Search results for Guanosine triphosphate

1152 hits were found for Guanosine triphosphate

# Family MCID Name MIFTS Score
1
P HYP605 Hyperphenylalaninemia, Bh4-Deficient, B 44 22.674
2
INS015 Inosine Triphosphatase Deficiency 22 16.869
3
PRT037 Pertussis 49 14.109
4
CHL014 Cholera 62 8.422
5
HMN044 Human Immunodeficiency Virus Type 1 76 8.088
6
IMM167 Immune Deficiency Disease 76 6.394
7
P HRP006 Herpes Simplex 65 6.393
8
P NRB001 Neuroblastoma 66 6.265
9
HLX001 Helix Syndrome 47 5.149
10
IMP005 Impotence 52 5.136
11
PRN001 Purine Nucleoside Phosphorylase Deficiency 53 5.119
12
VCC001 Vaccinia 49 5.111
13
c HPT001 Hepatitis C 61 4.938
14
P PHC003 Pheochromocytoma 70 4.855
15
ADR040 Adrenal Gland Pheochromocytoma 45 4.850
16
P DYS154 Dystonia 64 4.747
17
ISC004 Ischemia 61 4.669
18
P PLM037 Pulmonary Hypertension 69 4.421
19
c HPT073 Hepatitis C Virus 70 4.349
20
48X005 48,xyyy 39 4.292
21
ANX004 Anoxia 40 4.218
22
P LKM062 Leukemia, Acute Lymphoblastic 69 4.164
23
RPD005 Rapidly Involuting Congenital Hemangioma 48 4.118
24
P LKM071 Leukemia, Chronic Lymphocytic 74 4.000
25
P ATR011 Atrial Fibrillation 66 3.986
26
STM007 Stomatitis 52 3.939
27
P LNG032 Lung Cancer 98 3.904
28
CYS001 Cystic Fibrosis 77 3.863
29
HYP266 Hypoxia 56 3.839
30
P LKM002 Leukemia 65 3.773
31
P HPT021 Hepatitis 68 3.686
32
ACQ007 Acquired Immunodeficiency Syndrome 58 3.679
33
GLM045 Glioma 62 3.675
34
GLL048 Glial Tumor 51 3.644
35
TXC005 Toxic Shock Syndrome 61 3.563
36
c LKM061 Leukemia, Acute Myeloid 83 3.535
37
P ALZ034 Alzheimer Disease 87 3.445
38
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 3.425
39
SPN186 Spinal Cord Injury 60 3.375
40
GLB002 Glioblastoma 67 3.370
41
CYT002 Cytokine Deficiency 43 3.360
42
c SML038 Small Cell Cancer of the Lung 68 3.282
43
AGN016 Aging 53 3.271
44
BRN071 Brain Injury 50 3.265
45
P HPT023 Hepatocellular Carcinoma 95 3.262
46
HMN014 Human Immunodeficiency Virus Infectious Disease 54 3.253
47
c HYP807 Hyperinsulinemic Hypoglycemia, Familial, 6 52 3.248
48
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 3.169
49
HYP060 Hyperinsulinism 53 3.110
50
P GLM040 Glioma Susceptibility 1 70 3.107
51
MLG169 Malignant Astrocytoma 57 3.078
52
HYP141 Hyperphenylalaninemia 42 3.064
53
TRM010 Traumatic Brain Injury 50 3.059
54
PLM129 Pulmonary Disease, Chronic Obstructive 74 3.003
55
c ACT073 Acute Leukemia 59 2.990
56
P MYL006 Myeloid Leukemia 60 2.983
57
47X002 47,xyy 47 2.947
58
CLT003 Colitis 63 2.938
59
CRB004 Cerebral Artery Occlusion 45 2.934
60
c PLM164 Pulmonary Hypertension, Primary, 1 75 2.919
61
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 2.917
62
DFC004 Deficiency Anemia 74 2.904
63
OST159 Osteogenic Sarcoma 66 2.881
64
c PRC016 Pre-Eclampsia 64 2.853
65
PRS045 Prostatic Hypertrophy 53 2.852
66
CHC001 Chickenpox 56 2.842
67
c TYP009 Type 2 Diabetes Mellitus 91 2.829
68
P INF037 Inflammatory Bowel Disease 53 2.828
69
NRR001 Neuroretinitis 42 2.814
70
RTN023 Retinitis 45 2.814
71
c HPT016 Hepatitis B 62 2.801
72
END086 End Stage Renal Disease 54 2.799
73
c MGR028 Migraine with or Without Aura 1 63 2.695
74
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 2.670
75
c LKM005 Leukemia, T-Cell, Chronic 33 2.670
76
P GST053 Gastric Cancer 82 2.660
77
PRS021 Prostatic Adenoma 43 2.643
78
FTT001 Fatty Liver Disease 61 2.636
79
PRS129 Prostatic Hyperplasia, Benign 48 2.630
80
HYP056 Hypoglycemia 65 2.603
81
P TRM003 Tremor 50 2.592
82
P HRT032 Heart Disease 84 2.582
83
P MLN008 Melanoma 75 2.576
84
CRH001 Crohn's Disease 80 2.571
85
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 59 2.570
86
CRN030 Coronary Stenosis 50 2.515
87
P MYP004 Myopathy 67 2.509
88
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 2.502
89
c MCR133 Microvascular Complications of Diabetes 4 41 2.501
90
c MCR113 Microvascular Complications of Diabetes 3 52 2.501
91
c MCR130 Microvascular Complications of Diabetes 6 41 2.501
92
c MCR120 Microvascular Complications of Diabetes 7 47 2.501
93
ANG054 Angina Pectoris 65 2.500
94
TTN003 Tetanus 64 2.478
95
MNT002 Mental Depression 56 2.471
96
c HYP595 Hypertension, Essential 84 2.468
97
DPR016 Depression 64 2.463
98
ALL029 Allergic Disease 61 2.457
99
P MJR001 Major Depressive Disorder 68 2.445
100
PPL052 Papillomatosis, Confluent and Reticulated 34 2.440
101
NNL005 Non-Alcoholic Fatty Liver Disease 63 2.420
102
c DLT002 Dilated Cardiomyopathy 79 2.419
103
TTR005 Tetrahydrobiopterin Deficiency 49 2.410
104
DYS192 Dystonia, Dopa-Responsive 56 2.390
105
GTP002 Gtp Cyclohydrolase 1-Deficient Dopa-Responsive Dystonia 17 2.381
106
MDD018 Middle East Respiratory Syndrome 44 2.375
107
HYP066 Hyperglycemia 60 2.367
108
LPP008 Lipoprotein Quantitative Trait Locus 65 2.357
109
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 44 2.314
110
ULC004 Ulcerative Colitis 74 2.306
111
SYN036 Syncope 44 2.302
112
P VSC007 Vascular Disease 62 2.299
113
P ENC018 Encephalopathy 62 2.298
114
LWC001 Low Compliance Bladder 44 2.298
115
BRN004 Brain Edema 54 2.294
116
HYP005 Hypokalemia 55 2.275
117
ATH013 Atherosclerosis Susceptibility 63 2.272
118
ART140 Arteries, Anomalies of 52 2.270
119
PHN003 Phenylketonuria 76 2.265
120
P DBT009 Diabetes Mellitus 67 2.265
121
BNR002 Bone Resorption Disease 47 2.263
122
LVR012 Liver Cirrhosis 62 2.246
123
c ACT071 Acute Kidney Failure 60 2.231
124
P HML002 Hemolytic Anemia 62 2.220
125
OCL069 Ocular Motor Apraxia 57 2.216
126
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 2.212
127
P PRK039 Parkinsonism 55 2.204
128
P RTN008 Retinitis Pigmentosa 79 2.201
129
P LVR013 Liver Disease 68 2.201
130
P HYP265 Hypotonia 42 2.199
131
MDD011 Mood Disorder 61 2.199
132
c CHR684 Chronic Kidney Disease 73 2.194
133
SVR001 Severe Acute Respiratory Syndrome 68 2.188
134
CHG001 Chagas Disease 65 2.175
135
INS001 Insulinoma 59 2.169
136
P OVR042 Ovarian Cancer 88 2.150
137
SVR004 Severe Combined Immunodeficiency 70 2.118
138
P SZR006 Seizure Disorder 69 2.086
139
c BRN108 Branchiootic Syndrome 1 63 2.080
140
P KLZ004 Kala-Azar 1 41 2.077
141
LSH001 Leishmaniasis 63 2.077
142
P CRN300 Coronary Heart Disease 1 73 2.075
143
HPT004 Hepatic Coma 43 2.054
144
c SYS001 Systemic Lupus Erythematosus 85 2.051
145
P RTN016 Retinal Degeneration 52 2.038
146
P AST005 Asthma 75 2.037
147
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 2.035
148
OVR094 Ovarian Epithelial Cancer 39 2.029
149
INS024 Insulin-Like Growth Factor I 77 2.017
150
P LNG064 Lung Cancer Susceptibility 3 69 1.994
151
CHL068 Cholestasis 61 1.994
152
LNG099 Lung Disease 62 1.983
153
P GLM007 Glomerulonephritis 59 1.982
154
PRT013 Portal Hypertension 59 1.978
155
c HYP836 Hypercholesterolemia, Familial, 1 73 1.965
156
P HYP076 Hyperthyroidism 53 1.953
157
P EXN002 Exanthem 58 1.947
158
P LCT001 Lactic Acidosis 50 1.935
159
GT001 Gout 63 1.924
160
P LPS004 Lupus Erythematosus 61 1.911
161
PLY150 Polykaryocytosis Inducer 29 1.906
162
HYP014 Hyperuricemia 51 1.889
163
c MCR115 Microvascular Complications of Diabetes 5 65 1.888
164
P HYP098 Hypereosinophilic Syndrome 66 1.876
165
P ADL010 Adult Respiratory Distress Syndrome 70 1.865
166
CNG034 Congestive Heart Failure 69 1.844
167
P CHR345 Chronic Pain 50 1.837
168
LPD008 Lipid Metabolism Disorder 61 1.835
169
RNL114 Renal Cell Carcinoma, Nonpapillary 79 1.835
170
c DNT047 Dentinogenesis Imperfecta Type 2 35 1.829
171
PST011 Pustulosis of Palm and Sole 52 1.828
172
P PSR002 Psoriasis 63 1.828
173
P KDN018 Kidney Disease 71 1.824
174
P CRD119 Cardiac Arrest 68 1.821
175
c TYP008 Type 1 Diabetes Mellitus 77 1.807
176
P THR014 Thrombocytopenia 66 1.794
177
c ATR087 Atrial Standstill 1 74 1.785
178
MYL009 Myelodysplastic Syndrome 67 1.785
179
P MYC084 Mycobacterium Tuberculosis 1 68 1.779
180
P INF038 Influenza 68 1.779
181
c LKM063 Leukemia, Chronic Myeloid 70 1.776
182
c VRL010 Viral Hepatitis 52 1.768
183
LSC001 Lesch-Nyhan Syndrome 62 1.759
184
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 1.758
185
CRV035 Cervical Cancer 72 1.756
186
P MLT020 Multiple Sclerosis 79 1.749
187
c HYP326 Hyperinsulinemic Hypoglycemia, Familial, 5 50 1.747
188
c HYP271 Hyperinsulinemic Hypoglycemia, Familial, 4 52 1.747
189
P CTN015 Cutaneous T Cell Lymphoma 48 1.744
190
ALC007 Alcohol Dependence 65 1.735
191
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 1.734
192
P RHN004 Rhinitis 56 1.730
193
P FLL037 Follicular Lymphoma 66 1.729
194
NNL006 Non-Alcoholic Steatohepatitis 54 1.721
195
P PNC035 Pancreatic Cancer 87 1.710
196
CHL123 Chlamydia 58 1.709
197
P OBS001 Obstructive Jaundice 49 1.709
198
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 1.705
199
P INF032 Infertility 60 1.702
200
P NRF002 Neurofibromatosis 60 1.701
201
P SCK005 Sickle Cell Disease 56 1.701
202
P NTR004 Neutropenia 62 1.698
203
PNG002 Pain Agnosia 51 1.687
204
P INT143 Interstitial Cystitis 59 1.681
205
SPL018 Splenomegaly 47 1.681
206
DPH001 Diphtheria 59 1.676
207
HGH043 High Grade Glioma 46 1.674
208
P MYC007 Myocardial Infarction 69 1.667
209
BRN024 Bronchitis 67 1.663
210
P ADL017 Adult T-Cell Leukemia 53 1.661
211
ADN001 Adenosine Deaminase Deficiency 59 1.659
212
P BCL017 B-Cell Lymphoma 57 1.656
213
GST033 Gestational Diabetes 60 1.650
214
P MSC005 Muscular Dystrophy 66 1.641
215
P CYS018 Cystitis 58 1.638
216
ESP021 Esophageal Cancer 84 1.633
217
MTB004 Metabolic Acidosis 48 1.614
218
P DNG005 Dengue Virus 55 1.611
219
P SKN015 Skin Carcinoma 71 1.604
220
P OPT006 Optic Nerve Disease 57 1.599
221
MSL001 Measles 61 1.594
222
FBR047 Fibromyalgia 57 1.593
223
c PCH010 Pachyonychia Congenita 3 43 1.575
224
P PRD008 Periodontitis 63 1.575
225
HMP009 Haemophilus Influenzae 41 1.569
226
CLN015 Colon Adenocarcinoma 64 1.560
227
P EPL164 Epilepsy 70 1.544
228
RNL077 Renal Fibrosis 46 1.529
229
P MYC008 Myocarditis 59 1.528
230
TRC003 Trichomoniasis 53 1.527
231
LYM019 Lymphosarcoma 46 1.523
232
PRT251 Proteinuria, Chronic Benign 58 1.505
233
P PRP019 Peripheral Nervous System Disease 57 1.504
234
P MLG056 Malignant Hyperthermia 65 1.503
235
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 1.502
236
P NRP001 Neuropathy 59 1.493
237
SLP001 Sleeping Sickness 56 1.493
238
P CNR004 Cone-Rod Dystrophy 2 74 1.488
239
MYC005 Myocardial Stunning 45 1.487
240
BRK010 Burkitt Lymphoma 65 1.478
241
TCL027 T-Cell Acute Lymphoblastic Leukemia 52 1.473
242
P SCH015 Schizophrenia 74 1.472
243
P BND020 Bone Disease 60 1.468
244
c MJR022 Major Affective Disorder 8 37 1.468
245
c MJR024 Major Affective Disorder 9 40 1.468
246
P BPL003 Bipolar Disorder 56 1.468
247
CMB007 Combined Immunodeficiency 56 1.461
248
HRY003 Hairy Cell Leukemia 53 1.458
249
HPT019 Hepatic Encephalopathy 59 1.455
250
P HNT016 Huntington Disease 73 1.452
251
c OPT053 Optic Atrophy 1 62 1.451
252
DBT010 Diabetic Neuropathy 54 1.449
253
TRY001 Trypanosomiasis 50 1.443
254
c FML001 Familial Atrial Fibrillation 65 1.440
255
MLR004 Malaria 77 1.438
256
MTC005 Mitochondrial Metabolism Disease 44 1.437
257
P MVM001 Movement Disease 61 1.430
258
SGW002 Segawa Syndrome, Autosomal Recessive 44 1.429
259
MST004 Mast Cell Neoplasm 41 1.427
260
EXT007 Extracutaneous Mastocytoma 38 1.427
261
P PRS040 Prostate Cancer 95 1.427
262
HMN047 Human Cytomegalovirus Infection 59 1.425
263
HRW001 Hair Whorl 35 1.424
264
P TTR001 Tetralogy of Fallot 69 1.419
266
P BRN022 Bronchiectasis 59 1.396
267
P PRK057 Parkinson Disease, Late-Onset 79 1.390
268
VLK001 Volkmann Contracture 23 1.386
269
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 1.383
270
P BRS047 Breast Cancer 97 1.381
271
P CHN059 Chondrocalcinosis 51 1.380
272
BLR008 Bilirubin Metabolic Disorder 57 1.377
273
BCT022 Bacterial Infectious Disease 55 1.377
274
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 1.376
275
CRT015 Carotid Artery Occlusion 45 1.366
276
ADR016 Adrenal Cortical Carcinoma 61 1.363
277
ADR054 Adrenocortical Carcinoma, Hereditary 47 1.363
278
ADR004 Adrenal Cortical Adenocarcinoma 38 1.363
279
c AMY091 Amyotrophic Lateral Sclerosis 1 87 1.360
280
P LTR001 Lateral Sclerosis 57 1.360
281
c ACT134 Acute Liver Failure 57 1.358
282
P BRB001 Beriberi 44 1.353
283
ALL014 Allergic Encephalomyelitis 34 1.339
284
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 40 1.339
285
CHR073 Choreatic Disease 53 1.339
286
P OLG002 Oligodendroglioma 66 1.338
287
c INH030 Inherited Retinal Disorder 28 1.336
288
P NPH012 Nephrotic Syndrome 61 1.334
289
IRR002 Irritable Bowel Syndrome 64 1.332
290
ORL015 Oral Squamous Cell Carcinoma 43 1.331
291
P GLL022 Guillain-Barre Syndrome 59 1.318
292
LYM040 Lymphoblastic Lymphoma 53 1.317
293
ARG004 Argyria 26 1.317
294
P UVT001 Uveitis 57 1.314
295
P ECL001 Eclampsia 52 1.311
296
c SCN036 Secondary Progressive Multiple Sclerosis 55 1.311
297
DGN001 Degenerative Disc Disease 48 1.291
298
P MLN007 Male Infertility 56 1.289
299
VRL011 Viral Infectious Disease 60 1.287
300
P CLR023 Colorectal Cancer 100 1.286
301
IRN002 Iron Metabolism Disease 56 1.284
302
P MYP006 Myopia 55 1.282
303
SXL003 Sexual Disorder 49 1.280
304
DMY004 Demyelinating Disease 50 1.278
305
P URN019 Urinary Tract Infection 48 1.276
306
P MTC133 Mitochondrial Myopathy 51 1.275
307
PRT036 Peritonitis 65 1.273
308
ACT098 Acute Erythroid Leukemia 55 1.273
309
P NNT058 Neonatal Diabetes 52 1.273
310
P HRD217 Hereditary Optic Neuropathy 36 1.265
311
CLS049 Classic Phenylketonuria 34 1.264
312
P ENC004 Encephalitis 61 1.260
313
c ACT027 Acute Pancreatitis 60 1.258
314
INT007 Intermediate Coronary Syndrome 53 1.256
315
P GRV001 Graves' Disease 54 1.244
316
WLL004 Wallerian Degeneration 38 1.227
317
VSC003 Visceral Leishmaniasis 54 1.227
318
SKN019 Skin Melanoma 70 1.225
319
SPN035 Spindle Cell Sarcoma 51 1.224
320
SRC014 Sarcoma 64 1.224
321
GRW007 Growth Hormone Deficiency 47 1.219
322
P BLD134 Bladder Cancer 79 1.214
323
P ADN016 Adenocarcinoma 63 1.214
324
P MYC033 Myoclonus 46 1.213
325
ATM095 Autoimmune Disease 61 1.208
326
P NSP012 Nasopharyngeal Carcinoma 60 1.200
327
CNS004 Constipation 56 1.198
328
P ESN008 Eosinophilic Pneumonia 50 1.195
329
URT010 Ureteral Obstruction 44 1.193
330
P MSC003 Muscular Atrophy 52 1.186
331
P END044 Endometriosis 62 1.178
332
HYP264 Hypertonia 35 1.176
333
ATS010 Autosomal Recessive Disease 42 1.176
334
CHD001 Chediak-Higashi Syndrome 66 1.172
335
ALL003 Allergic Rhinitis 66 1.169
336
P PLM036 Pulmonary Fibrosis 65 1.168
337
LWG006 Low Grade Glioma 41 1.167
338
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 1.167
339
SQM006 Squamous Cell Carcinoma 59 1.157
340
P ATX030 Ataxia-Telangiectasia 80 1.157
341
TLN003 Telangiectasis 51 1.157
342
STR067 Stroke, Ischemic 79 1.153
343
PLS011 Plasmacytoma 56 1.148
344
ADN018 Adenoma 58 1.143
345
P BRS044 Breast Adenocarcinoma 58 1.140
346
GRY002 Gray Platelet Syndrome 57 1.135
347
PLM010 Pulmonary Edema 54 1.134
348
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 36 1.133
349
MSC157 Muscular Dystrophy, Duchenne Type 78 1.131
350
MTB016 Metabolic Myopathy 30 1.128
351
CHL004 Cholelithiasis 48 1.126
352
RSP007 Respiratory Distress Syndrome, Infant 41 1.126
353
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 1.124
354
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 1.120
355
P ALP008 Alopecia 53 1.110
356
BRN056 Bronchopulmonary Dysplasia 57 1.108
357
P RHM011 Rheumatoid Arthritis 81 1.105
358
P VSC011 Vasculitis 61 1.104
359
GN1001 Gnao1 Encephalopathy 11 1.099
360
P SRC025 Sarcoidosis 1 70 1.098
361
P SCK002 Sick Sinus Syndrome 55 1.095
362
CRB090 Cerebral Hypoxia 42 1.095
363
OST012 Osteoarthritis 77 1.095
364
PNC041 Pancreatic Ductal Adenocarcinoma 51 1.093
365
GNT003 Genital Herpes 54 1.091
366
THY029 Thyroid Carcinoma 55 1.091
367
P LPR021 Leprosy 3 71 1.086
368
HNS001 Hansen's Disease 32 1.086
369
P PNC044 Pancreatitis 61 1.077
370
THR004 Thrombocytosis 52 1.077
371
P GRF003 Graft-Versus-Host Disease 71 1.069
372
P MCR010 Microcephaly 59 1.062
373
ACT119 Acute Promyelocytic Leukemia 62 1.059
374
P HDC001 Headache 56 1.056
375
P RTN024 Retinoblastoma 72 1.055
376
MTH009 Mouth Disease 57 1.053
377
CRD132 Cardiac Conduction Defect 59 1.049
378
KRT009 Keratosis 52 1.047
379
ANT024 Anthrax Disease 57 1.047
380
THR024 Thrombosis 56 1.047
381
LYM027 Lymphopenia 56 1.041
382
P ART022 Arthritis 70 1.039
383
GLC003 Glucose Intolerance 53 1.037
384
MYL069 Myeloma, Multiple 76 1.032
385
c HYP604 Hyperinsulinemic Hypoglycemia, Familial, 2 65 1.031
386
P FBR017 Fibrosarcoma 55 1.024
387
P TMP001 Temporal Lobe Epilepsy 49 1.024
388
c ATM011 Autoimmune Hepatitis 62 1.023
389
TRS021 Triosephosphate Isomerase Deficiency 44 1.011
390
P LYM118 Lymphoma 66 1.006
391
P RSP003 Respiratory Failure 73 0.999
392
P HYP086 Hypothyroidism 68 0.998
393
PLG002 Plague 58 0.996
394
PYR041 Pyruvate Kinase Deficiency of Red Cells 56 0.993
395
LBR038 Leber Hereditary Optic Neuropathy, Modifier of 62 0.993
396
c GLL024 Gallbladder Disease 1 53 0.993
397
INT066 Interstitial Lung Disease 60 0.993
398
P HYP061 Hypertrophic Cardiomyopathy 68 0.991
399
PPT005 Peptic Ulcer Disease 58 0.990
400
KRN002 Kearns-Sayre Syndrome 62 0.989
401
CRN019 Coronary Artery Vasospasm 47 0.986
402
MST005 Mastitis 52 0.986
403
SFT003 Soft Tissue Sarcoma 43 0.983
404
P BDY004 Body Mass Index Quantitative Trait Locus 11 82 0.981
405
P MYS003 Myasthenia Gravis 67 0.980
406
END057 Endometrial Cancer 76 0.977
407
P SLP006 Sleep Apnea 69 0.973
408
P EYD002 Eye Disease 57 0.972
409
P MTC010 Mitochondrial Dna Depletion Syndrome 46 0.972
410
SKN016 Skin Disease 63 0.969
411
YLL002 Yellow Fever 61 0.967
412
c CHR688 Chronic Acquired Demyelinating Polyneuropathy 16 0.966
413
HRP004 Herpes Zoster 60 0.964
414
P ACT008 Actinic Keratosis 53 0.964
415
c GRV008 Graves Disease 1 54 0.958
416
PTH003 Pathologic Nystagmus 52 0.957
417
ALL006 Allergic Asthma 55 0.954
418
BRN032 Brain Glioma 45 0.951
419
P MNN013 Meningitis 65 0.944
420
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 0.943
421
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 0.943
422
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.943
423
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.943
424
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.943
425
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 0.943
426
c BDY019 Body Mass Index Quantitative Trait Locus 18 46 0.943
427
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.943
428
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.943
429
P CHL066 Cholangitis 51 0.942
430
RTN020 Retinal Vascular Disease 45 0.941
431
DSS032 Disease by Infectious Agent 55 0.936
432
MSN001 Mesangial Proliferative Glomerulonephritis 44 0.935
433
P PRL003 Proliferative Glomerulonephritis 43 0.935
434
c CHR095 Chronic Progressive External Ophthalmoplegia 48 0.930
435
MRP001 Morphine Dependence 41 0.925
436
P SNS001 Sensorineural Hearing Loss 60 0.921
437
P BNG032 Benign Mesothelioma 53 0.921
438
CRB039 Cerebrovascular Disease 65 0.916
439
URM002 Uremia 47 0.914
440
NCL008 Nuclear Ribonucleic Acid 15 0.912
441
PST092 Posttransplant Acute Limbic Encephalitis 29 0.911
442
LMB062 Limb Ischemia 55 0.911
443
c BCT007 Bacterial Meningitis 55 0.910
444
NRM005 Neuromuscular Disease 62 0.906
445
P FML011 Familial Adenomatous Polyposis 70 0.904
446
c RTN047 Retinitis Pigmentosa 18 45 0.901
447
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 0.900
448
P HYP069 Hyperparathyroidism 62 0.900
449
GST045 Gastroenteritis 58 0.900
450
HND015 Hand Skill, Relative 29 0.899
451
DWN001 Down Syndrome 70 0.892
452
P CHR012 Chronic Granulomatous Disease 69 0.888
453
KRT019 Keratitis, Hereditary 66 0.885
454
P PTS002 Ptosis 52 0.885
455
LYM017 Lyme Disease 63 0.880
456
CHL065 Cholangiocarcinoma 57 0.879
457
INT079 Intrahepatic Cholangiocarcinoma 51 0.879
458
KRT002 Keratomalacia 54 0.877
459
RTN017 Retinal Detachment 60 0.877
460
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 44 0.873
461
CTN007 Cutaneous Leishmaniasis 61 0.873
462
TRN015 Transient Cerebral Ischemia 62 0.869
463
c TBR025 Tuberous Sclerosis 1 84 0.869
464
P SLP005 Sleep Disorder 61 0.867
465
PLM134 Pulmonary Fibrosis, Idiopathic 76 0.866
466
MLD018 Mild Cognitive Impairment 48 0.864
467
NRL005 Neurilemmoma 60 0.858
468
HMG002 Hemoglobinuria 50 0.858
469
MSC007 Muscle Hypertrophy 64 0.855
470
RBS001 Rabies 57 0.850
471
CHR066 Chronic Fatigue Syndrome 59 0.843
473
P PRD021 Periodic Paralysis 42 0.837
474
P OVR082 Overgrowth Syndrome 41 0.836
475
ART016 Aortic Aneurysm 68 0.833
476
SCK003 Sickle Cell Anemia 74 0.832
477
DST006 Diastolic Heart Failure 45 0.829
478
WTH001 Withdrawal Disorder 47 0.829
479
CRB037 Cerebral Palsy 66 0.828
480
P SCL018 Scoliosis 57 0.824
481
MST020 Mast Cell Activation Syndrome 27 0.823
482
FND002 Fundus Dystrophy 54 0.822
483
HPT022 Hepatoblastoma 54 0.819
484
P LMY004 Leiomyosarcoma 62 0.816
485
PPL002 Papillary Carcinoma 46 0.815
486
CRY035 Cryptorchidism, Unilateral or Bilateral 57 0.813
487
SDD001 Sudden Infant Death Syndrome 60 0.813
488
CCC002 Coccidiosis 50 0.808
489
c SVR005 Severe Pre-Eclampsia 49 0.808
490
SCR003 Secretory Diarrhea 35 0.808
491
RYN005 Raynaud Phenomenon 45 0.808
492
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 0.806
493
SCH014 Schistosomiasis 56 0.806
494
CHL067 Cholecystitis 59 0.806
495
CVD001 Covid-19 59 0.806
496
c HPT003 Hepatitis a 63 0.806
497
c HPT015 Hepatitis D 49 0.805
498
AZS001 Azoospermia 45 0.804
499
P SLM003 Salmonellosis 54 0.804
500
HPT070 Hepatosplenic T-Cell Lymphoma 35 0.804
501
GRN017 Granulocytopenia 42 0.802
502
P DRM053 Dermatitis, Atopic 65 0.800
503
MCS002 Mucositis 55 0.798
504
P ESP024 Esophagitis 60 0.792
505
PRP030 Purpura 54 0.792
506
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 51 0.791
507
MTB008 Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 42 0.791
508
VRC001 Varicocele 48 0.791
509
ANR040 Aneurysm 60 0.791
510
c ACT135 Acute Graft Versus Host Disease 51 0.788
512
IGR001 Ige Responsiveness, Atopic 58 0.785
513
CHK001 Chikungunya 60 0.785
514
LGN006 Legionnaire Disease 52 0.784
515
SNL007 Senile Cataract 40 0.780
516
c FML021 Familial Hypercholesterolemia 71 0.780
517
P MTR014 Motor Neuron Disease 65 0.778
518
CRV002 Cervix Uteri Carcinoma in Situ 48 0.778
519
CRV045 Cervical Intraepithelial Neoplasia 38 0.778
520
MNT001 Mantle Cell Lymphoma 65 0.777
521
BRN028 Brain Cancer 73 0.777
522
DWR001 Dwarfism 44 0.772
523
RCK004 Rickets 64 0.768
524
HRT011 Heart Septal Defect 49 0.765
525
LNG039 Lung Squamous Cell Carcinoma 57 0.765
526
LSS003 Lassa Fever 49 0.765
527
P ART023 Arthropathy 59 0.764
528
P PRM011 Primary Ciliary Dyskinesia 68 0.764
529
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 0.762
530
HRT012 Heart Valve Disease 53 0.760
531
GST023 Gastric Ulcer 52 0.760
532
c ATS025 Autosomal Dominant Progressive External Ophthalmoplegia 45 0.760
533
P ACN011 Acne 55 0.755
534
PNC129 Pancreatic Adenocarcinoma 64 0.755
535
MYL031 Myeloproliferative Neoplasm 66 0.745
536
NPH009 Nephrolithiasis 54 0.744
537
NWC001 Newcastle Disease 47 0.744
538
P HRD011 Hereditary Spherocytosis 63 0.742
539
OTT002 Otitis Media 70 0.742
540
SLC006 Silicosis 55 0.742
541
IDP070 Idiopathic Scoliosis 41 0.741
542
ASP004 Asphyxia Neonatorum 50 0.741
543
ADG002 Audiogenic Seizures 25 0.741
544
P PMP001 Pemphigus 54 0.732
545
PST053 Postherpetic Neuralgia 39 0.732
546
STT041 Stuttering 52 0.728
547
PYR010 Peyronie's Disease 50 0.728
548
P MTR012 Mitral Valve Disease 57 0.728
549
PLM035 Pulmonary Eosinophilia 49 0.728
550
P INS002 in Situ Carcinoma 52 0.728
551
P HMN010 Hemangioma 61 0.728
552
MYL005 Myelofibrosis 70 0.727
553
P RHB003 Rhabdomyosarcoma 66 0.721
554
TRN018 Transitional Cell Carcinoma 56 0.721
555
c MST023 Mesothelioma, Malignant 56 0.718
556
P ANP001 Anaplastic Large Cell Lymphoma 59 0.718
557
TCK001 Tick-Borne Encephalitis 58 0.714
558
PRT058 Pure Autonomic Failure 58 0.714
559
CYN003 Cyanide Poisoning 22 0.714
560
P ACR001 Aicardi-Goutieres Syndrome 63 0.713
561
P NRN021 Neuronal Ceroid Lipofuscinosis 64 0.713
562
P HYP035 Hypophosphatasia 61 0.713
563
P ART018 Aortic Valve Insufficiency 52 0.713
564
CYT005 Cytomegalovirus Retinitis 50 0.705
565
KPS004 Kaposi Sarcoma 76 0.698
566
P AMY004 Amyloidosis 69 0.698
567
c ATM006 Autoimmune Lymphoproliferative Syndrome 75 0.696
568
WST001 West Syndrome 64 0.696
569
c PRM005 Primary Hyperparathyroidism 59 0.696
570
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.696
571
GST092 Gastroesophageal Reflux 59 0.696
572
P SPN046 Spinal Muscular Atrophy 62 0.696
573
TST014 Testicular Cancer 51 0.696
574
P BRT004 Bartter Disease 58 0.696
575
c THR092 Thrombophilia Due to Thrombin Defect 74 0.693
576
HRN029 Hearing Loss, Noise-Induced 37 0.693
577
P LNG028 Long Qt Syndrome 63 0.693
578
NRT004 Neuritis 53 0.693
579
NRT001 Neurotic Disorder 56 0.691
580
MLG079 Malignant Pleural Mesothelioma 42 0.682
581
c ACT068 Acute Cystitis 60 0.681
582
LYM133 Lymphoma, Hodgkin, Classic 69 0.679
583
P MCR129 Microvascular Complications of Diabetes 1 67 0.678
584
c MCR112 Microvascular Complications of Diabetes 2 42 0.678
585
PNM008 Pneumothorax 54 0.678
586
P MTC069 Mitochondrial Disorders 57 0.672
587
P ATR010 Atrial Heart Septal Defect 58 0.669
588
IRN001 Iron Deficiency Anemia 58 0.669
589
P OVR049 Ovarian Disease 50 0.669
590
IGG001 Iga Glomerulonephritis 50 0.669
591
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 0.668
592
CRV040 Cervix Carcinoma 50 0.664
593
c PLM163 Palmoplantar Keratoderma, Punctate Type Ii 28 0.664
594
c INF023 Inflammatory Breast Carcinoma 48 0.664
595
ALC009 Alcoholic Liver Cirrhosis 54 0.664
596
PNC060 Punctate Porokeratosis 28 0.664
597
MNG007 Manganese Poisoning 28 0.664
598
P APL001 Aplastic Anemia 72 0.663
599
ADN027 Adenomyosis 59 0.657
600
END041 Endometrial Adenocarcinoma 63 0.657
601
GTR002 Goiter 52 0.657
602
P CRB059 Cerebellar Degeneration 36 0.657
603
MCR088 Microscopic Polyangiitis 51 0.657
604
PRP016 Paraplegia 52 0.651
605
JVN004 Juvenile Myelomonocytic Leukemia 66 0.650
606
P SPN301 Spinocerebellar Ataxia 2 59 0.636
607
CHL147 Chlamydia Pneumonia 47 0.636
608
P MTR003 Mitral Valve Stenosis 53 0.636
609
c ACT075 Acute Myocardial Infarction 55 0.635
610
FBR054 Fibroma 44 0.632
611
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 64 0.632
612
P PRN023 Prion Disease 60 0.632
613
P NRC002 Narcolepsy 55 0.632
614
MLD001 Melioidosis 67 0.631
615
PLM033 Pulmonary Embolism 58 0.631
616
PTT037 Pituitary Tumors 44 0.623
617
P DRR001 Diarrhea 55 0.619
618
P LYM033 Lymphoproliferative Syndrome 59 0.618
619
FDL002 Food Allergy 47 0.618
620
GST050 Gastrointestinal System Disease 55 0.618
621
HPT067 Hepatocellular Adenoma 42 0.600
622
c ANM038 Anemia, Autoimmune Hemolytic 63 0.600
623
DGR001 Digeorge Syndrome 62 0.600
624
c HYP292 Hypophosphatasia, Infantile 56 0.600
625
SDD008 Sudden Sensorineural Hearing Loss 41 0.600
626
PRM236 Primary Biliary Cholangitis 62 0.596
627
HMC014 Homocysteinemia 52 0.595
628
c SCL052 Scleroderma, Familial Progressive 60 0.591
629
P GST044 Gastritis 55 0.587
630
EPD015 Epidemic Typhus 44 0.587
631
NSP002 Nasopharyngitis 45 0.585
632
P RTN018 Retinal Disease 53 0.583
633
ANR004 Anuria 44 0.576
634
INT323 Intraocular Pressure Quantitative Trait Locus 63 0.559
635
P ART021 Arteriosclerosis 53 0.542
636
XRD010 Xeroderma Pigmentosum, Variant Type 72 0.540
637
P CRD246 Cardiovascular System Disease 55 0.534
638
P NNN008 Noonan Syndrome 1 76 0.529
639
P BCK002 Beckwith-Wiedemann Syndrome 61 0.522
640
SMN007 Seminoma 42 0.522
641
CHL045 Choline Deficiency Disease 39 0.522
642
P HYP750 Hypertriglyceridemia, Familial 61 0.522
643
c PSD047 Pseudo-Turner Syndrome 52 0.518
644
P CTR002 Cataract 59 0.513
645
GST040 Gastric Adenocarcinoma 66 0.513
646
KRT006 Keratoconjunctivitis 53 0.508
647
STT001 Status Epilepticus 58 0.506
648
P TBR001 Tuberous Sclerosis 69 0.496
649
P DMN002 Dementia 65 0.493
650
P KDN017 Kidney Cancer 60 0.489
651
c NRB010 Neuroblastoma 1 59 0.480
652
c THY107 Thymoma, Familial 42 0.477
653
P THY023 Thymoma 64 0.477
654
P SPP010 Suppressor of Tumorigenicity 3 50 0.472
655
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.467
656
c ATS007 Autism Spectrum Disorder 71 0.465
657
CST001 Costello Syndrome 68 0.464
658
HDN002 Head Injury 44 0.462
659
ACT003 Acute Kidney Tubular Necrosis 46 0.453
660
PRP027 Peripheral Vascular Disease 71 0.452
661
DRM006 Dermatitis 61 0.444
662
MNN009 Meningoencephalitis 47 0.444
663
PRP007 Priapism 46 0.438
664
WST005 West Nile Virus 55 0.438
665
DYS161 Dystonia, Dopa-Responsive, Due to Sepiapterin Reductase Deficiency 57 0.437
666
c HRD010 Hereditary Spastic Paraplegia 65 0.434
667
P CRD224 Cardiofaciocutaneous Syndrome 1 71 0.432
668
P TMR010 Tumor Predisposition Syndrome 69 0.429
669
P OPN001 Open-Angle Glaucoma 55 0.429
670
P HYD006 Hydrocephalus 62 0.420
671
OCL006 Ocular Hypertension 53 0.420
672
OBS002 Obsessive-Compulsive Disorder 67 0.420
673
EPD052 Epidermolysis Bullosa Simplex Superficialis 17 0.420
674
GLM044 Glomerular Disease 34 0.418
675
c HMC039 Hemochromatosis, Type 1 73 0.415
676
P MLN069 Melanoma, Uveal 59 0.415
677
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 70 0.408
678
INH023 Inherited Cancer-Predisposing Syndrome 53 0.408
679
c ATS307 Autosomal Recessive Cerebellar Ataxia 38 0.405
680
P PTT006 Pituitary Adenoma 55 0.405
681
P RNV001 Renovascular Hypertension 48 0.404
682
P WSK001 Wiskott-Aldrich Syndrome 72 0.403
683
RTN003 Retinal Ischemia 48 0.398
684
PPL022 Papilloma 53 0.397
685
SQM002 Squamous Cell Papilloma 45 0.397
686
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 0.395
687
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 0.395
688
P FRG001 Fragile X Syndrome 70 0.395
689
CHR074 Choriocarcinoma 46 0.395
690
P VTR007 Vitreoretinopathy 45 0.395
691
c NRF024 Neurofibromatosis, Type I 76 0.387
692
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 55 0.386
693
RSP002 Respiratory Syncytial Virus Infectious Disease 51 0.386
694
P PLY014 Polycystic Kidney Disease 71 0.384
695
HMP005 Hemiplegia 53 0.371
696
LKC009 Leukocyte Adhesion Deficiency, Type I 69 0.370
697
MCR013 Microphthalmia 59 0.370
698
ANX010 Anxiety 70 0.369
699
P MYT002 Myotonic Dystrophy 51 0.369
700
SQM013 Squamous Cell Carcinoma, Head and Neck 75 0.369
701
c SPR086 Spermatogenic Failure 3 47 0.369
702
P ALC033 Alcohol Use Disorder 67 0.369
703
P PLY019 Polyneuropathy 52 0.369
704
PRM329 Premature Aging 36 0.369
705
P MGR001 Migraine Without Aura 48 0.366
706
P SYS005 Systemic Scleroderma 73 0.365
707
ORL011 Oral Cancer 60 0.365
708
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.357
709
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.357
710
P STR022 Stargardt Disease 61 0.357
711
OST003 Osteonecrosis 60 0.356
712
P SCL009 Sclerosing Cholangitis 46 0.356
713
LNN001 Lennox-Gastaut Syndrome 61 0.351
714
P MDL005 Medulloblastoma 75 0.351
715
AVN001 Avian Influenza 61 0.351
716
c HRD198 Hereditary Dystonia 29 0.351
717
P PSD015 Pseudohypoparathyroidism 54 0.349
718
HYP080 Hypogonadism 49 0.349
719
JPN002 Japanese Encephalitis 61 0.349
720
ILS001 Ileus 49 0.349
721
ALB002 Albinism 46 0.349
722
P ATS364 Autism 72 0.345
723
HMS001 Hemosiderosis 48 0.345
724
P RRH023 Rare Hereditary Hemochromatosis 52 0.345
725
c GLC092 Glaucoma, Primary Open Angle 60 0.343
726
P PLY011 Polycystic Ovary Syndrome 57 0.343
727
c ACR088 Aicardi-Goutieres Syndrome 3 39 0.341
728
GST037 Gastroparesis 52 0.341
729
P DBT005 Diabetes Insipidus 54 0.340
730
c CHL119 Cholangitis, Primary Sclerosing 57 0.333
731
TST044 Testicular Torsion 45 0.333
732
P ICH004 Ichthyosis 56 0.333
733
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 0.330
734
P OST002 Osteoporosis 76 0.330
735
P MJR007 Major Affective Disorder 1 42 0.330
736
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.330
737
LPT014 Leptin Deficiency or Dysfunction 77 0.330
738
P MGR003 Migraine with Aura 51 0.330
739
EMB004 Embryonal Carcinoma 55 0.330
740
SYS003 Systolic Heart Failure 49 0.330
741
RSP023 Rasopathy 54 0.330
742
AMN003 Amnestic Disorder 53 0.330
743
NRL016 Neural Tube Defects 80 0.329
744
PRP080 Peripheral Artery Disease 54 0.329
745
P HRM001 Hermansky-Pudlak Syndrome 65 0.329
746
BLR001 Biliary Atresia 55 0.329
747
ATN004 Autonomic Neuropathy 42 0.329
748
ART002 Arts Syndrome 66 0.325
749
HLC007 Helicobacter Pylori Infection 67 0.325
750
c INH020 Inherited Metabolic Disorder 47 0.325
751
INT002 Intermittent Claudication 61 0.324
752
SPS057 Spasticity 43 0.324
753
P MYS005 Myositis 55 0.320
754
P END033 Endocarditis 58 0.314
755
BRN018 Borna Disease 36 0.314
756
c HMN021 Human T-Cell Leukemia Virus Type 1 46 0.314
757
P NRV007 Nervous System Disease 65 0.309
758
P FBR031 Febrile Seizures 52 0.309
759
GNT167 Genetic Obesity 33 0.309
760
P RTT002 Rett Syndrome 79 0.309
761
c ART115 Aortic Valve Disease 1 72 0.307
762
P ALT001 Alternating Hemiplegia of Childhood 56 0.307
763
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 62 0.307
764
ENT004 Enthesopathy 51 0.307
765
P ATR005 Atrophic Gastritis 50 0.307
766
CHR178 Chromosomal Triplication 33 0.307
767
MTR002 Mitral Valve Insufficiency 51 0.307
768
CRC021 Carcinosarcoma 62 0.307
769
SPS019 Spastic Paraparesis 38 0.307
770
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.305
771
P LMB006 Limb-Girdle Muscular Dystrophy 52 0.305
772
PHS004 Phosphoribosylpyrophosphate Synthetase Superactivity 48 0.297
773
c CHR711 Chronic Asthma 41 0.297
774
TTH006 Tooth Disease 51 0.297
775
MNK002 Monkeypox 41 0.297
776
HYP006 Hypertensive Heart Disease 48 0.297
777
P TRC031 Trichorhinophalangeal Syndrome 37 0.297
778
P CRB088 Cerebral Atrophy 32 0.297
779
P XRD029 Xeroderma Pigmentosum, Complementation Group a 55 0.293
780
PST028 Post-Traumatic Stress Disorder 58 0.293
781
P MTH008 Methylmalonic Acidemia 52 0.293
782
ACT200 Acute Monoblastic Leukemia 40 0.293
783
c VRL012 Viral Meningitis 46 0.292
784
GRD001 Giardiasis 46 0.292
785
ARM002 Aromatic L-Amino Acid Decarboxylase Deficiency 55 0.286
786
c PSD108 Pseudohypoparathyroidism, Type Ia 64 0.286
787
EPL131 Epilepsy, Pyridoxine-Dependent 46 0.286
788
c THY109 Thyroid Cancer, Nonmedullary, 1 55 0.286
789
P MMB011 Membranous Nephropathy 50 0.286
790
FCL022 Focal Dystonia 41 0.286
791
P VNT002 Ventricular Septal Defect 58 0.286
792
OPT003 Opiate Dependence 49 0.286
793
c BPL002 Bipolar I Disorder 47 0.286
794
BRS051 Breast Disease 58 0.286
795
NRF007 Neurofibroma 63 0.286
796
ATN005 Autonomic Dysfunction 45 0.286
797
c WLM013 Wilms Tumor 1 65 0.285
798
FRN006 Frontotemporal Dementia 68 0.285
799
P SPR120 Supranuclear Palsy, Progressive, 1 68 0.285
800
MCL006 Macular Retinal Edema 56 0.285
801
CHR100 Chronic Ulcer of Skin 57 0.279
802
c ATM099 Autoimmune Uveitis 44 0.279
803
BRC012 Brucellosis 66 0.279
804
P CHR071 Charcot-Marie-Tooth Disease 64 0.279
805
c HPT007 Hepatitis E 50 0.279
806
LRN003 Learning Disability 49 0.279
807
BRK012 Broken Heart Syndrome 42 0.279
808
c HYP331 Hyperphenylalaninemia, Bh4-Deficient, a 59 0.278
809
c BRS111 Breast-Ovarian Cancer, Familial 2 53 0.278
810
P MYG005 Myoglobinuria 40 0.278
811
P DDN001 Duodenal Ulcer 52 0.278
812
PNC001 Pancytopenia 52 0.278
813
SNS003 Sensory Peripheral Neuropathy 51 0.278
815
P CND005 Cone Dystrophy 47 0.273
816
P CRG003 Crigler-Najjar Syndrome, Type I 64 0.273
817
SMT008 Smith-Magenis Syndrome 53 0.273
818
c CNG411 Congenital Disorder of Glycosylation, Type in 66 0.273
819
LBR036 Leber Plus Disease 67 0.273
820
ACH005 Achalasia 54 0.273
821
P ACT105 Acute Mountain Sickness 52 0.273
822
P FML023 Familial Hemiplegic Migraine 53 0.261
823
P PLY006 Polydactyly 58 0.261
824
c SPN294 Spinocerebellar Ataxia 1 53 0.261
825
P KRN004 Kernicterus 47 0.261
826
NPH010 Nephrosclerosis 50 0.261
827
PLR005 Pleuropneumonia 33 0.261
828
PRS047 Prostatitis 57 0.261
829
DYS015 Dysentery 49 0.261
830
BCT021 Bacterial Sepsis 43 0.261
831
DNT012 Dental Caries 53 0.261
832
P BNC003 Bone Cancer 58 0.261
833
P PYL005 Pyelonephritis 56 0.261
834
P PGT001 Paget's Disease of Bone 60 0.261
835
LCH001 Leech Infestation 37 0.261
836
P PRP029 Porphyria 60 0.261
837
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.261
838
P ART005 Arteriovenous Malformation 64 0.261
839
P DRM010 Dermatomyositis 61 0.261
840
CRY005 Cryptococcosis 61 0.261
841
c CHR417 Chronic Graft Versus Host Disease 55 0.261
842
ZLL002 Zollinger-Ellison Syndrome 55 0.258
843
CRV043 Cervical Dystonia 46 0.258
844
P HRD021 Hereditary Sensory Neuropathy 48 0.258
845
P CLC063 Celiac Disease 1 65 0.258
846
VRC005 Varicose Veins 59 0.258
847
CLB010 Coloboma of Macula 53 0.258
848
c SCH079 Schizophrenia 1 44 0.258
849
NPH091 Nephrolithiasis, Calcium Oxalate 61 0.258
850
PNS018 Pain Sensitivity Quantitative Trait Locus 1 23 0.258
851
MSC152 Muscular Dystrophy, Becker Type 69 0.258
852
CLF027 Cleft Palate, Isolated 64 0.258
853
OBS082 Obstructive Nephropathy 41 0.258
854
PLM001 Pulmonary Tuberculosis 69 0.258
855
P CCK001 Cockayne Syndrome 67 0.258
856
P MTH007 Methemoglobinemia 46 0.258
857
FLR002 Filariasis 55 0.258
858
URL001 Urolithiasis 45 0.258
859
P HML001 Hemolytic-Uremic Syndrome 52 0.258
860
BRN026 Branch Retinal Artery Occlusion 41 0.258
861
TCL001 T-Cell Adult Acute Lymphocytic Leukemia 42 0.258
862
CWP001 Cowpox 44 0.258
863
P RTN014 Retinal Artery Occlusion 46 0.258
864
CLP005 Ciliopathy 40 0.258
865
c DPH024 Diaphragmatic Hernia, Congenital 63 0.253
866
c CNT035 Central Nervous System Disease 53 0.253
867
P RNL015 Renal Hypertension 45 0.253
869
P QLT041 Qualitative or Quantitative Defects of Alpha-Dystroglycan 18 0.253
870
c CNG441 Congenital Muscular Dystrophy Due to Dystroglycanopathy 28 0.253
871
LNG108 Langerhans Cell Histiocytosis 57 0.243
872
DNT005 Dentatorubral-Pallidoluysian Atrophy 59 0.243
873
P FML018 Familial Mediterranean Fever 73 0.243
874
HYP457 Hypertrophic Scars 42 0.243
875
ENT011 Enterocolitis 55 0.243
877
OST017 Osteomyelitis 63 0.243
878
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.243
879
HST010 Histiocytosis 49 0.243
880
P CND004 Candidiasis 57 0.243
881
PSY004 Psychotic Disorder 66 0.243
882
P SBS003 Substance Abuse 54 0.243
883
PRM013 Premature Menopause 57 0.243
884
NPH003 Nephrocalcinosis 49 0.243
885
ACT084 Acute Stress Disorder 53 0.243
886
c ATS347 Autosomal Dominant Polycystic Kidney Disease 64 0.243
887
PRN019 Perinatal Necrotizing Enterocolitis 60 0.243
888
VSC002 Vascular Dementia 59 0.243
889
PLT016 Platelet Adenylate Cyclase Activity 16 0.234
890
SCC001 Succinic Semialdehyde Dehydrogenase Deficiency 59 0.234
891
TRD006 Tardive Dyskinesia 53 0.234
892
GBT001 Gaba-Transaminase Deficiency 37 0.234
893
P MCP040 Mucopolysaccharidosis-Plus Syndrome 70 0.234
894
P LSS002 Lissencephaly 52 0.234
895
URT049 Urate Oxidase, Pseudogene 24 0.234
896
c HYP368 Hyperphenylalaninemia, Bh4-Deficient, C 35 0.234
897
P SJG008 Sjogren Syndrome 60 0.234
898
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.234
899
c ACR091 Aicardi-Goutieres Syndrome 4 35 0.234
900
c SVR003 Severe Congenital Neutropenia 59 0.234
901
c ATM024 Autoimmune Pancreatitis 52 0.234
902
P GRS003 Griscelli Syndrome 54 0.234
903
PRP036 Peripheral T-Cell Lymphoma 52 0.234
904
TBL035 Tubulinopathy 34 0.234
905
P TCD001 Tic Disorder 50 0.234
906
CRT004 Carotid Artery Thrombosis 39 0.234
907
P INT068 Intestinal Disease 53 0.234
908
GST030 Gastrinoma 45 0.234
909
RTR008 Root Resorption 44 0.234
910
CCN002 Cocaine Abuse 49 0.234
911
CRC006 Carcinoid Syndrome 55 0.234
912
CRR012 Cirrhotic Cardiomyopathy 22 0.234
913
DYS073 Dysphagia 53 0.234
914
c LBR004 Leber Congenital Amaurosis 1 53 0.229
915
SCH078 Schimmelpenning-Feuerstein-Mims Syndrome 59 0.229
916
HYP114 Hypertensive Nephropathy 35 0.229
917
P JBR020 Joubert Syndrome 1 74 0.229
918
NVS017 Nevus, Epidermal 66 0.229
919
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 57 0.229
920
CLN019 Colonic Disease 47 0.229
921
P ANG015 Angioedema 56 0.229
922
PNC013 Pancreatic Ductal Carcinoma 48 0.229
923
CRN017 Coronary Thrombosis 46 0.229
924
c MLG069 Malignant Hypertension 46 0.229
925
ANC002 Anca-Associated Vasculitis 44 0.229
926
WBR001 Weber Syndrome 38 0.229
927
INF034 Infective Endocarditis 53 0.222
928
PSR001 Psoriatic Arthritis 61 0.222
929
CRH005 Crohn's Colitis 53 0.222
930
RTC012 Reticuloendotheliosis, X-Linked 35 0.222
931
c PNS012 Paine Syndrome 60 0.222
932
c EXD008 Exudative Vitreoretinopathy 1 71 0.222
933
BRT054 Brittle Bone Disorder 74 0.222
934
c CRT089 Cortical Dysplasia, Complex, with Other Brain Malformations 10 39 0.222
935