Search results for Oxidized glutathione

2538 hits were found for Oxidized glutathione

# Family MCID Name MIFTS Score
1
GLT007 Glutathione Synthetase Deficiency 48 56.141
2
GLT034 Glutathione Transferase Activity Toward Trans-Stilbene Oxide 4 38.503
3
GLT039 Glutathione Peroxidase Deficiency 33 35.459
4
HML010 Hemolytic Anemia Due to Glutathione Reductase Deficiency 21 34.406
5
ISC004 Ischemia 61 21.169
6
HYP066 Hyperglycemia 60 20.874
7
HYP266 Hypoxia 56 20.125
8
NNL005 Non-Alcoholic Fatty Liver Disease 63 19.821
9
AGN016 Aging 53 19.526
10
FTT001 Fatty Liver Disease 61 17.883
11
ATH013 Atherosclerosis Susceptibility 63 17.520
12
RPD005 Rapidly Involuting Congenital Hemangioma 48 17.298
13
P PLM037 Pulmonary Hypertension 69 17.240
14
c TYP009 Type 2 Diabetes Mellitus 91 16.683
15
P NRB001 Neuroblastoma 66 16.218
16
c PRC016 Pre-Eclampsia 64 16.154
17
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 16.074
18
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 15.951
19
P MTC069 Mitochondrial Disorders 57 15.836
20
c MCR120 Microvascular Complications of Diabetes 7 47 15.578
21
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 15.502
22
c MCR130 Microvascular Complications of Diabetes 6 41 15.487
23
c MCR133 Microvascular Complications of Diabetes 4 41 15.450
24
c MCR113 Microvascular Complications of Diabetes 3 52 15.450
25
CYT002 Cytokine Deficiency 43 14.995
26
c AMY091 Amyotrophic Lateral Sclerosis 1 87 14.965
27
P VSC007 Vascular Disease 62 14.865
28
c HYP836 Hypercholesterolemia, Familial, 1 73 14.818
29
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 14.595
30
DFC004 Deficiency Anemia 74 14.574
31
P AST005 Asthma 75 14.561
32
P LTR001 Lateral Sclerosis 57 14.523
33
48X005 48,xyyy 39 14.456
34
PLM129 Pulmonary Disease, Chronic Obstructive 74 14.395
35
P LVR013 Liver Disease 68 14.319
36
LPD008 Lipid Metabolism Disorder 61 14.277
37
P ALZ034 Alzheimer Disease 87 14.235
38
P DBT009 Diabetes Mellitus 67 14.187
39
P PRK057 Parkinson Disease, Late-Onset 79 14.103
40
CHN055 Chanarin-Dorfman Syndrome 61 13.841
41
P INF032 Infertility 60 13.772
42
P KDN018 Kidney Disease 71 13.696
43
c CHR684 Chronic Kidney Disease 73 13.546
44
c HYP595 Hypertension, Essential 84 13.443
46
CYS001 Cystic Fibrosis 77 12.926
47
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 12.838
48
TXC005 Toxic Shock Syndrome 61 12.826
49
P ADL010 Adult Respiratory Distress Syndrome 70 12.814
50
LPP008 Lipoprotein Quantitative Trait Locus 65 12.737
51
ART140 Arteries, Anomalies of 52 12.703
52
c ATR087 Atrial Standstill 1 74 12.679
53
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 12.669
54
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 12.669
55
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 12.669
56
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 12.669
57
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 12.669
58
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 12.669
59
c BDY019 Body Mass Index Quantitative Trait Locus 18 46 12.669
60
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 12.669
61
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 12.669
62
P BDY004 Body Mass Index Quantitative Trait Locus 11 82 12.648
63
c MCR115 Microvascular Complications of Diabetes 5 65 12.499
64
CLT003 Colitis 63 12.478
65
HMS001 Hemosiderosis 48 12.357
66
P CTR002 Cataract 59 12.337
67
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 12.332
68
P RRH023 Rare Hereditary Hemochromatosis 52 12.267
69
LNG099 Lung Disease 62 12.205
70
P PRD008 Periodontitis 63 11.890
71
LVR012 Liver Cirrhosis 62 11.844
72
BRN071 Brain Injury 50 11.637
73
PRT251 Proteinuria, Chronic Benign 58 11.603
74
IRN002 Iron Metabolism Disease 56 11.555
75
GLL048 Glial Tumor 51 11.505
76
P PNC044 Pancreatitis 61 11.484
77
GLM045 Glioma 62 11.458
78
END086 End Stage Renal Disease 54 11.425
79
P MLN007 Male Infertility 56 11.424
80
P RSP003 Respiratory Failure 73 11.340
81
P PRK039 Parkinsonism 55 11.273
82
PPL052 Papillomatosis, Confluent and Reticulated 34 11.144
83
P NRP001 Neuropathy 59 11.040
84
CRB004 Cerebral Artery Occlusion 45 11.032
85
c ACT027 Acute Pancreatitis 60 11.022
86
NNL006 Non-Alcoholic Steatohepatitis 54 10.960
87
P SZR006 Seizure Disorder 69 10.859
88
P BCL017 B-Cell Lymphoma 57 10.791
89
P MYP004 Myopathy 67 10.706
90
P CRN300 Coronary Heart Disease 1 73 10.650
91
P MYC007 Myocardial Infarction 69 10.599
92
PHN011 Phenytoin Toxicity 32 10.595
93
P SCK005 Sickle Cell Disease 56 10.476
94
P RHN004 Rhinitis 56 10.397
95
c TYP008 Type 1 Diabetes Mellitus 77 10.338
96
ANX004 Anoxia 40 10.329
97
ANP008 Anaplastic Oligoastrocytoma 31 10.308
98
P PLM036 Pulmonary Fibrosis 65 10.260
99
P SCH015 Schizophrenia 74 10.213
100
P ENC018 Encephalopathy 62 10.063
101
TRM010 Traumatic Brain Injury 50 10.044
102
P HNT016 Huntington Disease 73 9.976
103
P OVR042 Ovarian Cancer 88 9.954
104
P HYP086 Hypothyroidism 68 9.933
105
P ATS364 Autism 72 9.898
106
GLB002 Glioblastoma 67 9.883
107
P HRT032 Heart Disease 84 9.864
108
HMC014 Homocysteinemia 52 9.861
109
c ACT071 Acute Kidney Failure 60 9.859
110
P ALC033 Alcohol Use Disorder 67 9.848
111
P HML002 Hemolytic Anemia 62 9.846
112
P PRP019 Peripheral Nervous System Disease 57 9.774
113
HLX001 Helix Syndrome 47 9.757
114
CHL068 Cholestasis 61 9.706
115
P BRS047 Breast Cancer 97 9.644
116
BRN056 Bronchopulmonary Dysplasia 57 9.606
117
P ECL001 Eclampsia 52 9.585
118
HYP056 Hypoglycemia 65 9.566
119
P SLP006 Sleep Apnea 69 9.464
120
IMP005 Impotence 52 9.448
121
47X002 47,xyy 47 9.447
122
SPN186 Spinal Cord Injury 60 9.361
123
PNG002 Pain Agnosia 51 9.352
124
HYP060 Hyperinsulinism 53 9.347
125
P THL005 Thalassemia 56 9.342
126
P MSC005 Muscular Dystrophy 66 9.312
127
ULC004 Ulcerative Colitis 74 9.263
128
P BLD134 Bladder Cancer 79 9.253
129
P HPT023 Hepatocellular Carcinoma 95 9.218
130
P BPL003 Bipolar Disorder 56 9.173
131
c MJR022 Major Affective Disorder 8 37 9.172
132
c MJR024 Major Affective Disorder 9 40 9.172
133
STR067 Stroke, Ischemic 79 9.079
134
ALC007 Alcohol Dependence 65 9.047
135
P LCT001 Lactic Acidosis 50 9.046
136
CNG034 Congestive Heart Failure 69 9.043
137
P INF037 Inflammatory Bowel Disease 53 9.005
138
ALL003 Allergic Rhinitis 66 9.002
139
INT323 Intraocular Pressure Quantitative Trait Locus 63 9.002
140
P PHC003 Pheochromocytoma 70 8.919
141
ADR040 Adrenal Gland Pheochromocytoma 45 8.913
142
P MLT020 Multiple Sclerosis 79 8.853
143
MTB004 Metabolic Acidosis 48 8.669
144
ORL011 Oral Cancer 60 8.578
145
BCT022 Bacterial Infectious Disease 55 8.547
146
DWN001 Down Syndrome 70 8.539
147
P PRS040 Prostate Cancer 95 8.515
148
P PLY011 Polycystic Ovary Syndrome 57 8.512
149
P SKN015 Skin Carcinoma 71 8.459
150
GLC003 Glucose Intolerance 53 8.425
151
DPR016 Depression 64 8.387
152
URM002 Uremia 47 8.362
153
P CRD246 Cardiovascular System Disease 55 8.362
154
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 8.348
155
P HYP076 Hyperthyroidism 53 8.338
156
P MLN008 Melanoma 75 8.334
157
P ADN016 Adenocarcinoma 63 8.333
158
P CLR023 Colorectal Cancer 100 8.332
159
SKN016 Skin Disease 63 8.313
160
P LNG032 Lung Cancer 98 8.261
161
OST012 Osteoarthritis 77 8.255
162
MLR004 Malaria 77 8.206
163
P END044 Endometriosis 62 8.177
164
MNT002 Mental Depression 56 8.100
165
P KLZ004 Kala-Azar 1 41 8.096
166
LSH001 Leishmaniasis 63 8.096
167
c DLT002 Dilated Cardiomyopathy 79 8.087
168
KRT002 Keratomalacia 54 8.072
169
P PNC035 Pancreatic Cancer 87 8.071
170
MLD018 Mild Cognitive Impairment 48 8.043
171
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 8.043
172
SCK003 Sickle Cell Anemia 74 8.034
173
SQM006 Squamous Cell Carcinoma 59 8.024
174
DBT010 Diabetic Neuropathy 54 7.996
175
ALL006 Allergic Asthma 55 7.979
176
OST159 Osteogenic Sarcoma 66 7.967
177
c ACT075 Acute Myocardial Infarction 55 7.926
178
c PLM164 Pulmonary Hypertension, Primary, 1 75 7.893
179
CRB039 Cerebrovascular Disease 65 7.871
180
ATS010 Autosomal Recessive Disease 42 7.826
181
P ART021 Arteriosclerosis 53 7.801
182
c DNT047 Dentinogenesis Imperfecta Type 2 35 7.779
183
P ART022 Arthritis 70 7.739
184
P LNG064 Lung Cancer Susceptibility 3 69 7.726
185
P RHM011 Rheumatoid Arthritis 81 7.669
186
ATM095 Autoimmune Disease 61 7.641
187
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 7.637
188
PRT036 Peritonitis 65 7.627
189
TLN003 Telangiectasis 51 7.568
190
BRN004 Brain Edema 54 7.522
191
c ACT134 Acute Liver Failure 57 7.508
192
ANX010 Anxiety 70 7.504
193
P PSR002 Psoriasis 63 7.491
194
PST011 Pustulosis of Palm and Sole 52 7.487
195
PLM010 Pulmonary Edema 54 7.418
196
PRT013 Portal Hypertension 59 7.378
197
ALL029 Allergic Disease 61 7.373
198
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 7.372
199
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 7.372
200
P EPL164 Epilepsy 70 7.369
201
P MSC003 Muscular Atrophy 52 7.363
202
SCH014 Schistosomiasis 56 7.336
203
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 7.312
204
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 7.272
205
IGR001 Ige Responsiveness, Atopic 58 7.267
206
HPT019 Hepatic Encephalopathy 59 7.194
207
P ATX030 Ataxia-Telangiectasia 80 7.173
208
c SYS001 Systemic Lupus Erythematosus 85 7.167
209
HMN044 Human Immunodeficiency Virus Type 1 76 7.161
210
HRW001 Hair Whorl 35 7.134
211
ALL014 Allergic Encephalomyelitis 34 7.083
212
P HYP750 Hypertriglyceridemia, Familial 61 7.071
213
P LPS004 Lupus Erythematosus 61 7.070
214
GST023 Gastric Ulcer 52 7.057
215
CRH001 Crohn's Disease 80 7.055
216
P LKM002 Leukemia 65 7.026
217
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 7.023
218
BNR002 Bone Resorption Disease 47 7.015
219
c HPT001 Hepatitis C 61 7.013
220
c MGR028 Migraine with or Without Aura 1 63 6.980
221
P MJR001 Major Depressive Disorder 68 6.968
222
PRP027 Peripheral Vascular Disease 71 6.906
223
c BTT014 Beta-Thalassemia 72 6.898
224
P GLM007 Glomerulonephritis 59 6.884
225
P GST044 Gastritis 55 6.818
226
CHG001 Chagas Disease 65 6.800
227
c HPT073 Hepatitis C Virus 70 6.764
228
PLM134 Pulmonary Fibrosis, Idiopathic 76 6.762
229
P OPN001 Open-Angle Glaucoma 55 6.741
230
ANG054 Angina Pectoris 65 6.737
231
P RTN016 Retinal Degeneration 52 6.719
232
DRM006 Dermatitis 61 6.716
233
P GLM040 Glioma Susceptibility 1 70 6.700
234
P RTN018 Retinal Disease 53 6.690
235
c ATS007 Autism Spectrum Disorder 71 6.681
236
c PRD040 Periodontitis, Chronic 52 6.657
237
P CHR012 Chronic Granulomatous Disease 69 6.657
238
ORL015 Oral Squamous Cell Carcinoma 43 6.649
239
PRT037 Pertussis 49 6.648
240
GST033 Gestational Diabetes 60 6.638
241
P MYL006 Myeloid Leukemia 60 6.596
242
CRV035 Cervical Cancer 72 6.581
243
P GST053 Gastric Cancer 82 6.551
244
ADL002 Adult Syndrome 69 6.548
245
P LKM062 Leukemia, Acute Lymphoblastic 69 6.521
246
c INH020 Inherited Metabolic Disorder 47 6.489
247
RNL077 Renal Fibrosis 46 6.479
248
P MYC008 Myocarditis 59 6.469
249
STT001 Status Epilepticus 58 6.447
250
MCS002 Mucositis 55 6.424
251
P HPT021 Hepatitis 68 6.422
252
BLR008 Bilirubin Metabolic Disorder 57 6.418
253
P CRD119 Cardiac Arrest 68 6.388
254
MSC157 Muscular Dystrophy, Duchenne Type 78 6.376
255
ESP021 Esophageal Cancer 84 6.373
256
c PCH010 Pachyonychia Congenita 3 43 6.350
257
RNL114 Renal Cell Carcinoma, Nonpapillary 79 6.348
258
c LKM061 Leukemia, Acute Myeloid 83 6.314
259
MLG169 Malignant Astrocytoma 57 6.283
260
BRN024 Bronchitis 67 6.277
261
MTC005 Mitochondrial Metabolism Disease 44 6.255
262
ENT011 Enterocolitis 55 6.255
263
P DMN002 Dementia 65 6.237
264
c SCL052 Scleroderma, Familial Progressive 60 6.163
265
P FBR017 Fibrosarcoma 55 6.160
266
HPT004 Hepatic Coma 43 6.158
267
CNT047 Contact Dermatitis 56 6.103
268
P DRM053 Dermatitis, Atopic 65 6.084
269
c VRL010 Viral Hepatitis 52 6.052
270
ADN018 Adenoma 58 6.049
271
INS001 Insulinoma 59 6.023
272
CLN015 Colon Adenocarcinoma 64 5.997
273
PRM329 Premature Aging 36 5.994
274
IMM167 Immune Deficiency Disease 76 5.987
275
OCL069 Ocular Motor Apraxia 57 5.987
276
ADR007 Adrenoleukodystrophy 73 5.983
277
HLC007 Helicobacter Pylori Infection 67 5.978
278
PRN019 Perinatal Necrotizing Enterocolitis 60 5.951
279
PRS045 Prostatic Hypertrophy 53 5.946
280
VRC001 Varicocele 48 5.892
281
P BRS044 Breast Adenocarcinoma 58 5.864
282
P HYP265 Hypotonia 42 5.846
283
P MYC084 Mycobacterium Tuberculosis 1 68 5.838
284
P OPT006 Optic Nerve Disease 57 5.837
285
c GLC092 Glaucoma, Primary Open Angle 60 5.836
286
P MTH007 Methemoglobinemia 46 5.822
287
P ATR011 Atrial Fibrillation 66 5.796
288
ACQ007 Acquired Immunodeficiency Syndrome 58 5.771
289
GST092 Gastroesophageal Reflux 59 5.766
290
P CYS018 Cystitis 58 5.757
291
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 5.720
292
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 5.720
293
PRS021 Prostatic Adenoma 43 5.706
294
HYP781 Hypoascorbemia 52 5.706
295
VSC002 Vascular Dementia 59 5.682
296
P OST002 Osteoporosis 76 5.675
297
P MTR014 Motor Neuron Disease 65 5.675
298
c SML038 Small Cell Cancer of the Lung 68 5.661
299
P HYP061 Hypertrophic Cardiomyopathy 68 5.628
300
P EYD002 Eye Disease 57 5.627
301
NRR001 Neuroretinitis 42 5.627
302
P PNM007 Pneumonia 64 5.624
303
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 5.620
304
ART016 Aortic Aneurysm 68 5.597
305
THR024 Thrombosis 56 5.559
306
PRS129 Prostatic Hyperplasia, Benign 48 5.519
307
P HYP098 Hypereosinophilic Syndrome 66 5.514
308
PHN003 Phenylketonuria 76 5.504
309
INS024 Insulin-Like Growth Factor I 77 5.499
310
P MCR129 Microvascular Complications of Diabetes 1 67 5.486
311
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 51 5.478
312
MTB008 Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 42 5.478
313
MDD011 Mood Disorder 61 5.475
314
P RTN008 Retinitis Pigmentosa 79 5.467
315
LGH007 Leigh Syndrome 70 5.461
316
MYL069 Myeloma, Multiple 76 5.457
317
ACT119 Acute Promyelocytic Leukemia 62 5.449
318
ADR022 Adrenomyeloneuropathy 38 5.445
319
P THY032 Thyroiditis 56 5.438
320
PRP080 Peripheral Artery Disease 54 5.435
321
RTN023 Retinitis 45 5.427
322
GNG013 Gingivitis 59 5.411
323
CRT015 Carotid Artery Occlusion 45 5.409
324
P NPH012 Nephrotic Syndrome 61 5.404
325
c HPT016 Hepatitis B 62 5.384
326
SVR004 Severe Combined Immunodeficiency 70 5.369
327
PLC008 Placenta Disease 48 5.368
328
RCK004 Rickets 64 5.339
329
IRN001 Iron Deficiency Anemia 58 5.327
330
OVR094 Ovarian Epithelial Cancer 39 5.321
331
c MCR112 Microvascular Complications of Diabetes 2 42 5.321
332
INT007 Intermediate Coronary Syndrome 53 5.271
333
URT010 Ureteral Obstruction 44 5.266
334
CHL014 Cholera 62 5.262
335
c EXD008 Exudative Vitreoretinopathy 1 71 5.258
336
APN008 Apnea, Obstructive Sleep 66 5.253
337
P PRN023 Prion Disease 60 5.235
338
MYL009 Myelodysplastic Syndrome 67 5.200
339
BRR014 Barrett Esophagus 66 5.185
340
HVY002 Heavy Metal Poisoning 22 5.182
341
P AMY004 Amyloidosis 69 5.148
342
THY029 Thyroid Carcinoma 55 5.111
343
PST092 Posttransplant Acute Limbic Encephalitis 29 5.083
344
CHL065 Cholangiocarcinoma 57 5.069
345
INT079 Intrahepatic Cholangiocarcinoma 51 5.063
346
ALC006 Alcoholic Hepatitis 61 5.052
347
CHR066 Chronic Fatigue Syndrome 59 5.033
348
GT001 Gout 63 5.028
349
VTM002 Vitamin B12 Deficiency 48 5.018
350
NRL016 Neural Tube Defects 80 5.002
351
ACY009 Acyl-Coa Dehydrogenase, Medium-Chain, Deficiency of 58 4.999
352
TRN015 Transient Cerebral Ischemia 62 4.997
353
P KDN017 Kidney Cancer 60 4.988
354
P SNS001 Sensorineural Hearing Loss 60 4.982
355
ANR040 Aneurysm 60 4.959
356
P ANP001 Anaplastic Large Cell Lymphoma 59 4.958
357
P RTN024 Retinoblastoma 72 4.958
358
PPT005 Peptic Ulcer Disease 58 4.936
359
MST005 Mastitis 52 4.933
360
P PRP029 Porphyria 60 4.924
361
P HDC001 Headache 56 4.921
362
SVR001 Severe Acute Respiratory Syndrome 68 4.916
363
P LYM118 Lymphoma 66 4.897
364
NTR005 Nutritional Deficiency Disease 60 4.893
365
MTH071 Methane Production 24 4.885
366
XRD010 Xeroderma Pigmentosum, Variant Type 72 4.883
367
P MTC133 Mitochondrial Myopathy 51 4.882
368
P PLY019 Polyneuropathy 52 4.880
369
RBF001 Riboflavin Deficiency 49 4.879
370
P SPP010 Suppressor of Tumorigenicity 3 50 4.877
371
CHR178 Chromosomal Triplication 33 4.852
372
P CHR345 Chronic Pain 50 4.838
373
P NSP012 Nasopharyngeal Carcinoma 60 4.831
374
RLP002 Relapsing-Remitting Multiple Sclerosis 56 4.828
375
LMB062 Limb Ischemia 55 4.825
376
P MNN013 Meningitis 65 4.821
377
P LKM071 Leukemia, Chronic Lymphocytic 74 4.781
378
c LKM063 Leukemia, Chronic Myeloid 70 4.779
379
HGH043 High Grade Glioma 46 4.764
380
P UVT001 Uveitis 57 4.762
381
ACT098 Acute Erythroid Leukemia 55 4.744
382
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 4.717
383
P HMC002 Homocystinuria 52 4.715
384
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 4.714
385
P TRM003 Tremor 50 4.708
386
P HRP006 Herpes Simplex 65 4.696
387
PSY004 Psychotic Disorder 66 4.693
388
P BNG032 Benign Mesothelioma 53 4.691
389
P CND004 Candidiasis 57 4.687
390
ACY011 Acyl-Coa Dehydrogenase Deficiency 31 4.663
391
ALL010 Allergic Contact Dermatitis 55 4.652
392
AMN003 Amnestic Disorder 53 4.650
393
ACY010 Acyl-Coa Dehydrogenase, Very Long-Chain, Deficiency of 63 4.650
394
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 62 4.646
395
SPL018 Splenomegaly 47 4.643
396
ANT039 Antisynthetase Syndrome 55 4.641
397
PPL022 Papilloma 53 4.632
398
P DRR001 Diarrhea 55 4.631
399
SQM002 Squamous Cell Papilloma 45 4.621
400
CVD001 Covid-19 59 4.613
401
c SVR005 Severe Pre-Eclampsia 49 4.612
402
HYP014 Hyperuricemia 51 4.607
403
P ESP024 Esophagitis 60 4.606
404
VSC003 Visceral Leishmaniasis 54 4.593
405
HNS001 Hansen's Disease 32 4.581
406
ADP007 Adie Pupil 40 4.576
407
HNM002 Hinman Syndrome 29 4.576
408
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 4.544
409
P VSC011 Vasculitis 61 4.541
410
P ALP008 Alopecia 53 4.541
411
P LPR021 Leprosy 3 71 4.534
412
ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 35 4.530
413
P BND020 Bone Disease 60 4.516
414
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 4.509
415
P OBS001 Obstructive Jaundice 49 4.508
416
CNS004 Constipation 56 4.508
417
P GRF003 Graft-Versus-Host Disease 71 4.506
418
PLM001 Pulmonary Tuberculosis 69 4.494
419
DNT012 Dental Caries 53 4.487
420
c OPT053 Optic Atrophy 1 62 4.485
421
P ENC004 Encephalitis 61 4.477
422
NPH009 Nephrolithiasis 54 4.474
423
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 4.469
424
c DWL002 Dowling-Degos Disease 1 58 4.466
425
PNC041 Pancreatic Ductal Adenocarcinoma 51 4.460
426
OTT002 Otitis Media 70 4.448
427
SLC006 Silicosis 55 4.437
428
DSS032 Disease by Infectious Agent 55 4.429
429
P TRN020 Turner Syndrome 67 4.427
430
SNL007 Senile Cataract 40 4.420
431
P PLY014 Polycystic Kidney Disease 71 4.419
432
INT066 Interstitial Lung Disease 60 4.402
433
CHL123 Chlamydia 58 4.395
434
BRN002 Bronchiolitis 57 4.368
435
MTC004 Mitochondrial Encephalomyopathy 42 4.361
436
CHR100 Chronic Ulcer of Skin 57 4.344
437
END057 Endometrial Cancer 76 4.335
438
TRD006 Tardive Dyskinesia 53 4.328
439
BRN028 Brain Cancer 73 4.321
440
RTN020 Retinal Vascular Disease 45 4.319
441
HPT022 Hepatoblastoma 54 4.319
442
TBC004 Tobacco Addiction 63 4.310
443
DSS008 Disease of Mental Health 74 4.299
445
SRC014 Sarcoma 64 4.273
446
DMY004 Demyelinating Disease 50 4.271
447
SPN035 Spindle Cell Sarcoma 51 4.265
448
CRB090 Cerebral Hypoxia 42 4.263
449
HMG005 Hemoglobinopathy 55 4.251
450
CLR109 Colorectal Adenocarcinoma 50 4.250
451
c BRN108 Branchiootic Syndrome 1 63 4.244
452
P MPL001 Maple Syrup Urine Disease 69 4.241
453
P BRN022 Bronchiectasis 59 4.231
454
P PLM034 Pulmonary Emphysema 58 4.210
455
CRB037 Cerebral Palsy 66 4.203
456
KRN002 Kearns-Sayre Syndrome 62 4.203
457
FBR047 Fibromyalgia 57 4.199
458
P ANT006 Antiphospholipid Syndrome 55 4.185
459
c PRM108 Primary Progressive Multiple Sclerosis 51 4.175
460
TST044 Testicular Torsion 45 4.175
461
HYP005 Hypokalemia 55 4.175
462
HRN029 Hearing Loss, Noise-Induced 37 4.173
463
c HPT003 Hepatitis a 63 4.162
464
P SYS005 Systemic Scleroderma 73 4.157
465
GST050 Gastrointestinal System Disease 55 4.156
466
SQM013 Squamous Cell Carcinoma, Head and Neck 75 4.136
467
c PLM127 Pulmonary Hypertension, Primary, 3 34 4.132
468
HMP009 Haemophilus Influenzae 41 4.123
469
MSC007 Muscle Hypertrophy 64 4.122
470
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 4.120
471
c HMC039 Hemochromatosis, Type 1 73 4.110
472
P ATT013 Attention Deficit-Hyperactivity Disorder 65 4.087
473
PRM236 Primary Biliary Cholangitis 62 4.073
474
ARG004 Argyria 26 4.069
475
P MRC003 Mercury Poisoning 48 4.066
476
P SRC025 Sarcoidosis 1 70 4.062
477
c DPH024 Diaphragmatic Hernia, Congenital 63 4.055
478
P PRM011 Primary Ciliary Dyskinesia 68 4.053
479
P LRY044 Larynx Cancer 53 4.050
480
LKP003 Leukoplakia 39 4.050
481
ANM045 Anemia, Nonspherocytic Hemolytic, Due to G6pd Deficiency 50 4.047
482
P THR014 Thrombocytopenia 66 4.041
483
THY030 Thyroid Gland Disease 50 4.041
484
P RNV001 Renovascular Hypertension 48 4.034
485
TRY001 Trypanosomiasis 50 4.032
486
c ACT073 Acute Leukemia 59 4.012
487
GMM011 Gamma-Glutamylcysteine Synthetase Deficiency, Hemolytic Anemia Due to 25 4.007
488
P BRB001 Beriberi 44 4.006
489
P SBS003 Substance Abuse 54 4.004
490
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 4.003
491
P ACN011 Acne 55 4.001
492
TTN003 Tetanus 64 4.000
493
GST040 Gastric Adenocarcinoma 66 3.994
494
PRT038 Protein-Energy Malnutrition 53 3.992
495
RTN003 Retinal Ischemia 48 3.978
496
HDN002 Head Injury 44 3.973
497
c LKM005 Leukemia, T-Cell, Chronic 33 3.970
498
P KRT007 Keratoconus 49 3.969
499
P FRD001 Friedreich Ataxia 62 3.964
500
DBT007 Diabetic Cataract 36 3.953
501
TRN018 Transitional Cell Carcinoma 56 3.940
502
KRT009 Keratosis 52 3.939
503
P DDN001 Duodenal Ulcer 52 3.923
504
PRX001 Peroxisomal Disease 46 3.917
505
P OVR082 Overgrowth Syndrome 41 3.915
506
c BLD140 Blood Group, I System 47 3.914
507
GLT014 Glutathionuria 37 3.908
508
P INT068 Intestinal Disease 53 3.894
509
CLR108 Colorectal Adenoma 63 3.850
510
c FML021 Familial Hypercholesterolemia 71 3.844
511
CYS010 Cystinosis 61 3.832
512
P INF038 Influenza 68 3.821
513
P EXN002 Exanthem 58 3.818
514
CRN030 Coronary Stenosis 50 3.816
515
P TYR004 Tyrosinemia 49 3.816
516
P ART023 Arthropathy 59 3.801
517
P TMP001 Temporal Lobe Epilepsy 49 3.796
518
PST028 Post-Traumatic Stress Disorder 58 3.794
519
P ZLL001 Zellweger Syndrome 65 3.777
520
P CLC063 Celiac Disease 1 65 3.755
521
URT049 Urate Oxidase, Pseudogene 24 3.746
522
SLP001 Sleeping Sickness 56 3.745
523
c HNT011 Huntington Disease-Like 3 33 3.740
524
PRS047 Prostatitis 57 3.729
525
PLS007 Plasmodium Falciparum Malaria 52 3.722
526
c SPR086 Spermatogenic Failure 3 47 3.722
527
c BCT007 Bacterial Meningitis 55 3.711
528
MYC005 Myocardial Stunning 45 3.709
529
NNT012 Neonatal Jaundice 53 3.708
530
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 3.707
531
P NTR004 Neutropenia 62 3.704
532
PLM033 Pulmonary Embolism 58 3.700
533
c BSL007 Basal Cell Carcinoma 67 3.697
534
P RHB003 Rhabdomyosarcoma 66 3.695
535
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 3.687
536
INT002 Intermittent Claudication 61 3.683
537
STM007 Stomatitis 52 3.682
538
P MLG056 Malignant Hyperthermia 65 3.672
539
VLV047 Volvulus of Midgut 55 3.664
540
OCC016 Occupational Asthma 33 3.655
541
BTT017 Beta-Thalassemia Major 54 3.633
542
P HRD144 Hereditary Mixed Polyposis Syndrome 54 3.633
543
ACT149 Acetaminophen Metabolism 37 3.632
544
c ATM011 Autoimmune Hepatitis 62 3.627
545
P INS002 in Situ Carcinoma 52 3.625
546
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 62 3.607
547
MCL006 Macular Retinal Edema 56 3.600
548
ANT018 Anthracosis 50 3.599
549
HLL004 Hellp Syndrome 53 3.595
550
P TXP001 Toxoplasmosis 59 3.589
551
VCC001 Vaccinia 49 3.581
552
TST015 Testicular Disease 42 3.574
553
P PNM006 Pneumoconiosis 55 3.571
554
P URN019 Urinary Tract Infection 48 3.550
555
HMN014 Human Immunodeficiency Virus Infectious Disease 54 3.543
556
ENT004 Enthesopathy 51 3.531
557
P RCT021 Rectum Cancer 54 3.527
558
MDM001 Medium-Chain Acyl-Coenzyme a Dehydrogenase Deficiency 34 3.515
560
CND006 Candida Glabrata 29 3.505
561
P DNG005 Dengue Virus 55 3.499
562
P GRV001 Graves' Disease 54 3.494
563
SDD001 Sudden Infant Death Syndrome 60 3.488
564
GST045 Gastroenteritis 58 3.481
565
P ACT105 Acute Mountain Sickness 52 3.477
566
FLR002 Filariasis 55 3.474
567
CHL152 Childhood Acute Lymphocytic Leukemia 50 3.471
568
FND002 Fundus Dystrophy 54 3.463
569
P APL001 Aplastic Anemia 72 3.459
571
CTN007 Cutaneous Leishmaniasis 61 3.451
572
P SPR120 Supranuclear Palsy, Progressive, 1 68 3.447
573
HMG002 Hemoglobinuria 50 3.446
574
NRM005 Neuromuscular Disease 62 3.445
575
GRN017 Granulocytopenia 42 3.443
576
MST004 Mast Cell Neoplasm 41 3.436
577
EXT007 Extracutaneous Mastocytoma 38 3.436
578
MTC146 Mitochondrial Complex I Deficiency, Nuclear Type 1 59 3.428
579
PRV004 Periventricular Leukomalacia 52 3.419
580
MLT157 Multiple System Atrophy 1 69 3.419
581
c EPS039 Episodic Pain Syndrome, Familial, 1 42 3.406
582
CHD004 Chudley-Mccullough Syndrome 47 3.405
583
P GLC113 Galactosemia I 65 3.403
584
P LCH002 Lichen Planus 54 3.388
585
P MNC007 Monocytic Leukemia 48 3.381
586
URL001 Urolithiasis 45 3.372
587
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 3.369
588
AZS001 Azoospermia 45 3.363
589
GTR002 Goiter 52 3.361
590
HYP080 Hypogonadism 49 3.361
591
DGN001 Degenerative Disc Disease 48 3.356
592
c PNS012 Paine Syndrome 60 3.355
593
P FML011 Familial Adenomatous Polyposis 70 3.352
594
SKN019 Skin Melanoma 70 3.344
595
CRT013 Carotid Stenosis 51 3.344
596
LPT014 Leptin Deficiency or Dysfunction 77 3.340
597
c ATS347 Autosomal Dominant Polycystic Kidney Disease 64 3.338
598
RFS006 Refsum Disease, Classic 63 3.338
599
WLS001 Wilson Disease 70 3.334
600
SCR011 Scrapie 39 3.333
601
IGG001 Iga Glomerulonephritis 50 3.332
602
BRN012 Bronchiolitis Obliterans 56 3.330
603
PPT001 Peptic Esophagitis 51 3.307
604
KRT019 Keratitis, Hereditary 66 3.307
605
PNC129 Pancreatic Adenocarcinoma 64 3.300
606
P NRV007 Nervous System Disease 65 3.300
607
P SLP005 Sleep Disorder 61 3.291
608
CRH005 Crohn's Colitis 53 3.277
609
P RTT002 Rett Syndrome 79 3.276
610
HRT012 Heart Valve Disease 53 3.276
611
LYM133 Lymphoma, Hodgkin, Classic 69 3.270
612
c ACT249 Acute Asthma 40 3.268
613
ORL012 Oral Leukoplakia 35 3.266
614
PLR008 Pleurisy 49 3.264
615
KWS001 Kwashiorkor 44 3.262
616
P FTL001 Fetal Alcohol Syndrome 55 3.260
617
IRR002 Irritable Bowel Syndrome 64 3.258
618
LYM027 Lymphopenia 56 3.248
619
BRC012 Brucellosis 66 3.239
620
MNG007 Manganese Poisoning 28 3.237
621
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 3.233
622
c ACT068 Acute Cystitis 60 3.231
623
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 3.222
624
P MCR010 Microcephaly 59 3.222
625
HRT011 Heart Septal Defect 49 3.221
626
MTC023 Mitochondrial Encephalomyopathy Lactic Acidosis and Stroke-Like Episodes 44 3.219
627
PLY150 Polykaryocytosis Inducer 29 3.206
628
c SCN036 Secondary Progressive Multiple Sclerosis 55 3.202
629
P MDL005 Medulloblastoma 75 3.195
630
P DYS154 Dystonia 64 3.180
631
CRD137 Cardiogenic Shock 56 3.177
632
c SPN225 Spondyloarthropathy 1 70 3.173
633
OST003 Osteonecrosis 60 3.172
634
PRP030 Purpura 54 3.167
635
CRY035 Cryptorchidism, Unilateral or Bilateral 57 3.158
636
c MST023 Mesothelioma, Malignant 56 3.153
637
ACT017 Acute Chest Syndrome 50 3.141
638
MNN043 Meningioma, Familial 79 3.141
639
LYM002 Lymphoplasmacyte-Rich Meningioma 35 3.141
640
SCR001 Secretory Meningioma 40 3.141
641
INT395 Intracranial Meningioma 47 3.141
642
c FNC027 Fanconi Anemia, Complementation Group a 80 3.131
643
P PRS038 Personality Disorder 65 3.128
644
c HNT004 Huntington Disease-Like 2 51 3.105
645
P PLY018 Polycythemia 56 3.097
646
LYM143 Lymphoma, Non-Hodgkin, Familial 74 3.096
647
P CHL066 Cholangitis 51 3.096
648
END040 Endogenous Depression 54 3.093
649
P ADL017 Adult T-Cell Leukemia 53 3.087
650
P ALP009 Alopecia Areata 59 3.085
651
DFF005 Diffuse Large B-Cell Lymphoma 55 3.082
652
P MVM001 Movement Disease 61 3.080
653
BRS051 Breast Disease 58 3.080
654
SPN051 Spondylitis 51 3.079
655
INF009 Inflammatory Spondylopathy 30 3.079
656
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 3.071
657
LNG015 Lingual-Facial-Buccal Dyskinesia 47 3.068
658
ANR007 Anorexia Nervosa 59 3.064
659
HYP043 Hyperandrogenism 47 3.058
660
P MYS005 Myositis 55 3.053
661
WRN001 Werner Syndrome 69 3.048
662
NPH091 Nephrolithiasis, Calcium Oxalate 61 3.047
663
RHB024 Rhabdomyosarcoma 2 65 3.043
664
ALC009 Alcoholic Liver Cirrhosis 54 3.040
665
END072 Endotheliitis 36 3.037
666
P ANR048 Aniridia 1 66 3.035
667
PRP016 Paraplegia 52 3.029
668
ACT084 Acute Stress Disorder 53 3.020
669
CHL067 Cholecystitis 59 3.020
670
HPT046 Hepatic Veno-Occlusive Disease 54 3.008
671
ACT003 Acute Kidney Tubular Necrosis 46 2.998
672
OBS002 Obsessive-Compulsive Disorder 67 2.996
673
LBR038 Leber Hereditary Optic Neuropathy, Modifier of 62 2.984
674
DXR001 Doxorubicin Induced Cardiomyopathy 32 2.984
675
DPH001 Diphtheria 59 2.979
676
FSC002 Fascioliasis 43 2.971
677
c ALP101 Alpha-Thalassemia 62 2.966
678
CHR074 Choriocarcinoma 46 2.956
679
CRD132 Cardiac Conduction Defect 59 2.947
680
ASB001 Asbestosis 47 2.944
681
ASB003 Asbestos Intoxication 32 2.944
682
P URT039 Urticaria 57 2.943
683
P PTN014 Patent Ductus Arteriosus 1 59 2.940
684
HMR023 Hemorrhagic Cystitis 43 2.928
685
CRD223 Cardiac Arrhythmia 63 2.924
686
P CNJ013 Conjunctivitis 66 2.920
687
c ART101 Aortic Valve Disease 2 65 2.915
688
ATN004 Autonomic Neuropathy 42 2.914
689
SXL003 Sexual Disorder 49 2.913
690
CMM005 Common Cold 55 2.908
691
LRY018 Laryngeal Squamous Cell Carcinoma 47 2.907
692
P PYL005 Pyelonephritis 56 2.890
693
KSH001 Keshan Disease 31 2.889
694
RYS001 Reye Syndrome 49 2.887
695
P HRD217 Hereditary Optic Neuropathy 36 2.885
696
EMB004 Embryonal Carcinoma 55 2.880
697
SNS003 Sensory Peripheral Neuropathy 51 2.878
698
ALP103 Alpha-1-Antitrypsin Deficiency 67 2.877
699
P MYP006 Myopia 55 2.873
700
c LNG109 Lung Cancer Susceptibility 1 26 2.870
701
WTH001 Withdrawal Disorder 47 2.855
702
ACY005 Acyl-Coa Dehydrogenase, Short-Chain, Deficiency of 54 2.845
703
HSH003 Hashimoto Thyroiditis 60 2.840
704
BLR001 Biliary Atresia 55 2.829
705
P GLY013 Glycogen Storage Disease 59 2.829
706
ATN005 Autonomic Dysfunction 45 2.828
707
CHL147 Chlamydia Pneumonia 47 2.826
708
c JVN010 Juvenile Rheumatoid Arthritis 52 2.820
709
MCR013 Microphthalmia 59 2.814
710
P INT143 Interstitial Cystitis 59 2.813
711
ORL013 Oral Lichen Planus 45 2.803
712
P ATR005 Atrophic Gastritis 50 2.801
713
TNS005 Tonsillitis 57 2.797
714
VSL002 Visual Epilepsy 39 2.792
715
MTC205 Mitochondrial Complex Iv Deficiency, Nuclear Type 1 57 2.783
716
P VNT002 Ventricular Septal Defect 58 2.781
717
ORL004 Oral Submucous Fibrosis 56 2.772
718
SPP011 Suppression of Tumorigenicity 12 61 2.772
719
P LKD001 Leukodystrophy 58 2.765
720
PRP001 Propionic Acidemia 65 2.765
721
ALK013 Alkaptonuria 58 2.760
722
P SMK004 Smoking As a Quantitative Trait Locus 3 44 2.755
723
PRD004 Prediabetes Syndrome 52 2.753
724
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 2.744
725
KPS004 Kaposi Sarcoma 76 2.740
726
P ASP006 Aspergillosis 71 2.733
727
FLR001 Filarial Elephantiasis 59 2.733
728
P MGR001 Migraine Without Aura 48 2.726
729
DNG003 Dengue Disease 65 2.726
730
GRS011 Gerstmann-Straussler Disease 56 2.722
731
IRR003 Irritant Dermatitis 47 2.722
732
DMP001 Dumping Syndrome 43 2.715
733
P RNL015 Renal Hypertension 45 2.714
734
CYN002 Cyanosis, Transient Neonatal 43 2.710
735
P THY023 Thymoma 64 2.701
736
VRL011 Viral Infectious Disease 60 2.694
737
c THY107 Thymoma, Familial 42 2.693
738
NNT017 Neonatal Adrenoleukodystrophy 51 2.683
739
CMP010 Complex Regional Pain Syndrome 59 2.680
740
TNG007 Tongue Carcinoma 55 2.676
741
P MCP040 Mucopolysaccharidosis-Plus Syndrome 70 2.673
742
c INH030 Inherited Retinal Disorder 28 2.670
743
DYS015 Dysentery 49 2.661
744
RYN005 Raynaud Phenomenon 45 2.660
745
P GCH001 Gaucher's Disease 69 2.641
746
ASP004 Asphyxia Neonatorum 50 2.637
747
TYP007 Typhoid Fever 63 2.637
748
APH001 Aphthous Stomatitis 57 2.633
749
DBT081 Diabetic Encephalopathy 36 2.632
750
LYM019 Lymphosarcoma 46 2.632
751
P OVR046 Ovarian Cyst 43 2.629
752
MLD001 Melioidosis 67 2.613
753
FTL006 Fetal Alcohol Spectrum Disorder 43 2.612
754
CRV002 Cervix Uteri Carcinoma in Situ 48 2.611
755
CRV045 Cervical Intraepithelial Neoplasia 38 2.611
756
P CHR071 Charcot-Marie-Tooth Disease 64 2.610
757
CLR030 Clear Cell Renal Cell Carcinoma 53 2.601
758
SYN007 Synovitis 54 2.600
759
PLC002 Plica Syndrome 35 2.600
760
SBC016 Subacute Delirium 42 2.594
761
P PMP001 Pemphigus 54 2.592
762
P TBR001 Tuberous Sclerosis 69 2.591
763
CHL004 Cholelithiasis 48 2.589
764
DBT004 Diabetic Polyneuropathy 50 2.580
765
LYM017 Lyme Disease 63 2.567
766
c WLM013 Wilms Tumor 1 65 2.567
767
HMN047 Human Cytomegalovirus Infection 59 2.562
769
HPT014 Hepatorenal Syndrome 49 2.556
770
HYP141 Hyperphenylalaninemia 42 2.554
771
OCL006 Ocular Hypertension 53 2.553
772
P MYC033 Myoclonus 46 2.545
773
CHL045 Choline Deficiency Disease 39 2.541
774
c THY109 Thyroid Cancer, Nonmedullary, 1 55 2.540
775
DSS009 Disseminated Intravascular Coagulation 56 2.536
776
P PNC025 Panic Disorder 52 2.534
777
TRC023 Trichinosis 53 2.531
778
P SML001 Small Cell Carcinoma 52 2.528
779
TST014 Testicular Cancer 51 2.523
780
P VNS003 Venous Insufficiency 54 2.521
781
P MTH008 Methylmalonic Acidemia 52 2.519
782
ILT001 Ileitis 49 2.519
783
OLG001 Oligospermia 45 2.517
784
ABT001 Abetalipoproteinemia 68 2.511
785
MLT118 Multiple Acyl-Coa Dehydrogenase Deficiency 64 2.499
786
c CNG027 Congenital Hemolytic Anemia 49 2.497
787
NWB001 Newborn Respiratory Distress Syndrome 56 2.497
788
c THR092 Thrombophilia Due to Thrombin Defect 74 2.496
789
OVR063 Overnutrition 42 2.484
790
P FNC004 Fanconi Syndrome 60 2.484
792
INT067 Interstitial Nephritis 46 2.477
793
GLB001 Gilbert Syndrome 53 2.475
794
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 2.473
795
ACH005 Achalasia 54 2.471
796
P HYP069 Hyperparathyroidism 62 2.470
797
WLL004 Wallerian Degeneration 38 2.468
798
CRV040 Cervix Carcinoma 50 2.467
799
P END046 Endometritis 46 2.465
800
P HYD006 Hydrocephalus 62 2.464
801
c CHR095 Chronic Progressive External Ophthalmoplegia 48 2.464
802
CRT084 Creatinine Clearance Quantitative Trait Locus 25 2.463
803
PRC002 Paracoccidioidomycosis 53 2.459
804
NWC001 Newcastle Disease 47 2.456
806
P CRC039 Coarctation of Aorta 46 2.455
807
P TRT010 Teratoma 50 2.455
808
P ATR010 Atrial Heart Septal Defect 58 2.454
809
P FML018 Familial Mediterranean Fever 73 2.452
810
TNG009 Tongue Squamous Cell Carcinoma 43 2.451
811
PRT082 Preterm Premature Rupture of the Membranes 56 2.447
812
c HMG003 Hemoglobin E Disease 41 2.445
813
LMY002 Leiomyoma 51 2.442
814
P INT099 Intrahepatic Cholestasis of Pregnancy 61 2.440
815
MYM001 Myoma 54 2.438
816
PLY001 Polycythemia Vera 69 2.437
817
CYS005 Cysticercosis 60 2.430
818
INT075 Intracranial Hypertension 52 2.429
819
PLM031 Poliomyelitis 62 2.428
820
RSC001 Rosacea 55 2.427
821
P NRN021 Neuronal Ceroid Lipofuscinosis 64 2.426
822
ILS001 Ileus 49 2.423
823
c ATS307 Autosomal Recessive Cerebellar Ataxia 38 2.421
824
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 2.412
825
P AGG001 Aggressive Periodontitis 55 2.408
826
APP008 Appendicitis 62 2.406
827
PLC005 Placental Insufficiency 55 2.398
828
ART004 Aortic Atherosclerosis 46 2.395
829
P BRY005 Beryllium Disease 39 2.394
830
PRP007 Priapism 46 2.392
831
FML035 Familial Hyperlipidemia 54 2.389
832
c ATM006 Autoimmune Lymphoproliferative Syndrome 75 2.388
833
TTH006 Tooth Disease 51 2.382
834
OPT003 Opiate Dependence 49 2.381
835
PNC001 Pancytopenia 52 2.380
836
c TBR025 Tuberous Sclerosis 1 84 2.378
837
P FCL005 Focal Segmental Glomerulosclerosis 57 2.370
838
BRK010 Burkitt Lymphoma 65 2.367
839
P FML187 Familial Hypertension 34 2.355
840
NRT001 Neurotic Disorder 56 2.354
841
CRB086 Cerebral Aneurysms 40 2.352
842
P HRD011 Hereditary Spherocytosis 63 2.351
843
PSR001 Psoriatic Arthritis 61 2.350
844
PRX085 Preaxial Hallucal Polydactyly 28 2.350
845
ANT024 Anthrax Disease 57 2.348
846
FDL002 Food Allergy 47 2.347
847
OLG022 Oligoasthenoteratozoospermia 36 2.343
848
P TTR001 Tetralogy of Fallot 69 2.340
849
ECH003 Echinococcosis 52 2.339
850
LWC001 Low Compliance Bladder 44 2.339
851
NRT004 Neuritis 53 2.337
852
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 2.336
853
ISL099 Isolated Methylmalonic Acidemia 35 2.334
854
SFT003 Soft Tissue Sarcoma 43 2.332
855
EXR010 Exercise-Induced Bronchoconstriction 34 2.328
856
RSP019 Respiratory Distress Syndrome in Premature Infants 52 2.328
857
PLG002 Plague 58 2.323
858
GLM044 Glomerular Disease 34 2.320
859
CHR005 Chorioamnionitis 50 2.303
860
HNZ004 Heinz Body Anemias 40 2.300
861
P MMB011 Membranous Nephropathy 50 2.293
862
MSL001 Measles 61 2.290
863
OBS082 Obstructive Nephropathy 41 2.284
864
MYL080 Myalgic Encephalomyelitis/chronic Fatigue Syndrome 32 2.283
865
BCK006 Back Pain 43 2.282
866
RTN017 Retinal Detachment 60 2.276
867
GRW007 Growth Hormone Deficiency 47 2.276
868
SYS003 Systolic Heart Failure 49 2.274
869
CRC021 Carcinosarcoma 62 2.273
870
c GRV008 Graves Disease 1 54 2.272
871
c CNG006 Congenital Hypothyroidism 63 2.271
872
CCC002 Coccidiosis 50 2.265
873
CLF027 Cleft Palate, Isolated 64 2.264
874
P PRP003 Porphyria Cutanea Tarda 66 2.262
875
JPN002 Japanese Encephalitis 61 2.262
876
ALC005 Alcoholic Pancreatitis 38 2.262
877
ALC016 Alcohol Sensitivity, Acute 27 2.262
878
VRC005 Varicose Veins 59 2.254
879
EXT006 Extrahepatic Cholestasis 41 2.253
880
P PRL003 Proliferative Glomerulonephritis 43 2.244
881
INT030 Intracranial Aneurysm 55 2.240
882
P GLL018 Gallbladder Cancer 59 2.235
883
P END033 Endocarditis 58 2.232
884
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 2.231
885
PRQ002 Paraquat Poisoning 28 2.231
886
c PNC108 Pancreatitis, Hereditary 68 2.229
887
PLY100 Polyploidy 36 2.228
888
P CRN024 Corneal Disease 43 2.227
889
c GLL024 Gallbladder Disease 1 53 2.226
890
c BRS111 Breast-Ovarian Cancer, Familial 2 53 2.219
891
MCR018 Microcytic Anemia 46 2.218
892
FRN006 Frontotemporal Dementia 68 2.213
893
PRP083 Porphyria, Acute Intermittent 64 2.206
894
c TYR012 Tyrosinemia, Type I 61 2.201
895
P MJR007 Major Affective Disorder 1 42 2.199
896
PNM008 Pneumothorax 54 2.196
897
P ACT008 Actinic Keratosis 53 2.191
898
CHR576 Chronic Beryllium Disease 42 2.191
899
P SPN046 Spinal Muscular Atrophy 62 2.185
900
ART074 Aortic Dissection 53 2.182
901
EXF001 Exfoliation Syndrome 55 2.180
902
MNN009 Meningoencephalitis 47 2.176
903
DYS073 Dysphagia 53 2.167
904
PLP001 Pulpitis 48 2.163
905
CLF001 Cleft Lip 54 2.160
906
c PRG020 Paragangliomas 3 39 2.160
907
OPS001 Opisthorchiasis 41 2.159
908
P SCL009 Sclerosing Cholangitis 46 2.158
909
ETN001 Eating Disorder 59 2.154
910
LNG031 Lung Benign Neoplasm 51 2.151
911
PLM012 Pulmonary Sarcoidosis 52 2.149
912
P PTS002 Ptosis 52 2.139
913
PRM013 Premature Menopause 57 2.132
914
P HMN010 Hemangioma 61 2.131
915
HTT002 Hutterite Cerebroosteonephrodysplasia Syndrome 25 2.129
916
HYP025 Hyperphosphatemia 47 2.128
917
P MGR003 Migraine with Aura 51 2.128
918
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 42 2.128
919
MTR002 Mitral Valve Insufficiency 51 2.128
920
MYL005 Myelofibrosis 70 2.125
921
SDD008 Sudden Sensorineural Hearing Loss 41 2.117
922
OST017 Osteomyelitis 63 2.114
923
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 2.112
924
P CRN026 Corneal Edema 42 2.112
925
LNG039 Lung Squamous Cell Carcinoma 57 2.112
926
MTG002 Mutagen Sensitivity 34 2.111
927
PPL002 Papillary Carcinoma 46 2.111
928
c CHL119 Cholangitis, Primary Sclerosing 57 2.104
929
BLD131 Bladder Urothelial Carcinoma 59 2.102
930
P SCL018 Scoliosis 57 2.097
931
PRC051 Paracetamol Poisoning 29 2.096
932
EPT021 Epithelial Recurrent Erosion Dystrophy 45 2.085
933
YLL002 Yellow Fever 61 2.085
934
INT017 Intestinal Schistosomiasis 51 2.083
935
PMP006 Pemphigus Vulgaris, Familial 57 2.075
936
SRF006 Surfactant Dysfunction 33 2.068
937
INV001 Invasive Aspergillosis 48 2.068
938
ARG007 Argininemia 58 2.066
939
GSG001 Gas Gangrene 52 2.063
940
ANT078 Antipyrine Metabolism 24 2.062
941
TLR001 Tularemia 56 2.061
942
KWS002 Kawasaki Disease 65 2.061