Search results for Guanosine monophosphate

1117 hits were found for Guanosine monophosphate

# Family MCID Name MIFTS Score
1
PRT037 Pertussis 49 13.461
2
CHL014 Cholera 62 13.111
3
P NRB001 Neuroblastoma 66 8.370
4
IMP005 Impotence 52 7.612
5
P PLM037 Pulmonary Hypertension 69 5.990
6
P HRP006 Herpes Simplex 65 5.489
7
P LKM002 Leukemia 65 5.285
8
HLX001 Helix Syndrome 47 5.162
9
P PHC003 Pheochromocytoma 70 4.949
10
ADR040 Adrenal Gland Pheochromocytoma 45 4.949
11
P LKM071 Leukemia, Chronic Lymphocytic 74 4.823
12
GLL048 Glial Tumor 51 4.732
13
GLM045 Glioma 62 4.707
14
48X005 48,xyyy 39 4.467
15
PRN001 Purine Nucleoside Phosphorylase Deficiency 53 4.406
16
c PRC016 Pre-Eclampsia 64 4.399
17
P RHN004 Rhinitis 56 4.269
18
HMN044 Human Immunodeficiency Virus Type 1 76 4.155
19
P AST005 Asthma 75 4.111
20
ALL003 Allergic Rhinitis 66 4.109
21
RPD005 Rapidly Involuting Congenital Hemangioma 48 4.068
22
P MYL006 Myeloid Leukemia 60 4.059
23
IMM167 Immune Deficiency Disease 76 4.011
24
P LKM062 Leukemia, Acute Lymphoblastic 69 3.919
25
c HPT073 Hepatitis C Virus 70 3.913
26
OST159 Osteogenic Sarcoma 66 3.901
27
c HYP595 Hypertension, Essential 84 3.796
28
c PLM164 Pulmonary Hypertension, Primary, 1 75 3.790
29
ISC004 Ischemia 61 3.764
30
NRR001 Neuroretinitis 42 3.726
31
RTN023 Retinitis 45 3.726
32
NNL005 Non-Alcoholic Fatty Liver Disease 63 3.677
33
INS024 Insulin-Like Growth Factor I 77 3.671
34
BNR002 Bone Resorption Disease 47 3.670
35
VCC001 Vaccinia 49 3.650
36
P HYP069 Hyperparathyroidism 62 3.629
37
HYP266 Hypoxia 56 3.616
38
c HPT001 Hepatitis C 61 3.547
39
P TRM003 Tremor 50 3.526
40
c LKM061 Leukemia, Acute Myeloid 83 3.525
41
c MCR113 Microvascular Complications of Diabetes 3 52 3.493
42
c MCR133 Microvascular Complications of Diabetes 4 41 3.489
43
c MCR130 Microvascular Complications of Diabetes 6 41 3.489
44
c MCR120 Microvascular Complications of Diabetes 7 47 3.489
45
DFC004 Deficiency Anemia 74 3.483
46
P HYP076 Hyperthyroidism 53 3.468
47
c ACT073 Acute Leukemia 59 3.442
48
P DYS154 Dystonia 64 3.421
49
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 3.412
50
P RTN008 Retinitis Pigmentosa 79 3.399
51
CYS001 Cystic Fibrosis 77 3.398
52
FTT001 Fatty Liver Disease 61 3.364
53
TXC005 Toxic Shock Syndrome 61 3.353
54
ANX004 Anoxia 40 3.329
55
P GLM040 Glioma Susceptibility 1 70 3.289
56
CHC001 Chickenpox 56 3.278
57
MLG169 Malignant Astrocytoma 57 3.267
58
HYP066 Hyperglycemia 60 3.253
59
HYP060 Hyperinsulinism 53 3.218
60
P VSC007 Vascular Disease 62 3.203
61
SPN186 Spinal Cord Injury 60 3.202
62
P HML002 Hemolytic Anemia 62 3.184
63
MYL069 Myeloma, Multiple 76 3.146
64
P SZR006 Seizure Disorder 69 3.142
65
P HPT023 Hepatocellular Carcinoma 95 3.128
66
CNG034 Congestive Heart Failure 69 3.042
67
ADR016 Adrenal Cortical Carcinoma 61 3.039
68
BRN071 Brain Injury 50 3.000
69
P GRV001 Graves' Disease 54 2.998
70
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 59 2.987
71
GLB002 Glioblastoma 67 2.967
72
P SCK005 Sickle Cell Disease 56 2.964
73
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 2.960
74
PRS045 Prostatic Hypertrophy 53 2.949
75
c TYP009 Type 2 Diabetes Mellitus 91 2.909
76
CRB004 Cerebral Artery Occlusion 45 2.906
77
ADR054 Adrenocortical Carcinoma, Hereditary 47 2.902
78
ADR004 Adrenal Cortical Adenocarcinoma 38 2.902
79
P GRF003 Graft-Versus-Host Disease 71 2.894
80
ALL006 Allergic Asthma 55 2.864
81
P MLN008 Melanoma 75 2.845
82
c PRM005 Primary Hyperparathyroidism 59 2.834
83
P HPT021 Hepatitis 68 2.812
84
ALL029 Allergic Disease 61 2.805
85
P LYM118 Lymphoma 66 2.804
86
TRM010 Traumatic Brain Injury 50 2.780
87
STM007 Stomatitis 52 2.733
88
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 2.705
89
c HPT016 Hepatitis B 62 2.700
90
HYP056 Hypoglycemia 65 2.697
91
LVR012 Liver Cirrhosis 62 2.650
92
47X002 47,xyy 47 2.649
93
P GST053 Gastric Cancer 82 2.636
94
PRS021 Prostatic Adenoma 43 2.616
95
OCL069 Ocular Motor Apraxia 57 2.606
96
PRS129 Prostatic Hyperplasia, Benign 48 2.604
97
P ADL010 Adult Respiratory Distress Syndrome 70 2.557
98
CHR074 Choriocarcinoma 46 2.550
99
P ECL001 Eclampsia 52 2.544
100
P HYP098 Hypereosinophilic Syndrome 66 2.538
101
c MJR022 Major Affective Disorder 8 37 2.536
102
c MJR024 Major Affective Disorder 9 40 2.536
103
P BPL003 Bipolar Disorder 56 2.536
104
PTT037 Pituitary Tumors 44 2.535
105
PLM129 Pulmonary Disease, Chronic Obstructive 74 2.529
106
CYT002 Cytokine Deficiency 43 2.518
107
IGR001 Ige Responsiveness, Atopic 58 2.508
108
MST004 Mast Cell Neoplasm 41 2.503
109
EXT007 Extracutaneous Mastocytoma 38 2.503
110
LYM019 Lymphosarcoma 46 2.498
111
PPT005 Peptic Ulcer Disease 58 2.494
112
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 2.487
113
PRT251 Proteinuria, Chronic Benign 58 2.480
114
P PSR002 Psoriasis 63 2.461
115
P LVR013 Liver Disease 68 2.455
116
PRT013 Portal Hypertension 59 2.443
117
PST011 Pustulosis of Palm and Sole 52 2.442
118
P RTN016 Retinal Degeneration 52 2.432
119
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 2.429
120
MDD011 Mood Disorder 61 2.422
121
P PSD015 Pseudohypoparathyroidism 54 2.418
122
P DBT005 Diabetes Insipidus 54 2.409
123
c SYS001 Systemic Lupus Erythematosus 85 2.406
124
P DRM053 Dermatitis, Atopic 65 2.403
125
P NPH012 Nephrotic Syndrome 61 2.390
126
c DLT002 Dilated Cardiomyopathy 79 2.388
127
BRN004 Brain Edema 54 2.387
128
P GLM007 Glomerulonephritis 59 2.383
129
AGN016 Aging 53 2.381
130
P ENC018 Encephalopathy 62 2.370
131
INS001 Insulinoma 59 2.369
132
P LPS004 Lupus Erythematosus 61 2.347
133
c LKM063 Leukemia, Chronic Myeloid 70 2.327
134
CLT003 Colitis 63 2.295
135
P HYP024 Hypoparathyroidism 55 2.290
136
c GRV008 Graves Disease 1 54 2.288
137
LPD008 Lipid Metabolism Disorder 61 2.285
138
SXL003 Sexual Disorder 49 2.283
139
P HRT032 Heart Disease 84 2.283
140
TTN003 Tetanus 64 2.273
141
HPT004 Hepatic Coma 43 2.267
142
MNT002 Mental Depression 56 2.260
143
DBT010 Diabetic Neuropathy 54 2.229
144
MDD018 Middle East Respiratory Syndrome 44 2.214
145
P MJR001 Major Depressive Disorder 68 2.211
146
PPL052 Papillomatosis, Confluent and Reticulated 34 2.208
147
DPR016 Depression 64 2.207
148
P MYC084 Mycobacterium Tuberculosis 1 68 2.201
149
P MYP004 Myopathy 67 2.187
150
DPH001 Diphtheria 59 2.174
151
HYP014 Hyperuricemia 51 2.165
152
P HYP086 Hypothyroidism 68 2.128
153
c PCH010 Pachyonychia Congenita 3 43 2.128
154
ATH013 Atherosclerosis Susceptibility 63 2.127
155
ACT098 Acute Erythroid Leukemia 55 2.121
156
c VRL010 Viral Hepatitis 52 2.103
157
MYL009 Myelodysplastic Syndrome 67 2.076
158
P ADN016 Adenocarcinoma 63 2.064
159
HPT019 Hepatic Encephalopathy 59 2.055
160
ADN018 Adenoma 58 2.055
161
LSC001 Lesch-Nyhan Syndrome 62 2.051
162
PNG002 Pain Agnosia 51 2.049
163
IRR002 Irritable Bowel Syndrome 64 2.045
164
GST033 Gestational Diabetes 60 2.042
165
P INF037 Inflammatory Bowel Disease 53 2.036
166
c TBR025 Tuberous Sclerosis 1 84 2.031
167
CLN015 Colon Adenocarcinoma 64 2.029
168
P ALZ034 Alzheimer Disease 87 2.026
169
DRM006 Dermatitis 61 2.024
170
THY029 Thyroid Carcinoma 55 2.024
171
c HYP836 Hypercholesterolemia, Familial, 1 73 2.024
172
RNL077 Renal Fibrosis 46 2.020
173
P CLR023 Colorectal Cancer 100 2.008
174
CHG001 Chagas Disease 65 2.008
175
HND015 Hand Skill, Relative 29 1.972
176
P PRS040 Prostate Cancer 95 1.972
177
RNL114 Renal Cell Carcinoma, Nonpapillary 79 1.967
178
URT010 Ureteral Obstruction 44 1.966
179
P PNC035 Pancreatic Cancer 87 1.963
180
END086 End Stage Renal Disease 54 1.947
181
OVR094 Ovarian Epithelial Cancer 39 1.945
182
P DBT009 Diabetes Mellitus 67 1.938
183
ACT119 Acute Promyelocytic Leukemia 62 1.938
184
CRV035 Cervical Cancer 72 1.937
185
BRN056 Bronchopulmonary Dysplasia 57 1.935
186
PLY150 Polykaryocytosis Inducer 29 1.927
187
P BCL017 B-Cell Lymphoma 57 1.923
188
GLC003 Glucose Intolerance 53 1.914
189
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 1.905
190
c LKM005 Leukemia, T-Cell, Chronic 33 1.905
191
HRW001 Hair Whorl 35 1.898
192
c MCR115 Microvascular Complications of Diabetes 5 65 1.896
193
P MNN013 Meningitis 65 1.885
194
SPL018 Splenomegaly 47 1.885
195
CHD001 Chediak-Higashi Syndrome 66 1.878
196
LWC001 Low Compliance Bladder 44 1.878
197
MSL001 Measles 61 1.869
198
NNL006 Non-Alcoholic Steatohepatitis 54 1.865
199
WTH001 Withdrawal Disorder 47 1.851
200
c CHR684 Chronic Kidney Disease 73 1.848
201
ACQ007 Acquired Immunodeficiency Syndrome 58 1.848
202
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 1.848
203
P MYC007 Myocardial Infarction 69 1.832
204
PST028 Post-Traumatic Stress Disorder 58 1.826
205
ACT084 Acute Stress Disorder 53 1.826
206
c MGR028 Migraine with or Without Aura 1 63 1.826
207
SDD001 Sudden Infant Death Syndrome 60 1.815
208
P ENC004 Encephalitis 61 1.799
209
BRN024 Bronchitis 67 1.795
210
GT001 Gout 63 1.794
211
P CHR012 Chronic Granulomatous Disease 69 1.788
212
LYM017 Lyme Disease 63 1.784
213
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 1.784
214
DYS192 Dystonia, Dopa-Responsive 56 1.782
215
P CHR345 Chronic Pain 50 1.778
216
P THR014 Thrombocytopenia 66 1.777
217
CNS004 Constipation 56 1.776
218
SLP001 Sleeping Sickness 56 1.774
219
P PLY014 Polycystic Kidney Disease 71 1.761
220
c AMY091 Amyotrophic Lateral Sclerosis 1 87 1.757
221
P LTR001 Lateral Sclerosis 57 1.757
222
P BDY004 Body Mass Index Quantitative Trait Locus 11 82 1.757
223
ULC004 Ulcerative Colitis 74 1.753
224
P PRD008 Periodontitis 63 1.750
225
MYL031 Myeloproliferative Neoplasm 66 1.747
226
c BCT007 Bacterial Meningitis 55 1.744
227
TRY001 Trypanosomiasis 50 1.742
228
c DNT047 Dentinogenesis Imperfecta Type 2 35 1.742
229
P LNG032 Lung Cancer 98 1.738
230
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 1.734
231
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 1.734
232
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 1.734
233
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 1.734
234
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 1.734
235
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 1.734
236
c BDY019 Body Mass Index Quantitative Trait Locus 18 46 1.734
237
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 1.734
238
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 1.734
239
P PRP019 Peripheral Nervous System Disease 57 1.724
240
ANG054 Angina Pectoris 65 1.724
241
CHL004 Cholelithiasis 48 1.713
242
P CRD119 Cardiac Arrest 68 1.711
243
P HYP265 Hypotonia 42 1.705
244
P BND020 Bone Disease 60 1.704
245
P NRF002 Neurofibromatosis 60 1.694
246
DWR001 Dwarfism 44 1.690
247
P CTN015 Cutaneous T Cell Lymphoma 48 1.689
248
P MYC008 Myocarditis 59 1.685
249
c SML038 Small Cell Cancer of the Lung 68 1.679
250
DMY004 Demyelinating Disease 50 1.677
251
SCR003 Secretory Diarrhea 35 1.669
252
P CNR004 Cone-Rod Dystrophy 2 74 1.656
253
HGH043 High Grade Glioma 46 1.648
254
P PRK039 Parkinsonism 55 1.647
255
LNG099 Lung Disease 62 1.645
256
P LNG064 Lung Cancer Susceptibility 3 69 1.644
257
MLY001 Molybdenum Cofactor Deficiency 40 1.634
258
ESP021 Esophageal Cancer 84 1.627
259
P MYP006 Myopia 55 1.627
260
ILT001 Ileitis 49 1.614
261
STR067 Stroke, Ischemic 79 1.605
262
P ATR011 Atrial Fibrillation 66 1.603
263
P CRN300 Coronary Heart Disease 1 73 1.590
264
PPL002 Papillary Carcinoma 46 1.584
265
BCT022 Bacterial Infectious Disease 55 1.582
266
P INF038 Influenza 68 1.574
267
KRT019 Keratitis, Hereditary 66 1.565
268
P NRP001 Neuropathy 59 1.560
269
CRY035 Cryptorchidism, Unilateral or Bilateral 57 1.542
270
NRM005 Neuromuscular Disease 62 1.540
271
P SKN015 Skin Carcinoma 71 1.530
272
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 44 1.528
273
GNT003 Genital Herpes 54 1.527
274
HRP004 Herpes Zoster 60 1.522
275
RCK004 Rickets 64 1.522
276
DSS032 Disease by Infectious Agent 55 1.512
277
PLS011 Plasmacytoma 56 1.496
278
P OVR042 Ovarian Cancer 88 1.493
279
HRY003 Hairy Cell Leukemia 53 1.492
280
MLR004 Malaria 77 1.488
281
P UVT001 Uveitis 57 1.482
282
P LCT001 Lactic Acidosis 50 1.466
283
CRT015 Carotid Artery Occlusion 45 1.465
284
CRY003 Cryptosporidiosis 55 1.457
285
SKN016 Skin Disease 63 1.455
286
TRT001 Teratocarcinoma 41 1.436
287
P RTN024 Retinoblastoma 72 1.436
288
RYN005 Raynaud Phenomenon 45 1.427
289
THR024 Thrombosis 56 1.425
290
P PRL003 Proliferative Glomerulonephritis 43 1.424
291
HYP005 Hypokalemia 55 1.419
292
HMP009 Haemophilus Influenzae 41 1.415
293
c ATR087 Atrial Standstill 1 74 1.408
294
GST023 Gastric Ulcer 52 1.404
295
P KDN018 Kidney Disease 71 1.402
296
MSN001 Mesangial Proliferative Glomerulonephritis 44 1.398
297
P GLL022 Guillain-Barre Syndrome 59 1.394
298
c INH030 Inherited Retinal Disorder 28 1.388
299
LYM133 Lymphoma, Hodgkin, Classic 69 1.386
300
MLD018 Mild Cognitive Impairment 48 1.382
301
PLM010 Pulmonary Edema 54 1.381
302
c ATS347 Autosomal Dominant Polycystic Kidney Disease 64 1.378
303
P INS002 in Situ Carcinoma 52 1.370
304
MTB004 Metabolic Acidosis 48 1.367
305
GTR002 Goiter 52 1.366
306
P TMP001 Temporal Lobe Epilepsy 49 1.365
307
P TBR001 Tuberous Sclerosis 69 1.361
308
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 1.356
309
ASP003 Aseptic Meningitis 50 1.352
310
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 1.349
311
SCH014 Schistosomiasis 56 1.349
312
c ACT075 Acute Myocardial Infarction 55 1.346
313
CHL068 Cholestasis 61 1.340
314
P OBS001 Obstructive Jaundice 49 1.339
315
P PTS002 Ptosis 52 1.336
316
P SLM003 Salmonellosis 54 1.320
317
P FML011 Familial Adenomatous Polyposis 70 1.319
318
GRW007 Growth Hormone Deficiency 47 1.315
319
SCK003 Sickle Cell Anemia 74 1.311
320
P MSC005 Muscular Dystrophy 66 1.309
321
RSP007 Respiratory Distress Syndrome, Infant 41 1.308
322
RTN020 Retinal Vascular Disease 45 1.307
323
P DRR001 Diarrhea 55 1.306
324
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 1.303
325
P EXN002 Exanthem 58 1.299
326
P TTR001 Tetralogy of Fallot 69 1.299
327
c ATM011 Autoimmune Hepatitis 62 1.285
328
c SVR005 Severe Pre-Eclampsia 49 1.282
329
DST006 Diastolic Heart Failure 45 1.282
330
PHN003 Phenylketonuria 76 1.273
331
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 1.271
332
P VTR007 Vitreoretinopathy 45 1.271
333
SGW002 Segawa Syndrome, Autosomal Recessive 44 1.269
334
PNC001 Pancytopenia 52 1.266
335
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 1.264
336
LYM040 Lymphoblastic Lymphoma 53 1.263
337
P MTR012 Mitral Valve Disease 57 1.259
338
P ART022 Arthritis 70 1.258
339
P PLM036 Pulmonary Fibrosis 65 1.257
340
END057 Endometrial Cancer 76 1.252
341
P FBR017 Fibrosarcoma 55 1.244
342
P PLY011 Polycystic Ovary Syndrome 57 1.244
343
P INF032 Infertility 60 1.240
344
P VSC011 Vasculitis 61 1.240
345
P SCL018 Scoliosis 57 1.239
346
PYR010 Peyronie's Disease 50 1.239
347
P MLN007 Male Infertility 56 1.238
348
LYM027 Lymphopenia 56 1.230
349
ATS010 Autosomal Recessive Disease 42 1.230
350
P RTN034 Retinal Cone Dystrophy 3a 29 1.217
351
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 1.216
352
MCR013 Microphthalmia 59 1.211
353
MYL005 Myelofibrosis 70 1.209
354
c CHR711 Chronic Asthma 41 1.206
355
GRN017 Granulocytopenia 42 1.197
356
ORL015 Oral Squamous Cell Carcinoma 43 1.192
357
P PTT006 Pituitary Adenoma 55 1.185
358
ARG004 Argyria 26 1.182
359
DWN001 Down Syndrome 70 1.181
360
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 1.181
361
GST045 Gastroenteritis 58 1.178
362
ALC009 Alcoholic Liver Cirrhosis 54 1.175
363
ADG002 Audiogenic Seizures 25 1.175
364
SVR001 Severe Acute Respiratory Syndrome 68 1.175
365
SVR004 Severe Combined Immunodeficiency 70 1.174
366
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 1.171
367
URM002 Uremia 47 1.167
368
PRT036 Peritonitis 65 1.166
369
CRB090 Cerebral Hypoxia 42 1.164
370
KRN002 Kearns-Sayre Syndrome 62 1.158
371
c CHR095 Chronic Progressive External Ophthalmoplegia 48 1.158
372
TRN015 Transient Cerebral Ischemia 62 1.155
373
P END044 Endometriosis 62 1.155
374
P BRT004 Bartter Disease 58 1.153
375
LKC009 Leukocyte Adhesion Deficiency, Type I 69 1.152
376
P SLP006 Sleep Apnea 69 1.144
377
P NTR004 Neutropenia 62 1.143
378
PYR041 Pyruvate Kinase Deficiency of Red Cells 56 1.139
379
P ART021 Arteriosclerosis 53 1.135
380
CRV002 Cervix Uteri Carcinoma in Situ 48 1.130
381
CRV045 Cervical Intraepithelial Neoplasia 38 1.130
382
IDP070 Idiopathic Scoliosis 41 1.127
383
P PNV001 Panuveitis 48 1.127
384
WLL004 Wallerian Degeneration 38 1.127
385
CRH001 Crohn's Disease 80 1.107
386
P BRB001 Beriberi 44 1.106
387
P BRS047 Breast Cancer 97 1.104
389
AMN003 Amnestic Disorder 53 1.103
390
P DNG005 Dengue Virus 55 1.103
391
P PRP029 Porphyria 60 1.102
392
PNC129 Pancreatic Adenocarcinoma 64 1.096
393
c ACT135 Acute Graft Versus Host Disease 51 1.096
394
ACR016 Acromesomelic Dysplasia 35 1.094
395
ASP004 Asphyxia Neonatorum 50 1.094
396
APC001 Apical Myocardial Infarction 16 1.094
397
ACT058 Active Peptic Ulcer Disease 55 1.094
398
c ATS025 Autosomal Dominant Progressive External Ophthalmoplegia 45 1.094
399
SMT007 Smith-Fineman-Myers Syndrome 32 1.094
400
c SCL052 Scleroderma, Familial Progressive 60 1.081
401
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 1.081
402
P BRS044 Breast Adenocarcinoma 58 1.080
403
c ACT071 Acute Kidney Failure 60 1.080
404
TRC003 Trichomoniasis 53 1.078
405
c INH020 Inherited Metabolic Disorder 47 1.060
406
c PSD108 Pseudohypoparathyroidism, Type Ia 64 1.059
407
P EYD002 Eye Disease 57 1.059
408
P EPL164 Epilepsy 70 1.049
409
NWC001 Newcastle Disease 47 1.048
410
P PRK057 Parkinson Disease, Late-Onset 79 1.046
411
SPN035 Spindle Cell Sarcoma 51 1.044
412
SRC014 Sarcoma 64 1.044
413
P OPN001 Open-Angle Glaucoma 55 1.043
414
PLR008 Pleurisy 49 1.041
415
P SCH015 Schizophrenia 74 1.040
416
FBR047 Fibromyalgia 57 1.039
417
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 1.036
418
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 1.036
419
MRP001 Morphine Dependence 41 1.035
420
GST040 Gastric Adenocarcinoma 66 1.035
421
P RNV001 Renovascular Hypertension 48 1.032
422
c BRN108 Branchiootic Syndrome 1 63 1.030
423
ALC007 Alcohol Dependence 65 1.029
424
PLG002 Plague 58 1.022
425
CHL123 Chlamydia 58 1.021
426
P MVM001 Movement Disease 61 1.020
427
P RHM011 Rheumatoid Arthritis 81 1.012
428
ALL014 Allergic Encephalomyelitis 34 1.010
429
P ALC033 Alcohol Use Disorder 67 1.009
430
URL001 Urolithiasis 45 1.009
431
P CTR002 Cataract 59 1.008
432
P OVR082 Overgrowth Syndrome 41 0.995
433
NPH009 Nephrolithiasis 54 0.992
434
P PLY019 Polyneuropathy 52 0.984
435
P HYP750 Hypertriglyceridemia, Familial 61 0.984
436
P GST044 Gastritis 55 0.984
437
P HNT016 Huntington Disease 73 0.982
438
INT007 Intermediate Coronary Syndrome 53 0.973
439
P MTC133 Mitochondrial Myopathy 51 0.970
440
P BLD134 Bladder Cancer 79 0.968
441
P ACT105 Acute Mountain Sickness 52 0.963
442
P RTN018 Retinal Disease 53 0.959
443
P INT068 Intestinal Disease 53 0.957
444
BRN002 Bronchiolitis 57 0.957
445
CWP001 Cowpox 44 0.957
446
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 0.954
447
P RSP003 Respiratory Failure 73 0.951
448
HMN047 Human Cytomegalovirus Infection 59 0.951
449
P ADL017 Adult T-Cell Leukemia 53 0.944
450
HMC014 Homocysteinemia 52 0.944
451
P THP004 Thiopurines, Poor Metabolism of, 1 41 0.944
452
c THY107 Thymoma, Familial 42 0.940
453
P THY023 Thymoma 64 0.940
454
KRT009 Keratosis 52 0.938
455
PSD014 Pseudopseudohypoparathyroidism 54 0.934
456
NRL005 Neurilemmoma 60 0.934
457
P OPT006 Optic Nerve Disease 57 0.933
458
FBR009 Fibrous Dysplasia 48 0.933
459
DNH001 Donohue Syndrome 60 0.925
460
ACR011 Acromesomelic Dysplasia, Maroteaux Type 44 0.925
461
ANR004 Anuria 44 0.925
462
P MLT020 Multiple Sclerosis 79 0.924
463
P PRM051 Primary Pigmented Nodular Adrenocortical Disease 55 0.920
464
MTH009 Mouth Disease 57 0.919
465
P MCR010 Microcephaly 59 0.919
466
HPT022 Hepatoblastoma 54 0.917
467
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 40 0.913
468
CHR073 Choreatic Disease 53 0.913
469
PLM001 Pulmonary Tuberculosis 69 0.908
470
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 0.906
471
P OST002 Osteoporosis 76 0.906
472
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.906
473
PST092 Posttransplant Acute Limbic Encephalitis 29 0.895
474
ANT024 Anthrax Disease 57 0.893
475
THY111 Thyroid Carcinoma, Familial Medullary 67 0.890
476
THY125 Thyroid Gland Medullary Carcinoma 48 0.890
477
BRN012 Bronchiolitis Obliterans 56 0.889
478
NRT004 Neuritis 53 0.889
479
THR004 Thrombocytosis 52 0.888
480
MCC012 Mccune-Albright Syndrome 69 0.886
481
P HYP061 Hypertrophic Cardiomyopathy 68 0.886
482
MSC007 Muscle Hypertrophy 64 0.885
483
P HDC001 Headache 56 0.877
484
WST005 West Nile Virus 55 0.873
485
c ACT027 Acute Pancreatitis 60 0.872
486
c ACT134 Acute Liver Failure 57 0.860
487
SBC016 Subacute Delirium 42 0.853
488
DGN001 Degenerative Disc Disease 48 0.850
489
LKS001 Leukostasis 40 0.848
490
PLT016 Platelet Adenylate Cyclase Activity 16 0.841
491
P SRC025 Sarcoidosis 1 70 0.840
492
PRM236 Primary Biliary Cholangitis 62 0.840
493
PRP016 Paraplegia 52 0.836
494
c ACT249 Acute Asthma 40 0.835
495
STT041 Stuttering 52 0.833
496
P SYS005 Systemic Scleroderma 73 0.832
497
ADN001 Adenosine Deaminase Deficiency 59 0.832
498
P FLL037 Follicular Lymphoma 66 0.831
499
MYT011 Myotonia 37 0.831
500
P OLG002 Oligodendroglioma 66 0.828
501
P PNC044 Pancreatitis 61 0.822
502
OST012 Osteoarthritis 77 0.820
503
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 51 0.819
504
MTB008 Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 42 0.819
505
c HYP331 Hyperphenylalaninemia, Bh4-Deficient, a 59 0.818
506
TCL027 T-Cell Acute Lymphoblastic Leukemia 52 0.813
507
CNN003 Conn's Syndrome 77 0.808
508
CLF027 Cleft Palate, Isolated 64 0.808
509
STT001 Status Epilepticus 58 0.807
510
RTH007 Rothmund-Thomson Syndrome, Type 1 37 0.805
511
LBR036 Leber Plus Disease 67 0.804
512
P FRG001 Fragile X Syndrome 70 0.801
513
NRF007 Neurofibroma 63 0.793
514
SYN036 Syncope 44 0.793
515
CHK001 Chikungunya 60 0.792
516
P ESN008 Eosinophilic Pneumonia 50 0.792
517
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.785
518
AVN001 Avian Influenza 61 0.785
519
c WLM013 Wilms Tumor 1 65 0.783
520
RTN017 Retinal Detachment 60 0.777
521
c VRL007 Viral Encephalitis 50 0.771
522
CNG486 Congenital Disorders of N-Linked Glycosylation and Multiple Pathway 29 0.766
523
c GLC092 Glaucoma, Primary Open Angle 60 0.765
524
P MMB011 Membranous Nephropathy 50 0.760
525
P RHB003 Rhabdomyosarcoma 66 0.760
526
P BNC003 Bone Cancer 58 0.744
527
P ACN011 Acne 55 0.744
528
MCL006 Macular Retinal Edema 56 0.742
529
c RTN047 Retinitis Pigmentosa 18 45 0.741
530
P SPP010 Suppressor of Tumorigenicity 3 50 0.741
531
GRY002 Gray Platelet Syndrome 57 0.738
532
JVN004 Juvenile Myelomonocytic Leukemia 66 0.736
533
c HPT003 Hepatitis a 63 0.732
534
PLM035 Pulmonary Eosinophilia 49 0.732
535
BRN028 Brain Cancer 73 0.729
536
PRN029 Parainfluenza Virus Type 3 32 0.729
537
P PRC019 Precocious Puberty 48 0.729
538
c THY109 Thyroid Cancer, Nonmedullary, 1 55 0.719
539
P KRN004 Kernicterus 47 0.719
540
CRN019 Coronary Artery Vasospasm 47 0.719
541
P CRD246 Cardiovascular System Disease 55 0.716
542
PRP007 Priapism 46 0.716
543
P FTL001 Fetal Alcohol Syndrome 55 0.713
544
LMB062 Limb Ischemia 55 0.713
545
P LCH002 Lichen Planus 54 0.713
546
VRC005 Varicose Veins 59 0.713
547
P CHR071 Charcot-Marie-Tooth Disease 64 0.713
548
P MTH007 Methemoglobinemia 46 0.713
549
CRC006 Carcinoid Syndrome 55 0.713
550
c NRB010 Neuroblastoma 1 59 0.712
551
HPT070 Hepatosplenic T-Cell Lymphoma 35 0.712
552
ATM095 Autoimmune Disease 61 0.710
553
CRB037 Cerebral Palsy 66 0.704
554
CHL067 Cholecystitis 59 0.702
555
OST003 Osteonecrosis 60 0.696
556
INT066 Interstitial Lung Disease 60 0.696
557
RNL011 Renal Osteodystrophy 48 0.696
558
TCK001 Tick-Borne Encephalitis 58 0.691
559
TTH006 Tooth Disease 51 0.691
560
IDP033 Idiopathic Edema 41 0.691
561
PRP083 Porphyria, Acute Intermittent 64 0.690
562
P HRD011 Hereditary Spherocytosis 63 0.676
563
OPD006 Opioid Addiction 48 0.676
564
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 54 0.672
565
PRL045 Proline-Negative Auxotroph of Hamster, Complementation of 16 0.668
566
ACL001 Acalculous Cholecystitis 34 0.668
567
CVD001 Covid-19 59 0.668
568
GN1001 Gnao1 Encephalopathy 11 0.668
569
HYP264 Hypertonia 35 0.668
570
KRT002 Keratomalacia 54 0.665
571
P PMP001 Pemphigus 54 0.665
572
ANC002 Anca-Associated Vasculitis 44 0.659
573
c MCR112 Microvascular Complications of Diabetes 2 42 0.655
574
BYS001 Byssinosis 27 0.655
575
GNG005 Gangliocytoma 54 0.655
576
DNT012 Dental Caries 53 0.655
577
GNG002 Ganglioneuroma 52 0.655
578
P OPT009 Optic Neuritis 57 0.655
579
DSR013 Disorders of Gnas Inactivation 15 0.655
580
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.645
581
P ACH003 Achromatopsia 61 0.642
582
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 0.640
583
PRT058 Pure Autonomic Failure 58 0.631
584
PST053 Postherpetic Neuralgia 39 0.631
585
P MCR129 Microvascular Complications of Diabetes 1 67 0.629
586
c CNG223 Congenital Methemoglobinemia 39 0.629
587
c PLY172 Polycystic Kidney Disease 2 with or Without Polycystic Liver Disease 53 0.629
588
RTR001 Retrograde Amnesia 41 0.629
589
END041 Endometrial Adenocarcinoma 63 0.629
590
DSM004 Desmoid Tumor 65 0.629
591
ACT200 Acute Monoblastic Leukemia 40 0.629
592
DNG002 Dengue Hemorrhagic Fever 59 0.601
593
TLN003 Telangiectasis 51 0.596
594
c PRG020 Paragangliomas 3 39 0.595
595
P GLL020 Gallbladder Disease 57 0.595
596
c ANM038 Anemia, Autoimmune Hemolytic 63 0.595
597
HND002 Hand, Foot and Mouth Disease 50 0.595
598
SNS003 Sensory Peripheral Neuropathy 51 0.595
599
DBT006 Diabetic Macular Edema 48 0.595
600
CLF001 Cleft Lip 54 0.595
601
P PRD021 Periodic Paralysis 42 0.595
602
RSP002 Respiratory Syncytial Virus Infectious Disease 51 0.588
603
LPP008 Lipoprotein Quantitative Trait Locus 65 0.584
604
c OPT053 Optic Atrophy 1 62 0.574
605
CHR466 Chronic Thromboembolic Pulmonary Hypertension 47 0.573
606
P KLZ004 Kala-Azar 1 41 0.571
607
LSH001 Leishmaniasis 63 0.571
608
P ATX030 Ataxia-Telangiectasia 80 0.568
609
PRM003 Premature Ejaculation 44 0.568
610
PLM101 Pulmonary Hypertension, Chronic Thromboembolic, Without Deep Vein Thrombosis 37 0.561
611
INT002 Intermittent Claudication 61 0.560
612
P CYS018 Cystitis 58 0.559
613
CMB007 Combined Immunodeficiency 56 0.558
614
NCL008 Nuclear Ribonucleic Acid 15 0.550
615
SQM013 Squamous Cell Carcinoma, Head and Neck 75 0.550
616
INT323 Intraocular Pressure Quantitative Trait Locus 63 0.548
617
P MDL005 Medulloblastoma 75 0.542
618
SQM006 Squamous Cell Carcinoma 59 0.535
619
ART140 Arteries, Anomalies of 52 0.533
620
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 0.532
621
P MSC003 Muscular Atrophy 52 0.531
622
c TYP008 Type 1 Diabetes Mellitus 77 0.530
623
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.530
624
P MGR001 Migraine Without Aura 48 0.526
625
P INT143 Interstitial Cystitis 59 0.520
626
IFP003 Ifap Syndrome 2 41 0.514
627
SNL007 Senile Cataract 40 0.513
628
MSC157 Muscular Dystrophy, Duchenne Type 78 0.512
629
GLM044 Glomerular Disease 34 0.507
630
HYP080 Hypogonadism 49 0.491
631
P DMN002 Dementia 65 0.478
632
GST037 Gastroparesis 52 0.476
633
YLL002 Yellow Fever 61 0.476
634
PSR001 Psoriatic Arthritis 61 0.470
635
EMB004 Embryonal Carcinoma 55 0.469
636
PRP027 Peripheral Vascular Disease 71 0.467
637
ACT003 Acute Kidney Tubular Necrosis 46 0.466
638
P KDN017 Kidney Cancer 60 0.462
639
BRK010 Burkitt Lymphoma 65 0.457
640
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.447
641
ENC038 Encephalopathy, Progressive, with or Without Lipodystrophy 40 0.447
642
P BNG032 Benign Mesothelioma 53 0.447
643
c ATS007 Autism Spectrum Disorder 71 0.446
644
c HMC039 Hemochromatosis, Type 1 73 0.440
645
P FBR031 Febrile Seizures 52 0.433
646
FND002 Fundus Dystrophy 54 0.431
647
MYC005 Myocardial Stunning 45 0.426
648
XRD010 Xeroderma Pigmentosum, Variant Type 72 0.422
649
HRT011 Heart Septal Defect 49 0.420
650
P RNL015 Renal Hypertension 45 0.420
651
ILS001 Ileus 49 0.420
652
OCL006 Ocular Hypertension 53 0.420
653
BLR008 Bilirubin Metabolic Disorder 57 0.418
654
CRD132 Cardiac Conduction Defect 59 0.418
655
CHL065 Cholangiocarcinoma 57 0.418
656
INT079 Intrahepatic Cholangiocarcinoma 51 0.418
657
c ACT004 Acute Diarrhea 40 0.396
658
OPT003 Opiate Dependence 49 0.396
659
P CRC039 Coarctation of Aorta 46 0.395
660
ANX010 Anxiety 70 0.395
661
PLM033 Pulmonary Embolism 58 0.395
662
LWF001 Low-Flow Priapism 16 0.395
663
P RTT002 Rett Syndrome 79 0.395
664
P MYS003 Myasthenia Gravis 67 0.391
665
IRN002 Iron Metabolism Disease 56 0.391
666
P MLG056 Malignant Hyperthermia 65 0.391
667
FCS014 Fucosidase Regulator 15 0.385
668
HLC007 Helicobacter Pylori Infection 67 0.382
669
PPL022 Papilloma 53 0.382
670
P ESP024 Esophagitis 60 0.382
671
SQM002 Squamous Cell Papilloma 45 0.382
672
DYS015 Dysentery 49 0.382
673
P CND005 Cone Dystrophy 47 0.378
674
c CNG411 Congenital Disorder of Glycosylation, Type in 66 0.378
675
HPT009 Hepatopulmonary Syndrome 48 0.378
676
c HPT015 Hepatitis D 49 0.378
677
SPS057 Spasticity 43 0.378
678
c DPH024 Diaphragmatic Hernia, Congenital 63 0.375
679
P MGR003 Migraine with Aura 51 0.375
681
c GLL024 Gallbladder Disease 1 53 0.370
682
PLM134 Pulmonary Fibrosis, Idiopathic 76 0.367
683
CRC021 Carcinosarcoma 62 0.367
684
CRB039 Cerebrovascular Disease 65 0.367
685
HMN014 Human Immunodeficiency Virus Infectious Disease 54 0.363
686
RBS001 Rabies 57 0.359
687
ACH005 Achalasia 54 0.359
688
LSS003 Lassa Fever 49 0.359
689
c CHR688 Chronic Acquired Demyelinating Polyneuropathy 16 0.359
690
P MJR007 Major Affective Disorder 1 42 0.357
691
P HYD006 Hydrocephalus 62 0.357
692
SYS003 Systolic Heart Failure 49 0.357
693
ORL011 Oral Cancer 60 0.357
694
OBS002 Obsessive-Compulsive Disorder 67 0.356
695
EPD052 Epidermolysis Bullosa Simplex Superficialis 17 0.356
696
c ATM006 Autoimmune Lymphoproliferative Syndrome 75 0.351
697
ATN005 Autonomic Dysfunction 45 0.351
698
c ATS307 Autosomal Recessive Cerebellar Ataxia 38 0.347
699
P ATS364 Autism 72 0.345
700
c SCH079 Schizophrenia 1 44 0.340
701
NRL016 Neural Tube Defects 80 0.340
702
TRD006 Tardive Dyskinesia 53 0.340
703
P LNG028 Long Qt Syndrome 63 0.340
704
c HMN021 Human T-Cell Leukemia Virus Type 1 46 0.340
705
P PTN014 Patent Ductus Arteriosus 1 59 0.338
706
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 0.338
707
CYT005 Cytomegalovirus Retinitis 50 0.338
708
P MLN069 Melanoma, Uveal 59 0.337
709
P SNS001 Sensorineural Hearing Loss 60 0.337
710
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 0.337
711
P MYT002 Myotonic Dystrophy 51 0.337
712
OTT002 Otitis Media 70 0.334
713
MNT001 Mantle Cell Lymphoma 65 0.334
714
P VNT002 Ventricular Septal Defect 58 0.334
715
CNN005 Connective Tissue Disease 66 0.334
716
P URN019 Urinary Tract Infection 48 0.334
717
CRN017 Coronary Thrombosis 46 0.334
718
MST005 Mastitis 52 0.334
719
BRS051 Breast Disease 58 0.334
720
PTH003 Pathologic Nystagmus 52 0.334
721
SPS019 Spastic Paraparesis 38 0.334
722
P NSP012 Nasopharyngeal Carcinoma 60 0.332
723
P ALP008 Alopecia 53 0.332
724
CHR178 Chromosomal Triplication 33 0.332
725
LGN006 Legionnaire Disease 52 0.330
726
c VRL012 Viral Meningitis 46 0.330
727
c HRD010 Hereditary Spastic Paraplegia 65 0.330
728
TBR011 Tuberculous Meningitis 48 0.330
729
P ATR010 Atrial Heart Septal Defect 58 0.324
730
CLC006 Calcinosis 47 0.318
731
FRN006 Frontotemporal Dementia 68 0.316
732
LPT014 Leptin Deficiency or Dysfunction 77 0.316
733
GNT167 Genetic Obesity 33 0.316
734
P ATR001 Atrioventricular Septal Defect 54 0.315
735
P FML023 Familial Hemiplegic Migraine 53 0.315
736
ART002 Arts Syndrome 66 0.315
737
EPP011 Epiphyseal Chondrodysplasia, Miura Type 36 0.315
738
P SCK002 Sick Sinus Syndrome 55 0.315
739
MTR002 Mitral Valve Insufficiency 51 0.315
740
HMP005 Hemiplegia 53 0.315
741
P CLR019 Color Blindness 47 0.315
742
HRT012 Heart Valve Disease 53 0.315
743
NPH010 Nephrosclerosis 50 0.315
744
TRN012 Transient Global Amnesia 38 0.315
745
P BRN022 Bronchiectasis 59 0.315
746
c NRF024 Neurofibromatosis, Type I 76 0.313
747
c HRD198 Hereditary Dystonia 29 0.311
748
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 44 0.306
749
P MTC010 Mitochondrial Dna Depletion Syndrome 46 0.306
750
P TCD001 Tic Disorder 50 0.306
751
BRN018 Borna Disease 36 0.306
752
P PRM011 Primary Ciliary Dyskinesia 68 0.306
753
BRK012 Broken Heart Syndrome 42 0.306
754
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 0.306
755
NPH003 Nephrocalcinosis 49 0.303
756
ANR040 Aneurysm 60 0.303
757
GRD001 Giardiasis 46 0.296
758
HYP114 Hypertensive Nephropathy 35 0.293
759
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 57 0.293
760
CLN019 Colonic Disease 47 0.293
761
CRV040 Cervix Carcinoma 50 0.293
762
GRM005 Germ Cell Cancer 46 0.293
763
P ANG015 Angioedema 56 0.293
764
CRN030 Coronary Stenosis 50 0.293
765
c MLG069 Malignant Hypertension 46 0.293
766
PRS047 Prostatitis 57 0.293
767
P TST026 Testicular Germ Cell Cancer 42 0.293
768
P CHL066 Cholangitis 51 0.293
769
MNN009 Meningoencephalitis 47 0.290
770
P SLP005 Sleep Disorder 61 0.290
771
P NGH001 Night Blindness 52 0.290
772
c ART115 Aortic Valve Disease 1 72 0.287
773
P LPR021 Leprosy 3 71 0.287
774
MCN017 Meconium Ileus 52 0.287
775
MCS002 Mucositis 55 0.287
776
P DDN001 Duodenal Ulcer 52 0.287
777
ART016 Aortic Aneurysm 68 0.287
778
P PRN023 Prion Disease 60 0.287
779
CHR066 Chronic Fatigue Syndrome 59 0.287
780
HNS001 Hansen's Disease 32 0.287
781
ZLL002 Zollinger-Ellison Syndrome 55 0.287
782
c THR092 Thrombophilia Due to Thrombin Defect 74 0.287
783
HRN029 Hearing Loss, Noise-Induced 37 0.287
784
c ATM099 Autoimmune Uveitis 44 0.287
785
CRT004 Carotid Artery Thrombosis 39 0.287
786
CHL147 Chlamydia Pneumonia 47 0.287
787
GST030 Gastrinoma 45 0.287
788
SKN019 Skin Melanoma 70 0.287
789
CRR012 Cirrhotic Cardiomyopathy 22 0.287
790
MLK004 Malakoplakia 33 0.287
791
P CRB088 Cerebral Atrophy 32 0.287
792
P TMR010 Tumor Predisposition Syndrome 69 0.277
793
P LMB006 Limb-Girdle Muscular Dystrophy 52 0.277
794
P BRC006 Brachydactyly 52 0.270
795
P SML001 Small Cell Carcinoma 52 0.270
796
ENT011 Enterocolitis 55 0.270
797
KPS004 Kaposi Sarcoma 76 0.270
798
BRS099 Breast Ductal Carcinoma 61 0.270
799
HMS001 Hemosiderosis 48 0.270
800
P SPN046 Spinal Muscular Atrophy 62 0.270
801
P CND004 Candidiasis 57 0.270
802
ENT004 Enthesopathy 51 0.270
803
HYP043 Hyperandrogenism 47 0.270
804
VSC002 Vascular Dementia 59 0.270
805
P AMY004 Amyloidosis 69 0.270
806
DRG003 Drug Dependence 46 0.270
807
P RRH023 Rare Hereditary Hemochromatosis 52 0.270
808
c LBR004 Leber Congenital Amaurosis 1 53 0.267
809
P USH001 Usher Syndrome 63 0.267
810
c SPN294 Spinocerebellar Ataxia 1 53 0.267
811
PLM061 Pulmonary Edema of Mountaineers 25 0.265
812
NPH091 Nephrolithiasis, Calcium Oxalate 61 0.265
813
INT392 Intellectual Developmental Disorder with Paroxysmal Dyskinesia or Seizures 14 0.265
814
MSC152 Muscular Dystrophy, Becker Type 69 0.265
815
c SPR086 Spermatogenic Failure 3 47 0.265
816
c FML001 Familial Atrial Fibrillation 65 0.265
817
OBS082 Obstructive Nephropathy 41 0.265
818
P ANP001 Anaplastic Large Cell Lymphoma 59 0.265
819
PRP080 Peripheral Artery Disease 54 0.265
820
PRP030 Purpura 54 0.265
821
BRB002 Barbiturate Dependence 27 0.265
822
P MTR014 Motor Neuron Disease 65 0.265
823
RTR008 Root Resorption 44 0.265
824
IRN001 Iron Deficiency Anemia 58 0.265
825
c ATM022 Autoimmune Myocarditis 35 0.265
826
P MTR003 Mitral Valve Stenosis 53 0.265
827
BLR001 Biliary Atresia 55 0.265
828
BRC012 Brucellosis 66 0.265
829
BLD131 Bladder Urothelial Carcinoma 59 0.265
830
P ART023 Arthropathy 59 0.265
831
P CCK001 Cockayne Syndrome 67 0.265
832
AZS001 Azoospermia 45 0.265
833
VSC003 Visceral Leishmaniasis 54 0.265
834
P PLM034 Pulmonary Emphysema 58 0.265
835
MTB016 Metabolic Myopathy 30 0.265
836
P DYS021 Dysautonomia 38 0.265
837
DYS073 Dysphagia 53 0.265
838
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 70 0.257
839
P SPR120 Supranuclear Palsy, Progressive, 1 68 0.257
840
c CNT035 Central Nervous System Disease 53 0.257
841
LNG039 Lung Squamous Cell Carcinoma 57 0.257
842
ALB002 Albinism 46 0.257
843
P QLT041 Qualitative or Quantitative Defects of Alpha-Dystroglycan 18 0.257
844
c CNG441 Congenital Muscular Dystrophy Due to Dystroglycanopathy 28 0.257
845
INH023 Inherited Cancer-Predisposing Syndrome 53 0.257
846
P BCK002 Beckwith-Wiedemann Syndrome 61 0.251
847
GLL008 Gilles De La Tourette Syndrome 64 0.251
848
c EXD008 Exudative Vitreoretinopathy 1 71 0.251
849
ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 35 0.251
850
P GCH001 Gaucher's Disease 69 0.251
851
PSY004 Psychotic Disorder 66 0.251
852
P HYP035 Hypophosphatasia 61 0.251
853
CRY005 Cryptococcosis 61 0.251
854
PRM020 Premenstrual Tension 39 0.251
855
PRN019 Perinatal Necrotizing Enterocolitis 60 0.251
856
c BCT013 Bacterial Pneumonia 47 0.251
857
c CHR417 Chronic Graft Versus Host Disease 55 0.251
858
MST020 Mast Cell Activation Syndrome 27 0.251
859
c RTN032 Retinal Cone Dystrophy 1 24 0.239
860
VNH007 Von Hippel-Lindau Syndrome 72 0.239
861
P MCR364 Macrodactyly 41 0.239
862
c CND011 Cone Dystrophy 3 41 0.239
863
CHR100 Chronic Ulcer of Skin 57 0.239
864
MND031 Mandibuloacral Dysplasia Progeroid Syndrome 33 0.239
865
P MCP040 Mucopolysaccharidosis-Plus Syndrome 70 0.239
866
URT049 Urate Oxidase, Pseudogene 24 0.239
867
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.239
868
c PLM127 Pulmonary Hypertension, Primary, 3 34 0.239
869
c MST023 Mesothelioma, Malignant 56 0.239
870
GNY003 Guanylate Cyclase 2e, Pseudogene 12 0.239
871
HYP006 Hypertensive Heart Disease 48 0.239
872
MCN007 Meconium Aspiration Syndrome 53 0.239
873
P OVR049 Ovarian Disease 50 0.239
874
IGG001 Iga Glomerulonephritis 50 0.239
875
FLR002 Filariasis 55 0.239
876
BRN026 Branch Retinal Artery Occlusion 41 0.239
877
c HPT007 Hepatitis E 50 0.239
878
SBV001 Subvalvular Aortic Stenosis 31 0.239
879
P RTN014 Retinal Artery Occlusion 46 0.239
880
P NNS072 Nonsyndromic Hearing Loss 42 0.239
881
ESN011 Eisenmenger Syndrome 46 0.239
882
CYN003 Cyanide Poisoning 22 0.239
883
CLR033 Color Vision Deficiency 41 0.239
884
CLP005 Ciliopathy 40 0.239
885
PRM329 Premature Aging 36 0.239
886
CLS016 Clostridium Difficile Colitis 49 0.233
887
WST001 West Syndrome 64 0.233
888
c CNG415 Congenital Disorder of Glycosylation, Type Ia 58 0.233
889
MLD001 Melioidosis 67 0.233
890
EPD015 Epidemic Typhus 44 0.233
891
HMN048 Human Papillomavirus Infectious Disease 45 0.233
892
SLC006 Silicosis 55 0.233
893
MLG079 Malignant Pleural Mesothelioma 42 0.233
895
c CNG006 Congenital Hypothyroidism 63 0.229
896
LWC002 Lowe Oculocerebrorenal Syndrome 68 0.229
897
STR101 Striatal Degeneration, Autosomal Dominant 1 32 0.229
898
P ASP006 Aspergillosis 71 0.229
899
MRF001 Marfan Syndrome 76 0.229
900
c ACR090 Aicardi-Goutieres Syndrome 2 32 0.229
901
c CHR418 Chronic Leukemia 48 0.229
902
RDC002 Radiculopathy 51 0.229
903
OLG001 Oligospermia 45 0.229
904
SHG001 Shigellosis 61 0.229
905
BLR013 Biliary Tract Cancer 43 0.229
906
P HMC002 Homocystinuria 52 0.229
907
ADC009 Adcy5 Dyskinesia 8 0.229
908
CND006 Candida Glabrata 29 0.229
909
KRT006 Keratoconjunctivitis 53 0.229
910
P STR022 Stargardt Disease 61 0.205
911
ACH004 Achondroplasia 65 0.205
912
P CLC063 Celiac Disease 1 65 0.205
913
c CRB175 Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1 70 0.205
914
c CNR007 Cone-Rod Dystrophy 6 53 0.205
915
PHS004 Phosphoribosylpyrophosphate Synthetase Superactivity 48 0.205
916
OST032 Osteofibrous Dysplasia 52 0.205
917
c MCR312 Microphthalmia, Syndromic 10 39 0.205
918
PNS018 Pain Sensitivity Quantitative Trait Locus 1 23 0.205
919
c XNT010 Xanthinuria, Type I 52 0.205
920
P SJG008 Sjogren Syndrome 60 0.205
921
RTN187 Retinitis Pigmentosa-Deafness Syndrome 48 0.205
922
P CNG010 Congenital Stationary Night Blindness 56 0.205
923
c SVR003 Severe Congenital Neutropenia 59 0.205
924
FML035 Familial Hyperlipidemia 54 0.205
925
PTN001 Patent Foramen Ovale 61 0.205
926
MNK002 Monkeypox 41 0.205
927
P BRD002 Bardet-Biedl Syndrome 66 0.205
928
STR103 Streptococcus Pneumonia 47 0.205
929
P HRM001 Hermansky-Pudlak Syndrome 65 0.205
930
VLK001 Volkmann Contracture 23 0.205
931
P END033 Endocarditis 58 0.205
932
ATN004 Autonomic Neuropathy 42 0.205
933
SCB001 Scabies 49 0.205
934
TCL001 T-Cell Adult Acute Lymphocytic Leukemia 42 0.205
935
LRN003 Learning Disability 49 0.205
936
P TRC031 Trichorhinophalangeal Syndrome 37 0.205