Search results for Oxidized glutathione

1190 hits were found for Oxidized glutathione

# Family MCID Name MIFTS Score
1
GLT034 Glutathione Transferase Activity Toward Trans-Stilbene Oxide 4 3.678
2
HYP066 Hyperglycemia 61 0.384
3
ISC004 Ischemia 58 0.358
4
P LVR013 Liver Disease 68 0.350
5
HYP266 Hypoxia 57 0.348
6
P NRB001 Neuroblastoma 72 0.345
7
c PRC016 Pre-Eclampsia 63 0.336
8
P VSC007 Vascular Disease 63 0.335
9
ATH013 Atherosclerosis Susceptibility 65 0.332
10
P KDN018 Kidney Disease 72 0.322
11
P PLM037 Pulmonary Hypertension 67 0.320
12
LNG099 Lung Disease 60 0.317
13
P CTR002 Cataract 60 0.312
14
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.309
15
P CLR023 Colorectal Cancer 99 0.308
16
P ALZ034 Alzheimer Disease 88 0.307
17
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.307
18
FTT001 Fatty Liver Disease 61 0.294
19
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.286
20
c MCR130 Microvascular Complications of Diabetes 6 41 0.275
21
48X005 48,xyyy 39 0.275
22
c MCR120 Microvascular Complications of Diabetes 7 47 0.275
23
AGN016 Aging 56 0.274
24
c MCR113 Microvascular Complications of Diabetes 3 52 0.274
25
c MCR133 Microvascular Complications of Diabetes 4 41 0.274
26
CYT002 Cytokine Deficiency 42 0.272
27
LVR012 Liver Cirrhosis 62 0.269
28
P GLM045 Glioma 63 0.264
29
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.262
30
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.262
31
GLL048 Glial Tumor 45 0.259
32
c CHR684 Chronic Kidney Disease 70 0.259
33
c HYP836 Hypercholesterolemia, Familial, 1 73 0.259
34
P BRS047 Breast Cancer 97 0.258
35
P LTR001 Lateral Sclerosis 54 0.258
36
P LNG032 Lung Cancer 98 0.257
37
TXC005 Toxic Shock Syndrome 62 0.256
38
P HPT023 Hepatocellular Carcinoma 100 0.255
39
LPP008 Lipoprotein Quantitative Trait Locus 62 0.244
40
P OVR042 Ovarian Cancer 88 0.242
41
P BLD134 Bladder Cancer 79 0.241
42
LPD008 Lipid Metabolism Disorder 62 0.240
43
CYS001 Cystic Fibrosis 81 0.239
44
P INF032 Infertility 57 0.239
45
c HYP595 Hypertension, Essential 84 0.236
46
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.234
48
ART140 Arteries, Anomalies of 52 0.231
49
AST005 Asthma 76 0.230
50
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.229
51
DFC004 Deficiency Anemia 70 0.227
52
P CRN300 Coronary Heart Disease 1 63 0.225
53
P MLN007 Male Infertility 55 0.222
54
P PRK057 Parkinson Disease, Late-Onset 78 0.222
55
P ADN016 Adenocarcinoma 64 0.221
56
GLB015 Glioblastoma Multiforme 75 0.221
57
HMS001 Hemosiderosis 54 0.220
58
P RRH023 Rare Hereditary Hemochromatosis 41 0.218
59
PPL052 Papillomatosis, Confluent and Reticulated 33 0.218
60
P NRP001 Neuropathy 56 0.217
61
P HRT032 Heart Disease 75 0.214
62
ANX004 Anoxia 40 0.211
63
END086 End Stage Renal Disease 51 0.210
64
SQM006 Squamous Cell Carcinoma 60 0.210
65
P INF037 Inflammatory Bowel Disease 54 0.208
66
ANP008 Anaplastic Oligoastrocytoma 30 0.207
67
P PRD008 Periodontitis 64 0.207
68
P MCR115 Microvascular Complications of Diabetes 5 66 0.207
69
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.206
70
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.206
71
P DBT009 Diabetes Mellitus 64 0.206
72
P PRS040 Prostate Cancer 97 0.206
73
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.204
74
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.203
75
47X002 47,xyy 49 0.203
76
CRB004 Cerebral Artery Occlusion 45 0.202
77
ATM095 Autoimmune Disease 62 0.202
78
IRN002 Iron Metabolism Disease 57 0.201
79
P BCL017 B-Cell Lymphoma 58 0.200
80
CNG034 Congestive Heart Failure 69 0.200
81
CHL068 Cholestasis 61 0.199
82
P RSP003 Respiratory Failure 74 0.198
83
P MSC005 Muscular Dystrophy 66 0.197
84
P HML002 Hemolytic Anemia 63 0.197
85
PNG002 Pain Agnosia 51 0.196
86
HLX001 Helix Syndrome 47 0.195
87
P HNT016 Huntington Disease 72 0.194
88
P GST053 Gastric Cancer 83 0.194
89
BRN071 Brain Injury 49 0.194
90
P ECL001 Eclampsia 50 0.189
91
HYP056 Hypoglycemia 66 0.187
92
P PLM036 Pulmonary Fibrosis 65 0.186
93
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.186
94
c ACT027 Acute Pancreatitis 60 0.186
95
CLT003 Colitis 62 0.184
96
HMC014 Homocysteinemia 53 0.184
97
P RHN004 Rhinitis 57 0.184
98
P HYP086 Hypothyroidism 69 0.183
99
c ACT071 Acute Kidney Failure 60 0.182
100
P SCK005 Sickle Cell Disease 50 0.182
101
GLT007 Glutathione Synthetase Deficiency 47 0.181
102
NNL006 Non-Alcoholic Steatohepatitis 54 0.181
103
P PHC003 Pheochromocytoma 71 0.181
104
ADR040 Adrenal Gland Pheochromocytoma 46 0.181
105
P MYC007 Myocardial Infarction 70 0.179
106
IMP005 Impotence 52 0.178
107
TRM010 Traumatic Brain Injury 51 0.178
108
P SZR006 Seizure Disorder 56 0.178
109
P BPL003 Bipolar Disorder 56 0.178
110
c MJR024 Major Affective Disorder 9 41 0.178
111
c MJR022 Major Affective Disorder 8 38 0.178
112
P CRD246 Cardiovascular System Disease 57 0.176
113
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.176
114
P MYL006 Myeloid Leukemia 60 0.175
115
VSL002 Visual Epilepsy 59 0.174
116
ORL011 Oral Cancer 60 0.173
117
P END044 Endometriosis 63 0.173
118
P LKM002 Leukemia 68 0.173
119
SCH014 Schistosomiasis 57 0.172
120
P THL005 Thalassemia 60 0.172
121
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.171
122
SPN186 Spinal Cord Injury 60 0.170
123
P ATS364 Autism 70 0.170
124
P SKN015 Skin Carcinoma 66 0.170
125
DWN001 Down Syndrome 70 0.169
126
ADN018 Adenoma 59 0.168
127
P HYP076 Hyperthyroidism 55 0.168
128
P ENC018 Encephalopathy 61 0.168
129
P LNG064 Lung Cancer Susceptibility 3 78 0.167
130
DPR016 Depression 63 0.167
131
ULC004 Ulcerative Colitis 73 0.166
132
P PNC044 Pancreatitis 61 0.166
133
URM002 Uremia 49 0.166
134
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.165
135
HYP060 Hyperinsulinism 54 0.164
136
BRN056 Bronchopulmonary Dysplasia 57 0.163
137
OST159 Osteogenic Sarcoma 66 0.162
138
ALL006 Allergic Asthma 56 0.161
139
DRM006 Dermatitis 61 0.161
140
IGR001 Ige Responsiveness, Atopic 59 0.161
141
ALL003 Allergic Rhinitis 67 0.160
142
MLR004 Malaria 81 0.159
143
LSH001 Leishmaniasis 63 0.159
144
P KLZ004 Kala-Azar 1 41 0.159
145
c ATR087 Atrial Standstill 1 75 0.159
146
P MYP004 Myopathy 70 0.159
147
P PSR002 Psoriasis 62 0.158
148
PST011 Pustulosis of Palm and Sole 52 0.158
149
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.158
150
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.158
151
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.157
152
ALL026 Allergic Hypersensitivity Disease 62 0.157
153
P SLP006 Sleep Apnea 69 0.156
154
P ALC033 Alcohol Use Disorder 58 0.156
155
MNT002 Mental Depression 58 0.155
156
SKN016 Skin Disease 63 0.155
157
c ACT075 Acute Myocardial Infarction 57 0.155
158
OST012 Osteoarthritis 78 0.154
159
BCT022 Bacterial Infectious Disease 56 0.154
160
PLM010 Pulmonary Edema 54 0.154
161
P RHM011 Rheumatoid Arthritis 80 0.153
162
P PRP019 Peripheral Nervous System Disease 58 0.152
163
P ART021 Arteriosclerosis 54 0.151
164
P LKM062 Leukemia, Acute Lymphoblastic 69 0.151
165
P MLN008 Melanoma 69 0.150
166
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.150
167
P SCH015 Schizophrenia 74 0.148
168
P GLM007 Glomerulonephritis 57 0.148
169
P AST007 Astrocytoma 51 0.148
170
DBT010 Diabetic Neuropathy 54 0.148
171
c LKM061 Leukemia, Acute Myeloid 84 0.147
172
c SYS001 Systemic Lupus Erythematosus 86 0.147
173
SCK003 Sickle Cell Anemia 74 0.146
174
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.146
175
STR067 Stroke, Ischemic 81 0.146
176
ALC007 Alcohol Dependence 66 0.146
177
TLN003 Telangiectasis 52 0.146
178
CRV035 Cervical Cancer 76 0.145
179
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.144
180
P MLT020 Multiple Sclerosis 72 0.143
181
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.143
182
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.143
183
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.143
184
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.143
185
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.143
186
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.143
187
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.143
188
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.143
189
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.143
190
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.143
191
ALL014 Allergic Encephalomyelitis 38 0.143
192
PRT013 Portal Hypertension 59 0.142
193
P ATX030 Ataxia-Telangiectasia 82 0.142
194
MTB004 Metabolic Acidosis 50 0.141
195
ESP021 Esophageal Cancer 90 0.141
196
P PLY011 Polycystic Ovary Syndrome 56 0.141
197
P PNC035 Pancreatic Cancer 84 0.141
198
P ADL010 Adult Respiratory Distress Syndrome 65 0.141
199
P OPN001 Open-Angle Glaucoma 49 0.140
200
BRN004 Brain Edema 56 0.140
201
c DLT002 Dilated Cardiomyopathy 79 0.139
202
GLC003 Glucose Intolerance 54 0.139
203
c SML038 Small Cell Cancer of the Lung 65 0.139
204
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.138
205
P MTC069 Mitochondrial Disorders 56 0.138
206
HMN044 Human Immunodeficiency Virus Type 1 71 0.138
207
ORL015 Oral Squamous Cell Carcinoma 43 0.138
208
c HPT073 Hepatitis C Virus 72 0.138
209
ANX010 Anxiety 73 0.137
210
P GST044 Gastritis 56 0.137
211
ANG054 Angina Pectoris 66 0.136
212
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.136
213
BNR002 Bone Resorption Disease 48 0.134
214
HRW001 Hair Whorl 36 0.134
215
PRT037 Pertussis 65 0.133
216
P FBR017 Fibrosarcoma 56 0.133
217
c PCH010 Pachyonychia Congenita 3 44 0.133
218
CLN015 Colon Adenocarcinoma 65 0.132
219
P MJR001 Major Depressive Disorder 68 0.132
220
PRT036 Peritonitis 64 0.131
221
c HPT001 Hepatitis C 62 0.131
222
P CRD119 Cardiac Arrest 67 0.131
223
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.131
224
HLC007 Helicobacter Pylori Infection 59 0.131
225
CHG001 Chagas Disease 66 0.131
226
P LCT001 Lactic Acidosis 51 0.131
227
c PRD040 Periodontitis, Chronic 53 0.130
228
MSC157 Muscular Dystrophy, Duchenne Type 72 0.130
229
P HYP750 Hypertriglyceridemia, Familial 62 0.129
230
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.129
231
c GLC092 Glaucoma, Primary Open Angle 62 0.129
232
c VRL010 Viral Hepatitis 52 0.129
233
NTR005 Nutritional Deficiency Disease 62 0.129
234
c MGR028 Migraine with or Without Aura 1 67 0.129
235
c BTT014 Beta-Thalassemia 74 0.127
236
CRB039 Cerebrovascular Disease 67 0.127
237
P BRS044 Breast Adenocarcinoma 59 0.127
238
P MYC008 Myocarditis 59 0.126
239
VRC001 Varicocele 49 0.126
240
c SCL052 Scleroderma, Familial Progressive 61 0.125
241
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.125
242
c ACT134 Acute Liver Failure 56 0.125
243
P PNM007 Pneumonia 68 0.124
244
CRH001 Crohn's Disease 74 0.124
245
GST023 Gastric Ulcer 53 0.123
246
INS001 Insulinoma 60 0.123
247
P CHR012 Chronic Granulomatous Disease 67 0.123
248
P DRR001 Diarrhea 55 0.123
249
c DBT099 Diabetes Mellitus, Type I 65 0.122
250
P LPS004 Lupus Erythematosus 61 0.122
251
GLT039 Glutathione Peroxidase Deficiency 34 0.122
252
CNT047 Contact Dermatitis 58 0.121
253
PRS045 Prostatic Hypertrophy 53 0.121
254
P MSC003 Muscular Atrophy 52 0.121
255
BLR008 Bilirubin Metabolic Disorder 57 0.120
256
IMM167 Immune Deficiency Disease 78 0.120
257
THY029 Thyroid Carcinoma 59 0.120
258
BRR014 Barrett Esophagus 65 0.119
259
ACT119 Acute Promyelocytic Leukemia 63 0.117
260
BRN024 Bronchitis 68 0.117
261
P DRM053 Dermatitis, Atopic 66 0.117
262
SVR004 Severe Combined Immunodeficiency 73 0.117
263
ENT011 Enterocolitis 51 0.117
264
RNL077 Renal Fibrosis 47 0.117
265
ATS010 Autosomal Recessive Disease 48 0.117
266
INT007 Intermediate Coronary Syndrome 55 0.116
267
P NTR004 Neutropenia 63 0.116
268
CHR178 Chromosomal Triplication 35 0.116
269
PRS021 Prostatic Adenoma 51 0.115
270
P HYP098 Hypereosinophilic Syndrome 67 0.115
271
P RTN018 Retinal Disease 53 0.115
272
P LYM118 Lymphoma 68 0.115
273
MYL069 Myeloma, Multiple 85 0.115
274
PRM329 Premature Aging 35 0.114
275
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.114
276
MYL009 Myelodysplastic Syndrome 70 0.114
277
HPT019 Hepatic Encephalopathy 60 0.113
278
P CYS018 Cystitis 59 0.112
279
RBF001 Riboflavin Deficiency 49 0.112
280
GST033 Gestational Diabetes 61 0.112
281
PST092 Posttransplant Acute Limbic Encephalitis 29 0.112
282
HPT004 Hepatic Coma 45 0.112
283
PRN019 Perinatal Necrotizing Enterocolitis 59 0.112
284
ERY051 Erythroleukemia, Familial 56 0.111
285
P RTN016 Retinal Degeneration 53 0.111
286
c ATS007 Autism Spectrum Disorder 67 0.111
287
PRS129 Prostatic Hyperplasia, Benign 49 0.110
288
P LKM071 Leukemia, Chronic Lymphocytic 79 0.110
289
CHL014 Cholera 59 0.110
290
OVR094 Ovarian Epithelial Cancer 38 0.110
291
STT001 Status Epilepticus 60 0.110
292
ACQ007 Acquired Immunodeficiency Syndrome 60 0.110
293
IRN001 Iron Deficiency Anemia 59 0.109
294
MDD011 Mood Disorder 62 0.109
295
P KDN017 Kidney Cancer 60 0.109
296
P ART022 Arthritis 69 0.108
297
c LKM063 Leukemia, Chronic Myeloid 72 0.108
298
CHL065 Cholangiocarcinoma 68 0.107
299
INT079 Intrahepatic Cholangiocarcinoma 51 0.107
300
TRN018 Transitional Cell Carcinoma 56 0.107
301
HVY002 Heavy Metal Poisoning 22 0.106
302
P NSP012 Nasopharyngeal Carcinoma 66 0.106
303
PHN003 Phenylketonuria 75 0.106
304
HYP781 Hypoascorbemia 51 0.106
305
P LRY044 Larynx Cancer 55 0.105
306
VTM002 Vitamin B12 Deficiency 48 0.105
307
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.105
308
PRP027 Peripheral Vascular Disease 71 0.105
309
P TRM003 Tremor 54 0.104
310
CRT015 Carotid Artery Occlusion 45 0.104
311
P HPT021 Hepatitis 67 0.104
312
P SPP010 Suppressor of Tumorigenicity 3 51 0.104
313
PPT005 Peptic Ulcer Disease 59 0.104
314
EYD002 Eye Disease 58 0.103
315
c INH020 Inherited Metabolic Disorder 47 0.103
316
SNL007 Senile Cataract 42 0.103
317
OCL069 Ocular Motor Apraxia 51 0.103
318
GST092 Gastroesophageal Reflux 67 0.103
319
P MTH007 Methemoglobinemia 46 0.103
320
INS024 Insulin-Like Growth Factor I 79 0.103
321
P NPH012 Nephrotic Syndrome 60 0.103
322
P MNN013 Meningitis 66 0.103
323
CHR066 Chronic Fatigue Syndrome 61 0.102
324
P PRP029 Porphyria 62 0.102
325
c MLG068 Malignant Glioma 46 0.101
326
P DMN002 Dementia 66 0.100
327
KRT002 Keratomalacia 47 0.100
328
P BNG032 Benign Mesothelioma 46 0.100
329
URT010 Ureteral Obstruction 45 0.100
330
END057 Endometrial Cancer 74 0.100
331
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.099
332
TRN015 Transient Cerebral Ischemia 63 0.099
333
c SVR005 Severe Pre-Eclampsia 50 0.099
334
VSC002 Vascular Dementia 57 0.099
335
P OPT006 Optic Nerve Disease 60 0.099
336
P HDC001 Headache 57 0.099
337
PPL022 Papilloma 54 0.098
338
SQM002 Squamous Cell Papilloma 46 0.098
339
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.098
340
ART016 Aortic Aneurysm 69 0.098
341
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.098
342
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.097
343
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.097
344
c HPT016 Hepatitis B 59 0.097
345
P UVT001 Uveitis 57 0.096
346
c ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 35 0.096
347
PLM001 Pulmonary Tuberculosis 69 0.096
348
GST040 Gastric Adenocarcinoma 70 0.096
349
c MCR129 Microvascular Complications of Diabetes 1 66 0.096
350
VSC003 Visceral Leishmaniasis 55 0.096
351
OTT002 Otitis Media 72 0.096
352
VLV047 Volvulus of Midgut 49 0.095
353
ALC006 Alcoholic Hepatitis 61 0.095
354
P RTN008 Retinitis Pigmentosa 79 0.095
355
MST005 Mastitis 53 0.095
356
P MTR014 Motor Neuron Disease 65 0.095
357
P CND004 Candidiasis 58 0.095
358
P VSC011 Vasculitis 62 0.095
359
ADR007 Adrenoleukodystrophy 75 0.094
360
RTN023 Retinitis 46 0.094
361
NRR001 Neuroretinitis 42 0.094
362
THR024 Thrombosis 57 0.094
363
HPT022 Hepatoblastoma 56 0.094
364
ADR022 Adrenomyeloneuropathy 38 0.093
365
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.092
366
c ACT073 Acute Leukemia 58 0.092
367
P AMY004 Amyloidosis 70 0.092
368
P PLY019 Polyneuropathy 56 0.092
370
P PRN023 Prion Disease 57 0.092
371
c MCR112 Microvascular Complications of Diabetes 2 41 0.092
372
ALL010 Allergic Contact Dermatitis 56 0.091
373
ANR040 Aneurysm 59 0.091
374
P ANT006 Antiphospholipid Syndrome 55 0.091
375
NTR046 Neutrophil Migration 50 0.091
376
P RTN024 Retinoblastoma 73 0.091
377
c FML008 Familial Retinoblastoma 53 0.091
378
NRL016 Neural Tube Defects 82 0.091
379
CLR108 Colorectal Adenoma 64 0.091
380
HMP009 Haemophilus Influenzae 43 0.091
381
P PRM006 Primary Biliary Cirrhosis 62 0.090
382
LMB062 Limb Ischemia 55 0.090
383
MTC005 Mitochondrial Metabolism Disease 49 0.090
384
BRN028 Brain Cancer 74 0.090
385
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.090
386
c EXD008 Exudative Vitreoretinopathy 1 71 0.090
387
HNS001 Hansen's Disease 34 0.090
388
CNS004 Constipation 58 0.090
389
ANR007 Anorexia Nervosa 63 0.090
390
PLC008 Placenta Disease 50 0.089
391
P GRF003 Graft-Versus-Host Disease 72 0.089
392
P LPR021 Leprosy 3 69 0.089
393
P HRP006 Herpes Simplex 65 0.089
394
c LKM005 Leukemia, T-Cell, Chronic 34 0.089
395
GT001 Gout 64 0.089
396
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.088
397
CLR109 Colorectal Adenocarcinoma 51 0.088
398
XRD010 Xeroderma Pigmentosum, Variant Type 73 0.088
399
SRC014 Sarcoma 65 0.088
400
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 54 0.088
401
LKP003 Leukoplakia 39 0.088
402
c BSL007 Basal Cell Carcinoma 68 0.088
403
c ATM011 Autoimmune Hepatitis 63 0.087
404
P EPL164 Epilepsy 71 0.087
405
TTN003 Tetanus 65 0.087
406
ATX019 Ataxia with Vitamin E Deficiency 42 0.087
407
CHL152 Childhood Acute Lymphocytic Leukemia 44 0.087
408
P SYS005 Systemic Scleroderma 68 0.086
409
P OBS001 Obstructive Jaundice 50 0.086
410
RTN020 Retinal Vascular Disease 46 0.086
411
CHL123 Chlamydia 59 0.086
412
P TRC086 Trichohepatoenteric Syndrome 1 62 0.086
413
c RHB024 Rhabdomyosarcoma 2 67 0.086
414
LYM133 Lymphoma, Hodgkin, Classic 69 0.086
415
HRN029 Hearing Loss, Noise-Induced 37 0.086
416
RCK004 Rickets 68 0.086
417
c DWL002 Dowling-Degos Disease 1 58 0.086
418
SPN035 Spindle Cell Sarcoma 53 0.086
419
P DDN001 Duodenal Ulcer 52 0.086
420
SPL018 Splenomegaly 48 0.085
421
TRY001 Trypanosomiasis 50 0.085
422
P ANP001 Anaplastic Large Cell Lymphoma 58 0.085
423
P CHR345 Chronic Pain 44 0.085
424
ADL002 Adult Syndrome 70 0.085
425
NPH009 Nephrolithiasis 55 0.085
426
P MRC003 Mercury Poisoning 48 0.084
427
PSY004 Psychotic Disorder 67 0.084
428
P ESP024 Esophagitis 62 0.084
429
CRN030 Coronary Stenosis 50 0.084
430
TRD006 Tardive Dyskinesia 54 0.084
431
TBC004 Tobacco Addiction 64 0.084
432
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.084
433
ANM045 Anemia, Nonspherocytic Hemolytic, Due to G6pd Deficiency 49 0.084
434
P APL001 Aplastic Anemia 74 0.083
435
INT066 Interstitial Lung Disease 60 0.083
436
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.083
437
P ALP008 Alopecia 54 0.083
438
P BRN022 Bronchiectasis 59 0.083
439
P INS002 in Situ Carcinoma 53 0.083
440
c BCT007 Bacterial Meningitis 55 0.083
441
c NRF023 Neurofibromatosis, Type Ii 80 0.082
442
SLC006 Silicosis 56 0.082
443
P TRN020 Turner Syndrome 67 0.082
444
P SBS003 Substance Abuse 55 0.082
445
DNT012 Dental Caries 53 0.082
446
ARG004 Argyria 27 0.082
447
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.082
448
PRP080 Peripheral Artery Disease 53 0.082
449
P HMC002 Homocystinuria 53 0.082
450
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.081
451
CRB037 Cerebral Palsy 69 0.081
452
FLR002 Filariasis 55 0.080
453
c PLM127 Pulmonary Hypertension, Primary, 3 34 0.080
454
P RCT021 Rectum Cancer 52 0.080
455
P KRT007 Keratoconus 50 0.080
456
c OPT053 Optic Atrophy 1 63 0.080
457
HMG005 Hemoglobinopathy 56 0.080
458
MST004 Mast Cell Neoplasm 42 0.080
459
EXT007 Extracutaneous Mastocytoma 38 0.080
460
HML010 Hemolytic Anemia Due to Glutathione Reductase Deficiency 19 0.080
461
P SRC025 Sarcoidosis 1 70 0.080
462
P ENC004 Encephalitis 61 0.080
463
GST050 Gastrointestinal System Disease 56 0.080
464
THR013 Thoracic Outlet Syndrome 54 0.080
465
P RHB003 Rhabdomyosarcoma 63 0.079
466
P HRD144 Hereditary Mixed Polyposis Syndrome 51 0.079
467
P BRB001 Beriberi 46 0.079
468
P FRD001 Friedreich Ataxia 64 0.079
469
DSS008 Disease of Mental Health 58 0.079
470
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.079
471
P THY032 Thyroiditis 52 0.079
472
CVD001 Covid-19 44 0.079
473
HLL004 Hellp Syndrome 54 0.079
474
HDN002 Head Injury 46 0.078
475
ANT018 Anthracosis 48 0.078
476
P PLY014 Polycystic Kidney Disease 62 0.078
477
c MNN043 Meningioma, Familial 74 0.078
478
MNN042 Meningioma, Radiation-Induced 62 0.078
479
SPN021 Spinal Meningioma 50 0.078
480
SCR001 Secretory Meningioma 41 0.078
481
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.078
482
MCS002 Mucositis 56 0.078
483
P SNS001 Sensorineural Hearing Loss 60 0.078
484
P PNM006 Pneumoconiosis 56 0.078
485
RTN003 Retinal Ischemia 50 0.078
486
CHR100 Chronic Ulcer of Skin 55 0.077
487
GNG013 Gingivitis 59 0.077
488
HYP005 Hypokalemia 55 0.077
489
P BND020 Bone Disease 59 0.077
490
c LNG109 Lung Cancer Susceptibility 1 27 0.077
491
P PLM034 Pulmonary Emphysema 55 0.076
492
MYC005 Myocardial Stunning 46 0.076
493
P GLM040 Glioma Susceptibility 1 81 0.076
494
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.076
495
CRB090 Cerebral Hypoxia 44 0.076
496
c HPT003 Hepatitis a 62 0.076
497
DBT007 Diabetic Cataract 38 0.076
498
NWB001 Newborn Respiratory Distress Syndrome 58 0.076
499
P MPL001 Maple Syrup Urine Disease 69 0.076
500
P CLC063 Celiac Disease 1 66 0.076
501
AZS001 Azoospermia 50 0.075
502
c SPN225 Spondyloarthropathy 1 73 0.075
503
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.075
504
c SPR086 Spermatogenic Failure 3 44 0.075
505
c SVR001 Severe Acute Respiratory Syndrome 62 0.074
506
HPT046 Hepatic Veno-Occlusive Disease 56 0.074
507
c HMC039 Hemochromatosis, Type 1 74 0.074
508
PNC129 Pancreatic Adenocarcinoma 68 0.074
509
SLP001 Sleeping Sickness 54 0.074
510
c HNT011 Huntington Disease-Like 3 38 0.074
511
PLS007 Plasmodium Falciparum Malaria 52 0.073
512
KRT009 Keratosis 51 0.073
513
P INT068 Intestinal Disease 53 0.073
514
c THR092 Thrombophilia Due to Thrombin Defect 73 0.073
515
P ANR048 Aniridia 1 63 0.073
516
LPT014 Leptin Deficiency or Dysfunction 74 0.073
517
P ART023 Arthropathy 62 0.073
518
CYS010 Cystinosis 59 0.073
519
ORL012 Oral Leukoplakia 39 0.073
520
DFF005 Diffuse Large B-Cell Lymphoma 55 0.073
521
P OVR082 Overgrowth Syndrome 50 0.073
522
KRT019 Keratitis, Hereditary 65 0.073
523
P ADL017 Adult T-Cell Leukemia 56 0.073
524
ACT017 Acute Chest Syndrome 51 0.072
525
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.072
526
P HYP061 Hypertrophic Cardiomyopathy 70 0.072
527
TST044 Testicular Torsion 47 0.072
528
P TXP001 Toxoplasmosis 60 0.072
529
P TMP001 Temporal Lobe Epilepsy 50 0.072
530
P MDL005 Medulloblastoma 77 0.072
531
MSC007 Muscle Hypertrophy 64 0.072
532
c FNC043 Fanconi Anemia, Complementation Group E 62 0.072
533
P HYP265 Hypotonia 43 0.072
534
P TYR004 Tyrosinemia 58 0.071
535
P DNG005 Dengue Virus 59 0.071
536
IGG001 Iga Glomerulonephritis 48 0.071
537
HYP081 Hypolipoproteinemia 51 0.071
538
P EXN002 Exanthem 57 0.071
539
FSC002 Fascioliasis 42 0.071
540
ALC009 Alcoholic Liver Cirrhosis 53 0.070
541
HRT011 Heart Septal Defect 50 0.070
542
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.070
543
ATX010 Ataxia Neuropathy Spectrum 34 0.070
544
c FML021 Familial Hypercholesterolemia 66 0.070
545
FBR047 Fibromyalgia 58 0.070
546
ACN002 Acanthosis Nigricans 60 0.070
547
ACT064 Acute Necrotizing Encephalitis 33 0.070
548
BLD137 Blood Group--Ahonen 16 0.070
549
HMG002 Hemoglobinuria 50 0.070
550
P PLY018 Polycythemia 56 0.069
551
PPT001 Peptic Esophagitis 52 0.069
552
MCN007 Meconium Aspiration Syndrome 55 0.069
553
VCC001 Vaccinia 49 0.069
554
KSH001 Keshan Disease 34 0.069
555
P FML011 Familial Adenomatous Polyposis 72 0.068
556
P SPR120 Supranuclear Palsy, Progressive, 1 68 0.068
557
STM007 Stomatitis 50 0.068
558
INT002 Intermittent Claudication 61 0.068
559
CND006 Candida Glabrata 32 0.068
560
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.068
561
CHL067 Cholecystitis 57 0.068
562
c MST023 Mesothelioma, Malignant 57 0.068
563
MNG007 Manganese Poisoning 29 0.068
564
EMB004 Embryonal Carcinoma 56 0.067
565
CMM005 Common Cold 57 0.067
566
MLT157 Multiple System Atrophy 1 70 0.067
567
TNS005 Tonsillitis 57 0.067
568
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.067
569
GST045 Gastroenteritis 59 0.067
571
BRC012 Brucellosis 64 0.066
572
PRV004 Periventricular Leukomalacia 52 0.066
573
c HNT004 Huntington Disease-Like 2 50 0.066
574
ENT004 Enthesopathy 49 0.066
575
SCR011 Scrapie 39 0.066
576
P MYC084 Mycobacterium Tuberculosis 1 68 0.066
577
PRT038 Protein-Energy Malnutrition 54 0.066
578
P SML001 Small Cell Carcinoma 52 0.066
579
P INF038 Influenza 68 0.065
580
DPH001 Diphtheria 60 0.065
581
P THR014 Thrombocytopenia 67 0.065
582
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 67 0.065
583
HPT082 Hepatic Adenomas, Familial 44 0.065
584
ADP007 Adie Pupil 39 0.065
585
HNM002 Hinman Syndrome 27 0.065
586
TRC023 Trichinosis 53 0.065
587
LGH007 Leigh Syndrome 70 0.065
588
P FTL001 Fetal Alcohol Syndrome 57 0.065
589
THY030 Thyroid Gland Disease 52 0.065
590
END040 Endogenous Depression 55 0.064
591
PLR008 Pleurisy 50 0.064
592
CHD004 Chudley-Mccullough Syndrome 46 0.064
593
PLY150 Polykaryocytosis Inducer 31 0.064
594
FLR001 Filarial Elephantiasis 55 0.064
595
BLR001 Biliary Atresia 50 0.064
596
P CHL066 Cholangitis 51 0.064
597
LYM027 Lymphopenia 58 0.064
598
SDD001 Sudden Infant Death Syndrome 61 0.063
599
P ACT105 Acute Mountain Sickness 52 0.063
600
IRR003 Irritant Dermatitis 49 0.063
601
GTR002 Goiter 53 0.063
602
c CRV002 Cervix Uteri Carcinoma in Situ 46 0.063
603
CRV045 Cervical Intraepithelial Neoplasia 39 0.063
604
WRN001 Werner Syndrome 69 0.063
605
GRN017 Granulocytopenia 44 0.063
606
WLS001 Wilson Disease 71 0.063
607
NNT012 Neonatal Jaundice 53 0.063
608
LYM019 Lymphosarcoma 46 0.063
609
P GRV001 Graves' Disease 55 0.063
610
CRY035 Cryptorchidism, Unilateral or Bilateral 58 0.063
611
ASB001 Asbestosis 47 0.063
612
ASB003 Asbestos Intoxication 26 0.063
613
LRY018 Laryngeal Squamous Cell Carcinoma 44 0.062
615
OBS002 Obsessive-Compulsive Disorder 68 0.062
616
NRM005 Neuromuscular Disease 64 0.062
617
CHR074 Choriocarcinoma 47 0.062
618
P MYP006 Myopia 55 0.062
619
P MTC004 Mitochondrial Encephalomyopathy 44 0.062
620
P MNC007 Monocytic Leukemia 53 0.061
621
URL001 Urolithiasis 45 0.061
622
BRS051 Breast Disease 58 0.061
623
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.061
624
P ATR005 Atrophic Gastritis 50 0.061
625
c ATS347 Autosomal Dominant Polycystic Kidney Disease 65 0.061
626
JNT004 Joint Laxity, Short Stature, and Myopia 45 0.061
627
SPP011 Suppression of Tumorigenicity 12 59 0.061
628
WTH001 Withdrawal Disorder 48 0.061
629
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.060
630
P INT099 Intrahepatic Cholestasis of Pregnancy 51 0.060
631
P TRT010 Teratoma 52 0.060
632
KWS001 Kwashiorkor 44 0.060
633
P RTT002 Rett Syndrome 80 0.060
634
P PYL005 Pyelonephritis 56 0.060
635
c BRN108 Branchiootic Syndrome 1 62 0.060
636
P MGR001 Migraine Without Aura 49 0.060
637
ORL004 Oral Submucous Fibrosis 55 0.059
638
OST003 Osteonecrosis 61 0.059
639
PRP030 Purpura 54 0.059
640
SKN019 Skin Melanoma 68 0.059
641
CRH005 Crohn's Colitis 53 0.059
642
DXR001 Doxorubicin Induced Cardiomyopathy 33 0.059
643
LYM017 Lyme Disease 64 0.058
644
BLD131 Bladder Urothelial Carcinoma 62 0.058
645
P GLC113 Galactosemia I 64 0.058
646
MCL006 Macular Retinal Edema 55 0.058
647
CRV040 Cervix Carcinoma 51 0.058
648
P CNR004 Cone-Rod Dystrophy 2 73 0.058
649
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.058
650
VRL011 Viral Infectious Disease 61 0.058
651
SNS003 Sensory Peripheral Neuropathy 54 0.058
652
CYS005 Cysticercosis 53 0.057
653
MLD001 Melioidosis 68 0.057
654
HMR023 Hemorrhagic Cystitis 45 0.057
655
CRD223 Cardiac Arrhythmia 60 0.057
656
URT049 Urate Oxidase, Pseudogene 25 0.057
657
c SCN036 Secondary Progressive Multiple Sclerosis 51 0.057
658
ASP004 Asphyxia Neonatorum 46 0.057
659
P HRD217 Hereditary Optic Neuropathy 36 0.057
660
P THY023 Thymoma 65 0.057
661
P ATS308 Autosomal Dominant Cerebellar Ataxia 60 0.057
662
c THY107 Thymoma, Familial 52 0.057
663
P PNC025 Panic Disorder 53 0.056
664
c WLM013 Wilms Tumor 1 65 0.056
665
P CHR071 Charcot-Marie-Tooth Disease 65 0.056
666
KPS004 Kaposi Sarcoma 75 0.056
667
c ALP101 Alpha-Thalassemia 62 0.056
668
P ATR010 Atrial Heart Septal Defect 60 0.056
669
NPH091 Nephrolithiasis, Calcium Oxalate 60 0.056
670
P SLP005 Sleep Disorder 59 0.056
671
P VNS003 Venous Insufficiency 55 0.056
672
CHL147 Chlamydia Pneumonia 48 0.056
673
PLY001 Polycythemia Vera 69 0.056
674
MYM001 Myoma 54 0.056
675
FND002 Fundus Dystrophy 55 0.055
676
c INH030 Inherited Retinal Disorder 51 0.055
677
P TTR001 Tetralogy of Fallot 70 0.055
678
c JVN010 Juvenile Rheumatoid Arthritis 64 0.055
679
HPT014 Hepatorenal Syndrome 50 0.055
680
P OVR046 Ovarian Cyst 47 0.055
681
PRS047 Prostatitis 56 0.055
682
NRT001 Neurotic Disorder 53 0.055
683
ACT003 Acute Kidney Tubular Necrosis 45 0.055
684
P GLL018 Gallbladder Cancer 57 0.055
685
TST014 Testicular Cancer 46 0.055
686
ATN004 Autonomic Neuropathy 45 0.055
687
DMP001 Dumping Syndrome 44 0.055
688
CHL045 Choline Deficiency Disease 39 0.055
689
CLR030 Clear Cell Renal Cell Carcinoma 53 0.054
690
INT017 Intestinal Schistosomiasis 48 0.054
691
P VNT002 Ventricular Septal Defect 60 0.054
692
P MYS005 Myositis 56 0.054
693
ACH005 Achalasia 51 0.054
694
HYP080 Hypogonadism 50 0.054
695
P PMP001 Pemphigus 54 0.054
696
P SMK004 Smoking As a Quantitative Trait Locus 3 44 0.054
697
P ACT008 Actinic Keratosis 53 0.054
698
P MLG056 Malignant Hyperthermia 67 0.053
699
c ART101 Aortic Valve Disease 2 65 0.053
700
P ALP009 Alopecia Areata 60 0.053
701
APH001 Aphthous Stomatitis 57 0.053
702
ACT084 Acute Stress Disorder 47 0.053
703
P MCP040 Mucopolysaccharidosis-Plus Syndrome 69 0.053
704
P CNJ013 Conjunctivitis 65 0.053
705
LMY002 Leiomyoma 52 0.053
706
LNG031 Lung Benign Neoplasm 51 0.052
707
P FNC004 Fanconi Syndrome 50 0.052
708
P FNC034 Fanconi Renotubular Syndrome 2 40 0.052
709
P PTN014 Patent Ductus Arteriosus 1 60 0.052
710
P NRV007 Nervous System Disease 66 0.052
711
P GCH001 Gaucher's Disease 63 0.052
712
PNC001 Pancytopenia 54 0.052
713
CHL004 Cholelithiasis 49 0.052
714
P FML018 Familial Mediterranean Fever 73 0.052
715
P TBR001 Tuberous Sclerosis 70 0.052
716
PRC002 Paracoccidioidomycosis 54 0.052
717
P MYC033 Myoclonus 46 0.052
718
P PRL003 Proliferative Glomerulonephritis 44 0.052
719
OLG022 Oligoasthenoteratozoospermia 36 0.052
720
PST028 Post-Traumatic Stress Disorder 58 0.052
721
WLL004 Wallerian Degeneration 39 0.052
722
LNG039 Lung Squamous Cell Carcinoma 66 0.051
723
OPS001 Opisthorchiasis 41 0.051
724
P ANG001 Angelman Syndrome 69 0.051
725
P BRY005 Beryllium Disease 40 0.051
726
ABT001 Abetalipoproteinemia 69 0.051
727
TTH006 Tooth Disease 46 0.051
728
c PRG020 Paragangliomas 3 39 0.051
729
P NRN021 Neuronal Ceroid Lipofuscinosis 64 0.051
730
PLM031 Poliomyelitis 64 0.051
731
ETN001 Eating Disorder 60 0.051
732
GLB001 Gilbert Syndrome 58 0.051
733
GRD007 Grade Iii Astrocytoma 59 0.051
734
PRP016 Paraplegia 52 0.051
735
P END046 Endometritis 49 0.051
736
P CRC039 Coarctation of Aorta 47 0.051
737
MSL001 Measles 62 0.050
738
c THY109 Thyroid Cancer, Nonmedullary, 1 56 0.050
739
HYP141 Hyperphenylalaninemia 39 0.050
740
CLF027 Cleft Palate, Isolated 64 0.050
741
OLG001 Oligospermia 45 0.050
742
ALC005 Alcoholic Pancreatitis 40 0.050
743
P ASP006 Aspergillosis 69 0.050
745
RYN005 Raynaud Phenomenon 47 0.050
747
c PNC108 Pancreatitis, Hereditary 70 0.050
748
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.049
749
P FCL005 Focal Segmental Glomerulosclerosis 57 0.049
750
HYP043 Hyperandrogenism 48 0.049
751
c HMG003 Hemoglobin E Disease 45 0.049
752
c TBR025 Tuberous Sclerosis 1 77 0.049
753
CRC021 Carcinosarcoma 62 0.049
754
P HRD011 Hereditary Spherocytosis 60 0.049
755
ECH003 Echinococcosis 53 0.049
756
c INF145 Infantile Liver Failure Syndrome 1 50 0.049
757
ILT001 Ileitis 50 0.049
759
MYC088 Mycobacterium Avium Complex Infections 29 0.049
760
ANT078 Antipyrine Metabolism 24 0.049
761
AND005 Androgen Insensitivity Syndrome, Mild 19 0.049
762
MYL005 Myelofibrosis 70 0.049
763
BRK010 Burkitt Lymphoma 67 0.049
764
LPR001 Lepromatous Leprosy 50 0.049
765
P CRN024 Corneal Disease 44 0.049
766
SDD008 Sudden Sensorineural Hearing Loss 43 0.048
767
MTG002 Mutagen Sensitivity 35 0.048
768
DSS009 Disseminated Intravascular Coagulation 57 0.048
769
DYS015 Dysentery 52 0.048
770
OVR059 Ovary Adenocarcinoma 53 0.048
771
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 60 0.048
772
P MTH008 Methylmalonic Acidemia 50 0.048
773
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 49 0.048
774
MYL080 Myalgic Encephalomyelitis/chronic Fatigue Syndrome 27 0.048
775
DRG003 Drug Dependence 47 0.047
776
c CHR576 Chronic Beryllium Disease 42 0.047
777
EXT006 Extrahepatic Cholestasis 39 0.047
778
P HYD006 Hydrocephalus 66 0.047
779
TYP007 Typhoid Fever 63 0.047
780
P MGR003 Migraine with Aura 52 0.047
781
P AGG001 Aggressive Periodontitis 50 0.047
782
c FTL006 Fetal Alcohol Spectrum Disorder 43 0.047
783
c GCH015 Gaucher Disease, Type I 70 0.047
784
PRP001 Propionic Acidemia 65 0.047
785
JPN002 Japanese Encephalitis 57 0.047
786
c PRM038 Primary Agammaglobulinemia 44 0.047
787
ISL099 Isolated Methylmalonic Acidemia 29 0.047
788
c CNG027 Congenital Hemolytic Anemia 50 0.046
789
CMP010 Complex Regional Pain Syndrome 58 0.046
790
EXF001 Exfoliation Syndrome 56 0.046
791
P MMB011 Membranous Nephropathy 50 0.046
792
DYS073 Dysphagia 50 0.046
793
DBT081 Diabetic Encephalopathy 37 0.046
794
ONC002 Onchocerciasis 52 0.046
795
c CHL119 Cholangitis, Primary Sclerosing 57 0.046
796
P SCL009 Sclerosing Cholangitis 48 0.046
797
PPL002 Papillary Carcinoma 47 0.046
798
CLN044 Colon Adenoma 44 0.046
799
PRM020 Premenstrual Tension 40 0.046
800
c OVR114 Ovarian Cancer 1 38 0.046
801
YLL002 Yellow Fever 61 0.046
802
c SPR009 Sporadic Breast Cancer 45 0.046
803
ACT149 Acetaminophen Metabolism 35 0.046
804
c WLM018 Wilms Tumor 5 61 0.045
805
RHM001 Rheumatic Fever 60 0.045
806
P PLY041 Polymyositis 57 0.045
807
P CRN026 Corneal Edema 43 0.045
808
c ATM006 Autoimmune Lymphoproliferative Syndrome 74 0.045
809
KHL003 Kohlschutter-Tonz Syndrome 65 0.045
810
ALK013 Alkaptonuria 58 0.045
811
DBT004 Diabetic Polyneuropathy 49 0.045
812
MTC023 Mitochondrial Encephalomyopathy Lactic Acidosis and Stroke-Like Episodes 34 0.045
813
SCB001 Scabies 50 0.045
814
CLF001 Cleft Lip 53 0.044
815
IDP091 Idiopathic Nephrotic Syndrome 42 0.044
816
GNR004 Generalized Anxiety Disorder 56 0.044
817
PLS006 Plasmodium Vivax Malaria 51 0.044
818
MTY003 Mutyh Polyposis 30 0.044
819
LBR030 Leber Optic Atrophy 60 0.044
820
MCR013 Microphthalmia 57 0.044
821
CRN017 Coronary Thrombosis 47 0.044
822
GRW007 Growth Hormone Deficiency 46 0.044
823
P MJR007 Major Affective Disorder 1 43 0.044
824
ORP003 Oropharynx Cancer 55 0.043
825
P DRM007 Dermatitis Herpetiformis 55 0.043
826
c DRM040 Dermatitis Herpetiformis, Familial 35 0.043
827
SCH012 Schizoaffective Disorder 50 0.043
828
PLG002 Plague 63 0.043
829
OST011 Osteomalacia 52 0.043
830
c ACT135 Acute Graft Versus Host Disease 52 0.043
831
TLR001 Tularemia 51 0.043
832
MGC001 Megacolon 46 0.043
833
RSP021 Respiratory Allergy 45 0.043
834
c ATM099 Autoimmune Uveitis 45 0.043
835
ADS004 Aids Dementia Complex 40 0.043
836
P PRC031 Preeclampsia/eclampsia 1 38 0.043
837
P PRP003 Porphyria Cutanea Tarda 67 0.043
838
CHL122 Cholesteatoma of Middle Ear 50 0.043
839
ATN011 Autoinflammation with Infantile Enterocolitis 44 0.043
840
BLL006 Bullous Pemphigoid 62 0.042
841
P BRS053 Breast Fibroadenoma 49 0.042
842
SMN007 Seminoma 43 0.042
843
P RRT020 Rare Tumor 41 0.042
844
ALP103 Alpha-1-Antitrypsin Deficiency 64 0.042
845
PSR001 Psoriatic Arthritis 61 0.042
846
P GLY013 Glycogen Storage Disease 60 0.042
847
PMP006 Pemphigus Vulgaris, Familial 57 0.042
848
RSC001 Rosacea 54 0.042
849
FDL002 Food Allergy 51 0.042
850
PRQ002 Paraquat Poisoning 26 0.042
851
ART001 Arterial Tortuosity Syndrome 66 0.041
852
MCR018 Microcytic Anemia 47 0.041
853
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 47 0.041
854
MLT001 Multiple Chemical Sensitivity 40 0.041
855
KSH004 Kashin-Beck Disease 38 0.041
856
BRS099 Breast Ductal Carcinoma 62 0.041
857
DRG002 Drug-Induced Hepatitis 43 0.041
858
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 32 0.041
859
P END033 Endocarditis 57 0.041
860
CCC002 Coccidiosis 51 0.041
861
TTR005 Tetrahydrobiopterin Deficiency 45 0.041
862
MSN001 Mesangial Proliferative Glomerulonephritis 45 0.041
863
TNG009 Tongue Squamous Cell Carcinoma 44 0.041
864
TXC002 Toxic Encephalopathy 53 0.040
865
PRS131 Prostate Cancer/brain Cancer Susceptibility 25 0.040
866
MNT001 Mantle Cell Lymphoma 69 0.040
867
P SYP003 Syphilis 58 0.040
868
FML037 Female Breast Cancer 52 0.040
869
c BPL002 Bipolar I Disorder 49 0.040
870
CHL061 Childhood Leukemia 48 0.040
871
c HMN021 Human T-Cell Leukemia Virus Type 1 47 0.040
872
EWN003 Ewing Sarcoma 69 0.039
873
P MYS003 Myasthenia Gravis 68 0.039
874
P PRS038 Personality Disorder 65 0.039
875
c CNG006 Congenital Hypothyroidism 64 0.039
876
EXT034 Extrinsic Allergic Alveolitis 58 0.039
877
RHM028 Rheumatic Heart Disease 53 0.039
878
P LMB006 Limb-Girdle Muscular Dystrophy 53 0.039
879
MGL001 Megaloblastic Anemia 51 0.039
880
c INV001 Invasive Aspergillosis 49 0.039
881
TBR011 Tuberculous Meningitis 48 0.039
882
PRS042 Prostate Disease 43 0.039
883
PLY100 Polyploidy 40 0.039
884
SRF006 Surfactant Dysfunction 35 0.039
885
P OLG002 Oligodendroglioma 67 0.039
886
c TYR012 Tyrosinemia, Type I 66 0.039
887
CYT008 Cytomegalovirus Infection 57 0.039
888
P HMG032 Hemoglobin H Disease 52 0.039
889
c LRG001 Large Cell Carcinoma 50 0.039
890
c GRN049 Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type I 46 0.039
891
TBR006 Tuberculoid Leprosy 44 0.039
892
MRS001 Marasmus 42 0.039
893
SYS071 Systemic Autoimmune Disease 37 0.039
894
CRY005 Cryptococcosis 58 0.038
895
SFT003 Soft Tissue Sarcoma 56 0.038
896
c CNT035 Central Nervous System Disease 52 0.038
897
CHR073 Choreatic Disease 52 0.038
898
NRM004 Neuroma 51 0.038
899
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 47 0.038
900
P VTR007 Vitreoretinopathy 46 0.038
901
PTT037 Pituitary Tumors 44 0.038
902
CRB008 Cerebral Atherosclerosis 44 0.038
903
ACT209 Acatalasemia 44 0.038
904
DBT002 Diabetic Autonomic Neuropathy 41 0.038
905
RDN001 Reading Disorder 40 0.038
906
P FLL037 Follicular Lymphoma 67 0.038
907
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 65 0.038
908
ADN027 Adenomyosis 56 0.038
909
P ALP106 Alport Syndrome 1, X-Linked 55 0.038
910
ASP003 Aseptic Meningitis 51 0.038
911
GLC106 Glucocorticoid Resistance, Generalized 48 0.038
912
BWN006 Bowen's Disease 32 0.038
913
MTR001 Mature Cataract 28 0.038
914
MRF001 Marfan Syndrome 77 0.037
915
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 0.037
916
MNR012 Meniere Disease 57 0.037
917
CHK001 Chikungunya 57 0.037
918
MTH009 Mouth Disease 56 0.037
919
P ORL007 Oral Cavity Cancer 53 0.037
920
THR004 Thrombocytosis 51 0.037
921
c MLG069 Malignant Hypertension 47 0.037
922
PCD001 Pica Disease 41 0.037
923
SPN362 Spondylometaphyseal Dysplasia, Sedaghatian Type 41 0.037
924
ABD010 Abdominal Wall Defect 36 0.037
925
THL004 Theileriasis 30 0.037
926
c RNG015 Ring Chromosome 2 26 0.037
927
P RNL017 Renal Oncocytoma 53 0.037
928
BRR002 Barrett's Adenocarcinoma 36 0.037
929
FLL027 Fallopian Tube Carcinoma 67 0.036
930
P LYM033 Lymphoproliferative Syndrome 59 0.036
931
THY122 Thyroid Gland Cancer 57 0.036
932
c ACT078 Acute Porphyria 51 0.036
933
END062 Endometrial Hyperplasia 48 0.036
934
P SDR002 Siderosis 44 0.036
935
HML018 Homologous Wasting Disease 22 0.036
936
THY128 Thyroid Tumor 47 0.036
937
ALB002 Albinism 46 0.036
938
CLN003 Clonorchiasis 44 0.036
939
PLY068 Polysubstance Abuse 43 0.036
940
PRC051 Paracetamol Poisoning 30 0.036
941
BRD005 Borderline Leprosy 27 0.036
942
SCH003 Schizophreniform Disorder 56 0.035
943
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 55 0.035
944
BRN014 Bronchopneumonia 54 0.035
945
GST009 Gastroschisis 53 0.035
946
P SHR001 Short Bowel Syndrome 53 0.035
947
c GLL024 Gallbladder Disease 1 53 0.035
948
P HMR005 Hemorrhoid 46 0.035
949
MYF001 Myofibroma 45 0.035
950
NRN005 Neuronal Ceroid-Lipofuscinoses 41 0.035
951
c ERL056 Early-Onset Parkinson's Disease 39 0.035
952
MLD002 Mild Pre-Eclampsia 36 0.035
953
PYR009 Pyridoxine Deficiency Anemia 34 0.035
954
EPL050 Epilepsy, Partial, with Pericentral Spikes 25 0.035
955
CYN003 Cyanide Poisoning 24 0.035
956
P BLD062 Bile Duct Cancer 67 0.034
957
PLS011 Plasmacytoma 56 0.034
958
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 54 0.034
959
HMC040 Homocystinuria Due to Cystathionine Beta-Synthase Deficiency 52 0.034
960
CCN001 Cocaine Dependence 48 0.034
961
CLF056 Cleft Lip with or Without Cleft Palate 47 0.034
962
AGR002 Agoraphobia 45 0.034
963
P SBR004 Seborrheic Dermatitis 45 0.034
964
c MLG079 Malignant Pleural Mesothelioma 42 0.034
965
c HMG001 Hemoglobin C Disease 40 0.034
966
HNZ004 Heinz Body Anemias 39 0.034
967
FTL007 Fetal Hydantoin Syndrome 29 0.034
968
ACT133 Acetylation, Slow 23 0.034
969
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 58 0.034
970
c BNG091 Benign Chronic Pemphigus 58 0.034
971
P PLV020 Pelvic Organ Prolapse 57 0.034
972
TCK001 Tick-Borne Encephalitis 56 0.034
973
P PTT006 Pituitary Adenoma 55 0.034
974
WST005 West Nile Virus 54 0.034
975
ENC055 Encephalopathy, Ethylmalonic 53 0.034
976
PRN011 Pernicious Anemia 53 0.034
977
PLS009 Plasma Cell Neoplasm 51 0.034
978
DRY001 Dry Eye Syndrome 47 0.034
979
ORG002 Organic Acidemia 44 0.034
980
CRD043 Ceroid Storage Disease 44 0.034
981
CRN020 Coronary Restenosis 39 0.034
982
c PRG106 Progressive Muscular Dystrophy 33 0.034
983
P BLR006 Biliary Tract Disease 47 0.033
984
THR035 Thrombasthenia 40 0.033
985
RNL065 Renal Cell Carcinoma, Papillary, 1 73 0.032
986
P RBL001 Rubella 59 0.032
987
SRC027 Sarcoma, Synovial 58 0.032
988
CCC001 Coccidioidomycosis 58 0.032
989
DFF036 Differentiated Thyroid Carcinoma 52 0.032
990
MLL001 Molluscum Contagiosum 50 0.032
991
c INF023 Inflammatory Breast Carcinoma 50 0.032
992
P CRV031 Cervical Adenocarcinoma 49 0.032
993
c TYR013 Tyrosinemia, Type Ii 47 0.032
994
ELS001 Eales Disease 45 0.032
995
BRY001 Berylliosis 40 0.032
996
CVT001 Cavitary Optic Disc Anomalies 38 0.032
997
SLW005 Slowed Nerve Conduction Velocity, Autosomal Dominant 32 0.032
998
NNT021 Neonatal Meningitis 25 0.032
999
ORL006 Oral Mucosa Leukoplakia 23 0.032
1000
THY020 Thyroid Hyalinizing Trabecular Adenoma 21 0.032
1001
LSC001 Lesch-Nyhan Syndrome 62 0.031
1002
c SPN301 Spinocerebellar Ataxia 2 58 0.031
1003
HRY003 Hairy Cell Leukemia 55 0.031
1004
c HPT007 Hepatitis E 53 0.031
1005
LNT004 Lentigines 50 0.031
1006
ONC007 Oncocytoma 49 0.031
1007
EPT021 Epithelial Recurrent Erosion Dystrophy 42 0.031
1008
EXC002 Exocrine Pancreatic Insufficiency 42 0.031
1009
PRP075 Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss 37 0.031
1010
PRS011 Persian Gulf Syndrome 36 0.031
1011
c ALC016 Alcohol Sensitivity, Acute 31 0.031
1012
PRX092 Peroxidase, Salivary 9 0.031
1013
GTL001 Gitelman Syndrome 65 0.030
1014
MNK001 Menkes Disease 64 0.030
1015
NRF007 Neurofibroma 64 0.030
1016
END041 Endometrial Adenocarcinoma 63 0.030
1017
ESP020 Esophageal Atresia 62 0.030
1018
P EMR001 Emery-Dreifuss Muscular Dystrophy 60 0.030
1019
ERY003 Erythema Multiforme 58 0.030
1020
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 57 0.030
1021
MMM001 Mammary Paget's Disease 53 0.030
1022
P EPD016 Epidermolysis Bullosa 53 0.030
1023
PLM014 Pleomorphic Adenoma 52 0.030
1024
P EST001 Estrogen-Receptor Positive Breast Cancer 49 0.030
1025
P CLL015 Collagen Disease 47 0.030
1026
KRT013 Keratolytic Winter Erythema 46 0.030
1027
ENC005 Encephalomalacia 43 0.030
1028
P PLM025 Pulmonary Venoocclusive Disease 42 0.030
1029
c PRK021 Parkinson Disease 7, Autosomal Recessive Early-Onset 40 0.030
1030
P SPR119 Spermatogenic Failure, X-Linked, 1 39 0.030
1031
HYP264 Hypertonia 38 0.030
1032
SPS019 Spastic Paraparesis 38 0.030
1033
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 38 0.030
1034
CRY036 Cryptogenic Cirrhosis 36 0.030
1035
NNT024 Neonatal Stroke 34 0.030
1036
PHN011 Phenytoin Toxicity 33 0.030
1037
QLT008 Qualitative or Quantitative Defects of Dysferlin 30 0.030
1038
DYS030 Dysferlinopathy 29 0.030
1039
P PRG139 Progeroid Syndrome 28 0.030
1040
SRN001 Serine Deficiency 24 0.030
1041
NRM021 Neurometabolic Disorder Due to Serine Deficiency 15 0.030
1042
MYC006 Mycosis Fungoides 66 0.028
1043
c PRK089 Parkinson Disease 2, Autosomal Recessive Juvenile 59 0.028
1044
DBN001 Dubin-Johnson Syndrome 59 0.028
1045
CRV038 Cervical Squamous Cell Carcinoma 58 0.028
1046
PRN009 Paranoid Schizophrenia 50 0.028
1047
PRT035 Peritoneum Cancer 44 0.028
1048
RDC006 Red Cell Aplasia 43 0.028
1049
SKN020 Skin Papilloma 39 0.028
1050
c CHR020 Chronic Interstitial Cystitis 37 0.028
1051
WHT017 Wheat Allergy 32 0.028
1052
FNT004 Fainting 30 0.028
1053
TRN002 Transitional Meningioma 25 0.028
1054
PHC015 Phacoanaphylactic Uveitis 19 0.028
1055
CNN003 Conn's Syndrome 79 0.028
1056
SVR097 Severe Cutaneous Adverse Reaction 69 0.028
1057
CMM004 Common Variable Immunodeficiency 68 0.028
1058
CHD001 Chediak-Higashi Syndrome 66 0.028
1059
HMT002 Hematologic Cancer 62 0.028
1060
c CRD186 Ceroid Lipofuscinosis, Neuronal, 3 60 0.028
1061
P NRF002 Neurofibromatosis 56 0.028
1062
HMP005 Hemiplegia 55 0.028
1063
ESP023 Esophageal Disease 52 0.028
1064
MRG003 Marginal Zone B-Cell Lymphoma 52 0.028
1065
TRC010 Trichotillomania 51 0.028
1066
c PNC106 Pancreatic Agenesis 1 51 0.028
1067
P RNL007 Renal Tubular Acidosis 51 0.028
1068
MCP006 Mucoepidermoid Carcinoma 50 0.028
1069
AMB002 Amblyopia 49 0.028
1070
P SDR003 Sideroblastic Anemia 49 0.028
1071
HST010 Histiocytosis 48 0.028