Search results for Liver Extracts

2650 hits were found for Liver Extracts

# Family MCID Name MIFTS Score
1
P LVR013 Liver Disease 71 1.303
2
FTT001 Fatty Liver Disease 63 0.891
3
LVR012 Liver Cirrhosis 67 0.884
4
P HPT023 Hepatocellular Carcinoma 99 0.746
5
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.724
6
P CTR002 Cataract 62 0.526
7
c ACT134 Acute Liver Failure 53 0.479
8
P FTT008 Fatty Liver Disease, Nonalcoholic 1 58 0.454
9
P CLR023 Colorectal Cancer 100 0.427
10
NNL006 Non-Alcoholic Steatohepatitis 53 0.417
11
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.412
12
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 0.383
13
CHL068 Cholestasis 61 0.376
14
c HPT001 Hepatitis C 62 0.363
15
PRT013 Portal Hypertension 61 0.361
16
c VRL010 Viral Hepatitis 56 0.360
17
c HPT073 Hepatitis C Virus 74 0.358
18
c HPT016 Hepatitis B 63 0.339
19
HYP066 Hyperglycemia 63 0.325
20
P CHL066 Cholangitis 53 0.318
21
LPD008 Lipid Metabolism Disorder 64 0.306
22
P HPT021 Hepatitis 69 0.297
23
P ENC018 Encephalopathy 64 0.292
24
ISC004 Ischemia 62 0.289
25
TRD008 Triiodothyronine Receptor Auxiliary Protein 35 0.286
26
HPT004 Hepatic Coma 42 0.283
27
48X005 48,xyyy 37 0.280
28
HPT019 Hepatic Encephalopathy 60 0.265
29
CHL065 Cholangiocarcinoma 68 0.265
30
PRM236 Primary Biliary Cholangitis 57 0.265
31
INT079 Intrahepatic Cholangiocarcinoma 54 0.264
32
P PRM006 Primary Biliary Cirrhosis 54 0.257
33
VRC005 Varicose Veins 61 0.257
34
c ATM011 Autoimmune Hepatitis 63 0.256
35
PRT036 Peritonitis 66 0.252
36
P DRR001 Diarrhea 55 0.249
37
ADN018 Adenoma 60 0.245
38
c HYP836 Hypercholesterolemia, Familial, 1 74 0.244
39
P HMN010 Hemangioma 62 0.243
40
CYT002 Cytokine Deficiency 46 0.243
41
P KDN018 Kidney Disease 73 0.239
42
P SCL009 Sclerosing Cholangitis 47 0.234
43
ALC007 Alcohol Dependence 68 0.234
44
ALL026 Allergic Hypersensitivity Disease 65 0.229
45
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.226
46
c HPT003 Hepatitis a 60 0.225
47
HYP056 Hypoglycemia 68 0.222
48
ALC006 Alcoholic Hepatitis 60 0.220
49
P ALC033 Alcohol Use Disorder 58 0.219
50
HMS001 Hemosiderosis 54 0.218
51
OCL069 Ocular Motor Apraxia 53 0.217
52
BLR001 Biliary Atresia 51 0.212
53
P RRH023 Rare Hereditary Hemochromatosis 41 0.211
54
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 82 0.209
55
P GST053 Gastric Cancer 85 0.207
56
HRW001 Hair Whorl 36 0.207
57
P DBT009 Diabetes Mellitus 66 0.206
58
c CHL119 Cholangitis, Primary Sclerosing 59 0.206
59
BCT022 Bacterial Infectious Disease 57 0.205
60
P BDY004 Body Mass Index Quantitative Trait Locus 11 78 0.204
61
ECH003 Echinococcosis 54 0.204
62
P PNC035 Pancreatic Cancer 86 0.204
63
DRM006 Dermatitis 63 0.203
64
P BRS047 Breast Cancer 99 0.203
65
P ADN016 Adenocarcinoma 65 0.201
66
SCH014 Schistosomiasis 57 0.197
67
P INF037 Inflammatory Bowel Disease 57 0.197
68
ATM095 Autoimmune Disease 62 0.196
69
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 40 0.196
70
c DNT047 Dentinogenesis Imperfecta Type 2 34 0.194
71
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.194
72
c BDY021 Body Mass Index Quantitative Trait Locus 20 50 0.194
73
c BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.194
74
c BDY010 Body Mass Index Quantitative Trait Locus 4 48 0.194
75
c BDY015 Body Mass Index Quantitative Trait Locus 12 48 0.194
76
c BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.194
77
c BDY011 Body Mass Index Quantitative Trait Locus 10 47 0.194
78
c BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.194
79
c BDY006 Body Mass Index Quantitative Trait Locus 8 45 0.194
80
c BDY012 Body Mass Index Quantitative Trait Locus 7 45 0.194
81
BNR002 Bone Resorption Disease 51 0.193
82
HYP060 Hyperinsulinism 55 0.192
83
P THR014 Thrombocytopenia 67 0.192
84
47X002 47,xyy 49 0.192
85
DFC004 Deficiency Anemia 77 0.192
86
ATH013 Atherosclerosis Susceptibility 68 0.190
87
PRT018 Portal Vein Thrombosis 50 0.190
88
CLT003 Colitis 63 0.188
89
PLM017 Pulmonary Alveolar Microlithiasis 54 0.188
90
GLC003 Glucose Intolerance 55 0.187
91
HYP266 Hypoxia 58 0.187
92
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 91 0.185
93
P HYP750 Hypertriglyceridemia, Familial 62 0.185
94
ESP002 Esophageal Varix 49 0.185
95
GST023 Gastric Ulcer 53 0.184
96
ULC004 Ulcerative Colitis 75 0.184
97
SPL018 Splenomegaly 48 0.184
98
P HRP006 Herpes Simplex 66 0.183
99
P BCL017 B-Cell Lymphoma 61 0.183
100
PPL052 Papillomatosis, Confluent and Reticulated 34 0.181
101
c BDY007 Body Mass Index Quantitative Trait Locus 1 43 0.181
102
ALC009 Alcoholic Liver Cirrhosis 53 0.180
103
SKN016 Skin Disease 64 0.179
104
THR024 Thrombosis 58 0.178
105
P RHN004 Rhinitis 59 0.177
106
P OST002 Osteoporosis 79 0.175
107
c HMC039 Hemochromatosis, Type 1 73 0.175
108
SPN035 Spindle Cell Sarcoma 57 0.175
109
SRC014 Sarcoma 67 0.174
110
P PRD008 Periodontitis 66 0.172
111
P VSC007 Vascular Disease 65 0.171
112
RHM027 Rheumatic Disease 56 0.171
113
BLR008 Bilirubin Metabolic Disorder 58 0.171
114
P RCT021 Rectum Cancer 54 0.169
115
c ACT071 Acute Kidney Failure 60 0.168
116
P GST044 Gastritis 58 0.166
117
HPT022 Hepatoblastoma 58 0.165
118
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 51 0.165
119
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 43 0.165
120
P DRM053 Dermatitis, Atopic 68 0.164
121
P PSR002 Psoriasis 63 0.164
122
CYS001 Cystic Fibrosis 84 0.164
123
TXC005 Toxic Shock Syndrome 63 0.164
124
ALL003 Allergic Rhinitis 69 0.163
125
P OBS001 Obstructive Jaundice 49 0.163
126
P NRB010 Neuroblastoma 1 66 0.163
127
PST011 Pustulosis of Palm and Sole 51 0.162
128
P NTR004 Neutropenia 64 0.162
129
P HYP086 Hypothyroidism 70 0.161
130
P MYP006 Myopia 58 0.161
131
c HYP595 Hypertension, Essential 87 0.161
132
END030 End Stage Renal Failure 60 0.160
133
AZS001 Azoospermia 51 0.160
134
c CHR684 Chronic Kidney Disease 68 0.159
135
ENT004 Enthesopathy 46 0.158
136
P AMY004 Amyloidosis 71 0.158
137
CNG034 Congestive Heart Failure 69 0.158
138
HPT014 Hepatorenal Syndrome 49 0.158
139
PPT005 Peptic Ulcer Disease 60 0.156
140
LSH001 Leishmaniasis 64 0.154
141
CHL067 Cholecystitis 60 0.152
142
c MCR113 Microvascular Complications of Diabetes 3 55 0.152
143
c MCR130 Microvascular Complications of Diabetes 6 42 0.152
144
c MCR133 Microvascular Complications of Diabetes 4 42 0.152
145
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.152
146
c MCR120 Microvascular Complications of Diabetes 7 48 0.152
147
P KLZ004 Kala-Azar 1 43 0.152
148
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.151
149
P END033 Endocarditis 58 0.151
150
P NRP001 Neuropathy 57 0.151
151
BRN024 Bronchitis 70 0.150
152
P LYM118 Lymphoma 70 0.150
153
c PRC016 Pre-Eclampsia 63 0.150
154
SVR004 Severe Combined Immunodeficiency 74 0.150
155
P HMP007 Hemophilia 58 0.149
156
P HYP098 Hypereosinophilic Syndrome 67 0.148
157
DYS014 Dyspepsia 51 0.147
158
INT323 Intraocular Pressure Quantitative Trait Locus 64 0.147
159
DYS015 Dysentery 45 0.147
160
PRS045 Prostatic Hypertrophy 55 0.147
161
PLY023 Polycystic Liver Disease 55 0.147
162
P END047 Endophthalmitis 50 0.147
163
PRS021 Prostatic Adenoma 52 0.147
164
CLN015 Colon Adenocarcinoma 65 0.146
165
MLN008 Melanoma 68 0.146
166
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 67 0.145
167
P HRT032 Heart Disease 78 0.144
168
c ACT027 Acute Pancreatitis 60 0.143
169
P CRD119 Cardiac Arrest 71 0.143
170
c GLL024 Gallbladder Disease 1 53 0.143
171
INS024 Insulin-Like Growth Factor I 79 0.142
172
P SKN015 Skin Carcinoma 67 0.141
173
P PRS040 Prostate Cancer 97 0.141
174
OST012 Osteoarthritis 80 0.141
175
BND020 Bone Disease 60 0.141
176
ANX010 Anxiety 75 0.140
177
P GRF003 Graft-Versus-Host Disease 71 0.140
178
PRS129 Prostatic Hyperplasia, Benign 49 0.139
179
AGN016 Aging 58 0.139
180
P CND004 Candidiasis 61 0.138
181
DNT012 Dental Caries 52 0.138
182
BDD001 Budd-Chiari Syndrome 62 0.138
183
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.138
184
P LNG032 Lung Cancer 99 0.138
185
CRY036 Cryptogenic Cirrhosis 38 0.137
186
CYT008 Cytomegalovirus Infection 58 0.137
187
CNS004 Constipation 59 0.136
188
P PLY019 Polyneuropathy 55 0.136
189
P HYP076 Hyperthyroidism 55 0.135
190
PNG002 Pain Agnosia 52 0.135
191
c ACT210 Acute Respiratory Distress Syndrome 59 0.135
192
LNG099 Lung Disease 62 0.135
193
P PNC044 Pancreatitis 61 0.134
194
MLR004 Malaria 82 0.134
195
IMM167 Immune Deficiency Disease 79 0.134
196
P RSP003 Respiratory Failure 75 0.134
197
CHL014 Cholera 58 0.134
198
CHL004 Cholelithiasis 50 0.134
199
HYP014 Hyperuricemia 52 0.133
200
DSS009 Disseminated Intravascular Coagulation 58 0.133
201
ALP103 Alpha-1-Antitrypsin Deficiency 63 0.132
202
OVR082 Overgrowth Syndrome 51 0.132
203
PLM033 Pulmonary Embolism 60 0.131
204
RTN017 Retinal Detachment 62 0.131
205
P BLD134 Bladder Cancer 79 0.131
206
c INF145 Infantile Liver Failure Syndrome 1 50 0.130
207
GT001 Gout 63 0.130
208
HLX001 Helix Syndrome 46 0.130
209
P OVR042 Ovarian Cancer 89 0.129
210
P EXN002 Exanthem 58 0.129
211
PRT037 Pertussis 66 0.127
212
P LKM002 Leukemia 69 0.127
213
GLB002 Glioblastoma 74 0.127
214
GLB015 Glioblastoma Multiforme 60 0.126
215
P PLM037 Pulmonary Hypertension 69 0.126
216
P FBR017 Fibrosarcoma 57 0.125
217
P THL005 Thalassemia 62 0.125
218
c HPT007 Hepatitis E 53 0.125
219
c LRG017 Large Intestine Cancer 53 0.125
220
IMP005 Impotence 53 0.124
221
P LYM031 Lymphocytic Leukemia 56 0.124
222
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.123
223
P DDN001 Duodenal Ulcer 50 0.123
224
IRN002 Iron Metabolism Disease 58 0.123
225
LPT014 Leptin Deficiency or Dysfunction 72 0.123
226
P GLY013 Glycogen Storage Disease 59 0.122
227
P ALZ034 Alzheimer Disease 90 0.122
228
P ASP006 Aspergillosis 67 0.121
229
CRB039 Cerebrovascular Disease 71 0.121
230
P PRP029 Porphyria 58 0.121
231
TLN003 Telangiectasis 53 0.121
232
CRH001 Crohn's Disease 75 0.120
233
WLS001 Wilson Disease 69 0.120
234
P UVT001 Uveitis 58 0.120
235
NDL013 Nodular Regenerative Hyperplasia 48 0.120
236
P MCR115 Microvascular Complications of Diabetes 5 67 0.118
237
HLL004 Hellp Syndrome 53 0.118
238
P NRF023 Neurofibromatosis, Type Ii 77 0.118
239
CLR109 Colorectal Adenocarcinoma 51 0.118
240
STM007 Stomatitis 51 0.118
241
OST003 Osteonecrosis 62 0.118
242
NTR005 Nutritional Deficiency Disease 61 0.118
243
SQM006 Squamous Cell Carcinoma 60 0.118
244
PLM001 Pulmonary Tuberculosis 72 0.118
245
GST019 Gastrointestinal Stromal Tumor 76 0.117
246
P TRM003 Tremor 55 0.117
247
ANG020 Angiosarcoma 59 0.117
248
P PLY014 Polycystic Kidney Disease 61 0.117
249
ORL011 Oral Cancer 62 0.116
250
OST159 Osteogenic Sarcoma 67 0.116
251
HPT046 Hepatic Veno-Occlusive Disease 56 0.115
252
HMN044 Human Immunodeficiency Virus Type 1 73 0.115
253
c PCH010 Pachyonychia Congenita 3 43 0.115
254
P SRC025 Sarcoidosis 1 72 0.115
255
P ART021 Arteriosclerosis 56 0.115
256
P SYP003 Syphilis 59 0.114
257
P BRS044 Breast Adenocarcinoma 59 0.114
258
P HML002 Hemolytic Anemia 64 0.114
259
c SYS001 Systemic Lupus Erythematosus 88 0.114
260
HPT009 Hepatopulmonary Syndrome 49 0.114
261
P CRN300 Coronary Heart Disease 1 59 0.114
262
c THR092 Thrombophilia Due to Thrombin Defect 74 0.113
263
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 56 0.113
264
c RHB024 Rhabdomyosarcoma 2 64 0.113
265
P INF032 Infertility 60 0.113
266
P ART022 Arthritis 71 0.113
267
ESP021 Esophageal Cancer 90 0.112
268
P SZR006 Seizure Disorder 59 0.112
269
ATX038 Ataxia and Polyneuropathy, Adult-Onset 51 0.112
270
CVR006 Cavernous Hemangioma 49 0.112
271
P HYP724 Hyperlipoproteinemia, Type Iii 74 0.112
272
P CRN018 Coronary Artery Anomaly 67 0.112
273
PNM008 Pneumothorax 56 0.111
274
DPR016 Depression 64 0.111
275
PRN011 Pernicious Anemia 51 0.111
276
P RHM011 Rheumatoid Arthritis 82 0.111
277
NRN004 Neuroendocrine Tumor 59 0.111
278
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.111
279
BRN004 Brain Edema 57 0.111
280
P LNG064 Lung Cancer Susceptibility 3 79 0.111
281
P PRP019 Peripheral Nervous System Disease 64 0.110
282
c CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 59 0.109
283
GST045 Gastroenteritis 60 0.109
284
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 65 0.109
285
P GLM007 Glomerulonephritis 58 0.109
286
PST092 Posttransplant Acute Limbic Encephalitis 29 0.109
287
FDL002 Food Allergy 52 0.109
288
DWN001 Down Syndrome 70 0.109
289
P LPR021 Leprosy 3 67 0.108
290
HNS001 Hansen's Disease 35 0.108
291
ART140 Arteries, Anomalies of 60 0.108
292
GST050 Gastrointestinal System Disease 57 0.108
293
VCC001 Vaccinia 50 0.108
294
PST046 Post-Transplant Lymphoproliferative Disease 55 0.108
295
ALV002 Alveolar Echinococcosis 50 0.108
296
HPT067 Hepatocellular Adenoma 45 0.107
297
VSL002 Visual Epilepsy 58 0.107
298
ARG004 Argyria 28 0.107
299
ANX004 Anoxia 44 0.107
300
HYP063 Hypersplenism 51 0.106
301
MYL069 Myeloma, Multiple 85 0.106
302
ACQ007 Acquired Immunodeficiency Syndrome 61 0.106
303
P ECL001 Eclampsia 53 0.106
304
CNT047 Contact Dermatitis 58 0.106
305
P TRN020 Turner Syndrome 66 0.106
306
P LPS004 Lupus Erythematosus 62 0.106
307
P PLY011 Polycystic Ovary Syndrome 58 0.105
308
PLL012 Pollen Allergy 46 0.105
309
P LYM033 Lymphoproliferative Syndrome 62 0.105
310
P PHC003 Pheochromocytoma 71 0.104
311
CHL079 Children's Interstitial Lung Disease 27 0.104
312
PRP030 Purpura 56 0.104
313
c ATR087 Atrial Standstill 1 76 0.104
314
P ALP008 Alopecia 58 0.104
315
CHL039 Choledocholithiasis 37 0.103
316
ADR040 Adrenal Gland Pheochromocytoma 51 0.103
317
P LMY004 Leiomyosarcoma 63 0.103
318
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 62 0.103
319
ALL006 Allergic Asthma 56 0.103
320
CRV035 Cervical Cancer 77 0.103
321
c ACT068 Acute Cystitis 63 0.103
322
GNG013 Gingivitis 60 0.102
323
P RTN024 Retinoblastoma 74 0.102
324
MCL006 Macular Retinal Edema 52 0.102
325
P INF038 Influenza 69 0.101
326
P APL001 Aplastic Anemia 76 0.101
327
GST040 Gastric Adenocarcinoma 67 0.101
328
MTB004 Metabolic Acidosis 48 0.101
329
c FML008 Familial Retinoblastoma 46 0.101
331
P SLP006 Sleep Apnea 71 0.100
332
HYP080 Hypogonadism 51 0.100
333
GLL048 Glial Tumor 48 0.100
334
MNT002 Mental Depression 60 0.100
335
P NSP012 Nasopharyngeal Carcinoma 67 0.099
336
P VSC011 Vasculitis 64 0.099
337
P BLR006 Biliary Tract Disease 49 0.099
338
AMB001 Amebiasis 44 0.099
339
P GLM045 Glioma 64 0.099
340
TYP007 Typhoid Fever 61 0.099
341
ADL002 Adult Syndrome 62 0.099
342
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 61 0.099
343
THY029 Thyroid Carcinoma 62 0.099
344
HYP005 Hypokalemia 55 0.099
345
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 46 0.098
346
P MYL006 Myeloid Leukemia 61 0.098
347
HYP064 Hypogonadotropism 40 0.098
348
ATX019 Ataxia with Vitamin E Deficiency 46 0.098
349
P MYC007 Myocardial Infarction 74 0.098
350
P PLM036 Pulmonary Fibrosis 66 0.097
351
IDP011 Idiopathic Interstitial Pneumonia 65 0.097
352
c SML038 Small Cell Cancer of the Lung 67 0.097
353
P SDR002 Siderosis 42 0.096
354
KLB003 Klebsiella Pneumonia 36 0.096
355
FCT001 Factor Viii Deficiency 54 0.096
356
P DNG005 Dengue Virus 57 0.096
357
P LCT001 Lactic Acidosis 52 0.096
358
P URT039 Urticaria 61 0.096
359
AMN003 Amnestic Disorder 55 0.096
360
SNL007 Senile Cataract 41 0.096
361
INS001 Insulinoma 60 0.096
362
c DWL002 Dowling-Degos Disease 1 59 0.096
363
HLC007 Helicobacter Pylori Infection 61 0.096
364
CNN005 Connective Tissue Disease 68 0.095
365
P RRT020 Rare Tumor 43 0.095
366
URM002 Uremia 50 0.095
367
c ATS347 Autosomal Dominant Polycystic Kidney Disease 61 0.095
368
MCS002 Mucositis 56 0.094
369
OST017 Osteomyelitis 65 0.094
370
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 56 0.094
371
TTN003 Tetanus 62 0.094
372
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 0.094
373
c HMP029 Hemophilia a 69 0.094
374
VSC003 Visceral Leishmaniasis 55 0.093
375
MST021 Meester-Loeys Syndrome 32 0.093
376
ILS001 Ileus 51 0.093
377
CRB004 Cerebral Artery Occlusion 38 0.093
378
P SCK005 Sickle Cell Disease 53 0.093
379
c HPT015 Hepatitis D 49 0.093
380
c LKM061 Leukemia, Acute Myeloid 84 0.093
381
P TYR004 Tyrosinemia 54 0.093
382
INF034 Infective Endocarditis 53 0.092
383
c ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 36 0.092
384
FSC002 Fascioliasis 44 0.092
385
P MYP004 Myopathy 63 0.091
386
CHC001 Chickenpox 53 0.091
387
c PNS012 Paine Syndrome 61 0.091
388
NTR046 Neutrophil Migration 49 0.091
390
PLY150 Polykaryocytosis Inducer 31 0.091
391
c EPS039 Episodic Pain Syndrome, Familial, 1 40 0.091
392
P BLD062 Bile Duct Cancer 66 0.090
393
STR067 Stroke, Ischemic 82 0.090
394
P LKM062 Leukemia, Acute Lymphoblastic 68 0.090
395
PLM010 Pulmonary Edema 56 0.090
396
P PRM002 Primary Hyperoxaluria 60 0.090
397
ATS010 Autosomal Recessive Disease 49 0.089
398
P TXP001 Toxoplasmosis 61 0.089
399
c INH020 Inherited Metabolic Disorder 51 0.089
400
P CHR345 Chronic Pain 52 0.089
401
AST005 Asthma 80 0.089
402
c DNG003 Dengue Disease 61 0.089
403
P PNM007 Pneumonia 71 0.089
404
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 61 0.089
405
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.089
406
SPP010 Suppressor of Tumorigenicity 3 54 0.089
407
P ENC004 Encephalitis 64 0.089
408
c MGR028 Migraine with or Without Aura 1 70 0.089
409
KRT002 Keratomalacia 47 0.088
410
HPT082 Hepatic Adenomas, Familial 40 0.088
411
P CNJ013 Conjunctivitis 67 0.088
412
KRT019 Keratitis, Hereditary 69 0.088
413
CND006 Candida Glabrata 33 0.088
414
P CLC063 Celiac Disease 1 66 0.087
415
P END044 Endometriosis 63 0.087
416
CMB003 Combined T Cell and B Cell Immunodeficiency 53 0.087
417
c GRV008 Graves Disease 1 55 0.087
418
CYS008 Cystic Echinococcosis 47 0.087
419
P TRT010 Teratoma 52 0.087
420
YLL002 Yellow Fever 58 0.087
421
HMC014 Homocysteinemia 54 0.087
422
MSL001 Measles 61 0.087
423
P MSC003 Muscular Atrophy 52 0.086
424
SKN019 Skin Melanoma 68 0.086
425
ENT011 Enterocolitis 51 0.086
426
SXL003 Sexual Disorder 49 0.086
427
IRR002 Irritable Bowel Syndrome 65 0.086
428
SPN186 Spinal Cord Injury 63 0.086
429
INT075 Intracranial Hypertension 54 0.086
430
PPL022 Papilloma 56 0.085
431
c ACT073 Acute Leukemia 59 0.085
432
VRL011 Viral Infectious Disease 62 0.085
433
LYM133 Lymphoma, Hodgkin, Classic 70 0.085
434
APP008 Appendicitis 61 0.085
435
CMM005 Common Cold 57 0.085
436
SBC016 Subacute Delirium 43 0.085
437
P ATR011 Atrial Fibrillation 67 0.085
438
c AMY091 Amyotrophic Lateral Sclerosis 1 88 0.085
439
CYS014 Cystadenocarcinoma 51 0.085
440
PNC129 Pancreatic Adenocarcinoma 69 0.085
441
PLR007 Pleural Empyema 44 0.085
442
GLL018 Gallbladder Cancer 57 0.085
443
PNC001 Pancytopenia 54 0.085
444
HMT018 Hematopoietic Stem Cell Transplantation 54 0.085
445
FLR002 Filariasis 56 0.084
446
END057 Endometrial Cancer 74 0.084
447
P MLN069 Melanoma, Uveal 59 0.084
449
CRD001 Cardiac Tamponade 45 0.084
450
CYS009 Cystadenoma 43 0.084
451
RCK004 Rickets 70 0.084
452
PRS047 Prostatitis 57 0.084
453
P KDN017 Kidney Cancer 60 0.084
454
DPH001 Diphtheria 61 0.084
455
PLM186 Pulmonary Arterial Hypertension Associated with Portal Hypertension 26 0.084
456
PLR008 Pleurisy 50 0.084
457
BRN071 Brain Injury 51 0.083
458
LYM019 Lymphosarcoma 48 0.083
459
ANR040 Aneurysm 60 0.083
460
LMY002 Leiomyoma 52 0.083
461
P INT068 Intestinal Disease 56 0.083
462
OPS001 Opisthorchiasis 39 0.082
463
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 55 0.082
464
EXT006 Extrahepatic Cholestasis 38 0.082
465
PLY100 Polyploidy 41 0.082
466
BRC012 Brucellosis 62 0.082
467
ENC038 Encephalopathy, Progressive, with or Without Lipodystrophy 38 0.081
468
P NPH012 Nephrotic Syndrome 65 0.081
469
c TRC022 Tricuspid Valve Insufficiency 41 0.081
470
P CRN026 Corneal Edema 44 0.081
471
P MSC005 Muscular Dystrophy 68 0.081
472
P GCH001 Gaucher's Disease 63 0.081
473
NPH091 Nephrolithiasis, Calcium Oxalate 66 0.081
474
P RHB003 Rhabdomyosarcoma 62 0.081
475
P ALG028 Alagille Syndrome 1 70 0.081
476
P MLN007 Male Infertility 57 0.081
477
MCR013 Microphthalmia 62 0.081
478
P SHR001 Short Bowel Syndrome 50 0.080
479
LYM143 Lymphoma, Non-Hodgkin, Familial 74 0.080
480
c FML035 Familial Hyperlipidemia 56 0.080
481
LVR002 Liver Angiosarcoma 52 0.080
482
BNN003 Bone Inflammation Disease 51 0.080
483
P LTR001 Lateral Sclerosis 56 0.080
484
CHG001 Chagas Disease 66 0.079
485
SQM002 Squamous Cell Papilloma 49 0.079
486
P ATX030 Ataxia-Telangiectasia 83 0.079
487
MST005 Mastitis 55 0.079
488
CRC021 Carcinosarcoma 62 0.079
489
c LKM060 Leukemia, Acute Lymphoblastic 3 57 0.079
490
P SLP005 Sleep Disorder 58 0.079
491
NWC001 Newcastle Disease 45 0.079
492
P HDC001 Headache 59 0.079
493
P MYC008 Myocarditis 60 0.079
494
DRG002 Drug-Induced Hepatitis 41 0.078
495
ANG018 Angiomyolipoma 46 0.078
496
HRP004 Herpes Zoster 58 0.078
497
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 62 0.078
498
P MLT020 Multiple Sclerosis 73 0.078
499
P MYC084 Mycobacterium Tuberculosis 1 69 0.078
500
c PRM038 Primary Agammaglobulinemia 45 0.078
501
ANG054 Angina Pectoris 66 0.078
502
P DMN002 Dementia 68 0.077
503
INT052 Intestinal Volvulus 44 0.077
504
HYP081 Hypolipoproteinemia 51 0.077
505
CCC002 Coccidiosis 46 0.077
506
c INV001 Invasive Aspergillosis 48 0.076
507
SCK003 Sickle Cell Anemia 74 0.076
508
P ADL010 Adult Respiratory Distress Syndrome 61 0.076
509
P BLD124 Bleeding Disorder, Platelet-Type, 11 66 0.076
510
HMP001 Hemopericardium 44 0.076
511
EYD002 Eye Disease 59 0.076
512
c PRG047 Progressive Familial Intrahepatic Cholestasis 59 0.076
513
c ACT075 Acute Myocardial Infarction 59 0.076
514
HMN004 Hemangioma of Liver 35 0.076
515
P HMR005 Hemorrhoid 47 0.075
516
P VNS003 Venous Insufficiency 55 0.075
517
P MNN013 Meningitis 67 0.075
518
ORL015 Oral Squamous Cell Carcinoma 44 0.075
519
DFF005 Diffuse Large B-Cell Lymphoma 56 0.075
520
CHL045 Choline Deficiency Disease 39 0.075
521
ALL010 Allergic Contact Dermatitis 56 0.074
522
P HST010 Histiocytosis 54 0.074
523
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.074
524
CYN002 Cyanosis, Transient Neonatal 45 0.074
525
P FML355 Familial Intrahepatic Cholestasis 49 0.073
526
P SBS003 Substance Abuse 56 0.073
527
ACT003 Acute Kidney Tubular Necrosis 42 0.073
528
ACT055 Actinomycosis 43 0.073
529
WTH001 Withdrawal Disorder 47 0.073
530
PRT038 Protein-Energy Malnutrition 56 0.073
531
CTN007 Cutaneous Leishmaniasis 61 0.072
532
MDD011 Mood Disorder 62 0.072
533
ALL014 Allergic Encephalomyelitis 40 0.072
534
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 61 0.072
535
P SYS005 Systemic Scleroderma 68 0.072
536
P PRC012 Pericardial Effusion 51 0.072
537
DYS073 Dysphagia 52 0.072
538
P HYP069 Hyperparathyroidism 64 0.072
539
KRT009 Keratosis 52 0.072
540
c PRT132 Protoporphyria, Erythropoietic, 1 59 0.072
541
P CNG048 Congenital Hepatic Fibrosis 39 0.072
542
KPS004 Kaposi Sarcoma 75 0.072
543
c FML021 Familial Hypercholesterolemia 67 0.072
544
MSC007 Muscle Hypertrophy 65 0.071
545
CHL123 Chlamydia 60 0.071
546
GTR002 Goiter 54 0.071
547
IMM064 Immunodeficiency, Common Variable, 10 51 0.071
548
CLL003 Cellulitis 56 0.071
549
BNT001 Banti's Syndrome 22 0.071
550
IGR001 Ige Responsiveness, Atopic 61 0.070
551
P ESP024 Esophagitis 62 0.070
552
RYS001 Reye Syndrome 49 0.070
553
NRN001 Neuroendocrine Carcinoma 48 0.070
554
P CYS018 Cystitis 59 0.070
555
BRK010 Burkitt Lymphoma 68 0.070
556
BCK006 Back Pain 44 0.070
557
c CHR431 Chronic Venous Insufficiency 48 0.070
558
XRD010 Xeroderma Pigmentosum, Variant Type 72 0.070
559
AMN001 Amenorrhea 54 0.070
560
c HMP004 Hemophilia B 66 0.070
561
INT017 Intestinal Schistosomiasis 49 0.070
562
P THY032 Thyroiditis 52 0.070
563
P DBT085 Diabetes Mellitus, Insulin-Dependent 68 0.069
564
P SLM003 Salmonellosis 54 0.069
565
P AST007 Astrocytoma 52 0.069
566
P THY023 Thymoma 64 0.069
567
c THY107 Thymoma, Familial 55 0.069
568
P DBT005 Diabetes Insipidus 54 0.069
569
P HRD008 Hereditary Hemorrhagic Telangiectasia 64 0.069
570
P ATT013 Attention Deficit-Hyperactivity Disorder 66 0.069
571
HMP009 Haemophilus Influenzae 46 0.069
572
P ART023 Arthropathy 61 0.069
573
c SVR005 Severe Pre-Eclampsia 50 0.069
574
c SCL052 Scleroderma, Familial Progressive 62 0.069
575
c LKM071 Leukemia, Chronic Lymphocytic 81 0.069
576
ANR007 Anorexia Nervosa 64 0.068
577
MCR141 Mucormycosis 48 0.068
578
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 41 0.068
579
c BTT014 Beta-Thalassemia 73 0.068
580
P MJR001 Major Depressive Disorder 69 0.068
581
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.068
582
PRC051 Paracetamol Poisoning 31 0.068
583
FCT007 Factor Vii Deficiency 65 0.068
585
PFF001 Pfeiffer Syndrome 79 0.068
586
P GLL020 Gallbladder Disease 60 0.068
587
CHR074 Choriocarcinoma 47 0.067
588
PRP027 Peripheral Vascular Disease 72 0.067
589
c GCH015 Gaucher Disease, Type I 65 0.067
590
CRR012 Cirrhotic Cardiomyopathy 23 0.067
591
ZLL002 Zollinger-Ellison Syndrome 54 0.067
592
PRN019 Perinatal Necrotizing Enterocolitis 55 0.067
593
P CRG003 Crigler-Najjar Syndrome, Type I 61 0.067
594
GLB001 Gilbert Syndrome 58 0.067
595
PLS002 Peliosis Hepatis 37 0.067
596
P OPT006 Optic Nerve Disease 59 0.067
597
PRM127 Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type 38 0.066
598
P TCL004 T-Cell Leukemia 48 0.066
599
CRY004 Cryoglobulinemia 47 0.066
600
ASC001 Ascaridiasis 36 0.066
601
c MCR129 Microvascular Complications of Diabetes 1 67 0.066
602
CYS005 Cysticercosis 55 0.066
603
PLS011 Plasmacytoma 57 0.066
604
GSG001 Gas Gangrene 52 0.066
605
VSC002 Vascular Dementia 57 0.066
606
DBT010 Diabetic Neuropathy 56 0.066
607
ASC010 Ascaris Lumbricoides Infection 51 0.066
608
P NMN002 Niemann-Pick Disease 60 0.066
609
GST033 Gestational Diabetes 58 0.066
610
P INT070 Intestinal Obstruction 60 0.066
611
RTR008 Root Resorption 44 0.066
612
PTT037 Pituitary Tumors 47 0.066
613
P INS002 in Situ Carcinoma 55 0.066
614
OST011 Osteomalacia 51 0.066
615
P ART005 Arteriovenous Malformation 63 0.065
616
c PRD040 Periodontitis, Chronic 56 0.065
617
c ANT034 Anterior Uveitis 48 0.065
618
P PYL005 Pyelonephritis 58 0.065
619
P RNL015 Renal Hypertension 47 0.065
620
LPT001 Leptospirosis 60 0.065
621
HDN002 Head Injury 47 0.065
622
TRM010 Traumatic Brain Injury 54 0.065
623
c DLT002 Dilated Cardiomyopathy 81 0.065
624
P BNG032 Benign Mesothelioma 47 0.065
625
c LKM005 Leukemia, T-Cell, Chronic 35 0.065
626
MYL009 Myelodysplastic Syndrome 72 0.065
627
c LPM012 Lipomatosis, Multiple 60 0.065
628
P CRD132 Cardiac Conduction Defect 61 0.065
629
ACT119 Acute Promyelocytic Leukemia 63 0.065
630
FSC004 Fasciitis 47 0.065
631
HMN014 Human Immunodeficiency Virus Infectious Disease 56 0.064
632
c LKM063 Leukemia, Chronic Myeloid 74 0.064
633
P PRK057 Parkinson Disease, Late-Onset 77 0.064
634
ACT058 Active Peptic Ulcer Disease 55 0.064
635
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.064
636
IRN001 Iron Deficiency Anemia 59 0.064
637
c LKM004 Leukemia, B-Cell, Chronic 35 0.064
638
URT049 Urate Oxidase, Pseudogene 26 0.064
639
STS002 Situs Inversus 46 0.063
640
MTH009 Mouth Disease 56 0.063
641
PRC013 Pericarditis 54 0.063
642
CRC006 Carcinoid Syndrome 55 0.063
643
c PRS136 Prostate Cancer, Hereditary, 6 34 0.063
644
c PRS130 Prostate Cancer, Hereditary, 8 33 0.063
645
CRD223 Cardiac Arrhythmia 61 0.063
646
P SJG008 Sjogren Syndrome 57 0.063
647
c PLM164 Pulmonary Hypertension, Primary, 1 79 0.063
648
OVR063 Overnutrition 47 0.063
649
P ANG015 Angioedema 54 0.063
650
P ATS364 Autism 68 0.063
651
CRD137 Cardiogenic Shock 50 0.063
652
CLR108 Colorectal Adenoma 64 0.063
653
RNL077 Renal Fibrosis 49 0.063
654
ART016 Aortic Aneurysm 71 0.063
655
PLG002 Plague 54 0.062
656
LYM027 Lymphopenia 58 0.062
657
PRS063 Paresthesia 46 0.062
658
NNT012 Neonatal Jaundice 48 0.062
659
P INT099 Intrahepatic Cholestasis of Pregnancy 50 0.062
660
ORL005 Oral Candidiasis 56 0.062
661
P FML011 Familial Adenomatous Polyposis 73 0.062
662
P RBL001 Rubella 56 0.062
663
P HNT016 Huntington Disease 72 0.062
664
P EPL164 Epilepsy 73 0.061
665
TST014 Testicular Cancer 49 0.061
666
c WLM018 Wilms Tumor 5 63 0.061
667
P PLY018 Polycythemia 56 0.061
668
PNC034 Pancreas Disease 51 0.061
669
ENH001 Enhanced S-Cone Syndrome 56 0.061
670
GRN017 Granulocytopenia 46 0.061
671
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 54 0.061
672
THR016 Thrombophlebitis 50 0.061
673
LNG108 Langerhans Cell Histiocytosis 60 0.061
674
DNG002 Dengue Hemorrhagic Fever 59 0.061
675
PLM031 Poliomyelitis 58 0.061
676
STT001 Status Epilepticus 61 0.060
677
c SVR001 Severe Acute Respiratory Syndrome 56 0.060
678
CTR172 Citrullinemia, Classic 62 0.060
679
P ANR048 Aniridia 1 64 0.060
680
HRT011 Heart Septal Defect 52 0.060
681
GST092 Gastroesophageal Reflux 68 0.060
682
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 63 0.060
683
P SML001 Small Cell Carcinoma 55 0.060
684
c ACT135 Acute Graft Versus Host Disease 52 0.059
685
P PLM034 Pulmonary Emphysema 55 0.059
686
LST001 Listeriosis 55 0.059
687
THR004 Thrombocytosis 52 0.059
688
CRY005 Cryptococcosis 51 0.059
689
c FNC043 Fanconi Anemia, Complementation Group E 64 0.059
690
NRR001 Neuroretinitis 46 0.059
691
PHR003 Pharyngitis 56 0.059
692
HYP781 Hypoascorbemia 48 0.059
693
RTN020 Retinal Vascular Disease 49 0.059
694
P LCH002 Lichen Planus 55 0.059
695
ATN005 Autonomic Dysfunction 48 0.059
696
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 36 0.059
697
AVN001 Avian Influenza 56 0.059
698
c MCR112 Microvascular Complications of Diabetes 2 42 0.059
699
P VNW001 Von Willebrand's Disease 64 0.059
700
P BLD036 Bile Duct Disease 46 0.059
701
IGG001 Iga Glomerulonephritis 50 0.059
702
c SPN225 Spondyloarthropathy 1 74 0.058
703
P HYP061 Hypertrophic Cardiomyopathy 68 0.058
704
RTN023 Retinitis 46 0.058
705
TXC011 Toxocariasis 43 0.058
706
SFT003 Soft Tissue Sarcoma 57 0.058
707
QFV001 Q Fever 58 0.058
708
NCR007 Necrotizing Fasciitis 47 0.058
709
VTM033 Vitamin K Deficiency Bleeding 47 0.058
710
c PNC106 Pancreatic Agenesis 1 50 0.058
711
THR100 Thrombocytopenic Purpura, Autoimmune 61 0.058
712
c CHR682 Chronic Bilirubin Encephalopathy 36 0.058
713
RSP021 Respiratory Allergy 45 0.057
714
P SCH015 Schizophrenia 76 0.057
715
c ACT036 Acute Cholangitis 37 0.057
716
CHK001 Chikungunya 55 0.057
717
UND005 Undifferentiated Pleomorphic Sarcoma 66 0.057
718
DVR002 Diverticulitis 44 0.057
719
CNT025 Central Pontine Myelinolysis 45 0.057
720
OCL022 Ocular Melanoma 54 0.057
721
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 33 0.057
722
CRT015 Carotid Artery Occlusion 44 0.057
723
c HNT011 Huntington Disease-Like 3 37 0.057
724
PLC008 Placenta Disease 51 0.056
725
c TYR012 Tyrosinemia, Type I 61 0.056
726
P BPL003 Bipolar Disorder 59 0.056
727
PLM005 Pleomorphic Lipoma 41 0.056
728
c DPH024 Diaphragmatic Hernia, Congenital 66 0.056
729
CRY035 Cryptorchidism, Unilateral or Bilateral 61 0.056
730
P PTS002 Ptosis 53 0.056
731
CRY003 Cryptosporidiosis 50 0.056
732
P GRV001 Graves' Disease 57 0.056
733
ATN004 Autonomic Neuropathy 43 0.056
734
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.056
735
ERY051 Erythroleukemia, Familial 58 0.056
736
STT004 Steatorrhea 39 0.056
737
c ALM001 Al Amyloidosis 50 0.055
738
P MCP040 Mucopolysaccharidosis-Plus Syndrome 62 0.055
739
P HYP024 Hypoparathyroidism 56 0.055
740
TRY001 Trypanosomiasis 50 0.055
741
PRM020 Premenstrual Tension 48 0.055
742
PRD004 Prediabetes Syndrome 49 0.055
743
SCB001 Scabies 50 0.055
744
TRN018 Transitional Cell Carcinoma 57 0.055
745
MDS022 Mediastinitis 42 0.055
746
LYM021 Lymphadenitis 58 0.055
747
PRP083 Porphyria, Acute Intermittent 62 0.055
748
HST009 Histiocytoma 47 0.055
749
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 49 0.055
750
P MRC003 Mercury Poisoning 47 0.055
751
c PLY170 Polycystic Kidney Disease 4 with or Without Polycystic Liver Disease 62 0.054
752
THR123 Thrombotic Microangiopathy 41 0.054
753
MCR017 Macrocytic Anemia 41 0.054
754
PHN003 Phenylketonuria 73 0.054
755
P HYP730 Hypogonadotropic Hypogonadism 54 0.054
756
GST030 Gastrinoma 43 0.054
757
ACT162 Acute Sensory Ataxic Neuropathy 27 0.054
758
P BLD051 Blood Coagulation Disease 48 0.054
759
c CNG216 Congenital Hydrocephalus 55 0.054
760
RYN005 Raynaud Phenomenon 50 0.054
761
P RTN018 Retinal Disease 53 0.054
762
THY111 Thyroid Carcinoma, Familial Medullary 68 0.054
763
SYN036 Syncope 46 0.054
764
RDN001 Reading Disorder 42 0.054
765
P THR015 Thrombophilia 51 0.054
766
MXD005 Mixed Connective Tissue Disease 55 0.054
767
P LPS002 Liposarcoma 62 0.054
768
P HMR003 Hemorrhagic Disease 54 0.054
769
c CHR417 Chronic Graft Versus Host Disease 56 0.054
770
JPN002 Japanese Encephalitis 56 0.054
771
DSS008 Disease of Mental Health 66 0.054
772
OBS525 Obsolete: Squamous Cell Carcinoma of Head and Neck 58 0.054
773
THY125 Thyroid Gland Medullary Carcinoma 52 0.053
774
P HYD006 Hydrocephalus 68 0.053
775
PSY004 Psychotic Disorder 68 0.053
776
LMB062 Limb Ischemia 50 0.053
777
BCT021 Bacterial Sepsis 44 0.053
778
FBR003 Fibrous Histiocytoma 43 0.053
779
LYS012 Lysosomal Acid Lipase Deficiency 63 0.053
780
P CRY007 Cryoglobulinemia, Familial Mixed 50 0.053
781
c HNT004 Huntington Disease-Like 2 48 0.053
782
NRF026 Neurofibromatosis, Type Iv, of Riccardi 65 0.053
783
DRM011 Dermatophytosis 49 0.053
784
c MJR024 Major Affective Disorder 9 42 0.053
785
c MJR022 Major Affective Disorder 8 39 0.053
786
PLS007 Plasmodium Falciparum Malaria 53 0.053
787
MCR011 Microinvasive Gastric Cancer 43 0.053
788
TRN015 Transient Cerebral Ischemia 62 0.053
789
P MYS003 Myasthenia Gravis 68 0.052
790
P HYP083 Hypopituitarism 53 0.052
791
ATR057 Atrioventricular Block 56 0.052
792
P MNC007 Monocytic Leukemia 52 0.052
793
P TBR001 Tuberous Sclerosis 72 0.052
794
P HML001 Hemolytic-Uremic Syndrome 54 0.052
795
MSN004 Mesenchymal Cell Neoplasm 45 0.052
796
P BRB001 Beriberi 41 0.052
797
LYS002 Lysosomal Storage Disease 52 0.052
798
SMN007 Seminoma 43 0.052
799
P HMP002 Hemophagocytic Lymphohistiocytosis 68 0.052
800
KLT001 Klatskin's Tumor 50 0.052
801
BLR028 Biliary Atresia, Extrahepatic 35 0.052
802
GST020 Gastric Antral Vascular Ectasia 42 0.052
803
HYP017 Hypophosphatemia 48 0.052
804
P TCD001 Tic Disorder 55 0.052
805
P TRC086 Trichohepatoenteric Syndrome 1 57 0.052
806
P MTH008 Methylmalonic Acidemia 50 0.052
807
BLR013 Biliary Tract Cancer 44 0.052
808
GRD001 Giardiasis 42 0.052
809
PRP001 Propionic Acidemia 63 0.052
810
MLG065 Malignant Fibroxanthoma 45 0.052
811
GYN001 Gynecomastia 49 0.052
812
INF021 Infant Gynecomastia 32 0.052
813
ING001 Inguinal Hernia 61 0.052
814
PNT038 Peanut Allergy 45 0.052
815
LNG031 Lung Benign Neoplasm 52 0.052
816
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 29 0.051
817
TNS005 Tonsillitis 58 0.051
818
FRC011 Fructose Intolerance, Hereditary 52 0.051
819
BLD063 Bile Duct Cysts 42 0.051
820
CRN030 Coronary Stenosis 49 0.051
821
P HYP058 Hypervitaminosis a 45 0.051
822
ANR004 Anuria 47 0.051
823
DBN001 Dubin-Johnson Syndrome 58 0.051
824
P AGM001 Agammaglobulinemia 66 0.051
825
HRT012 Heart Valve Disease 56 0.051
826
ADR016 Adrenal Cortical Carcinoma 51 0.051
827
c MLG074 Malignant Mesenchymoma 50 0.051
828
ACN002 Acanthosis Nigricans 62 0.051
829
NRT001 Neurotic Disorder 53 0.051
830
c WLM013 Wilms Tumor 1 69 0.051
831
ADR054 Adrenocortical Carcinoma, Hereditary 68 0.051
832
CCC001 Coccidioidomycosis 54 0.051
833
P SPR119 Spermatogenic Failure, X-Linked, 1 38 0.051
834
EXP004 Exophthalmos 53 0.051
835
P DRM010 Dermatomyositis 62 0.051
836
P MYS005 Myositis 54 0.051
837
P CNR004 Cone-Rod Dystrophy 2 72 0.050
838
c JVN010 Juvenile Rheumatoid Arthritis 67 0.050
839
HYP020 Hyperprolactinemia 62 0.050
840
PPL001 Papillary Adenoma 42 0.050
841
CLN045 Colonic Benign Neoplasm 52 0.050
842
ORN008 Ornithine Transcarbamylase Deficiency, Hyperammonemia Due to 60 0.050
843
c ATM006 Autoimmune Lymphoproliferative Syndrome 73 0.050
844
P MMP001 Mumps 57 0.050
845
c BRN108 Branchiootic Syndrome 1 62 0.050
846
PRM329 Premature Aging 41 0.050
847
c HYP555 Hypertriglyceridemia, Transient Infantile 38 0.050
848
ACR007 Acromegaly 70 0.050
849
VTM002 Vitamin B12 Deficiency 48 0.050
850
CHR178 Chromosomal Triplication 36 0.050
851
CHR100 Chronic Ulcer of Skin 53 0.050
852
c ATS007 Autism Spectrum Disorder 69 0.050
853
DMP001 Dumping Syndrome 44 0.050
854
INT002 Intermittent Claudication 60 0.050
855
SYN007 Synovitis 55 0.050
856
EMB004 Embryonal Carcinoma 57 0.050
857
c HYP272 Hypercholesterolemia, Familial, 3 44 0.050
858
BRR014 Barrett Esophagus 67 0.050
859
P CHN012 Chondrosarcoma 57 0.050
860
c MNN043 Meningioma, Familial 74 0.049
861
MNN042 Meningioma, Radiation-Induced 64 0.049
862
SPN021 Spinal Meningioma 40 0.049
863
END040 Endogenous Depression 55 0.049
864
P GND004 Gonadal Dysgenesis 47 0.049
865
PSR001 Psoriatic Arthritis 63 0.049
866
CLF027 Cleft Palate, Isolated 67 0.049
867
P OVR046 Ovarian Cyst 50 0.049
868
PRM024 Primary Angle-Closure Glaucoma 39 0.049
869
INT071 Intestinal Perforation 45 0.049
870
c ART138 Aortic Aneurysm, Familial Abdominal, 1 62 0.049
871
PTN001 Patent Foramen Ovale 57 0.049
872
P ACT008 Actinic Keratosis 50 0.049
873
SCR011 Scrapie 37 0.049
874
BRN028 Brain Cancer 75 0.049
875
SPS057 Spasticity 38 0.049
876
P BRN022 Bronchiectasis 60 0.048
877
SCR001 Secretory Meningioma 38 0.048
878
ADR007 Adrenoleukodystrophy 72 0.048
879
RRS014 Rare Surgical Neurologic Disease 33 0.048
880
EXT007 Extracutaneous Mastocytoma 39 0.048
881
STN013 Stenotrophomonas Maltophilia Infection 26 0.048
882
c BSL007 Basal Cell Carcinoma 68 0.048
883
c ANM038 Anemia, Autoimmune Hemolytic 61 0.048
884
PNC119 Pancreatic Neuroendocrine Tumor 48 0.048
885
PRT019 Protein-Losing Enteropathy 41 0.048
886
P RTN016 Retinal Degeneration 56 0.048
887
ART004 Aortic Atherosclerosis 47 0.048
888
LYM002 Lymphoplasmacyte-Rich Meningioma 40 0.048
889
P ZLL001 Zellweger Syndrome 56 0.048
890
ETN001 Eating Disorder 61 0.048
891
EXC002 Exocrine Pancreatic Insufficiency 41 0.048
892
c LVR030 Liver Failure, Infantile, Transient 33 0.048
893
ERY003 Erythema Multiforme 57 0.048
894
PRX001 Peroxisomal Disease 45 0.048
895
DST016 Distomatosis 27 0.048
896
CHR066 Chronic Fatigue Syndrome 61 0.048
897
SPP011 Suppression of Tumorigenicity 12 61 0.048
898
WST005 West Nile Virus 56 0.048
899
P LRY044 Larynx Cancer 59 0.047
900
P ATR010 Atrial Heart Septal Defect 61 0.047
901
ISL099 Isolated Methylmalonic Acidemia 30 0.047
902
BNG077 Benign Idiopathic Neonatal Seizures 27 0.047
903
PRC001 Pericoronitis 40 0.047
904
UMB002 Umbilical Hernia 45 0.047
905
P PLY041 Polymyositis 57 0.047
906
OTT002 Otitis Media 71 0.047
907
P PTN014 Patent Ductus Arteriosus 1 60 0.047
908
NRT004 Neuritis 52 0.047
909
P ALP061 Alopecia, Androgenetic, 1 51 0.047
910
c NMN015 Niemann-Pick Disease, Type C1 67 0.047
911
SLC006 Silicosis 55 0.047
912
c SCN007 Secondary Hyperparathyroidism 52 0.047
913
P CLL015 Collagen Disease 46 0.047
914
P MPL001 Maple Syrup Urine Disease 68 0.047
915
PRS034 Parasitic Helminthiasis Infectious Disease 48 0.047
916
ART002 Arts Syndrome 63 0.047
917
c PRG020 Paragangliomas 3 36 0.047
918
DBT007 Diabetic Cataract 42 0.047
919
CRH005 Crohn's Colitis 56 0.047
920
SQM013 Squamous Cell Carcinoma, Head and Neck 81 0.047
921
MSC157 Muscular Dystrophy, Duchenne Type 70 0.047
922
KWS002 Kawasaki Disease 65 0.047
923
BRN002 Bronchiolitis 60 0.047
924
ADR004 Adrenal Cortical Adenocarcinoma 44 0.047
925
MYL005 Myelofibrosis 69 0.047
926
MCP006 Mucoepidermoid Carcinoma 53 0.047
927
SPN051 Spondylitis 53 0.046
928
EPD015 Epidemic Typhus 47 0.046
929
PTH003 Pathologic Nystagmus 53 0.046
930
FLR001 Filarial Elephantiasis 51 0.046
931
GLC036 Glucagonoma 45 0.046
932
LNG073 Long-Chain 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 61 0.046
933
VRC001 Varicocele 51 0.046
934
KLD004 Keloid Disorder 41 0.046
935
INT007 Intermediate Coronary Syndrome 58 0.046
936
P ICH004 Ichthyosis 55 0.046
937
P ATR005 Atrophic Gastritis 49 0.046
938
TBC004 Tobacco Addiction 65 0.046
939
MST004 Mast Cell Neoplasm 40 0.046
940
KHL003 Kohlschutter-Tonz Syndrome 63 0.046
941
STM006 Stomach Disease 50 0.046
942
CNN003 Conn's Syndrome 78 0.046
943
MMB001 Membranoproliferative Glomerulonephritis 54 0.046
944
c HYP511 Hypogonadotropic Hypogonadism 15 with or Without Anosmia 29 0.046
945
GNG003 Gingival Recession 43 0.046
946
OBS168 Obsolete: Atypical Teratoid/rhabdoid Tumor 25 0.046
947
BRN014 Bronchopneumonia 47 0.046
948
P HMN036 Hemangiopericytoma, Malignant 57 0.045
949
P TTR001 Tetralogy of Fallot 70 0.045
950
P MGL001 Megaloblastic Anemia 54 0.045
951
INT051 Intussusception 48 0.045
952
c PSR017 Psoriasis 2 55 0.045
953
c PSR023 Psoriasis 1 50 0.045
954
c PSR028 Psoriasis 7 40 0.045
955
c PSR018 Psoriasis 13 40 0.045
956
c PSR032 Psoriasis 11 40 0.045
957
49X002 49,xxxxy Syndrome 39 0.045
958
P PLY168 Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease 66 0.045
959
APN008 Apnea, Obstructive Sleep 64 0.045
960
MYM001 Myoma 52 0.045
961
URT010 Ureteral Obstruction 46 0.045
962
c PLY105 Polycystic Ovary Syndrome 1 38 0.045
963
P CRV031 Cervical Adenocarcinoma 49 0.045
964
ARG002 Argininosuccinic Aciduria 59 0.045
965
P ANL018 Analbuminemia 51 0.045
966
INF058 Inflammatory Myofibroblastic Tumor 44 0.045
967
ANT078 Antipyrine Metabolism 24 0.045
968
RBS001 Rabies 57 0.045
969
IRD001 Iridocyclitis 42 0.045
970
IRT001 Iritis 37 0.045
971
MCN017 Meconium Ileus 54 0.045
972
CHL013 Cholecystolithiasis 37 0.045
973
CMM004 Common Variable Immunodeficiency 69 0.045
974
NRL005 Neurilemmoma 62 0.045
975
HMZ003 Homozygous Familial Hypercholesterolemia 48 0.045
976
P HYP265 Hypotonia 43 0.045
977
HPT066 Hepatoportal Sclerosis 24 0.045
978
THY030 Thyroid Gland Disease 53 0.045
979
SHW001 Shwartzman Phenomenon 35 0.045
980
INF009 Inflammatory Spondylopathy 29 0.045
981
ADN011 Adenoid Cystic Carcinoma 71 0.044
982
MLD001 Melioidosis 66 0.044
983
GLS018 Glass Syndrome 51 0.044
984
MNN009 Meningoencephalitis 50 0.044
985
BRN056 Bronchopulmonary Dysplasia 57 0.044
986
PPT001 Peptic Esophagitis 47 0.044
987
GNR004 Generalized Anxiety Disorder 55 0.044
988
P GNG009 Gangliosidosis 45 0.044
989
PYR016 Pyridoxine Deficiency 31 0.044
990
HYP084 Hypopyon 39 0.044
991
HMG002 Hemoglobinuria 49 0.044
992
P AVS003 Avascular Necrosis 43 0.044
993
CYT018 Cytochrome P450 2d6 Variant 28 0.044
994
ORL004 Oral Submucous Fibrosis 55 0.044
995
c FNC027 Fanconi Anemia, Complementation Group a 81 0.044
996
LYM017 Lyme Disease 64 0.044
997
CRT013 Carotid Stenosis 50 0.044
998
OVR094 Ovarian Epithelial Cancer 39 0.044
999
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 64 0.044
1000
P HRD207 Hereditary Transthyretin Amyloidosis 26 0.044
1001
VNT037 Ventral Hernia 31 0.044
1002
OCL006 Ocular Hypertension 52 0.044
1003
P STR020 Strabismus 57 0.044
1004
MCH006 Mechanical Strabismus 31 0.044
1005
PRT058 Pure Autonomic Failure 60 0.044
1006
P RNV001 Renovascular Hypertension 49 0.043
1007
BCT004 Bacteriuria 48 0.043
1008
CTS005 Catastrophic Antiphospholipid Syndrome 44 0.043
1009
GRM010 Germ Cells Tumors 35 0.043
1010
c CHL132 Cholestasis, Progressive Familial Intrahepatic, 1 54 0.043
1011
c CHL136 Cholestasis, Progressive Familial Intrahepatic, 2 54 0.043
1012
P MVM001 Movement Disease 63 0.043
1013
SRC027 Sarcoma, Synovial 60 0.043
1014
EXT034 Extrinsic Allergic Alveolitis 58 0.043
1015
P FLL037 Follicular Lymphoma 67 0.043
1016
ADR022 Adrenomyeloneuropathy 39 0.043
1017
MYF001 Myofibroma 40 0.043
1018
P CHR012 Chronic Granulomatous Disease 69 0.043
1019
P CTR177 Citrullinemia, Type Ii, Adult-Onset 44 0.043
1020
c VSC053 Visceral Steatosis, Congenital 22 0.043
1021
P SNS001 Sensorineural Hearing Loss 62 0.043
1022
IRR003 Irritant Dermatitis 46 0.043
1023
LKP003 Leukoplakia 40 0.043
1024
ABT001 Abetalipoproteinemia 68 0.043
1025
MYS004 Myiasis 39 0.043
1026
CRV040 Cervix Carcinoma 52 0.043
1027
P RTN008 Retinitis Pigmentosa 77 0.042
1028
FBR047 Fibromyalgia 60 0.042
1029
MYX004 Myxedema 41 0.042
1030
P MTC069 Mitochondrial Disorders 57 0.042
1031
c MCL062 Mucolipidosis Ii Alpha/beta 67 0.042
1032
NWB001 Newborn Respiratory Distress Syndrome 58 0.042
1033
NPH003 Nephrocalcinosis 52 0.042
1034
ISL001 Islet Cell Tumor 47 0.042
1035
GLC008 Glucose Metabolism Disease 47 0.042
1036
CRT084 Creatinine Clearance Quantitative Trait Locus 26 0.042
1037
c ADL017 Adult T-Cell Leukemia 59 0.042
1038
ORL013 Oral Lichen Planus 47 0.042
1039
P DYS154 Dystonia 65 0.042
1040
FBR054 Fibroma 45 0.042
1041
P PRS038 Personality Disorder 66 0.042
1042
GRW007 Growth Hormone Deficiency 48 0.042
1043
GST071 Gastrointestinal Carcinoma 42 0.042
1044
ATP014 Atp8b1 Deficiency 25 0.042
1045
CRB037 Cerebral Palsy 69 0.042
1046
ANT024 Anthrax Disease 56 0.042
1047
P KRT007 Keratoconus 51 0.042
1048
LTX001 Latex Allergy 42 0.042
1049
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.042
1050
P END039 Endodermal Sinus Tumor 44 0.042
1051
LPR001 Lepromatous Leprosy 50 0.042
1052
NCR004 Nocardiosis 44 0.042
1053
BRS099 Breast Ductal Carcinoma 63 0.042
1054
CHP002 Chops Syndrome 41 0.042
1055
P RHB008 Rhabdoid Tumor Predisposition Syndrome 1 65 0.041
1056
c CHL134 Cholestasis, Benign Recurrent Intrahepatic, 1 56 0.041
1057
c CHL116 Cholestasis, Intrahepatic, of Pregnancy, 1 50 0.041
1058
DXT002 Dextrocardia with Situs Inversus 44 0.041
1059
SNG003 Single Ventricular Heart 31 0.041
1060
PST028 Post-Traumatic Stress Disorder 60 0.041
1061
ACT084 Acute Stress Disorder 42 0.041
1062
c ART101 Aortic Valve Disease 2 67 0.041
1063
c ALP101 Alpha-Thalassemia 63 0.041
1064
MCP033 Mucopolysaccharidoses 39 0.041
1065
SVR097 Severe Cutaneous Adverse Reaction 66 0.041
1066
HYD002 Hydronephrosis 58 0.041
1067
HYP043 Hyperandrogenism 48 0.041
1068
LYM009 Lymphocytic Choriomeningitis 45 0.041
1069
INT066 Interstitial Lung Disease 61 0.041
1070
P MMB011 Membranous Nephropathy 54 0.041
1071
INT067 Interstitial Nephritis 46 0.041
1072
c MST023 Mesothelioma, Malignant 59 0.041
1073
P MYT002 Myotonic Dystrophy 52 0.041
1074
RHB001 Rhabdoid Cancer 62 0.041
1075
SLP001 Sleeping Sickness 47 0.041
1076
RHM001 Rheumatic Fever 56 0.041
1077
ATM052 Autoimmune Disease 1 38 0.041
1078
c BCT013 Bacterial Pneumonia 49 0.041
1079
HPR003 Heparin-Induced Thrombocytopenia 49 0.041
1080
BLR004 Biliary Dyskinesia 33 0.041
1081