Search results for (S)-2-Aceto-2-hydroxybutanoic acid

2843 hits were found for (S)-2-Aceto-2-hydroxybutanoic acid

# Family MCID Name MIFTS Score
1
P LVR013 Liver Disease 71 0.368
2
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.358
3
HLX001 Helix Syndrome 46 0.331
4
P CLR023 Colorectal Cancer 100 0.326
5
P NRB010 Neuroblastoma 1 66 0.309
6
LVR012 Liver Cirrhosis 67 0.305
7
P BRS047 Breast Cancer 99 0.298
8
CHL068 Cholestasis 61 0.293
9
48X005 48,xyyy 37 0.287
10
FTT001 Fatty Liver Disease 63 0.283
11
P DRR001 Diarrhea 55 0.277
12
P KDN018 Kidney Disease 73 0.266
13
TRD008 Triiodothyronine Receptor Auxiliary Protein 35 0.247
14
P GLM045 Glioma 64 0.247
15
PRT014 Protein S Deficiency 50 0.246
16
P HPT023 Hepatocellular Carcinoma 99 0.246
17
ISC004 Ischemia 62 0.246
18
GLL048 Glial Tumor 48 0.244
19
P SZR006 Seizure Disorder 59 0.241
20
OST012 Osteoarthritis 80 0.239
21
P BLD134 Bladder Cancer 79 0.238
22
P INF037 Inflammatory Bowel Disease 57 0.238
23
PRT037 Pertussis 66 0.237
24
P LKM002 Leukemia 69 0.236
25
ACT119 Acute Promyelocytic Leukemia 63 0.235
26
P PRS040 Prostate Cancer 97 0.234
27
VSL002 Visual Epilepsy 58 0.231
28
P ALZ034 Alzheimer Disease 90 0.230
29
P OVR042 Ovarian Cancer 89 0.228
30
P ADN016 Adenocarcinoma 65 0.228
31
ALL026 Allergic Hypersensitivity Disease 65 0.227
32
ATM095 Autoimmune Disease 62 0.226
33
P LNG032 Lung Cancer 99 0.226
34
P CRN300 Coronary Heart Disease 1 59 0.224
35
CLT003 Colitis 63 0.223
36
c THR092 Thrombophilia Due to Thrombin Defect 74 0.223
37
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.222
38
HYP014 Hyperuricemia 52 0.222
39
NRL016 Neural Tube Defects 83 0.222
40
DPR016 Depression 64 0.221
41
LPD008 Lipid Metabolism Disorder 64 0.219
42
ATH013 Atherosclerosis Susceptibility 68 0.215
43
ULC004 Ulcerative Colitis 75 0.215
44
GST092 Gastroesophageal Reflux 68 0.215
45
HMN044 Human Immunodeficiency Virus Type 1 73 0.215
46
HYP066 Hyperglycemia 63 0.214
47
P LYM031 Lymphocytic Leukemia 56 0.213
48
P MYL006 Myeloid Leukemia 61 0.212
49
47X002 47,xyy 49 0.212
50
BNR002 Bone Resorption Disease 51 0.211
51
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 82 0.210
52
GLB002 Glioblastoma 74 0.210
53
DFC004 Deficiency Anemia 77 0.209
54
P VSC007 Vascular Disease 65 0.209
55
GLB015 Glioblastoma Multiforme 60 0.209
56
MTB004 Metabolic Acidosis 48 0.208
57
DRM006 Dermatitis 63 0.207
58
HRW001 Hair Whorl 36 0.207
59
THR024 Thrombosis 58 0.207
60
P HRP006 Herpes Simplex 66 0.204
61
P FTT008 Fatty Liver Disease, Nonalcoholic 1 58 0.204
62
P DDN001 Duodenal Ulcer 50 0.203
63
P CRN018 Coronary Artery Anomaly 67 0.203
64
c HPT016 Hepatitis B 63 0.203
65
PLM017 Pulmonary Alveolar Microlithiasis 54 0.201
66
CYS001 Cystic Fibrosis 84 0.201
67
ATX038 Ataxia and Polyneuropathy, Adult-Onset 51 0.200
68
MNT002 Mental Depression 60 0.200
69
HYP056 Hypoglycemia 68 0.200
70
ADN018 Adenoma 60 0.200
71
P PNC035 Pancreatic Cancer 86 0.199
72
P PSR002 Psoriasis 63 0.199
73
CRH001 Crohn's Disease 75 0.199
74
c HYP595 Hypertension, Essential 87 0.197
75
PST011 Pustulosis of Palm and Sole 51 0.196
76
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 91 0.195
77
c PRC016 Pre-Eclampsia 63 0.195
78
SCH014 Schistosomiasis 57 0.194
79
CHL014 Cholera 58 0.194
80
P HYP724 Hyperlipoproteinemia, Type Iii 74 0.193
81
c CHR684 Chronic Kidney Disease 68 0.193
82
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 40 0.192
83
P GST053 Gastric Cancer 85 0.192
84
P ENC018 Encephalopathy 64 0.192
85
GT001 Gout 63 0.191
86
ART140 Arteries, Anomalies of 60 0.189
87
c HYP836 Hypercholesterolemia, Familial, 1 74 0.189
88
P DBT009 Diabetes Mellitus 66 0.188
89
c LKM061 Leukemia, Acute Myeloid 84 0.188
90
PRM236 Primary Biliary Cholangitis 57 0.187
91
P NRF023 Neurofibromatosis, Type Ii 77 0.186
92
P HNT016 Huntington Disease 72 0.186
93
P HYP750 Hypertriglyceridemia, Familial 62 0.186
94
P HRT032 Heart Disease 78 0.186
95
P RTN024 Retinoblastoma 74 0.184
96
LYM133 Lymphoma, Hodgkin, Classic 70 0.184
97
BRR014 Barrett Esophagus 67 0.183
98
HMC014 Homocysteinemia 54 0.183
99
c FML008 Familial Retinoblastoma 46 0.183
100
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.182
101
P BDY004 Body Mass Index Quantitative Trait Locus 11 78 0.182
102
P THL005 Thalassemia 62 0.182
103
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 0.181
104
SQM006 Squamous Cell Carcinoma 60 0.180
105
CYT002 Cytokine Deficiency 46 0.180
106
PPT005 Peptic Ulcer Disease 60 0.180
107
c ACT210 Acute Respiratory Distress Syndrome 59 0.179
108
OST159 Osteogenic Sarcoma 67 0.179
109
CRB039 Cerebrovascular Disease 71 0.178
110
LNG099 Lung Disease 62 0.178
111
c GLL024 Gallbladder Disease 1 53 0.177
112
P OST002 Osteoporosis 79 0.176
113
HYP266 Hypoxia 58 0.176
114
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 67 0.174
115
P LYM118 Lymphoma 70 0.174
116
P MJR001 Major Depressive Disorder 69 0.174
117
P PRM006 Primary Biliary Cirrhosis 54 0.174
118
P NTR004 Neutropenia 64 0.173
119
MYL069 Myeloma, Multiple 85 0.173
120
P NRP001 Neuropathy 57 0.173
121
PLM001 Pulmonary Tuberculosis 72 0.172
122
P MYC007 Myocardial Infarction 74 0.170
123
VCC001 Vaccinia 50 0.170
124
c HPT073 Hepatitis C Virus 74 0.170
125
DWN001 Down Syndrome 70 0.170
126
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.168
127
P BPL003 Bipolar Disorder 59 0.168
128
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 51 0.167
129
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 43 0.167
130
c MJR024 Major Affective Disorder 9 42 0.166
131
c MJR022 Major Affective Disorder 8 39 0.166
132
P GST044 Gastritis 58 0.166
133
c DNT047 Dentinogenesis Imperfecta Type 2 34 0.166
134
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.165
135
P ESP024 Esophagitis 62 0.165
136
P SCK005 Sickle Cell Disease 53 0.165
137
c SYS001 Systemic Lupus Erythematosus 88 0.165
138
P CTR002 Cataract 62 0.164
139
CRV035 Cervical Cancer 77 0.163
140
ALC007 Alcohol Dependence 68 0.163
141
BRN071 Brain Injury 51 0.163
142
PLM033 Pulmonary Embolism 60 0.163
143
BRK010 Burkitt Lymphoma 68 0.162
144
NNL006 Non-Alcoholic Steatohepatitis 53 0.161
145
END030 End Stage Renal Failure 60 0.161
146
STR067 Stroke, Ischemic 82 0.160
147
c BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.159
148
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.159
149
c BDY021 Body Mass Index Quantitative Trait Locus 20 50 0.159
150
c BDY010 Body Mass Index Quantitative Trait Locus 4 48 0.159
151
c BDY015 Body Mass Index Quantitative Trait Locus 12 48 0.159
152
c BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.159
153
c BDY011 Body Mass Index Quantitative Trait Locus 10 47 0.159
154
c BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.159
155
c BDY006 Body Mass Index Quantitative Trait Locus 8 45 0.159
156
c BDY012 Body Mass Index Quantitative Trait Locus 7 45 0.159
157
c PCH010 Pachyonychia Congenita 3 43 0.159
158
STM007 Stomatitis 51 0.158
159
c SML038 Small Cell Cancer of the Lung 67 0.158
160
SRC014 Sarcoma 67 0.158
161
HMP009 Haemophilus Influenzae 46 0.158
162
SKN016 Skin Disease 64 0.158
163
SPN035 Spindle Cell Sarcoma 57 0.157
164
c RHB024 Rhabdomyosarcoma 2 64 0.157
165
IRN002 Iron Metabolism Disease 58 0.157
166
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.157
167
P RHM011 Rheumatoid Arthritis 82 0.157
168
PPL052 Papillomatosis, Confluent and Reticulated 34 0.157
169
P TRN020 Turner Syndrome 66 0.157
170
CNG034 Congestive Heart Failure 69 0.156
171
P DRM053 Dermatitis, Atopic 68 0.155
172
BCT022 Bacterial Infectious Disease 57 0.155
173
TXC005 Toxic Shock Syndrome 63 0.154
174
c AMY091 Amyotrophic Lateral Sclerosis 1 88 0.154
175
P HPT021 Hepatitis 69 0.154
176
HYP060 Hyperinsulinism 55 0.153
177
OCL069 Ocular Motor Apraxia 53 0.153
178
MLN008 Melanoma 68 0.153
179
c ACT075 Acute Myocardial Infarction 59 0.152
180
GST023 Gastric Ulcer 53 0.152
181
P LKM062 Leukemia, Acute Lymphoblastic 68 0.152
182
SCK003 Sickle Cell Anemia 74 0.152
183
P LTR001 Lateral Sclerosis 56 0.151
184
INS024 Insulin-Like Growth Factor I 79 0.151
185
ADL002 Adult Syndrome 62 0.150
186
TRM010 Traumatic Brain Injury 54 0.150
187
P BCL017 B-Cell Lymphoma 61 0.149
188
PNG002 Pain Agnosia 52 0.148
189
P UVT001 Uveitis 58 0.148
190
P MYP004 Myopathy 63 0.148
191
PRT036 Peritonitis 66 0.147
192
MLR004 Malaria 82 0.147
193
P CHL066 Cholangitis 53 0.147
194
IMM167 Immune Deficiency Disease 79 0.147
195
P LPS004 Lupus Erythematosus 62 0.147
196
ANX010 Anxiety 75 0.146
197
P ATS364 Autism 68 0.146
198
c ACT071 Acute Kidney Failure 60 0.146
199
P PRD008 Periodontitis 66 0.146
200
DNT012 Dental Caries 52 0.146
201
EWN003 Ewing Sarcoma 69 0.145
202
P HYP086 Hypothyroidism 70 0.145
203
P THR014 Thrombocytopenia 67 0.145
204
c MGR028 Migraine with or Without Aura 1 70 0.145
205
c BDY007 Body Mass Index Quantitative Trait Locus 1 43 0.144
206
c MCR120 Microvascular Complications of Diabetes 7 48 0.144
207
c MCR113 Microvascular Complications of Diabetes 3 55 0.143
208
P ART022 Arthritis 71 0.143
209
P BLD124 Bleeding Disorder, Platelet-Type, 11 66 0.143
210
P CHR345 Chronic Pain 52 0.143
211
c MCR130 Microvascular Complications of Diabetes 6 42 0.143
212
c MCR133 Microvascular Complications of Diabetes 4 42 0.143
213
HPT004 Hepatic Coma 42 0.143
214
AGN016 Aging 58 0.142
215
GST045 Gastroenteritis 60 0.142
216
P MNN013 Meningitis 67 0.141
217
SPN186 Spinal Cord Injury 63 0.141
218
PRS045 Prostatic Hypertrophy 55 0.140
219
P PRK057 Parkinson Disease, Late-Onset 77 0.140
220
URM002 Uremia 50 0.140
221
PHN003 Phenylketonuria 73 0.140
222
P INF038 Influenza 69 0.139
223
STT001 Status Epilepticus 61 0.139
224
AST005 Asthma 80 0.139
225
NTR005 Nutritional Deficiency Disease 61 0.139
226
ESP021 Esophageal Cancer 90 0.138
227
THY029 Thyroid Carcinoma 62 0.138
228
BRN024 Bronchitis 70 0.138
229
c SVR001 Severe Acute Respiratory Syndrome 56 0.138
230
TYP007 Typhoid Fever 61 0.137
231
EMB004 Embryonal Carcinoma 57 0.137
232
P EPL164 Epilepsy 73 0.137
233
TLN003 Telangiectasis 53 0.137
234
P TRM003 Tremor 55 0.137
235
SVR004 Severe Combined Immunodeficiency 74 0.136
236
P SKN015 Skin Carcinoma 67 0.136
237
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 0.136
238
P INF032 Infertility 60 0.136
239
P ENC004 Encephalitis 64 0.135
240
BND020 Bone Disease 60 0.135
241
P AST007 Astrocytoma 52 0.135
242
CRB004 Cerebral Artery Occlusion 38 0.135
243
P SCH015 Schizophrenia 76 0.135
244
P PNM007 Pneumonia 71 0.134
245
c HPT001 Hepatitis C 62 0.134
246
ENH001 Enhanced S-Cone Syndrome 56 0.134
247
c ACT068 Acute Cystitis 63 0.134
248
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.134
249
PRP030 Purpura 56 0.133
250
HPT019 Hepatic Encephalopathy 60 0.133
251
ANG054 Angina Pectoris 66 0.132
252
MYL009 Myelodysplastic Syndrome 72 0.132
253
P GLM007 Glomerulonephritis 58 0.132
254
ATX019 Ataxia with Vitamin E Deficiency 46 0.132
255
MST005 Mastitis 55 0.132
256
c ACT027 Acute Pancreatitis 60 0.131
257
P DMN002 Dementia 68 0.131
258
P DBT085 Diabetes Mellitus, Insulin-Dependent 68 0.130
259
P END033 Endocarditis 58 0.130
260
c ATS007 Autism Spectrum Disorder 69 0.130
261
ANX004 Anoxia 44 0.130
262
ALL014 Allergic Encephalomyelitis 40 0.130
263
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.129
264
OVR082 Overgrowth Syndrome 51 0.129
265
c PNS012 Paine Syndrome 61 0.129
266
P FBR017 Fibrosarcoma 57 0.128
267
PRS021 Prostatic Adenoma 52 0.128
268
CHL123 Chlamydia 60 0.128
269
GLC003 Glucose Intolerance 55 0.127
270
ACQ007 Acquired Immunodeficiency Syndrome 61 0.127
271
P RSP003 Respiratory Failure 75 0.127
272
P PHC003 Pheochromocytoma 71 0.127
273
P PRP019 Peripheral Nervous System Disease 64 0.127
274
ORL011 Oral Cancer 62 0.126
275
DYS014 Dyspepsia 51 0.126
276
P CRD132 Cardiac Conduction Defect 61 0.125
277
ADR040 Adrenal Gland Pheochromocytoma 51 0.125
278
P ATT013 Attention Deficit-Hyperactivity Disorder 66 0.125
279
TTN003 Tetanus 62 0.125
280
CLN015 Colon Adenocarcinoma 65 0.125
281
VTM002 Vitamin B12 Deficiency 48 0.125
282
P ART021 Arteriosclerosis 56 0.125
283
c EPS039 Episodic Pain Syndrome, Familial, 1 40 0.125
284
P MLT020 Multiple Sclerosis 73 0.125
285
c BTT014 Beta-Thalassemia 73 0.125
286
PPL022 Papilloma 56 0.124
287
PRS129 Prostatic Hyperplasia, Benign 49 0.124
288
HNS001 Hansen's Disease 35 0.124
289
P ALC033 Alcohol Use Disorder 58 0.123
290
URT049 Urate Oxidase, Pseudogene 26 0.123
291
c ACT073 Acute Leukemia 59 0.123
292
HYP781 Hypoascorbemia 48 0.123
293
P THR015 Thrombophilia 51 0.123
294
P LPR021 Leprosy 3 67 0.123
295
P ATX030 Ataxia-Telangiectasia 83 0.123
296
P ECL001 Eclampsia 53 0.122
297
KRT009 Keratosis 52 0.122
298
RHM027 Rheumatic Disease 56 0.122
299
P PNC044 Pancreatitis 61 0.122
301
P EXN002 Exanthem 58 0.122
302
P CRD119 Cardiac Arrest 71 0.121
303
OST003 Osteonecrosis 62 0.121
304
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 41 0.121
305
c LKM071 Leukemia, Chronic Lymphocytic 81 0.121
306
P MCR115 Microvascular Complications of Diabetes 5 67 0.120
307
HMG005 Hemoglobinopathy 57 0.120
308
LYM019 Lymphosarcoma 48 0.119
309
P NPH012 Nephrotic Syndrome 65 0.119
310
SQM002 Squamous Cell Papilloma 49 0.119
311
PLM010 Pulmonary Edema 56 0.119
312
MDD011 Mood Disorder 62 0.119
313
P CYS018 Cystitis 59 0.119
314
P MSC003 Muscular Atrophy 52 0.118
315
HLC007 Helicobacter Pylori Infection 61 0.118
316
P HDC001 Headache 59 0.118
317
P PLM037 Pulmonary Hypertension 69 0.118
318
END057 Endometrial Cancer 74 0.118
319
RTN023 Retinitis 46 0.117
320
NRR001 Neuroretinitis 46 0.117
321
c VRL010 Viral Hepatitis 56 0.117
322
P PRP029 Porphyria 58 0.117
323
DPH001 Diphtheria 61 0.116
324
c LKM004 Leukemia, B-Cell, Chronic 35 0.115
325
P MSC005 Muscular Dystrophy 68 0.115
326
P LNG064 Lung Cancer Susceptibility 3 79 0.115
327
HYP005 Hypokalemia 55 0.115
328
PPT001 Peptic Esophagitis 47 0.115
329
P ATR011 Atrial Fibrillation 67 0.115
330
END040 Endogenous Depression 55 0.115
331
ADR007 Adrenoleukodystrophy 72 0.114
332
P HYP076 Hyperthyroidism 55 0.114
333
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 56 0.114
334
c ATR087 Atrial Standstill 1 76 0.113
335
DSS009 Disseminated Intravascular Coagulation 58 0.113
336
P HYP098 Hypereosinophilic Syndrome 67 0.113
337
RCK004 Rickets 70 0.113
338
DBT010 Diabetic Neuropathy 56 0.113
339
P SLM003 Salmonellosis 54 0.113
340
c INH020 Inherited Metabolic Disorder 51 0.113
341
MCS002 Mucositis 56 0.113
342
P END044 Endometriosis 63 0.113
343
P MPL001 Maple Syrup Urine Disease 68 0.112
344
c MLG068 Malignant Glioma 46 0.112
345
ERY051 Erythroleukemia, Familial 58 0.112
346
P INT099 Intrahepatic Cholestasis of Pregnancy 50 0.112
347
CHL079 Children's Interstitial Lung Disease 27 0.112
348
P RTN016 Retinal Degeneration 56 0.112
349
P TMP001 Temporal Lobe Epilepsy 53 0.111
350
P LCT001 Lactic Acidosis 52 0.111
351
P NSP012 Nasopharyngeal Carcinoma 67 0.111
352
SPP010 Suppressor of Tumorigenicity 3 54 0.111
353
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 62 0.111
354
NRT001 Neurotic Disorder 53 0.110
355
c DWL002 Dowling-Degos Disease 1 59 0.110
356
IDP011 Idiopathic Interstitial Pneumonia 65 0.110
357
CNS004 Constipation 59 0.110
358
CHC001 Chickenpox 53 0.109
359
P RHN004 Rhinitis 59 0.109
360
P PLM036 Pulmonary Fibrosis 66 0.109
361
c HPT003 Hepatitis a 60 0.109
362
c PLM127 Pulmonary Hypertension, Primary, 3 33 0.109
363
ADR022 Adrenomyeloneuropathy 39 0.109
364
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 61 0.109
365
CHL065 Cholangiocarcinoma 68 0.108
366
CLF027 Cleft Palate, Isolated 67 0.108
367
P PLY019 Polyneuropathy 55 0.108
368
DYS015 Dysentery 45 0.108
369
P RTN008 Retinitis Pigmentosa 77 0.108
370
CHL004 Cholelithiasis 50 0.107
371
LSH001 Leishmaniasis 64 0.107
372
P KLZ004 Kala-Azar 1 43 0.107
373
P CNR004 Cone-Rod Dystrophy 2 72 0.107
374
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.107
375
c LRG017 Large Intestine Cancer 53 0.106
376
GST033 Gestational Diabetes 58 0.106
377
TRT001 Teratocarcinoma 44 0.106
378
c BSL007 Basal Cell Carcinoma 68 0.106
379
INT007 Intermediate Coronary Syndrome 58 0.106
380
P SCL009 Sclerosing Cholangitis 47 0.106
381
P VSC011 Vasculitis 64 0.106
382
OBS525 Obsolete: Squamous Cell Carcinoma of Head and Neck 58 0.105
383
c FNC043 Fanconi Anemia, Complementation Group E 64 0.105
384
INT079 Intrahepatic Cholangiocarcinoma 54 0.105
385
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 65 0.105
386
KRT002 Keratomalacia 47 0.105
387
ENT011 Enterocolitis 51 0.105
388
P BRS044 Breast Adenocarcinoma 59 0.105
389
INT323 Intraocular Pressure Quantitative Trait Locus 64 0.105
390
CNT047 Contact Dermatitis 58 0.104
391
PLY150 Polykaryocytosis Inducer 31 0.104
392
MTH009 Mouth Disease 56 0.104
393
ARG004 Argyria 28 0.104
394
P INS002 in Situ Carcinoma 55 0.104
395
TRN018 Transitional Cell Carcinoma 57 0.104
396
c CHL119 Cholangitis, Primary Sclerosing 59 0.103
397
EYD002 Eye Disease 59 0.103
398
ORL015 Oral Squamous Cell Carcinoma 44 0.103
399
P KDN017 Kidney Cancer 60 0.103
400
c PRM038 Primary Agammaglobulinemia 45 0.103
401
P SCL018 Scoliosis 61 0.103
402
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 46 0.102
403
P HYP069 Hyperparathyroidism 64 0.102
404
ATS010 Autosomal Recessive Disease 49 0.102
405
P TCL004 T-Cell Leukemia 48 0.101
406
c LKM005 Leukemia, T-Cell, Chronic 35 0.101
407
P ALP008 Alopecia 58 0.101
408
NPH091 Nephrolithiasis, Calcium Oxalate 66 0.101
409
SQM013 Squamous Cell Carcinoma, Head and Neck 81 0.101
410
P MYC084 Mycobacterium Tuberculosis 1 69 0.101
411
AVN001 Avian Influenza 56 0.100
412
MSL001 Measles 61 0.100
413
OST017 Osteomyelitis 65 0.100
414
IMM064 Immunodeficiency, Common Variable, 10 51 0.100
415
c FTL070 Fetal Akinesia Deformation Sequence 2 33 0.100
416
c LKM063 Leukemia, Chronic Myeloid 74 0.100
417
P MLN007 Male Infertility 57 0.099
418
OTT002 Otitis Media 71 0.099
419
LPT014 Leptin Deficiency or Dysfunction 72 0.099
420
P PLY011 Polycystic Ovary Syndrome 58 0.099
421
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.099
422
PRP027 Peripheral Vascular Disease 72 0.098
423
AMN003 Amnestic Disorder 55 0.098
424
c ACT134 Acute Liver Failure 53 0.098
425
P BNG032 Benign Mesothelioma 47 0.098
426
P HML002 Hemolytic Anemia 64 0.097
427
CHG001 Chagas Disease 66 0.097
428
P HMC002 Homocystinuria 52 0.097
429
P ART023 Arthropathy 61 0.097
430
HMS001 Hemosiderosis 54 0.097
431
SPL018 Splenomegaly 48 0.097
432
PRT013 Portal Hypertension 61 0.097
433
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 36 0.096
434
LYS012 Lysosomal Acid Lipase Deficiency 63 0.096
435
ENT004 Enthesopathy 46 0.096
436
MTH071 Methane Production 26 0.096
437
P RRH023 Rare Hereditary Hemochromatosis 41 0.096
438
FBR047 Fibromyalgia 60 0.096
439
NWC001 Newcastle Disease 45 0.095
440
BRN004 Brain Edema 57 0.095
441
OVR094 Ovarian Epithelial Cancer 39 0.095
442
P RCT021 Rectum Cancer 54 0.095
443
P AMY004 Amyloidosis 71 0.095
444
IGR001 Ige Responsiveness, Atopic 61 0.095
445
c ALP101 Alpha-Thalassemia 63 0.095
446
LYM143 Lymphoma, Non-Hodgkin, Familial 74 0.095
448
c DLT002 Dilated Cardiomyopathy 81 0.094
449
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 55 0.094
450
DYS073 Dysphagia 52 0.094
451
c CRV002 Cervix Uteri Carcinoma in Situ 47 0.094
452
CRV045 Cervical Intraepithelial Neoplasia 41 0.094
453
HMN014 Human Immunodeficiency Virus Infectious Disease 56 0.094
454
c LKM060 Leukemia, Acute Lymphoblastic 3 57 0.093
455
KPS004 Kaposi Sarcoma 75 0.093
456
P HMP007 Hemophilia 58 0.093
457
P MDL005 Medulloblastoma 78 0.093
458
CRH005 Crohn's Colitis 56 0.093
459
RRS014 Rare Surgical Neurologic Disease 33 0.093
460
TRN015 Transient Cerebral Ischemia 62 0.093
461
HMT018 Hematopoietic Stem Cell Transplantation 54 0.093
462
LNG031 Lung Benign Neoplasm 52 0.092
463
P SRC025 Sarcoidosis 1 72 0.092
464
ANT024 Anthrax Disease 56 0.092
465
c GLY008 Glycogen Storage Disease Ii 68 0.092
466
VRC005 Varicose Veins 61 0.092
467
c PRS136 Prostate Cancer, Hereditary, 6 34 0.091
468
c PRS130 Prostate Cancer, Hereditary, 8 33 0.091
469
c VSC019 Vesicoureteral Reflux 1 62 0.091
470
GST040 Gastric Adenocarcinoma 67 0.091
471
IMP005 Impotence 53 0.091
472
P GCH001 Gaucher's Disease 63 0.091
473
P ACT008 Actinic Keratosis 50 0.091
474
P GRF003 Graft-Versus-Host Disease 71 0.091
475
PSY004 Psychotic Disorder 68 0.091
476
P DYS154 Dystonia 65 0.091
477
PST092 Posttransplant Acute Limbic Encephalitis 29 0.091
478
IRR002 Irritable Bowel Syndrome 65 0.090
479
BLR008 Bilirubin Metabolic Disorder 58 0.090
480
ALL003 Allergic Rhinitis 69 0.090
481
P PYL005 Pyelonephritis 58 0.090
482
P URT039 Urticaria 61 0.090
483
c ATM099 Autoimmune Uveitis 45 0.090
484
PLM031 Poliomyelitis 58 0.090
485
BRR002 Barrett's Adenocarcinoma 36 0.089
486
RHM001 Rheumatic Fever 56 0.089
487
CLR108 Colorectal Adenoma 64 0.089
488
GST050 Gastrointestinal System Disease 57 0.088
489
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 62 0.088
490
c SPN225 Spondyloarthropathy 1 74 0.088
491
P HYP061 Hypertrophic Cardiomyopathy 68 0.088
492
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 56 0.088
493
INS001 Insulinoma 60 0.088
494
DSS008 Disease of Mental Health 66 0.088
495
c FML035 Familial Hyperlipidemia 56 0.087
496
ALL006 Allergic Asthma 56 0.087
497
PRN019 Perinatal Necrotizing Enterocolitis 55 0.086
498
P CND004 Candidiasis 61 0.085
499
WLL004 Wallerian Degeneration 40 0.085
500
BRN028 Brain Cancer 75 0.085
501
P OPN001 Open-Angle Glaucoma 50 0.084
502
SFT003 Soft Tissue Sarcoma 57 0.084
503
P ZLL001 Zellweger Syndrome 56 0.084
504
c INF071 Inflammatory Bowel Disease 1 66 0.084
505
VSC002 Vascular Dementia 57 0.084
506
c SCL052 Scleroderma, Familial Progressive 62 0.084
507
P PLY014 Polycystic Kidney Disease 61 0.084
508
INT052 Intestinal Volvulus 44 0.084
509
BCK006 Back Pain 44 0.084
510
P HYP265 Hypotonia 43 0.084
511
GNG013 Gingivitis 60 0.084
512
ZLL002 Zollinger-Ellison Syndrome 54 0.083
513
HDN002 Head Injury 47 0.083
514
SBC016 Subacute Delirium 43 0.083
515
c ATM011 Autoimmune Hepatitis 63 0.083
516
P SLP006 Sleep Apnea 71 0.083
517
TRY001 Trypanosomiasis 50 0.083
518
P SYS005 Systemic Scleroderma 68 0.082
519
PHR003 Pharyngitis 56 0.082
520
PLS011 Plasmacytoma 57 0.082
521
P MGL001 Megaloblastic Anemia 54 0.082
522
P RTN018 Retinal Disease 53 0.082
523
c MCR129 Microvascular Complications of Diabetes 1 67 0.082
524
HYP081 Hypolipoproteinemia 51 0.082
525
ALL010 Allergic Contact Dermatitis 56 0.082
526
PLG002 Plague 54 0.082
527
CYS013 Cystinuria 66 0.082
528
OST115 Osteonecrosis of the Jaw 40 0.081
529
ANR040 Aneurysm 60 0.081
530
P LRY044 Larynx Cancer 59 0.081
531
P OBS001 Obstructive Jaundice 49 0.081
532
ANR007 Anorexia Nervosa 64 0.081
533
c BRN108 Branchiootic Syndrome 1 62 0.081
534
RSC001 Rosacea 55 0.081
535
P HRS035 Hirschsprung Disease 1 65 0.081
536
FDL002 Food Allergy 52 0.081
537
P PRS038 Personality Disorder 66 0.081
538
CHR074 Choriocarcinoma 47 0.081
539
PRN011 Pernicious Anemia 51 0.080
540
PNC129 Pancreatic Adenocarcinoma 69 0.080
541
P THY032 Thyroiditis 52 0.080
542
P FML011 Familial Adenomatous Polyposis 73 0.080
543
PRT011 Protein C Deficiency 45 0.080
544
c PLM164 Pulmonary Hypertension, Primary, 1 79 0.080
545
P INT068 Intestinal Disease 56 0.080
546
P PRN023 Prion Disease 57 0.080
547
PTT037 Pituitary Tumors 47 0.079
548
CHL067 Cholecystitis 60 0.079
549
P NMN002 Niemann-Pick Disease 60 0.079
550
RNL077 Renal Fibrosis 49 0.079
551
CHR073 Choreatic Disease 52 0.079
552
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 45 0.079
553
P CNJ013 Conjunctivitis 67 0.079
554
c GCH015 Gaucher Disease, Type I 65 0.079
555
P SBS003 Substance Abuse 56 0.078
556
CLR109 Colorectal Adenocarcinoma 51 0.078
557
CYT008 Cytomegalovirus Infection 58 0.078
558
DFF005 Diffuse Large B-Cell Lymphoma 56 0.078
559
P RHB003 Rhabdomyosarcoma 62 0.078
560
SPN051 Spondylitis 53 0.078
561
INF009 Inflammatory Spondylopathy 29 0.078
562
MNN042 Meningioma, Radiation-Induced 64 0.078
563
INT017 Intestinal Schistosomiasis 49 0.078
564
HND015 Hand Skill, Relative 33 0.078
565
c CHR064 Chronic Monocytic Leukemia 43 0.077
566
SYN007 Synovitis 55 0.077
567
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.077
568
IRN001 Iron Deficiency Anemia 59 0.077
569
c MNN043 Meningioma, Familial 74 0.077
570
SPN021 Spinal Meningioma 40 0.077
571
LYM002 Lymphoplasmacyte-Rich Meningioma 40 0.077
572
SCR001 Secretory Meningioma 38 0.077
573
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 63 0.077
574
CNN005 Connective Tissue Disease 68 0.077
575
SLP001 Sleeping Sickness 47 0.077
576
P INT143 Interstitial Cystitis 62 0.076
577
HPT022 Hepatoblastoma 58 0.076
578
P MVM001 Movement Disease 63 0.076
579
P NRV007 Nervous System Disease 68 0.076
580
P CLC063 Celiac Disease 1 66 0.076
581
CRN030 Coronary Stenosis 49 0.075
582
HRP004 Herpes Zoster 58 0.075
583
P DNG005 Dengue Virus 57 0.075
584
RFS006 Refsum Disease, Classic 62 0.075
585
PLC008 Placenta Disease 51 0.075
586
P HYD006 Hydrocephalus 68 0.075
587
c CNG216 Congenital Hydrocephalus 55 0.075
588
P PNC025 Panic Disorder 53 0.075
589
XRD010 Xeroderma Pigmentosum, Variant Type 72 0.075
590
c ADL017 Adult T-Cell Leukemia 59 0.075
591
BLR001 Biliary Atresia 51 0.075
592
ACR006 Aceruloplasminemia 74 0.074
593
YLL002 Yellow Fever 58 0.074
594
P MCP040 Mucopolysaccharidosis-Plus Syndrome 62 0.074
595
P ANT006 Antiphospholipid Syndrome 56 0.074
596
KRT013 Keratolytic Winter Erythema 45 0.074
597
P PLY018 Polycythemia 56 0.074
598
P RBL001 Rubella 56 0.074
599
P MYC008 Myocarditis 60 0.073
600
KRT019 Keratitis, Hereditary 69 0.073
601
SPT004 Septic Arthritis 55 0.073
602
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 54 0.073
603
RLP002 Relapsing-Remitting Multiple Sclerosis 57 0.073
604
HYD002 Hydronephrosis 58 0.073
605
CHL152 Childhood Acute Lymphocytic Leukemia 50 0.073
606
RTN017 Retinal Detachment 62 0.073
607
c GLC092 Glaucoma, Primary Open Angle 63 0.073
608
GRN017 Granulocytopenia 46 0.073
609
PRP080 Peripheral Artery Disease 51 0.073
610
INF034 Infective Endocarditis 53 0.072
611
P SYP003 Syphilis 59 0.072
612
LKP003 Leukoplakia 40 0.072
613
c FML021 Familial Hypercholesterolemia 67 0.072
614
MMM001 Mammary Paget's Disease 53 0.072
615
c WLM018 Wilms Tumor 5 63 0.072
616
SCR011 Scrapie 37 0.072
617
TBC004 Tobacco Addiction 65 0.072
618
GTR002 Goiter 54 0.072
619
CHR178 Chromosomal Triplication 36 0.072
620
P ADL010 Adult Respiratory Distress Syndrome 61 0.072
621
KRT006 Keratoconjunctivitis 53 0.072
622
P ATR005 Atrophic Gastritis 49 0.072
623
SKN019 Skin Melanoma 68 0.071
624
IDP070 Idiopathic Scoliosis 39 0.071
625
THR016 Thrombophlebitis 50 0.071
626
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.071
627
CMM005 Common Cold 57 0.071
628
RBS001 Rabies 57 0.071
629
P GLM040 Glioma Susceptibility 1 68 0.071
630
ACT113 Acute Myeloblastic Leukemia with Maturation 48 0.071
631
TBR011 Tuberculous Meningitis 50 0.071
632
KHL003 Kohlschutter-Tonz Syndrome 63 0.071
633
STN013 Stenotrophomonas Maltophilia Infection 26 0.071
634
RYS001 Reye Syndrome 49 0.071
635
NCL008 Nuclear Ribonucleic Acid 16 0.071
636
LYS002 Lysosomal Storage Disease 52 0.071
637
LYM027 Lymphopenia 58 0.070
638
P FLL037 Follicular Lymphoma 67 0.070
639
P MYS005 Myositis 54 0.070
640
P SLP005 Sleep Disorder 58 0.070
641
WST005 West Nile Virus 56 0.070
642
P MNC007 Monocytic Leukemia 52 0.070
643
PLS007 Plasmodium Falciparum Malaria 53 0.070
644
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.070
645
P TXP001 Toxoplasmosis 61 0.070
646
STF001 Stiff-Person Syndrome 60 0.069
647
ILS001 Ileus 51 0.069
648
ALP103 Alpha-1-Antitrypsin Deficiency 63 0.069
649
DMY004 Demyelinating Disease 54 0.069
650
MSC007 Muscle Hypertrophy 65 0.069
651
c HYP272 Hypercholesterolemia, Familial, 3 44 0.069
652
CRB037 Cerebral Palsy 69 0.068
653
c MLG074 Malignant Mesenchymoma 50 0.068
654
MSC157 Muscular Dystrophy, Duchenne Type 70 0.068
655
ETN001 Eating Disorder 61 0.068
656
PNC001 Pancytopenia 54 0.068
657
CMB003 Combined T Cell and B Cell Immunodeficiency 53 0.068
658
CLF001 Cleft Lip 53 0.068
659
P MTR014 Motor Neuron Disease 66 0.068
660
XNT003 Xanthomatosis 48 0.068
661
IGG001 Iga Glomerulonephritis 50 0.068
662
P TBR001 Tuberous Sclerosis 72 0.068
663
CHR100 Chronic Ulcer of Skin 53 0.068
664
MLK006 Milk Allergy 44 0.068
665
P SHR001 Short Bowel Syndrome 50 0.068
666
PST021 Postpartum Depression 51 0.068
667
P MCR010 Microcephaly 56 0.068
668
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 49 0.067
669
c SVR005 Severe Pre-Eclampsia 50 0.067
670
LMY002 Leiomyoma 52 0.067
671
P APL001 Aplastic Anemia 76 0.067
672
PRS047 Prostatitis 57 0.067
673
GLS001 Gliosarcoma 56 0.067
674
P MYS003 Myasthenia Gravis 68 0.067
675
49X002 49,xxxxy Syndrome 39 0.067
676
c SCN007 Secondary Hyperparathyroidism 52 0.067
677
HRT011 Heart Septal Defect 52 0.067
678
IMM165 Immunoglobulin Switch Sequences 16 0.067
680
TNS005 Tonsillitis 58 0.067
681
c PRD040 Periodontitis, Chronic 56 0.067
682
INT075 Intracranial Hypertension 54 0.067
683
P MYC033 Myoclonus 47 0.067
684
P TRC086 Trichohepatoenteric Syndrome 1 57 0.066
685
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 48 0.066
686
CRT015 Carotid Artery Occlusion 44 0.066
687
RRD056 Rare Disease in Surgical Orthopedic 29 0.066
688
GRD007 Grade Iii Astrocytoma 59 0.066
689
P BNC003 Bone Cancer 56 0.066
690
WTH001 Withdrawal Disorder 47 0.066
691
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 61 0.066
692
BRN056 Bronchopulmonary Dysplasia 57 0.066
693
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.066
694
P BRB001 Beriberi 41 0.066
695
P PRP034 Purpura Fulminans 42 0.066
696
MYF002 Myofascial Pain Syndrome 39 0.066
697
CND006 Candida Glabrata 33 0.066
698
THY030 Thyroid Gland Disease 53 0.066
699
CRB011 Cerebrotendinous Xanthomatosis 61 0.066
700
P SPN046 Spinal Muscular Atrophy 65 0.066
701
c FML001 Familial Atrial Fibrillation 67 0.066
702
DRY001 Dry Eye Syndrome 50 0.066
703
BCT004 Bacteriuria 48 0.065
704
HRY003 Hairy Cell Leukemia 57 0.065
705
c GRV008 Graves Disease 1 55 0.065
706
P MJR007 Major Affective Disorder 1 44 0.065
707
SHG001 Shigellosis 54 0.065
708
JPN002 Japanese Encephalitis 56 0.065
709
CRC021 Carcinosarcoma 62 0.065
710
NRT004 Neuritis 52 0.065
711
PST053 Postherpetic Neuralgia 43 0.065
712
FCT001 Factor Viii Deficiency 54 0.065
713
P ICH004 Ichthyosis 55 0.065
714
ART016 Aortic Aneurysm 71 0.065
715
MST004 Mast Cell Neoplasm 40 0.065
716
EXT007 Extracutaneous Mastocytoma 39 0.065
717
URT010 Ureteral Obstruction 46 0.065
718
P GRV001 Graves' Disease 57 0.065
719
IMP004 Impetigo 47 0.064
720
PTH003 Pathologic Nystagmus 53 0.064
721
P TRT010 Teratoma 52 0.064
722
P VNT002 Ventricular Septal Defect 61 0.064
723
P ASP006 Aspergillosis 67 0.064
724
LYM040 Lymphoblastic Lymphoma 54 0.064
725
P CTN015 Cutaneous T Cell Lymphoma 52 0.064
726
CLL003 Cellulitis 56 0.064
727
VRL011 Viral Infectious Disease 62 0.064
728
VSC003 Visceral Leishmaniasis 55 0.064
729
c EXD008 Exudative Vitreoretinopathy 1 69 0.064
730
THY122 Thyroid Gland Cancer 59 0.063
731
c HMP029 Hemophilia a 69 0.063
732
P HMN010 Hemangioma 62 0.063
733
SPS057 Spasticity 38 0.063
734
DWR001 Dwarfism 45 0.063
735
ALC006 Alcoholic Hepatitis 60 0.063
736
c HPT015 Hepatitis D 49 0.063
737
SLC006 Silicosis 55 0.063
738
P PTT006 Pituitary Adenoma 53 0.063
739
HYP017 Hypophosphatemia 48 0.063
740
OBS168 Obsolete: Atypical Teratoid/rhabdoid Tumor 25 0.063
741
P SJG008 Sjogren Syndrome 57 0.063
742
KWS001 Kwashiorkor 46 0.063
743
APP008 Appendicitis 61 0.063
744
ACT084 Acute Stress Disorder 42 0.063
745
c OVR114 Ovarian Cancer 1 39 0.063
746
c HMC039 Hemochromatosis, Type 1 73 0.063
747
ACN002 Acanthosis Nigricans 62 0.063
748
SDD001 Sudden Infant Death Syndrome 61 0.063
749
FCT007 Factor Vii Deficiency 65 0.063
750
HRN026 Hernia, Hiatus 46 0.063
751
P THY023 Thymoma 64 0.062
752
P MYP006 Myopia 58 0.062
753
P MMP001 Mumps 57 0.062
754
c THY107 Thymoma, Familial 55 0.062
755
BCT002 Bacterial Vaginosis 52 0.062
756
GLS018 Glass Syndrome 51 0.062
757
c BCT007 Bacterial Meningitis 56 0.062
758
P PTS002 Ptosis 53 0.062
759
P PLM034 Pulmonary Emphysema 55 0.062
760
DBT002 Diabetic Autonomic Neuropathy 45 0.062
761
NTR046 Neutrophil Migration 49 0.062
762
AMN001 Amenorrhea 54 0.062
763
P VSC018 Visceral Steatosis 34 0.062
764
P INT070 Intestinal Obstruction 60 0.062
765
EXN003 Exencephaly 32 0.062
766
c HNT004 Huntington Disease-Like 2 48 0.062
767
c HNT011 Huntington Disease-Like 3 37 0.062
768
SPP011 Suppression of Tumorigenicity 12 61 0.061
769
PRP016 Paraplegia 54 0.061
770
RTC005 Reticulosarcoma 48 0.061
771
PYR009 Pyridoxine Deficiency Anemia 32 0.061
772
P PMP001 Pemphigus 56 0.061
773
PST028 Post-Traumatic Stress Disorder 60 0.061
774
MCL006 Macular Retinal Edema 52 0.061
775
ALC009 Alcoholic Liver Cirrhosis 53 0.061
776
ONC002 Onchocerciasis 50 0.061
777
MCR013 Microphthalmia 62 0.061
778
c PSR023 Psoriasis 1 50 0.061
779
c ACT135 Acute Graft Versus Host Disease 52 0.061
780
GLL018 Gallbladder Cancer 57 0.060
781
P OLG002 Oligodendroglioma 67 0.060
782
OBS002 Obsessive-Compulsive Disorder 69 0.060
783
MNN009 Meningoencephalitis 50 0.060
784
RHM028 Rheumatic Heart Disease 54 0.060
785
LWC001 Low Compliance Bladder 45 0.060
786
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.060
787
c MST023 Mesothelioma, Malignant 59 0.060
788
INT002 Intermittent Claudication 60 0.060
789
FCL014 Focal Epilepsy 56 0.060
790
P OPT006 Optic Nerve Disease 59 0.060
791
P BRN022 Bronchiectasis 60 0.059
792
KRT001 Keratoconjunctivitis Sicca 53 0.059
793
MXD026 Mixed Glioma 36 0.059
794
LYM009 Lymphocytic Choriomeningitis 45 0.059
795
HPT082 Hepatic Adenomas, Familial 40 0.059
796
P LCH002 Lichen Planus 55 0.059
797
AZS001 Azoospermia 51 0.059
798
ESP002 Esophageal Varix 49 0.059
799
FSC004 Fasciitis 47 0.059
800
P PLL002 Pellagra 47 0.059
801
MNT001 Mantle Cell Lymphoma 69 0.059
802
NRN004 Neuroendocrine Tumor 59 0.059
803
ATN005 Autonomic Dysfunction 48 0.059
804
PLC007 Placental Abruption 47 0.059
805
TRD006 Tardive Dyskinesia 58 0.059
806
VTM033 Vitamin K Deficiency Bleeding 47 0.059
807
PLY001 Polycythemia Vera 70 0.059
808
INC002 Inclusion Body Myositis 66 0.059
809
P ANR048 Aniridia 1 64 0.059
810
CTN007 Cutaneous Leishmaniasis 61 0.059
811
P NGH001 Night Blindness 48 0.058
812
P ALP009 Alopecia Areata 61 0.058
813
ADG002 Audiogenic Seizures 25 0.058
814
P SCL057 Scoliosis, Isolated 1 41 0.058
815
c HMG029 Hemoglobin Se Disease 40 0.058
816
ACR007 Acromegaly 70 0.058
817
VRC001 Varicocele 51 0.058
818
HYP080 Hypogonadism 51 0.058
819
PLR007 Pleural Empyema 44 0.058
820
c BLR024 Biliary Cirrhosis, Primary, 1 30 0.058
821
NWB001 Newborn Respiratory Distress Syndrome 58 0.058
822
PNM008 Pneumothorax 56 0.058
823
FLR002 Filariasis 56 0.058
824
THR004 Thrombocytosis 52 0.058
825
CHL056 Cheilitis 46 0.058
826
P AVS003 Avascular Necrosis 43 0.058
827
P SML001 Small Cell Carcinoma 55 0.058
828
HYP064 Hypogonadotropism 40 0.058
829
NRF026 Neurofibromatosis, Type Iv, of Riccardi 65 0.058
830
P HMN032 Human Herpesvirus 8 49 0.058
831
THR013 Thoracic Outlet Syndrome 49 0.058
832
SCH003 Schizophreniform Disorder 49 0.058
833
CRT017 Cartilage Disease 54 0.058
834
ATN004 Autonomic Neuropathy 43 0.057
835
c MJR008 Major Affective Disorder 2 35 0.057
836
P SNS001 Sensorineural Hearing Loss 62 0.057
837
P EPD016 Epidermolysis Bullosa 54 0.057
838
ING001 Inguinal Hernia 61 0.057
839
c FNC027 Fanconi Anemia, Complementation Group a 81 0.057
840
PRP083 Porphyria, Acute Intermittent 62 0.057
841
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 61 0.057
842
CLR030 Clear Cell Renal Cell Carcinoma 54 0.057
843
P CHN012 Chondrosarcoma 57 0.057
844
SCH012 Schizoaffective Disorder 50 0.057
845
c PRM005 Primary Hyperparathyroidism 60 0.057
846
PSR001 Psoriatic Arthritis 63 0.057
847
APH002 Aphasia 56 0.057
848
ACT003 Acute Kidney Tubular Necrosis 42 0.057
849
P CRN037 Craniosynostosis 69 0.057
850
BLD131 Bladder Urothelial Carcinoma 62 0.057
851
SCH036 Scheie Syndrome 68 0.057
852
LMB062 Limb Ischemia 50 0.057
853
c WLM013 Wilms Tumor 1 69 0.057
854
SNL007 Senile Cataract 41 0.057
855
MCR004 Macroglobulinemia 50 0.057
856
PLY100 Polyploidy 41 0.057
857
c ART138 Aortic Aneurysm, Familial Abdominal, 1 62 0.057
858
P FRD012 Friedreich Ataxia 1 65 0.057
859
P MTC069 Mitochondrial Disorders 57 0.056
860
c MCR112 Microvascular Complications of Diabetes 2 42 0.056
861
PLR008 Pleurisy 50 0.056
862
c PSR017 Psoriasis 2 55 0.056
863
c PSR028 Psoriasis 7 40 0.056
864
c PSR018 Psoriasis 13 40 0.056
865
c PSR032 Psoriasis 11 40 0.056
866
c THR082 Thrombophilia Due to Activated Protein C Resistance 61 0.056
867
PRT018 Portal Vein Thrombosis 50 0.056
868
BRS099 Breast Ductal Carcinoma 63 0.056
869
P EPN002 Ependymoma 61 0.056
870
TCK001 Tick-Borne Encephalitis 53 0.056
871
c CHR682 Chronic Bilirubin Encephalopathy 36 0.056
872
c INF145 Infantile Liver Failure Syndrome 1 50 0.056
873
ANP008 Anaplastic Oligoastrocytoma 31 0.056
874
TST014 Testicular Cancer 49 0.056
875
c MJR003 Major Affective Disorder 6 34 0.056
876
c MJR006 Major Affective Disorder 5 34 0.056
877
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 49 0.056
878
ORL012 Oral Leukoplakia 42 0.056
879
INT066 Interstitial Lung Disease 61 0.056
880
LPR001 Lepromatous Leprosy 50 0.056
881
LST001 Listeriosis 55 0.056
882
CRD223 Cardiac Arrhythmia 61 0.056
883
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 65 0.055
884
c BNG030 Benign Ependymoma 48 0.055
885
LKD001 Leukodystrophy 61 0.055
886
LNT004 Lentigines 47 0.055
887
BRT054 Brittle Bone Disorder 71 0.055
888
c SCN036 Secondary Progressive Multiple Sclerosis 54 0.055
889
WRN001 Werner Syndrome 68 0.055
890
c THY109 Thyroid Cancer, Nonmedullary, 1 58 0.055
891
GLB001 Gilbert Syndrome 58 0.055
892
P ART106 Arterial Calcification, Generalized, of Infancy, 1 49 0.055
893
P MYT002 Myotonic Dystrophy 52 0.055
894
ART002 Arts Syndrome 63 0.055
896
c MJR023 Major Affective Disorder 7 34 0.055
897
c MJR004 Major Affective Disorder 4 29 0.055
898
c ATM006 Autoimmune Lymphoproliferative Syndrome 73 0.055
899
DCB001 Decubitus Ulcer 54 0.055
900
LYM017 Lyme Disease 64 0.055
901
THY111 Thyroid Carcinoma, Familial Medullary 68 0.054
902
P FTL001 Fetal Alcohol Syndrome 56 0.054
903
MYT026 Myotonia Atrophica 25 0.054
904
P EHL001 Ehlers-Danlos Syndrome 60 0.054
905
c BCT013 Bacterial Pneumonia 49 0.054
906
P SMK004 Smoking As a Quantitative Trait Locus 3 46 0.054
907
VGN023 Vaginitis 54 0.054
908
P CLL015 Collagen Disease 46 0.054
909
CRD137 Cardiogenic Shock 50 0.054
910
P FNC004 Fanconi Syndrome 48 0.054
911
P MTH007 Methemoglobinemia 47 0.054
912
BWN006 Bowen's Disease 34 0.054
913
P RTN022 Retinal Vein Occlusion 50 0.054
914
HRT012 Heart Valve Disease 56 0.054
915
SPN041 Spinal Cord Disease 57 0.054
916
HMT002 Hematologic Cancer 64 0.054
917
INT067 Interstitial Nephritis 46 0.054
918
PYR016 Pyridoxine Deficiency 31 0.054
919
c FLL041 Follicular Lymphoma 1 50 0.054
920
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 52 0.054
921
CCC001 Coccidioidomycosis 54 0.053
922
HPT014 Hepatorenal Syndrome 49 0.053
923
c HMP004 Hemophilia B 66 0.053
924
LPT006 Leptin Receptor Deficiency 47 0.053
925
RTN020 Retinal Vascular Disease 49 0.053
926
CHL013 Cholecystolithiasis 37 0.053
927
RYN005 Raynaud Phenomenon 50 0.053
928
P ANG015 Angioedema 54 0.053
929
ATX010 Ataxia Neuropathy Spectrum 39 0.053
930
P ACT232 Acute Necrotizing Encephalopathy 28 0.053
931
BLD137 Blood Group--Ahonen 17 0.053
932
P GLL022 Guillain-Barre Syndrome 56 0.053
933
P HML001 Hemolytic-Uremic Syndrome 54 0.053
934
HLL004 Hellp Syndrome 53 0.053
935
TXC002 Toxic Encephalopathy 54 0.053
936
ASP007 Aspiration Pneumonia 46 0.053
937
P FRG001 Fragile X Syndrome 69 0.053
938
KRN002 Kearns-Sayre Syndrome 64 0.053
939
P VNW001 Von Willebrand's Disease 64 0.053
940
c LKM056 Leukemia, Chronic Lymphocytic 2 49 0.053
941
c ANT034 Anterior Uveitis 48 0.052
942
BLC012 Bile Acid Malabsorption, Primary 29 0.052
943
CMP010 Complex Regional Pain Syndrome 57 0.052
944
FSC002 Fascioliasis 44 0.052
945
MCR017 Macrocytic Anemia 41 0.052
946
EPD015 Epidemic Typhus 47 0.052
947
RNL065 Renal Cell Carcinoma, Papillary, 1 75 0.052
948
MYL005 Myelofibrosis 69 0.052
949
HYP043 Hyperandrogenism 48 0.052
950
KWS002 Kawasaki Disease 65 0.052
951
CRT013 Carotid Stenosis 50 0.052
952
PPL001 Papillary Adenoma 42 0.052
953
HYP003 Hypermethioninemia 42 0.052
954
PRM329 Premature Aging 41 0.052
955
CYS005 Cysticercosis 55 0.052
956
c ART101 Aortic Valve Disease 2 67 0.052
957
P HRD011 Hereditary Spherocytosis 59 0.052
958
LSC001 Lesch-Nyhan Syndrome 61 0.052
959
P ANG001 Angelman Syndrome 65 0.052
960
END041 Endometrial Adenocarcinoma 64 0.052
961
CMR002 Coumarin Resistance 56 0.052
962
P OPT009 Optic Neuritis 55 0.052
963
HMP005 Hemiplegia 55 0.052
964
HYP814 Hypermethioninemia with S-Adenosylhomocysteine Hydrolase Deficiency 27 0.051
965
P SPR120 Supranuclear Palsy, Progressive, 1 68 0.051
966
CYN002 Cyanosis, Transient Neonatal 45 0.051
967
AND002 Androgen Insensitivity Syndrome 66 0.051
968
PPL049 Papillon-Lefevre Syndrome 63 0.051
969
c ATS347 Autosomal Dominant Polycystic Kidney Disease 61 0.051
970
LRN003 Learning Disability 51 0.051
971
P PRP003 Porphyria Cutanea Tarda 66 0.051
972
P MMB011 Membranous Nephropathy 54 0.051
973
TRN044 Transposition of the Great Arteries 44 0.051
974
VTR007 Vitreoretinopathy 48 0.051
975
ILT001 Ileitis 50 0.051
976
URN003 Urinary Schistosomiasis 45 0.051
977
c ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 36 0.051
978
HRN029 Hearing Loss, Noise-Induced 38 0.051
979
DCT002 Ductal Carcinoma in Situ 57 0.051
980
c JVN010 Juvenile Rheumatoid Arthritis 67 0.051
981
NRM005 Neuromuscular Disease 62 0.051
982
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 44 0.051
983
HRL004 Hurler-Scheie Syndrome 43 0.050
984
CRY035 Cryptorchidism, Unilateral or Bilateral 61 0.050
985
SXL003 Sexual Disorder 49 0.050
986
THY125 Thyroid Gland Medullary Carcinoma 52 0.050
987
CRN017 Coronary Thrombosis 45 0.050
988
GNG003 Gingival Recession 43 0.050
989
HYP025 Hyperphosphatemia 47 0.050
990
c RNG015 Ring Chromosome 2 27 0.050
991
OST011 Osteomalacia 51 0.050
992
RDN001 Reading Disorder 42 0.050
993
FRN006 Frontotemporal Dementia 70 0.050
994
P HYP040 Hypospadias 54 0.050
995
CHR066 Chronic Fatigue Syndrome 61 0.050
996
BRC012 Brucellosis 62 0.050
997
ACT058 Active Peptic Ulcer Disease 55 0.050
998
BRS051 Breast Disease 59 0.050
999
P RNL015 Renal Hypertension 47 0.050
1000
P PRC017 Precursor Lymphoblastic Lymphoma/leukemia 28 0.050
1001
THR100 Thrombocytopenic Purpura, Autoimmune 61 0.050
1002
P GNG009 Gangliosidosis 45 0.050
1003
MYT011 Myotonia 37 0.050
1004
CHK001 Chikungunya 55 0.050
1005
P DBT005 Diabetes Insipidus 54 0.050
1006
CHL147 Chlamydia Pneumonia 39 0.050
1007
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 29 0.050
1008
RSP019 Respiratory Distress Syndrome in Premature Infants 58 0.050
1009
MSC190 Muscular Disease 54 0.050
1010
EXC002 Exocrine Pancreatic Insufficiency 41 0.050
1011
CRC006 Carcinoid Syndrome 55 0.049
1012
BRN002 Bronchiolitis 60 0.049
1013
KLD004 Keloid Disorder 41 0.049
1014
P ESS003 Essential Thrombocythemia 69 0.049
1015
OPT003 Opiate Dependence 50 0.049
1016
SYN036 Syncope 46 0.049
1017
P TTR001 Tetralogy of Fallot 70 0.049
1018
SCB001 Scabies 50 0.049
1019
NCR007 Necrotizing Fasciitis 47 0.049
1020
BLL006 Bullous Pemphigoid 63 0.049
1021
OCL006 Ocular Hypertension 52 0.049
1022
PRM020 Premenstrual Tension 48 0.049
1023
ATM052 Autoimmune Disease 1 38 0.049
1024
ALX003 Alexander Disease 58 0.049
1025
HSH003 Hashimoto Thyroiditis 63 0.049
1026
P LMY004 Leiomyosarcoma 63 0.049
1027
LRY018 Laryngeal Squamous Cell Carcinoma 44 0.049
1028
P CHR012 Chronic Granulomatous Disease 69 0.049
1029
BNN003 Bone Inflammation Disease 51 0.049
1030
P STR092 Striatal Degeneration, Autosomal Dominant 2 42 0.049
1031
P OCL013 Oculodentodigital Dysplasia 65 0.049
1032
VTR013 Vitreoretinopathy, Neovascular Inflammatory 61 0.049
1033
ANR004 Anuria 47 0.049
1034
CRP001 Carpal Tunnel Syndrome 68 0.049
1035
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 53 0.049
1036
CCC002 Coccidiosis 46 0.049
1037
c MCL062 Mucolipidosis Ii Alpha/beta 67 0.049
1038
CRV040 Cervix Carcinoma 52 0.049
1039
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 44 0.049
1040
DMP001 Dumping Syndrome 44 0.049
1041
TRY004 Trypanosomiasis, Human East-African 25 0.049
1042
P STR020 Strabismus 57 0.049
1043
MCH006 Mechanical Strabismus 31 0.049
1044
SNS003 Sensory Peripheral Neuropathy 56 0.048
1045
GST071 Gastrointestinal Carcinoma 42 0.048
1046
PYL006 Pyloric Stenosis 47 0.048
1047
GST037 Gastroparesis 52 0.048
1048
c PNC106 Pancreatic Agenesis 1 50 0.048
1049
HML018 Homologous Wasting Disease 22 0.048
1050
P NRC002 Narcolepsy 56 0.048
1051
c PST005 Posterior Uveitis 52 0.048
1052
P CHR285 Chronic Myelomonocytic Leukemia 60 0.048
1053
DRM011 Dermatophytosis 49 0.048
1054
HYP457 Hypertrophic Scars 44 0.048
1055
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 33 0.048
1056
APN008 Apnea, Obstructive Sleep 64 0.048
1057