Search results for Guanosine diphosphate

958 hits were found for Guanosine diphosphate

# Family MCID Name MIFTS Score
1
PRT037 Pertussis 49 11.264
2
CHL014 Cholera 62 7.845
3
P NRB001 Neuroblastoma 66 5.650
4
HLX001 Helix Syndrome 47 4.934
5
ISC004 Ischemia 61 4.927
6
RPD005 Rapidly Involuting Congenital Hemangioma 48 4.856
7
IMP005 Impotence 52 4.788
8
HMN044 Human Immunodeficiency Virus Type 1 76 4.690
9
PRN001 Purine Nucleoside Phosphorylase Deficiency 53 4.373
10
P HRP006 Herpes Simplex 65 4.350
11
P PLM037 Pulmonary Hypertension 69 4.193
12
P MYC084 Mycobacterium Tuberculosis 1 68 4.122
13
NRR001 Neuroretinitis 42 3.913
14
RTN023 Retinitis 45 3.913
15
BNR002 Bone Resorption Disease 47 3.891
16
P HPT023 Hepatocellular Carcinoma 95 3.855
17
IMM167 Immune Deficiency Disease 76 3.830
18
48X005 48,xyyy 39 3.792
19
TRM010 Traumatic Brain Injury 50 3.780
20
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 3.746
21
P HPT021 Hepatitis 68 3.699
22
BLR008 Bilirubin Metabolic Disorder 57 3.698
23
BRN071 Brain Injury 50 3.647
24
P OVR042 Ovarian Cancer 88 3.523
25
GLM045 Glioma 62 3.498
26
P CRG003 Crigler-Najjar Syndrome, Type I 64 3.490
27
P LNG032 Lung Cancer 98 3.486
28
SVR001 Severe Acute Respiratory Syndrome 68 3.468
29
GLL048 Glial Tumor 51 3.451
30
c HPT001 Hepatitis C 61 3.296
31
GLB002 Glioblastoma 67 3.270
32
P VSC007 Vascular Disease 62 3.239
33
47X002 47,xyy 47 3.236
34
c HPT073 Hepatitis C Virus 70 3.223
35
CHG001 Chagas Disease 65 3.208
36
c SML038 Small Cell Cancer of the Lung 68 3.206
37
GLB001 Gilbert Syndrome 53 3.191
38
HYP266 Hypoxia 56 3.177
39
P THR014 Thrombocytopenia 66 3.110
40
P MLN008 Melanoma 75 3.022
41
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 59 3.009
42
P RTN008 Retinitis Pigmentosa 79 2.991
43
VCC001 Vaccinia 49 2.945
44
LPP008 Lipoprotein Quantitative Trait Locus 65 2.922
45
P MYC007 Myocardial Infarction 69 2.921
46
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 2.910
47
TXC005 Toxic Shock Syndrome 61 2.896
48
P LKM002 Leukemia 65 2.882
49
P ADL010 Adult Respiratory Distress Syndrome 70 2.861
50
P PHC003 Pheochromocytoma 70 2.854
51
ADR040 Adrenal Gland Pheochromocytoma 45 2.854
52
ANX004 Anoxia 40 2.800
53
DPH001 Diphtheria 59 2.785
54
P SZR006 Seizure Disorder 69 2.781
55
c SYS001 Systemic Lupus Erythematosus 85 2.766
56
c MCR115 Microvascular Complications of Diabetes 5 65 2.755
57
STM007 Stomatitis 52 2.721
58
P DRR001 Diarrhea 55 2.707
59
OST159 Osteogenic Sarcoma 66 2.706
60
c HPT003 Hepatitis a 63 2.705
61
ACQ007 Acquired Immunodeficiency Syndrome 58 2.614
62
P ENC018 Encephalopathy 62 2.606
63
P BRB001 Beriberi 44 2.588
64
MLR004 Malaria 77 2.562
65
P DYS154 Dystonia 64 2.560
66
P MYP004 Myopathy 67 2.559
67
P LPS004 Lupus Erythematosus 61 2.524
68
TRY001 Trypanosomiasis 50 2.506
69
LVR012 Liver Cirrhosis 62 2.488
70
OVR094 Ovarian Epithelial Cancer 39 2.481
71
c TYP009 Type 2 Diabetes Mellitus 91 2.449
72
SPN186 Spinal Cord Injury 60 2.438
73
PRT036 Peritonitis 65 2.426
74
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 2.422
75
P NTR004 Neutropenia 62 2.403
76
CNG034 Congestive Heart Failure 69 2.391
77
DFC004 Deficiency Anemia 74 2.390
78
c PRC016 Pre-Eclampsia 64 2.381
79
P SCK005 Sickle Cell Disease 56 2.380
80
c ATM011 Autoimmune Hepatitis 62 2.349
81
PRS021 Prostatic Adenoma 43 2.344
82
CVD001 Covid-19 59 2.333
83
P DBT009 Diabetes Mellitus 67 2.315
84
THR024 Thrombosis 56 2.315
85
c MJR022 Major Affective Disorder 8 37 2.312
86
c MJR024 Major Affective Disorder 9 40 2.312
87
P BPL003 Bipolar Disorder 56 2.312
88
MYL069 Myeloma, Multiple 76 2.302
89
ANG054 Angina Pectoris 65 2.301
90
CRH001 Crohn's Disease 80 2.301
91
P BND020 Bone Disease 60 2.294
92
P GST053 Gastric Cancer 82 2.282
93
P RTN016 Retinal Degeneration 52 2.277
94
ART140 Arteries, Anomalies of 52 2.261
95
P PNC035 Pancreatic Cancer 87 2.250
96
P GLM040 Glioma Susceptibility 1 70 2.229
97
P LKM071 Leukemia, Chronic Lymphocytic 74 2.216
98
MLG169 Malignant Astrocytoma 57 2.214
99
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 2.212
100
SLP001 Sleeping Sickness 56 2.206
101
c LKM061 Leukemia, Acute Myeloid 83 2.202
102
PRS045 Prostatic Hypertrophy 53 2.196
103
DWN001 Down Syndrome 70 2.190
104
c ACT073 Acute Leukemia 59 2.185
105
CLT003 Colitis 63 2.184
106
c ACT075 Acute Myocardial Infarction 55 2.183
107
OCL069 Ocular Motor Apraxia 57 2.172
108
P MYL006 Myeloid Leukemia 60 2.161
109
P ADN016 Adenocarcinoma 63 2.160
110
MDD018 Middle East Respiratory Syndrome 44 2.159
111
HYP060 Hyperinsulinism 53 2.144
112
ADN018 Adenoma 58 2.124
113
CYS001 Cystic Fibrosis 77 2.100
114
P LKM062 Leukemia, Acute Lymphoblastic 69 2.096
115
NNL005 Non-Alcoholic Fatty Liver Disease 63 2.091
116
P PRS040 Prostate Cancer 95 2.084
117
c MCR133 Microvascular Complications of Diabetes 4 41 2.083
118
c MCR113 Microvascular Complications of Diabetes 3 52 2.083
119
c MCR130 Microvascular Complications of Diabetes 6 41 2.083
120
c MCR120 Microvascular Complications of Diabetes 7 47 2.083
121
c HYP595 Hypertension, Essential 84 2.082
122
HYP056 Hypoglycemia 65 2.077
123
c PCH010 Pachyonychia Congenita 3 43 2.073
124
ALL029 Allergic Disease 61 2.072
125
BRN004 Brain Edema 54 2.072
126
HRW001 Hair Whorl 35 2.069
127
ALC007 Alcohol Dependence 65 2.058
128
c PLM164 Pulmonary Hypertension, Primary, 1 75 2.046
129
ATH013 Atherosclerosis Susceptibility 63 2.035
130
P TRM003 Tremor 50 2.029
131
INT007 Intermediate Coronary Syndrome 53 2.021
132
FTT001 Fatty Liver Disease 61 2.016
133
c CHR684 Chronic Kidney Disease 73 2.013
134
CRB004 Cerebral Artery Occlusion 45 2.013
135
c HPT016 Hepatitis B 62 2.010
136
HMN014 Human Immunodeficiency Virus Infectious Disease 54 2.009
137
c VRL010 Viral Hepatitis 52 1.999
138
PRS129 Prostatic Hyperplasia, Benign 48 1.996
139
P LNG064 Lung Cancer Susceptibility 3 69 1.994
140
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 1.990
141
P CLR023 Colorectal Cancer 100 1.985
142
P GLM007 Glomerulonephritis 59 1.953
143
c CHR688 Chronic Acquired Demyelinating Polyneuropathy 16 1.952
144
HGH043 High Grade Glioma 46 1.936
145
P ATR011 Atrial Fibrillation 66 1.894
146
P EPL164 Epilepsy 70 1.885
147
CYT002 Cytokine Deficiency 43 1.875
148
c HYP807 Hyperinsulinemic Hypoglycemia, Familial, 6 52 1.874
149
c HYP836 Hypercholesterolemia, Familial, 1 73 1.870
150
ULC004 Ulcerative Colitis 74 1.863
151
END086 End Stage Renal Disease 54 1.863
152
AGN016 Aging 53 1.862
153
CLN015 Colon Adenocarcinoma 64 1.854
154
P PRK039 Parkinsonism 55 1.831
155
P MYC008 Myocarditis 59 1.827
156
CHL004 Cholelithiasis 48 1.825
157
P MSC005 Muscular Dystrophy 66 1.824
158
P ALZ034 Alzheimer Disease 87 1.814
159
P NPH012 Nephrotic Syndrome 61 1.801
160
c BRN108 Branchiootic Syndrome 1 63 1.795
161
PRT251 Proteinuria, Chronic Benign 58 1.783
162
DWR001 Dwarfism 44 1.774
163
ORL015 Oral Squamous Cell Carcinoma 43 1.768
164
PRP027 Peripheral Vascular Disease 71 1.762
165
P BRS047 Breast Cancer 97 1.760
166
CHC001 Chickenpox 56 1.746
167
c DLT002 Dilated Cardiomyopathy 79 1.745
168
P EXN002 Exanthem 58 1.737
169
ACT098 Acute Erythroid Leukemia 55 1.721
170
MND023 Mend Syndrome 49 1.715
171
MST004 Mast Cell Neoplasm 41 1.695
172
EXT007 Extracutaneous Mastocytoma 38 1.695
173
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 1.694
174
BRN028 Brain Cancer 73 1.689
175
P KLZ004 Kala-Azar 1 41 1.684
176
LSH001 Leishmaniasis 63 1.684
177
P RSP003 Respiratory Failure 73 1.682
178
BCT022 Bacterial Infectious Disease 55 1.660
179
P HYP265 Hypotonia 42 1.659
180
P LVR013 Liver Disease 68 1.653
181
P INF037 Inflammatory Bowel Disease 53 1.648
182
GT001 Gout 63 1.646
183
CHD001 Chediak-Higashi Syndrome 66 1.641
184
P HRT032 Heart Disease 84 1.615
185
INS024 Insulin-Like Growth Factor I 77 1.611
186
CNG486 Congenital Disorders of N-Linked Glycosylation and Multiple Pathway 29 1.608
187
P RTN018 Retinal Disease 53 1.607
188
PST011 Pustulosis of Palm and Sole 52 1.606
189
P PSR002 Psoriasis 63 1.606
190
HYP066 Hyperglycemia 60 1.604
191
P HML002 Hemolytic Anemia 62 1.599
192
LYM019 Lymphosarcoma 46 1.597
193
PLY150 Polykaryocytosis Inducer 29 1.595
194
PLM010 Pulmonary Edema 54 1.590
195
STR067 Stroke, Ischemic 79 1.589
196
PLM129 Pulmonary Disease, Chronic Obstructive 74 1.589
197
HDN002 Head Injury 44 1.587
198
CRB039 Cerebrovascular Disease 65 1.582
199
CRT015 Carotid Artery Occlusion 45 1.581
200
THY029 Thyroid Carcinoma 55 1.578
201
P HYP086 Hypothyroidism 68 1.565
202
P OBS001 Obstructive Jaundice 49 1.565
203
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 1.549
204
INS001 Insulinoma 59 1.546
205
c MGR028 Migraine with or Without Aura 1 63 1.536
206
LPD008 Lipid Metabolism Disorder 61 1.535
207
URM002 Uremia 47 1.535
208
SQM006 Squamous Cell Carcinoma 59 1.533
209
P HDC001 Headache 56 1.525
210
P LCT001 Lactic Acidosis 50 1.515
211
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 44 1.507
212
P CRD119 Cardiac Arrest 68 1.505
213
P KDN018 Kidney Disease 71 1.499
214
MNT002 Mental Depression 56 1.491
215
LNG099 Lung Disease 62 1.490
216
P MJR001 Major Depressive Disorder 68 1.462
217
CRV035 Cervical Cancer 72 1.455
218
PNG002 Pain Agnosia 51 1.452
219
DPR016 Depression 64 1.452
220
P ALC033 Alcohol Use Disorder 67 1.441
221
c DNT047 Dentinogenesis Imperfecta Type 2 35 1.440
222
P HYP076 Hyperthyroidism 53 1.440
223
CHL068 Cholestasis 61 1.439
224
P ART021 Arteriosclerosis 53 1.435
225
SPL018 Splenomegaly 47 1.434
226
c GRV008 Graves Disease 1 54 1.432
227
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 1.429
228
P OST002 Osteoporosis 76 1.429
229
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 1.429
230
IRN002 Iron Metabolism Disease 56 1.426
231
PNC041 Pancreatic Ductal Adenocarcinoma 51 1.425
232
PRT013 Portal Hypertension 59 1.423
233
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 1.419
234
MDD011 Mood Disorder 61 1.418
235
HPT004 Hepatic Coma 43 1.414
236
P SKN015 Skin Carcinoma 71 1.407
237
DSS032 Disease by Infectious Agent 55 1.402
238
HPT019 Hepatic Encephalopathy 59 1.387
239
c ACT071 Acute Kidney Failure 60 1.386
240
END057 Endometrial Cancer 76 1.383
241
MYL009 Myelodysplastic Syndrome 67 1.382
242
SCK003 Sickle Cell Anemia 74 1.382
243
MTB004 Metabolic Acidosis 48 1.366
244
ALL006 Allergic Asthma 55 1.351
245
P RHN004 Rhinitis 56 1.349
246
KRN002 Kearns-Sayre Syndrome 62 1.344
247
RTN020 Retinal Vascular Disease 45 1.327
248
c AMY091 Amyotrophic Lateral Sclerosis 1 87 1.313
249
P LTR001 Lateral Sclerosis 57 1.313
250
P TMP001 Temporal Lobe Epilepsy 49 1.309
251
HYP014 Hyperuricemia 51 1.308
252
IRR002 Irritable Bowel Syndrome 64 1.298
253
CRN017 Coronary Thrombosis 46 1.290
254
HMP009 Haemophilus Influenzae 41 1.284
255
P PTS002 Ptosis 52 1.282
256
P RTN024 Retinoblastoma 72 1.282
257
PHN003 Phenylketonuria 76 1.277
258
TTN003 Tetanus 64 1.277
259
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 1.276
260
c LKM005 Leukemia, T-Cell, Chronic 33 1.276
261
P CRN300 Coronary Heart Disease 1 73 1.275
262
c DRR009 Diarrhea 6 46 1.274
263
P PNC044 Pancreatitis 61 1.261
264
ADR016 Adrenal Cortical Carcinoma 61 1.259
265
ADR054 Adrenocortical Carcinoma, Hereditary 47 1.259
266
ADR004 Adrenal Cortical Adenocarcinoma 38 1.259
267
P FBR031 Febrile Seizures 52 1.254
268
P ATX030 Ataxia-Telangiectasia 80 1.246
269
TLN003 Telangiectasis 51 1.246
270
ALL003 Allergic Rhinitis 66 1.239
271
RNL114 Renal Cell Carcinoma, Nonpapillary 79 1.226
272
P INS002 in Situ Carcinoma 52 1.222
273
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 1.217
274
SCH014 Schistosomiasis 56 1.217
275
P ECL001 Eclampsia 52 1.213
276
SVR004 Severe Combined Immunodeficiency 70 1.213
277
P SBS003 Substance Abuse 54 1.211
278
CRY035 Cryptorchidism, Unilateral or Bilateral 57 1.210
279
GST033 Gestational Diabetes 60 1.209
280
PLS011 Plasmacytoma 56 1.202
281
TCL027 T-Cell Acute Lymphoblastic Leukemia 52 1.202
282
CHK001 Chikungunya 60 1.199
283
P OLG002 Oligodendroglioma 66 1.199
284
HYP005 Hypokalemia 55 1.197
285
P CTN015 Cutaneous T Cell Lymphoma 48 1.182
286
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 1.181
287
HYP080 Hypogonadism 49 1.175
288
LWG006 Low Grade Glioma 41 1.175
289
CRV002 Cervix Uteri Carcinoma in Situ 48 1.175
290
CRV045 Cervical Intraepithelial Neoplasia 38 1.175
291
CNS004 Constipation 56 1.162
292
TRN015 Transient Cerebral Ischemia 62 1.148
293
P CHR345 Chronic Pain 50 1.147
294
P SCH015 Schizophrenia 74 1.146
295
c CNG192 Congenital Disorder of Glycosylation, Type Ik 37 1.138
296
ALG025 Alg1-Congenital Disorder of Glycosylation 19 1.138
297
HYP264 Hypertonia 35 1.138
298
PRP016 Paraplegia 52 1.134
299
CYT005 Cytomegalovirus Retinitis 50 1.132
300
P MTC133 Mitochondrial Myopathy 51 1.127
301
P BRS044 Breast Adenocarcinoma 58 1.127
302
P LMB006 Limb-Girdle Muscular Dystrophy 52 1.113
303
P ANP001 Anaplastic Large Cell Lymphoma 59 1.110
304
P NRF002 Neurofibromatosis 60 1.108
305
DMY004 Demyelinating Disease 50 1.107
306
P MSC003 Muscular Atrophy 52 1.106
307
ENT004 Enthesopathy 51 1.102
308
c HPT015 Hepatitis D 49 1.101
309
P LYM118 Lymphoma 66 1.093
310
c THY107 Thymoma, Familial 42 1.083
311
P THY023 Thymoma 64 1.083
312
PRM236 Primary Biliary Cholangitis 62 1.083
313
P LYM033 Lymphoproliferative Syndrome 59 1.074
314
c OPT053 Optic Atrophy 1 62 1.069
315
HPT022 Hepatoblastoma 54 1.069
316
TST044 Testicular Torsion 45 1.067
317
PST092 Posttransplant Acute Limbic Encephalitis 29 1.063
318
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 1.062
319
TRC003 Trichomoniasis 53 1.059
320
PNC129 Pancreatic Adenocarcinoma 64 1.057
321
P BCL017 B-Cell Lymphoma 57 1.055
322
P SPP010 Suppressor of Tumorigenicity 3 50 1.054
323
LWC001 Low Compliance Bladder 44 1.052
324
WLL004 Wallerian Degeneration 38 1.052
325
P PRD008 Periodontitis 63 1.046
326
c GLL024 Gallbladder Disease 1 53 1.045
327
BRN056 Bronchopulmonary Dysplasia 57 1.039
328
P NRP001 Neuropathy 59 1.031
329
RYN005 Raynaud Phenomenon 45 1.029
330
P HYP098 Hypereosinophilic Syndrome 66 1.019
331
ACT119 Acute Promyelocytic Leukemia 62 1.019
332
c SCL052 Scleroderma, Familial Progressive 60 1.015
333
P CRD246 Cardiovascular System Disease 55 1.004
334
PPT005 Peptic Ulcer Disease 58 1.002
335
c ATR087 Atrial Standstill 1 74 0.997
336
BRN024 Bronchitis 67 0.994
337
ARG004 Argyria 26 0.987
338
ASP004 Asphyxia Neonatorum 50 0.986
339
PRP030 Purpura 54 0.984
340
P ESP024 Esophagitis 60 0.983
341
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 0.982
342
KRT009 Keratosis 52 0.979
343
PYR041 Pyruvate Kinase Deficiency of Red Cells 56 0.975
344
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 51 0.974
345
MTB008 Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 42 0.974
346
P SLP006 Sleep Apnea 69 0.972
347
LYM027 Lymphopenia 56 0.971
348
P CNR004 Cone-Rod Dystrophy 2 74 0.967
349
URT010 Ureteral Obstruction 44 0.959
350
PPL052 Papillomatosis, Confluent and Reticulated 34 0.957
351
MND031 Mandibuloacral Dysplasia Progeroid Syndrome 33 0.955
352
LYM017 Lyme Disease 63 0.951
353
P ACT008 Actinic Keratosis 53 0.951
354
KRT002 Keratomalacia 54 0.947
355
FBR047 Fibromyalgia 57 0.943
356
P FML011 Familial Adenomatous Polyposis 70 0.941
357
P BNG032 Benign Mesothelioma 53 0.941
358
P PLM036 Pulmonary Fibrosis 65 0.939
359
DBT010 Diabetic Neuropathy 54 0.938
360
RNL077 Renal Fibrosis 46 0.936
361
MSL001 Measles 61 0.935
362
P INF038 Influenza 68 0.926
363
c THR092 Thrombophilia Due to Thrombin Defect 74 0.923
364
GLC003 Glucose Intolerance 53 0.919
365
P MNN013 Meningitis 65 0.911
366
YLL002 Yellow Fever 61 0.908
367
NNL006 Non-Alcoholic Steatohepatitis 54 0.902
368
P SYS005 Systemic Scleroderma 73 0.899
369
c BCT007 Bacterial Meningitis 55 0.897
370
WLK001 Walker-Warburg Syndrome 62 0.896
371
PTT037 Pituitary Tumors 44 0.891
372
HMN047 Human Cytomegalovirus Infection 59 0.890
373
DYS015 Dysentery 49 0.890
374
PRP080 Peripheral Artery Disease 54 0.888
375
INT323 Intraocular Pressure Quantitative Trait Locus 63 0.882
376
HND015 Hand Skill, Relative 29 0.875
377
P OPT006 Optic Nerve Disease 57 0.869
378
ORL011 Oral Cancer 60 0.869
379
c INH030 Inherited Retinal Disorder 28 0.868
380
RCK004 Rickets 64 0.864
381
THR004 Thrombocytosis 52 0.863
382
XRD010 Xeroderma Pigmentosum, Variant Type 72 0.861
383
c TYP008 Type 1 Diabetes Mellitus 77 0.858
384
PPL002 Papillary Carcinoma 46 0.854
385
GST045 Gastroenteritis 58 0.854
386
HRP004 Herpes Zoster 60 0.853
387
LMB062 Limb Ischemia 55 0.852
388
P FBR017 Fibrosarcoma 55 0.848
389
SPN035 Spindle Cell Sarcoma 51 0.848
390
SRC014 Sarcoma 64 0.848
391
P MLT020 Multiple Sclerosis 79 0.847
392
P UVT001 Uveitis 57 0.846
393
PTH003 Pathologic Nystagmus 52 0.845
394
WTH001 Withdrawal Disorder 47 0.844
395
P SCL018 Scoliosis 57 0.843
396
P ADL017 Adult T-Cell Leukemia 53 0.843
397
P ART022 Arthritis 70 0.842
398
CRD132 Cardiac Conduction Defect 59 0.833
399
TRN018 Transitional Cell Carcinoma 56 0.830
400
SPS057 Spasticity 43 0.829
401
c TBR025 Tuberous Sclerosis 1 84 0.828
402
MLD018 Mild Cognitive Impairment 48 0.823
403
CCC002 Coccidiosis 50 0.823
404
SCR003 Secretory Diarrhea 35 0.816
405
P SLM003 Salmonellosis 54 0.816
406
HRT011 Heart Septal Defect 49 0.813
407
KRT019 Keratitis, Hereditary 66 0.811
408
P VNT002 Ventricular Septal Defect 58 0.810
409
P EYD002 Eye Disease 57 0.810
410
P URN019 Urinary Tract Infection 48 0.810
411
CRC021 Carcinosarcoma 62 0.810
413
ALC009 Alcoholic Liver Cirrhosis 54 0.797
414
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 0.797
415
P TTR001 Tetralogy of Fallot 69 0.796
416
c HYP326 Hyperinsulinemic Hypoglycemia, Familial, 5 50 0.796
417
c HYP271 Hyperinsulinemic Hypoglycemia, Familial, 4 52 0.796
418
ESP021 Esophageal Cancer 84 0.796
419
c ACT027 Acute Pancreatitis 60 0.795
420
GRY002 Gray Platelet Syndrome 57 0.795
421
CRB090 Cerebral Hypoxia 42 0.795
422
c ATS007 Autism Spectrum Disorder 71 0.790
423
FRN006 Frontotemporal Dementia 68 0.790
424
c THY109 Thyroid Cancer, Nonmedullary, 1 55 0.790
425
P OPN001 Open-Angle Glaucoma 55 0.788
426
P VSC011 Vasculitis 61 0.784
427
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 0.781
428
GST023 Gastric Ulcer 52 0.779
429
NRM005 Neuromuscular Disease 62 0.779
430
STT041 Stuttering 52 0.772
431
IGR001 Ige Responsiveness, Atopic 58 0.772
432
c CHR095 Chronic Progressive External Ophthalmoplegia 48 0.772
433
PLM134 Pulmonary Fibrosis, Idiopathic 76 0.767
434
RTN017 Retinal Detachment 60 0.767
435
c RTN047 Retinitis Pigmentosa 18 45 0.767
436
P RHB003 Rhabdomyosarcoma 66 0.767
437
P RNV001 Renovascular Hypertension 48 0.766
438
P AMY004 Amyloidosis 69 0.764
439
NWC001 Newcastle Disease 47 0.763
440
LNG039 Lung Squamous Cell Carcinoma 57 0.763
441
GST040 Gastric Adenocarcinoma 66 0.763
442
ILS001 Ileus 49 0.763
443
TTH006 Tooth Disease 51 0.762
444
P CHR071 Charcot-Marie-Tooth Disease 64 0.762
445
DYS073 Dysphagia 53 0.762
446
P MYP006 Myopia 55 0.760
447
GRW007 Growth Hormone Deficiency 47 0.760
448
c PLM163 Palmoplantar Keratoderma, Punctate Type Ii 28 0.759
449
PNC060 Punctate Porokeratosis 28 0.759
450
CHL065 Cholangiocarcinoma 57 0.751
451
INT079 Intrahepatic Cholangiocarcinoma 51 0.751
452
P HMR003 Hemorrhagic Disease 59 0.746
453
P PGT001 Paget's Disease of Bone 60 0.746
454
VSC002 Vascular Dementia 59 0.746
455
MYL005 Myelofibrosis 70 0.746
456
RBS001 Rabies 57 0.745
457
SDD001 Sudden Infant Death Syndrome 60 0.744
458
P MYC033 Myoclonus 46 0.744
459
P RHM011 Rheumatoid Arthritis 81 0.744
460
PNC013 Pancreatic Ductal Carcinoma 48 0.739
461
P GRV001 Graves' Disease 54 0.736
462
P MTR012 Mitral Valve Disease 57 0.736
463
DGN001 Degenerative Disc Disease 48 0.736
464
CRC006 Carcinoid Syndrome 55 0.734
465
P MYS005 Myositis 55 0.726
466
STT001 Status Epilepticus 58 0.726
467
P DRM010 Dermatomyositis 61 0.726
468
PLR008 Pleurisy 49 0.726
469
P MLN069 Melanoma, Uveal 59 0.717
470
c MST023 Mesothelioma, Malignant 56 0.711
471
P MTR003 Mitral Valve Stenosis 53 0.711
472
PST053 Postherpetic Neuralgia 39 0.711
473
CTN007 Cutaneous Leishmaniasis 61 0.711
474
CLP005 Ciliopathy 40 0.711
475
CRB037 Cerebral Palsy 66 0.709
476
IDP070 Idiopathic Scoliosis 41 0.708
477
c ATS025 Autosomal Dominant Progressive External Ophthalmoplegia 45 0.708
478
MNG007 Manganese Poisoning 28 0.708
479
P ATS364 Autism 72 0.703
480
THM002 Thiamine-Responsive Megaloblastic Anemia Syndrome 50 0.703
481
P ASP006 Aspergillosis 71 0.703
482
OST017 Osteomyelitis 63 0.703
483
DNT012 Dental Caries 53 0.703
484
P CRN026 Corneal Edema 42 0.703
485
P RCT021 Rectum Cancer 54 0.698
486
BRS099 Breast Ductal Carcinoma 61 0.698
487
P MJR007 Major Affective Disorder 1 42 0.696
488
P NRV007 Nervous System Disease 65 0.696
489
c GLC092 Glaucoma, Primary Open Angle 60 0.696
490
OST012 Osteoarthritis 77 0.696
491
SKN019 Skin Melanoma 70 0.689
492
P ALP008 Alopecia 53 0.680
493
P INT068 Intestinal Disease 53 0.676
494
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 0.676
495
ATS010 Autosomal Recessive Disease 42 0.676
496
c HNT011 Huntington Disease-Like 3 33 0.675
497
P MCR129 Microvascular Complications of Diabetes 1 67 0.675
498
c CNG006 Congenital Hypothyroidism 63 0.675
499
c MCR112 Microvascular Complications of Diabetes 2 42 0.675
500
PRN035 Perniosis 27 0.675
501
INF021 Infant Gynecomastia 30 0.675
502
TYP007 Typhoid Fever 63 0.675
503
GYN001 Gynecomastia 48 0.675
504
P FCL005 Focal Segmental Glomerulosclerosis 57 0.675
505
CRY003 Cryptosporidiosis 55 0.675
506
PRC051 Paracetamol Poisoning 29 0.675
507
c SCN036 Secondary Progressive Multiple Sclerosis 55 0.672
508
P SYP003 Syphilis 59 0.672
509
P HNT016 Huntington Disease 73 0.652
510
MTC005 Mitochondrial Metabolism Disease 44 0.648
511
FCS014 Fucosidase Regulator 15 0.648
512
P PRP019 Peripheral Nervous System Disease 57 0.648
513
P LNG028 Long Qt Syndrome 63 0.645
514
VLL006 Villous Adenoma 40 0.640
515
BCT021 Bacterial Sepsis 43 0.640
516
P CND004 Candidiasis 57 0.640
517
P CLL015 Collagen Disease 47 0.640
518
MST020 Mast Cell Activation Syndrome 27 0.640
519
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 57 0.637
520
SPR010 Sporotrichosis 45 0.621
521
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 0.611
522
CCN002 Cocaine Abuse 49 0.610
523
PSR001 Psoriatic Arthritis 61 0.609
524
PLM001 Pulmonary Tuberculosis 69 0.595
525
CMB007 Combined Immunodeficiency 56 0.586
526
TRS021 Triosephosphate Isomerase Deficiency 44 0.585
527
P PRK057 Parkinson Disease, Late-Onset 79 0.578
528
EPT021 Epithelial Recurrent Erosion Dystrophy 45 0.573
529
c EXD008 Exudative Vitreoretinopathy 1 71 0.573
530
LWC002 Lowe Oculocerebrorenal Syndrome 68 0.573
531
GST071 Gastrointestinal Carcinoma 46 0.573
532
NRT001 Neurotic Disorder 56 0.573
533
PRD004 Prediabetes Syndrome 52 0.573
534
DNG003 Dengue Disease 65 0.573
535
CHL123 Chlamydia 58 0.563
536
ATM095 Autoimmune Disease 61 0.555
537
P STN012 Sting-Associated Vasculopathy, Infantile-Onset 42 0.553
538
STN011 Sting-Associated Vasculopathy with Onset in Infancy 44 0.553
539
P ECT006 Ectodermal Dysplasia 62 0.553
540
RNL011 Renal Osteodystrophy 48 0.553
541
P HYP024 Hypoparathyroidism 55 0.553
542
c BPL002 Bipolar I Disorder 47 0.551
543
VRL011 Viral Infectious Disease 60 0.551
544
P BDY004 Body Mass Index Quantitative Trait Locus 11 82 0.535
545
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 0.535
546
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 0.535
547
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.535
548
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.535
549
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.535
550
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 0.535
551
c BDY019 Body Mass Index Quantitative Trait Locus 18 46 0.535
552
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.535
553
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.535
554
P DNG005 Dengue Virus 55 0.533
555
P NNN008 Noonan Syndrome 1 76 0.532
556
ZLL002 Zollinger-Ellison Syndrome 55 0.523
557
c FML001 Familial Atrial Fibrillation 65 0.523
558
GST030 Gastrinoma 45 0.523
559
c PSD047 Pseudo-Turner Syndrome 52 0.520
560
c LKM063 Leukemia, Chronic Myeloid 70 0.517
561
P KRN004 Kernicterus 47 0.517
562
P BLD134 Bladder Cancer 79 0.506
563
INT002 Intermittent Claudication 61 0.500
564
c CNG411 Congenital Disorder of Glycosylation, Type in 66 0.494
565
CRC014 Carcinoid Tumors, Intestinal 46 0.487
566
c PNS012 Paine Syndrome 60 0.487
567
PTT048 Pituitary Adenoma, Prolactin-Secreting 64 0.487
568
ANP005 Anaplastic Astrocytoma 59 0.487
569
SMT003 Somatostatinoma 52 0.487
570
P INF032 Infertility 60 0.487
571
P CTR002 Cataract 59 0.486
572
P TBR001 Tuberous Sclerosis 69 0.463
573
P HYP750 Hypertriglyceridemia, Familial 61 0.459
574
HMC014 Homocysteinemia 52 0.458
575
SKN016 Skin Disease 63 0.454
576
PLM033 Pulmonary Embolism 58 0.454
577
P CRD224 Cardiofaciocutaneous Syndrome 1 71 0.449
578
P AST005 Asthma 75 0.449
579
P CYS018 Cystitis 58 0.449
580
P GST044 Gastritis 55 0.443
581
CST001 Costello Syndrome 68 0.439
582
P MTC069 Mitochondrial Disorders 57 0.437
583
P MCR010 Microcephaly 59 0.435
584
CRT004 Carotid Artery Thrombosis 39 0.434
585
LKC009 Leukocyte Adhesion Deficiency, Type I 69 0.425
586
BRK010 Burkitt Lymphoma 65 0.424
587
P OVR082 Overgrowth Syndrome 41 0.424
588
P DMN002 Dementia 65 0.420
589
P PTN014 Patent Ductus Arteriosus 1 59 0.419
590
MTH009 Mouth Disease 57 0.412
591
ART002 Arts Syndrome 66 0.410
592
ANT024 Anthrax Disease 57 0.410
593
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.404
594
P KDN017 Kidney Cancer 60 0.404
596
P HYP069 Hyperparathyroidism 62 0.403
597
P QLT041 Qualitative or Quantitative Defects of Alpha-Dystroglycan 18 0.403
598
c CNG441 Congenital Muscular Dystrophy Due to Dystroglycanopathy 28 0.403
599
P CHR012 Chronic Granulomatous Disease 69 0.397
600
ALL014 Allergic Encephalomyelitis 34 0.397
601
P HRM001 Hermansky-Pudlak Syndrome 65 0.396
602
P TMR010 Tumor Predisposition Syndrome 69 0.388
603
P MLN007 Male Infertility 56 0.388
604
P ENC004 Encephalitis 61 0.388
605
LPT014 Leptin Deficiency or Dysfunction 77 0.386
606
ALB002 Albinism 46 0.386
607
PLM101 Pulmonary Hypertension, Chronic Thromboembolic, Without Deep Vein Thrombosis 37 0.376
608
CHR466 Chronic Thromboembolic Pulmonary Hypertension 47 0.376
609
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.369
610
P GRF003 Graft-Versus-Host Disease 71 0.368
611
ACT003 Acute Kidney Tubular Necrosis 46 0.368
612
P MYT002 Myotonic Dystrophy 51 0.368
613
MNN009 Meningoencephalitis 47 0.368
614
ADN001 Adenosine Deaminase Deficiency 59 0.368
615
OCL006 Ocular Hypertension 53 0.368
616
P PLY019 Polyneuropathy 52 0.367
617
EPD052 Epidermolysis Bullosa Simplex Superficialis 17 0.364
618
LGN006 Legionnaire Disease 52 0.364
619
P HRD011 Hereditary Spherocytosis 63 0.360
620
c ATS307 Autosomal Recessive Cerebellar Ataxia 38 0.353
621
FND002 Fundus Dystrophy 54 0.353
622
P HML001 Hemolytic-Uremic Syndrome 52 0.352
623
P INT143 Interstitial Cystitis 59 0.349
624
P DBT005 Diabetes Insipidus 54 0.349
625
GLM044 Glomerular Disease 34 0.349
626
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 0.347
627
c MSC097 Muscular Dystrophy-Dystroglycanopathy , Type a, 14 29 0.347
628
c MSC099 Muscular Dystrophy-Dystroglycanopathy , Type B, 14 29 0.347
629
c MSC098 Muscular Dystrophy-Dystroglycanopathy , Type C, 14 41 0.347
630
P SPR120 Supranuclear Palsy, Progressive, 1 68 0.347
631
c CNG550 Congenital Muscular Dystrophy-Dystroglycanopathy A14 29 0.347
632
P MLG056 Malignant Hyperthermia 65 0.347
633
MSC077 Muscle Eye Brain Disease 53 0.347
634
GNT167 Genetic Obesity 33 0.347
635
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 60 0.346
636
MSC157 Muscular Dystrophy, Duchenne Type 78 0.345
637
ANX010 Anxiety 70 0.345
638
P SNS001 Sensorineural Hearing Loss 60 0.345
639
MYC005 Myocardial Stunning 45 0.345
640
MLD001 Melioidosis 67 0.344
641
MYL031 Myeloproliferative Neoplasm 66 0.344
642
c HRD010 Hereditary Spastic Paraplegia 65 0.336
643
GRD001 Giardiasis 46 0.336
644
P MTC010 Mitochondrial Dna Depletion Syndrome 46 0.335
645
BLR001 Biliary Atresia 55 0.335
646
FLR002 Filariasis 55 0.335
647
CWP001 Cowpox 44 0.335
648
P WSK001 Wiskott-Aldrich Syndrome 72 0.334
649
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.331
650
HMS001 Hemosiderosis 48 0.331
651
P RRH023 Rare Hereditary Hemochromatosis 52 0.331
652
P DRM053 Dermatitis, Atopic 65 0.324
653
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 70 0.324
654
P MGR003 Migraine with Aura 51 0.324
655
DRM006 Dermatitis 61 0.324
656
DNG002 Dengue Hemorrhagic Fever 59 0.324
657
INH023 Inherited Cancer-Predisposing Syndrome 53 0.324
658
CRN019 Coronary Artery Vasospasm 47 0.324
659
CRN030 Coronary Stenosis 50 0.324
660
c INH020 Inherited Metabolic Disorder 47 0.324
661
c ACT134 Acute Liver Failure 57 0.324
662
c ACR088 Aicardi-Goutieres Syndrome 3 39 0.318
663
P PTT006 Pituitary Adenoma 55 0.318
664
P MGR001 Migraine Without Aura 48 0.318
665
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 55 0.317
666
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.317
667
c HMC039 Hemochromatosis, Type 1 73 0.317
668
AVN001 Avian Influenza 61 0.317
669
AMN003 Amnestic Disorder 53 0.317
670
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 0.317
671
ACH005 Achalasia 54 0.317
672
P ACT105 Acute Mountain Sickness 52 0.317
673
IRN001 Iron Deficiency Anemia 58 0.316
674
ART016 Aortic Aneurysm 68 0.315
675
WST001 West Syndrome 64 0.301
676
c SPN294 Spinocerebellar Ataxia 1 53 0.301
677
HLC007 Helicobacter Pylori Infection 67 0.301
678
MNT001 Mantle Cell Lymphoma 65 0.301
679
c PRM005 Primary Hyperparathyroidism 59 0.301
680
PLR005 Pleuropneumonia 33 0.301
681
BRS051 Breast Disease 58 0.301
682
TBR011 Tuberculous Meningitis 48 0.300
683
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.296
684
P PLY011 Polycystic Ovary Syndrome 57 0.296
685
P OVR049 Ovarian Disease 50 0.296
686
P HYP061 Hypertrophic Cardiomyopathy 68 0.296
687
P CND005 Cone Dystrophy 47 0.282
688
LNN001 Lennox-Gastaut Syndrome 61 0.282
689
P MDL005 Medulloblastoma 75 0.282
690
P CRC039 Coarctation of Aorta 46 0.282
691
SMT008 Smith-Magenis Syndrome 53 0.282
692
LBR036 Leber Plus Disease 67 0.282
693
RSP023 Rasopathy 54 0.282
694
LSS003 Lassa Fever 49 0.282
695
OST003 Osteonecrosis 60 0.280
696
P DDN001 Duodenal Ulcer 52 0.280
697
c FML021 Familial Hypercholesterolemia 71 0.280
698
ANR040 Aneurysm 60 0.280
699
CLS016 Clostridium Difficile Colitis 49 0.273
700
OTT002 Otitis Media 70 0.273
701
c CNG415 Congenital Disorder of Glycosylation, Type Ia 58 0.273
702
MTR002 Mitral Valve Insufficiency 51 0.273
703
HMP005 Hemiplegia 53 0.273
704
P ANG015 Angioedema 56 0.273
705
MST005 Mastitis 52 0.273
706
P CHL066 Cholangitis 51 0.273
707
MLG079 Malignant Pleural Mesothelioma 42 0.273
708
SYN036 Syncope 44 0.273
709
NCL008 Nuclear Ribonucleic Acid 15 0.273
710
PHS004 Phosphoribosylpyrophosphate Synthetase Superactivity 48 0.273
711
SQM013 Squamous Cell Carcinoma, Head and Neck 75 0.273
712
P END044 Endometriosis 62 0.273
713
PRM329 Premature Aging 36 0.273
714
c WLM013 Wilms Tumor 1 65 0.261
715
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 0.261
716
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 0.261
717
c CNT035 Central Nervous System Disease 53 0.261
718
EMB004 Embryonal Carcinoma 55 0.261
719
P RNL015 Renal Hypertension 45 0.261
720
P HYD006 Hydrocephalus 62 0.261
722
P VTR007 Vitreoretinopathy 45 0.261
723
DCT002 Ductal Carcinoma in Situ 58 0.260
724
c ANM038 Anemia, Autoimmune Hemolytic 63 0.260
725
KPS004 Kaposi Sarcoma 76 0.260
726
P HMN010 Hemangioma 61 0.260
727
P ACN011 Acne 55 0.260
728
LCH001 Leech Infestation 37 0.260
729
P PRP029 Porphyria 60 0.260
730
FLR001 Filarial Elephantiasis 59 0.260
731
HMG002 Hemoglobinuria 50 0.260
732
GRN017 Granulocytopenia 42 0.260
733
CNG506 Congenital Amyoplasia 27 0.260
734
P CLC063 Celiac Disease 1 65 0.246
735
VRC005 Varicose Veins 59 0.246
736
PLT016 Platelet Adenylate Cyclase Activity 16 0.246
737
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 44 0.246
738
CLF027 Cleft Palate, Isolated 64 0.246
739
MVL001 Mevalonic Aciduria 65 0.246
740
c CHR711 Chronic Asthma 41 0.246
741
PRP036 Peripheral T-Cell Lymphoma 52 0.246
742
BRN012 Bronchiolitis Obliterans 56 0.246
743
STR103 Streptococcus Pneumonia 47 0.246
744
VLK001 Volkmann Contracture 23 0.246
745
P END033 Endocarditis 58 0.246
746
BRN002 Bronchiolitis 57 0.246
747
BLD131 Bladder Urothelial Carcinoma 59 0.246
748
GNG013 Gingivitis 59 0.246
749
P ART023 Arthropathy 59 0.246
750
VSC003 Visceral Leishmaniasis 54 0.246
751
P PLM034 Pulmonary Emphysema 58 0.246
752
HYP835 Hypothalamic Obesity 38 0.246
753
MTB016 Metabolic Myopathy 30 0.246
754
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.238
755
P FML023 Familial Hemiplegic Migraine 53 0.238
756
DNG001 Dengue Shock Syndrome 40 0.238
757
SCH078 Schimmelpenning-Feuerstein-Mims Syndrome 59 0.238
758
P PLY006 Polydactyly 58 0.238
759
HYP114 Hypertensive Nephropathy 35 0.238
760
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.238
761
P JBR020 Joubert Syndrome 1 74 0.238
762
P MMB011 Membranous Nephropathy 50 0.238
763
NVS017 Nevus, Epidermal 66 0.238
764
EPD015 Epidemic Typhus 44 0.238
765
FCT005 Factor Xiii Deficiency 55 0.238
766
PPL022 Papilloma 53 0.238
767
CNN005 Connective Tissue Disease 66 0.238
768
SQM002 Squamous Cell Papilloma 45 0.238
769
CRV040 Cervix Carcinoma 50 0.238
770
HRT012 Heart Valve Disease 53 0.238
771
ATN005 Autonomic Dysfunction 45 0.238
772
WBR001 Weber Syndrome 38 0.238
773
SPS019 Spastic Paraparesis 38 0.238
774
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 64 0.237
775
c ART115 Aortic Valve Disease 1 72 0.237
776
SPP011 Suppression of Tumorigenicity 12 61 0.237
777
BRT054 Brittle Bone Disorder 74 0.237
778
P NSP012 Nasopharyngeal Carcinoma 60 0.237
779
HTC003 Hutchinson-Gilford Progeria Syndrome 65 0.237
780
THY111 Thyroid Carcinoma, Familial Medullary 67 0.237
781
HMR023 Hemorrhagic Cystitis 43 0.237
782
PNC001 Pancytopenia 52 0.237
783
OST015 Osteochondrodysplasia 60 0.237
784
PST028 Post-Traumatic Stress Disorder 58 0.237
785
P GCH001 Gaucher's Disease 69 0.237
786
P LRY044 Larynx Cancer 53 0.237
787
THY125 Thyroid Gland Medullary Carcinoma 48 0.237
788
GTR002 Goiter 52 0.237
789
HLL004 Hellp Syndrome 53 0.237
790
BLR013 Biliary Tract Cancer 43 0.237
791
P CRB059 Cerebellar Degeneration 36 0.237
792
c GRS014 Griscelli Syndrome, Type 2 52 0.210
793
c SPS151 Spastic Paraplegia 11, Autosomal Recessive 52 0.210
794
P HRD021 Hereditary Sensory Neuropathy 48 0.210
795
CLB010 Coloboma of Macula 53 0.210
796
BRT002 Birt-Hogg-Dube Syndrome 64 0.210
797
NRL016 Neural Tube Defects 80 0.210
798
LYM133 Lymphoma, Hodgkin, Classic 69 0.210
799
STR039 Sturge-Weber Syndrome 60 0.210
800
c CHR408 Charcot-Marie-Tooth Disease, X-Linked Recessive, 5 43 0.210
801
TRD006 Tardive Dyskinesia 53 0.210
802
P PRV002 Periventricular Nodular Heterotopia 52 0.210
803
PNS018 Pain Sensitivity Quantitative Trait Locus 1 23 0.210
804
P LSS002 Lissencephaly 52 0.210
805
c SPS125 Spastic Paraplegia 15, Autosomal Recessive 51 0.210
806
PBL005 Piebald Trait 60 0.210
807
P SJG008 Sjogren Syndrome 60 0.210
808
c PLM127 Pulmonary Hypertension, Primary, 3 34 0.210
809
PRV020 Periventricular Heterotopia with Microcephaly, Autosomal Recessive 26 0.210
810
c SVR003 Severe Congenital Neutropenia 59 0.210
811
OBS082 Obstructive Nephropathy 41 0.210
812
P GRS003 Griscelli Syndrome 54 0.210
813
PTN001 Patent Foramen Ovale 61 0.210
814
MNK002 Monkeypox 41 0.210
815
NRT004 Neuritis 53 0.210
816
P ATR010 Atrial Heart Septal Defect 58 0.210
817
P BRD002 Bardet-Biedl Syndrome 66 0.210
818
BRC012 Brucellosis 66 0.210
819
IGG001 Iga Glomerulonephritis 50 0.210
820
ATN004 Autonomic Neuropathy 42 0.210
821
P MTH007 Methemoglobinemia 46 0.210
822
AZS001 Azoospermia 45 0.210
823
c SVR107 Severe Congenital Neutropenia 3 20 0.210
824
BRN026 Branch Retinal Artery Occlusion 41 0.210
825
SCB001 Scabies 49 0.210
826
TCL001 T-Cell Adult Acute Lymphocytic Leukemia 42 0.210
827
P PMP001 Pemphigus 54 0.210
828
P TRC031 Trichorhinophalangeal Syndrome 37 0.210
829
P RTN014 Retinal Artery Occlusion 46 0.210
830
P PRM011 Primary Ciliary Dyskinesia 68 0.210
831
c RNG019 Ring Chromosome 3 19 0.210
832
c SPS025 Spastic Paraplegia 15 30 0.210
833
NDL022 Nodular Neuronal Heterotopia 30 0.210
834
P HRD217 Hereditary Optic Neuropathy 36 0.210
835
c HMN021 Human T-Cell Leukemia Virus Type 1 46 0.210
836
INF034 Infective Endocarditis 53 0.209
837
P APL001 Aplastic Anemia 72 0.209
838
P HML033 Hemolytic Uremic Syndrome, Atypical 1 67 0.209
839
P MCH002 Machado-Joseph Disease 62 0.209
840
GST092 Gastroesophageal Reflux 59 0.209
841
c HYP604 Hyperinsulinemic Hypoglycemia, Familial, 2 65 0.209
842
MLG141 Malignant Atrophic Papulosis 35 0.209
843
HYP457 Hypertrophic Scars 42 0.209
844
P SML001 Small Cell Carcinoma 52 0.209
845
P OCL002 Oculocutaneous Albinism 59 0.209
846
P XRD029 Xeroderma Pigmentosum, Complementation Group a 55 0.209
847
ENT011 Enterocolitis 55 0.209
848
c MSC037 Muscular Dystrophy-Dystroglycanopathy , Type a, 4 59 0.209
850
c BRS111 Breast-Ovarian Cancer, Familial 2 53 0.209
851
P MYG005 Myoglobinuria 40 0.209
852
INV001 Invasive Aspergillosis 48 0.209
853
PRS119 Persistent Genital Arousal Disorder 18 0.209
854
QFV001 Q Fever 61 0.209
855
HND002 Hand, Foot and Mouth Disease 50 0.209
856
P LPS002 Liposarcoma 64 0.209
857
CLC006 Calcinosis 47 0.209
858
c MLG084 Malignant Fibrous Histiocytoma 62 0.209
859
DYS018 Dysostosis 43 0.209
860
P RTN022 Retinal Vein Occlusion 54 0.209
861
P SPN046 Spinal Muscular Atrophy 62 0.209
862
P PYL005 Pyelonephritis 56 0.209
863
SMN007 Seminoma 42 0.209
864
INT066 Interstitial Lung Disease 60 0.209
865
LST001 Listeriosis 59 0.209
866
RTN003 Retinal Ischemia 48 0.209
867
c ACT068 Acute Cystitis 60 0.209
868
PRM013 Premature Menopause 57 0.209
869
P ART018 Aortic Valve Insufficiency 52 0.209
870
ACT084 Acute Stress Disorder 53 0.209
871
P FBR003 Fibrous Histiocytoma 43 0.209
872
P ATR005 Atrophic Gastritis 50 0.209
873
CHL045 Choline Deficiency Disease 39 0.209
874
CHR066 Chronic Fatigue Syndrome 59 0.209
875
PRN019 Perinatal Necrotizing Enterocolitis 60 0.209
876
CND006 Candida Glabrata 29 0.209
877
CHR178 Chromosomal Triplication 33 0.209
878
P ACT241 Acute Bilirubin Encephalopathy 26 0.209
879
MYT011 Myotonia 37 0.209
880
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.174
881
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 33 0.174
882
P NNS032 Non-Syndromic X-Linked Intellectual Disability 46 0.174
883
c HNT004 Huntington Disease-Like 2 51 0.174
884
HPT067 Hepatocellular Adenoma 42 0.174
885
FBR054 Fibroma 44 0.174
886
c SYN064 Syndromic X-Linked Intellectual Disability 25 0.174
887
CRN048 Craniofacial-Deafness-Hand Syndrome 52 0.174
888
P SRC025 Sarcoidosis 1 70 0.174
889
P PLV020 Pelvic Organ Prolapse 57 0.174
890
RYN001 Raynaud Disease 49 0.174
891
DGR001 Digeorge Syndrome 62 0.174
892
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 64 0.174
893
c GLY008 Glycogen Storage Disease Ii 72 0.174
894
LKN001 Leukoencephalopathy with Vanishing White Matter 63 0.174
895
c LNG048 Long Qt Syndrome 3 52 0.174
896
ISL014 Isolated Growth Hormone Deficiency, Type Ia 54 0.174
897
c XRD030 Xeroderma Pigmentosum, Complementation Group C 55 0.174
898
HYP611 Hypoparathyroidism, X-Linked 29 0.174
899
P BRC006 Brachydactyly 52 0.174
900
P MSC002 Muscular Dystrophy-Dystroglycanopathy 36 0.174
901
P ALT001 Alternating Hemiplegia of Childhood 56 0.174
902
c MTC062 Mitochondrial Dna Depletion Syndrome 2 44 0.174
903
BLD171 Blood Group, Lewis System 21 0.174
904
c CHL119 Cholangitis, Primary Sclerosing 57 0.174
905
c CNG208 Congenital Disorder of Glycosylation, Type Iic 47 0.174
906
c PRX094 Paroxysmal Nocturnal Hemoglobinuria 1 30 0.174
907
CHR081 Choroideremia 58 0.174
908
PRP083 Porphyria, Acute Intermittent 64 0.174
909
P LPR021 Leprosy 3 71 0.174
910
WRN001 Werner Syndrome 69 0.174
911
c TBR026 Tuberous Sclerosis 2 71 0.174
912
ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 35 0.174
913
c PRG038 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 2 49 0.174
914
c NPH073 Nephrotic Syndrome, Type 8 26 0.174
915
c PRG040 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 4 52 0.174
916
c MSC182 Muscular Dystrophy-Dystroglycanopathy , Type C, 15 31 0.174
917
INS015 Inosine Triphosphatase Deficiency 22 0.174
918
c LKM056 Leukemia, Chronic Lymphocytic 2 47 0.174
919
P PRG130 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 1 54 0.174
920
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 62 0.174
921
MCS002 Mucositis 55 0.174
922
P MMP001 Mumps 56 0.174
923
TLR001 Tularemia 56 0.174
924
NRL005 Neurilemmoma 60 0.174
925
LPT001 Leptospirosis 65 0.174
926
P SCL009 Sclerosing Cholangitis 46 0.174
927
c FML015 Familial Nephrotic Syndrome 48 0.174
928
PRS042 Prostate Disease 42 0.174
929
END041 Endometrial Adenocarcinoma 63 0.174
930
CYS014 Cystadenocarcinoma 51 0.174
931
TRT001 Teratocarcinoma 41 0.174
932