Search results for Thrombin

1987 hits were found for Thrombin

# Family MCID Name MIFTS Score
1
c THR092 Thrombophilia Due to Thrombin Defect 73 6.140
2
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.207
3
THR024 Thrombosis 57 0.179
4
DSS009 Disseminated Intravascular Coagulation 57 0.178
5
PRT037 Pertussis 65 0.172
6
P HMP007 Hemophilia 51 0.160
7
HPR003 Heparin-Induced Thrombocytopenia 48 0.150
8
ISC004 Ischemia 58 0.149
9
P THR014 Thrombocytopenia 67 0.145
10
INT007 Intermediate Coronary Syndrome 55 0.139
11
P THR015 Thrombophilia 51 0.136
12
c HMP029 Hemophilia a 67 0.128
13
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.125
14
P VSC007 Vascular Disease 63 0.121
15
LPP008 Lipoprotein Quantitative Trait Locus 62 0.119
16
BRN004 Brain Edema 56 0.114
17
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.112
18
PLM033 Pulmonary Embolism 59 0.111
19
ART140 Arteries, Anomalies of 52 0.108
20
LVR012 Liver Cirrhosis 62 0.107
21
P ATR011 Atrial Fibrillation 66 0.104
22
P MYC007 Myocardial Infarction 70 0.103
23
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.101
24
P ANT006 Antiphospholipid Syndrome 55 0.100
25
ATH013 Atherosclerosis Susceptibility 65 0.099
26
c ACT075 Acute Myocardial Infarction 57 0.099
27
ANR040 Aneurysm 59 0.093
28
STR067 Stroke, Ischemic 81 0.092
29
ANG054 Angina Pectoris 66 0.091
30
c PRC016 Pre-Eclampsia 63 0.088
31
CRN017 Coronary Thrombosis 47 0.087
32
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.084
33
LNG099 Lung Disease 60 0.082
34
VRC005 Varicose Veins 60 0.082
35
c HYP836 Hypercholesterolemia, Familial, 1 73 0.081
36
PRP027 Peripheral Vascular Disease 71 0.081
37
P PLM036 Pulmonary Fibrosis 65 0.079
38
ANT009 Antithrombin Iii Deficiency 59 0.079
39
47X002 47,xyy 49 0.079
40
THR035 Thrombasthenia 40 0.076
41
P LVR013 Liver Disease 68 0.075
42
c THR082 Thrombophilia Due to Activated Protein C Resistance 61 0.075
43
P NRB001 Neuroblastoma 72 0.073
44
ART016 Aortic Aneurysm 69 0.073
45
TXC005 Toxic Shock Syndrome 62 0.073
46
P GLM007 Glomerulonephritis 57 0.073
47
P PNC035 Pancreatic Cancer 84 0.072
48
CRB039 Cerebrovascular Disease 67 0.072
49
P GLM045 Glioma 63 0.072
50
P CRN300 Coronary Heart Disease 1 63 0.072
51
GLL048 Glial Tumor 45 0.072
52
BRN071 Brain Injury 49 0.070
53
CYT002 Cytokine Deficiency 42 0.070
54
GLB015 Glioblastoma Multiforme 75 0.068
55
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.068
56
P SCK005 Sickle Cell Disease 50 0.068
57
c HMP004 Hemophilia B 68 0.067
58
P AST007 Astrocytoma 51 0.067
59
P VNW001 Von Willebrand's Disease 65 0.065
60
CRB004 Cerebral Artery Occlusion 45 0.065
61
MYL069 Myeloma, Multiple 85 0.063
62
P RHM011 Rheumatoid Arthritis 80 0.063
63
OST159 Osteogenic Sarcoma 66 0.063
64
P BRN019 Bernard-Soulier Syndrome 60 0.063
65
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.061
66
PRT129 Prothrombin Deficiency, Congenital 50 0.061
67
48X005 48,xyyy 39 0.061
68
P PRS040 Prostate Cancer 97 0.059
69
P BRS047 Breast Cancer 97 0.059
70
P ALZ034 Alzheimer Disease 88 0.059
71
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 0.059
72
LPD008 Lipid Metabolism Disorder 62 0.059
73
P INF037 Inflammatory Bowel Disease 54 0.059
74
FCT001 Factor Viii Deficiency 51 0.059
75
P VTR007 Vitreoretinopathy 46 0.059
76
PRT014 Protein S Deficiency 44 0.059
77
P HRT032 Heart Disease 75 0.057
78
HYP066 Hyperglycemia 61 0.057
79
P NPH012 Nephrotic Syndrome 60 0.057
80
P HMR003 Hemorrhagic Disease 53 0.057
81
P ART022 Arthritis 69 0.055
82
P SYS005 Systemic Scleroderma 68 0.055
83
GLN010 Glanzmann Thrombasthenia 66 0.055
84
P MCR115 Microvascular Complications of Diabetes 5 66 0.055
85
c SCL052 Scleroderma, Familial Progressive 61 0.055
86
P PNC044 Pancreatitis 61 0.055
87
c ACT027 Acute Pancreatitis 60 0.055
88
P END033 Endocarditis 57 0.055
89
P ART021 Arteriosclerosis 54 0.055
90
END086 End Stage Renal Disease 51 0.055
91
HMG002 Hemoglobinuria 50 0.055
92
c SYS001 Systemic Lupus Erythematosus 86 0.053
93
CNG034 Congestive Heart Failure 69 0.053
94
AFB002 Afibrinogenemia, Congenital 65 0.053
95
ALL026 Allergic Hypersensitivity Disease 62 0.053
96
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 60 0.053
97
P CRD246 Cardiovascular System Disease 57 0.053
98
P PLY018 Polycythemia 56 0.053
99
LMB062 Limb Ischemia 55 0.053
100
PLM010 Pulmonary Edema 54 0.053
101
TRM010 Traumatic Brain Injury 51 0.053
102
CRN030 Coronary Stenosis 50 0.053
103
PLY001 Polycythemia Vera 69 0.051
104
P ESS003 Essential Thrombocythemia 68 0.051
105
P PLM037 Pulmonary Hypertension 67 0.051
106
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.051
107
P NTR004 Neutropenia 63 0.051
108
FCT002 Factor Xi Deficiency 60 0.051
109
CHL014 Cholera 59 0.051
110
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.051
111
INF034 Infective Endocarditis 53 0.051
112
P ECL001 Eclampsia 50 0.051
113
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.048
114
P OVR042 Ovarian Cancer 88 0.048
115
OST012 Osteoarthritis 78 0.048
116
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.048
117
c CHR684 Chronic Kidney Disease 70 0.048
118
P LKM062 Leukemia, Acute Lymphoblastic 69 0.048
119
ACT119 Acute Promyelocytic Leukemia 63 0.048
120
TRN015 Transient Cerebral Ischemia 63 0.048
121
RTN017 Retinal Detachment 61 0.048
122
PPT005 Peptic Ulcer Disease 59 0.048
123
FCT006 Factor V Deficiency 57 0.048
124
P PLY011 Polycystic Ovary Syndrome 56 0.048
125
PRP030 Purpura 54 0.048
126
ESP002 Esophageal Varix 51 0.048
127
P BLD051 Blood Coagulation Disease 46 0.048
128
PRT012 Prothrombin Deficiency 40 0.048
129
CRT004 Carotid Artery Thrombosis 38 0.048
130
c HYP595 Hypertension, Essential 84 0.046
131
SCK003 Sickle Cell Anemia 74 0.046
132
CRH001 Crohn's Disease 74 0.046
133
ULC004 Ulcerative Colitis 73 0.046
134
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.046
135
HYP056 Hypoglycemia 66 0.046
136
P HYD006 Hydrocephalus 66 0.046
137
CLT003 Colitis 62 0.046
138
P VSC011 Vasculitis 62 0.046
139
ATM095 Autoimmune Disease 62 0.046
140
P LPS004 Lupus Erythematosus 61 0.046
141
INT066 Interstitial Lung Disease 60 0.046
142
PRT013 Portal Hypertension 59 0.046
143
c ACT134 Acute Liver Failure 56 0.046
144
BNR002 Bone Resorption Disease 48 0.046
145
VTM033 Vitamin K Deficiency Bleeding 48 0.046
146
PLC007 Placental Abruption 48 0.046
147
HLX001 Helix Syndrome 47 0.046
148
PRT011 Protein C Deficiency 44 0.046
149
CRS001 Crescentic Glomerulonephritis 43 0.046
150
HPR006 Heparin Cofactor Ii Deficiency 40 0.046
151
MCL003 Macular Holes 40 0.046
152
LCH001 Leech Infestation 35 0.046
153
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.043
154
AST005 Asthma 76 0.043
155
END057 Endometrial Cancer 74 0.043
156
P KDN018 Kidney Disease 72 0.043
157
DFC004 Deficiency Anemia 70 0.043
158
DWN001 Down Syndrome 70 0.043
159
P MLN008 Melanoma 69 0.043
160
P HYP086 Hypothyroidism 69 0.043
161
P LKM002 Leukemia 68 0.043
162
PNC129 Pancreatic Adenocarcinoma 68 0.043
163
c FML001 Familial Atrial Fibrillation 65 0.043
164
P DBT009 Diabetes Mellitus 64 0.043
165
P ART023 Arthropathy 62 0.043
166
SPN186 Spinal Cord Injury 60 0.043
167
GRY002 Gray Platelet Syndrome 59 0.043
168
P URT039 Urticaria 58 0.043
169
EYD002 Eye Disease 58 0.043
170
P FBR017 Fibrosarcoma 56 0.043
171
PRT082 Preterm Premature Rupture of the Membranes 54 0.043
172
c MCR113 Microvascular Complications of Diabetes 3 52 0.043
173
THR004 Thrombocytosis 51 0.043
174
PRT018 Portal Vein Thrombosis 50 0.043
175
c MCR120 Microvascular Complications of Diabetes 7 47 0.043
176
c MCR130 Microvascular Complications of Diabetes 6 41 0.043
177
c MCR133 Microvascular Complications of Diabetes 4 41 0.043
178
P HPT023 Hepatocellular Carcinoma 100 0.040
179
P GLM040 Glioma Susceptibility 1 81 0.040
180
LPT014 Leptin Deficiency or Dysfunction 74 0.040
181
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.040
182
P AMY004 Amyloidosis 70 0.040
183
ADL002 Adult Syndrome 70 0.040
184
P CRD119 Cardiac Arrest 67 0.040
185
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.040
186
CLN015 Colon Adenocarcinoma 65 0.040
187
P ADN016 Adenocarcinoma 64 0.040
188
c FNC043 Fanconi Anemia, Complementation Group E 62 0.040
189
c SVR001 Severe Acute Respiratory Syndrome 62 0.040
190
GST033 Gestational Diabetes 61 0.040
191
P HMN010 Hemangioma 61 0.040
192
VSL002 Visual Epilepsy 59 0.040
193
HYP266 Hypoxia 57 0.040
194
BCT022 Bacterial Infectious Disease 56 0.040
195
P SZR006 Seizure Disorder 56 0.040
196
FCT003 Factor X Deficiency 54 0.040
197
P RTN022 Retinal Vein Occlusion 53 0.040
198
PRP080 Peripheral Artery Disease 53 0.040
199
BLD053 Blood Platelet Disease 49 0.040
200
c PRM038 Primary Agammaglobulinemia 44 0.040
201
P TRC031 Trichorhinophalangeal Syndrome 40 0.040
202
ALL014 Allergic Encephalomyelitis 38 0.040
203
THR123 Thrombotic Microangiopathy 36 0.040
204
LYM005 Lymphocele 35 0.040
205
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.037
206
P MCP040 Mucopolysaccharidosis-Plus Syndrome 69 0.037
207
c MCR129 Microvascular Complications of Diabetes 1 66 0.037
208
PRT036 Peritonitis 64 0.037
209
P END044 Endometriosis 63 0.037
210
INT002 Intermittent Claudication 61 0.037
211
P THR005 Thrombotic Thrombocytopenic Purpura 61 0.037
212
c ACT071 Acute Kidney Failure 60 0.037
213
P THL005 Thalassemia 60 0.037
214
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.037
215
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.037
216
P NRP001 Neuropathy 56 0.037
217
CHR100 Chronic Ulcer of Skin 55 0.037
218
P HYP076 Hyperthyroidism 55 0.037
219
FCT004 Factor Xii Deficiency 55 0.037
220
HMS001 Hemosiderosis 54 0.037
221
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.037
222
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.037
223
OCL069 Ocular Motor Apraxia 51 0.037
224
THR016 Thrombophlebitis 51 0.037
225
CRT013 Carotid Stenosis 50 0.037
226
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.037
227
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.037
228
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.037
229
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.037
230
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.037
231
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.037
232
c PCH010 Pachyonychia Congenita 3 44 0.037
233
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.037
234
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.037
235
c MCR112 Microvascular Complications of Diabetes 2 41 0.037
236
ASP030 Aspirin Resistance 39 0.037
238
P CLR023 Colorectal Cancer 99 0.034
239
P LNG032 Lung Cancer 98 0.034
240
P GST053 Gastric Cancer 83 0.034
241
INS024 Insulin-Like Growth Factor I 79 0.034
242
c MNN043 Meningioma, Familial 74 0.034
243
MYL005 Myelofibrosis 70 0.034
244
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.034
245
P PNM007 Pneumonia 68 0.034
246
RCK004 Rickets 68 0.034
247
MYL031 Myeloproliferative Neoplasm 66 0.034
248
P ART005 Arteriovenous Malformation 65 0.034
249
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.034
250
BDD001 Budd-Chiari Syndrome 63 0.034
251
P HYP750 Hypertriglyceridemia, Familial 62 0.034
252
MNN042 Meningioma, Radiation-Induced 62 0.034
253
NTR005 Nutritional Deficiency Disease 62 0.034
254
P ENC018 Encephalopathy 61 0.034
255
P KDN017 Kidney Cancer 60 0.034
256
STT001 Status Epilepticus 60 0.034
257
P DNG005 Dengue Virus 59 0.034
258
P BCL017 B-Cell Lymphoma 58 0.034
259
P PRP019 Peripheral Nervous System Disease 58 0.034
260
P ANG015 Angioedema 57 0.034
261
ERY051 Erythroleukemia, Familial 56 0.034
262
AMN003 Amnestic Disorder 54 0.034
263
GST023 Gastric Ulcer 53 0.034
264
P DDN001 Duodenal Ulcer 52 0.034
265
FCT005 Factor Xiii Deficiency 52 0.034
266
P PST095 Post-Thrombotic Syndrome 51 0.034
267
SPN021 Spinal Meningioma 50 0.034
268
NTR046 Neutrophil Migration 50 0.034
269
HDN002 Head Injury 46 0.034
270
CHR466 Chronic Thromboembolic Pulmonary Hypertension 45 0.034
271
c ACQ014 Acquired Hemophilia 45 0.034
272
P BCT020 Bacteremia 2 44 0.034
273
CVD001 Covid-19 44 0.034
274
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.034
275
P RRH023 Rare Hereditary Hemochromatosis 41 0.034
276
SHW001 Shwartzman Phenomenon 37 0.034
277
PLM101 Pulmonary Hypertension, Chronic Thromboembolic, Without Deep Vein Thrombosis 37 0.034
278
PLY150 Polykaryocytosis Inducer 31 0.034
279
CNG486 Congenital Disorders of N-Linked Glycosylation and Multiple Pathway 30 0.034
280
c RRH015 Rare Hemorrhagic Disorder 23 0.034
281
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.031
283
P BLD134 Bladder Cancer 79 0.031
284
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.031
285
c ATR087 Atrial Standstill 1 75 0.031
286
P RSP003 Respiratory Failure 74 0.031
287
c BTT014 Beta-Thalassemia 74 0.031
288
P MLT020 Multiple Sclerosis 72 0.031
289
c HPT073 Hepatitis C Virus 72 0.031
290
c PNC108 Pancreatitis, Hereditary 70 0.031
291
P LYM118 Lymphoma 68 0.031
292
c CNG411 Congenital Disorder of Glycosylation, Type in 68 0.031
293
FCT007 Factor Vii Deficiency 67 0.031
294
BRK010 Burkitt Lymphoma 67 0.031
295
P TRN020 Turner Syndrome 67 0.031
296
c MGR028 Migraine with or Without Aura 1 67 0.031
297
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.031
298
c ART101 Aortic Valve Disease 2 65 0.031
299
P ADL010 Adult Respiratory Distress Syndrome 65 0.031
300
OST017 Osteomyelitis 64 0.031
301
CRC021 Carcinosarcoma 62 0.031
302
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.031
303
FTT001 Fatty Liver Disease 61 0.031
304
VRL011 Viral Infectious Disease 61 0.031
305
NRL005 Neurilemmoma 60 0.031
306
P SCL018 Scoliosis 60 0.031
307
CRD223 Cardiac Arrhythmia 60 0.031
308
SQM006 Squamous Cell Carcinoma 60 0.031
309
DNG002 Dengue Hemorrhagic Fever 60 0.031
310
PRT058 Pure Autonomic Failure 59 0.031
311
IRN001 Iron Deficiency Anemia 59 0.031
312
IRN002 Iron Metabolism Disease 57 0.031
313
P HDC001 Headache 57 0.031
314
PNM008 Pneumothorax 56 0.031
315
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.031
316
ALL006 Allergic Asthma 56 0.031
317
AGN016 Aging 56 0.031
318
SYN007 Synovitis 54 0.031
319
HYP060 Hyperinsulinism 54 0.031
320
P LTR001 Lateral Sclerosis 54 0.031
321
PRS045 Prostatic Hypertrophy 53 0.031
322
CRH005 Crohn's Colitis 53 0.031
323
P HML001 Hemolytic-Uremic Syndrome 53 0.031
324
GTR002 Goiter 53 0.031
325
HMC014 Homocysteinemia 53 0.031
326
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.031
327
c VRL010 Viral Hepatitis 52 0.031
328
P SML001 Small Cell Carcinoma 52 0.031
329
NTR018 Neutrophilia, Hereditary 52 0.031
330
P SPP010 Suppressor of Tumorigenicity 3 51 0.031
331
PRS021 Prostatic Adenoma 51 0.031
332
PLS009 Plasma Cell Neoplasm 51 0.031
333
DYS165 Dysfibrinogenemia, Congenital 51 0.031
334
CHR635 Chromosome 5q Deletion Syndrome 50 0.031
335
c SVR005 Severe Pre-Eclampsia 50 0.031
336
P MTR003 Mitral Valve Stenosis 50 0.031
337
PLC008 Placenta Disease 50 0.031
338
PRS129 Prostatic Hyperplasia, Benign 49 0.031
339
INT078 Intracranial Thrombosis 49 0.031
340
SCT005 Scott Syndrome 49 0.031
341
URM002 Uremia 49 0.031
342
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.031
343
NSS002 Neisseria Meningitidis Infection 47 0.031
344
P PRL003 Proliferative Glomerulonephritis 44 0.031
345
IDP070 Idiopathic Scoliosis 42 0.031
346
SCR001 Secretory Meningioma 41 0.031
347
OVR094 Ovarian Epithelial Cancer 38 0.031
348
PLC002 Plica Syndrome 36 0.031
349
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.031
350
c LKM061 Leukemia, Acute Myeloid 84 0.026
351
BRN028 Brain Cancer 74 0.026
352
P OST002 Osteoporosis 74 0.026
353
SVR004 Severe Combined Immunodeficiency 73 0.026
354
P FML018 Familial Mediterranean Fever 73 0.026
355
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.026
356
P HYP061 Hypertrophic Cardiomyopathy 70 0.026
357
P TBR001 Tuberous Sclerosis 70 0.026
358
CRB037 Cerebral Palsy 69 0.026
359
LYM133 Lymphoma, Hodgkin, Classic 69 0.026
360
c MCL062 Mucolipidosis Ii Alpha/beta 68 0.026
361
P HPT021 Hepatitis 67 0.026
362
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.026
363
c INF071 Inflammatory Bowel Disease 1 67 0.026
364
c RHB024 Rhabdomyosarcoma 2 67 0.026
365
LPT001 Leptospirosis 66 0.026
366
P CLC063 Celiac Disease 1 66 0.026
367
P DMN002 Dementia 66 0.026
368
KHL003 Kohlschutter-Tonz Syndrome 65 0.026
369
P HRP006 Herpes Simplex 65 0.026
370
c DBT099 Diabetes Mellitus, Type I 65 0.026
371
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.026
372
P RHB003 Rhabdomyosarcoma 63 0.026
373
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 63 0.026
374
PLG002 Plague 63 0.026
375
P HRD008 Hereditary Hemorrhagic Telangiectasia 63 0.026
376
c HPT001 Hepatitis C 62 0.026
377
P PSR002 Psoriasis 62 0.026
378
P ART067 Aortic Aneurysm, Familial Thoracic 1 61 0.026
379
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.026
380
IDP011 Idiopathic Interstitial Pneumonia 59 0.026
381
c DNG003 Dengue Disease 59 0.026
382
HLC007 Helicobacter Pylori Infection 59 0.026
383
CRD132 Cardiac Conduction Defect 58 0.026
384
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.026
385
BRG013 Buerger Disease 58 0.026
386
P PRN023 Prion Disease 57 0.026
387
c MST023 Mesothelioma, Malignant 57 0.026
388
P PLY019 Polyneuropathy 56 0.026
389
c THY109 Thyroid Cancer, Nonmedullary, 1 56 0.026
390
c CRD184 Ceroid Lipofuscinosis, Neuronal, 5 55 0.026
391
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 55 0.026
392
GLC003 Glucose Intolerance 54 0.026
393
PSD007 Pseudomyxoma Peritonei 54 0.026
394
HLL004 Hellp Syndrome 54 0.026
395
CLL003 Cellulitis 54 0.026
396
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.026
397
P END047 Endophthalmitis 53 0.026
398
P RTN018 Retinal Disease 53 0.026
399
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.026
400
DMY004 Demyelinating Disease 52 0.026
401
NRT004 Neuritis 52 0.026
402
PST011 Pustulosis of Palm and Sole 52 0.026
403
PLS007 Plasmodium Falciparum Malaria 52 0.026
404
IMP005 Impotence 52 0.026
405
ART074 Aortic Dissection 52 0.026
406
LMY002 Leiomyoma 52 0.026
407
c ALM001 Al Amyloidosis 50 0.026
408
P OVR082 Overgrowth Syndrome 50 0.026
409
c HRD202 Hereditary Lymphedema I 50 0.026
410
ECT026 Ectopic Pregnancy 50 0.026
411
P CMP008 Compartment Syndrome 49 0.026
412
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.026
413
SPL018 Splenomegaly 48 0.026
414
BBS001 Babesiosis 48 0.026
415
RNL077 Renal Fibrosis 47 0.026
416
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.026
417
LYM019 Lymphosarcoma 46 0.026
418
RTN023 Retinitis 46 0.026
419
P BNG032 Benign Mesothelioma 46 0.026
420
c MLG068 Malignant Glioma 46 0.026
421
PLC001 Placenta Accreta 46 0.026
422
HMR002 Hemarthrosis 45 0.026
423
CRT015 Carotid Artery Occlusion 45 0.026
424
c GZP005 Gaze Palsy, Familial Horizontal, with Progressive Scoliosis 1 44 0.026
425
HYP084 Hypopyon 43 0.026
426
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.026
427
ATX019 Ataxia with Vitamin E Deficiency 42 0.026
428
NRR001 Neuroretinitis 42 0.026
429
ANC002 Anca-Associated Vasculitis 41 0.026
430
P SCL057 Scoliosis, Isolated 1 41 0.026
431
SPR126 Superior Semicircular Canal Dehiscence 40 0.026
432
PLC009 Placenta Praevia 39 0.026
433
AML001 Amelanotic Melanoma 39 0.026
434
c CHR682 Chronic Bilirubin Encephalopathy 39 0.026
435
FRN014 Fournier Gangrene 37 0.026
436
MNN021 Meningococcemia 37 0.026
437
PHM001 Phimosis 37 0.026
438
c PRS136 Prostate Cancer, Hereditary, 6 33 0.026
439
c PRS130 Prostate Cancer, Hereditary, 8 32 0.026
440
P CRN133 Coronary Artery Disease, Autosomal Dominant, 1 32 0.026
441
c INH004 Inherited Blood Coagulation Disease 30 0.026
442
ARG004 Argyria 27 0.026
443
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.026
444
ESP021 Esophageal Cancer 90 0.022
445
MLR004 Malaria 81 0.022
446
CYS001 Cystic Fibrosis 81 0.022
447
P RTT002 Rett Syndrome 80 0.022
448
c DLT002 Dilated Cardiomyopathy 79 0.022
449
IMM167 Immune Deficiency Disease 78 0.022
450
CRV035 Cervical Cancer 76 0.022
451
ADR007 Adrenoleukodystrophy 75 0.022
452
c HMC039 Hemochromatosis, Type 1 74 0.022
453
c SPN225 Spondyloarthropathy 1 73 0.022
454
P RTN024 Retinoblastoma 73 0.022
455
ANX010 Anxiety 73 0.022
456
c TBR026 Tuberous Sclerosis 2 72 0.022
457
P GRF003 Graft-Versus-Host Disease 72 0.022
458
HMN044 Human Immunodeficiency Virus Type 1 71 0.022
459
P EPL164 Epilepsy 71 0.022
460
P SRC025 Sarcoidosis 1 70 0.022
461
GST040 Gastric Adenocarcinoma 70 0.022
462
P MYP004 Myopathy 70 0.022
463
CRT072 Creutzfeldt-Jakob Disease 70 0.022
464
ABT001 Abetalipoproteinemia 69 0.022
465
P OCL013 Oculodentodigital Dysplasia 69 0.022
466
P HYP802 Hypocalcemia, Autosomal Dominant 1 69 0.022
467
CHL065 Cholangiocarcinoma 68 0.022
468
P INF038 Influenza 68 0.022
469
P HYP098 Hypereosinophilic Syndrome 67 0.022
470
P BLD062 Bile Duct Cancer 67 0.022
471
ALC007 Alcohol Dependence 66 0.022
472
c FML021 Familial Hypercholesterolemia 66 0.022
473
P NSP012 Nasopharyngeal Carcinoma 66 0.022
474
P MNN013 Meningitis 66 0.022
475
c SML038 Small Cell Cancer of the Lung 65 0.022
476
TTN003 Tetanus 65 0.022
477
P CNJ013 Conjunctivitis 65 0.022
478
PPL049 Papillon-Lefevre Syndrome 65 0.022
479
GRN037 Granulomatosis with Polyangiitis 65 0.022
480
ANG020 Angiosarcoma 64 0.022
481
P HRM001 Hermansky-Pudlak Syndrome 64 0.022
482
OVR029 Ovarian Hyperstimulation Syndrome 64 0.022
483
TBC004 Tobacco Addiction 64 0.022
484
GT001 Gout 64 0.022
485
BRC012 Brucellosis 64 0.022
486
MSC007 Muscle Hypertrophy 64 0.022
487
MGK001 Megakaryocytic Leukemia 64 0.022
488
P HML002 Hemolytic Anemia 63 0.022
489
P HYP069 Hyperparathyroidism 63 0.022
490
c ACT068 Acute Cystitis 63 0.022
491
c LCL006 Localized Scleroderma 62 0.022
492
c HPT003 Hepatitis a 62 0.022
493
HSH003 Hashimoto Thyroiditis 62 0.022
494
MDD011 Mood Disorder 62 0.022
495
PSR001 Psoriatic Arthritis 61 0.022
496
P INT143 Interstitial Cystitis 61 0.022
497
DRM006 Dermatitis 61 0.022
498
CHR001 Churg-Strauss Syndrome 61 0.022
499
P MYL006 Myeloid Leukemia 60 0.022
500
HRP004 Herpes Zoster 60 0.022
501
PNM010 Pneumothorax, Primary Spontaneous 60 0.022
502
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.022
503
P VNT002 Ventricular Septal Defect 60 0.022
504
HPT019 Hepatic Encephalopathy 60 0.022
505
P SNS001 Sensorineural Hearing Loss 60 0.022
506
CHC001 Chickenpox 60 0.022
507
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.022
508
ING001 Inguinal Hernia 60 0.022
509
P HRD011 Hereditary Spherocytosis 60 0.022
510
c HRD002 Hereditary Angioedema 60 0.022
511
P MYC008 Myocarditis 59 0.022
512
c HPT016 Hepatitis B 59 0.022
513
DCT002 Ductal Carcinoma in Situ 59 0.022
514
P CYS018 Cystitis 59 0.022
515
BRN002 Bronchiolitis 59 0.022
516
P GLL022 Guillain-Barre Syndrome 59 0.022
517
c ACT073 Acute Leukemia 58 0.022
518
P SYP003 Syphilis 58 0.022
519
c PRM005 Primary Hyperparathyroidism 58 0.022
520
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.022
521
CNS004 Constipation 58 0.022
522
P INF032 Infertility 57 0.022
523
P UVT001 Uveitis 57 0.022
524
P GLL020 Gallbladder Disease 57 0.022
525
GLS018 Glass Syndrome 57 0.022
526
BRN056 Bronchopulmonary Dysplasia 57 0.022
527
P EXN002 Exanthem 57 0.022
528
BLR008 Bilirubin Metabolic Disorder 57 0.022
529
VSC002 Vascular Dementia 57 0.022
530
HMR039 Hemorrhage, Intracerebral 57 0.022
531
CYT008 Cytomegalovirus Infection 57 0.022
532
PLC005 Placental Insufficiency 57 0.022
533
SCH014 Schistosomiasis 57 0.022
534
P BPL003 Bipolar Disorder 56 0.022
535
P CHN012 Chondrosarcoma 56 0.022
536
HPT046 Hepatic Veno-Occlusive Disease 56 0.022
537
HMT008 Hematuria, Benign Familial 56 0.022
538
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.022
539
HMG005 Hemoglobinopathy 56 0.022
540
GST050 Gastrointestinal System Disease 56 0.022
541
INT030 Intracranial Aneurysm 56 0.022
542
P HYP838 Hyperlipidemia, Familial Combined, 3 56 0.022
543
AND020 Androgen Insensitivity, Partial 56 0.022
544
P GST044 Gastritis 56 0.022
545
MCL006 Macular Retinal Edema 55 0.022
546
ORL004 Oral Submucous Fibrosis 55 0.022
547
P DRR001 Diarrhea 55 0.022
548
c BCT007 Bacterial Meningitis 55 0.022
549
P ACT010 Acth-Secreting Pituitary Adenoma 55 0.022
550
P GRV001 Graves' Disease 55 0.022
551
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.022
552
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.022
553
GNG005 Gangliocytoma 55 0.022
554
ACT058 Active Peptic Ulcer Disease 55 0.022
555
P VNS003 Venous Insufficiency 55 0.022
556
JVN009 Juvenile Pilocytic Astrocytoma 55 0.022
557
P DRM007 Dermatitis Herpetiformis 55 0.022
558
VGN023 Vaginitis 54 0.022
559
PRT038 Protein-Energy Malnutrition 54 0.022
560
P TRM003 Tremor 54 0.022
561
NNL006 Non-Alcoholic Steatohepatitis 54 0.022
562
PNC001 Pancytopenia 54 0.022
563
CRM001 Crimean-Congo Hemorrhagic Fever 53 0.022
564
c CNT016 Central Retinal Vein Occlusion 53 0.022
565
RHM028 Rheumatic Heart Disease 53 0.022
566
P INS002 in Situ Carcinoma 53 0.022
567
HRT012 Heart Valve Disease 53 0.022
568
P CRB194 Cerebroretinal Microangiopathy with Calcifications and Cysts 1 53 0.022
569
INT075 Intracranial Hypertension 53 0.022
570
P PNC025 Panic Disorder 53 0.022
571
c FML008 Familial Retinoblastoma 53 0.022
572
c PSR017 Psoriasis 2 53 0.022
573
c CNT035 Central Nervous System Disease 52 0.022
574
THY030 Thyroid Gland Disease 52 0.022
575
P THY032 Thyroiditis 52 0.022
576
P ACT105 Acute Mountain Sickness 52 0.022
577
c PSR023 Psoriasis 1 52 0.022
578
c CNG189 Congenital Disorder of Glycosylation, Type Ib 52 0.022
579
TLN003 Telangiectasis 52 0.022
580
c ACT135 Acute Graft Versus Host Disease 52 0.022
581
PNG002 Pain Agnosia 51 0.022
582
SPN051 Spondylitis 51 0.022
583
SPS003 Spastic Diplegia 51 0.022
585
ILS001 Ileus 51 0.022
586
CLR109 Colorectal Adenocarcinoma 51 0.022
587
ENT011 Enterocolitis 51 0.022
588
P LCT001 Lactic Acidosis 51 0.022
589
ACT049 Acute Disseminated Encephalomyelitis 51 0.022
590
CYS014 Cystadenocarcinoma 51 0.022
591
INT079 Intrahepatic Cholangiocarcinoma 51 0.022
592
LNG031 Lung Benign Neoplasm 51 0.022
593
SPN019 Spondylolisthesis 51 0.022
594
c PTT057 Pituitary Adenoma 4, Acth-Secreting 51 0.022
595
GNG012 Gingival Overgrowth 51 0.022
596
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.022
597
CRV040 Cervix Carcinoma 51 0.022
598
P CHL066 Cholangitis 51 0.022
599
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.022
600
HYP081 Hypolipoproteinemia 51 0.022
601
PLR007 Pleural Empyema 50 0.022
602
RDC002 Radiculopathy 50 0.022
603
FSC004 Fasciitis 50 0.022
604
STM007 Stomatitis 50 0.022
605
c INF145 Infantile Liver Failure Syndrome 1 50 0.022
606
MTB004 Metabolic Acidosis 50 0.022
607
DYS073 Dysphagia 50 0.022
608
HRT011 Heart Septal Defect 50 0.022
609
c INF023 Inflammatory Breast Carcinoma 50 0.022
610
CVR006 Cavernous Hemangioma 49 0.022
611
DFF035 Diffuse Cutaneous Systemic Sclerosis 49 0.022
612
QDR001 Quadriplegia 48 0.022
613
CHL061 Childhood Leukemia 48 0.022
614
NCR007 Necrotizing Fasciitis 48 0.022
615
P CPL014 Capillary Malformation-Arteriovenous Malformation 1 48 0.022
616
RFR010 Refractory Anemia 48 0.022
617
MNC006 Monoclonal Gammopathy of Uncertain Significance 48 0.022
618
P PRN026 Porencephaly 48 0.022
619
IGG001 Iga Glomerulonephritis 48 0.022
620
BNN003 Bone Inflammation Disease 48 0.022
621
LPT006 Leptin Receptor Deficiency 48 0.022
622
PRP007 Priapism 47 0.022
623
CRD001 Cardiac Tamponade 47 0.022
624
P RNL015 Renal Hypertension 47 0.022
625
NDL007 Nodular Goiter 47 0.022
626
c PSR032 Psoriasis 11 47 0.022
627
STM006 Stomach Disease 47 0.022
628
P CRC039 Coarctation of Aorta 47 0.022
629
CRD137 Cardiogenic Shock 47 0.022
630
P OVR046 Ovarian Cyst 47 0.022
631
ATN005 Autonomic Dysfunction 46 0.022
632
RTN020 Retinal Vascular Disease 46 0.022
633
MDS022 Mediastinitis 46 0.022
634
MNN020 Meningococcal Infection 46 0.022
635
c VNW008 Von Willebrand Disease, Type 3 46 0.022
636
CRN019 Coronary Artery Vasospasm 46 0.022
637
ANG018 Angiomyolipoma 46 0.022
638
ANR004 Anuria 46 0.022
639
P HRN001 Horner's Syndrome 45 0.022
640
c TRC022 Tricuspid Valve Insufficiency 45 0.022
641
URT010 Ureteral Obstruction 45 0.022
642
HPT004 Hepatic Coma 45 0.022
643
PRL008 Paralytic Ileus 45 0.022
644
P CMM008 Communicating Hydrocephalus 45 0.022
645
KDN015 Kidney Angiomyolipoma 45 0.022
646
PLS029 Plasminogen Activator Inhibitor-1 Deficiency 45 0.022
647
RTR001 Retrograde Amnesia 44 0.022
648
P CHR345 Chronic Pain 44 0.022
649
DBT008 Diabetic Angiopathy 44 0.022
650
ISC015 Ischemic Colitis 44 0.022
651
PRT035 Peritoneum Cancer 44 0.022
652
c HYP272 Hypercholesterolemia, Familial, 3 44 0.022
653
ALP043 Alpha-2-Plasmin Inhibitor Deficiency 44 0.022
654
BCT021 Bacterial Sepsis 44 0.022
655
SDD008 Sudden Sensorineural Hearing Loss 43 0.022
656
ANG011 Angiodysplasia 43 0.022
657
P PRP034 Purpura Fulminans 43 0.022
658
ILC002 Ileocolitis 43 0.022
659
BLR013 Biliary Tract Cancer 42 0.022
660
HYP457 Hypertrophic Scars 42 0.022
661
MST004 Mast Cell Neoplasm 42 0.022
662
BNS003 Binswanger's Disease 42 0.022
663
PNM013 Pneumococcal Meningitis 42 0.022
664
c PSR028 Psoriasis 7 42 0.022
665
BCK006 Back Pain 42 0.022
666
CTS005 Catastrophic Antiphospholipid Syndrome 42 0.022
667
OBS082 Obstructive Nephropathy 42 0.022
668
IDP091 Idiopathic Nephrotic Syndrome 42 0.022
669
49X006 49, Xxxxy Syndrome 41 0.022
670
DFF003 Diffuse Scleroderma 41 0.022
671
c PSR018 Psoriasis 13 41 0.022
672
PRS063 Paresthesia 41 0.022
673
ANG049 Angioedema Induced by Ace Inhibitors 40 0.022
674
P PRG092 Pregnancy Loss, Recurrent 1 40 0.022
675
CLP006 Clopidogrel Resistance 40 0.022
676
TRN012 Transient Global Amnesia 39 0.022
677
c HMG029 Hemoglobin Se Disease 39 0.022
678
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.022
679
PRM127 Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type 38 0.022
680
EXT007 Extracutaneous Mastocytoma 38 0.022
681
P PRC031 Preeclampsia/eclampsia 1 38 0.022
682
c SYS043 Systemic Lupus Erythematosus 1 38 0.022
683
MCP033 Mucopolysaccharidoses 38 0.022
684
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 37 0.022
685
CRD016 Cardiac Rupture 37 0.022
686
GLM044 Glomerular Disease 37 0.022
687
c ACQ042 Acquired Hemophilia a 37 0.022
688
CHL013 Cholecystolithiasis 37 0.022
689
VRL017 Viral Hemorrhagic Fever 36 0.022
690
c DRM040 Dermatitis Herpetiformis, Familial 35 0.022
691
CRB079 Cerebrospinal Fluid Leak 35 0.022
692
PLN026 Pilonidal Sinus 35 0.022
693
AMR003 Amaurosis Fugax 34 0.022
694
NNT024 Neonatal Stroke 34 0.022
696
HPT081 Hepatic Infarction 33 0.022
697
SGT001 Sagittal Sinus Thrombosis 32 0.022
698
SNG003 Single Ventricular Heart 30 0.022
699
PLX004 Plexopathy 30 0.022
700
PLT031 Platelet Membrane Fluidity 29 0.022
701
DSC004 Discitis 29 0.022
702
PST092 Posttransplant Acute Limbic Encephalitis 29 0.022
703
SBS002 Substernal Goiter 27 0.022
704
c RNG015 Ring Chromosome 2 26 0.022
705
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.022
706
SPL005 Splenic Artery Aneurysm 25 0.022
707
HRP008 Herpes Simiae 25 0.022
708
PRT130 Protein Z Deficiency 24 0.022
709
JVN026 Jeavons Syndrome 24 0.022
710
SBC002 Subclavian Artery Aneurysm 24 0.022
711
NCR014 Necrotizing Soft Tissue Infection 23 0.022
712
FCT013 Factor V Leiden Thrombophilia 22 0.022
713
CNG171 Congenital Plasminogen Deficiency 18 0.022
714
P ANT080 Antigen Defined by Monoclonal Antibody Aj9 18 0.022
715
PRL045 Proline-Negative Auxotroph of Hamster, Complementation of 18 0.022
716
PLT016 Platelet Adenylate Cyclase Activity 16 0.022
717
MTH081 Mthfr Gene Variant 14 0.022
718
NRL016 Neural Tube Defects 82 0.015
719
P ATX030 Ataxia-Telangiectasia 82 0.015
720
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.015
721
P RTN008 Retinitis Pigmentosa 79 0.015
722
P LKM071 Leukemia, Chronic Lymphocytic 79 0.015
723
PFF001 Pfeiffer Syndrome 79 0.015
724
CNN003 Conn's Syndrome 79 0.015
725
c CWD006 Cowden Syndrome 1 78 0.015
726
GST019 Gastrointestinal Stromal Tumor 78 0.015
727
P LNG064 Lung Cancer Susceptibility 3 78 0.015
728
P PRK057 Parkinson Disease, Late-Onset 78 0.015
729
P MDL005 Medulloblastoma 77 0.015
730
MRF001 Marfan Syndrome 77 0.015
731
c TBR025 Tuberous Sclerosis 1 77 0.015
732
c NRF024 Neurofibromatosis, Type I 77 0.015
733
KPS004 Kaposi Sarcoma 75 0.015
734
P APL001 Aplastic Anemia 74 0.015
735
P SCH015 Schizophrenia 74 0.015
736
VNH007 Von Hippel-Lindau Syndrome 73 0.015
737
P CNR004 Cone-Rod Dystrophy 2 73 0.015
738
P JBR020 Joubert Syndrome 1 72 0.015
739
P LFR001 Li-Fraumeni Syndrome 72 0.015
740
P HNT016 Huntington Disease 72 0.015
741
c MLT156 Multiple Endocrine Neoplasia, Type I 72 0.015
742
P FML011 Familial Adenomatous Polyposis 72 0.015
743
OTT002 Otitis Media 72 0.015
744
FBR012 Fabry Disease 72 0.015
745
c LKM063 Leukemia, Chronic Myeloid 72 0.015
746
P PHC003 Pheochromocytoma 71 0.015
747
ACR007 Acromegaly 71 0.015
748
c EXD008 Exudative Vitreoretinopathy 1 71 0.015
749
CNT097 Central Hypoventilation Syndrome, Congenital 71 0.015
750
BHC003 Behcet Syndrome 71 0.015
751
MYL009 Myelodysplastic Syndrome 70 0.015
752
MLT157 Multiple System Atrophy 1 70 0.015
753
APR006 Apert Syndrome 70 0.015
754
c GLY008 Glycogen Storage Disease Ii 70 0.015
755
c GCH015 Gaucher Disease, Type I 70 0.015
756
PTZ001 Peutz-Jeghers Syndrome 70 0.015
757
P FRG001 Fragile X Syndrome 70 0.015
758
P TTR001 Tetralogy of Fallot 70 0.015
759
P ASP006 Aspergillosis 69 0.015
760
PLM001 Pulmonary Tuberculosis 69 0.015
761
P RTH006 Rothmund-Thomson Syndrome, Type 2 69 0.015
762
ACR008 Acrocallosal Syndrome 69 0.015
763
SVR097 Severe Cutaneous Adverse Reaction 69 0.015
764
P PRM011 Primary Ciliary Dyskinesia 69 0.015
765
P SLP006 Sleep Apnea 69 0.015
766
c PRG042 Progressive Familial Heart Block, Type Ia 69 0.015
767
P LPR021 Leprosy 3 69 0.015
768
EWN003 Ewing Sarcoma 69 0.015
769
P ANG001 Angelman Syndrome 69 0.015
770
MNT001 Mantle Cell Lymphoma 69 0.015
771
c MYT021 Myotonic Dystrophy 1 69 0.015
772
P TMP003 Temporal Arteritis 68 0.015
773
P MYC084 Mycobacterium Tuberculosis 1 68 0.015
774
SND001 Sandhoff Disease 68 0.015
775
c BSL007 Basal Cell Carcinoma 68 0.015
776
OBS002 Obsessive-Compulsive Disorder 68 0.015
777
CRZ001 Crouzon Syndrome 68 0.015
778
SKN019 Skin Melanoma 68 0.015
779
P MYS003 Myasthenia Gravis 68 0.015
780
P HML033 Hemolytic Uremic Syndrome, Atypical 1 68 0.015
781
c CRD086 Cardiomyopathy, Familial Hypertrophic, 1 68 0.015
782
BRN024 Bronchitis 68 0.015
783
CNN005 Connective Tissue Disease 68 0.015
784
P ALP004 Alport Syndrome 68 0.015
785
MLD001 Melioidosis 68 0.015
786
MLT118 Multiple Acyl-Coa Dehydrogenase Deficiency 68 0.015
787
P KBK002 Kabuki Syndrome 1 67 0.015
788
HYL004 Hyaline Fibromatosis Syndrome 67 0.015
789
P CWD010 Cowden Syndrome 67 0.015
790
GST092 Gastroesophageal Reflux 67 0.015
791
P CRB048 Cerebral Cavernous Malformations 67 0.015
792
CHR103 Charge Syndrome 67 0.015
793
c PRD013 Periodic Fever, Familial, Autosomal Dominant 67 0.015
794
P OLG002 Oligodendroglioma 67 0.015
795
BLM001 Bloom Syndrome 67 0.015
796
P FLL037 Follicular Lymphoma 67 0.015
797
ALL003 Allergic Rhinitis 67 0.015
798
OMN001 Omenn Syndrome 67 0.015
799
THY111 Thyroid Carcinoma, Familial Medullary 67 0.015
800
P SHW006 Shwachman-Diamond Syndrome 1 67 0.015
801
P CHR012 Chronic Granulomatous Disease 67 0.015
802
PSY004 Psychotic Disorder 67 0.015
803
c ATS007 Autism Spectrum Disorder 67 0.015
804
CRP001 Carpal Tunnel Syndrome 67 0.015
805
FBR011 Fibrodysplasia Ossificans Progressiva 67 0.015
806
P MLG056 Malignant Hyperthermia 67 0.015
807
c PLY168 Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease 66 0.015
808
P TRC072 Treacher Collins Syndrome 1 66 0.015
809
P SKN015 Skin Carcinoma 66 0.015
810
MYX005 Myxoid Liposarcoma 66 0.015
811
ART001 Arterial Tortuosity Syndrome 66 0.015
812
c FML346 Familial Adenomatous Polyposis 1 66 0.015
813
ADR054 Adrenocortical Carcinoma, Hereditary 66 0.015
814
ACH004 Achondroplasia 66 0.015
815
AND002 Androgen Insensitivity Syndrome 66 0.015
816
CHR593 Chromosome 16p13.3 Deletion Syndrome, Proximal 66 0.015
817
CHG001 Chagas Disease 66 0.015
818
P CCK001 Cockayne Syndrome 66 0.015
819
LNG039 Lung Squamous Cell Carcinoma 66 0.015
820
P NRV007 Nervous System Disease 66 0.015
821
P BRD002 Bardet-Biedl Syndrome 66 0.015
822
CRN036 Craniopharyngioma 65 0.015
823
GTL001 Gitelman Syndrome 65 0.015
824
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.015
825
LWC002 Lowe Oculocerebrorenal Syndrome 65 0.015
826
P MCK013 Meckel Syndrome, Type 1 65 0.015
827
KRT019 Keratitis, Hereditary 65 0.015
828
ACR006 Aceruloplasminemia 65 0.015
829
SRC014 Sarcoma 65 0.015
830
P LPS002 Liposarcoma 65 0.015
831
ATM096 Autoimmune Polyendocrine Syndrome, Type I, with or Without Reversible Metaphyseal Dysplasia 65 0.015
832
TNG002 Tangier Disease 65 0.015
833
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 65 0.015
834
BRR014 Barrett Esophagus 65 0.015
835
PND002 Pendred Syndrome 65 0.015
836
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 65 0.015
837
c WLM013 Wilms Tumor 1 65 0.015
838
P PRS038 Personality Disorder 65 0.015
839
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 65 0.015
840
P THY023 Thymoma 65 0.015
841
c ATS347 Autosomal Dominant Polycystic Kidney Disease 65 0.015
842
APN008 Apnea, Obstructive Sleep 64 0.015
843
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.015
844
PLL001 Pallister-Hall Syndrome 64 0.015
845
P PRT008 Proteus Syndrome 64 0.015
846
BRK001 Brooke-Spiegler Syndrome 64 0.015
847
c JVN010 Juvenile Rheumatoid Arthritis 64 0.015
848
CNG510 Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi 64 0.015
849
ART002 Arts Syndrome 64 0.015
850
DGR001 Digeorge Syndrome 64 0.015
851
MLT163 Multiple Pterygium Syndrome, Escobar Variant 64 0.015
852
P PRD008 Periodontitis 64 0.015
853
PLM031 Poliomyelitis 64 0.015
854
DSM004 Desmoid Tumor 64 0.015
855
LYM017 Lyme Disease 64 0.015
856
RFS006 Refsum Disease, Classic 64 0.015
857
c EPS035 Episodic Ataxia, Type 2 63 0.015
858
c DPH024 Diaphragmatic Hernia, Congenital 63 0.015
859
KRN002 Kearns-Sayre Syndrome 63 0.015
860
P GCH001 Gaucher's Disease 63 0.015
861
P ANR048 Aniridia 1 63 0.015
862
TYP007 Typhoid Fever 63 0.015
863
CNT061 Conotruncal Heart Malformations 63 0.015
864
c MLG084 Malignant Fibrous Histiocytoma 63 0.015
865
P DST002 Distal Arthrogryposis 63 0.015
866
SKN016 Skin Disease 63 0.015
867
P SHR029 Short Syndrome 63 0.015
868
INT146 Intervertebral Disc Disease 63 0.015
869
PTR032 Peters-Plus Syndrome 63 0.015
870
CHN016 Cohen Syndrome 63 0.015
871
P PTT014 Pitt-Hopkins Syndrome 63 0.015
872
END041 Endometrial Adenocarcinoma 63 0.015
873
HYP780 Hypoadrenocorticism, Familial 63 0.015
874
P LMY004 Leiomyosarcoma 63 0.015
875
ANR007 Anorexia Nervosa 63 0.015
876
DPR016 Depression 63 0.015
877
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 62 0.015
878
c GLC092 Glaucoma, Primary Open Angle 62 0.015
879
c ALP101 Alpha-Thalassemia 62 0.015
880
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.015
881
HMT002 Hematologic Cancer 62 0.015
882
LRN002 Laron Syndrome 62 0.015
883
P PLY014 Polycystic Kidney Disease 62 0.015
884
P EPL140 Epilepsy, Idiopathic Generalized 62 0.015
885
c BRN108 Branchiootic Syndrome 1 62 0.015
886
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.015
887
TKY002 Takayasu Arteritis 62 0.015
888
P SPN046 Spinal Muscular Atrophy 62 0.015
889
P ESP024 Esophagitis 62 0.015
890
P TRC086 Trichohepatoenteric Syndrome 1 62 0.015
891
BLL006 Bullous Pemphigoid 62 0.015
892
c BRD010 Bardet-Biedl Syndrome 1 62 0.015
893
HYD038 Hydrops Fetalis, Nonimmune 62 0.015
894
P BCK002 Beckwith-Wiedemann Syndrome 62 0.015
895
c ANM038 Anemia, Autoimmune Hemolytic 62 0.015
896
P ACR001 Aicardi-Goutieres Syndrome 62 0.015
897
CRN239 Carnitine Deficiency, Systemic Primary 62 0.015
898
HYP810 Hypereosinophilic Syndrome, Idiopathic 62 0.015
899
P OST009 Osteochondritis Dissecans 62 0.015
900
P PRM006 Primary Biliary Cirrhosis 62 0.015
901
SCH078 Schimmelpenning-Feuerstein-Mims Syndrome 62 0.015
902
CHL068 Cholestasis 61 0.015
903
P DRM010 Dermatomyositis 61 0.015
904
c NRD017 Neurodegeneration with Brain Iron Accumulation 1 61 0.015
906
NRM001 Neuromyelitis Optica 61 0.015
907
P LYM113 Lymphoproliferative Syndrome, X-Linked, 1 61 0.015
908
OST003 Osteonecrosis 61 0.015
909
CHN055 Chanarin-Dorfman Syndrome 61 0.015
910
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 61 0.015
911
c PNS012 Paine Syndrome 61 0.015
912
WST001 West Syndrome 61 0.015
913
P ENC004 Encephalitis 61 0.015
914
OSS012 Osseous Heteroplasia, Progressive 61 0.015
915
WLD007 Waldenstroem's Macroglobulinemia 61 0.015
916
c WLM018 Wilms Tumor 5 61 0.015
917
ART141 Arteriovenous Malformations of the Brain 61 0.015
918
WHM001 Whim Syndrome 61 0.015
919
P ACH003 Achromatopsia 61 0.015
920
RCT015 Reactive Arthritis 61 0.015
921
P SJG008 Sjogren Syndrome 61 0.015
922
ARG002 Argininosuccinic Aciduria 61 0.015
923
SDD001 Sudden Infant Death Syndrome 61 0.015
924
APP008 Appendicitis 61 0.015
925
DCB001 Decubitus Ulcer 61 0.015
926
LGN002 Legionellosis 60 0.015
927
NTH001 Netherton Syndrome 60 0.015
928
NPH091 Nephrolithiasis, Calcium Oxalate 60 0.015
929
PTN001 Patent Foramen Ovale 60 0.015
930
WLL001 Williams-Beuren Syndrome 60 0.015
931
RGH009 Right Atrial Isomerism 60 0.015
932
CFF002 Coffin-Lowry Syndrome 60 0.015
933
HST017 Histiocytosis-Lymphadenopathy Plus Syndrome 60 0.015
934
P TST021 Testicular Germ Cell Tumor 60 0.015
935
DPH001 Diphtheria 60 0.015
936
c LPM012 Lipomatosis, Multiple 60 0.015
937
CHR288 Chronic Recurrent Multifocal Osteomyelitis 60 0.015
938
c JVN061 Juvenile Arthritis 60 0.015
939
P ATS308 Autosomal Dominant Cerebellar Ataxia 60 0.015
940
P BNG030 Benign Ependymoma 60 0.015
941
ACN002 Acanthosis Nigricans 60 0.015
942
ACQ007 Acquired Immunodeficiency Syndrome 60 0.015
943
P ALP009 Alopecia Areata 60 0.015
944
LGG001 Legg-Calve-Perthes Disease 60 0.015
945
STR039 Sturge-Weber Syndrome 60 0.015
946
P ATR010 Atrial Heart Septal Defect 60 0.015
947
END081 Endosteal Hyperostosis, Autosomal Dominant 60 0.015
948
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.015
949
PMS001 Poems Syndrome 60 0.015
950
P CTR002 Cataract 60 0.015
951
P PTN014 Patent Ductus Arteriosus 1 60 0.015
952
ORL011 Oral Cancer 60 0.015
953
HYD002 Hydronephrosis 60 0.015
954
QFV001 Q Fever 60 0.015
955
STF001 Stiff-Person Syndrome 60 0.015
956
P GLY013 Glycogen Storage Disease 60 0.015
957
DRR014 Darier-White Disease 60 0.015
958
VGN017 Vaginal Cancer 60 0.015
959
NLP001 Nail-Patella Syndrome 60 0.015
960
P OPT006 Optic Nerve Disease 60 0.015
961
SPP011 Suppression of Tumorigenicity 12 59 0.015
962
P AXN002 Axenfeld-Rieger Syndrome 59 0.015
963
c PSD114 Pseudohypoaldosteronism, Type I, Autosomal Recessive 59 0.015
964
P BND020 Bone Disease 59 0.015
965
THY029 Thyroid Carcinoma 59 0.015
966
IGR001 Ige Responsiveness, Atopic 59 0.015
967
SPN027 Spinal Stenosis 59 0.015
968
P SPN309 Spinocerebellar Ataxia 6 59 0.015
969
CHL123 Chlamydia 59 0.015
970
PRN019 Perinatal Necrotizing Enterocolitis 59 0.015
971
P PRD006 Prader-Willi Syndrome 59 0.015
972
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 59 0.015
973
c LTN004 Late-Onset Retinal Degeneration 59 0.015
974
DBN001 Dubin-Johnson Syndrome 59 0.015
975
P BRS044 Breast Adenocarcinoma 59 0.015
976
GRD007 Grade Iii Astrocytoma 59 0.015
977
c HYD046 Hydatidiform Mole, Recurrent, 1 59 0.015
978
KLP010 Klippel-Trenaunay-Weber Syndrome 59 0.015
979
P HMN036 Hemangiopericytoma, Malignant 59 0.015
980
ACH043 Achondroplasia, Severe, with Developmental Delay and Acanthosis Nigricans 59 0.015
981
ADN018 Adenoma 59 0.015
982
VLV032 Vulva Cancer 59 0.015
983
c CLR131 Ciliary Dyskinesia, Primary, 1 59 0.015
984
SRC027 Sarcoma, Synovial 58 0.015
985
RNL024 Renal Glucosuria 58 0.015
986
DBT087 Diabetes Insipidus, Neurohypophyseal 58 0.015
987
P PLY017 Polyarteritis Nodosa 58 0.015
988
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 58 0.015
989
P INT070 Intestinal Obstruction 58 0.015
990
P HYP726 Hypercalcemia, Infantile, 1 58 0.015
991
CMP010 Complex Regional Pain Syndrome 58 0.015
992
P MLT007 Multiple Epiphyseal Dysplasia 58 0.015
993
SCR008 Scrub Typhus 58 0.015
994
DST005 Diastrophic Dysplasia 58 0.015
995
c PRG018 Paragangliomas 1 58 0.015
996
c PTT056 Pituitary Adenoma 1, Multiple Types 58 0.015
997
SPT004 Septic Arthritis 58 0.015
998
P ALC033 Alcohol Use Disorder 58 0.015
999
MYR002 Mayer-Rokitansky-Kuster-Hauser Syndrome 58 0.015
1000
CCC001 Coccidioidomycosis 58 0.015
1001
P EPD083 Epidermodysplasia Verruciformis 1 58 0.015
1002
HYP458 Hyper Ige Syndrome 58 0.015
1003
RSP019 Respiratory Distress Syndrome in Premature Infants 58 0.015
1004
CNT047 Contact Dermatitis 58 0.015
1005
P EHL001 Ehlers-Danlos Syndrome 58 0.015
1006
NWB001 Newborn Respiratory Distress Syndrome 58 0.015
1007
DSS008 Disease of Mental Health 58 0.015
1008
MNT002 Mental Depression 58 0.015
1009
P BNC003 Bone Cancer 58 0.015
1010
c DWL002 Dowling-Degos Disease 1 58 0.015
1011
P CND004 Candidiasis 58 0.015
1012
EXT034 Extrinsic Allergic Alveolitis 58 0.015
1013
MXD005 Mixed Connective Tissue Disease 58 0.015
1014
P VND007 Van Der Woude Syndrome 1 58 0.015
1015
c THY102 Thyroid Cancer, Nonmedullary, 2 58 0.015
1016
CHR081 Choroideremia 57 0.015
1017
PMP006 Pemphigus Vulgaris, Familial 57 0.015
1018
DNY001 Denys-Drash Syndrome 57 0.015
1019
P OPT009 Optic Neuritis 57 0.015
1020
TTL012 Total Anomalous Pulmonary Venous Return 1 57 0.015
1021
P PLV020 Pelvic Organ Prolapse 57 0.015
1022
CST005 Castleman Disease 57 0.015
1023
c CHL119 Cholangitis, Primary Sclerosing 57 0.015
1024
CHL067 Cholecystitis 57 0.015
1025
c ANM036 Anemia, Sideroblastic, 1 57 0.015
1026
c VSC019 Vesicoureteral Reflux 1 57 0.015
1027
P MYM013 Moyamoya Disease 1 57 0.015
1028
P PLY041 Polymyositis 57 0.015
1029
CHK001 Chikungunya 57 0.015
1030
P RHN004 Rhinitis 57 0.015
1031
MBS002 Moebius Syndrome 57 0.015
1032
THY122 Thyroid Gland Cancer 57 0.015
1033
BRD001 Brody Myopathy 57 0.015
1034
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 57 0.015
1035
LYM021 Lymphadenitis 57 0.015
1036
c ALZ056 Alzheimer Disease 3 57 0.015
1037
APH001 Aphthous Stomatitis 57 0.015
1038
c ART061 Arthrogryposis, Distal, Type 2a 57 0.015
1039
P FCL005 Focal Segmental Glomerulosclerosis 57 0.015
1040
TNS005 Tonsillitis 57 0.015
1041
APH002 Aphasia 57 0.015
1042
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.015
1043
CMM005 Common Cold 57 0.015
1044
ARS001 Aarskog-Scott Syndrome 57 0.015
1045
c ANG068 Angioedema, Hereditary, Type I 57 0.015
1046
GLT035 Glutaric Acidemia I 57 0.015
1047
ENC044 Enchondromatosis, Multiple, Ollier Type 57 0.015
1048
JPN002 Japanese Encephalitis 57 0.015
1049
AMY082 Amyloidosis, Familial Visceral 57 0.015
1050
INT303 Intracranial Hypertension, Idiopathic 57 0.015
1051
PHR003 Pharyngitis 57 0.015
1052
AYM001 Ayme-Gripp Syndrome 57 0.015
1053
PGM001 Pigmented Villonodular Synovitis 56 0.015
1054
c GLC112 Galactosemia Iii 56 0.015
1055
P PYL005 Pyelonephritis 56 0.015
1056
c BSL024 Basal Cell Carcinoma 1 56 0.015
1057
P MYS005 Myositis 56 0.015
1058
c LSS005 Lissencephaly 1 56 0.015
1059
CMR002 Coumarin Resistance 56 0.015
1060
P MLT074 Multiple Endocrine Neoplasia 56 0.015
1061
TRN018 Transitional Cell Carcinoma 56 0.015
1062
PLS011 Plasmacytoma 56 0.015
1063
EXF001 Exfoliation Syndrome 56 0.015
1064
c INT072 Intestinal Pseudo-Obstruction 56 0.015
1065
LMY014 Leiomyoma, Uterine 56 0.015
1066
ADN027 Adenomyosis 56 0.015
1067
P PNL012 Penile Cancer 56 0.015
1068
SPN041 Spinal Cord Disease 56 0.015
1069
SFT003 Soft Tissue Sarcoma 56 0.015
1070
ALL010 Allergic Contact Dermatitis 56 0.015
1071
ALL001 Allan-Herndon-Dudley Syndrome 56 0.015
1072
PRS047 Prostatitis 56 0.015
1073
ISL001 Islet Cell Tumor 56 0.015
1074
VRG001 Variegate Porphyria 56 0.015
1075
ACS001 Acoustic Neuroma 56 0.015
1076
INS023 Insensitivity to Pain, Congenital, with Anhidrosis 56 0.015
1077
CYS008 Cystic Echinococcosis 56 0.015
1078