Search results for Antioxidants

2354 hits were found for Antioxidants

# Family MCID Name MIFTS Score
1
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.290
2
HYP066 Hyperglycemia 61 0.261
3
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.242
4
ISC004 Ischemia 58 0.217
5
ATH013 Atherosclerosis Susceptibility 65 0.212
6
c HYP836 Hypercholesterolemia, Familial, 1 73 0.200
7
P LVR013 Liver Disease 68 0.200
8
P CTR002 Cataract 60 0.198
10
c PRC016 Pre-Eclampsia 63 0.191
11
P CRN300 Coronary Heart Disease 1 63 0.180
12
PPL052 Papillomatosis, Confluent and Reticulated 33 0.177
13
P ALZ034 Alzheimer Disease 88 0.171
14
P INF032 Infertility 57 0.169
15
AGN016 Aging 56 0.168
16
P KDN018 Kidney Disease 72 0.166
17
FTT001 Fatty Liver Disease 61 0.166
18
LPD008 Lipid Metabolism Disorder 62 0.163
19
P MLN007 Male Infertility 55 0.160
20
P NRB001 Neuroblastoma 72 0.159
21
P CLR023 Colorectal Cancer 99 0.156
22
P PRD008 Periodontitis 64 0.154
23
HYP266 Hypoxia 57 0.149
24
P MCR115 Microvascular Complications of Diabetes 5 66 0.146
25
P VSC007 Vascular Disease 63 0.146
26
LNG099 Lung Disease 60 0.145
27
c MCR120 Microvascular Complications of Diabetes 7 47 0.144
28
CRB004 Cerebral Artery Occlusion 45 0.142
29
P DBT009 Diabetes Mellitus 64 0.140
30
SKN016 Skin Disease 63 0.140
31
P PNC044 Pancreatitis 61 0.140
32
c MCR113 Microvascular Complications of Diabetes 3 52 0.139
33
c MCR130 Microvascular Complications of Diabetes 6 41 0.139
34
c MCR133 Microvascular Complications of Diabetes 4 41 0.139
35
48X005 48,xyyy 39 0.139
36
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.137
37
HMS001 Hemosiderosis 54 0.137
38
P RRH023 Rare Hereditary Hemochromatosis 41 0.137
39
P SKN015 Skin Carcinoma 66 0.133
40
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.132
41
c ACT027 Acute Pancreatitis 60 0.131
42
P HPT023 Hepatocellular Carcinoma 100 0.130
43
P LTR001 Lateral Sclerosis 54 0.130
44
CYT002 Cytokine Deficiency 42 0.130
45
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.130
46
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.129
47
P BRS047 Breast Cancer 97 0.128
48
GST023 Gastric Ulcer 53 0.128
49
BRN071 Brain Injury 49 0.128
50
LPP008 Lipoprotein Quantitative Trait Locus 62 0.127
51
c CHR684 Chronic Kidney Disease 70 0.124
52
EYD002 Eye Disease 58 0.124
53
ART140 Arteries, Anomalies of 52 0.124
54
P HRT032 Heart Disease 75 0.123
55
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.123
56
c HYP595 Hypertension, Essential 84 0.119
57
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.119
58
P INF037 Inflammatory Bowel Disease 54 0.119
59
P ECL001 Eclampsia 50 0.119
60
END086 End Stage Renal Disease 51 0.116
61
HYP781 Hypoascorbemia 51 0.115
62
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.115
63
CLT003 Colitis 62 0.114
64
ULC004 Ulcerative Colitis 73 0.112
65
SPN186 Spinal Cord Injury 60 0.111
66
P CRD246 Cardiovascular System Disease 57 0.111
67
NNL006 Non-Alcoholic Steatohepatitis 54 0.111
68
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.109
69
P THL005 Thalassemia 60 0.108
70
P PRS040 Prostate Cancer 97 0.107
71
P MYC007 Myocardial Infarction 70 0.106
72
P ART021 Arteriosclerosis 54 0.106
73
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.106
74
TRM010 Traumatic Brain Injury 51 0.106
75
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.105
76
ATM095 Autoimmune Disease 62 0.104
77
DRM006 Dermatitis 61 0.104
78
ORL011 Oral Cancer 60 0.103
79
c ACT071 Acute Kidney Failure 60 0.103
80
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.103
81
c PCH010 Pachyonychia Congenita 3 44 0.103
82
P HYP086 Hypothyroidism 69 0.102
83
LVR012 Liver Cirrhosis 62 0.102
84
c PRD040 Periodontitis, Chronic 53 0.101
85
P PLM036 Pulmonary Fibrosis 65 0.100
86
P NRP001 Neuropathy 56 0.100
87
P PHC003 Pheochromocytoma 71 0.099
88
ADR040 Adrenal Gland Pheochromocytoma 46 0.099
89
P BCL017 B-Cell Lymphoma 58 0.097
90
P HYP076 Hyperthyroidism 55 0.097
91
c ATR087 Atrial Standstill 1 75 0.096
92
P HNT016 Huntington Disease 72 0.096
93
IRN002 Iron Metabolism Disease 57 0.096
94
BRN056 Bronchopulmonary Dysplasia 57 0.096
95
P DRR001 Diarrhea 55 0.095
96
ANX004 Anoxia 40 0.095
97
OST012 Osteoarthritis 78 0.094
98
CNG034 Congestive Heart Failure 69 0.094
99
P GST044 Gastritis 56 0.094
100
P GST053 Gastric Cancer 83 0.093
101
AST005 Asthma 76 0.093
102
c ACT075 Acute Myocardial Infarction 57 0.093
103
ENT004 Enthesopathy 49 0.093
104
BRN024 Bronchitis 68 0.092
105
PPT005 Peptic Ulcer Disease 59 0.092
106
CYS001 Cystic Fibrosis 81 0.091
107
DFC004 Deficiency Anemia 70 0.091
108
IMP005 Impotence 52 0.090
109
VRC001 Varicocele 49 0.090
110
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.089
111
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.089
112
CRB039 Cerebrovascular Disease 67 0.088
113
P ENC018 Encephalopathy 61 0.088
114
P BRS044 Breast Adenocarcinoma 59 0.088
115
HMC014 Homocysteinemia 53 0.088
116
PRM329 Premature Aging 35 0.088
117
CHL068 Cholestasis 61 0.087
118
c DWL002 Dowling-Degos Disease 1 58 0.087
119
47X002 47,xyy 49 0.087
120
P RHM011 Rheumatoid Arthritis 80 0.085
121
PRP027 Peripheral Vascular Disease 71 0.085
122
STR067 Stroke, Ischemic 81 0.084
123
P SCH015 Schizophrenia 74 0.084
124
CRH001 Crohn's Disease 74 0.084
125
c BTT014 Beta-Thalassemia 74 0.083
126
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.083
127
P BLD134 Bladder Cancer 79 0.082
128
DWN001 Down Syndrome 70 0.082
129
P SLP006 Sleep Apnea 69 0.082
130
c HPT001 Hepatitis C 62 0.082
131
TXC005 Toxic Shock Syndrome 62 0.082
132
BRN004 Brain Edema 56 0.082
133
DBT010 Diabetic Neuropathy 54 0.082
134
c VRL010 Viral Hepatitis 52 0.082
135
ORL015 Oral Squamous Cell Carcinoma 43 0.082
136
P ATS364 Autism 70 0.081
137
P MYP004 Myopathy 70 0.081
138
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.081
139
P HYP750 Hypertriglyceridemia, Familial 62 0.081
140
VSL002 Visual Epilepsy 59 0.081
141
ADN018 Adenoma 59 0.081
142
P PLY011 Polycystic Ovary Syndrome 56 0.081
143
P SZR006 Seizure Disorder 56 0.081
144
GLC003 Glucose Intolerance 54 0.081
145
P SCK005 Sickle Cell Disease 50 0.081
146
BNR002 Bone Resorption Disease 48 0.081
147
P OVR042 Ovarian Cancer 88 0.080
148
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.080
149
P MLT020 Multiple Sclerosis 72 0.080
150
P ANP001 Anaplastic Large Cell Lymphoma 58 0.080
151
GT001 Gout 64 0.079
152
DPR016 Depression 63 0.079
153
P PSR002 Psoriasis 62 0.079
154
NTR005 Nutritional Deficiency Disease 62 0.079
155
BCT022 Bacterial Infectious Disease 56 0.079
156
P RTN016 Retinal Degeneration 53 0.079
157
P OPN001 Open-Angle Glaucoma 49 0.079
158
CRV035 Cervical Cancer 76 0.078
159
ANG054 Angina Pectoris 66 0.078
160
c DBT099 Diabetes Mellitus, Type I 65 0.078
161
P ADN016 Adenocarcinoma 64 0.078
162
GST033 Gestational Diabetes 61 0.078
163
c ACT134 Acute Liver Failure 56 0.078
164
PST011 Pustulosis of Palm and Sole 52 0.078
165
P PNC035 Pancreatic Cancer 84 0.076
166
P PLM037 Pulmonary Hypertension 67 0.076
167
P MSC005 Muscular Dystrophy 66 0.076
168
P NPH012 Nephrotic Syndrome 60 0.076
169
CNT047 Contact Dermatitis 58 0.076
170
P PRK057 Parkinson Disease, Late-Onset 78 0.075
171
ALC007 Alcohol Dependence 66 0.075
172
P DMN002 Dementia 66 0.075
173
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.075
174
NPH009 Nephrolithiasis 55 0.075
175
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.075
176
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.075
177
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.075
178
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.075
179
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.075
180
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.075
181
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.075
182
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.075
183
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.075
184
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.075
185
ALL014 Allergic Encephalomyelitis 38 0.075
186
HRW001 Hair Whorl 36 0.075
187
c MCR129 Microvascular Complications of Diabetes 1 66 0.074
188
HYP056 Hypoglycemia 66 0.074
189
CLN015 Colon Adenocarcinoma 65 0.074
190
PRT036 Peritonitis 64 0.074
191
P GLM045 Glioma 63 0.074
192
c GLC092 Glaucoma, Primary Open Angle 62 0.074
193
THY029 Thyroid Carcinoma 59 0.074
194
P UVT001 Uveitis 57 0.074
195
KRT002 Keratomalacia 47 0.074
196
GLL048 Glial Tumor 45 0.074
197
P LNG032 Lung Cancer 98 0.073
198
c SYS001 Systemic Lupus Erythematosus 86 0.073
199
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.073
200
MNT002 Mental Depression 58 0.073
201
P BPL003 Bipolar Disorder 56 0.073
202
CLR109 Colorectal Adenocarcinoma 51 0.073
203
c MJR024 Major Affective Disorder 9 41 0.073
204
c MJR022 Major Affective Disorder 8 38 0.073
205
P OST002 Osteoporosis 74 0.072
206
PLM001 Pulmonary Tuberculosis 69 0.072
207
P ADL010 Adult Respiratory Distress Syndrome 65 0.072
208
AMN003 Amnestic Disorder 54 0.072
209
P SPP010 Suppressor of Tumorigenicity 3 51 0.072
210
c SVR005 Severe Pre-Eclampsia 50 0.072
211
HVY002 Heavy Metal Poisoning 22 0.072
212
LSH001 Leishmaniasis 63 0.070
213
HYP014 Hyperuricemia 52 0.070
214
TLN003 Telangiectasis 52 0.070
215
P KLZ004 Kala-Azar 1 41 0.070
216
c MCR112 Microvascular Complications of Diabetes 2 41 0.070
217
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.070
218
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.069
219
SCK003 Sickle Cell Anemia 74 0.069
220
c EXD008 Exudative Vitreoretinopathy 1 71 0.069
221
P DRM053 Dermatitis, Atopic 66 0.069
222
ALL026 Allergic Hypersensitivity Disease 62 0.069
223
c SCL052 Scleroderma, Familial Progressive 61 0.069
224
P MYL006 Myeloid Leukemia 60 0.069
225
SQM006 Squamous Cell Carcinoma 60 0.069
226
PRS045 Prostatic Hypertrophy 53 0.069
227
PRS021 Prostatic Adenoma 51 0.069
228
URM002 Uremia 49 0.069
229
URL001 Urolithiasis 45 0.069
230
P ATX030 Ataxia-Telangiectasia 82 0.068
231
GLB015 Glioblastoma Multiforme 75 0.068
232
OST159 Osteogenic Sarcoma 66 0.068
233
P ATR011 Atrial Fibrillation 66 0.068
234
P LPS004 Lupus Erythematosus 61 0.068
235
HLC007 Helicobacter Pylori Infection 59 0.068
236
P PRP019 Peripheral Nervous System Disease 58 0.068
237
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.068
238
KLB003 Klebsiella Pneumonia 41 0.068
239
LKP003 Leukoplakia 39 0.068
240
PST092 Posttransplant Acute Limbic Encephalitis 29 0.068
241
P MJR001 Major Depressive Disorder 68 0.066
242
P HML002 Hemolytic Anemia 63 0.066
243
P END044 Endometriosis 63 0.066
244
GNG013 Gingivitis 59 0.066
245
P GLM007 Glomerulonephritis 57 0.066
246
P RHN004 Rhinitis 57 0.066
247
P PLY019 Polyneuropathy 56 0.066
248
HYP060 Hyperinsulinism 54 0.066
249
DNT012 Dental Caries 53 0.066
250
ESP021 Esophageal Cancer 90 0.065
251
c DLT002 Dilated Cardiomyopathy 79 0.065
252
P LNG064 Lung Cancer Susceptibility 3 78 0.065
253
P RTN018 Retinal Disease 53 0.065
254
OCL069 Ocular Motor Apraxia 51 0.065
255
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.065
256
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.065
257
P LKM062 Leukemia, Acute Lymphoblastic 69 0.063
258
c ATS007 Autism Spectrum Disorder 67 0.063
259
CHG001 Chagas Disease 66 0.063
260
CLR108 Colorectal Adenoma 64 0.063
261
IRN001 Iron Deficiency Anemia 59 0.063
262
P FBR017 Fibrosarcoma 56 0.063
263
MCS002 Mucositis 56 0.063
264
P ALP008 Alopecia 54 0.063
265
PLM010 Pulmonary Edema 54 0.063
266
P DDN001 Duodenal Ulcer 52 0.063
267
DYS015 Dysentery 52 0.063
268
PRS129 Prostatic Hyperplasia, Benign 49 0.063
269
OLG022 Oligoasthenoteratozoospermia 36 0.063
270
c LKM061 Leukemia, Acute Myeloid 84 0.062
271
c NRF023 Neurofibromatosis, Type Ii 80 0.062
272
c SVR001 Severe Acute Respiratory Syndrome 62 0.062
273
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.062
274
P MTC069 Mitochondrial Disorders 56 0.062
275
GST050 Gastrointestinal System Disease 56 0.062
276
INT007 Intermediate Coronary Syndrome 55 0.062
277
TRD006 Tardive Dyskinesia 54 0.062
278
GTR002 Goiter 53 0.062
279
STM007 Stomatitis 50 0.062
280
SNL007 Senile Cataract 42 0.062
281
ORL012 Oral Leukoplakia 39 0.062
282
HRN029 Hearing Loss, Noise-Induced 37 0.062
283
MLR004 Malaria 81 0.060
284
P RSP003 Respiratory Failure 74 0.060
285
P MLN008 Melanoma 69 0.060
286
P PNM007 Pneumonia 68 0.060
287
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.060
288
P ESP024 Esophagitis 62 0.060
289
CNS004 Constipation 58 0.060
290
BLR008 Bilirubin Metabolic Disorder 57 0.060
291
VSC002 Vascular Dementia 57 0.060
292
P GRV001 Graves' Disease 55 0.060
293
KRT009 Keratosis 51 0.060
294
HYP081 Hypolipoproteinemia 51 0.060
295
HDN002 Head Injury 46 0.060
297
P RTN008 Retinitis Pigmentosa 79 0.059
298
c HPT073 Hepatitis C Virus 72 0.059
299
P EPL164 Epilepsy 71 0.059
300
ALL003 Allergic Rhinitis 67 0.059
301
NPH091 Nephrolithiasis, Calcium Oxalate 60 0.059
302
STT001 Status Epilepticus 60 0.059
303
ALL006 Allergic Asthma 56 0.059
304
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.059
305
CHR100 Chronic Ulcer of Skin 55 0.059
306
P AST007 Astrocytoma 51 0.059
307
IMM167 Immune Deficiency Disease 78 0.057
308
P LKM002 Leukemia 68 0.057
309
c MGR028 Migraine with or Without Aura 1 67 0.057
310
P ALC033 Alcohol Use Disorder 58 0.057
311
MCR013 Microphthalmia 57 0.057
312
SCH014 Schistosomiasis 57 0.057
313
PPL022 Papilloma 54 0.057
314
SQM002 Squamous Cell Papilloma 46 0.057
315
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.057
316
c HNT011 Huntington Disease-Like 3 38 0.057
317
CND006 Candida Glabrata 32 0.057
318
URT049 Urate Oxidase, Pseudogene 25 0.057
319
P ART022 Arthritis 69 0.056
320
RCK004 Rickets 68 0.056
321
P FRD001 Friedreich Ataxia 64 0.056
322
P VSC011 Vasculitis 62 0.056
323
ACQ007 Acquired Immunodeficiency Syndrome 60 0.056
324
P BND020 Bone Disease 59 0.056
325
IGR001 Ige Responsiveness, Atopic 59 0.056
326
P TRM003 Tremor 54 0.056
327
P LCH002 Lichen Planus 53 0.056
328
MST005 Mastitis 53 0.056
329
PLR008 Pleurisy 50 0.056
330
TST044 Testicular Torsion 47 0.056
331
RTN023 Retinitis 46 0.056
332
NRR001 Neuroretinitis 42 0.056
333
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.054
334
PHN003 Phenylketonuria 75 0.054
335
ANX010 Anxiety 73 0.054
336
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.054
337
P MNN013 Meningitis 66 0.054
338
TRN015 Transient Cerebral Ischemia 63 0.054
339
c HPT003 Hepatitis a 62 0.054
340
APH001 Aphthous Stomatitis 57 0.054
341
ERY051 Erythroleukemia, Familial 56 0.054
342
ENT011 Enterocolitis 51 0.054
343
P ATR005 Atrophic Gastritis 50 0.054
344
HLX001 Helix Syndrome 47 0.054
345
RTN020 Retinal Vascular Disease 46 0.054
346
STT009 Sutton Disease 2 30 0.054
347
P HPT021 Hepatitis 67 0.052
348
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.052
349
c FML021 Familial Hypercholesterolemia 66 0.052
350
APN008 Apnea, Obstructive Sleep 64 0.052
351
HPT019 Hepatic Encephalopathy 60 0.052
352
P OPT006 Optic Nerve Disease 60 0.052
353
ALL010 Allergic Contact Dermatitis 56 0.052
354
PRS047 Prostatitis 56 0.052
355
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.052
356
P MSC003 Muscular Atrophy 52 0.052
357
P CRV031 Cervical Adenocarcinoma 49 0.052
358
ATS010 Autosomal Recessive Disease 48 0.052
359
DRY001 Dry Eye Syndrome 47 0.052
360
BCK003 Background Diabetic Retinopathy 46 0.052
361
HPT004 Hepatic Coma 45 0.052
362
CRT015 Carotid Artery Occlusion 45 0.052
363
INS024 Insulin-Like Growth Factor I 79 0.051
364
END057 Endometrial Cancer 74 0.051
365
IRR002 Irritable Bowel Syndrome 65 0.051
366
P ENC004 Encephalitis 61 0.051
367
CHR066 Chronic Fatigue Syndrome 61 0.051
368
P SNS001 Sensorineural Hearing Loss 60 0.051
369
c HPT016 Hepatitis B 59 0.051
370
FBR047 Fibromyalgia 58 0.051
371
CHL067 Cholecystitis 57 0.051
372
P FTL001 Fetal Alcohol Syndrome 57 0.051
373
P PYL005 Pyelonephritis 56 0.051
374
PLC008 Placenta Disease 50 0.051
375
MTC005 Mitochondrial Metabolism Disease 49 0.051
376
NWC001 Newcastle Disease 45 0.051
377
KWS001 Kwashiorkor 44 0.051
379
MYL069 Myeloma, Multiple 85 0.049
380
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.049
381
c ATM006 Autoimmune Lymphoproliferative Syndrome 74 0.049
382
OTT002 Otitis Media 72 0.049
383
HMN044 Human Immunodeficiency Virus Type 1 71 0.049
384
P LYM118 Lymphoma 68 0.049
385
P CRD119 Cardiac Arrest 67 0.049
386
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.049
387
P MTR014 Motor Neuron Disease 65 0.049
388
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.049
389
P PRP029 Porphyria 62 0.049
390
ALC006 Alcoholic Hepatitis 61 0.049
391
P MYC008 Myocarditis 59 0.049
392
PRN019 Perinatal Necrotizing Enterocolitis 59 0.049
393
P PRN023 Prion Disease 57 0.049
394
ORL004 Oral Submucous Fibrosis 55 0.049
395
CRH005 Crohn's Colitis 53 0.049
396
PRP080 Peripheral Artery Disease 53 0.049
397
P INT068 Intestinal Disease 53 0.049
398
RNL077 Renal Fibrosis 47 0.049
399
c CRV002 Cervix Uteri Carcinoma in Situ 46 0.049
400
MYC005 Myocardial Stunning 46 0.049
401
MLC004 Mulchandani-Bhoj-Conlin Syndrome 44 0.049
402
P CHR345 Chronic Pain 44 0.049
403
CRV045 Cervical Intraepithelial Neoplasia 39 0.049
404
LPT014 Leptin Deficiency or Dysfunction 74 0.047
405
CRB037 Cerebral Palsy 69 0.047
406
P INF038 Influenza 68 0.047
407
GST092 Gastroesophageal Reflux 67 0.047
408
BRR014 Barrett Esophagus 65 0.047
409
P HRP006 Herpes Simplex 65 0.047
410
NRM005 Neuromuscular Disease 64 0.047
411
P NTR004 Neutropenia 63 0.047
412
c BRN108 Branchiootic Syndrome 1 62 0.047
413
CTN007 Cutaneous Leishmaniasis 62 0.047
414
MDD011 Mood Disorder 62 0.047
415
P KDN017 Kidney Cancer 60 0.047
416
P SLP005 Sleep Disorder 59 0.047
417
HPT022 Hepatoblastoma 56 0.047
418
P RCT021 Rectum Cancer 52 0.047
419
PPT001 Peptic Esophagitis 52 0.047
420
CCC002 Coccidiosis 51 0.047
421
MTB004 Metabolic Acidosis 50 0.047
422
OLG001 Oligospermia 45 0.047
423
ORL013 Oral Lichen Planus 45 0.047
424
c SPR086 Spermatogenic Failure 3 44 0.047
425
ATX019 Ataxia with Vitamin E Deficiency 42 0.047
426
c FNC027 Fanconi Anemia, Complementation Group a 81 0.045
427
ADR007 Adrenoleukodystrophy 75 0.045
428
MSC157 Muscular Dystrophy, Duchenne Type 72 0.045
429
GST040 Gastric Adenocarcinoma 70 0.045
430
c PNC108 Pancreatitis, Hereditary 70 0.045
431
c SML038 Small Cell Cancer of the Lung 65 0.045
432
P RHB003 Rhabdomyosarcoma 63 0.045
433
VRC005 Varicose Veins 60 0.045
434
P CYS018 Cystitis 59 0.045
435
BRS051 Breast Disease 58 0.045
436
LMB062 Limb Ischemia 55 0.045
437
PRT038 Protein-Energy Malnutrition 54 0.045
438
NNT012 Neonatal Jaundice 53 0.045
439
DBT004 Diabetic Polyneuropathy 49 0.045
440
P MRC003 Mercury Poisoning 48 0.045
441
TST015 Testicular Disease 43 0.045
442
HMP009 Haemophilus Influenzae 43 0.045
443
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.045
444
DBT007 Diabetic Cataract 38 0.045
445
ADR022 Adrenomyeloneuropathy 38 0.045
447
CHR178 Chromosomal Triplication 35 0.045
448
c LKM063 Leukemia, Chronic Myeloid 72 0.043
449
P SRC025 Sarcoidosis 1 70 0.043
450
P AMY004 Amyloidosis 70 0.043
451
ART016 Aortic Aneurysm 69 0.043
452
P CLC063 Celiac Disease 1 66 0.043
453
ACT119 Acute Promyelocytic Leukemia 63 0.043
454
P PRM006 Primary Biliary Cirrhosis 62 0.043
455
RTN017 Retinal Detachment 61 0.043
456
P ALP009 Alopecia Areata 60 0.043
457
c DNG003 Dengue Disease 59 0.043
458
GST045 Gastroenteritis 59 0.043
459
ANR040 Aneurysm 59 0.043
460
P HDC001 Headache 57 0.043
461
TNS005 Tonsillitis 57 0.043
462
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.043
463
SLC006 Silicosis 56 0.043
464
P LRY044 Larynx Cancer 55 0.043
465
MYM001 Myoma 54 0.043
466
FDL002 Food Allergy 51 0.043
467
P LCT001 Lactic Acidosis 51 0.043
468
c HNT004 Huntington Disease-Like 2 50 0.043
469
SPL018 Splenomegaly 48 0.043
470
ART004 Aortic Atherosclerosis 47 0.043
471
P HMR005 Hemorrhoid 46 0.043
472
c HMG003 Hemoglobin E Disease 45 0.043
473
DBT008 Diabetic Angiopathy 44 0.043
474
OVR094 Ovarian Epithelial Cancer 38 0.043
475
P RTN024 Retinoblastoma 73 0.041
476
WLS001 Wilson Disease 71 0.041
477
ADL002 Adult Syndrome 70 0.041
478
P LPR021 Leprosy 3 69 0.041
479
c BSL007 Basal Cell Carcinoma 68 0.041
480
PNC129 Pancreatic Adenocarcinoma 68 0.041
481
P GLC113 Galactosemia I 64 0.041
482
INT066 Interstitial Lung Disease 60 0.041
483
P CND004 Candidiasis 58 0.041
484
CMM005 Common Cold 57 0.041
485
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 54 0.041
486
c FML008 Familial Retinoblastoma 53 0.041
487
DMY004 Demyelinating Disease 52 0.041
488
CRT013 Carotid Stenosis 50 0.041
489
LNG015 Lingual-Facial-Buccal Dyskinesia 50 0.041
490
P RNV001 Renovascular Hypertension 48 0.041
491
P BNG032 Benign Mesothelioma 46 0.041
492
URT010 Ureteral Obstruction 45 0.041
493
CRB090 Cerebral Hypoxia 44 0.041
494
HYP141 Hyperphenylalaninemia 39 0.041
495
HNS001 Hansen's Disease 34 0.041
496
PRQ002 Paraquat Poisoning 26 0.041
497
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.041
498
NRL016 Neural Tube Defects 82 0.038
499
SVR004 Severe Combined Immunodeficiency 73 0.038
500
P CNR004 Cone-Rod Dystrophy 2 73 0.038
501
OBS002 Obsessive-Compulsive Disorder 68 0.038
502
P THR014 Thrombocytopenia 67 0.038
503
PSY004 Psychotic Disorder 67 0.038
504
P NRV007 Nervous System Disease 66 0.038
505
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.038
506
P NRN021 Neuronal Ceroid Lipofuscinosis 64 0.038
507
c JVN010 Juvenile Rheumatoid Arthritis 64 0.038
508
ANR007 Anorexia Nervosa 63 0.038
509
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.038
510
INT002 Intermittent Claudication 61 0.038
511
INS001 Insulinoma 60 0.038
512
CHL014 Cholera 59 0.038
513
P BRN022 Bronchiectasis 59 0.038
514
P URT039 Urticaria 58 0.038
515
THR024 Thrombosis 57 0.038
516
P PNM006 Pneumoconiosis 56 0.038
517
c THY109 Thyroid Cancer, Nonmedullary, 1 56 0.038
518
c FML035 Familial Hyperlipidemia 55 0.038
519
c BCT007 Bacterial Meningitis 55 0.038
520
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.038
521
P MYP006 Myopia 55 0.038
522
PRP030 Purpura 54 0.038
523
P MNC007 Monocytic Leukemia 53 0.038
524
P THY032 Thyroiditis 52 0.038
525
CRV040 Cervix Carcinoma 51 0.038
526
c PYR010 Peyronie's Disease 50 0.038
527
RTN003 Retinal Ischemia 50 0.038
528
P TMP001 Temporal Lobe Epilepsy 50 0.038
529
P KRT007 Keratoconus 50 0.038
530
NTR046 Neutrophil Migration 50 0.038
531
BBS001 Babesiosis 48 0.038
532
ANT018 Anthracosis 48 0.038
533
KHN001 Kuhnt-Junius Degeneration 47 0.038
534
P MTH007 Methemoglobinemia 46 0.038
535
ELS001 Eales Disease 45 0.038
536
JNT004 Joint Laxity, Short Stature, and Myopia 45 0.038
537
P PRC031 Preeclampsia/eclampsia 1 38 0.038
538
BRN028 Brain Cancer 74 0.036
539
c SPN225 Spondyloarthropathy 1 73 0.036
540
P HYP061 Hypertrophic Cardiomyopathy 70 0.036
541
LYM133 Lymphoma, Hodgkin, Classic 69 0.036
542
KRT019 Keratitis, Hereditary 65 0.036
543
PRP083 Porphyria, Acute Intermittent 64 0.036
544
c ACT068 Acute Cystitis 63 0.036
545
c ATM011 Autoimmune Hepatitis 63 0.036
546
c OPT053 Optic Atrophy 1 63 0.036
547
ING001 Inguinal Hernia 60 0.036
548
SPP011 Suppression of Tumorigenicity 12 59 0.036
549
PRT013 Portal Hypertension 59 0.036
550
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.036
551
CHL123 Chlamydia 59 0.036
552
EXF001 Exfoliation Syndrome 56 0.036
553
MCL006 Macular Retinal Edema 55 0.036
554
P PLM034 Pulmonary Emphysema 55 0.036
555
P SBS003 Substance Abuse 55 0.036
556
P VNS003 Venous Insufficiency 55 0.036
557
P PMP001 Pemphigus 54 0.036
558
OCL006 Ocular Hypertension 53 0.036
559
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.036
560
FML037 Female Breast Cancer 52 0.036
561
SPN051 Spondylitis 51 0.036
563
CHR005 Chorioamnionitis 51 0.036
564
P OBS001 Obstructive Jaundice 50 0.036
565
WTH001 Withdrawal Disorder 48 0.036
566
RYN005 Raynaud Phenomenon 47 0.036
567
c MLG068 Malignant Glioma 46 0.036
568
ATN004 Autonomic Neuropathy 45 0.036
569
P MTC004 Mitochondrial Encephalomyopathy 44 0.036
570
MRS001 Marasmus 42 0.036
571
PRM020 Premenstrual Tension 40 0.036
572
CNT060 Central Serous Chorioretinopathy 38 0.036
573
c CHR098 Chronic Pyelonephritis 38 0.036
574
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 37 0.036
575
P HRD217 Hereditary Optic Neuropathy 36 0.036
576
INF009 Inflammatory Spondylopathy 31 0.036
577
THL004 Theileriasis 30 0.036
578
P LKM071 Leukemia, Chronic Lymphocytic 79 0.033
579
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.033
580
P GRF003 Graft-Versus-Host Disease 72 0.033
581
SMT004 Smith-Lemli-Opitz Syndrome 70 0.033
582
P TBR001 Tuberous Sclerosis 70 0.033
583
P SYS005 Systemic Scleroderma 68 0.033
584
BRK010 Burkitt Lymphoma 67 0.033
585
P MLG056 Malignant Hyperthermia 67 0.033
586
c RHB024 Rhabdomyosarcoma 2 67 0.033
587
P NSP012 Nasopharyngeal Carcinoma 66 0.033
588
SRC014 Sarcoma 65 0.033
589
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.033
590
BRC012 Brucellosis 64 0.033
591
MSC007 Muscle Hypertrophy 64 0.033
592
c DPH024 Diaphragmatic Hernia, Congenital 63 0.033
593
PLG002 Plague 63 0.033
594
P ART023 Arthropathy 62 0.033
595
c PRT132 Protoporphyria, Erythropoietic, 1 61 0.033
596
DCB001 Decubitus Ulcer 61 0.033
597
c JVN061 Juvenile Arthritis 60 0.033
598
P TXP001 Toxoplasmosis 60 0.033
599
BRN002 Bronchiolitis 59 0.033
600
CRY035 Cryptorchidism, Unilateral or Bilateral 58 0.033
601
P SYP003 Syphilis 58 0.033
602
LYM027 Lymphopenia 58 0.033
603
PMP006 Pemphigus Vulgaris, Familial 57 0.033
604
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.033
605
HMG005 Hemoglobinopathy 56 0.033
606
SYN007 Synovitis 54 0.033
607
PRT082 Preterm Premature Rupture of the Membranes 54 0.033
608
AMN001 Amenorrhea 54 0.033
609
P INS002 in Situ Carcinoma 53 0.033
610
P HMC002 Homocystinuria 53 0.033
611
SPN035 Spindle Cell Sarcoma 53 0.033
612
NRT004 Neuritis 52 0.033
613
PLS007 Plasmodium Falciparum Malaria 52 0.033
614
THY030 Thyroid Gland Disease 52 0.033
615
P ACT105 Acute Mountain Sickness 52 0.033
616
c SCN036 Secondary Progressive Multiple Sclerosis 51 0.033
617
HYP080 Hypogonadism 50 0.033
618
RBF001 Riboflavin Deficiency 49 0.033
619
c CHR431 Chronic Venous Insufficiency 49 0.033
620
IRR003 Irritant Dermatitis 49 0.033
621
CHL004 Cholelithiasis 49 0.033
622
IGG001 Iga Glomerulonephritis 48 0.033
623
P KRN004 Kernicterus 47 0.033
624
ANV001 Anovulation 47 0.033
625
c OPT051 Opitz Gbbb Syndrome, Type I 47 0.033
626
TST014 Testicular Cancer 46 0.033
627
CHP002 Chops Syndrome 44 0.033
628
c FTL006 Fetal Alcohol Spectrum Disorder 43 0.033
629
P MLT008 Multinodular Goiter 42 0.033
630
CRD118 Cardiovascular Cancer 41 0.033
631
SPN362 Spondylometaphyseal Dysplasia, Sedaghatian Type 41 0.033
632
AML001 Amelanotic Melanoma 39 0.033
633
GLM044 Glomerular Disease 37 0.033
634
PLC002 Plica Syndrome 36 0.033
635
GST039 Gastroduodenitis 31 0.033
636
MNG007 Manganese Poisoning 29 0.033
637
PRX085 Preaxial Hallucal Polydactyly 28 0.033
638
INF118 Inflammatory Myopathy with Abundant Macrophages 28 0.033
639
c TBR025 Tuberous Sclerosis 1 77 0.030
640
c HMC039 Hemochromatosis, Type 1 74 0.030
641
P TTR001 Tetralogy of Fallot 70 0.030
642
P MYC084 Mycobacterium Tuberculosis 1 68 0.030
643
CHL065 Cholangiocarcinoma 68 0.030
644
CNN005 Connective Tissue Disease 68 0.030
645
P TRN020 Turner Syndrome 67 0.030
646
P HYP098 Hypereosinophilic Syndrome 67 0.030
647
PRP001 Propionic Acidemia 65 0.030
648
PRT037 Pertussis 65 0.030
649
c WLM013 Wilms Tumor 1 65 0.030
650
P PRS038 Personality Disorder 65 0.030
651
P THY023 Thymoma 65 0.030
652
TYP007 Typhoid Fever 63 0.030
653
P PLY014 Polycystic Kidney Disease 62 0.030
654
DPH001 Diphtheria 60 0.030
655
CRD223 Cardiac Arrhythmia 60 0.030
656
RHM001 Rheumatic Fever 60 0.030
657
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.030
658
c ACT073 Acute Leukemia 58 0.030
659
CRD132 Cardiac Conduction Defect 58 0.030
660
NWB001 Newborn Respiratory Distress Syndrome 58 0.030
661
P OPT009 Optic Neuritis 57 0.030
662
PLC005 Placental Insufficiency 57 0.030
663
JPN002 Japanese Encephalitis 57 0.030
664
GNR004 Generalized Anxiety Disorder 56 0.030
665
SCH003 Schizophreniform Disorder 56 0.030
666
HYP005 Hypokalemia 55 0.030
667
VSC003 Visceral Leishmaniasis 55 0.030
668
P SLM003 Salmonellosis 55 0.030
669
RSC001 Rosacea 54 0.030
670
TND005 Tendinitis 54 0.030
671
P END047 Endophthalmitis 53 0.030
672
RHM028 Rheumatic Heart Disease 53 0.030
673
HRT012 Heart Valve Disease 53 0.030
674
NRT001 Neurotic Disorder 53 0.030
675
ALC009 Alcoholic Liver Cirrhosis 53 0.030
676
c GLL024 Gallbladder Disease 1 53 0.030
677
PRP016 Paraplegia 52 0.030
678
c THY107 Thymoma, Familial 52 0.030
679
c PNC106 Pancreatic Agenesis 1 51 0.030
680
INT079 Intrahepatic Cholangiocarcinoma 51 0.030
681
TLR001 Tularemia 51 0.030
682
P CHL066 Cholangitis 51 0.030
683
SCH012 Schizoaffective Disorder 50 0.030
684
P OVR082 Overgrowth Syndrome 50 0.030
685
CRN030 Coronary Stenosis 50 0.030
686
P AGG001 Aggressive Periodontitis 50 0.030
687
KRT001 Keratoconjunctivitis Sicca 49 0.030
688
HYP006 Hypertensive Heart Disease 49 0.030
689
PRN014 Paronychia 49 0.030
690
P BRS053 Breast Fibroadenoma 49 0.030
691
DBT006 Diabetic Macular Edema 48 0.030
692
PNC034 Pancreas Disease 48 0.030
693
SXL003 Sexual Disorder 47 0.030
694
CRN017 Coronary Thrombosis 47 0.030
695
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.030
696
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.030
697
c ACT042 Acute Pyelonephritis 46 0.030
698
ACT003 Acute Kidney Tubular Necrosis 45 0.030
699
c STN011 Sting-Associated Vasculopathy with Onset in Infancy 45 0.030
700
OVR063 Overnutrition 44 0.030
701
c SRC023 Sarcoidosis 2 43 0.030
702
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 43 0.030
703
PNM013 Pneumococcal Meningitis 42 0.030
704
P STN012 Sting-Associated Vasculopathy, Infantile-Onset 42 0.030
705
c ATS307 Autosomal Recessive Cerebellar Ataxia 42 0.030
706
PCD001 Pica Disease 41 0.030
707
NPH098 Nephrolithiasis, X-Linked Recessive, with Renal Failure 41 0.030
708
VSL013 Visual Impairment and Progressive Phthisis Bulbi 41 0.030
709
CHL045 Choline Deficiency Disease 39 0.030
710
SCR011 Scrapie 39 0.030
711
KSH004 Kashin-Beck Disease 38 0.030
712
DBT081 Diabetic Encephalopathy 37 0.030
713
P MXL015 Maxillary Sinusitis 36 0.030
714
c ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 35 0.030
715
KSH001 Keshan Disease 34 0.030
716
c LKM005 Leukemia, T-Cell, Chronic 34 0.030
717
DXR001 Doxorubicin Induced Cardiomyopathy 33 0.030
718
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 32 0.030
719
P SKN067 Skin/hair/eye Pigmentation, Variation in, 2 31 0.030
720
ACT228 Acute Radiation Syndrome 29 0.030
721
EPL050 Epilepsy, Partial, with Pericentral Spikes 25 0.030
722
KPS004 Kaposi Sarcoma 75 0.027
723
P APL001 Aplastic Anemia 74 0.027
724
c THR092 Thrombophilia Due to Thrombin Defect 73 0.027
725
XRD010 Xeroderma Pigmentosum, Variant Type 73 0.027
726
P FRG001 Fragile X Syndrome 70 0.027
727
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.027
728
PLY001 Polycythemia Vera 69 0.027
729
SKN019 Skin Melanoma 68 0.027
730
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 67 0.027
731
HTC003 Hutchinson-Gilford Progeria Syndrome 65 0.027
732
P CNJ013 Conjunctivitis 65 0.027
733
PPL049 Papillon-Lefevre Syndrome 65 0.027
734
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 0.027
735
KWS002 Kawasaki Disease 65 0.027
736
c CNG006 Congenital Hypothyroidism 64 0.027
737
OST017 Osteomyelitis 64 0.027
738
P MVM001 Movement Disease 63 0.027
739
c ALP101 Alpha-Thalassemia 62 0.027
740
HSH003 Hashimoto Thyroiditis 62 0.027
741
CRC021 Carcinosarcoma 62 0.027
742
MSL001 Measles 62 0.027
743
c PNS012 Paine Syndrome 61 0.027
744
YLL002 Yellow Fever 61 0.027
745
P SJG008 Sjogren Syndrome 61 0.027
746
APP008 Appendicitis 61 0.027
747
P TST021 Testicular Germ Cell Tumor 60 0.027
748
P SCL018 Scoliosis 60 0.027
749
HYD002 Hydronephrosis 60 0.027
750
P GLY013 Glycogen Storage Disease 60 0.027
751
IDP011 Idiopathic Interstitial Pneumonia 59 0.027
752
AVN001 Avian Influenza 59 0.027
753
P DNG005 Dengue Virus 59 0.027
754
P TYR004 Tyrosinemia 58 0.027
755
DSS008 Disease of Mental Health 58 0.027
756
ACY009 Acyl-Coa Dehydrogenase, Medium-Chain, Deficiency of 58 0.027
757
BRG013 Buerger Disease 58 0.027
758
GLS018 Glass Syndrome 57 0.027
759
c CHL119 Cholangitis, Primary Sclerosing 57 0.027
760
P EXN002 Exanthem 57 0.027
761
DSS009 Disseminated Intravascular Coagulation 57 0.027
762
c MST023 Mesothelioma, Malignant 57 0.027
763
P END033 Endocarditis 57 0.027
764
P FCL005 Focal Segmental Glomerulosclerosis 57 0.027
765
P PLY018 Polycythemia 56 0.027
766
TCK001 Tick-Borne Encephalitis 56 0.027
767
VRG001 Variegate Porphyria 56 0.027
768
MTH009 Mouth Disease 56 0.027
769
c GRV008 Graves Disease 1 56 0.027
770
ORP003 Oropharynx Cancer 55 0.027
771
FND002 Fundus Dystrophy 55 0.027
772
FLR002 Filariasis 55 0.027
773
PLM012 Pulmonary Sarcoidosis 53 0.027
774
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.027
775
P TCD001 Tic Disorder 53 0.027
776
KRT006 Keratoconjunctivitis 53 0.027
777
ECH003 Echinococcosis 53 0.027
778
CLF001 Cleft Lip 53 0.027
779
P PNC025 Panic Disorder 53 0.027
780
P RTN022 Retinal Vein Occlusion 53 0.027
781
OVR059 Ovary Adenocarcinoma 53 0.027
782
P LRY019 Laryngitis 52 0.027
783
DRM011 Dermatophytosis 52 0.027
784
PRV004 Periventricular Leukomalacia 52 0.027
785
LMY002 Leiomyoma 52 0.027
786
c INH030 Inherited Retinal Disorder 51 0.027
787
PLS006 Plasmodium Vivax Malaria 51 0.027
788
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.027
789
P MMB011 Membranous Nephropathy 50 0.027
790
AZS001 Azoospermia 50 0.027
791
c HRD202 Hereditary Lymphedema I 50 0.027
792
BLR001 Biliary Atresia 50 0.027
793
P CRV039 Cervicitis 49 0.027
794
HYP043 Hyperandrogenism 48 0.027
795
P SCL009 Sclerosing Cholangitis 48 0.027
796
CHL147 Chlamydia Pneumonia 48 0.027
797
VTM002 Vitamin B12 Deficiency 48 0.027
798
c TYR013 Tyrosinemia, Type Ii 47 0.027
799
PRC003 Proctitis 47 0.027
800
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.027
801
CRD137 Cardiogenic Shock 47 0.027
802
EXS001 Exostosis 46 0.027
803
CHD004 Chudley-Mccullough Syndrome 46 0.027
804
PGM003 Pigmentation Disease 46 0.027
805
P PRD037 Periodontal Ehlers-Danlos Syndrome 45 0.027
807
CRB008 Cerebral Atherosclerosis 44 0.027
808
P HYP111 Hyperprolinemia 44 0.027
809
c HYP272 Hypercholesterolemia, Familial, 3 44 0.027
810
CHL152 Childhood Acute Lymphocytic Leukemia 44 0.027
811
BCT021 Bacterial Sepsis 44 0.027
812
CVD001 Covid-19 44 0.027
813
TND004 Tendinopathy 43 0.027
814
P TST026 Testicular Germ Cell Cancer 43 0.027
815
P HYP265 Hypotonia 43 0.027
816
HYP457 Hypertrophic Scars 42 0.027
817
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.027
818
OBS082 Obstructive Nephropathy 42 0.027
819
P PHT010 Photoparoxysmal Response 1 42 0.027
820
OPS001 Opisthorchiasis 41 0.027
821
PLY100 Polyploidy 40 0.027
822
SPS019 Spastic Paraparesis 38 0.027
823
c SYS043 Systemic Lupus Erythematosus 1 38 0.027
824
ACY011 Acyl-Coa Dehydrogenase Deficiency 38 0.027
825
MLD002 Mild Pre-Eclampsia 36 0.027
826
c ATM022 Autoimmune Myocarditis 35 0.027
827
GRM010 Germ Cells Tumors 34 0.027
828
MDM001 Medium-Chain Acyl-Coenzyme a Dehydrogenase Deficiency 33 0.027
829
P VSC018 Visceral Steatosis 33 0.027
830
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 28 0.027
831
c CLB022 Coloboma, Ocular, Autosomal Recessive 28 0.027
832
CHL079 Children's Interstitial Lung Disease 26 0.027
833
HTT002 Hutterite Cerebroosteonephrodysplasia Syndrome 26 0.027
834
NRM022 Neurometabolic Disease 25 0.027
835
ADG002 Audiogenic Seizures 25 0.027
836
MTC015 Mitochondrial Dna-Associated Leigh Syndrome and Narp 24 0.027
837
P RTT002 Rett Syndrome 80 0.023
838
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.023
839
c MNN043 Meningioma, Familial 74 0.023
840
P NJM001 Nijmegen Breakage Syndrome 74 0.023
841
RNL065 Renal Cell Carcinoma, Papillary, 1 73 0.023
842
P FML018 Familial Mediterranean Fever 73 0.023
843
ACR007 Acromegaly 71 0.023
844
MYL005 Myelofibrosis 70 0.023
845
P MPL001 Maple Syrup Urine Disease 69 0.023
846
MNT001 Mantle Cell Lymphoma 69 0.023
847
P SPR120 Supranuclear Palsy, Progressive, 1 68 0.023
848
P MYS003 Myasthenia Gravis 68 0.023
849
c HYP768 Hyperlipoproteinemia, Type I 67 0.023
850
CRP001 Carpal Tunnel Syndrome 67 0.023
851
P HYD006 Hydrocephalus 66 0.023
852
LNG039 Lung Squamous Cell Carcinoma 66 0.023
853
MYL031 Myeloproliferative Neoplasm 66 0.023
854
KHL003 Kohlschutter-Tonz Syndrome 65 0.023
855
P DYS154 Dystonia 65 0.023
856
DMN031 Dementia, Lewy Body 65 0.023
857
ATM096 Autoimmune Polyendocrine Syndrome, Type I, with or Without Reversible Metaphyseal Dysplasia 65 0.023
858
c ATS347 Autosomal Dominant Polycystic Kidney Disease 65 0.023
859
CLF027 Cleft Palate, Isolated 64 0.023
860
TBC004 Tobacco Addiction 64 0.023
861
HYP020 Hyperprolactinemia 64 0.023
862
KRN002 Kearns-Sayre Syndrome 63 0.023
863
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.023
864
c FNC043 Fanconi Anemia, Complementation Group E 62 0.023
865
P SPN046 Spinal Muscular Atrophy 62 0.023
866
P FCS012 Facioscapulohumeral Muscular Dystrophy 1 62 0.023
867
MNN042 Meningioma, Radiation-Induced 62 0.023
868
PSR001 Psoriatic Arthritis 61 0.023
869
P INT143 Interstitial Cystitis 61 0.023
870
ALV005 Alveolar Soft Part Sarcoma 61 0.023
871
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.023
872
CNT105 Central Core Disease of Muscle 60 0.023
873
P ATS308 Autosomal Dominant Cerebellar Ataxia 60 0.023
874
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.023
875
CHC001 Chickenpox 60 0.023
876
P PTN014 Patent Ductus Arteriosus 1 60 0.023
877
PLM033 Pulmonary Embolism 59 0.023
878
c LTN004 Late-Onset Retinal Degeneration 59 0.023
879
P GLL022 Guillain-Barre Syndrome 59 0.023
880
ALK013 Alkaptonuria 58 0.023
881
PST028 Post-Traumatic Stress Disorder 58 0.023
882
RBS001 Rabies 58 0.023
883
CMP010 Complex Regional Pain Syndrome 58 0.023
884
SPS150 Spastic Ataxia, Charlevoix-Saguenay Type 58 0.023
885
P PLY041 Polymyositis 57 0.023
886
ARG007 Argininemia 57 0.023
887
HMR039 Hemorrhage, Intracerebral 57 0.023
888
CYT008 Cytomegalovirus Infection 57 0.023
889
AYM001 Ayme-Gripp Syndrome 57 0.023
890
P VNB005 Van Buchem Disease 56 0.023
891
TRN018 Transitional Cell Carcinoma 56 0.023
892
LMY014 Leiomyoma, Uterine 56 0.023
893
CYS008 Cystic Echinococcosis 56 0.023
894
SBC001 Subacute Sclerosing Panencephalitis 56 0.023
895
P HYP838 Hyperlipidemia, Familial Combined, 3 56 0.023
896
DFF005 Diffuse Large B-Cell Lymphoma 55 0.023
897
ACT058 Active Peptic Ulcer Disease 55 0.023
898
c MYP132 Myopathy, Congenital 55 0.023
899
FLT006 Floating-Harbor Syndrome 55 0.023
900
VGN023 Vaginitis 54 0.023
901
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 0.023
902
HLL004 Hellp Syndrome 54 0.023
903
SNS003 Sensory Peripheral Neuropathy 54 0.023
904
SLP001 Sleeping Sickness 54 0.023
905
TRC023 Trichinosis 53 0.023
906
BCT002 Bacterial Vaginosis 53 0.023
907
P HML001 Hemolytic-Uremic Syndrome 53 0.023
908
INF034 Infective Endocarditis 53 0.023
909
P ORL007 Oral Cavity Cancer 53 0.023
910
P HMR003 Hemorrhagic Disease 53 0.023
911
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 53 0.023
912
P ACT008 Actinic Keratosis 53 0.023
913
c CNT035 Central Nervous System Disease 52 0.023
914
P SML001 Small Cell Carcinoma 52 0.023
915
CRT016 Carotid Artery Disease 52 0.023
916
NRP045 Neuropathy, Ataxia, and Retinitis Pigmentosa 52 0.023
917
c ACT135 Acute Graft Versus Host Disease 52 0.023
918
THR004 Thrombocytosis 51 0.023
919
P HRD144 Hereditary Mixed Polyposis Syndrome 51 0.023
920
MYL020 Myelomeningocele 51 0.023
921
P THR015 Thrombophilia 51 0.023
922
P HYP040 Hypospadias 51 0.023
923
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.023
924
SCB001 Scabies 50 0.023
925
LNT004 Lentigines 50 0.023
926
SPN021 Spinal Meningioma 50 0.023
927
MCL027 Macular Dystrophy, Dominant Cystoid 50 0.023
928
TRY001 Trypanosomiasis 50 0.023
929
HMG002 Hemoglobinuria 50 0.023
930
HYP748 Hypertelorism 50 0.023
931
P MYT002 Myotonic Dystrophy 49 0.023
932
P CRN025 Corneal Dystrophy 49 0.023
933
P MTC133 Mitochondrial Myopathy 49 0.023
934
c BPL002 Bipolar I Disorder 49 0.023
935
P MGR001 Migraine Without Aura 49 0.023
936
ACT029 Acute Interstitial Pneumonia 49 0.023
937
SBS004 Substance Dependence 48 0.023
938
VTM033 Vitamin K Deficiency Bleeding 48 0.023
939
DGN001 Degenerative Disc Disease 48 0.023
940
HYP025 Hyperphosphatemia 48 0.023
941
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 47 0.023
942
DRG003 Drug Dependence 47 0.023
943
P UTR058 Uterine Anomalies 47 0.023
944
ABD017 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 47 0.023
945
CLN019 Colonic Disease 47 0.023
946
c INH020 Inherited Metabolic Disorder 47 0.023
947
P CRC039 Coarctation of Aorta 47 0.023
948
CHR074 Choriocarcinoma 47 0.023
949
P BLD051 Blood Coagulation Disease 46 0.023
950
LYM019 Lymphosarcoma 46 0.023
951
ASP004 Asphyxia Neonatorum 46 0.023
952
P OPT048 Opitz-Gbbb Syndrome 46 0.023
953
MNN020 Meningococcal Infection 46 0.023
954
PLL012 Pollen Allergy 46 0.023
955
AND014 Androgenic Alopecia 46 0.023
956
TRP008 Tropical Calcific Pancreatitis 46 0.023
957
GRW007 Growth Hormone Deficiency 46 0.023
958
VGN019 Vaginal Discharge 46 0.023
959
LKS001 Leukostasis 46 0.023
960
CYN002 Cyanosis, Transient Neonatal 45 0.023
961
HMR023 Hemorrhagic Cystitis 45 0.023
962
P BRN120 Bronchus Cancer 45 0.023
963
P OCY003 Oocyte Maturation Defect 1 45 0.023
964
BRN032 Brain Glioma 45 0.023
965
GRD001 Giardiasis 45 0.023
966
MYF001 Myofibroma 45 0.023
967
GRN017 Granulocytopenia 44 0.023
968
FCH001 Fuchs' Endothelial Dystrophy 44 0.023
969
LRY018 Laryngeal Squamous Cell Carcinoma 44 0.023
970
ART006 Arthus Reaction 44 0.023
971
ENC005 Encephalomalacia 43 0.023
972
SDD008 Sudden Sensorineural Hearing Loss 43 0.023
973
TRP009 Triple X Syndrome 42 0.023
974
ALC010 Alcoholic Cardiomyopathy 42 0.023
975
c CHR576 Chronic Beryllium Disease 42 0.023
976
BCK006 Back Pain 42 0.023
977
c MLG079 Malignant Pleural Mesothelioma 42 0.023
978
IDP091 Idiopathic Nephrotic Syndrome 42 0.023
979
FSC002 Fascioliasis 42 0.023
980
EHR002 Ehrlichiosis 42 0.023
981
c BRT038 Baraitser-Winter Syndrome 1 41 0.023
982
RST023 Resting Heart Rate, Variation in 41 0.023
983
TTT001 Tatton-Brown-Rahman Syndrome 41 0.023
984
DBT002 Diabetic Autonomic Neuropathy 41 0.023
985
SCR001 Secretory Meningioma 41 0.023
986
MCL003 Macular Holes 40 0.023
987
ADS004 Aids Dementia Complex 40 0.023
988
ALC005 Alcoholic Pancreatitis 40 0.023
989
GLC008 Glucose Metabolism Disease 40 0.023
990
P BRY005 Beryllium Disease 40 0.023
991
CRD005 Cardia Cancer 40 0.023
992
CRN020 Coronary Restenosis 39 0.023
993
SKN020 Skin Papilloma 39 0.023
994
P DYS021 Dysautonomia 39 0.023
995
c PRG020 Paragangliomas 3 39 0.023
997
c PLY105 Polycystic Ovary Syndrome 1 38 0.023
998
c OVR114 Ovarian Cancer 1 38 0.023
999
P FML187 Familial Hypertension 37 0.023
1000
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.023
1001
PYR009 Pyridoxine Deficiency Anemia 34 0.023
1002
c PLM127 Pulmonary Hypertension, Primary, 3 34 0.023
1003
c PRS136 Prostate Cancer, Hereditary, 6 33 0.023
1004
c PRS130 Prostate Cancer, Hereditary, 8 32 0.023
1005
KDN013 Kidney Hypertrophy 32 0.023
1006
DGN002 Degenerative Myopia 32 0.023
1007
PRC051 Paracetamol Poisoning 30 0.023
1008
MTR001 Mature Cataract 28 0.023
1009
HYP561 Hypertelorism, Preauricular Sinus, Punctal Pits, and Deafness 28 0.023
1010
CYT018 Cytochrome P450 2d6 Variant 27 0.023
1011
VLK001 Volkmann Contracture 25 0.023
1012
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.023
1013
DRM046 Dermal Ridges-off-the-End 24 0.023
1014
DRG025 Drug-Induced Hearing Loss 22 0.023
1015
c RNG019 Ring Chromosome 3 22 0.023
1016
PHC015 Phacoanaphylactic Uveitis 19 0.023
1017
PRX092 Peroxidase, Salivary 9 0.023
1018
CNN003 Conn's Syndrome 79 0.019
1019
P MDL005 Medulloblastoma 77 0.019
1020
MRF001 Marfan Syndrome 77 0.019
1021
c NRF024 Neurofibromatosis, Type I 77 0.019
1022
c TBR026 Tuberous Sclerosis 2 72 0.019
1023
P FML011 Familial Adenomatous Polyposis 72 0.019
1024
BHC003 Behcet Syndrome 71 0.019
1025
MYL009 Myelodysplastic Syndrome 70 0.019
1026
MLT157 Multiple System Atrophy 1 70 0.019
1027
c GCH015 Gaucher Disease, Type I 70 0.019
1028
P ASP006 Aspergillosis 69 0.019
1029
WRN001 Werner Syndrome 69 0.019
1030
ABT001 Abetalipoproteinemia 69 0.019
1031
P OCL013 Oculodentodigital Dysplasia 69 0.019
1032
CST001 Costello Syndrome 68 0.019
1033
P ESS003 Essential Thrombocythemia 68 0.019
1034
c MCL062 Mucolipidosis Ii Alpha/beta 68 0.019
1035
P DYS007 Dyskeratosis Congenita 67 0.019
1036
c PRD013 Periodic Fever, Familial, Autosomal Dominant 67 0.019
1037
c INF071 Inflammatory Bowel Disease 1 67 0.019
1038
FCT007 Factor Vii Deficiency 67 0.019
1039
P OLG002 Oligodendroglioma 67 0.019
1040
P FLL037 Follicular Lymphoma 67 0.019
1041
P PRP003 Porphyria Cutanea Tarda 67 0.019
1042
P BLD062 Bile Duct Cancer 67 0.019
1043
GLL008 Gilles De La Tourette Syndrome 66 0.019
1044
TTN003 Tetanus 65 0.019
1045
ACR006 Aceruloplasminemia 65 0.019
1046
P LPS002 Liposarcoma 65 0.019
1047
P PSD087 Pseudoxanthoma Elasticum 65 0.019
1048
MSM014 Mismatch Repair Cancer Syndrome 65 0.019
1049
P CHR071 Charcot-Marie-Tooth Disease 65 0.019
1050
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.019
1051
MYC079 Myoclonic Epilepsy of Lafora 64 0.019
1052
OVR029 Ovarian Hyperstimulation Syndrome 64 0.019
1053
ART002 Arts Syndrome 64 0.019
1054
ALP103 Alpha-1-Antitrypsin Deficiency 64 0.019
1055
P CRN015 Cornelia De Lange Syndrome 64 0.019
1056
LYM017 Lyme Disease 64 0.019
1057
P GCH001 Gaucher's Disease 63 0.019
1058
c PLY162 Polyposis Syndrome, Hereditary Mixed, 1 63 0.019
1059
END041 Endometrial Adenocarcinoma 63 0.019
1060
P LMY004 Leiomyosarcoma 63 0.019
1061
HMT002 Hematologic Cancer 62 0.019
1062
P BCK002 Beckwith-Wiedemann Syndrome 62 0.019
1063
P ORT004 Orthostatic Intolerance 62 0.019
1064
OST003 Osteonecrosis 61 0.019
1065
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 61 0.019
1066
CNV004 Canavan Disease 61 0.019
1067
c WLM018 Wilms Tumor 5 61 0.019
1068
VRL011 Viral Infectious Disease 61 0.019
1069
P HMN010 Hemangioma 61 0.019
1070
SHG001 Shigellosis 60 0.019
1071
HRP004 Herpes Zoster 60 0.019
1072
DNG002 Dengue Hemorrhagic Fever 60 0.019
1073
LBR030 Leber Optic Atrophy 60 0.019
1074
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.019
1075
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 60 0.019
1076
c CRD186 Ceroid Lipofuscinosis, Neuronal, 3 60 0.019
1077
PNM001 Pneumocystosis 59 0.019