy 31 0.846
822
CLC017 Calcification of Joints and Arteries 45 0.843
823
SCR003 Secretory Diarrhea 35 0.840
824
LWC002 Lowe Oculocerebrorenal Syndrome 68 0.839
825
MCR013 Microphthalmia 59 0.839
826
c BLD140 Blood Group, I System 47 0.837
827
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.835
828
PRP036 Peripheral T-Cell Lymphoma 52 0.835
829
P FML355 Familial Intrahepatic Cholestasis 38 0.833
830
CLF027 Cleft Palate, Isolated 64 0.832
831
PRP083 Porphyria, Acute Intermittent 64 0.828
832
RBF001 Riboflavin Deficiency 49 0.828
833
PLS007 Plasmodium Falciparum Malaria 52 0.825
834
c SVR005 Severe Pre-Eclampsia 49 0.825
835
PRX097 Paroxysmal Dystonia 32 0.825
836
P INF038 Influenza 68 0.824
837
PLT016 Platelet Adenylate Cyclase Activity 16 0.821
838
KPS004 Kaposi Sarcoma 76 0.821
839
ACR007 Acromegaly 70 0.821
840
DRY001 Dry Eye Syndrome 49 0.821
841
BSL008 Basal Ganglia Disease 41 0.821
842
PLM035 Pulmonary Eosinophilia 49 0.821
843
P HYP263 Hypersomnia 40 0.821
844
INT075 Intracranial Hypertension 52 0.818
845
BLM002 Bulimia Nervosa 56 0.816
846
ANG020 Angiosarcoma 63 0.816
847
APH001 Aphthous Stomatitis 57 0.816
848
c PRG047 Progressive Familial Intrahepatic Cholestasis 64 0.810
849
P BNC003 Bone Cancer 58 0.810
850
VSC004 Vasculogenic Impotence 29 0.810
851
P ANT006 Antiphospholipid Syndrome 55 0.810
852
MNN009 Meningoencephalitis 47 0.810
853
HYP114 Hypertensive Nephropathy 35 0.809
854
TRN030 Transient Erythroblastopenia of Childhood 34 0.809
855
P PRM030 Permanent Neonatal Diabetes Mellitus 59 0.809
856
TNS005 Tonsillitis 57 0.809
857
INT394 Intermittent Asthma 21 0.809
858
MST020 Mast Cell Activation Syndrome 27 0.809
859
MYT011 Myotonia 37 0.809
860
P PRD021 Periodic Paralysis 42 0.809
861
P GCH001 Gaucher's Disease 69 0.804
862
ADR007 Adrenoleukodystrophy 73 0.803
863
c HYP326 Hyperinsulinemic Hypoglycemia, Familial, 5 50 0.803
864
c HYP271 Hyperinsulinemic Hypoglycemia, Familial, 4 52 0.803
865
CNT047 Contact Dermatitis 56 0.803
866
P HRM001 Hermansky-Pudlak Syndrome 65 0.803
867
HYP072 Hypersensitivity Reaction Type Iii Disease 39 0.803
868
ADR022 Adrenomyeloneuropathy 38 0.803
869
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.798
870
c INF071 Inflammatory Bowel Disease 1 65 0.798
871
TSY002 Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations 52 0.798
872
P PRC031 Preeclampsia/eclampsia 1 43 0.798
873
BRN038 Bronchial Disease 51 0.798
874
PRM008 Parametritis 40 0.798
875
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.798
876
CHR682 Chronic Bilirubin Encephalopathy 37 0.798
877
c ANM038 Anemia, Autoimmune Hemolytic 63 0.796
878
c HYP604 Hyperinsulinemic Hypoglycemia, Familial, 2 65 0.796
879
c CHR418 Chronic Leukemia 48 0.796
881
GST045 Gastroenteritis 58 0.794
882
P PLY019 Polyneuropathy 52 0.794
883
MMM001 Mammary Paget's Disease 53 0.794
884
P AMY004 Amyloidosis 69 0.794
885
WLD007 Waldenstroem's Macroglobulinemia 59 0.794
886
c ACR081 Aicardi-Goutieres Syndrome 6 32 0.786
887
URL001 Urolithiasis 45 0.786
888
P NRF002 Neurofibromatosis 60 0.786
889
HPR003 Heparin-Induced Thrombocytopenia 47 0.786
890
PRT038 Protein-Energy Malnutrition 53 0.783
891
c VRL007 Viral Encephalitis 50 0.783
892
c DWL002 Dowling-Degos Disease 1 58 0.778
893
c PSD108 Pseudohypoparathyroidism, Type Ia 64 0.778
894
c PLY168 Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease 65 0.778
895
c ACT249 Acute Asthma 40 0.778
896
HMN047 Human Cytomegalovirus Infection 59 0.778
897
OST011 Osteomalacia 52 0.778
898
MTC037 Mitochondrial Phosphate Carrier Deficiency 35 0.774
899
MLK003 Melkersson-Rosenthal Syndrome 44 0.770
900
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 58 0.770
901
P SPP010 Suppressor of Tumorigenicity 3 50 0.769
902
CNS002 Constrictive Pericarditis 39 0.769
903
PSY004 Psychotic Disorder 66 0.769
904
P GLL022 Guillain-Barre Syndrome 59 0.769
905
PLY023 Polycystic Liver Disease 62 0.768
906
P HMP002 Hemophagocytic Lymphohistiocytosis 60 0.768
907
END041 Endometrial Adenocarcinoma 63 0.768
908
WBR001 Weber Syndrome 38 0.768
909
DSS032 Disease by Infectious Agent 55 0.764
910
P CTR002 Cataract 59 0.764
911
MST005 Mastitis 52 0.760
912
SNG003 Single Ventricular Heart 30 0.760
913
DWR001 Dwarfism 44 0.760
914
GNT167 Genetic Obesity 33 0.760
915
BRN028 Brain Cancer 73 0.752
916
CRY035 Cryptorchidism, Unilateral or Bilateral 57 0.751
917
RCT015 Reactive Arthritis 60 0.751
918
P PMP001 Pemphigus 54 0.751
919
PLS037 Plasma Cell Tumor 20 0.751
920
STT041 Stuttering 52 0.750
921
c THY109 Thyroid Cancer, Nonmedullary, 1 55 0.750
922
LBR038 Leber Hereditary Optic Neuropathy, Modifier of 62 0.750
923
BCT021 Bacterial Sepsis 43 0.750
924
PLY100 Polyploidy 36 0.750
925
VRC005 Varicose Veins 59 0.740
926
NPH091 Nephrolithiasis, Calcium Oxalate 61 0.740
927
DYS192 Dystonia, Dopa-Responsive 56 0.740
928
P MGR003 Migraine with Aura 51 0.740
929
P MTR003 Mitral Valve Stenosis 53 0.740
930
P PRN023 Prion Disease 60 0.740
931
HPT022 Hepatoblastoma 54 0.740
932
MTC005 Mitochondrial Metabolism Disease 44 0.733
933
P PLY018 Polycythemia 56 0.733
934
MTC029 Mitochondrial Complex V Deficiency, Nuclear Type 1 40 0.733
935
P PTS002 Ptosis 52 0.730
936
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 0.730
937
IRN001 Iron Deficiency Anemia 58 0.730
938
P DRM010 Dermatomyositis 61 0.730
939
VRC001 Varicocele 48 0.730
940
SML019 Smallpox 55 0.730
941
PRQ002 Paraquat Poisoning 28 0.730
942
P VTR007 Vitreoretinopathy 45 0.730
943
c RNG015 Ring Chromosome 2 22 0.730
944
c DMN047 Diamond-Blackfan Anemia 18 19 0.729
945
P DMN043 Diamond-Blackfan Anemia 15 with Mandibulofacial Dysostosis 31 0.729
946
DMN037 Diamond-Blackfan Anemia 14 with Mandibulofacial Dysostosis 19 0.729
947
P CTN015 Cutaneous T Cell Lymphoma 48 0.722
948
P MDL005 Medulloblastoma 75