Search results for superoxide

1092 hits were found for superoxide

# Family MCID Name MIFTS Score
1
P LTR001 Lateral Sclerosis 54 0.591
2
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.591
3
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.221
4
ISC004 Ischemia 58 0.212
5
DWN001 Down Syndrome 70 0.194
6
P MTR014 Motor Neuron Disease 65 0.181
7
HYP266 Hypoxia 57 0.181
8
P VSC007 Vascular Disease 63 0.172
9
P CHR012 Chronic Granulomatous Disease 67 0.170
10
HYP066 Hyperglycemia 61 0.169
11
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.166
12
P NRB001 Neuroblastoma 72 0.162
13
PRT037 Pertussis 65 0.147
14
CHR178 Chromosomal Triplication 35 0.147
15
P BRS047 Breast Cancer 97 0.138
16
P PLM037 Pulmonary Hypertension 67 0.136
17
c MCR130 Microvascular Complications of Diabetes 6 41 0.136
18
P PLM036 Pulmonary Fibrosis 65 0.135
19
c MCR113 Microvascular Complications of Diabetes 3 52 0.135
20
c MCR120 Microvascular Complications of Diabetes 7 47 0.133
21
c MCR133 Microvascular Complications of Diabetes 4 41 0.133
22
c HYP836 Hypercholesterolemia, Familial, 1 73 0.131
23
c PRC016 Pre-Eclampsia 63 0.131
24
P ALZ034 Alzheimer Disease 88 0.130
25
ATH013 Atherosclerosis Susceptibility 65 0.130
26
P PRD008 Periodontitis 64 0.130
27
LNG099 Lung Disease 60 0.130
28
P KDN018 Kidney Disease 72 0.128
29
48X005 48,xyyy 39 0.126
30
BRN071 Brain Injury 49 0.125
31
CRB004 Cerebral Artery Occlusion 45 0.125
32
P CTR002 Cataract 60 0.123
33
P PRK057 Parkinson Disease, Late-Onset 78 0.121
34
P LVR013 Liver Disease 68 0.121
35
HRW001 Hair Whorl 36 0.119
36
P MCR115 Microvascular Complications of Diabetes 5 66 0.117
37
P ADN016 Adenocarcinoma 64 0.114
38
BRN004 Brain Edema 56 0.114
39
AGN016 Aging 56 0.114
40
ANX004 Anoxia 40 0.114
41
CYT002 Cytokine Deficiency 42 0.108
42
P PRS040 Prostate Cancer 97 0.106
43
c CHR684 Chronic Kidney Disease 70 0.106
44
BRN056 Bronchopulmonary Dysplasia 57 0.106
45
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.106
46
P INF032 Infertility 57 0.104
47
TXC005 Toxic Shock Syndrome 62 0.102
48
LVR012 Liver Cirrhosis 62 0.102
49
P HPT023 Hepatocellular Carcinoma 100 0.100
50
P CLR023 Colorectal Cancer 99 0.100
51
LPP008 Lipoprotein Quantitative Trait Locus 62 0.100
52
P GLM007 Glomerulonephritis 57 0.100
53
BNR002 Bone Resorption Disease 48 0.100
54
SQM006 Squamous Cell Carcinoma 60 0.097
55
P INF037 Inflammatory Bowel Disease 54 0.097
56
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.095
57
P GST053 Gastric Cancer 83 0.095
58
P OVR042 Ovarian Cancer 88 0.093
59
P MLN008 Melanoma 69 0.093
60
P DBT009 Diabetes Mellitus 64 0.093
61
LSH001 Leishmaniasis 63 0.093
62
P FBR017 Fibrosarcoma 56 0.093
63
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.093
64
P KLZ004 Kala-Azar 1 41 0.093
65
c HYP595 Hypertension, Essential 84 0.091
66
P GLM045 Glioma 63 0.091
67
P NTR004 Neutropenia 63 0.091
68
FTT001 Fatty Liver Disease 61 0.091
69
DRM006 Dermatitis 61 0.091
70
SPN186 Spinal Cord Injury 60 0.091
71
c PRD040 Periodontitis, Chronic 53 0.091
72
c SYS001 Systemic Lupus Erythematosus 86 0.088
73
P PNC035 Pancreatic Cancer 84 0.088
74
OST012 Osteoarthritis 78 0.088
75
SKN016 Skin Disease 63 0.088
76
CLT003 Colitis 62 0.088
77
47X002 47,xyy 49 0.088
78
GLL048 Glial Tumor 45 0.088
79
c DLT002 Dilated Cardiomyopathy 79 0.086
80
P HRT032 Heart Disease 75 0.086
81
ULC004 Ulcerative Colitis 73 0.086
82
P MSC005 Muscular Dystrophy 66 0.086
83
BRC012 Brucellosis 64 0.086
84
TRD006 Tardive Dyskinesia 54 0.086
85
CRH001 Crohn's Disease 74 0.083
86
P PHC003 Pheochromocytoma 71 0.083
87
ATM095 Autoimmune Disease 62 0.083
88
BCT022 Bacterial Infectious Disease 56 0.083
89
HMS001 Hemosiderosis 54 0.083
90
HMC014 Homocysteinemia 53 0.083
91
ADR040 Adrenal Gland Pheochromocytoma 46 0.083
92
P RRH023 Rare Hereditary Hemochromatosis 41 0.083
93
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.080
94
P RSP003 Respiratory Failure 74 0.080
95
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.080
96
DFC004 Deficiency Anemia 70 0.080
97
CNG034 Congestive Heart Failure 69 0.080
98
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.080
99
P PSR002 Psoriasis 62 0.080
100
c ACT027 Acute Pancreatitis 60 0.080
101
P MLN007 Male Infertility 55 0.080
102
PST011 Pustulosis of Palm and Sole 52 0.080
103
ART140 Arteries, Anomalies of 52 0.080
104
P LNG064 Lung Cancer Susceptibility 3 78 0.078
105
c ATR087 Atrial Standstill 1 75 0.078
106
P SRC025 Sarcoidosis 1 70 0.078
107
ALC007 Alcohol Dependence 66 0.078
108
P DRM053 Dermatitis, Atopic 66 0.078
109
PRT036 Peritonitis 64 0.078
110
P CRN300 Coronary Heart Disease 1 63 0.078
111
P ESP024 Esophagitis 62 0.078
112
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.078
113
c ACT075 Acute Myocardial Infarction 57 0.078
114
P NRP001 Neuropathy 56 0.078
115
P ECL001 Eclampsia 50 0.078
116
NTR046 Neutrophil Migration 50 0.078
117
P BNG032 Benign Mesothelioma 46 0.078
118
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.078
119
PRM329 Premature Aging 35 0.078
120
P SCH015 Schizophrenia 74 0.075
121
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.075
122
HMN044 Human Immunodeficiency Virus Type 1 71 0.075
123
P LPR021 Leprosy 3 69 0.075
124
c DBT099 Diabetes Mellitus, Type I 65 0.075
125
P PNC044 Pancreatitis 61 0.075
126
ADN018 Adenoma 59 0.075
127
IRN002 Iron Metabolism Disease 57 0.075
128
ALL006 Allergic Asthma 56 0.075
129
P GST044 Gastritis 56 0.075
130
TRM010 Traumatic Brain Injury 51 0.075
131
VLV047 Volvulus of Midgut 49 0.075
132
HNS001 Hansen's Disease 34 0.075
133
P LNG032 Lung Cancer 98 0.072
134
ESP021 Esophageal Cancer 90 0.072
135
GLB015 Glioblastoma Multiforme 75 0.072
136
CHG001 Chagas Disease 66 0.072
137
ALL026 Allergic Hypersensitivity Disease 62 0.072
138
P MYL006 Myeloid Leukemia 60 0.072
139
P UVT001 Uveitis 57 0.072
140
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.072
141
IMP005 Impotence 52 0.072
142
CRT015 Carotid Artery Occlusion 45 0.072
143
P RHM011 Rheumatoid Arthritis 80 0.069
144
P HNT016 Huntington Disease 72 0.069
145
P MYC007 Myocardial Infarction 70 0.069
146
P ART022 Arthritis 69 0.069
147
ANG054 Angina Pectoris 66 0.069
148
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.069
149
c SCL052 Scleroderma, Familial Progressive 61 0.069
150
P LPS004 Lupus Erythematosus 61 0.069
151
c ACT071 Acute Kidney Failure 60 0.069
152
P RHN004 Rhinitis 57 0.069
153
PLM010 Pulmonary Edema 54 0.069
154
MYL069 Myeloma, Multiple 85 0.066
156
c LKM061 Leukemia, Acute Myeloid 84 0.066
157
P ATX030 Ataxia-Telangiectasia 82 0.066
158
P LKM002 Leukemia 68 0.066
159
P CRD119 Cardiac Arrest 67 0.066
160
ALL003 Allergic Rhinitis 67 0.066
161
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.066
162
P SKN015 Skin Carcinoma 66 0.066
163
P ADL010 Adult Respiratory Distress Syndrome 65 0.066
164
CHL014 Cholera 59 0.066
165
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.066
166
P HYP076 Hyperthyroidism 55 0.066
167
DBT010 Diabetic Neuropathy 54 0.066
168
c VRL010 Viral Hepatitis 52 0.066
169
TLN003 Telangiectasis 52 0.066
170
HMP009 Haemophilus Influenzae 43 0.066
171
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.062
172
P PNM007 Pneumonia 68 0.062
173
GT001 Gout 64 0.062
174
LPD008 Lipid Metabolism Disorder 62 0.062
175
IRN001 Iron Deficiency Anemia 59 0.062
176
EXT034 Extrinsic Allergic Alveolitis 58 0.062
177
c MST023 Mesothelioma, Malignant 57 0.062
178
P ART021 Arteriosclerosis 54 0.062
179
PRP016 Paraplegia 52 0.062
180
MYC005 Myocardial Stunning 46 0.062
181
PPL052 Papillomatosis, Confluent and Reticulated 33 0.062
182
CYS001 Cystic Fibrosis 81 0.059
183
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.059
184
P LKM062 Leukemia, Acute Lymphoblastic 69 0.059
185
P HML002 Hemolytic Anemia 63 0.059
186
CTN007 Cutaneous Leishmaniasis 62 0.059
187
P ENC018 Encephalopathy 61 0.059
188
P THL005 Thalassemia 60 0.059
189
HLC007 Helicobacter Pylori Infection 59 0.059
190
P SYP003 Syphilis 58 0.059
191
RSP019 Respiratory Distress Syndrome in Premature Infants 58 0.059
192
NWB001 Newborn Respiratory Distress Syndrome 58 0.059
193
TNS005 Tonsillitis 57 0.059
194
SCH014 Schistosomiasis 57 0.059
195
END086 End Stage Renal Disease 51 0.059
196
PLR008 Pleurisy 50 0.059
197
P RNV001 Renovascular Hypertension 48 0.059
198
IGG001 Iga Glomerulonephritis 48 0.059
199
HDN002 Head Injury 46 0.059
200
ORL015 Oral Squamous Cell Carcinoma 43 0.059
201
SNL007 Senile Cataract 42 0.059
202
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.059
203
c NRF023 Neurofibromatosis, Type Ii 80 0.055
204
IMM167 Immune Deficiency Disease 78 0.055
205
MSC157 Muscular Dystrophy, Duchenne Type 72 0.055
206
c HPT073 Hepatitis C Virus 72 0.055
207
MYL009 Myelodysplastic Syndrome 70 0.055
208
P SLP006 Sleep Apnea 69 0.055
209
P SYS005 Systemic Scleroderma 68 0.055
210
BRN024 Bronchitis 68 0.055
211
P NSP012 Nasopharyngeal Carcinoma 66 0.055
212
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.055
213
c HPT001 Hepatitis C 62 0.055
214
P VSC011 Vasculitis 62 0.055
215
INT066 Interstitial Lung Disease 60 0.055
216
P OPT006 Optic Nerve Disease 60 0.055
217
PRT013 Portal Hypertension 59 0.055
218
THY029 Thyroid Carcinoma 59 0.055
219
VSL002 Visual Epilepsy 59 0.055
220
P PRP019 Peripheral Nervous System Disease 58 0.055
221
P CRD246 Cardiovascular System Disease 57 0.055
222
P BPL003 Bipolar Disorder 56 0.055
223
ERY051 Erythroleukemia, Familial 56 0.055
224
P SZR006 Seizure Disorder 56 0.055
225
MCS002 Mucositis 56 0.055
226
SLC006 Silicosis 56 0.055
227
c BCT007 Bacterial Meningitis 55 0.055
228
INT007 Intermediate Coronary Syndrome 55 0.055
229
GST023 Gastric Ulcer 53 0.055
230
P LCT001 Lactic Acidosis 51 0.055
231
P OBS001 Obstructive Jaundice 50 0.055
232
URM002 Uremia 49 0.055
233
c MJR024 Major Affective Disorder 9 41 0.055
234
ALL014 Allergic Encephalomyelitis 38 0.055
235
c MJR022 Major Affective Disorder 8 38 0.055
236
HRN029 Hearing Loss, Noise-Induced 37 0.055
237
PST092 Posttransplant Acute Limbic Encephalitis 29 0.055
238
SVR004 Severe Combined Immunodeficiency 73 0.051
239
c SPN225 Spondyloarthropathy 1 73 0.051
240
OTT002 Otitis Media 72 0.051
241
P ATS364 Autism 70 0.051
242
P ASP006 Aspergillosis 69 0.051
243
P HYP086 Hypothyroidism 69 0.051
244
ART016 Aortic Aneurysm 69 0.051
245
P MYC084 Mycobacterium Tuberculosis 1 68 0.051
246
CRB039 Cerebrovascular Disease 67 0.051
247
P HYP098 Hypereosinophilic Syndrome 67 0.051
248
P MNN013 Meningitis 66 0.051
249
CLN015 Colon Adenocarcinoma 65 0.051
250
P NRN021 Neuronal Ceroid Lipofuscinosis 64 0.051
251
DPR016 Depression 63 0.051
252
P END044 Endometriosis 63 0.051
253
P HYP750 Hypertriglyceridemia, Familial 62 0.051
254
P ART023 Arthropathy 62 0.051
255
CHL068 Cholestasis 61 0.051
256
VRC005 Varicose Veins 60 0.051
257
STT001 Status Epilepticus 60 0.051
258
P MYC008 Myocarditis 59 0.051
259
MNT002 Mental Depression 58 0.051
260
P PRN023 Prion Disease 57 0.051
261
P PNM006 Pneumoconiosis 56 0.051
262
LMB062 Limb Ischemia 55 0.051
263
P GRV001 Graves' Disease 55 0.051
264
c PRM092 Primary Lateral Sclerosis, Adult, 1 53 0.051
265
P MSC003 Muscular Atrophy 52 0.051
266
SPN051 Spondylitis 51 0.051
267
ANT018 Anthracosis 48 0.051
268
HLX001 Helix Syndrome 47 0.051
269
ASB001 Asbestosis 47 0.051
270
CRD137 Cardiogenic Shock 47 0.051
271
c PCH010 Pachyonychia Congenita 3 44 0.051
272
c ATS307 Autosomal Recessive Cerebellar Ataxia 42 0.051
273
CHN002 Chancroid 40 0.051
274
INF009 Inflammatory Spondylopathy 31 0.051
275
ASB003 Asbestos Intoxication 26 0.051
276
MLR004 Malaria 81 0.046
277
PFF001 Pfeiffer Syndrome 79 0.046
278
P MDL005 Medulloblastoma 77 0.046
279
P OST002 Osteoporosis 74 0.046
280
c BTT014 Beta-Thalassemia 74 0.046
281
c EXD008 Exudative Vitreoretinopathy 1 71 0.046
282
P MYP004 Myopathy 70 0.046
283
P LYM118 Lymphoma 68 0.046
284
BRK010 Burkitt Lymphoma 67 0.046
285
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.046
286
TTN003 Tetanus 65 0.046
287
BRR014 Barrett Esophagus 65 0.046
288
P FRD001 Friedreich Ataxia 64 0.046
289
LYM017 Lyme Disease 64 0.046
290
TRN015 Transient Cerebral Ischemia 63 0.046
291
P PRM006 Primary Biliary Cirrhosis 62 0.046
292
P NPH012 Nephrotic Syndrome 60 0.046
293
P ALP009 Alopecia Areata 60 0.046
294
PPT005 Peptic Ulcer Disease 59 0.046
295
EYD002 Eye Disease 58 0.046
296
GRN051 Granulomatous Disease, Chronic, X-Linked 57 0.046
297
VSC002 Vascular Dementia 57 0.046
298
P PYL005 Pyelonephritis 56 0.046
299
c ACT134 Acute Liver Failure 56 0.046
300
P MTC069 Mitochondrial Disorders 56 0.046
301
SYN007 Synovitis 54 0.046
302
GLC003 Glucose Intolerance 54 0.046
303
P ALP008 Alopecia 54 0.046
304
PLM012 Pulmonary Sarcoidosis 53 0.046
305
P MNC007 Monocytic Leukemia 53 0.046
306
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.046
307
NRT004 Neuritis 52 0.046
308
FLT011 Felty Syndrome 52 0.046
309
P SPP010 Suppressor of Tumorigenicity 3 51 0.046
310
STM007 Stomatitis 50 0.046
311
P AGG001 Aggressive Periodontitis 50 0.046
312
ENT004 Enthesopathy 49 0.046
313
MTC005 Mitochondrial Metabolism Disease 49 0.046
314
VCC001 Vaccinia 49 0.046
315
RTN020 Retinal Vascular Disease 46 0.046
316
FBR054 Fibroma 44 0.046
317
c MLG079 Malignant Pleural Mesothelioma 42 0.046
318
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.046
319
DBT007 Diabetic Cataract 38 0.046
320
PLC002 Plica Syndrome 36 0.046
322
c FNC027 Fanconi Anemia, Complementation Group a 81 0.042
323
P LKM071 Leukemia, Chronic Lymphocytic 79 0.042
324
INS024 Insulin-Like Growth Factor I 79 0.042
325
AST005 Asthma 76 0.042
326
XRD010 Xeroderma Pigmentosum, Variant Type 73 0.042
327
P RTN024 Retinoblastoma 73 0.042
328
c LKM063 Leukemia, Chronic Myeloid 72 0.042
329
P AMY004 Amyloidosis 70 0.042
330
P OST001 Osteopetrosis 70 0.042
331
LKC009 Leukocyte Adhesion Deficiency, Type I 69 0.042
332
c ATS007 Autism Spectrum Disorder 67 0.042
333
c MGR028 Migraine with or Without Aura 1 67 0.042
334
OST159 Osteogenic Sarcoma 66 0.042
335
P DMN002 Dementia 66 0.042
336
P CNJ013 Conjunctivitis 65 0.042
337
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.042
338
CLR108 Colorectal Adenoma 64 0.042
339
MSC007 Muscle Hypertrophy 64 0.042
340
P DRM010 Dermatomyositis 61 0.042
341
INT002 Intermittent Claudication 61 0.042
342
ALC006 Alcoholic Hepatitis 61 0.042
343
RCT015 Reactive Arthritis 61 0.042
344
RTN017 Retinal Detachment 61 0.042
345
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.042
346
CHL123 Chlamydia 59 0.042
347
P CYS018 Cystitis 59 0.042
348
c ACT073 Acute Leukemia 58 0.042
349
P ALC033 Alcohol Use Disorder 58 0.042
350
CNT047 Contact Dermatitis 58 0.042
351
P CND004 Candidiasis 58 0.042
352
P PLY019 Polyneuropathy 56 0.042
353
ORL004 Oral Submucous Fibrosis 55 0.042
354
PPL022 Papilloma 54 0.042
355
NNL006 Non-Alcoholic Steatohepatitis 54 0.042
356
P RTN016 Retinal Degeneration 53 0.042
357
c FML008 Familial Retinoblastoma 53 0.042
358
P DDN001 Duodenal Ulcer 52 0.042
359
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.042
360
ENT011 Enterocolitis 51 0.042
361
P AST007 Astrocytoma 51 0.042
362
CHR005 Chorioamnionitis 51 0.042
363
c PYR010 Peyronie's Disease 50 0.042
364
RTN003 Retinal Ischemia 50 0.042
365
c SVR005 Severe Pre-Eclampsia 50 0.042
366
P KRT007 Keratoconus 50 0.042
367
MTB004 Metabolic Acidosis 50 0.042
368
VRC001 Varicocele 49 0.042
369
ATS010 Autosomal Recessive Disease 48 0.042
370
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.042
371
SPL018 Splenomegaly 48 0.042
372
P MRC003 Mercury Poisoning 48 0.042
373
RNL077 Renal Fibrosis 47 0.042
374
LYM019 Lymphosarcoma 46 0.042
375
RTN023 Retinitis 46 0.042
376
SQM002 Squamous Cell Papilloma 46 0.042
377
MSN001 Mesangial Proliferative Glomerulonephritis 45 0.042
378
ACT003 Acute Kidney Tubular Necrosis 45 0.042
379
CRD043 Ceroid Storage Disease 44 0.042
380
P PRL003 Proliferative Glomerulonephritis 44 0.042
381
CRB090 Cerebral Hypoxia 44 0.042
383
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.042
384
NRR001 Neuroretinitis 42 0.042
385
NRN005 Neuronal Ceroid-Lipofuscinoses 41 0.042
386
OVR094 Ovarian Epithelial Cancer 38 0.042
387
P FML187 Familial Hypertension 37 0.042
388
GLM044 Glomerular Disease 37 0.042
389
PLY150 Polykaryocytosis Inducer 31 0.042
390
HVY002 Heavy Metal Poisoning 22 0.042
391
P GLM040 Glioma Susceptibility 1 81 0.036
392
STR067 Stroke, Ischemic 81 0.036
393
P BLD134 Bladder Cancer 79 0.036
394
P RTN008 Retinitis Pigmentosa 79 0.036
395
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.036
396
CRV035 Cervical Cancer 76 0.036
397
PHN003 Phenylketonuria 75 0.036
398
BRN028 Brain Cancer 74 0.036
399
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.036
400
P MLT020 Multiple Sclerosis 72 0.036
401
PRP027 Peripheral Vascular Disease 71 0.036
402
GST040 Gastric Adenocarcinoma 70 0.036
403
WRN001 Werner Syndrome 69 0.036
404
LYM133 Lymphoma, Hodgkin, Classic 69 0.036
405
CNN005 Connective Tissue Disease 68 0.036
406
P MJR001 Major Depressive Disorder 68 0.036
407
PNC129 Pancreatic Adenocarcinoma 68 0.036
408
BLM001 Bloom Syndrome 67 0.036
409
c RHB024 Rhabdomyosarcoma 2 67 0.036
410
KRT019 Keratitis, Hereditary 65 0.036
411
c JVN010 Juvenile Rheumatoid Arthritis 64 0.036
412
OST017 Osteomyelitis 64 0.036
413
c ACT068 Acute Cystitis 63 0.036
414
c ATM011 Autoimmune Hepatitis 63 0.036
415
CYC010 Cyclic Neutropenia 62 0.036
416
c HPT003 Hepatitis a 62 0.036
417
P ENC004 Encephalitis 61 0.036
418
CHR066 Chronic Fatigue Syndrome 61 0.036
419
VRL011 Viral Infectious Disease 61 0.036
420
P KDN017 Kidney Cancer 60 0.036
421
P ATS308 Autosomal Dominant Cerebellar Ataxia 60 0.036
422
HPT019 Hepatic Encephalopathy 60 0.036
423
ACQ007 Acquired Immunodeficiency Syndrome 60 0.036
424
INS001 Insulinoma 60 0.036
425
c CRD186 Ceroid Lipofuscinosis, Neuronal, 3 60 0.036
426
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.036
427
c HPT016 Hepatitis B 59 0.036
428
IGR001 Ige Responsiveness, Atopic 59 0.036
429
PRN019 Perinatal Necrotizing Enterocolitis 59 0.036
430
GNG013 Gingivitis 59 0.036
431
BRN002 Bronchiolitis 59 0.036
432
ANR040 Aneurysm 59 0.036
433
P BCL017 B-Cell Lymphoma 58 0.036
434
P PLY041 Polymyositis 57 0.036
435
DSS009 Disseminated Intravascular Coagulation 57 0.036
436
LST001 Listeriosis 56 0.036
437
ATR057 Atrioventricular Block 55 0.036
438
P DRR001 Diarrhea 55 0.036
439
VSC003 Visceral Leishmaniasis 55 0.036
440
P PLM034 Pulmonary Emphysema 55 0.036
441
P VNS003 Venous Insufficiency 55 0.036
442
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 55 0.036
443
HYP060 Hyperinsulinism 54 0.036
444
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 54 0.036
445
BRN014 Bronchopneumonia 54 0.036
446
SNS003 Sensory Peripheral Neuropathy 54 0.036
447
P TRM003 Tremor 54 0.036
448
MST005 Mastitis 53 0.036
449
GTR002 Goiter 53 0.036
450
ALC009 Alcoholic Liver Cirrhosis 53 0.036
451
c GLL024 Gallbladder Disease 1 53 0.036
452
P PRG013 Paraganglioma 52 0.036
453
P THY032 Thyroiditis 52 0.036
454
PPT001 Peptic Esophagitis 52 0.036
455
P HRD144 Hereditary Mixed Polyposis Syndrome 51 0.036
456
MYL020 Myelomeningocele 51 0.036
457
P MMB011 Membranous Nephropathy 50 0.036
458
CRN030 Coronary Stenosis 50 0.036
459
P SCK005 Sickle Cell Disease 50 0.036
460
TRY001 Trypanosomiasis 50 0.036
461
DYS073 Dysphagia 50 0.036
462
LPR001 Lepromatous Leprosy 50 0.036
463
P ATR005 Atrophic Gastritis 50 0.036
464
ANM045 Anemia, Nonspherocytic Hemolytic, Due to G6pd Deficiency 49 0.036
465
SPT005 Spotted Fever 49 0.036
466
PPL002 Papillary Carcinoma 47 0.036
467
ADN001 Adenosine Deaminase Deficiency 47 0.036
468
RYN005 Raynaud Phenomenon 47 0.036
469
P VTR007 Vitreoretinopathy 46 0.036
470
MYL013 Myeloperoxidase Deficiency 46 0.036
471
LKS001 Leukostasis 46 0.036
472
c ACT042 Acute Pyelonephritis 46 0.036
473
HPT004 Hepatic Coma 45 0.036
474
P CHR345 Chronic Pain 44 0.036
475
TNG009 Tongue Squamous Cell Carcinoma 44 0.036
476
ART006 Arthus Reaction 44 0.036
477
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 43 0.036
478
P HRD018 Hair Disease 43 0.036
479
DRG002 Drug-Induced Hepatitis 43 0.036
480
KLD004 Keloid Disorder 40 0.036
481
RDT001 Radiation Cystitis 32 0.036
482
MYC015 Mycobacterium Fortuitum 32 0.036
483
PRX085 Preaxial Hallucal Polydactyly 28 0.036
484
ARG004 Argyria 27 0.036
485
PRQ002 Paraquat Poisoning 26 0.036
486
STN013 Stenotrophomonas Maltophilia Infection 25 0.036
487
NRL016 Neural Tube Defects 82 0.029
488
KPS004 Kaposi Sarcoma 75 0.029
489
c ART115 Aortic Valve Disease 1 75 0.029
490
SCK003 Sickle Cell Anemia 74 0.029
491
c THR092 Thrombophilia Due to Thrombin Defect 73 0.029
492
P FML018 Familial Mediterranean Fever 73 0.029
493
P GRF003 Graft-Versus-Host Disease 72 0.029
494
ACR007 Acromegaly 71 0.029
495
P EPL164 Epilepsy 71 0.029
496
ADL002 Adult Syndrome 70 0.029
497
PLY001 Polycythemia Vera 69 0.029
498
P SPR120 Supranuclear Palsy, Progressive, 1 68 0.029
499
P INF038 Influenza 68 0.029
500
MLD001 Melioidosis 68 0.029
501
P HPT021 Hepatitis 67 0.029
502
P FLL037 Follicular Lymphoma 67 0.029
503
PSY004 Psychotic Disorder 67 0.029
504
P MLG056 Malignant Hyperthermia 67 0.029
505
CHD001 Chediak-Higashi Syndrome 66 0.029
506
c MCR129 Microvascular Complications of Diabetes 1 66 0.029
507
P HYD006 Hydrocephalus 66 0.029
508
P NRV007 Nervous System Disease 66 0.029
509
c SML038 Small Cell Cancer of the Lung 65 0.029
510
SRC014 Sarcoma 65 0.029
511
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 65 0.029
512
P HRP006 Herpes Simplex 65 0.029
513
KWS002 Kawasaki Disease 65 0.029
514
NRM005 Neuromuscular Disease 64 0.029
515
CLF027 Cleft Palate, Isolated 64 0.029
516
P GLC113 Galactosemia I 64 0.029
517
KRN002 Kearns-Sayre Syndrome 63 0.029
518
c OPT053 Optic Atrophy 1 63 0.029
519
c GLC092 Glaucoma, Primary Open Angle 62 0.029
520
c LCL006 Localized Scleroderma 62 0.029
521
c BRN108 Branchiootic Syndrome 1 62 0.029
522
P SPN046 Spinal Muscular Atrophy 62 0.029
523
CRC021 Carcinosarcoma 62 0.029
524
MDD011 Mood Disorder 62 0.029
525
P PRP029 Porphyria 62 0.029
526
APP008 Appendicitis 61 0.029
527
NPH091 Nephrolithiasis, Calcium Oxalate 60 0.029
528
c JVN061 Juvenile Arthritis 60 0.029
529
MTC146 Mitochondrial Complex I Deficiency, Nuclear Type 1 60 0.029
530
LBR030 Leber Optic Atrophy 60 0.029
531
P PTN014 Patent Ductus Arteriosus 1 60 0.029
532
SPP011 Suppression of Tumorigenicity 12 59 0.029
533
P RBL001 Rubella 59 0.029
534
c DNG003 Dengue Disease 59 0.029
535
P BRS044 Breast Adenocarcinoma 59 0.029
536
GST045 Gastroenteritis 59 0.029
537
ALP097 Alopecia Universalis Congenita 59 0.029
538
CRY035 Cryptorchidism, Unilateral or Bilateral 58 0.029
539
P ANP001 Anaplastic Large Cell Lymphoma 58 0.029
540
ANT024 Anthrax Disease 58 0.029
541
CRD132 Cardiac Conduction Defect 58 0.029
542
SPT004 Septic Arthritis 58 0.029
543
BRS051 Breast Disease 58 0.029
544
P URT039 Urticaria 58 0.029
545
c DWL002 Dowling-Degos Disease 1 58 0.029
546
LYM027 Lymphopenia 58 0.029
547
P OPT009 Optic Neuritis 57 0.029
548
P END033 Endocarditis 57 0.029
549
P FTL001 Fetal Alcohol Syndrome 57 0.029
550
BLR008 Bilirubin Metabolic Disorder 57 0.029
551
JPN002 Japanese Encephalitis 57 0.029
552
PNM008 Pneumothorax 56 0.029
553
P PLY018 Polycythemia 56 0.029
554
TRN018 Transitional Cell Carcinoma 56 0.029
555
ADN027 Adenomyosis 56 0.029
556
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.029
557
BRN012 Bronchiolitis Obliterans 55 0.029
558
MCN007 Meconium Aspiration Syndrome 55 0.029
559
ORP003 Oropharynx Cancer 55 0.029
560
NPH009 Nephrolithiasis 55 0.029
561
CHR100 Chronic Ulcer of Skin 55 0.029
562
P PRG130 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 1 55 0.029
563
P SLM003 Salmonellosis 55 0.029
564
PRP030 Purpura 54 0.029
565
MYM001 Myoma 54 0.029
566
c PRG040 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 4 54 0.029
567
PRS045 Prostatic Hypertrophy 53 0.029
568
MMM001 Mammary Paget's Disease 53 0.029
569
RHM028 Rheumatic Heart Disease 53 0.029
570
KRT006 Keratoconjunctivitis 53 0.029
571
c BRS111 Breast-Ovarian Cancer, Familial 2 53 0.029
572
P HYP083 Hypopituitarism 53 0.029
573
P HML001 Hemolytic-Uremic Syndrome 53 0.029
574
P PNC025 Panic Disorder 53 0.029
575
PRP080 Peripheral Artery Disease 53 0.029
576
P RTN018 Retinal Disease 53 0.029
577
c CNT035 Central Nervous System Disease 52 0.029
578
LGN006 Legionnaire Disease 52 0.029
579
HYP014 Hyperuricemia 52 0.029
580
P MGR003 Migraine with Aura 52 0.029
581
ONC002 Onchocerciasis 52 0.029
582
PRL019 Prolidase Deficiency 52 0.029
583
P TRT010 Teratoma 52 0.029
584
PRV004 Periventricular Leukomalacia 52 0.029
585
THR004 Thrombocytosis 51 0.029
586
PRS021 Prostatic Adenoma 51 0.029
587
TNG007 Tongue Carcinoma 51 0.029
588
ASP003 Aseptic Meningitis 51 0.029
589
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.029
590
CRV040 Cervix Carcinoma 51 0.029
591
RDC002 Radiculopathy 50 0.029
592
ALL009 Allergic Conjunctivitis 50 0.029
593
c PRG038 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 2 50 0.029
594
CRT013 Carotid Stenosis 50 0.029
595
PRN009 Paranoid Schizophrenia 50 0.029
596
URT001 Urethritis 49 0.029
597
BLL004 Bullous Keratopathy 49 0.029
598
c CHR431 Chronic Venous Insufficiency 49 0.029
599
PLP001 Pulpitis 49 0.029
600
PRS129 Prostatic Hyperplasia, Benign 49 0.029
601
P OPN001 Open-Angle Glaucoma 49 0.029
602
MNN009 Meningoencephalitis 49 0.029
603
c BPL002 Bipolar I Disorder 49 0.029
604
P MGR001 Migraine Without Aura 49 0.029
605
c BCT013 Bacterial Pneumonia 48 0.029
606
MCC002 Mucocutaneous Leishmaniasis 47 0.029
607
THY128 Thyroid Tumor 47 0.029
608
P RNL015 Renal Hypertension 47 0.029
609
CRN017 Coronary Thrombosis 47 0.029
610
KRT008 Keratopathy 47 0.029
611
c INH020 Inherited Metabolic Disorder 47 0.029
612
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.029
613
c ACT076 Acute Myocarditis 46 0.029
614
c CRV002 Cervix Uteri Carcinoma in Situ 46 0.029
615
c SPL067 Split-Hand/foot Malformation 1 46 0.029
616
FCL012 Facial Paralysis 46 0.029
617
c CHR095 Chronic Progressive External Ophthalmoplegia 46 0.029
618
GRW007 Growth Hormone Deficiency 46 0.029
619
P HMR005 Hemorrhoid 46 0.029
620
CRN019 Coronary Artery Vasospasm 46 0.029
621
c MLG068 Malignant Glioma 46 0.029
622
CYS019 Cystathioninuria 45 0.029
623
ISL121 Isolated Split Hand-Split Foot Malformation 45 0.029
624
TBR006 Tuberculoid Leprosy 44 0.029
625
P MTC004 Mitochondrial Encephalomyopathy 44 0.029
626
BCT021 Bacterial Sepsis 44 0.029
627
P OVR106 Ovarian Clear Cell Carcinoma 44 0.029
628
CLN044 Colon Adenoma 44 0.029
629
SMN007 Seminoma 43 0.029
630
SKN005 Skin Atrophy 43 0.029
631
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.029
632
EHR002 Ehrlichiosis 42 0.029
633
PRS063 Paresthesia 41 0.029
634
c MCR112 Microvascular Complications of Diabetes 2 41 0.029
635
ALC005 Alcoholic Pancreatitis 40 0.029
636
c PRG020 Paragangliomas 3 39 0.029
637
RCK002 Rocky Mountain Spotted Fever 39 0.029
638
CRV045 Cervical Intraepithelial Neoplasia 39 0.029
639
PRG008 Paragonimiasis 38 0.029
640
P HRD217 Hereditary Optic Neuropathy 36 0.029
642
c LKM005 Leukemia, T-Cell, Chronic 34 0.029
643
PST010 Pasteurellosis 34 0.029
644
HMN002 Human Granulocytic Anaplasmosis 32 0.029
645
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.029
646
PLR005 Pleuropneumonia 31 0.029
647
P SKN067 Skin/hair/eye Pigmentation, Variation in, 2 31 0.029
648
MNN024 Meningitis and Encephalitis 29 0.029
649
P PRG139 Progeroid Syndrome 28 0.029
650
THY006 Thymus Lymphoma 26 0.029
651
URT049 Urate Oxidase, Pseudogene 25 0.029
652
P RTT002 Rett Syndrome 80 0.021
653
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.021
654
MRF001 Marfan Syndrome 77 0.021
655
ADR007 Adrenoleukodystrophy 75 0.021
656
P APL001 Aplastic Anemia 74 0.021
657
END057 Endometrial Cancer 74 0.021
658
c HMC039 Hemochromatosis, Type 1 74 0.021
659
P CNR004 Cone-Rod Dystrophy 2 73 0.021
660
P ALG028 Alagille Syndrome 1 73 0.021
661
WLS001 Wilson Disease 71 0.021
662
P BRG001 Brugada Syndrome 71 0.021
663
BHC003 Behcet Syndrome 71 0.021
664
MLT157 Multiple System Atrophy 1 70 0.021
665
MYL005 Myelofibrosis 70 0.021
666
c GCH015 Gaucher Disease, Type I 70 0.021
667
c PNC108 Pancreatitis, Hereditary 70 0.021
668
PLM001 Pulmonary Tuberculosis 69 0.021
669
CRB037 Cerebral Palsy 69 0.021
670
P ANG001 Angelman Syndrome 69 0.021
671
c BSL007 Basal Cell Carcinoma 68 0.021
672
P MYS003 Myasthenia Gravis 68 0.021
673
P ESS003 Essential Thrombocythemia 68 0.021
674
P FRN006 Frontotemporal Dementia 68 0.021
675
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 67 0.021
676
P DYS007 Dyskeratosis Congenita 67 0.021
677
P SHW006 Shwachman-Diamond Syndrome 1 67 0.021
678
P TRN020 Turner Syndrome 67 0.021
679
P CLC063 Celiac Disease 1 66 0.021
680
P LNG028 Long Qt Syndrome 66 0.021
681
GLL008 Gilles De La Tourette Syndrome 66 0.021
682
GRG001 Greig Cephalopolysyndactyly Syndrome 66 0.021
683
ADR054 Adrenocortical Carcinoma, Hereditary 66 0.021
684
HYP056 Hypoglycemia 66 0.021
685
c HRD010 Hereditary Spastic Paraplegia 66 0.021
686
P ATR011 Atrial Fibrillation 66 0.021
687
P CCK001 Cockayne Syndrome 66 0.021
688
HTC003 Hutchinson-Gilford Progeria Syndrome 65 0.021
689
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.021
690
P LPS002 Liposarcoma 65 0.021
691
c WLM013 Wilms Tumor 1 65 0.021
692
PTT048 Pituitary Adenoma, Prolactin-Secreting 65 0.021
693
P CHR071 Charcot-Marie-Tooth Disease 65 0.021
694
MNK001 Menkes Disease 64 0.021
695
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.021
696
ANG020 Angiosarcoma 64 0.021
697
TBC004 Tobacco Addiction 64 0.021
698
ART002 Arts Syndrome 64 0.021
699
PRP083 Porphyria, Acute Intermittent 64 0.021
700
P GCH001 Gaucher's Disease 63 0.021
701
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.021
702
P HYP069 Hyperparathyroidism 63 0.021
703
PLG002 Plague 63 0.021
704
ACT119 Acute Promyelocytic Leukemia 63 0.021
705
P MVM001 Movement Disease 63 0.021
706
ANR007 Anorexia Nervosa 63 0.021
707
BDD001 Budd-Chiari Syndrome 63 0.021
708
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.021
709
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.021
710
HMT002 Hematologic Cancer 62 0.021
711
P MCH002 Machado-Joseph Disease 62 0.021
712
LSC001 Lesch-Nyhan Syndrome 62 0.021
713
P ORT004 Orthostatic Intolerance 62 0.021
714
c ANM038 Anemia, Autoimmune Hemolytic 62 0.021
715
MSL001 Measles 62 0.021
716
c NRD017 Neurodegeneration with Brain Iron Accumulation 1 61 0.021
717
PSR001 Psoriatic Arthritis 61 0.021
718
P INT143 Interstitial Cystitis 61 0.021
719
YLL002 Yellow Fever 61 0.021
720
c WLM018 Wilms Tumor 5 61 0.021
721
P SJG008 Sjogren Syndrome 61 0.021
722
GST033 Gestational Diabetes 61 0.021
723
SDD001 Sudden Infant Death Syndrome 61 0.021
724
P ART067 Aortic Aneurysm, Familial Thoracic 1 61 0.021
725
NRL005 Neurilemmoma 60 0.021
726
PNM010 Pneumothorax, Primary Spontaneous 60 0.021
727
P TXP001 Toxoplasmosis 60 0.021
728
CRD223 Cardiac Arrhythmia 60 0.021
729
P SNS001 Sensorineural Hearing Loss 60 0.021
730
ORL011 Oral Cancer 60 0.021
731
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 60 0.021
732
P CHR285 Chronic Myelomonocytic Leukemia 60 0.021
733
P BND020 Bone Disease 59 0.021
734
IDP011 Idiopathic Interstitial Pneumonia 59 0.021
735
PNM001 Pneumocystosis 59 0.021
736
PLM033 Pulmonary Embolism 59 0.021
737
PRT058 Pure Autonomic Failure 59 0.021
738
P LYM033 Lymphoproliferative Syndrome 59 0.021
739
DCT002 Ductal Carcinoma in Situ 59 0.021
740
GRD007 Grade Iii Astrocytoma 59 0.021
741
AVN001 Avian Influenza 59 0.021
742
P HMN036 Hemangiopericytoma, Malignant 59 0.021
743
P DNG005 Dengue Virus 59 0.021
744
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.021
745
FRB001 Farber Lipogranulomatosis 59 0.021
746
c SVR003 Severe Congenital Neutropenia 59 0.021
747
INC002 Inclusion Body Myositis 58 0.021
748
c SPN301 Spinocerebellar Ataxia 2 58 0.021
749
CRY005 Cryptococcosis 58 0.021
750
P INT070 Intestinal Obstruction 58 0.021
751
FBR047 Fibromyalgia 58 0.021
752
CMP010 Complex Regional Pain Syndrome 58 0.021
753
CCC001 Coccidioidomycosis 58 0.021
754
P BNC003 Bone Cancer 58 0.021
755
CNS004 Constipation 58 0.021
756
MXD005 Mixed Connective Tissue Disease 58 0.021
757
P FNC044 Fanconi Anemia, Complementation Group C 57 0.021
758
MCR013 Microphthalmia 57 0.021
759
P ZLL001 Zellweger Syndrome 57 0.021
760
P EXN002 Exanthem 57 0.021
761
P HDC001 Headache 57 0.021
762
THR024 Thrombosis 57 0.021
763
APH001 Aphthous Stomatitis 57 0.021
764
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.021
765
CMM005 Common Cold 57 0.021
766
c LKM070 Leukemia, Acute Monocytic 57 0.021
767
CYT008 Cytomegalovirus Infection 57 0.021
768
P MYS005 Myositis 56 0.021
769
P ADL017 Adult T-Cell Leukemia 56 0.021
770
P PLY011 Polycystic Ovary Syndrome 56 0.021
771
PLS011 Plasmacytoma 56 0.021
772
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 56 0.021
773
GNR004 Generalized Anxiety Disorder 56 0.021
774
ACS001 Acoustic Neuroma 56 0.021
775
HMG005 Hemoglobinopathy 56 0.021
776
GST050 Gastrointestinal System Disease 56 0.021
777
ORL005 Oral Candidiasis 56 0.021
778
SML019 Smallpox 56 0.021
779
AND020 Androgen Insensitivity, Partial 56 0.021
780
c THY109 Thyroid Cancer, Nonmedullary, 1 56 0.021
781
FLR001 Filarial Elephantiasis 55 0.021
782
c FML035 Familial Hyperlipidemia 55 0.021
783
HYP005 Hypokalemia 55 0.021
784
NRN004 Neuroendocrine Tumor 55 0.021
785
MCL006 Macular Retinal Edema 55 0.021
786
AMB001 Amebiasis 55 0.021
787
DFF005 Diffuse Large B-Cell Lymphoma 55 0.021
788
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.021
789
CPL003 Capillary Leak Syndrome 55 0.021
790
P SBS003 Substance Abuse 55 0.021
791
FLR002 Filariasis 55 0.021
792
P DRM007 Dermatitis Herpetiformis 55 0.021
793
P XRD029 Xeroderma Pigmentosum, Complementation Group a 55 0.021
794
HNC001 Henoch-Schoenlein Purpura 55 0.021
795
P LRY044 Larynx Cancer 55 0.021
796
HRY003 Hairy Cell Leukemia 55 0.021
797
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 54 0.021
798
RSC001 Rosacea 54 0.021
799
AMN003 Amnestic Disorder 54 0.021
800
CRT017 Cartilage Disease 54 0.021
801
CRY003 Cryptosporidiosis 54 0.021
802
PRT038 Protein-Energy Malnutrition 54 0.021
803
ANL018 Analbuminemia 54 0.021
804
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 54 0.021
805
CLL003 Cellulitis 54 0.021
806
PNC001 Pancytopenia 54 0.021
807
c SPN294 Spinocerebellar Ataxia 1 53 0.021
808
CLR030 Clear Cell Renal Cell Carcinoma 53 0.021
809
c LNG048 Long Qt Syndrome 3 53 0.021
810
P LCH002 Lichen Planus 53 0.021
811
P END047 Endophthalmitis 53 0.021
812
P EPD016 Epidermolysis Bullosa 53 0.021
813
P INS002 in Situ Carcinoma 53 0.021
814
P HMC002 Homocystinuria 53 0.021
815
CRH005 Crohn's Colitis 53 0.021
816
ECH003 Echinococcosis 53 0.021
817
P ALL008 Allergic Bronchopulmonary Aspergillosis 53 0.021
818
OCL006 Ocular Hypertension 53 0.021
819
CYS005 Cysticercosis 53 0.021
820
INF034 Infective Endocarditis 53 0.021
821
CLF001 Cleft Lip 53 0.021
822
GSG001 Gas Gangrene 53 0.021
823
SPN035 Spindle Cell Sarcoma 53 0.021
824
IRD001 Iridocyclitis 53 0.021
825
DNT012 Dental Caries 53 0.021
826
PRN011 Pernicious Anemia 53 0.021
827
c HPT007 Hepatitis E 53 0.021
828
TRC003 Trichomoniasis 53 0.021
829
P INT068 Intestinal Disease 53 0.021
830
OVR059 Ovary Adenocarcinoma 53 0.021
831
c FML191 Familial Long Qt Syndrome 53 0.021
832
CHR073 Choreatic Disease 52 0.021
833
DMY004 Demyelinating Disease 52 0.021
834
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.021
835
MRG003 Marginal Zone B-Cell Lymphoma 52 0.021
836
P RCT021 Rectum Cancer 52 0.021
837
DYS015 Dysentery 52 0.021
838
THY030 Thyroid Gland Disease 52 0.021
839
NRP045 Neuropathy, Ataxia, and Retinitis Pigmentosa 52 0.021
840
ACT200 Acute Monoblastic Leukemia 52 0.021
841
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.021
842
PNG002 Pain Agnosia 51 0.021
844
OLG003 Oligohydramnios 51 0.021
845
OCL069 Ocular Motor Apraxia 51 0.021
846
UNV001 Unverricht-Lundborg Syndrome 51 0.021
847
RYS001 Reye Syndrome 51 0.021
848
ILS001 Ileus 51 0.021
849
LNG031 Lung Benign Neoplasm 51 0.021
850
ESP002 Esophageal Varix 51 0.021
851
NRM004 Neuroma 51 0.021
852
TLR001 Tularemia 51 0.021
853
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 51 0.021
854
P CHL066 Cholangitis 51 0.021
855
c ACT078 Acute Porphyria 51 0.021
856
c HNT004 Huntington Disease-Like 2 50 0.021
857
P MYS079 Miyoshi Muscular Dystrophy 50 0.021
858
P ESN008 Eosinophilic Pneumonia 50 0.021
859
FSC004 Fasciitis 50 0.021
860
MYC087 Mycoplasma Pneumoniae Pneumonia 50 0.021
861
P TMP001 Temporal Lobe Epilepsy 50 0.021
862
PRT018 Portal Vein Thrombosis 50 0.021
863
BLR001 Biliary Atresia 50 0.021
864
HMG002 Hemoglobinuria 50 0.021
865
LSS003 Lassa Fever 50 0.021
866
CLR003 Clear Cell Adenocarcinoma 50 0.021
867
ILT001 Ileitis 50 0.021
868
P OMP004 Omphalocele 50 0.021
869
HYP080 Hypogonadism 50 0.021
870
3HY007 3-Hydroxy-3-Methylglutaryl-Coa Lyase Deficiency 49 0.021
871
RBF001 Riboflavin Deficiency 49 0.021
872
P MYT002 Myotonic Dystrophy 49 0.021
873
c CHR418 Chronic Leukemia 49 0.021
874
P MTC133 Mitochondrial Myopathy 49 0.021
875
P ART018 Aortic Valve Insufficiency 49 0.021
876
IRR003 Irritant Dermatitis 49 0.021
877
MCR004 Macroglobulinemia 49 0.021
878
SCT005 Scott Syndrome 49 0.021
879
EPD006 Epidermolysis Bullosa Acquisita 49 0.021
880
P SDR003 Sideroblastic Anemia 49 0.021
881
P BRS053 Breast Fibroadenoma 49 0.021
882
c HPT015 Hepatitis D 49 0.021
883
ADR016 Adrenal Cortical Carcinoma 48 0.021
884
AMY086 Amyotrophy, Hereditary Neuralgic 48 0.021
885
INT017 Intestinal Schistosomiasis 48 0.021
886
ASP007 Aspiration Pneumonia 48 0.021
887
CLC006 Calcinosis 48 0.021
888
RFR010 Refractory Anemia 48 0.021
889
HPT009 Hepatopulmonary Syndrome 48 0.021
890
PLM035 Pulmonary Eosinophilia 48 0.021
891
DBT006 Diabetic Macular Edema 48 0.021
892
END062 Endometrial Hyperplasia 48 0.021
893
GLC106 Glucocorticoid Resistance, Generalized 48 0.021
894
CHL147 Chlamydia Pneumonia 48 0.021
895
c VRL012 Viral Meningitis 48 0.021
896
ESN015 Eosinophilic Fasciitis 48 0.021
897
VTM002 Vitamin B12 Deficiency 48 0.021
898
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.021
899
ART004 Aortic Atherosclerosis 47 0.021
900
RDT013 Radiation Proctitis 47 0.021
901
c MLG069 Malignant Hypertension 47 0.021
902
CLF056 Cleft Lip with or Without Cleft Palate 47 0.021
903
VRN004 Vernal Keratoconjunctivitis 47 0.021
904
PRC003 Proctitis 47 0.021
905
P HMN032 Human Herpesvirus 8 47 0.021
906
ACT055 Actinomycosis 47 0.021
907
P CLL015 Collagen Disease 47 0.021
908
KRT002 Keratomalacia 47 0.021
909
RFT001 Rift Valley Fever 47 0.021
910
c HMN021 Human T-Cell Leukemia Virus Type 1 47 0.021
911
c CNG216 Congenital Hydrocephalus 47 0.021
912
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.021
913
ANV001 Anovulation 47 0.021
914
P CRC039 Coarctation of Aorta 47 0.021
915
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 47 0.021
916
TST044 Testicular Torsion 47 0.021
917
NSS002 Neisseria Meningitidis Infection 47 0.021
918
CMP002 Campylobacteriosis 46 0.021
919
ATN005 Autonomic Dysfunction 46 0.021
920
PRP017 Periapical Periodontitis 46 0.021
921
TTH006 Tooth Disease 46 0.021
922
SPN020 Spondylosis 46 0.021
923
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.021
924
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.021
925
EXS001 Exostosis 46 0.021
926
KRT013 Keratolytic Winter Erythema 46 0.021
927
P MYC033 Myoclonus 46 0.021
928
CWP001 Cowpox 46 0.021
929
PRX001 Peroxisomal Disease 46 0.021
930
OLG001 Oligospermia 45 0.021
931
TTR005 Tetrahydrobiopterin Deficiency 45 0.021
932
RTR008 Root Resorption 45 0.021
933
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.021
934
URT010 Ureteral Obstruction 45 0.021
935
TRT001 Teratocarcinoma 45 0.021
936
PLR022 Pleural Disease 45 0.021
937
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.021
938
LYD001 Leydig Cell Tumor 45 0.021
939
CHR466 Chronic Thromboembolic Pulmonary Hypertension 45 0.021
940
INT304 Interstitial Pneumonitis, Desquamative, Familial 45 0.021
941
URL001 Urolithiasis 45 0.021
942
NNS002 Nonspecific Interstitial Pneumonia 45 0.021
943
AGR002 Agoraphobia 45 0.021
944
MLN073 Melanosis, Neurocutaneous 45 0.021
945
c ATM099 Autoimmune Uveitis 45 0.021
946
DBT008 Diabetic Angiopathy 44 0.021
947
GRN017 Granulocytopenia 44 0.021
948
P SMK004 Smoking As a Quantitative Trait Locus 3 44 0.021
949
ORG002 Organic Acidemia 44 0.021
950
IRT001 Iritis 44 0.021
951
P SDR002 Siderosis 44 0.021
952
ACT209 Acatalasemia 44 0.021
953
ART116 Arthropathy, Progressive Pseudorheumatoid, of Childhood 44 0.021
954
c SPR086 Spermatogenic Failure 3 44 0.021
955
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.021
956
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.021
957
P CRN024 Corneal Disease 44 0.021
958
ADR041 Adrenal Cortical Adenoma 43 0.021
959
MCR011 Microinvasive Gastric Cancer 43 0.021
960
P AMY106 Amyotrophic Lateral Sclerosis 10 with or Without Frontotemporal Dementia 43 0.021
961
PRS042 Prostate Disease 43 0.021
962
HYP457 Hypertrophic Scars 42 0.021
963
BNT003 Bent Bone Dysplasia Syndrome 42 0.021
964
MST004 Mast Cell Neoplasm 42 0.021
965
BNS003 Binswanger's Disease 42 0.021
966
PNM013 Pneumococcal Meningitis 42 0.021
967
PHY002 Physical Disorder 42 0.021
968
P VND001 Vein Disease 42 0.021
969
TRP014 Triploidy 42 0.021
970
EXC002 Exocrine Pancreatic Insufficiency 42 0.021
971
BCK006 Back Pain 42 0.021
972
BNB002 Bainbridge-Ropers Syndrome 42 0.021
973
BTN002 Boutonneuse Fever 42 0.021
974
IDP091 Idiopathic Nephrotic Syndrome 42 0.021
975
SPN050 Spinocerebellar Degeneration 42 0.021
976
FSC002 Fascioliasis 42 0.021
977
P RNG032 Ring Chromosome 42 0.021
978
ANC002 Anca-Associated Vasculitis 41 0.021
979
MTC029 Mitochondrial Complex V Deficiency, Nuclear Type 1 41 0.021
980
EPC002 Epicondylitis 41 0.021
981
LTX001 Latex Allergy 41 0.021
982
TTT001 Tatton-Brown-Rahman Syndrome 41 0.021
983
MMM006 Mammographic Density 41 0.021
984
P RRT020 Rare Tumor 41 0.021
985
c HYP072 Hypersensitivity Reaction Type Iii Disease 40 0.021
986
EXT006 Extrahepatic Cholestasis 39 0.021
987
c SPS097 Spastic Paraplegia 13, Autosomal Dominant 39 0.021
988
LKP003 Leukoplakia 39 0.021
989
PRP002 Periapical Granuloma 39 0.021
990
FLL031 Follicular Adenoma 39 0.021
991
ADR004 Adrenal Cortical Adenocarcinoma 39 0.021
992
P FML340 Familial Episodic Pain Syndrome 39 0.021
993
ORL012 Oral Leukoplakia 39 0.021
994
HYP141 Hyperphenylalaninemia 39 0.021
995
EXT007 Extracutaneous Mastocytoma 38 0.021
996
LWG005 Low-Grade Astrocytoma 38 0.021
997
CVT001 Cavitary Optic Disc Anomalies 38 0.021
998
ADR022 Adrenomyeloneuropathy 38 0.021
999
c DNR003 Duane Retraction Syndrome 1 38 0.021
1000
c MLG157 Malignant Pheochromocytoma 38 0.021
1001
SRT002 Sertoli Cell Tumor 38 0.021
1002
SPS019 Spastic Paraparesis 38 0.021
1003
KSH004 Kashin-Beck Disease 38 0.021
1004
CRT004 Carotid Artery Thrombosis 38 0.021
1005
c CHR098 Chronic Pyelonephritis 38 0.021
1006
NPH113 Nephroma 37 0.021
1007
P PLY187 Polyarticular Juvenile Idiopathic Arthritis 37 0.021
1008
c LPR022 Leprosy 2 37 0.021
1009
INC003 Inclusion Conjunctivitis 37 0.021
1010
END028 Endemic Goiter 37 0.021
1011
PNB004 Panbronchiolitis, Diffuse 37 0.021
1012
c BCT006 Bacterial Conjunctivitis 37 0.021
1013
PLM101 Pulmonary Hypertension, Chronic Thromboembolic, Without Deep Vein Thrombosis 37 0.021
1014
CHR463 Chronic Actinic Dermatitis 37 0.021
1015
BNG018 Benign Paroxysmal Positional Nystagmus 37 0.021
1016
SYS071 Systemic Autoimmune Disease 37 0.021
1017
P PYR039 Peyronie Disease 36 0.021
1018
NTL004 Nut Allergy 36 0.021
1019
P MXL015 Maxillary Sinusitis 36 0.021
1020
c GRN038 Granulomatous Disease, Chronic, Autosomal Recessive, Cytochrome B-Positive, Type Iii 36 0.021
1021
MLD002 Mild Pre-Eclampsia 36 0.021
1022
AMY003 Amyotrophic Neuralgia 35 0.021
1023
c DRM040 Dermatitis Herpetiformis, Familial 35 0.021
1024
c ATM022 Autoimmune Myocarditis 35 0.021
1025
RBS005 Ribose 5-Phosphate Isomerase Deficiency 35 0.021
1026
SRF006 Surfactant Dysfunction 35 0.021
1027
NND010 Nondisjunction 34 0.021
1028
NNT024 Neonatal Stroke 34 0.021
1029
RHM034 Rahman Syndrome 34 0.021
1030
PRG007 Progressive Bulbar Palsy 34 0.021
1031
SPR006 Sparganosis 34 0.021
1032
DXR001 Doxorubicin Induced Cardiomyopathy 33 0.021
1033
RTN004 Retinal Microaneurysm 33 0.021
1034
NNS011 Nonseminomatous Germ Cell Tumor 33 0.021
1035
TXC020 Toxic Oil Syndrome 33 0.021
1036
CND006 Candida Glabrata 32 0.021
1037
LYM043 Lymphocytic Hypophysitis 32 0.021
1038
c RTN140 Retinitis Pigmentosa 67 32 0.021
1039
MYC014 Mycobacterium Chelonae 31 0.021
1040
ALL007 Allergic Urticaria 31 0.021
1041
GST039 Gastroduodenitis 31 0.021
1042
c CRN221 Craniosynostosis 4 31 0.021
1043
ANM001 Anemia of Prematurity 31 0.021
1044
c PRG019 Paragangliomas 2 31 0.021
1045
STT009 Sutton Disease 2 30 0.021
1046
GRN004 Granulomatous Amebic Encephalitis 30 0.021
1047
c RTN143 Retinitis Pigmentosa 47 30 0.021
1048
c ACT059 Acute Maxillary Sinusitis 30 0.021
1049
SPN392 Spondylosis, Cervical 30 0.021
1050
ACT228 Acute Radiation Syndrome 29 0.021
1051
MTC150 Mitochondrial Complex V Deficiency, Mitochondrial Type 1 29 0.021
1052
MYC019 Mycobacterium Marinum 29 0.021
1053
IMM162 Immunoglobulin E Concentration, Serum 28 0.021
1054
MYP120 Myopathy, Distal, with Rimmed Vacuoles 28 0.021
1055
TMP019 Temporomandibular Joint Anomaly 28 0.021
1056
c RTN068 Retinitis Pigmentosa 6 28 0.021
1057
CNG382 Congenital Cataracts, Hearing Loss, and Neurodegeneration 28 0.021
1058
c RNG022 Ring Chromosome 6 28 0.021
1059
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 28 0.021
1060
SNL009 Senile Plaque Formation 28 0.021
1061
MTR001 Mature Cataract 28 0.021
1062
BRD005 Borderline Leprosy 27 0.021
1063
MST020 Mast Cell Activation Syndrome 26 0.021
1064
c RNG015 Ring Chromosome 2 26 0.021
1065
BNG077 Benign Idiopathic Neonatal Seizures 26 0.021
1066
HML021 Hemolytic Anemia, Nonspherocytic, Due to Glucose Phosphate Isomerase Deficiency 26 0.021
1067
OCL004 Ocular Hyperemia 26 0.021
1068
c MNS008 Monosomy 21 26 0.021
1069
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.021
1070
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.021
1071
RDT005 Radiation Induced Cancer 25 0.021
1072
MTC015 Mitochondrial Dna-Associated Leigh Syndrome and Narp 24 0.021
1073
c RTN032 Retinal Cone Dystrophy 1 24 0.021
1074
c PRS134 Prostate Cancer, Hereditary, 3 24 0.021
1075
P STR035 Streptococcal Group a Invasive Disease 23 0.021
1076
TXC008 Toxic Optic Neuropathy 23 0.021
1077
NCR014 Necrotizing Soft Tissue Infection 23 0.021
1078
c RNG021 Ring Chromosome 5 23 0.021
1079
CRB087 Cerebral Arteriosclerosis 22 0.021
1080
c CRN216 Craniosynostosis 5 21 0.021
1081
DSS012 Disseminated Infection with Mycobacterium Avium Complex 20 0.021
1082
c CHR688 Chronic Acquired Demyelinating Polyneuropathy