Search results for Guanosine monophosphate

1094 hits were found for Guanosine monophosphate

# Family MCID Name MIFTS Score
1
PRT037 Pertussis 65 28.948
2
CHL014 Cholera 62 25.273
3
IMP005 Impotence 52 18.562
4
P NRB001 Neuroblastoma 66 15.545
5
P PLM037 Pulmonary Hypertension 72 14.146
6
P HRP006 Herpes Simplex 65 10.972
7
HLX001 Helix Syndrome 48 10.052
8
P PHC003 Pheochromocytoma 69 9.748
9
ADR040 Adrenal Gland Pheochromocytoma 46 9.748
10
c PLM164 Pulmonary Hypertension, Primary, 1 76 9.186
11
P LKM002 Leukemia 67 9.165
12
GLL048 Glial Tumor 52 9.096
13
GLM045 Glioma 63 9.076
14
c PRC016 Pre-Eclampsia 65 8.458
15
HYP266 Hypoxia 57 8.453
16
P LKM071 Leukemia, Chronic Lymphocytic 75 8.398
17
HMN044 Human Immunodeficiency Virus Type 1 78 8.092
18
48X005 48,xyyy 39 8.048
19
ISC004 Ischemia 61 7.995
20
c HPT073 Hepatitis C Virus 71 7.891
21
CYS001 Cystic Fibrosis 78 7.658
22
NNL005 Non-Alcoholic Fatty Liver Disease 63 7.643
23
HYP066 Hyperglycemia 61 7.583
24
NRR001 Neuroretinitis 42 7.486
25
RTN023 Retinitis 46 7.486
26
VCC001 Vaccinia 47 7.443
27
c HYP595 Hypertension, Essential 85 7.434
28
OST159 Osteogenic Sarcoma 66 7.383
29
BNR002 Bone Resorption Disease 47 7.306
30
c HPT001 Hepatitis C 62 7.287
31
RPD005 Rapidly Involuting Congenital Hemangioma 46 7.273
32
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 7.252
33
P RHN004 Rhinitis 57 7.231
34
FTT001 Fatty Liver Disease 62 7.173
35
IMM167 Immune Deficiency Disease 78 7.159
36
CNG034 Congestive Heart Failure 69 7.133
37
c MCR113 Microvascular Complications of Diabetes 3 52 7.077
38
c MCR130 Microvascular Complications of Diabetes 6 41 7.057
39
c MCR120 Microvascular Complications of Diabetes 7 47 7.057
40
c MCR133 Microvascular Complications of Diabetes 4 41 7.057
41
P RTN008 Retinitis Pigmentosa 80 6.964
42
ALL003 Allergic Rhinitis 67 6.725
43
TXC005 Toxic Shock Syndrome 62 6.703
44
c TYP009 Type 2 Diabetes Mellitus 92 6.701
45
P LKM062 Leukemia, Acute Lymphoblastic 69 6.676
46
SPN186 Spinal Cord Injury 61 6.669
47
PRS045 Prostatic Hypertrophy 53 6.667
48
P VSC007 Vascular Disease 63 6.655
49
P MYL006 Myeloid Leukemia 61 6.624
50
P HYP069 Hyperparathyroidism 62 6.543
51
ANX004 Anoxia 40 6.484
52
P AST005 Asthma 76 6.475
53
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 60 6.430
54
P GLM040 Glioma Susceptibility 1 71 6.421
55
CYT002 Cytokine Deficiency 43 6.418
56
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 6.417
57
PRN001 Purine Nucleoside Phosphorylase Deficiency 53 6.391
58
c LKM061 Leukemia, Acute Myeloid 83 6.382
59
MLG169 Malignant Astrocytoma 57 6.332
60
CHC001 Chickenpox 57 6.266
61
HYP060 Hyperinsulinism 54 6.259
62
P DYS154 Dystonia 64 6.201
63
P HYP076 Hyperthyroidism 53 6.185
64
GLB002 Glioblastoma 67 6.162
65
PRS021 Prostatic Adenoma 43 6.154
66
PRS129 Prostatic Hyperplasia, Benign 49 6.104
67
INS024 Insulin-Like Growth Factor I 78 6.070
68
P SZR006 Seizure Disorder 70 6.051
69
P TRM003 Tremor 48 6.050
70
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 5.903
71
47X002 47,xyy 48 5.876
72
P HML002 Hemolytic Anemia 62 5.853
73
LVR012 Liver Cirrhosis 63 5.811
74
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 5.802
75
P SCK005 Sickle Cell Disease 56 5.782
76
AGN016 Aging 54 5.773
77
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 5.756
78
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 5.756
79
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 5.756
80
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 5.756
81
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 5.756
82
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 5.756
83
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 5.756
84
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 5.756
85
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 5.756
86
c ACT073 Acute Leukemia 58 5.749
87
CRB004 Cerebral Artery Occlusion 45 5.642
88
P ADL010 Adult Respiratory Distress Syndrome 71 5.572
89
BRN071 Brain Injury 50 5.567
90
PRT251 Proteinuria, Chronic Benign 57 5.547
91
DFC004 Deficiency Anemia 74 5.494
92
STM007 Stomatitis 54 5.472
93
PLM129 Pulmonary Disease, Chronic Obstructive 74 5.426
94
P RTN016 Retinal Degeneration 52 5.387
95
P HRT032 Heart Disease 81 5.367
96
P HPT023 Hepatocellular Carcinoma 96 5.348
97
P LVR013 Liver Disease 69 5.326
98
P MLN008 Melanoma 76 5.322
99
c MGR028 Migraine with or Without Aura 1 64 5.232
100
TRM010 Traumatic Brain Injury 51 5.223
101
c MJR022 Major Affective Disorder 8 38 5.185
102
c MJR024 Major Affective Disorder 9 41 5.185
103
P BPL003 Bipolar Disorder 56 5.185
104
ALL029 Allergic Disease 59 5.132
105
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 80 5.106
106
c HPT016 Hepatitis B 62 5.090
107
P GRV001 Graves' Disease 55 5.064
108
ALL006 Allergic Asthma 56 5.025
109
P HPT021 Hepatitis 69 5.012
110
LPD008 Lipid Metabolism Disorder 62 5.011
111
HYP056 Hypoglycemia 65 5.004
112
PRT013 Portal Hypertension 59 4.983
113
MNT002 Mental Depression 57 4.980
114
MYL069 Myeloma, Multiple 77 4.978
115
P GST053 Gastric Cancer 83 4.968
116
c PRM005 Primary Hyperparathyroidism 59 4.964
117
P DRM053 Dermatitis, Atopic 65 4.962
118
P ALZ034 Alzheimer Disease 87 4.956
119
CLT003 Colitis 63 4.930
120
P ENC018 Encephalopathy 62 4.920
121
P PSR002 Psoriasis 63 4.909
122
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 4.905
123
P NPH012 Nephrotic Syndrome 60 4.901
124
MDD011 Mood Disorder 62 4.897
125
c DLT002 Dilated Cardiomyopathy 78 4.896
126
PTT037 Pituitary Tumors 44 4.887
127
P PSD015 Pseudohypoparathyroidism 55 4.887
128
INS001 Insulinoma 59 4.866
129
P BCL017 B-Cell Lymphoma 59 4.853
130
P MYP004 Myopathy 67 4.838
131
PST011 Pustulosis of Palm and Sole 52 4.835
132
P DBT005 Diabetes Insipidus 54 4.824
133
SXL003 Sexual Disorder 49 4.817
134
DPR016 Depression 65 4.805
135
P HYP086 Hypothyroidism 69 4.799
136
P GRF003 Graft-Versus-Host Disease 71 4.790
137
P MJR001 Major Depressive Disorder 68 4.780
138
P PNC035 Pancreatic Cancer 86 4.764
139
c SYS001 Systemic Lupus Erythematosus 87 4.763
140
HYP014 Hyperuricemia 51 4.750
141
ADR016 Adrenal Cortical Carcinoma 62 4.746
142
EXT007 Extracutaneous Mastocytoma 38 4.697
143
MST004 Mast Cell Neoplasm 42 4.697
144
c HYP836 Hypercholesterolemia, Familial, 1 73 4.694
145
HPT004 Hepatic Coma 43 4.680
146
ADR054 Adrenocortical Carcinoma, Hereditary 47 4.583
147
ADR004 Adrenal Cortical Adenocarcinoma 38 4.583
148
P GLM007 Glomerulonephritis 60 4.572
149
P INF037 Inflammatory Bowel Disease 53 4.533
150
P MYC084 Mycobacterium Tuberculosis 1 68 4.518
151
P LPS004 Lupus Erythematosus 61 4.499
152
P PRK039 Parkinsonism 55 4.484
153
P LYM118 Lymphoma 67 4.474
154
PPL052 Papillomatosis, Confluent and Reticulated 34 4.465
155
ACT098 Acute Erythroid Leukemia 55 4.447
156
END086 End Stage Renal Disease 52 4.445
157
TTN003 Tetanus 65 4.434
158
P ECL001 Eclampsia 52 4.419
159
GT001 Gout 64 4.415
160
OCL069 Ocular Motor Apraxia 57 4.389
161
ADN018 Adenoma 59 4.388
162
P CHR345 Chronic Pain 50 4.384
163
HPT019 Hepatic Encephalopathy 59 4.364
164
CHR074 Choriocarcinoma 46 4.361
165
P DBT009 Diabetes Mellitus 67 4.361
166
P HYP098 Hypereosinophilic Syndrome 66 4.357
167
CNS004 Constipation 56 4.343
168
c CHR684 Chronic Kidney Disease 69 4.336
169
RNL077 Renal Fibrosis 46 4.328
170
P KDN018 Kidney Disease 72 4.327
171
P CHR012 Chronic Granulomatous Disease 69 4.310
172
THY029 Thyroid Carcinoma 51 4.298
173
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 4.295
174
LSC001 Lesch-Nyhan Syndrome 62 4.293
175
GLC003 Glucose Intolerance 54 4.276
176
IRR002 Irritable Bowel Syndrome 65 4.267
177
LWC001 Low Compliance Bladder 45 4.220
178
P HYP024 Hypoparathyroidism 55 4.201
179
c TBR025 Tuberous Sclerosis 1 84 4.189
180
c AMY091 Amyotrophic Lateral Sclerosis 1 88 4.189
181
P LTR001 Lateral Sclerosis 58 4.189
182
MDD018 Middle East Respiratory Syndrome 44 4.187
183
P PLY014 Polycystic Kidney Disease 69 4.183
184
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 4.161
185
c LKM005 Leukemia, T-Cell, Chronic 34 4.161
186
P ADN016 Adenocarcinoma 63 4.156
187
PNG002 Pain Agnosia 51 4.155
188
URT010 Ureteral Obstruction 45 4.134
189
ANG054 Angina Pectoris 66 4.134
190
BCT022 Bacterial Infectious Disease 56 4.129
191
IGR001 Ige Responsiveness, Atopic 59 4.121
192
ACQ007 Acquired Immunodeficiency Syndrome 59 4.102
193
CLN015 Colon Adenocarcinoma 65 4.075
194
P LNG032 Lung Cancer 98 4.067
195
BRN004 Brain Edema 54 4.062
196
ACT119 Acute Promyelocytic Leukemia 62 4.053
197
DBT010 Diabetic Neuropathy 54 4.050
198
PPT005 Peptic Ulcer Disease 58 4.037
199
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 4.036
200
DPH001 Diphtheria 59 4.033
201
P PRP019 Peripheral Nervous System Disease 58 4.025
202
P CLR023 Colorectal Cancer 100 4.020
203
P NRF002 Neurofibromatosis 57 4.016
204
c LKM063 Leukemia, Chronic Myeloid 71 4.011
205
PLY150 Polykaryocytosis Inducer 29 4.009
206
P MYC007 Myocardial Infarction 70 4.006
207
P OVR042 Ovarian Cancer 88 4.003
208
P MSC005 Muscular Dystrophy 67 3.973
209
P DRR001 Diarrhea 55 3.961
210
RNL114 Renal Cell Carcinoma, Nonpapillary 80 3.955
211
DRM006 Dermatitis 62 3.929
212
c GRV008 Graves Disease 1 54 3.916
213
BRN024 Bronchitis 67 3.889
214
c MCR115 Microvascular Complications of Diabetes 5 65 3.884
215
P HNT016 Huntington Disease 73 3.831
216
ATH013 Atherosclerosis Susceptibility 63 3.831
217
c ATR087 Atrial Standstill 1 74 3.814
218
P LNG064 Lung Cancer Susceptibility 3 70 3.812
219
SLP001 Sleeping Sickness 56 3.803
220
c ACT075 Acute Myocardial Infarction 56 3.795
221
MSL001 Measles 61 3.777
222
LNG099 Lung Disease 62 3.740
223
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 3.734
224
NNL006 Non-Alcoholic Steatohepatitis 54 3.733
225
HRW001 Hair Whorl 35 3.731
226
PLM010 Pulmonary Edema 55 3.731
227
P PRD008 Periodontitis 64 3.708
228
P CRD119 Cardiac Arrest 67 3.693
229
P BRS047 Breast Cancer 98 3.677
230
TRY001 Trypanosomiasis 50 3.677
231
LYM019 Lymphosarcoma 46 3.652
232
P TBR001 Tuberous Sclerosis 69 3.651
233
CHG001 Chagas Disease 66 3.640
234
MLR004 Malaria 80 3.614
235
P NRP001 Neuropathy 60 3.610
236
CHD001 Chediak-Higashi Syndrome 67 3.599
237
CHL068 Cholestasis 61 3.568
238
MCR013 Microphthalmia 60 3.557
239
HND015 Hand Skill, Relative 30 3.544
240
P BND020 Bone Disease 59 3.524
241
P MNN013 Meningitis 65 3.499
242
SPL018 Splenomegaly 49 3.498
243
P INF038 Influenza 68 3.493
244
c PCH010 Pachyonychia Congenita 3 43 3.484
245
DSS032 Disease by Infectious Agent 55 3.475
246
OVR094 Ovarian Epithelial Cancer 39 3.459
247
HMP009 Haemophilus Influenzae 41 3.458
248
P HDC001 Headache 57 3.454
249
P MYC008 Myocarditis 59 3.446
250
LYM017 Lyme Disease 62 3.437
251
P HYP265 Hypotonia 42 3.433
252
BRN056 Bronchopulmonary Dysplasia 56 3.419
253
P THR014 Thrombocytopenia 66 3.408
254
c VRL010 Viral Hepatitis 53 3.385
255
ULC004 Ulcerative Colitis 74 3.384
256
SCR003 Secretory Diarrhea 35 3.381
257
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 3.380
258
P ENC004 Encephalitis 61 3.377
259
P CTN015 Cutaneous T Cell Lymphoma 48 3.372
260
GST033 Gestational Diabetes 61 3.369
261
WTH001 Withdrawal Disorder 48 3.362
262
P SKN015 Skin Carcinoma 71 3.355
263
c SML038 Small Cell Cancer of the Lung 69 3.351
264
DMY004 Demyelinating Disease 50 3.324
265
P PRS040 Prostate Cancer 95 3.320
266
THR024 Thrombosis 56 3.316
267
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 3.299
268
c ATS347 Autosomal Dominant Polycystic Kidney Disease 66 3.288
269
SKN016 Skin Disease 63 3.277
270
c BCT007 Bacterial Meningitis 55 3.275
271
c DNT047 Dentinogenesis Imperfecta Type 2 35 3.267
272
P INF032 Infertility 57 3.259
273
HRP004 Herpes Zoster 61 3.243
274
P CRN300 Coronary Heart Disease 1 73 3.230
275
SVR004 Severe Combined Immunodeficiency 72 3.209
276
P RTN024 Retinoblastoma 73 3.198
277
P RHM011 Rheumatoid Arthritis 82 3.184
278
P ART022 Arthritis 71 3.167
279
P ATR011 Atrial Fibrillation 66 3.165
280
P UVT001 Uveitis 57 3.163
281
MYL009 Myelodysplastic Syndrome 67 3.150
282
P DNG005 Dengue Virus 56 3.145
283
ATS010 Autosomal Recessive Disease 42 3.123
284
SVR001 Severe Acute Respiratory Syndrome 67 3.123
285
PRT036 Peritonitis 65 3.084
286
P LCT001 Lactic Acidosis 51 3.060
287
DWR001 Dwarfism 44 3.058
288
c SCL052 Scleroderma, Familial Progressive 61 3.058
289
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 3.057
290
c ACT071 Acute Kidney Failure 60 3.052
291
KRT019 Keratitis, Hereditary 66 3.017
292
RCK004 Rickets 68 2.967
293
RYN005 Raynaud Phenomenon 45 2.940
294
CHL004 Cholelithiasis 49 2.936
295
P NTR004 Neutropenia 63 2.929
296
MTB004 Metabolic Acidosis 48 2.921
297
P PRK057 Parkinson Disease, Late-Onset 80 2.920
298
ACT084 Acute Stress Disorder 54 2.918
299
PST028 Post-Traumatic Stress Disorder 59 2.918
300
HGH043 High Grade Glioma 45 2.889
301
CRH001 Crohn's Disease 80 2.886
302
P SLP006 Sleep Apnea 69 2.884
303
PRP007 Priapism 47 2.878
304
P CRD246 Cardiovascular System Disease 56 2.878
305
STR067 Stroke, Ischemic 80 2.862
306
P CNR004 Cone-Rod Dystrophy 2 74 2.854
307
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 2.852
308
SCH014 Schistosomiasis 56 2.852
309
ATM095 Autoimmune Disease 61 2.852
310
P SCH015 Schizophrenia 74 2.842
311
CHL123 Chlamydia 58 2.819
312
ESP021 Esophageal Cancer 83 2.806
313
P MYP006 Myopia 56 2.806
314
END057 Endometrial Cancer 72 2.804
315
MLY001 Molybdenum Cofactor Deficiency 40 2.785
316
c INH030 Inherited Retinal Disorder 28 2.785
317
P PLM036 Pulmonary Fibrosis 66 2.781
318
P EPL164 Epilepsy 68 2.778
319
P FBR017 Fibrosarcoma 56 2.772
320
ALL014 Allergic Encephalomyelitis 34 2.772
321
MLD018 Mild Cognitive Impairment 48 2.762
322
P VSC011 Vasculitis 61 2.756
323
P MLN007 Male Infertility 56 2.751
324
P ART021 Arteriosclerosis 54 2.745
325
SDD001 Sudden Infant Death Syndrome 60 2.738
326
CRV035 Cervical Cancer 73 2.732
327
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 45 2.723
328
GNT003 Genital Herpes 54 2.718
329
LYM027 Lymphopenia 56 2.718
330
P OVR082 Overgrowth Syndrome 49 2.714
331
P INS002 in Situ Carcinoma 53 2.714
332
ALC007 Alcohol Dependence 66 2.709
333
CRY003 Cryptosporidiosis 56 2.707
334
P PLY011 Polycystic Ovary Syndrome 57 2.701
335
NPH009 Nephrolithiasis 54 2.701
336
P TMP001 Temporal Lobe Epilepsy 49 2.693
337
P BLD134 Bladder Cancer 79 2.678
338
c BRN108 Branchiootic Syndrome 1 62 2.632
339
P GST044 Gastritis 55 2.626
340
INT007 Intermediate Coronary Syndrome 54 2.625
341
P BRB001 Beriberi 44 2.625
342
TRT001 Teratocarcinoma 42 2.622
344
P MVM001 Movement Disease 61 2.592
345
PNC041 Pancreatic Ductal Adenocarcinoma 51 2.591
346
P OBS001 Obstructive Jaundice 48 2.587
347
P ACH003 Achromatopsia 62 2.578
348
P PTS002 Ptosis 52 2.577
349
GTR002 Goiter 53 2.574
350
P RTN018 Retinal Disease 53 2.568
351
P HYP750 Hypertriglyceridemia, Familial 62 2.557
352
P VTR007 Vitreoretinopathy 46 2.539
353
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 2.539
354
HMN047 Human Cytomegalovirus Infection 57 2.538
355
ILT001 Ileitis 48 2.536
356
P PTT006 Pituitary Adenoma 55 2.536
357
ARG004 Argyria 26 2.527
358
P BRS044 Breast Adenocarcinoma 58 2.524
359
GLC009 Glucosephosphate Dehydrogenase Deficiency 53 2.518
360
P SLM003 Salmonellosis 54 2.512
361
HRY003 Hairy Cell Leukemia 61 2.512
362
P FML011 Familial Adenomatous Polyposis 71 2.509
363
GST045 Gastroenteritis 58 2.508
364
HMC014 Homocysteinemia 52 2.508
365
PHN003 Phenylketonuria 76 2.504
366
GRW007 Growth Hormone Deficiency 46 2.494
367
P OST002 Osteoporosis 76 2.481
368
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 2.478
369
CRT015 Carotid Artery Occlusion 45 2.471
370
SCK003 Sickle Cell Anemia 74 2.466
371
CRY035 Cryptorchidism, Unilateral or Bilateral 58 2.466
372
FBR009 Fibrous Dysplasia 48 2.463
373
URM002 Uremia 47 2.462
374
RTN020 Retinal Vascular Disease 46 2.459
375
DWN001 Down Syndrome 70 2.455
376
NRM005 Neuromuscular Disease 63 2.454
377
MYL031 Myeloproliferative Neoplasm 66 2.452
378
c THY107 Thymoma, Familial 42 2.443
379
P THY023 Thymoma 64 2.443
380
P EYD002 Eye Disease 57 2.438
381
P EXN002 Exanthem 58 2.429
382
P TTR001 Tetralogy of Fallot 69 2.429
383
P RSP003 Respiratory Failure 74 2.423
384
TRN015 Transient Cerebral Ischemia 63 2.417
385
P END044 Endometriosis 62 2.417
386
MTH009 Mouth Disease 57 2.408
387
P MCR010 Microcephaly 60 2.408
388
LKC009 Leukocyte Adhesion Deficiency, Type I 70 2.403
389
TLN003 Telangiectasis 51 2.395
390
AMN003 Amnestic Disorder 54 2.394
391
c PSD108 Pseudohypoparathyroidism, Type Ia 65 2.393
392
NWC001 Newcastle Disease 47 2.393
393
P OPN001 Open-Angle Glaucoma 55 2.372
394
c SVR005 Severe Pre-Eclampsia 50 2.359
395
DST006 Diastolic Heart Failure 45 2.359
396
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 2.355
397
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 2.355
398
P OPT006 Optic Nerve Disease 58 2.348
399
LPP008 Lipoprotein Quantitative Trait Locus 65 2.347
400
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 2.347
401
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 2.347
402
GST040 Gastric Adenocarcinoma 67 2.342
403
MRP001 Morphine Dependence 42 2.342
404
GST023 Gastric Ulcer 52 2.319
405
PST092 Posttransplant Acute Limbic Encephalitis 28 2.311
406
PLS011 Plasmacytoma 56 2.311
407
c ATM011 Autoimmune Hepatitis 63 2.309
408
P PRL003 Proliferative Glomerulonephritis 43 2.306
409
c OPT053 Optic Atrophy 1 62 2.305
410
ANT024 Anthrax Disease 58 2.304
411
CHR466 Chronic Thromboembolic Pulmonary Hypertension 48 2.301
412
P KLZ004 Kala-Azar 1 41 2.293
413
LSH001 Leishmaniasis 64 2.293
414
PLG002 Plague 58 2.289
415
P ADL017 Adult T-Cell Leukemia 56 2.287
416
P ATX030 Ataxia-Telangiectasia 80 2.281
417
PRM003 Premature Ejaculation 44 2.280
418
c CHR711 Chronic Asthma 41 2.277
419
P GLL022 Guillain-Barre Syndrome 60 2.277
420
LYM040 Lymphoblastic Lymphoma 53 2.272
421
MSC007 Muscle Hypertrophy 64 2.271
422
P RNV001 Renovascular Hypertension 49 2.267
423
P MTR012 Mitral Valve Disease 57 2.265
424
PLM101 Pulmonary Hypertension, Chronic Thromboembolic, Without Deep Vein Thrombosis 37 2.253
425
INT002 Intermittent Claudication 61 2.251
426
SGW002 Segawa Syndrome, Autosomal Recessive 44 2.246
427
DYS192 Dystonia, Dopa-Responsive 55 2.244
428
CMB007 Combined Immunodeficiency 57 2.242
429
GRN017 Granulocytopenia 42 2.241
430
P ALC033 Alcohol Use Disorder 61 2.235
431
P HYP061 Hypertrophic Cardiomyopathy 69 2.234
432
WST005 West Nile Virus 57 2.224
433
c ACT027 Acute Pancreatitis 60 2.217
434
INT323 Intraocular Pressure Quantitative Trait Locus 64 2.202
435
MSN001 Mesangial Proliferative Glomerulonephritis 44 2.202
436
TRC003 Trichomoniasis 53 2.201
437
P CYS018 Cystitis 59 2.198
438
MCC012 Mccune-Albright Syndrome 70 2.192
439
PYR010 Peyronie's Disease 50 2.188
440
P SCL018 Scoliosis 57 2.188
441
URL001 Urolithiasis 46 2.187
442
LYM133 Lymphoma, Hodgkin, Classic 74 2.186
443
PNC001 Pancytopenia 53 2.182
444
PNC129 Pancreatic Adenocarcinoma 65 2.177
445
c ACT135 Acute Graft Versus Host Disease 51 2.177
446
P MLT020 Multiple Sclerosis 79 2.176
447
P MDL005 Medulloblastoma 75 2.176
448
P CTR002 Cataract 60 2.173
449
c ACT134 Acute Liver Failure 59 2.170
450
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 39 2.160
451
CHR073 Choreatic Disease 54 2.160
452
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 2.150
453
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 2.139
454
SPN035 Spindle Cell Sarcoma 54 2.139
455
SRC014 Sarcoma 65 2.139
456
P MSC003 Muscular Atrophy 52 2.131
457
c TYP008 Type 1 Diabetes Mellitus 70 2.129
458
P ATT013 Attention Deficit-Hyperactivity Disorder 64 2.129
459
LKS001 Leukostasis 41 2.122
460
P MGR001 Migraine Without Aura 49 2.111
461
ASP003 Aseptic Meningitis 50 2.107
462
P ACT105 Acute Mountain Sickness 52 2.103
463
P RTN034 Retinal Cone Dystrophy 3a 28 2.100
464
SQM006 Squamous Cell Carcinoma 60 2.093
465
ART140 Arteries, Anomalies of 53 2.091
466
P INT143 Interstitial Cystitis 60 2.091
467
PRM236 Primary Biliary Cholangitis 60 2.090
468
P PLY019 Polyneuropathy 52 2.083
469
PRP016 Paraplegia 52 2.076
470
c ACT249 Acute Asthma 40 2.071
471
P PNC044 Pancreatitis 61 2.071
472
ADN001 Adenosine Deaminase Deficiency 59 2.056
473
P SYS005 Systemic Scleroderma 74 2.056
474
MSC157 Muscular Dystrophy, Duchenne Type 79 2.055
475
FBR047 Fibromyalgia 58 2.044
476
GLM044 Glomerular Disease 35 2.038
477
CWP001 Cowpox 45 2.027
478
P INT068 Intestinal Disease 53 2.027
479
BRN002 Bronchiolitis 57 2.027
480
PPL002 Papillary Carcinoma 46 2.009
481
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 50 2.004
482
ORL015 Oral Squamous Cell Carcinoma 43 1.996
483
HYP080 Hypogonadism 50 1.972
484
STT001 Status Epilepticus 59 1.959
485
PLR008 Pleurisy 50 1.957
486
LBR036 Leber Plus Disease 66 1.945
487
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 1.938
488
PSD014 Pseudopseudohypoparathyroidism 54 1.938
489
NRL005 Neurilemmoma 60 1.938
490
P FRG001 Fragile X Syndrome 70 1.932
491
ADG002 Audiogenic Seizures 25 1.930
492
ALC009 Alcoholic Liver Cirrhosis 54 1.930
493
P DMN002 Dementia 66 1.921
494
YLL002 Yellow Fever 61 1.913
495
GST037 Gastroparesis 52 1.913
496
DGN001 Degenerative Disc Disease 49 1.908
497
SYN036 Syncope 45 1.902
498
NRF007 Neurofibroma 64 1.902
499
PYR041 Pyruvate Kinase Deficiency of Red Cells 57 1.894
500
CRB090 Cerebral Hypoxia 42 1.884
501
EMB004 Embryonal Carcinoma 56 1.884
502
P PRM051 Primary Pigmented Nodular Adrenocortical Disease 55 1.881
503
PRP027 Peripheral Vascular Disease 71 1.877
504
ACT003 Acute Kidney Tubular Necrosis 46 1.873
505
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 60 1.868
506
AVN001 Avian Influenza 61 1.868
507
HPT022 Hepatoblastoma 54 1.868
508
c WLM013 Wilms Tumor 1 66 1.862
509
KRN002 Kearns-Sayre Syndrome 63 1.860
510
c CHR095 Chronic Progressive External Ophthalmoplegia 49 1.860
511
P PRP029 Porphyria 60 1.860
512
P KDN017 Kidney Cancer 61 1.857
513
OST012 Osteoarthritis 77 1.850
514
STT041 Stuttering 52 1.838
515
RTN017 Retinal Detachment 60 1.838
516
BRK010 Burkitt Lymphoma 66 1.834
517
P OLG002 Oligodendroglioma 66 1.822
518
THR004 Thrombocytosis 53 1.802
519
P BNG032 Benign Mesothelioma 53 1.797
520
c GLC092 Glaucoma, Primary Open Angle 62 1.791
521
c ATS007 Autism Spectrum Disorder 72 1.789
522
c HMC039 Hemochromatosis, Type 1 73 1.769
523
P RHB003 Rhabdomyosarcoma 66 1.768
524
P MMB011 Membranous Nephropathy 50 1.768
525
P MTC133 Mitochondrial Myopathy 50 1.768
526
c INH020 Inherited Metabolic Disorder 48 1.763
527
TCL027 T-Cell Acute Lymphoblastic Leukemia 51 1.761
528
THY111 Thyroid Carcinoma, Familial Medullary 67 1.757
529
THY125 Thyroid Gland Medullary Carcinoma 48 1.757
530
BRN012 Bronchiolitis Obliterans 56 1.756
531
NRT004 Neuritis 53 1.756
532
P SRC025 Sarcoidosis 1 71 1.756
533
P FBR031 Febrile Seizures 52 1.739
534
P PNV001 Panuveitis 49 1.739
535
IDP070 Idiopathic Scoliosis 42 1.739
536
WLL004 Wallerian Degeneration 38 1.739
537
FND002 Fundus Dystrophy 55 1.733
538
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 1.733
539
MYC005 Myocardial Stunning 46 1.713
540
P ACN011 Acne 57 1.705
541
P BNC003 Bone Cancer 58 1.705
542
MCL006 Macular Retinal Edema 57 1.697
543
XRD010 Xeroderma Pigmentosum, Variant Type 73 1.695
544
c RTN047 Retinitis Pigmentosa 18 46 1.691
545
P SPP010 Suppressor of Tumorigenicity 3 51 1.691
546
HRT011 Heart Septal Defect 49 1.686
547
ILS001 Ileus 50 1.686
548
P RNL015 Renal Hypertension 45 1.686
549
BLR008 Bilirubin Metabolic Disorder 57 1.679
550
CRD132 Cardiac Conduction Defect 60 1.678
551
CHL065 Cholangiocarcinoma 58 1.678
552
INT079 Intrahepatic Cholangiocarcinoma 51 1.678
553
CHK001 Chikungunya 60 1.673
554
P ESN008 Eosinophilic Pneumonia 50 1.673
555
ENC038 Encephalopathy, Progressive, with or Without Lipodystrophy 40 1.664
556
PLM001 Pulmonary Tuberculosis 69 1.656
557
ANX010 Anxiety 70 1.653
558
BRN028 Brain Cancer 74 1.645
559
P PRC019 Precocious Puberty 47 1.645
560
PRN029 Parainfluenza Virus Type 3 32 1.645
561
KRT009 Keratosis 53 1.640
562
SBC016 Subacute Delirium 43 1.610
563
c THY109 Thyroid Cancer, Nonmedullary, 1 55 1.603
564
CRN019 Coronary Artery Vasospasm 47 1.603
565
P KRN004 Kernicterus 46 1.603
566
SMT007 Smith-Fineman-Myers Syndrome 32 1.603
567
c ATS025 Autosomal Dominant Progressive External Ophthalmoplegia 45 1.603
568
ACR016 Acromesomelic Dysplasia 35 1.603
569
ASP004 Asphyxia Neonatorum 50 1.603
570
APC001 Apical Myocardial Infarction 16 1.603
571
ACT058 Active Peptic Ulcer Disease 56 1.603
572
c ACT004 Acute Diarrhea 40 1.592
573
LWF001 Low-Flow Priapism 16 1.589
574
P CRC039 Coarctation of Aorta 46 1.589
575
P RTT002 Rett Syndrome 79 1.585
576
LMB062 Limb Ischemia 55 1.581
577
P FTL001 Fetal Alcohol Syndrome 55 1.581
578
P LCH002 Lichen Planus 54 1.581
579
VRC005 Varicose Veins 60 1.579
580
P CHR071 Charcot-Marie-Tooth Disease 64 1.579
581
P MTH007 Methemoglobinemia 46 1.579
582
CRC006 Carcinoid Syndrome 55 1.579
583
P MYS003 Myasthenia Gravis 68 1.570
584
P MLG056 Malignant Hyperthermia 66 1.570
585
IRN002 Iron Metabolism Disease 57 1.570
586
CNG486 Congenital Disorders of N-Linked Glycosylation and Multiple Pathway 29 1.569
587
PLT016 Platelet Adenylate Cyclase Activity 16 1.564
588
FCS014 Fucosidase Regulator 15 1.546
589
HLC007 Helicobacter Pylori Infection 67 1.535
590
OCL006 Ocular Hypertension 53 1.535
591
P ESP024 Esophagitis 60 1.535
592
DYS015 Dysentery 50 1.535
593
PPL022 Papilloma 53 1.535
594
SQM002 Squamous Cell Papilloma 46 1.535
595
OPT003 Opiate Dependence 49 1.535
596
P FLL037 Follicular Lymphoma 74 1.522
597
MYT011 Myotonia 39 1.522
598
P CND005 Cone Dystrophy 47 1.519
599
HPT009 Hepatopulmonary Syndrome 48 1.519
600
PLM033 Pulmonary Embolism 58 1.519
601
SPS057 Spasticity 42 1.516
602
c HPT015 Hepatitis D 49 1.516
603
OST003 Osteonecrosis 61 1.511
604
INT066 Interstitial Lung Disease 60 1.511
605
RNL011 Renal Osteodystrophy 49 1.511
606
c DPH024 Diaphragmatic Hernia, Congenital 64 1.506
607
P MGR003 Migraine with Aura 52 1.506
609
TCK001 Tick-Borne Encephalitis 59 1.491
610
TTH006 Tooth Disease 51 1.491
611
IDP033 Idiopathic Edema 41 1.491
612
c GLL024 Gallbladder Disease 1 52 1.486
613
CRC021 Carcinosarcoma 64 1.476
614
CRB039 Cerebrovascular Disease 66 1.476
615
MYL005 Myelofibrosis 71 1.473
616
HMN014 Human Immunodeficiency Virus Infectious Disease 54 1.458
617
GRY002 Gray Platelet Syndrome 58 1.458
618
LSS003 Lassa Fever 49 1.441
619
c CNG411 Congenital Disorder of Glycosylation, Type in 67 1.441
620
ACH005 Achalasia 55 1.441
621
c CHR688 Chronic Acquired Demyelinating Polyneuropathy 16 1.441
622
RBS001 Rabies 58 1.441
623
P MJR007 Major Affective Disorder 1 42 1.436
624
P HYD006 Hydrocephalus 61 1.436
625
SYS003 Systolic Heart Failure 49 1.436
626
ORL011 Oral Cancer 60 1.436
627
c HPT003 Hepatitis a 63 1.434
628
PLM035 Pulmonary Eosinophilia 49 1.434
629
P HRD011 Hereditary Spherocytosis 64 1.433
630
OPD006 Opioid Addiction 48 1.433
631
EPD052 Epidermolysis Bullosa Simplex Superficialis 17 1.429
632
OBS002 Obsessive-Compulsive Disorder 68 1.429
633
CLF027 Cleft Palate, Isolated 64 1.428
634
RSP002 Respiratory Syncytial Virus Infectious Disease 52 1.423
635
RTH007 Rothmund-Thomson Syndrome, Type 1 37 1.418
636
PLM134 Pulmonary Fibrosis, Idiopathic 76 1.411
637
c ATM006 Autoimmune Lymphoproliferative Syndrome 75 1.411
638
ATN005 Autonomic Dysfunction 46 1.411
639
c ATS307 Autosomal Recessive Cerebellar Ataxia 39 1.394
640
P PMP001 Pemphigus 55 1.387
641
KRT002 Keratomalacia 55 1.387
642
P ATS364 Autism 69 1.387
643
TRD006 Tardive Dyskinesia 53 1.364
644
NRL016 Neural Tube Defects 81 1.364
645
c SCH079 Schizophrenia 1 44 1.364
646
P LNG028 Long Qt Syndrome 64 1.364
647
c HMN021 Human T-Cell Leukemia Virus Type 1 47 1.364
648
ANC002 Anca-Associated Vasculitis 44 1.363
649
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 57 1.358
650
P PTN014 Patent Ductus Arteriosus 1 59 1.358
651
CYT005 Cytomegalovirus Retinitis 50 1.358
652
P SNS001 Sensorineural Hearing Loss 59 1.354
653
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 1.354
654
P MYT002 Myotonic Dystrophy 51 1.354
655
GNG002 Ganglioneuroma 52 1.346
656
BYS001 Byssinosis 28 1.346
657
c MCR112 Microvascular Complications of Diabetes 2 42 1.346
658
P OPT009 Optic Neuritis 57 1.346
659
DNT012 Dental Caries 53 1.346
660
GNG005 Gangliocytoma 55 1.346
661
DSR013 Disorders of Gnas Inactivation 15 1.346
662
SPS019 Spastic Paraparesis 38 1.341
663
OTT002 Otitis Media 71 1.341
664
MNT001 Mantle Cell Lymphoma 67 1.341
665
P URN019 Urinary Tract Infection 49 1.341
666
P VNT002 Ventricular Septal Defect 58 1.341
667
CNN005 Connective Tissue Disease 67 1.341
668
CRN017 Coronary Thrombosis 46 1.341
669
MST005 Mastitis 53 1.341
670
BRS051 Breast Disease 58 1.341
671
PTH003 Pathologic Nystagmus 52 1.341
672
P NSP012 Nasopharyngeal Carcinoma 61 1.334
673
P ALP008 Alopecia 54 1.334
674
CHR178 Chromosomal Triplication 34 1.334
675
TBR011 Tuberculous Meningitis 48 1.325
676
LGN006 Legionnaire Disease 52 1.325
677
c VRL012 Viral Meningitis 46 1.325
678
c HRD010 Hereditary Spastic Paraplegia 66 1.325
679
CRB037 Cerebral Palsy 67 1.322
680
CHL067 Cholecystitis 60 1.312
681
RSP007 Respiratory Distress Syndrome, Infant 40 1.306
682
CNN003 Conn's Syndrome 79 1.300
683
P ATR010 Atrial Heart Septal Defect 58 1.300
684
c VRL007 Viral Encephalitis 50 1.283
685
CLC006 Calcinosis 47 1.278
686
GNT167 Genetic Obesity 30 1.271
687
LPT014 Leptin Deficiency or Dysfunction 78 1.271
688
ART002 Arts Syndrome 66 1.264
689
P FML023 Familial Hemiplegic Migraine 53 1.264
690
P ATR001 Atrioventricular Septal Defect 55 1.264
691
EPP011 Epiphyseal Chondrodysplasia, Miura Type 36 1.264
692
HRT012 Heart Valve Disease 53 1.264
693
P CLR019 Color Blindness 48 1.264
694
HMP005 Hemiplegia 54 1.264
695
MTR002 Mitral Valve Insufficiency 52 1.264
696
NPH010 Nephrosclerosis 50 1.264
697
P SCK002 Sick Sinus Syndrome 55 1.264
698
TRN012 Transient Global Amnesia 38 1.264
699
P BRN022 Bronchiectasis 60 1.264
700
c NRF024 Neurofibromatosis, Type I 72 1.258
701
PST053 Postherpetic Neuralgia 40 1.252
702
PRT058 Pure Autonomic Failure 58 1.252
703
P MLN069 Melanoma, Uveal 61 1.250
704
c HRD198 Hereditary Dystonia 30 1.250
705
c CNG223 Congenital Methemoglobinemia 39 1.242
706
c PLY172 Polycystic Kidney Disease 2 with or Without Polycystic Liver Disease 53 1.242
707
DSM004 Desmoid Tumor 66 1.242
708
P MCR129 Microvascular Complications of Diabetes 1 68 1.242
709
END041 Endometrial Adenocarcinoma 64 1.242
710
ACT200 Acute Monoblastic Leukemia 41 1.242
711
P PRM011 Primary Ciliary Dyskinesia 69 1.230
712
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 1.230
713
BRN018 Borna Disease 36 1.230
714
P MTC010 Mitochondrial Dna Depletion Syndrome 47 1.230
715
P TCD001 Tic Disorder 49 1.230
716
BRK012 Broken Heart Syndrome 42 1.230
717
NPH003 Nephrocalcinosis 49 1.218
718
P THP004 Thiopurines, Poor Metabolism of, 1 42 1.207
719
JVN004 Juvenile Myelomonocytic Leukemia 67 1.193
720
GRD001 Giardiasis 46 1.189
721
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 57 1.176
722
HYP114 Hypertensive Nephropathy 36 1.176
723
CRN030 Coronary Stenosis 50 1.176
724
P CHL066 Cholangitis 52 1.176
725
PRS047 Prostatitis 58 1.176
726
CRV040 Cervix Carcinoma 50 1.176
727
P ANG015 Angioedema 56 1.176
728
c MLG069 Malignant Hypertension 46 1.176
729
CLN019 Colonic Disease 47 1.176
730
P TST026 Testicular Germ Cell Cancer 44 1.176
731
GRM005 Germ Cell Cancer 46 1.176
732
PRL045 Proline-Negative Auxotroph of Hamster, Complementation of 16 1.176
733
ACL001 Acalculous Cholecystitis 38 1.176
734
HYP264 Hypertonia 36 1.176
735
GN1001 Gnao1 Encephalopathy 11 1.176
736
FRN006 Frontotemporal Dementia 68 1.167
737
P NGH001 Night Blindness 52 1.167
738
MNN009 Meningoencephalitis 48 1.167
739
P SLP005 Sleep Disorder 61 1.167
740
c ART115 Aortic Valve Disease 1 74 1.154
741
P LPR021 Leprosy 3 71 1.154
742
CHR066 Chronic Fatigue Syndrome 60 1.154
743
ART016 Aortic Aneurysm 68 1.154
744
MCN017 Meconium Ileus 53 1.154
745
P DDN001 Duodenal Ulcer 53 1.154
746
MCS002 Mucositis 56 1.154
747
P PRN023 Prion Disease 60 1.154
748
HNS001 Hansen's Disease 32 1.154
749
ANR040 Aneurysm 61 1.154
750
c THR092 Thrombophilia Due to Thrombin Defect 74 1.152
751
c ATM099 Autoimmune Uveitis 45 1.152
752
ZLL002 Zollinger-Ellison Syndrome 55 1.152
753
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 44 1.152
754
HRN029 Hearing Loss, Noise-Induced 37 1.152
755
CRR012 Cirrhotic Cardiomyopathy 22 1.152
756
GST030 Gastrinoma 45 1.152
757
SKN019 Skin Melanoma 71 1.152
758
CHL147 Chlamydia Pneumonia 47 1.152
759
CRT004 Carotid Artery Thrombosis 39 1.152
760
P CRB088 Cerebral Atrophy 33 1.152
761
MLK004 Malakoplakia 33 1.152
762
DNG002 Dengue Hemorrhagic Fever 60 1.130
763
P LMB006 Limb-Girdle Muscular Dystrophy 52 1.114
764
c ANM038 Anemia, Autoimmune Hemolytic 64 1.106
765
c PRG020 Paragangliomas 3 39 1.106
766
P GLL020 Gallbladder Disease 56 1.106
767
CLF001 Cleft Lip 53 1.106
768
DBT006 Diabetic Macular Edema 48 1.106
769
P PRD021 Periodic Paralysis 41 1.106
770
SNS003 Sensory Peripheral Neuropathy 52 1.106
771
HND002 Hand, Foot and Mouth Disease 50 1.106
772
P SML001 Small Cell Carcinoma 52 1.084
773
KPS004 Kaposi Sarcoma 77 1.084
774
ENT011 Enterocolitis 55 1.084
775
P AMY004 Amyloidosis 70 1.084
776
P RRH023 Rare Hereditary Hemochromatosis 54 1.084
777
P CND004 Candidiasis 58 1.084
778
HMS001 Hemosiderosis 48 1.084
779
P SPN046 Spinal Muscular Atrophy 63 1.084
780
HYP043 Hyperandrogenism 48 1.084
781
BRS099 Breast Ductal Carcinoma 61 1.084
782
ENT004 Enthesopathy 51 1.084
783
VSC002 Vascular Dementia 60 1.084
784
DRG003 Drug Dependence 46 1.084
785
P USH001 Usher Syndrome 64 1.072
786
c LBR004 Leber Congenital Amaurosis 1 52 1.072
787
c SPN294 Spinocerebellar Ataxia 1 53 1.072
788
MTB016 Metabolic Myopathy 30 1.065
789
PLM061 Pulmonary Edema of Mountaineers 26 1.065
790
MSC152 Muscular Dystrophy, Becker Type 69 1.065
791
c SPR086 Spermatogenic Failure 3 46 1.065
792
P ANP001 Anaplastic Large Cell Lymphoma 61 1.065
793
PRP080 Peripheral Artery Disease 54 1.065
794
c FML001 Familial Atrial Fibrillation 65 1.065
795
c ATM022 Autoimmune Myocarditis 36 1.065
796
NPH091 Nephrolithiasis, Calcium Oxalate 61 1.065
797
OBS082 Obstructive Nephropathy 41 1.065
798
VSC003 Visceral Leishmaniasis 55 1.065
799
P PLM034 Pulmonary Emphysema 58 1.065
800
BLD131 Bladder Urothelial Carcinoma 60 1.065
801
P CCK001 Cockayne Syndrome 68 1.065
802
INT392 Intellectual Developmental Disorder with Paroxysmal Dyskinesia or Seizures 15 1.065
803
BLR001 Biliary Atresia 55 1.065
804
RTR008 Root Resorption 44 1.065
805
BRB002 Barbiturate Dependence 28 1.065
806
IRN001 Iron Deficiency Anemia 58 1.065
807
BRC012 Brucellosis 66 1.065
808
PRP030 Purpura 54 1.065
809
P MTR014 Motor Neuron Disease 65 1.065
810
AZS001 Azoospermia 45 1.065
811
P MTR003 Mitral Valve Stenosis 53 1.065
812
P DYS021 Dysautonomia 38 1.065
813
DYS073 Dysphagia 53 1.065
814
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 1.064
815
P SPR120 Supranuclear Palsy, Progressive, 1 69 1.031
816
P QLT041 Qualitative or Quantitative Defects of Alpha-Dystroglycan 18 1.031
817
LNG039 Lung Squamous Cell Carcinoma 57 1.031
818
c CNT035 Central Nervous System Disease 54 1.031
819
ALB002 Albinism 47 1.031
820
c CNG441 Congenital Muscular Dystrophy Due to Dystroglycanopathy 28 1.031
821
c EXD008 Exudative Vitreoretinopathy 1 71 1.007
822
P BCK002 Beckwith-Wiedemann Syndrome 62 1.007
823
GLL008 Gilles De La Tourette Syndrome 65 1.007
824
ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 36 1.007
825
P BRC006 Brachydactyly 51 1.007
826
c BCT013 Bacterial Pneumonia 48 1.007
827
CRY005 Cryptococcosis 60 1.007
828
P HYP035 Hypophosphatasia 62 1.007
829
PSY004 Psychotic Disorder 66 1.007
830
P GCH001 Gaucher's Disease 70 1.007
831
PRM020 Premenstrual Tension 39 1.007
832
MST020 Mast Cell Activation Syndrome 28 1.007
833
c CHR417 Chronic Graft Versus Host Disease 55 1.007
834
PRN019 Perinatal Necrotizing Enterocolitis 60 1.007
835
CLP005 Ciliopathy 41 0.960
836
CYN003 Cyanide Poisoning 22 0.960
837
P MCR364 Macrodactyly 40 0.960
838
c MST023 Mesothelioma, Malignant 56 0.960
839
CHR100 Chronic Ulcer of Skin 57 0.960
840
GNY003 Guanylate Cyclase 2e, Pseudogene 12 0.960
841
P MCP040 Mucopolysaccharidosis-Plus Syndrome 70 0.960
842
THR100 Thrombocytopenic Purpura, Autoimmune 61 0.960
843
c RTN032 Retinal Cone Dystrophy 1 24 0.960
844
URT049 Urate Oxidase, Pseudogene 24 0.960
845
SBV001 Subvalvular Aortic Stenosis 30 0.960
846
IGG001 Iga Glomerulonephritis 50 0.960
847
P RTN014 Retinal Artery Occlusion 47 0.960
848
c PLM127 Pulmonary Hypertension, Primary, 3 34 0.960
849
MND031 Mandibuloacral Dysplasia Progeroid Syndrome 33 0.960
850
BRN026 Branch Retinal Artery Occlusion 41 0.960
851
P FCL005 Focal Segmental Glomerulosclerosis 57 0.960
852
FLR002 Filariasis 55 0.960
853
MCN007 Meconium Aspiration Syndrome 53 0.960
854
HYP006 Hypertensive Heart Disease 49 0.960
855
c HPT007 Hepatitis E 51 0.960
856
P OVR049 Ovarian Disease 52 0.960
857
CLR033 Color Vision Deficiency 40 0.960
858
P NNS072 Nonsyndromic Hearing Loss 40 0.960
859
ESN011 Eisenmenger Syndrome 47 0.960
860
PRP083 Porphyria, Acute Intermittent 65 0.955
861
EPD015 Epidemic Typhus 44 0.937
862
WST001 West Syndrome 59 0.937
863
CLS016 Clostridium Difficile Colitis 49 0.937
864
MLD001 Melioidosis 67 0.937
865
MLG079 Malignant Pleural Mesothelioma 42 0.937
866
SLC006 Silicosis 56 0.937
867
HMN048 Human Papillomavirus Infectious Disease 46 0.937
868
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 54 0.936
869
NCL008 Nuclear Ribonucleic Acid 15 0.924
870
SQM013 Squamous Cell Carcinoma, Head and Neck 73 0.924
871
ACR011 Acromesomelic Dysplasia, Maroteaux Type 44 0.924
872
DNH001 Donohue Syndrome 61 0.924
873
ANR004 Anuria 44 0.924
874
MRF001 Marfan Syndrome 76 0.919
875
P ASP006 Aspergillosis 72 0.919
876
LWC002 Lowe Oculocerebrorenal Syndrome 68 0.919
877
STR101 Striatal Degeneration, Autosomal Dominant 1 32 0.919
878
c CHR418 Chronic Leukemia 48 0.919
879
P HMC002 Homocystinuria 53 0.919
880
KRT006 Keratoconjunctivitis 53 0.919
881
ADC009 Adcy5 Dyskinesia 8 0.919
882
RDC002 Radiculopathy 52 0.919
883
SHG001 Shigellosis 63 0.919
884
OLG001 Oligospermia 45 0.919
885
CND006 Candida Glabrata 30 0.919
886
BLR013 Biliary Tract Cancer 43 0.919
887
P HRD217 Hereditary Optic Neuropathy 36 0.825
888
RTN187 Retinitis Pigmentosa-Deafness Syndrome 48 0.825
889
PHS004 Phosphoribosylpyrophosphate Synthetase Superactivity 49 0.825
890
P SJG008 Sjogren Syndrome 61 0.825
891
P CLC063 Celiac Disease 1 66 0.825
892
c SVR003 Severe Congenital Neutropenia 59 0.825
893
P STR022 Stargardt Disease 61 0.825
894
c XNT010 Xanthinuria, Type I 52 0.825
895
c MCR312 Microphthalmia, Syndromic 10 40 0.825
896
ACH004 Achondroplasia 66 0.825
897
OST032 Osteofibrous Dysplasia 52 0.825
898
PNS018 Pain Sensitivity Quantitative Trait Locus 1 23 0.825
899
CTN007 Cutaneous Leishmaniasis 62 0.825
900
VLK001 Volkmann Contracture 23 0.825
901
LRN003 Learning Disability 49 0.825
902
P BRD002 Bardet-Biedl Syndrome 66 0.825
903
MNK002 Monkeypox 41 0.825
904
P HRM001 Hermansky-Pudlak Syndrome 65 0.825
905
SCB001 Scabies 50 0.825
906
STR103 Streptococcus Pneumonia 47 0.825
907
ATN004 Autonomic Neuropathy 42 0.825
908
P END033 Endocarditis 58 0.825
909
TCL001 T-Cell Adult Acute Lymphocytic Leukemia 43 0.825
910
CCN002 Cocaine Abuse 49 0.825
911
PTN001 Patent Foramen Ovale 62 0.825
912
FML035 Familial Hyperlipidemia 55 0.825
913
P TRC031 Trichorhinophalangeal Syndrome 38 0.825
914
c RNG019 Ring Chromosome 3 19 0.825
915
HDN002 Head Injury 44 0.825
916
SKL017 Skeletal Dysplasias 41 0.815
917
PRM163 Primary Mediastinal Large B-Cell Lymphoma 40 0.815
918
P MCH002 Machado-Joseph Disease 62 0.815
919
BCL014 B-Cell Growth Factor 33 0.815
920
PTT048 Pituitary Adenoma, Prolactin-Secreting 64 0.815
921
SPP011 Suppression of Tumorigenicity 12 61 0.815
922
LYM007 Lymphangioleiomyomatosis 68 0.815
923
OVR029 Ovarian Hyperstimulation Syndrome 63 0.815
924
P MYS005 Myositis 56 0.815
925
CRT072 Creutzfeldt-Jakob Disease 68 0.815
926
VNH007 Von Hippel-Lindau Syndrome 73 0.815
927
HYD038 Hydrops Fetalis, Nonimmune 59 0.815
928
P APL001 Aplastic Anemia 73 0.815
929
HYP457 Hypertrophic Scars 42 0.815
930
BCT021 Bacterial Sepsis 43 0.815
931
c CNG006 Congenital Hypothyroidism 63 0.815
932
c MGR030 Migraine, Familial Hemiplegic, 2 49 0.815
933
WRN001 Werner Syndrome 69 0.815
934
c CRD065 Cardiomyopathy, Familial Hypertrophic, 2 47 0.815
935
HTC003 Hutchinson-Gilford Progeria Syndrome 65 0.815
936
c HNT011 Huntington Disease-Like 3 34 0.815
937
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 32 0.815
938
c ACR084 Aicardi-Goutieres Syndrome 7 29 0.815
939