Search results for Guanosine diphosphate

943 hits were found for Guanosine diphosphate

# Family MCID Name MIFTS Score
1
PRT037 Pertussis 65 25.346
2
CHL014 Cholera 62 16.593
3
P NRB001 Neuroblastoma 66 11.200
4
IMP005 Impotence 52 11.002
5
P PLM037 Pulmonary Hypertension 72 9.592
6
HLX001 Helix Syndrome 48 9.481
7
ISC004 Ischemia 61 9.080
8
RPD005 Rapidly Involuting Congenital Hemangioma 46 8.869
9
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 8.819
10
P HRP006 Herpes Simplex 65 8.541
11
BNR002 Bone Resorption Disease 47 7.970
12
HMN044 Human Immunodeficiency Virus Type 1 78 7.946
13
BLR008 Bilirubin Metabolic Disorder 57 7.538
14
48X005 48,xyyy 39 7.396
15
P MYC084 Mycobacterium Tuberculosis 1 68 7.372
16
NRR001 Neuroretinitis 42 7.279
17
RTN023 Retinitis 46 7.279
18
GLM045 Glioma 63 6.985
19
P VSC007 Vascular Disease 63 6.979
20
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 60 6.969
21
P OVR042 Ovarian Cancer 88 6.916
22
GLL048 Glial Tumor 52 6.824
23
47X002 47,xyy 48 6.802
24
HYP266 Hypoxia 57 6.604
25
IMM167 Immune Deficiency Disease 78 6.595
26
TRM010 Traumatic Brain Injury 51 6.565
27
P THR014 Thrombocytopenia 66 6.561
28
VCC001 Vaccinia 47 6.469
29
P PHC003 Pheochromocytoma 69 6.466
30
ADR040 Adrenal Gland Pheochromocytoma 46 6.466
31
LPP008 Lipoprotein Quantitative Trait Locus 65 6.407
32
c HPT001 Hepatitis C 62 6.406
33
c HPT073 Hepatitis C Virus 71 6.287
34
PRN001 Purine Nucleoside Phosphorylase Deficiency 53 6.256
35
P MYC007 Myocardial Infarction 70 6.224
36
P HPT021 Hepatitis 69 6.058
37
P LKM002 Leukemia 67 6.055
38
P HPT023 Hepatocellular Carcinoma 96 6.018
39
P CRG003 Crigler-Najjar Syndrome, Type I 63 5.997
40
P RTN008 Retinitis Pigmentosa 80 5.956
41
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 5.944
42
BRN071 Brain Injury 50 5.923
43
GLB001 Gilbert Syndrome 53 5.922
44
TXC005 Toxic Shock Syndrome 62 5.826
45
ANX004 Anoxia 40 5.792
46
GLB002 Glioblastoma 67 5.760
47
ART140 Arteries, Anomalies of 53 5.610
48
CHG001 Chagas Disease 66 5.581
49
c PLM164 Pulmonary Hypertension, Primary, 1 76 5.540
50
P LNG032 Lung Cancer 98 5.539
51
c PRC016 Pre-Eclampsia 65 5.528
52
P BRB001 Beriberi 44 5.515
53
P NTR004 Neutropenia 63 5.428
54
c SML038 Small Cell Cancer of the Lung 69 5.383
55
P SZR006 Seizure Disorder 70 5.337
56
P DRR001 Diarrhea 55 5.302
57
THR024 Thrombosis 56 5.298
58
OST159 Osteogenic Sarcoma 66 5.291
59
c ACT075 Acute Myocardial Infarction 56 5.283
60
INT007 Intermediate Coronary Syndrome 54 5.279
61
STM007 Stomatitis 54 5.247
62
P ENC018 Encephalopathy 62 5.243
63
c TYP009 Type 2 Diabetes Mellitus 92 5.233
64
SVR001 Severe Acute Respiratory Syndrome 67 5.224
65
P MLN008 Melanoma 76 5.112
66
P GLM040 Glioma Susceptibility 1 71 5.086
67
c SYS001 Systemic Lupus Erythematosus 87 5.085
68
DPH001 Diphtheria 59 5.075
69
SPN186 Spinal Cord Injury 61 5.064
70
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 80 5.057
71
CNG034 Congestive Heart Failure 69 5.056
72
c HYP836 Hypercholesterolemia, Familial, 1 73 5.029
73
P DYS154 Dystonia 64 5.023
74
MLG169 Malignant Astrocytoma 57 5.022
75
P MYP004 Myopathy 67 5.000
76
c HYP595 Hypertension, Essential 85 4.990
77
ANG054 Angina Pectoris 66 4.921
78
c MCR115 Microvascular Complications of Diabetes 5 65 4.910
79
P GST053 Gastric Cancer 83 4.895
80
LVR012 Liver Cirrhosis 63 4.852
81
PRS021 Prostatic Adenoma 43 4.850
82
P ADL010 Adult Respiratory Distress Syndrome 71 4.849
83
P LKM071 Leukemia, Chronic Lymphocytic 75 4.841
84
PRS045 Prostatic Hypertrophy 53 4.803
85
P SCK005 Sickle Cell Disease 56 4.779
86
P DBT009 Diabetes Mellitus 67 4.714
87
P HRT032 Heart Disease 81 4.704
88
c MGR028 Migraine with or Without Aura 1 64 4.627
89
CYS001 Cystic Fibrosis 78 4.605
90
HYP060 Hyperinsulinism 54 4.594
91
P PNC035 Pancreatic Cancer 86 4.582
92
TRY001 Trypanosomiasis 50 4.580
93
P RTN016 Retinal Degeneration 52 4.580
94
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 4.567
95
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 4.566
96
P BND020 Bone Disease 59 4.533
97
DFC004 Deficiency Anemia 74 4.525
98
P LPS004 Lupus Erythematosus 61 4.520
99
OVR094 Ovarian Epithelial Cancer 39 4.516
100
P MSC005 Muscular Dystrophy 67 4.511
101
MYL069 Myeloma, Multiple 77 4.496
102
HYP066 Hyperglycemia 61 4.492
103
PRS129 Prostatic Hyperplasia, Benign 49 4.481
104
ACQ007 Acquired Immunodeficiency Syndrome 59 4.454
105
P ADN016 Adenocarcinoma 63 4.446
106
HYP056 Hypoglycemia 65 4.397
107
c CHR688 Chronic Acquired Demyelinating Polyneuropathy 16 4.390
108
PRT036 Peritonitis 65 4.326
109
c MCR130 Microvascular Complications of Diabetes 6 41 4.320
110
c MCR120 Microvascular Complications of Diabetes 7 47 4.320
111
c MCR113 Microvascular Complications of Diabetes 3 52 4.320
112
c MCR133 Microvascular Complications of Diabetes 4 41 4.320
113
c LKM061 Leukemia, Acute Myeloid 83 4.277
114
CLT003 Colitis 63 4.268
115
AGN016 Aging 54 4.267
116
ALL029 Allergic Disease 59 4.259
117
PRP027 Peripheral Vascular Disease 71 4.256
118
FTT001 Fatty Liver Disease 62 4.242
119
NNL005 Non-Alcoholic Fatty Liver Disease 63 4.242
120
c HPT016 Hepatitis B 62 4.235
121
P BCL017 B-Cell Lymphoma 59 4.230
122
MLR004 Malaria 80 4.219
123
STR067 Stroke, Ischemic 80 4.211
124
SLP001 Sleeping Sickness 56 4.208
125
ALC007 Alcohol Dependence 66 4.177
126
P MYL006 Myeloid Leukemia 61 4.161
127
CYT002 Cytokine Deficiency 43 4.150
128
ADN018 Adenoma 59 4.140
129
P CRN300 Coronary Heart Disease 1 73 4.139
130
P LKM062 Leukemia, Acute Lymphoblastic 69 4.106
131
CRB004 Cerebral Artery Occlusion 45 4.069
132
P BRS047 Breast Cancer 98 4.057
133
CRH001 Crohn's Disease 80 4.042
134
END086 End Stage Renal Disease 52 3.984
135
P HML002 Hemolytic Anemia 62 3.983
136
c MJR022 Major Affective Disorder 8 38 3.964
137
c MJR024 Major Affective Disorder 9 41 3.964
138
P BPL003 Bipolar Disorder 56 3.964
139
CHC001 Chickenpox 57 3.961
140
P CLR023 Colorectal Cancer 100 3.953
141
MDD018 Middle East Respiratory Syndrome 44 3.897
142
P PRS040 Prostate Cancer 95 3.891
143
P TRM003 Tremor 48 3.889
144
P ALZ034 Alzheimer Disease 87 3.865
145
BCT022 Bacterial Infectious Disease 56 3.853
146
PRT251 Proteinuria, Chronic Benign 57 3.807
147
c PCH010 Pachyonychia Congenita 3 43 3.798
148
P LNG064 Lung Cancer Susceptibility 3 70 3.796
149
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 3.783
150
P LVR013 Liver Disease 69 3.773
151
P INF037 Inflammatory Bowel Disease 53 3.749
152
c CHR684 Chronic Kidney Disease 69 3.735
153
c ACT073 Acute Leukemia 58 3.730
154
c ATM011 Autoimmune Hepatitis 63 3.728
155
P PRK039 Parkinsonism 55 3.724
156
P GLM007 Glomerulonephritis 60 3.724
157
OCL069 Ocular Motor Apraxia 57 3.724
158
BRN004 Brain Edema 54 3.722
159
c BRN108 Branchiootic Syndrome 1 62 3.714
160
HRW001 Hair Whorl 35 3.713
161
P EPL164 Epilepsy 68 3.697
162
GT001 Gout 64 3.697
163
P NPH012 Nephrotic Syndrome 60 3.695
164
P KLZ004 Kala-Azar 1 41 3.616
165
LSH001 Leishmaniasis 64 3.616
166
PLM129 Pulmonary Disease, Chronic Obstructive 74 3.613
167
PLM010 Pulmonary Edema 55 3.571
168
ATH013 Atherosclerosis Susceptibility 63 3.557
169
P ATR011 Atrial Fibrillation 66 3.538
170
HMN014 Human Immunodeficiency Virus Infectious Disease 54 3.530
171
P CRD119 Cardiac Arrest 67 3.499
172
INS001 Insulinoma 59 3.498
173
PLY150 Polykaryocytosis Inducer 29 3.494
174
P EXN002 Exanthem 58 3.477
175
P HDC001 Headache 57 3.475
176
c DLT002 Dilated Cardiomyopathy 78 3.471
177
c VRL010 Viral Hepatitis 53 3.461
178
ACT098 Acute Erythroid Leukemia 55 3.419
179
P KDN018 Kidney Disease 72 3.408
180
LPD008 Lipid Metabolism Disorder 62 3.401
181
SVR004 Severe Combined Immunodeficiency 72 3.363
182
URM002 Uremia 47 3.349
183
SQM006 Squamous Cell Carcinoma 60 3.341
184
CHL068 Cholestasis 61 3.341
185
CRB039 Cerebrovascular Disease 66 3.337
186
DWN001 Down Syndrome 70 3.328
187
P ART021 Arteriosclerosis 54 3.325
188
CLN015 Colon Adenocarcinoma 65 3.301
189
P RHN004 Rhinitis 57 3.286
190
c AMY091 Amyotrophic Lateral Sclerosis 1 88 3.282
191
P LTR001 Lateral Sclerosis 58 3.282
192
LNG099 Lung Disease 62 3.279
193
MNT002 Mental Depression 57 3.276
194
P RTN018 Retinal Disease 53 3.259
195
ULC004 Ulcerative Colitis 74 3.245
196
CHL004 Cholelithiasis 49 3.209
197
TRN015 Transient Cerebral Ischemia 63 3.198
198
PNC041 Pancreatic Ductal Adenocarcinoma 51 3.197
199
DSS032 Disease by Infectious Agent 55 3.190
200
CRN017 Coronary Thrombosis 46 3.188
201
THY029 Thyroid Carcinoma 51 3.185
202
c HYP807 Hyperinsulinemic Hypoglycemia, Familial, 6 52 3.182
203
DWR001 Dwarfism 44 3.180
204
P HYP076 Hyperthyroidism 53 3.172
205
P LCT001 Lactic Acidosis 51 3.171
206
HMP009 Haemophilus Influenzae 41 3.167
207
MND023 Mend Syndrome 49 3.164
208
P MJR001 Major Depressive Disorder 68 3.162
209
HGH043 High Grade Glioma 45 3.161
210
CNS004 Constipation 56 3.159
211
P RTN024 Retinoblastoma 73 3.157
212
ORL015 Oral Squamous Cell Carcinoma 43 3.156
213
P HYP086 Hypothyroidism 69 3.147
214
c HPT003 Hepatitis a 63 3.147
215
P HYP265 Hypotonia 42 3.126
216
HYP014 Hyperuricemia 51 3.124
217
END057 Endometrial Cancer 72 3.116
218
IRN002 Iron Metabolism Disease 57 3.113
219
PRT013 Portal Hypertension 59 3.108
220
P RSP003 Respiratory Failure 74 3.104
221
P OST002 Osteoporosis 76 3.097
222
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 3.088
223
MDD011 Mood Disorder 62 3.084
224
IRR002 Irritable Bowel Syndrome 65 3.081
225
HPT004 Hepatic Coma 43 3.070
226
DPR016 Depression 65 3.069
227
CHD001 Chediak-Higashi Syndrome 67 3.052
228
P CHR345 Chronic Pain 50 3.027
229
P MYC008 Myocarditis 59 3.020
230
P ATX030 Ataxia-Telangiectasia 80 3.011
231
TLN003 Telangiectasis 51 3.011
232
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 3.008
233
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 3.008
234
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 3.008
235
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 3.008
236
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 3.008
237
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 3.008
238
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 3.008
239
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 3.008
240
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 3.008
241
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 3.003
242
PNG002 Pain Agnosia 51 3.002
243
HPT019 Hepatic Encephalopathy 59 2.961
244
CNG486 Congenital Disorders of N-Linked Glycosylation and Multiple Pathway 29 2.959
245
c ACT071 Acute Kidney Failure 60 2.957
246
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 2.947
247
c LKM005 Leukemia, T-Cell, Chronic 34 2.947
248
P NRF002 Neurofibromatosis 57 2.943
249
INS024 Insulin-Like Growth Factor I 78 2.934
250
HDN002 Head Injury 44 2.928
251
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 2.925
252
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 2.925
253
TTN003 Tetanus 65 2.924
254
P PSR002 Psoriasis 63 2.913
255
PST011 Pustulosis of Palm and Sole 52 2.913
256
c OPT053 Optic Atrophy 1 62 2.886
257
P NRP001 Neuropathy 60 2.879
258
c DNT047 Dentinogenesis Imperfecta Type 2 35 2.870
259
EXT007 Extracutaneous Mastocytoma 38 2.866
260
MST004 Mast Cell Neoplasm 42 2.866
261
PST092 Posttransplant Acute Limbic Encephalitis 28 2.859
262
SPL018 Splenomegaly 49 2.846
263
ALL003 Allergic Rhinitis 67 2.845
264
P CRD246 Cardiovascular System Disease 56 2.827
265
CRT015 Carotid Artery Occlusion 45 2.812
266
RNL114 Renal Cell Carcinoma, Nonpapillary 80 2.791
267
P OBS001 Obstructive Jaundice 48 2.788
268
P INF038 Influenza 68 2.784
269
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 2.784
270
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 2.760
271
P SKN015 Skin Carcinoma 71 2.738
272
LWC001 Low Compliance Bladder 45 2.719
273
ATS010 Autosomal Recessive Disease 42 2.709
274
P ECL001 Eclampsia 52 2.693
275
P PRD008 Periodontitis 64 2.691
276
MTB004 Metabolic Acidosis 48 2.672
277
c SCL052 Scleroderma, Familial Progressive 61 2.667
278
LYM019 Lymphosarcoma 46 2.649
279
RYN005 Raynaud Phenomenon 45 2.623
280
P CTN015 Cutaneous T Cell Lymphoma 48 2.616
281
P LYM118 Lymphoma 67 2.610
282
P FBR031 Febrile Seizures 52 2.600
283
FCS014 Fucosidase Regulator 15 2.598
284
P PRP019 Peripheral Nervous System Disease 58 2.598
285
c ATR087 Atrial Standstill 1 74 2.596
286
P ALC033 Alcohol Use Disorder 61 2.592
287
P HYP098 Hypereosinophilic Syndrome 66 2.585
288
ACT119 Acute Promyelocytic Leukemia 62 2.584
289
P HNT016 Huntington Disease 73 2.584
290
PRP016 Paraplegia 52 2.566
291
CYT005 Cytomegalovirus Retinitis 50 2.557
292
P SLP006 Sleep Apnea 69 2.555
293
ARG004 Argyria 26 2.555
294
PRP030 Purpura 54 2.544
295
P BRS044 Breast Adenocarcinoma 58 2.535
296
P RHM011 Rheumatoid Arthritis 82 2.531
297
PHN003 Phenylketonuria 76 2.522
298
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 45 2.518
299
PYR041 Pyruvate Kinase Deficiency of Red Cells 57 2.507
300
LYM027 Lymphopenia 56 2.490
301
BRN024 Bronchitis 67 2.487
302
KRN002 Kearns-Sayre Syndrome 63 2.484
303
P LMB006 Limb-Girdle Muscular Dystrophy 52 2.479
304
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 2.453
305
P MSC003 Muscular Atrophy 52 2.452
306
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 2.450
307
SCH014 Schistosomiasis 56 2.450
308
c HPT015 Hepatitis D 49 2.432
309
CRV035 Cervical Cancer 73 2.418
310
RTN020 Retinal Vascular Disease 46 2.417
311
BRN028 Brain Cancer 74 2.397
312
P MTC133 Mitochondrial Myopathy 50 2.395
313
P BNG032 Benign Mesothelioma 53 2.372
314
P PLM036 Pulmonary Fibrosis 66 2.362
315
P INF032 Infertility 57 2.362
316
c THY107 Thymoma, Familial 42 2.360
317
P THY023 Thymoma 64 2.360
318
SCK003 Sickle Cell Anemia 74 2.359
319
CMB007 Combined Immunodeficiency 57 2.351
320
URT010 Ureteral Obstruction 45 2.347
321
P TMP001 Temporal Lobe Epilepsy 49 2.346
322
INT323 Intraocular Pressure Quantitative Trait Locus 64 2.339
323
PPL052 Papillomatosis, Confluent and Reticulated 34 2.337
324
P PRK057 Parkinson Disease, Late-Onset 80 2.319
325
DMY004 Demyelinating Disease 50 2.316
326
LYM017 Lyme Disease 62 2.313
327
HPT022 Hepatoblastoma 54 2.302
328
c THR092 Thrombophilia Due to Thrombin Defect 74 2.299
329
HYP080 Hypogonadism 50 2.281
330
PRM236 Primary Biliary Cholangitis 60 2.279
331
P FML011 Familial Adenomatous Polyposis 71 2.273
332
DBT010 Diabetic Neuropathy 54 2.259
333
THR004 Thrombocytosis 53 2.257
334
PNC129 Pancreatic Adenocarcinoma 65 2.254
335
RNL077 Renal Fibrosis 46 2.253
336
MSL001 Measles 61 2.249
337
GST033 Gestational Diabetes 61 2.245
338
c TYP008 Type 1 Diabetes Mellitus 70 2.241
339
YLL002 Yellow Fever 61 2.241
340
P PTS002 Ptosis 52 2.237
341
ATM095 Autoimmune Disease 61 2.229
342
P OPT006 Optic Nerve Disease 58 2.228
343
c GRV008 Graves Disease 1 54 2.217
344
c GLL024 Gallbladder Disease 1 52 2.205
345
P SYS005 Systemic Scleroderma 74 2.204
346
P INS002 in Situ Carcinoma 53 2.198
347
P SPP010 Suppressor of Tumorigenicity 3 51 2.180
348
P ART022 Arthritis 71 2.176
349
PTT037 Pituitary Tumors 44 2.172
350
HMN047 Human Cytomegalovirus Infection 57 2.167
351
DYS015 Dysentery 50 2.165
352
PRP080 Peripheral Artery Disease 54 2.158
353
MYL009 Myelodysplastic Syndrome 67 2.154
354
P MNN013 Meningitis 65 2.151
355
P DNG005 Dengue Virus 56 2.140
356
P NNN008 Noonan Syndrome 1 77 2.134
357
GLC009 Glucosephosphate Dehydrogenase Deficiency 53 2.131
358
TRC003 Trichomoniasis 53 2.121
359
GLC003 Glucose Intolerance 54 2.118
360
NNL006 Non-Alcoholic Steatohepatitis 54 2.113
361
c TBR025 Tuberous Sclerosis 1 84 2.110
362
SPN035 Spindle Cell Sarcoma 54 2.109
363
SRC014 Sarcoma 65 2.109
364
P BLD134 Bladder Cancer 79 2.105
365
CHK001 Chikungunya 60 2.105
366
P OLG002 Oligodendroglioma 66 2.105
367
KRT002 Keratomalacia 55 2.100
368
c BCT007 Bacterial Meningitis 55 2.097
369
c PSD047 Pseudo-Turner Syndrome 52 2.087
370
ORL011 Oral Cancer 60 2.081
371
c LKM063 Leukemia, Chronic Myeloid 71 2.075
372
P KRN004 Kernicterus 46 2.073
373
XRD010 Xeroderma Pigmentosum, Variant Type 73 2.050
374
ALL006 Allergic Asthma 56 2.045
375
BRN056 Bronchopulmonary Dysplasia 56 2.043
376
ADR016 Adrenal Cortical Carcinoma 62 2.043
377
ADR054 Adrenocortical Carcinoma, Hereditary 47 2.043
378
ADR004 Adrenal Cortical Adenocarcinoma 38 2.043
379
GST045 Gastroenteritis 58 2.023
381
HRP004 Herpes Zoster 61 2.017
382
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 2.014
383
LMB062 Limb Ischemia 55 2.012
384
CHL123 Chlamydia 58 2.011
385
HND015 Hand Skill, Relative 30 2.009
386
INT002 Intermittent Claudication 61 2.006
387
P FBR017 Fibrosarcoma 56 1.998
388
PTH003 Pathologic Nystagmus 52 1.987
389
c ACT027 Acute Pancreatitis 60 1.986
390
P PNC044 Pancreatitis 61 1.986
391
c DRR009 Diarrhea 6 45 1.984
392
c CNG411 Congenital Disorder of Glycosylation, Type in 67 1.981
393
c INH030 Inherited Retinal Disorder 28 1.980
394
P OPN001 Open-Angle Glaucoma 55 1.959
395
P ESP024 Esophagitis 60 1.957
396
P MLT020 Multiple Sclerosis 79 1.954
397
CRY035 Cryptorchidism, Unilateral or Bilateral 58 1.948
398
P CTR002 Cataract 60 1.947
399
CRD132 Cardiac Conduction Defect 60 1.938
400
SPS057 Spasticity 42 1.924
401
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 50 1.923
402
PLS011 Plasmacytoma 56 1.917
403
TCL027 T-Cell Acute Lymphoblastic Leukemia 51 1.917
404
PPT005 Peptic Ulcer Disease 58 1.894
405
P SCH015 Schizophrenia 74 1.893
406
P UVT001 Uveitis 57 1.890
407
WTH001 Withdrawal Disorder 48 1.881
408
P ADL017 Adult T-Cell Leukemia 56 1.878
409
P SCL018 Scoliosis 57 1.878
410
HRT011 Heart Septal Defect 49 1.859
411
P TBR001 Tuberous Sclerosis 69 1.856
412
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 1.852
413
TST044 Testicular Torsion 45 1.848
414
P URN019 Urinary Tract Infection 49 1.846
415
CRC021 Carcinosarcoma 64 1.846
416
P VNT002 Ventricular Septal Defect 58 1.846
417
P EYD002 Eye Disease 57 1.846
418
MND031 Mandibuloacral Dysplasia Progeroid Syndrome 33 1.845
419
HMC014 Homocysteinemia 52 1.840
420
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 1.833
421
TRN018 Transitional Cell Carcinoma 56 1.824
422
SKN016 Skin Disease 63 1.821
423
PLM033 Pulmonary Embolism 58 1.821
424
ENT004 Enthesopathy 51 1.816
425
CHL065 Cholangiocarcinoma 58 1.811
426
INT079 Intrahepatic Cholangiocarcinoma 51 1.811
427
LWG006 Low Grade Glioma 41 1.805
428
P CRD224 Cardiofaciocutaneous Syndrome 1 71 1.802
429
P CYS018 Cystitis 59 1.802
430
KRT009 Keratosis 53 1.800
431
MLD018 Mild Cognitive Impairment 48 1.798
432
CCC002 Coccidiosis 50 1.798
433
MYL005 Myelofibrosis 71 1.788
434
RBS001 Rabies 58 1.785
435
P GST044 Gastritis 55 1.775
436
P HYP750 Hypertriglyceridemia, Familial 62 1.774
437
SCR003 Secretory Diarrhea 35 1.773
438
P SLM003 Salmonellosis 54 1.771
439
FRN006 Frontotemporal Dementia 68 1.766
440
c ATS007 Autism Spectrum Disorder 72 1.766
441
KRT019 Keratitis, Hereditary 66 1.766
442
c THY109 Thyroid Cancer, Nonmedullary, 1 55 1.764
443
CST001 Costello Syndrome 68 1.764
444
P MTC069 Mitochondrial Disorders 57 1.753
445
P AST005 Asthma 76 1.745
446
P MCR010 Microcephaly 60 1.745
447
CRC006 Carcinoid Syndrome 55 1.744
448
CRT004 Carotid Artery Thrombosis 39 1.741
449
P VSC011 Vasculitis 61 1.741
450
P SBS003 Substance Abuse 54 1.732
451
LKC009 Leukocyte Adhesion Deficiency, Type I 70 1.706
452
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 1.702
453
BRK010 Burkitt Lymphoma 66 1.700
454
P OVR082 Overgrowth Syndrome 49 1.699
455
ALC009 Alcoholic Liver Cirrhosis 54 1.694
456
P TTR001 Tetralogy of Fallot 69 1.688
457
ESP021 Esophageal Cancer 83 1.688
458
c HYP326 Hyperinsulinemic Hypoglycemia, Familial, 5 51 1.688
459
c HYP271 Hyperinsulinemic Hypoglycemia, Familial, 4 53 1.688
460
P ACT008 Actinic Keratosis 54 1.688
461
P DMN002 Dementia 66 1.685
462
GRY002 Gray Platelet Syndrome 58 1.684
463
CRB090 Cerebral Hypoxia 42 1.684
464
P PTN014 Patent Ductus Arteriosus 1 59 1.679
465
P MLN069 Melanoma, Uveal 61 1.676
466
PLM134 Pulmonary Fibrosis, Idiopathic 76 1.672
467
c RTN047 Retinitis Pigmentosa 18 46 1.672
468
RTN017 Retinal Detachment 60 1.672
469
P RHB003 Rhabdomyosarcoma 66 1.672
470
P RNV001 Renovascular Hypertension 49 1.672
471
ALG025 Alg1-Congenital Disorder of Glycosylation 17 1.659
472
c CNG192 Congenital Disorder of Glycosylation, Type Ik 34 1.659
473
HYP264 Hypertonia 36 1.659
474
FBR047 Fibromyalgia 58 1.657
475
GST040 Gastric Adenocarcinoma 67 1.657
476
LNG039 Lung Squamous Cell Carcinoma 57 1.657
477
ILS001 Ileus 50 1.657
478
NWC001 Newcastle Disease 47 1.657
479
P CHR071 Charcot-Marie-Tooth Disease 64 1.653
480
TTH006 Tooth Disease 51 1.653
481
DYS073 Dysphagia 53 1.653
482
MTH009 Mouth Disease 57 1.653
483
ART002 Arts Syndrome 66 1.644
484
ANT024 Anthrax Disease 58 1.644
485
P ENC004 Encephalitis 61 1.631
486
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 1.628
488
P KDN017 Kidney Cancer 61 1.620
489
NRM005 Neuromuscular Disease 63 1.620
490
GST023 Gastric Ulcer 52 1.620
491
P QLT041 Qualitative or Quantitative Defects of Alpha-Dystroglycan 18 1.616
492
P HYP069 Hyperparathyroidism 62 1.616
493
c CNG441 Congenital Muscular Dystrophy Due to Dystroglycanopathy 28 1.616
494
RCK004 Rickets 68 1.598
495
BRS099 Breast Ductal Carcinoma 61 1.598
496
P RCT021 Rectum Cancer 54 1.598
497
IGR001 Ige Responsiveness, Atopic 59 1.594
498
STT041 Stuttering 52 1.594
499
c CHR095 Chronic Progressive External Ophthalmoplegia 49 1.594
500
P MJR007 Major Affective Disorder 1 42 1.593
501
P NRV007 Nervous System Disease 67 1.593
502
P CHR012 Chronic Granulomatous Disease 69 1.592
503
ALL014 Allergic Encephalomyelitis 34 1.592
504
c GLC092 Glaucoma, Primary Open Angle 62 1.589
505
OST012 Osteoarthritis 77 1.589
506
P AMY004 Amyloidosis 70 1.588
507
P HMR003 Hemorrhagic Disease 59 1.588
508
P PGT001 Paget's Disease of Bone 61 1.588
509
VSC002 Vascular Dementia 60 1.588
510
P HRM001 Hermansky-Pudlak Syndrome 65 1.588
511
PNC013 Pancreatic Ductal Carcinoma 48 1.562
512
P MLN007 Male Infertility 56 1.558
513
LPT014 Leptin Deficiency or Dysfunction 78 1.548
514
ALB002 Albinism 47 1.548
515
GRW007 Growth Hormone Deficiency 46 1.545
516
P MYP006 Myopia 56 1.545
517
c PLM163 Palmoplantar Keratoderma, Punctate Type Ii 29 1.539
518
PNC060 Punctate Porokeratosis 28 1.539
519
P ALP008 Alopecia 54 1.524
520
PLM101 Pulmonary Hypertension, Chronic Thromboembolic, Without Deep Vein Thrombosis 37 1.511
521
CHR466 Chronic Thromboembolic Pulmonary Hypertension 48 1.511
522
P MYS005 Myositis 56 1.507
523
P DRM010 Dermatomyositis 61 1.507
524
PLR008 Pleurisy 50 1.507
525
STT001 Status Epilepticus 59 1.507
526
WLK001 Walker-Warburg Syndrome 62 1.498
527
P ATT013 Attention Deficit-Hyperactivity Disorder 64 1.483
528
SDD001 Sudden Infant Death Syndrome 60 1.482
529
P MYC033 Myoclonus 47 1.482
530
P ANP001 Anaplastic Large Cell Lymphoma 61 1.479
531
ACT003 Acute Kidney Tubular Necrosis 46 1.476
532
P GRF003 Graft-Versus-Host Disease 71 1.476
533
P MYT002 Myotonic Dystrophy 51 1.476
534
ADN001 Adenosine Deaminase Deficiency 59 1.475
535
MNN009 Meningoencephalitis 48 1.475
536
P PLY019 Polyneuropathy 52 1.473
537
EPD052 Epidermolysis Bullosa Simplex Superficialis 17 1.459
538
LGN006 Legionnaire Disease 52 1.459
539
DGN001 Degenerative Disc Disease 49 1.451
540
P GRV001 Graves' Disease 55 1.451
541
P MTR012 Mitral Valve Disease 57 1.451
542
CLP005 Ciliopathy 41 1.451
543
c MST023 Mesothelioma, Malignant 56 1.451
544
CTN007 Cutaneous Leishmaniasis 62 1.451
545
P FCL005 Focal Segmental Glomerulosclerosis 57 1.451
546
P MTR003 Mitral Valve Stenosis 53 1.451
547
PST053 Postherpetic Neuralgia 40 1.451
548
P HRD011 Hereditary Spherocytosis 64 1.443
549
P CNR004 Cone-Rod Dystrophy 2 74 1.418
550
c ATS307 Autosomal Recessive Cerebellar Ataxia 39 1.418
551
FND002 Fundus Dystrophy 55 1.418
552
P ATS364 Autism 69 1.415
553
P ASP006 Aspergillosis 72 1.415
554
THM002 Thiamine-Responsive Megaloblastic Anemia Syndrome 50 1.415
555
OST017 Osteomyelitis 63 1.415
556
DNT012 Dental Caries 53 1.415
557
P CRN026 Corneal Edema 42 1.415
558
P HML001 Hemolytic-Uremic Syndrome 52 1.410
559
P DBT005 Diabetes Insipidus 54 1.400
560
GLM044 Glomerular Disease 35 1.400
561
P INT143 Interstitial Cystitis 60 1.400
562
GNT167 Genetic Obesity 30 1.393
563
P SPR120 Supranuclear Palsy, Progressive, 1 69 1.393
564
P MLG056 Malignant Hyperthermia 66 1.393
565
P LNG028 Long Qt Syndrome 64 1.387
566
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 60 1.387
567
MSC157 Muscular Dystrophy, Duchenne Type 79 1.384
568
ANX010 Anxiety 70 1.384
569
P SNS001 Sensorineural Hearing Loss 59 1.384
570
MYC005 Myocardial Stunning 46 1.384
571
MLD001 Melioidosis 67 1.381
572
OCL006 Ocular Hypertension 53 1.381
573
MYL031 Myeloproliferative Neoplasm 66 1.381
574
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 57 1.356
575
c HRD010 Hereditary Spastic Paraplegia 66 1.349
576
GRD001 Giardiasis 46 1.349
577
CWP001 Cowpox 45 1.342
578
BLR001 Biliary Atresia 55 1.342
579
FLR002 Filariasis 55 1.342
580
P WSK001 Wiskott-Aldrich Syndrome 72 1.340
581
CRB037 Cerebral Palsy 67 1.339
582
c ATS025 Autosomal Dominant Progressive External Ophthalmoplegia 45 1.337
583
MNG007 Manganese Poisoning 28 1.337
584
IDP070 Idiopathic Scoliosis 42 1.337
585
P LYM033 Lymphoproliferative Syndrome 59 1.334
586
P RRH023 Rare Hereditary Hemochromatosis 54 1.327
587
HMS001 Hemosiderosis 48 1.327
588
WLL004 Wallerian Degeneration 38 1.314
589
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 1.308
590
P INT068 Intestinal Disease 53 1.308
591
c CNG006 Congenital Hypothyroidism 63 1.305
592
c HNT011 Huntington Disease-Like 3 34 1.305
593
P MCR129 Microvascular Complications of Diabetes 1 68 1.305
594
GYN001 Gynecomastia 47 1.305
595
c MCR112 Microvascular Complications of Diabetes 2 42 1.305
596
CRY003 Cryptosporidiosis 56 1.305
597
INF021 Infant Gynecomastia 30 1.305
598
TYP007 Typhoid Fever 64 1.305
599
PRN035 Perniosis 27 1.305
600
P DRM053 Dermatitis, Atopic 65 1.301
601
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 1.301
602
P MGR003 Migraine with Aura 52 1.301
603
DNG002 Dengue Hemorrhagic Fever 60 1.301
604
DRM006 Dermatitis 62 1.301
605
PPL002 Papillary Carcinoma 46 1.300
606
c ACT134 Acute Liver Failure 59 1.299
607
CRN030 Coronary Stenosis 50 1.299
608
CRN019 Coronary Artery Vasospasm 47 1.299
609
c INH020 Inherited Metabolic Disorder 48 1.299
610
c ACR088 Aicardi-Goutieres Syndrome 3 39 1.275
611
P PTT006 Pituitary Adenoma 55 1.275
612
P MGR001 Migraine Without Aura 49 1.275
613
c HMC039 Hemochromatosis, Type 1 73 1.274
614
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 55 1.274
615
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 60 1.274
616
AVN001 Avian Influenza 61 1.274
617
ACH005 Achalasia 55 1.274
618
AMN003 Amnestic Disorder 54 1.274
619
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 1.274
620
P ACT105 Acute Mountain Sickness 52 1.274
621
IRN001 Iron Deficiency Anemia 58 1.269
622
P MTC010 Mitochondrial Dna Depletion Syndrome 47 1.269
623
ART016 Aortic Aneurysm 68 1.264
624
ANR040 Aneurysm 61 1.264
625
ASP004 Asphyxia Neonatorum 50 1.250
626
CCN002 Cocaine Abuse 49 1.244
627
MNT001 Mantle Cell Lymphoma 67 1.207
628
WST001 West Syndrome 59 1.207
629
HLC007 Helicobacter Pylori Infection 67 1.207
630
c SPN294 Spinocerebellar Ataxia 1 53 1.207
631
c PRM005 Primary Hyperparathyroidism 59 1.207
632
BRS051 Breast Disease 58 1.207
633
PLR005 Pleuropneumonia 33 1.207
634
TBR011 Tuberculous Meningitis 48 1.206
635
c SCN036 Secondary Progressive Multiple Sclerosis 55 1.194
636
P SYP003 Syphilis 59 1.194
637
THR100 Thrombocytopenic Purpura, Autoimmune 61 1.187
638
P HYP061 Hypertrophic Cardiomyopathy 69 1.187
639
P PLY011 Polycystic Ovary Syndrome 57 1.187
640
P OVR049 Ovarian Disease 52 1.187
641
BCT021 Bacterial Sepsis 43 1.162
642
VLL006 Villous Adenoma 41 1.162
643
CRV002 Cervix Uteri Carcinoma in Situ 47 1.162
644
P CND004 Candidiasis 58 1.162
645
P CLL015 Collagen Disease 48 1.162
646
MST020 Mast Cell Activation Syndrome 28 1.162
647
CRV045 Cervical Intraepithelial Neoplasia 39 1.162
648
LSS003 Lassa Fever 49 1.131
649
SMT008 Smith-Magenis Syndrome 54 1.131
650
P CND005 Cone Dystrophy 47 1.131
651
P CRC039 Coarctation of Aorta 46 1.131
652
P MDL005 Medulloblastoma 75 1.131
653
LBR036 Leber Plus Disease 66 1.131
654
OST003 Osteonecrosis 61 1.123
655
P DDN001 Duodenal Ulcer 53 1.123
656
c EXD008 Exudative Vitreoretinopathy 1 71 1.098
657
LWC002 Lowe Oculocerebrorenal Syndrome 68 1.098
658
EPT021 Epithelial Recurrent Erosion Dystrophy 46 1.098
659
GST071 Gastrointestinal Carcinoma 46 1.098
660
DNG003 Dengue Disease 65 1.098
661
PRD004 Prediabetes Syndrome 52 1.098
662
NRT001 Neurotic Disorder 56 1.098
663
OTT002 Otitis Media 71 1.097
664
CLS016 Clostridium Difficile Colitis 49 1.097
665
MLG079 Malignant Pleural Mesothelioma 42 1.097
666
P ANG015 Angioedema 56 1.097
667
MST005 Mastitis 53 1.097
668
HMP005 Hemiplegia 54 1.097
669
MTR002 Mitral Valve Insufficiency 52 1.097
670
NCL008 Nuclear Ribonucleic Acid 15 1.095
671
PHS004 Phosphoribosylpyrophosphate Synthetase Superactivity 49 1.095
672
SQM013 Squamous Cell Carcinoma, Head and Neck 73 1.095
673
P END044 Endometriosis 62 1.095
674
MTC005 Mitochondrial Metabolism Disease 45 1.095
675
SKN019 Skin Melanoma 71 1.065
676
P VTR007 Vitreoretinopathy 46 1.048
677
LNN001 Lennox-Gastaut Syndrome 61 1.048
678
c WLM013 Wilms Tumor 1 66 1.048
679
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 1.048
680
P HYD006 Hydrocephalus 61 1.048
681
EMB004 Embryonal Carcinoma 56 1.048
682
c CNT035 Central Nervous System Disease 54 1.048
684
CNG506 Congenital Amyoplasia 27 1.042
685
c ANM038 Anemia, Autoimmune Hemolytic 64 1.042
686
KPS004 Kaposi Sarcoma 77 1.042
687
DCT002 Ductal Carcinoma in Situ 58 1.042
688
HMG002 Hemoglobinuria 50 1.042
689
P ACN011 Acne 57 1.042
690
FLR001 Filarial Elephantiasis 59 1.042
691
P HMN010 Hemangioma 62 1.042
692
P PRP029 Porphyria 60 1.042
693
LCH001 Leech Infestation 38 1.042
694
GRN017 Granulocytopenia 42 1.042
695
VRL011 Viral Infectious Disease 61 1.011
696
c BPL002 Bipolar I Disorder 47 1.011
697
MTB016 Metabolic Myopathy 30 0.985
698
CLF027 Cleft Palate, Isolated 64 0.985
699
P CLC063 Celiac Disease 1 66 0.985
700
PRP036 Peripheral T-Cell Lymphoma 53 0.985
701
c CHR711 Chronic Asthma 41 0.985
702
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 44 0.985
703
MVL001 Mevalonic Aciduria 66 0.985
704
VRC005 Varicose Veins 60 0.985
705
PLT016 Platelet Adenylate Cyclase Activity 16 0.985
706
c MSC098 Muscular Dystrophy-Dystroglycanopathy , Type C, 14 39 0.985
707
VLK001 Volkmann Contracture 23 0.985
708
VSC003 Visceral Leishmaniasis 55 0.985
709
P PLM034 Pulmonary Emphysema 58 0.985
710
BLD131 Bladder Urothelial Carcinoma 60 0.985
711
STR103 Streptococcus Pneumonia 47 0.985
712
BRN012 Bronchiolitis Obliterans 56 0.985
713
P END033 Endocarditis 58 0.985
714
GNG013 Gingivitis 59 0.985
715
BRN002 Bronchiolitis 57 0.985
716
HYP835 Hypothalamic Obesity 38 0.985
717
SPR010 Sporotrichosis 46 0.985
718
PLM001 Pulmonary Tuberculosis 69 0.968
719
SPS019 Spastic Paraparesis 38 0.954
720
WBR001 Weber Syndrome 38 0.954
721
SCH078 Schimmelpenning-Feuerstein-Mims Syndrome 61 0.954
722
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.954
723
EPD015 Epidemic Typhus 44 0.954
724
P FML023 Familial Hemiplegic Migraine 53 0.954
725
P PLY006 Polydactyly 59 0.954
726
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.954
727
HYP114 Hypertensive Nephropathy 36 0.954
728
P JBR020 Joubert Syndrome 1 74 0.954
729
NVS017 Nevus, Epidermal 66 0.954
730
P CHL066 Cholangitis 52 0.954
731
SYN036 Syncope 45 0.954
732
HRT012 Heart Valve Disease 53 0.954
733
CNN005 Connective Tissue Disease 67 0.954
734
P MMB011 Membranous Nephropathy 50 0.954
735
DNG001 Dengue Shock Syndrome 40 0.954
736
PPL022 Papilloma 53 0.954
737
CRV040 Cervix Carcinoma 50 0.954
738
SQM002 Squamous Cell Papilloma 46 0.954
739
FCT005 Factor Xiii Deficiency 55 0.954
740
ATN005 Autonomic Dysfunction 46 0.954
741
c ART115 Aortic Valve Disease 1 74 0.949
742
P NSP012 Nasopharyngeal Carcinoma 61 0.949
743
SPP011 Suppression of Tumorigenicity 12 61 0.949
744
BRT054 Brittle Bone Disorder 74 0.949
745
HMR023 Hemorrhagic Cystitis 43 0.949
746
HTC003 Hutchinson-Gilford Progeria Syndrome 65 0.949
747
THY111 Thyroid Carcinoma, Familial Medullary 67 0.949
748
PRM329 Premature Aging 36 0.949
749
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 64 0.949
750
THY125 Thyroid Gland Medullary Carcinoma 48 0.949
751
GTR002 Goiter 53 0.949
752
PNC001 Pancytopenia 53 0.949
753
P GCH001 Gaucher's Disease 70 0.949
754
P LRY044 Larynx Cancer 54 0.949
755
PST028 Post-Traumatic Stress Disorder 59 0.949
756
HLL004 Hellp Syndrome 53 0.949
757
P CRB059 Cerebellar Degeneration 36 0.949
758
c FML001 Familial Atrial Fibrillation 65 0.899
759
ZLL002 Zollinger-Ellison Syndrome 55 0.899
760
GST030 Gastrinoma 45 0.899
761
LYM133 Lymphoma, Hodgkin, Classic 74 0.842
762
P PRM011 Primary Ciliary Dyskinesia 69 0.842
763
P HRD217 Hereditary Optic Neuropathy 36 0.842
764
c SPS025 Spastic Paraplegia 15 30 0.842
765
c CHR408 Charcot-Marie-Tooth Disease, X-Linked Recessive, 5 43 0.842
766
P SJG008 Sjogren Syndrome 61 0.842
767
c SPS125 Spastic Paraplegia 15, Autosomal Recessive 49 0.842
768
c SPS151 Spastic Paraplegia 11, Autosomal Recessive 49 0.842
769
PRV020 Periventricular Heterotopia with Microcephaly, Autosomal Recessive 26 0.842
770
STR039 Sturge-Weber Syndrome 61 0.842
771
c CNG415 Congenital Disorder of Glycosylation, Type Ia 59 0.842
772
P LSS002 Lissencephaly 50 0.842
773
P HRD021 Hereditary Sensory Neuropathy 48 0.842
774
c SVR003 Severe Congenital Neutropenia 59 0.842
775
P PRV002 Periventricular Nodular Heterotopia 52 0.842
776
TRD006 Tardive Dyskinesia 53 0.842
777
NRL016 Neural Tube Defects 81 0.842
778
BRT002 Birt-Hogg-Dube Syndrome 64 0.842
779
CLB010 Coloboma of Macula 53 0.842
780
PBL005 Piebald Trait 59 0.842
781
c GRS014 Griscelli Syndrome, Type 2 51 0.842
782
PNS018 Pain Sensitivity Quantitative Trait Locus 1 23 0.842
783
P GRS003 Griscelli Syndrome 53 0.842
784
OBS082 Obstructive Nephropathy 41 0.842
785
P PMP001 Pemphigus 55 0.842
786
NDL022 Nodular Neuronal Heterotopia 29 0.842
787
IGG001 Iga Glomerulonephritis 50 0.842
788
P BRD002 Bardet-Biedl Syndrome 66 0.842
789
MNK002 Monkeypox 41 0.842
790
SCB001 Scabies 50 0.842
791
P RTN014 Retinal Artery Occlusion 47 0.842
792
c PLM127 Pulmonary Hypertension, Primary, 3 34 0.842
793
BRN026 Branch Retinal Artery Occlusion 41 0.842
794
P ATR010 Atrial Heart Septal Defect 58 0.842
795
NRT004 Neuritis 53 0.842
796
ATN004 Autonomic Neuropathy 42 0.842
797
P MTH007 Methemoglobinemia 46 0.842
798
BRC012 Brucellosis 66 0.842
799
c SVR107 Severe Congenital Neutropenia 3 20 0.842
800
TCL001 T-Cell Adult Acute Lymphocytic Leukemia 43 0.842
801
PTN001 Patent Foramen Ovale 62 0.842
802
AZS001 Azoospermia 45 0.842
803
P TRC031 Trichorhinophalangeal Syndrome 38 0.842
804
c RNG019 Ring Chromosome 3 19 0.842
805
c HMN021 Human T-Cell Leukemia Virus Type 1 47 0.842
806
TRS021 Triosephosphate Isomerase Deficiency 45 0.842
807
P MCH002 Machado-Joseph Disease 62 0.840
808
c MSC037 Muscular Dystrophy-Dystroglycanopathy , Type a, 4 60 0.840
809
c HYP604 Hyperinsulinemic Hypoglycemia, Familial, 2 65 0.840
810
MLG141 Malignant Atrophic Papulosis 35 0.840
811
P HML033 Hemolytic Uremic Syndrome, Atypical 1 69 0.840
812
P APL001 Aplastic Anemia 73 0.840
813
HYP457 Hypertrophic Scars 42 0.840
814
P OCL002 Oculocutaneous Albinism 59 0.840
815
P TMR010 Tumor Predisposition Syndrome 67 0.840
816
INV001 Invasive Aspergillosis 49 0.840
817
INF034 Infective Endocarditis 54 0.840
818
P SML001 Small Cell Carcinoma 52 0.840
819
P XRD029 Xeroderma Pigmentosum, Complementation Group a 56 0.840
820
c BRS111 Breast-Ovarian Cancer, Familial 2 53 0.840
821
ENT011 Enterocolitis 55 0.840
822
P ACT241 Acute Bilirubin Encephalopathy 25 0.840
823
P FBR003 Fibrous Histiocytoma 43 0.840
824
P ART018 Aortic Valve Insufficiency 52 0.840
825
P ATR005 Atrophic Gastritis 50 0.840
826
CHR066 Chronic Fatigue Syndrome 60 0.840
827
DYS018 Dysostosis 44 0.840
828
P ART023 Arthropathy 61 0.840
829
SMN007 Seminoma 42 0.840
830
ACT084 Acute Stress Disorder 54 0.840
831
CHL045 Choline Deficiency Disease 39 0.840
833
RTN003 Retinal Ischemia 49 0.840
834
P SPN046 Spinal Muscular Atrophy 63 0.840
835
c ACT068 Acute Cystitis 61 0.840
836
c MLG084 Malignant Fibrous Histiocytoma 62 0.840
837
P MYG005 Myoglobinuria 40 0.840
838
P PYL005 Pyelonephritis 57 0.840
839
QFV001 Q Fever 62 0.840
840
INT066 Interstitial Lung Disease 60 0.840
841
P LPS002 Liposarcoma 64 0.840
842
LST001 Listeriosis 59 0.840
843
HND002 Hand, Foot and Mouth Disease 50 0.840
844
CLC006 Calcinosis 47 0.840
845
P RTN022 Retinal Vein Occlusion 54 0.840
846
MYT011 Myotonia 39 0.840
847
CND006 Candida Glabrata 30 0.840
848
BLR013 Biliary Tract Cancer 43 0.840
849
PRS119 Persistent Genital Arousal Disorder 18 0.840
850
CHR178 Chromosomal Triplication 34 0.840
851
PRN019 Perinatal Necrotizing Enterocolitis 60 0.840
852
P STN012 Sting-Associated Vasculopathy, Infantile-Onset 42 0.817
853
STN011 Sting-Associated Vasculopathy with Onset in Infancy 45 0.817
854
P ECT006 Ectodermal Dysplasia 63 0.817
855
P HYP024 Hypoparathyroidism 55 0.817
856
RNL011 Renal Osteodystrophy 49 0.817
857
PTT048 Pituitary Adenoma, Prolactin-Secreting 64 0.753
858
CRC014 Carcinoid Tumors, Intestinal 46 0.753
859
SMT003 Somatostatinoma 52 0.753
860
SKL017 Skeletal Dysplasias 41 0.697
861
PNM013 Pneumococcal Meningitis 43 0.697
862
c LKM056 Leukemia, Chronic Lymphocytic 2 48 0.697
863
c PRX094 Paroxysmal Nocturnal Hemoglobinuria 1 30 0.697
864
P LPR021 Leprosy 3 71 0.697
865
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.697
866
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 62 0.697
867
P PRG130 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 1 54 0.697
868
P ALT001 Alternating Hemiplegia of Childhood 57 0.697
869
P NNS032 Non-Syndromic X-Linked Intellectual Disability 46 0.697
870
ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 36 0.697
871
P BRC006 Brachydactyly 51 0.697
872
P MSC002 Muscular Dystrophy-Dystroglycanopathy 35 0.697
873
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 64 0.697
874
WRN001 Werner Syndrome 69 0.697
875
c XRD030 Xeroderma Pigmentosum, Complementation Group C 55 0.697
876
P PLV020 Pelvic Organ Prolapse 58 0.697
877
c LNG048 Long Qt Syndrome 3 53 0.697
878
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 32 0.697
879
LKN001 Leukoencephalopathy with Vanishing White Matter 63 0.697
880
c MSC182 Muscular Dystrophy-Dystroglycanopathy , Type C, 15 30 0.697
881
c NPH073 Nephrotic Syndrome, Type 8 25 0.697
882
c MTC062 Mitochondrial Dna Depletion Syndrome 2 43 0.697
883
c TBR026 Tuberous Sclerosis 2 71 0.697
884
c CHL119 Cholangitis, Primary Sclerosing 58 0.697
885
PRP083 Porphyria, Acute Intermittent 65 0.697
886
CHR081 Choroideremia 58 0.697
887
c HNT004 Huntington Disease-Like 2 52 0.697
888
HYP611 Hypoparathyroidism, X-Linked 30 0.697
889
c PRG038 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 2 49 0.697
890
c GLY008 Glycogen Storage Disease Ii 72 0.697
891
c CNG208 Congenital Disorder of Glycosylation, Type Iic 47 0.697
892
RYN001 Raynaud Disease 50 0.697
893
P SRC025 Sarcoidosis 1 71 0.697
894
ISL014 Isolated Growth Hormone Deficiency, Type Ia 54 0.697
895
DGR001 Digeorge Syndrome 62 0.697
896
CRN048 Craniofacial-Deafness-Hand Syndrome 52 0.697
897
c PRG040 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 4 53 0.697
898
c MSC097 Muscular Dystrophy-Dystroglycanopathy , Type a, 14 27 0.697
899
c MSC099 Muscular Dystrophy-Dystroglycanopathy , Type B, 14 26 0.697
900
HPT067 Hepatocellular Adenoma 43 0.697
901
FBR054 Fibroma 44 0.697
902
c CNG550 Congenital Muscular Dystrophy-Dystroglycanopathy A14 27 0.697
903
PRS042 Prostate Disease 42 0.697
904
P LCH002 Lichen Planus 54 0.697
905
P HMC002 Homocystinuria 53 0.697
906
P TYR004 Tyrosinemia 50 0.697
907
P PRD021 Periodic Paralysis 41 0.697
908
P MTH008 Methylmalonic Acidemia 52 0.697
909
TRT001 Teratocarcinoma 42 0.697
910
P OLV001 Olivopontocerebellar Atrophy 51 0.697
911
P MMP001 Mumps 57 0.697
912
BLD171 Blood Group, Lewis System 20 0.697
913
VRC001 Varicocele 48 0.697
914
END041 Endometrial Adenocarcinoma 64 0.697
915
P SCL009 Sclerosing Cholangitis 48 0.697
916
PYL006 Pyloric Stenosis 48 0.697
917
CLB002 Clubfoot 51 0.697
918
TST014 Testicular Cancer 52 0.697
919
CYS014 Cystadenocarcinoma 51 0.697
920
MCS002 Mucositis 56 0.697
921
PRT018 Portal Vein Thrombosis 50 0.697
922
PRM013 Premature Menopause 58 0.697
923
HYP043 Hyperandrogenism 48 0.697
924
GST050 Gastrointestinal System Disease 55 0.697
925
c FML015 Familial Nephrotic Syndrome 48 0.697
926
c GM2006 Gm2 Gangliosidosis 46 0.697
927
NRL005 Neurilemmoma 60 0.697
928
c SYN064 Syndromic X-Linked Intellectual Disability 25 0.697
929
P ART005 Arteriovenous Malformation 65 0.697
930
TLR001 Tularemia 56 0.697
931
LPT001 Leptospirosis 66 0.697
932
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 54 0.697
933
GNT179 Genetic Steroid-Resistant Nephrotic Syndrome 39