Search results for Apoptosis Activator 2

4911 hits were found for Apoptosis Activator 2

# Family MCID Name MIFTS Score
1
c TYP009 Type 2 Diabetes Mellitus 91 102.898
2
P DBT009 Diabetes Mellitus 67 67.340
3
SVR001 Severe Acute Respiratory Syndrome 68 53.207
4
P BCL017 B-Cell Lymphoma 57 52.132
5
P BRS047 Breast Cancer 97 50.688
6
HYP266 Hypoxia 56 49.077
7
P LNG032 Lung Cancer 98 47.133
8
ISC004 Ischemia 61 47.080
9
P LKM002 Leukemia 65 47.077
10
P NRB001 Neuroblastoma 66 46.343
11
CYT002 Cytokine Deficiency 43 46.187
12
P PRS040 Prostate Cancer 95 45.481
13
GLM045 Glioma 62 45.029
14
GLL048 Glial Tumor 51 44.823
15
P PNC035 Pancreatic Cancer 87 43.796
16
c LKM061 Leukemia, Acute Myeloid 83 43.143
17
P RHM011 Rheumatoid Arthritis 81 43.088
18
P OVR042 Ovarian Cancer 88 43.043
19
HYP066 Hyperglycemia 60 42.623
20
P ART022 Arthritis 70 42.559
21
P HRP006 Herpes Simplex 65 41.719
22
c SML038 Small Cell Cancer of the Lung 68 41.710
23
P MLN008 Melanoma 75 41.594
24
P LYM118 Lymphoma 66 41.497
25
HMN044 Human Immunodeficiency Virus Type 1 76 41.263
26
P CLR023 Colorectal Cancer 100 41.226
27
P HPT023 Hepatocellular Carcinoma 95 41.153
28
GLB002 Glioblastoma 67 41.141
29
48X005 48,xyyy 39 40.616
30
MYL069 Myeloma, Multiple 76 40.487
31
AGN016 Aging 53 40.482
32
OST159 Osteogenic Sarcoma 66 40.374
33
c DNT047 Dentinogenesis Imperfecta Type 2 35 40.298
34
P MYL006 Myeloid Leukemia 60 39.597
35
P GST053 Gastric Cancer 82 39.412
36
P ADN016 Adenocarcinoma 63 39.296
37
P BDY004 Body Mass Index Quantitative Trait Locus 11 82 38.458
38
RNL114 Renal Cell Carcinoma, Nonpapillary 79 38.429
39
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 38.169
40
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 38.115
41
c HYP595 Hypertension, Essential 84 38.008
42
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 37.851
43
SQM006 Squamous Cell Carcinoma 59 37.665
44
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 37.588
45
PRT037 Pertussis 49 37.234
46
c MCR113 Microvascular Complications of Diabetes 3 52 37.186
47
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 37.101
48
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 37.098
49
c BDY019 Body Mass Index Quantitative Trait Locus 18 46 37.098
50
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 37.095
51
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 37.095
52
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 37.095
53
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 37.093
54
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 37.092
55
IMM167 Immune Deficiency Disease 76 36.971
56
P LPS004 Lupus Erythematosus 61 36.258
57
c MCR120 Microvascular Complications of Diabetes 7 47 36.024
58
CVD001 Covid-19 59 35.731
59
CLT003 Colitis 63 35.698
60
c SYS001 Systemic Lupus Erythematosus 85 35.684
61
c MCR130 Microvascular Complications of Diabetes 6 41 35.535
62
c MCR133 Microvascular Complications of Diabetes 4 41 35.533
63
NNL005 Non-Alcoholic Fatty Liver Disease 63 35.526
64
P HPT021 Hepatitis 68 35.103
65
RPD005 Rapidly Involuting Congenital Hemangioma 48 34.764
66
P ALZ034 Alzheimer Disease 87 34.686
67
OST012 Osteoarthritis 77 34.606
68
FTT001 Fatty Liver Disease 61 34.520
69
RHB024 Rhabdomyosarcoma 2 65 34.462
70
P LKM071 Leukemia, Chronic Lymphocytic 74 34.426
71
P BLD134 Bladder Cancer 79 34.401
72
P LKM062 Leukemia, Acute Lymphoblastic 69 34.349
73
CRV035 Cervical Cancer 72 33.950
74
PLM129 Pulmonary Disease, Chronic Obstructive 74 33.710
75
CRH001 Crohn's Disease 80 33.555
76
ULC004 Ulcerative Colitis 74 33.301
77
ATH013 Atherosclerosis Susceptibility 63 33.258
78
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 33.191
79
MCR225 Macrophage Activation Syndrome 45 33.128
80
STR067 Stroke, Ischemic 79 33.099
81
P CNR004 Cone-Rod Dystrophy 2 74 32.916
82
c MCR115 Microvascular Complications of Diabetes 5 65 32.675
83
P MYC007 Myocardial Infarction 69 32.436
84
LPD008 Lipid Metabolism Disorder 61 31.868
85
ATM095 Autoimmune Disease 61 31.749
86
P KDN018 Kidney Disease 71 31.640
87
P PRD008 Periodontitis 63 31.606
88
HYP056 Hypoglycemia 65 31.505
89
c PCH010 Pachyonychia Congenita 3 43 31.253
90
P LNG064 Lung Cancer Susceptibility 3 69 31.077
91
c ACT027 Acute Pancreatitis 60 30.906
92
SPN186 Spinal Cord Injury 60 30.791
93
c HPT001 Hepatitis C 61 30.744
94
RCK004 Rickets 64 30.583
95
BNR002 Bone Resorption Disease 47 30.572
97
P LVR013 Liver Disease 68 30.407
98
c CHR684 Chronic Kidney Disease 73 30.401
99
SVR004 Severe Combined Immunodeficiency 70 30.377
100
HLX001 Helix Syndrome 47 30.287
101
P MYC084 Mycobacterium Tuberculosis 1 68 30.259
102
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 30.250
103
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 30.230
104
P HRT032 Heart Disease 84 30.179
105
P RTN024 Retinoblastoma 72 30.100
106
P PNC044 Pancreatitis 61 30.082
107
P VSC007 Vascular Disease 62 30.026
108
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 29.913
109
P CRN300 Coronary Heart Disease 1 73 29.885
110
c HPT073 Hepatitis C Virus 70 29.883
111
c LNG047 Long Qt Syndrome 2 59 29.796
112
c MCR112 Microvascular Complications of Diabetes 2 42 29.795
113
LPP008 Lipoprotein Quantitative Trait Locus 65 29.702
114
BRN071 Brain Injury 50 29.530
115
SPN035 Spindle Cell Sarcoma 51 29.296
116
PRT251 Proteinuria, Chronic Benign 58 29.153
117
SRC014 Sarcoma 64 29.076
118
P MLT020 Multiple Sclerosis 79 29.048
119
LNG099 Lung Disease 62 28.810
120
P MJR001 Major Depressive Disorder 68 28.750
121
P SPN301 Spinocerebellar Ataxia 2 59 28.737
122
c THR092 Thrombophilia Due to Thrombin Defect 74 28.729
123
c ATR087 Atrial Standstill 1 74 28.687
124
DPR016 Depression 64 28.615
125
THY029 Thyroid Carcinoma 55 28.589
126
END057 Endometrial Cancer 76 28.511
127
P AST005 Asthma 75 28.496
128
P INF037 Inflammatory Bowel Disease 53 28.482
129
P INF038 Influenza 68 28.422
130
c HPT016 Hepatitis B 62 28.362
131
CNG034 Congestive Heart Failure 69 28.250
132
ART140 Arteries, Anomalies of 52 28.148
133
CMP083 Complete Plasminogen Activator Inhibitor 1 Deficiency 27 27.894
134
P SZR006 Seizure Disorder 69 27.844
135
LYM133 Lymphoma, Hodgkin, Classic 69 27.778
136
P ADL010 Adult Respiratory Distress Syndrome 70 27.522
137
c HNT004 Huntington Disease-Like 2 51 27.419
138
c LKM063 Leukemia, Chronic Myeloid 70 27.401
139
DWN001 Down Syndrome 70 27.383
140
c HYP836 Hypercholesterolemia, Familial, 1 73 27.380
141
P PSR002 Psoriasis 63 27.362
142
CRB004 Cerebral Artery Occlusion 45 27.336
143
ESP021 Esophageal Cancer 84 27.320
144
PST011 Pustulosis of Palm and Sole 52 27.247
145
MNT002 Mental Depression 56 27.154
146
P PHC003 Pheochromocytoma 70 26.995
147
MYL009 Myelodysplastic Syndrome 67 26.973
148
ACQ007 Acquired Immunodeficiency Syndrome 58 26.950
149
P NTR004 Neutropenia 62 26.905
150
c TYP008 Type 1 Diabetes Mellitus 77 26.870
151
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 26.820
152
P NSP012 Nasopharyngeal Carcinoma 60 26.781
153
TRM010 Traumatic Brain Injury 50 26.646
154
ALL029 Allergic Disease 61 26.588
155
P KDN017 Kidney Cancer 60 26.340
156
c MYT020 Myotonic Dystrophy 2 57 26.270
157
INS024 Insulin-Like Growth Factor I 77 26.236
158
P SPN429 Spinocerebellar Ataxia, Autosomal Recessive, with Axonal Neuropathy 2 57 26.232
159
c NRF023 Neurofibromatosis, Type Ii 70 26.222
160
c AMY091 Amyotrophic Lateral Sclerosis 1 87 26.183
161
BCT022 Bacterial Infectious Disease 55 26.172
162
P NRP001 Neuropathy 59 26.040
163
ADN018 Adenoma 58 26.025
164
ACT058 Active Peptic Ulcer Disease 55 25.921
165
c PRC016 Pre-Eclampsia 64 25.897
167
P THR014 Thrombocytopenia 66 25.792
168
P GRF003 Graft-Versus-Host Disease 71 25.658
169
END086 End Stage Renal Disease 54 25.585
170
LVR012 Liver Cirrhosis 62 25.583
171
P PLM036 Pulmonary Fibrosis 65 25.535
172
47X002 47,xyy 47 25.497
173
DFC004 Deficiency Anemia 74 25.356
174
CHR276 Chronic Active Epstein-Barr Virus Infection 41 25.324
175
CRB039 Cerebrovascular Disease 65 25.261
176
P EPL164 Epilepsy 70 25.236
177
SKN016 Skin Disease 63 25.219
178
TXC005 Toxic Shock Syndrome 61 25.170
179
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 25.091
180
c ART101 Aortic Valve Disease 2 65 25.081
181
c GRS014 Griscelli Syndrome, Type 2 52 24.999
182
PRT036 Peritonitis 65 24.968
183
c ACT075 Acute Myocardial Infarction 55 24.888
184
P PLM037 Pulmonary Hypertension 69 24.859
185
c TBR026 Tuberous Sclerosis 2 71 24.847
186
P BPL003 Bipolar Disorder 56 24.829
187
P GLM040 Glioma Susceptibility 1 70 24.805
188
P SPS133 Spastic Paraplegia 2, X-Linked 50 24.776
189
P GLM007 Glomerulonephritis 59 24.687
190
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 24.678
191
P SKN015 Skin Carcinoma 71 24.578
192
P LTR001 Lateral Sclerosis 57 24.561
193
P DRM053 Dermatitis, Atopic 65 24.549
194
P PRK057 Parkinson Disease, Late-Onset 79 24.318
195
c MTR019 Maturity-Onset Diabetes of the Young, Type 2 53 24.232
196
ADR040 Adrenal Gland Pheochromocytoma 45 24.224
197
P END044 Endometriosis 62 24.211
198
c PSR017 Psoriasis 2 53 24.180
199
HMN014 Human Immunodeficiency Virus Infectious Disease 54 24.161
200
c LKM005 Leukemia, T-Cell, Chronic 33 24.153
201
TLN003 Telangiectasis 51 24.141
202
c BRS111 Breast-Ovarian Cancer, Familial 2 53 24.098
203
P OST002 Osteoporosis 76 24.074
204
HGH043 High Grade Glioma 46 24.048
205
c HMP012 Hemophagocytic Lymphohistiocytosis, Familial, 2 47 24.046
206
c LKM056 Leukemia, Chronic Lymphocytic 2 47 23.989
207
LYM143 Lymphoma, Non-Hodgkin, Familial 74 23.936
208
DRM006 Dermatitis 61 23.894
209
P PNM007 Pneumonia 64 23.867
210
P DRR001 Diarrhea 55 23.857
211
PLM001 Pulmonary Tuberculosis 69 23.829
212
CYS001 Cystic Fibrosis 77 23.720
213
BRK010 Burkitt Lymphoma 65 23.615
214
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 23.527
215
BCK006 Back Pain 43 23.498
216
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 23.485
217
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 23.485
218
CHL014 Cholera 62 23.480
219
c HPT003 Hepatitis a 63 23.379
220
THR024 Thrombosis 56 23.370
221
P DMN002 Dementia 65 23.316
222
P INF032 Infertility 60 23.266
223
NNL006 Non-Alcoholic Steatohepatitis 54 23.194
224
P HYP086 Hypothyroidism 68 23.189
225
ORL015 Oral Squamous Cell Carcinoma 43 23.186
226
P PRP019 Peripheral Nervous System Disease 57 23.180
227
c PLY172 Polycystic Kidney Disease 2 with or Without Polycystic Liver Disease 53 23.177
228
P FBR017 Fibrosarcoma 55 23.173
229
P SPP010 Suppressor of Tumorigenicity 3 50 23.133
230
P SCH015 Schizophrenia 74 23.122
231
c CRD183 Ceroid Lipofuscinosis, Neuronal, 2 56 22.996
232
VCC001 Vaccinia 49 22.941
233
c ACT073 Acute Leukemia 59 22.933
234
DFF005 Diffuse Large B-Cell Lymphoma 55 22.870
235
ALC007 Alcohol Dependence 65 22.848
236
LSH001 Leishmaniasis 63 22.822
237
c LPD033 Lipodystrophy, Congenital Generalized, Type 2 52 22.771
238
LYM114 Lymphoproliferative Syndrome, X-Linked, 2 51 22.704
239
P MYP004 Myopathy 67 22.681
240
c HRM017 Hermansky-Pudlak Syndrome 2 55 22.605
241
HYP060 Hyperinsulinism 53 22.412
242
CLN015 Colon Adenocarcinoma 64 22.293
243
P KLZ004 Kala-Azar 1 41 22.292
244
P SLP006 Sleep Apnea 69 22.257
245
P ATR011 Atrial Fibrillation 66 22.206
246
c CHL118 Cholestasis, Benign Recurrent Intrahepatic, 2 44 22.193
247
CHL065 Cholangiocarcinoma 57 22.186
248
c SPH014 Spherocytosis, Type 2 38 22.181
249
P HYP098 Hypereosinophilic Syndrome 66 22.177
250
c PRK089 Parkinson Disease 2, Autosomal Recessive Juvenile 60 22.123
251
P RSP003 Respiratory Failure 73 22.032
252
c SPN225 Spondyloarthropathy 1 70 21.924
253
P VSC011 Vasculitis 61 21.885
254
P GST044 Gastritis 55 21.878
255
P PRK039 Parkinsonism 55 21.749
256
P RHN004 Rhinitis 56 21.701
257
P CHR345 Chronic Pain 50 21.695
258
c DFN250 Deafness, Autosomal Recessive 2 45 21.643
259
c ARR046 Arrhythmogenic Right Ventricular Dysplasia, Familial, 2 45 21.628
260
ANX010 Anxiety 70 21.594
261
P MSC005 Muscular Dystrophy 66 21.570
262
TTN003 Tetanus 64 21.530
263
MST020 Mast Cell Activation Syndrome 27 21.497
264
P ATX030 Ataxia-Telangiectasia 80 21.454
265
c PRG019 Paragangliomas 2 30 21.448
266
STM007 Stomatitis 52 21.374
267
DSS032 Disease by Infectious Agent 55 21.351
268
P ANR048 Aniridia 1 66 21.273
269
GLC003 Glucose Intolerance 53 21.221
270
P TRN020 Turner Syndrome 67 21.203
271
c PRG038 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 2 49 21.183
272
ORL011 Oral Cancer 60 21.132
273
INT079 Intrahepatic Cholangiocarcinoma 51 21.109
274
P ENC004 Encephalitis 61 21.037
275
c MGR028 Migraine with or Without Aura 1 63 21.029
276
INT323 Intraocular Pressure Quantitative Trait Locus 63 21.023
277
OCL069 Ocular Motor Apraxia 57 20.952
278
P HNT016 Huntington Disease 73 20.952
279
c THR037 Thrombocytopenia 2 36 20.910
280
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 20.863
281
CHL123 Chlamydia 58 20.820
282
P SRC025 Sarcoidosis 1 70 20.812
283
SKN019 Skin Melanoma 70 20.807
285
MLT118 Multiple Acyl-Coa Dehydrogenase Deficiency 64 20.735
286
c PLM164 Pulmonary Hypertension, Primary, 1 75 20.733
287
ANR040 Aneurysm 60 20.674
288
P BRS044 Breast Adenocarcinoma 58 20.662
289
P ENC018 Encephalopathy 62 20.661
290
MLR004 Malaria 77 20.621
291
c DLT002 Dilated Cardiomyopathy 79 20.598
292
P ALC033 Alcohol Use Disorder 67 20.594
293
P CTR002 Cataract 59 20.587
294
c LFR007 Li-Fraumeni Syndrome 2 45 20.571
295
c ACT071 Acute Kidney Failure 60 20.525
296
OVR094 Ovarian Epithelial Cancer 39 20.496
297
HRW001 Hair Whorl 35 20.452
298
c LBR012 Leber Congenital Amaurosis 2 52 20.446
299
P DNG005 Dengue Virus 55 20.420
300
PRS045 Prostatic Hypertrophy 53 20.413
301
SPN051 Spondylitis 51 20.405
302
PNC041 Pancreatic Ductal Adenocarcinoma 51 20.342
303
FCS011 Facioscapulohumeral Muscular Dystrophy 2 42 20.228
304
HMC041 Homocystinuria Due to Deficiency of N -Methylenetetrahydrofolate Reductase Activity 48 20.222
305
P CRD119 Cardiac Arrest 68 20.211
306
HMP009 Haemophilus Influenzae 41 20.196
307
c MLT160 Multiple Endocrine Neoplasia, Type Iia 67 20.192
308
MLG169 Malignant Astrocytoma 57 20.111
309
P BNG032 Benign Mesothelioma 53 20.102
310
c 46X049 46,xy Sex Reversal 2 51 20.091
311
c AMY058 Amyotrophic Lateral Sclerosis 2, Juvenile 41 20.088
312
c RNG015 Ring Chromosome 2 22 20.038
313
P MYC008 Myocarditis 59 20.031
314
P BND020 Bone Disease 60 20.030
315
PRS021 Prostatic Adenoma 43 19.988
316
KPS004 Kaposi Sarcoma 76 19.944
317
c TLN011 Telangiectasia, Hereditary Hemorrhagic, Type 2 45 19.939
318
P EXN002 Exanthem 58 19.935
319
c FTL070 Fetal Akinesia Deformation Sequence 2 36 19.930
320
ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 35 19.853
321
ALL014 Allergic Encephalomyelitis 34 19.831
322
P FLL037 Follicular Lymphoma 66 19.798
323
P ERY048 Erythrocytosis, Familial, 2 57 19.782
324
INF009 Inflammatory Spondylopathy 30 19.754
325
CRB037 Cerebral Palsy 66 19.745
326
LYM019 Lymphosarcoma 46 19.731
327
PPL052 Papillomatosis, Confluent and Reticulated 34 19.726
328
PRS129 Prostatic Hyperplasia, Benign 48 19.714
329
SPN402 Spinal Muscular Atrophy, X-Linked 2 47 19.676
330
NRR001 Neuroretinitis 42 19.619
331
P PLY011 Polycystic Ovary Syndrome 57 19.542
332
RTN023 Retinitis 45 19.537
333
P CRD246 Cardiovascular System Disease 55 19.507
334
SFT003 Soft Tissue Sarcoma 43 19.495
335
PNG002 Pain Agnosia 51 19.467
336
c HYP604 Hyperinsulinemic Hypoglycemia, Familial, 2 65 19.447
337
DNN001 Danon Disease 59 19.431
338
P NRF002 Neurofibromatosis 60 19.425
339
IMP005 Impotence 52 19.412
340
P MSC003 Muscular Atrophy 52 19.407
341
c DMN005 Diamond-Blackfan Anemia 2 28 19.393
342
c CRB191 Cerebral Cavernous Malformations 2 45 19.380
343
ALL003 Allergic Rhinitis 66 19.365
344
GST033 Gestational Diabetes 60 19.339
345
P CHR654 Charcot-Marie-Tooth Disease, Axonal, Type 2e 63 19.326
346
ACT119 Acute Promyelocytic Leukemia 62 19.326
347
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 19.319
348
PPL022 Papilloma 53 19.313
349
IFP003 Ifap Syndrome 2 41 19.312
350
IMM056 Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome 2 35 19.207
351
c NPH030 Nephronophthisis 2 50 19.180
352
c ATM011 Autoimmune Hepatitis 62 19.178
353
P ATT013 Attention Deficit-Hyperactivity Disorder 65 19.069
354
c MJR022 Major Affective Disorder 8 37 19.061
355
c MJR024 Major Affective Disorder 9 40 19.061
356
PST028 Post-Traumatic Stress Disorder 58 19.036
357
c SCL052 Scleroderma, Familial Progressive 60 19.016
358
P URN019 Urinary Tract Infection 48 18.927
359
ADL002 Adult Syndrome 69 18.908
360
CNS004 Constipation 56 18.882
361
PRP027 Peripheral Vascular Disease 71 18.881
362
PNC129 Pancreatic Adenocarcinoma 64 18.866
363
P TRM003 Tremor 50 18.856
364
DPH001 Diphtheria 59 18.810
365
P HYP750 Hypertriglyceridemia, Familial 61 18.808
366
c PRS114 Prostate Cancer, Hereditary, 2 33 18.767
367
c WLF009 Wolfram Syndrome 2 43 18.728
368
IRN002 Iron Metabolism Disease 56 18.723
369
c DFN036 Deafness, X-Linked 2 44 18.702
370
P RHB003 Rhabdomyosarcoma 66 18.680
371
c BRD014 Bardet-Biedl Syndrome 2 53 18.653
372
CHL068 Cholestasis 61 18.637
373
VRL011 Viral Infectious Disease 60 18.630
374
c FML347 Familial Adenomatous Polyposis 2 56 18.623
375
c NRP064 Neuropathy, Congenital Hypomyelinating, 2 35 18.613
376
SQM002 Squamous Cell Papilloma 45 18.577
377
c CRN303 Corneal Dystrophy, Posterior Polymorphous, 2 29 18.571
378
P WSK001 Wiskott-Aldrich Syndrome 72 18.547
379
c LYM107 Lymphoproliferative Syndrome 2 50 18.535
380
c ATS007 Autism Spectrum Disorder 71 18.531
381
SQM013 Squamous Cell Carcinoma, Head and Neck 75 18.520
382
PRP030 Purpura 54 18.512
383
P ALP008 Alopecia 53 18.507
384
c ACT068 Acute Cystitis 60 18.471
385
P ATS364 Autism 72 18.468
386
P MDL005 Medulloblastoma 75 18.444
387
LYM027 Lymphopenia 56 18.442
388
MLD018 Mild Cognitive Impairment 48 18.410
389
c HMC009 Hemochromatosis Type 2 58 18.349
390
GST040 Gastric Adenocarcinoma 66 18.329
391
P CND004 Candidiasis 57 18.287
392
c NPH049 Nephrotic Syndrome, Type 2 49 18.239
393
c CRB170 Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 2 35 18.202
394
PLM134 Pulmonary Fibrosis, Idiopathic 76 18.170
395
P SKN067 Skin/hair/eye Pigmentation, Variation in, 2 30 18.139
396
P AMY004 Amyloidosis 69 18.126
397
P CNG499 Congenital Anomalies of Kidney and Urinary Tract 2 52 18.088
398
P RCT021 Rectum Cancer 54 18.057
399
DSS008 Disease of Mental Health 74 18.049
400
P THY032 Thyroiditis 56 18.044
401
PLM033 Pulmonary Embolism 58 17.994
402
MCL079 Macular Telangiectasia Type 2 28 17.973
403
ANX004 Anoxia 40 17.930
404
P INS002 in Situ Carcinoma 52 17.915
405
c VRL010 Viral Hepatitis 52 17.863
406
ANG054 Angina Pectoris 65 17.831
407
MCS002 Mucositis 55 17.830
408
BRN024 Bronchitis 67 17.801
409
P NJM001 Nijmegen Breakage Syndrome 75 17.794
410
NLX003 Neu-Laxova Syndrome 2 47 17.768
411
ALL006 Allergic Asthma 55 17.748
412
PRS047 Prostatitis 57 17.747
413
c DYS143 Dyskeratosis Congenita, Autosomal Dominant 2 39 17.734
414
P HYP760 Hypothyroidism, Congenital, Nongoitrous, 2 54 17.723
415
c OPT023 Optic Atrophy 2 31 17.704
416
P UVT001 Uveitis 57 17.667
417
PTT046 Pituitary Hormone Deficiency, Combined, 2 62 17.597
418
P EYD002 Eye Disease 57 17.590
419
c TRC073 Treacher Collins Syndrome 2 28 17.562
420
P PRS038 Personality Disorder 65 17.539
421
HYP290 Hypobetalipoproteinemia, Familial, 2 39 17.524
422
NNK001 Nonaka Myopathy 58 17.499
423
P ATS366 Autism X-Linked 2 41 17.495
424
c SPN326 Spinal Muscular Atrophy, Distal, Autosomal Recessive, 2 38 17.479
425
ART016 Aortic Aneurysm 68 17.419
426
c JVN010 Juvenile Rheumatoid Arthritis 52 17.397
427
P RTH006 Rothmund-Thomson Syndrome, Type 2 67 17.390
428
DBT010 Diabetic Neuropathy 54 17.365
429
P BRN140 Brain Small Vessel Disease 2 30 17.345
430
HLC007 Helicobacter Pylori Infection 67 17.338
431
c BRT029 Brittle Cornea Syndrome 2 33 17.312
432
P BCT020 Bacteremia 2 43 17.266
433
P GCH001 Gaucher's Disease 69 17.234
434
CHG001 Chagas Disease 65 17.214
435
c NTR051 Neutropenia, Severe Congenital, 2, Autosomal Dominant 27 17.177
436
P THL005 Thalassemia 56 17.155
437
ACT098 Acute Erythroid Leukemia 55 17.152
438
SMT018 Smith-Mccort Dysplasia 2 34 17.089
439
PFF001 Pfeiffer Syndrome 77 17.063
440
P PLY014 Polycystic Kidney Disease 71 17.056
441
P ACN011 Acne 55 17.051
442
BRT005 Barth Syndrome 55 17.048
443
ENT004 Enthesopathy 51 17.014
444
MNT001 Mantle Cell Lymphoma 65 16.998
445
c GLY008 Glycogen Storage Disease Ii 72 16.997
446
c CRN277 Craniosynostosis 2 37 16.926
447
P MNN013 Meningitis 65 16.913
448
TRC008 Trachoma 53 16.907
449
c EMR018 Emery-Dreifuss Muscular Dystrophy 2, Autosomal Dominant 54 16.878
450
MSL001 Measles 61 16.855
451
INS001 Insulinoma 59 16.815
452
HYP741 Hyperparathyroidism 2 with Jaw Tumors 51 16.808
453
P HYP076 Hyperthyroidism 53 16.776
454
c RBN017 Robinow Syndrome, Autosomal Dominant 2 45 16.754
455
P ADL017 Adult T-Cell Leukemia 53 16.702
456
ECT109 Ectodermal Dysplasia and Immunodeficiency 2 29 16.697
457
BRN004 Brain Edema 54 16.682
458
P SYS005 Systemic Scleroderma 73 16.680
459
IMM034 Immunodeficiency, Common Variable, 2 41 16.636
460
P ANP001 Anaplastic Large Cell Lymphoma 59 16.633
461
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 16.571
462
GLS018 Glass Syndrome 60 16.544
463
P HYP069 Hyperparathyroidism 62 16.532
464
c ACT202 Acth-Independent Macronodular Adrenal Hyperplasia 2 34 16.486
465
c ACT134 Acute Liver Failure 57 16.484
466
c THY102 Thyroid Cancer, Nonmedullary, 2 54 16.391
467
c SCH085 Schizophrenia 2 27 16.334
468
c HYP602 Hyperoxaluria, Primary, Type Ii 51 16.317
469
c PRT060 Parietal Foramina 2 31 16.305
470
c PRD040 Periodontitis, Chronic 52 16.288
471
CMB007 Combined Immunodeficiency 56 16.259
472
PSR001 Psoriatic Arthritis 61 16.247
473
DRR016 Diarrhea 2, with Microvillus Atrophy 55 16.196
474
GST045 Gastroenteritis 58 16.184
475
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 16.136
476
c BRN108 Branchiootic Syndrome 1 63 16.134
477
CHC001 Chickenpox 56 16.094
478
SPL018 Splenomegaly 47 16.091
479
BRN028 Brain Cancer 73 16.082
480
c MYS019 Miyoshi Muscular Dystrophy 2 20 16.053
481
RLP002 Relapsing-Remitting Multiple Sclerosis 56 16.043
482
P FML011 Familial Adenomatous Polyposis 70 15.996
483
SYN007 Synovitis 54 15.985
484
P HDC001 Headache 56 15.969
485
P NPH012 Nephrotic Syndrome 61 15.962
486
CLR109 Colorectal Adenocarcinoma 50 15.925
487
GT001 Gout 63 15.909
488
P HMP007 Hemophilia 52 15.873
489
RNL077 Renal Fibrosis 46 15.864
490
P EPS003 Episodic Ataxia 59 15.863
491
P MCR129 Microvascular Complications of Diabetes 1 67 15.843
492
P ECL001 Eclampsia 52 15.840
493
INT007 Intermediate Coronary Syndrome 53 15.829
494
P ESP024 Esophagitis 60 15.807
495
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 15.717
496
SCH014 Schistosomiasis 56 15.705
497
HMS001 Hemosiderosis 48 15.693
498
P HYP733 Hypercalciuria, Absorptive, 2 45 15.690
499
c HMN022 Human T-Cell Leukemia Virus Type 2 34 15.689
500
PPT005 Peptic Ulcer Disease 58 15.679
501
PLC002 Plica Syndrome 35 15.661
502
GST023 Gastric Ulcer 52 15.599
503
STT001 Status Epilepticus 58 15.586
504
P SCL018 Scoliosis 57 15.547
505
P RRH023 Rare Hereditary Hemochromatosis 52 15.527
506
P SMK004 Smoking As a Quantitative Trait Locus 3 44 15.500
507
P OPN001 Open-Angle Glaucoma 55 15.481
508
TRN018 Transitional Cell Carcinoma 56 15.463
509
P RTN016 Retinal Degeneration 52 15.423
510
P OVR082 Overgrowth Syndrome 41 15.423
511
c GCH016 Gaucher Disease, Type Ii 53 15.419
512
DNT012 Dental Caries 53 15.419
513
CHR074 Choriocarcinoma 46 15.402
514
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 15.392
515
P GRV001 Graves' Disease 54 15.379
516
c FRN048 Frontometaphyseal Dysplasia 2 35 15.365
517
MDD011 Mood Disorder 61 15.328
518
P THY023 Thymoma 64 15.316
519
P MPL001 Maple Syrup Urine Disease 69 15.275
520
c TBR025 Tuberous Sclerosis 1 84 15.270
521
KRT002 Keratomalacia 54 15.265
522
FBR047 Fibromyalgia 57 15.257
523
c THY107 Thymoma, Familial 42 15.253
524
HNS001 Hansen's Disease 32 15.246
525
P CNJ013 Conjunctivitis 66 15.241
526
CRH005 Crohn's Colitis 53 15.239
527
PLM031 Poliomyelitis 62 15.234
528
PLY150 Polykaryocytosis Inducer 29 15.203
529
KRT019 Keratitis, Hereditary 66 15.157
530
CRB150 Cerebral Creatine Deficiency Syndrome 2 54 15.141
532
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 15.112
533
P CTN015 Cutaneous T Cell Lymphoma 48 15.095
534
P ART021 Arteriosclerosis 53 15.093
535
LNG031 Lung Benign Neoplasm 51 15.083
536
DGN001 Degenerative Disc Disease 48 15.073
537
P CHL066 Cholangitis 51 15.027
538
MSC007 Muscle Hypertrophy 64 15.009
539
c GLM025 Glioma Susceptibility 2 30 14.997
540
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 14.968
541
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 44 14.933
542
P END033 Endocarditis 58 14.928
543
ART002 Arts Syndrome 66 14.922
544
c TBL031 Tubulointerstitial Kidney Disease, Autosomal Dominant, 1 48 14.908
545
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 14.866
546
c ACT135 Acute Graft Versus Host Disease 51 14.846
547
P ART023 Arthropathy 59 14.814
548
MDD018 Middle East Respiratory Syndrome 44 14.802
549
c RNL095 Renal-Hepatic-Pancreatic Dysplasia 2 26 14.791
550
ENT011 Enterocolitis 55 14.771
551
P RTN008 Retinitis Pigmentosa 79 14.763
552
c EXS020 Exostoses, Multiple, Type Ii 38 14.748
553
P MLN007 Male Infertility 56 14.732
554
P SCK005 Sickle Cell Disease 56 14.686
555
c HMP029 Hemophilia a 69 14.682
556
c ATM006 Autoimmune Lymphoproliferative Syndrome 75 14.679
557
P LPR021 Leprosy 3 71 14.678
558
P TBR001 Tuberous Sclerosis 69 14.674
559
CLS005 Clouston Syndrome 59 14.653
560
LMY002 Leiomyoma 51 14.612
561
DSS009 Disseminated Intravascular Coagulation 56 14.589
562
MSC157 Muscular Dystrophy, Duchenne Type 78 14.560
563
TRN015 Transient Cerebral Ischemia 62 14.536
564
MNN043 Meningioma, Familial 79 14.529
565
IRR002 Irritable Bowel Syndrome 64 14.506
566
PRM236 Primary Biliary Cholangitis 62 14.485
567
LRY018 Laryngeal Squamous Cell Carcinoma 47 14.419
568
c BSL007 Basal Cell Carcinoma 67 14.410
569
MCL006 Macular Retinal Edema 56 14.399
570
P HML002 Hemolytic Anemia 62 14.375
571
P LYM033 Lymphoproliferative Syndrome 59 14.370
572
P PLY019 Polyneuropathy 52 14.351
573
HDN002 Head Injury 44 14.330
574
HPT022 Hepatoblastoma 54 14.322
575
c ALB021 Albinism, Oculocutaneous, Type Ii 58 14.312
576
EWN003 Ewing Sarcoma 69 14.287
577
c THY109 Thyroid Cancer, Nonmedullary, 1 55 14.256
578
LPT014 Leptin Deficiency or Dysfunction 77 14.250
579
c NRP053 Neuropathy, Hereditary Sensory and Autonomic, Type Iia 67 14.244
580
c SPN395 Spinal Muscular Atrophy, Type Ii 55 14.232
581
P CYS018 Cystitis 58 14.226
582
PLM010 Pulmonary Edema 54 14.213
583
P LRY044 Larynx Cancer 53 14.198
584
INT395 Intracranial Meningioma 47 14.149
585
P HYD006 Hydrocephalus 62 14.133
586
P SBS003 Substance Abuse 54 14.131
587
IMM122 Immunodeficiency 41 with Lymphoproliferation and Autoimmunity 53 14.120
588
P ANT006 Antiphospholipid Syndrome 55 14.107
589
P TMP001 Temporal Lobe Epilepsy 49 14.101
590
MYL005 Myelofibrosis 70 14.097
591
NRL016 Neural Tube Defects 80 14.072
592
HYP080 Hypogonadism 49 14.070
593
CLR108 Colorectal Adenoma 63 14.060
594
HMC014 Homocysteinemia 52 14.051
595
c PRM038 Primary Agammaglobulinemia 47 14.042
596
c EPL115 Epilepsy, Familial Temporal Lobe, 2 36 14.002
597
GNG013 Gingivitis 59 13.994
598
c ART068 Aortic Aneurysm, Familial Thoracic 2 34 13.988
599
P RTN018 Retinal Disease 53 13.959
600
OST003 Osteonecrosis 60 13.954
601
P SLP005 Sleep Disorder 61 13.950
602
OTT002 Otitis Media 70 13.946
603
SPS057 Spasticity 43 13.944
604
VRC005 Varicose Veins 59 13.920
605
c CLC045 Celiac Disease 2 15 13.903
606
P TMR010 Tumor Predisposition Syndrome 69 13.878
607
HMN047 Human Cytomegalovirus Infection 59 13.867
608
HMT002 Hematologic Cancer 61 13.851
609
P PLY018 Polycythemia 56 13.850
610
P URT039 Urticaria 57 13.848
611
P DDN001 Duodenal Ulcer 52 13.844
612
P APL001 Aplastic Anemia 72 13.840
613
P CLC063 Celiac Disease 1 65 13.827
614
GST019 Gastrointestinal Stromal Tumor 78 13.815
615
c PLM163 Palmoplantar Keratoderma, Punctate Type Ii 28 13.775
616
ACT113 Acute Myeloblastic Leukemia with Maturation 46 13.765
617
c MST023 Mesothelioma, Malignant 56 13.754
618
OCL006 Ocular Hypertension 53 13.705
619
SCR001 Secretory Meningioma 40 13.702
620
LYM002 Lymphoplasmacyte-Rich Meningioma 35 13.702
621
c MLT093 Multiple Sclerosis 2 21 13.696
622
P HYP061 Hypertrophic Cardiomyopathy 68 13.673
623
ANT039 Antisynthetase Syndrome 55 13.670
624
ATN011 Autoinflammation with Infantile Enterocolitis 46 13.618
625
MST005 Mastitis 52 13.572
626
CRV045 Cervical Intraepithelial Neoplasia 38 13.539
627
CRV002 Cervix Uteri Carcinoma in Situ 48 13.513
628
CLR030 Clear Cell Renal Cell Carcinoma 53 13.496
629
DYS073 Dysphagia 53 13.481
630
CNV004 Canavan Disease 61 13.426
631
ACT084 Acute Stress Disorder 53 13.421
632
PRT013 Portal Hypertension 59 13.420
633
STT009 Sutton Disease 2 30 13.418
634
FCT001 Factor Viii Deficiency 61 13.383
635
GST092 Gastroesophageal Reflux 59 13.372
636
ATS010 Autosomal Recessive Disease 42 13.361
637
NWC001 Newcastle Disease 47 13.357
638
c DNC008 Diencephalic-Mesencephalic Junction Dysplasia Syndrome 2 22 13.315
639
c ANM042 Anemia, Congenital Dyserythropoietic, Type Ii 50 13.273
640
KRT009 Keratosis 52 13.265
641
THN010 Thanatophoric Dysplasia, Type Ii 44 13.231
642
CNN005 Connective Tissue Disease 66 13.230
643
P ATS406 Autosomal Recessive Pyridoxine-Refractory Sideroblastic Anemia 2 44 13.222
644
ACR007 Acromegaly 70 13.221
645
DNG003 Dengue Disease 65 13.197
646
c ART151 Aortic Aneurysm, Familial Abdominal, 2 13 13.195
647
URT010 Ureteral Obstruction 44 13.172
648
P MYS003 Myasthenia Gravis 67 13.140
649
P MYP006 Myopia 55 13.136
650
CTN007 Cutaneous Leishmaniasis 61 13.124
651
VSC003 Visceral Leishmaniasis 54 13.122
652
c MCL062 Mucolipidosis Ii Alpha/beta 69 13.122
653
P CTR177 Citrullinemia, Type Ii, Adult-Onset 56 13.119
654
VSC058 Vasculitis, Autoinflammation, Immunodeficiency, and Hematologic Defects Syndrome 49 13.091
655
P DYS154 Dystonia 64 13.081
656
P SPN046 Spinal Muscular Atrophy 62 13.051
657
PTT037 Pituitary Tumors 44 13.044
658
RTN017 Retinal Detachment 60 13.037
659
BLP046 Blepharophimosis, Ptosis, and Epicanthus Inversus 56 13.011
660
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 70 13.005
661
INH023 Inherited Cancer-Predisposing Syndrome 53 13.004
662
HYP005 Hypokalemia 55 12.980
663
GLL039 Galloway-Mowat Syndrome 2, X-Linked 21 12.958
664
P SJG008 Sjogren Syndrome 60 12.945
665
P LYN001 Lynch Syndrome 76 12.932
666
MYC079 Myoclonic Epilepsy of Lafora 63 12.921
667
IGG001 Iga Glomerulonephritis 50 12.915
668
MCR316 Microcephaly, Short Stature, and Impaired Glucose Metabolism 2 22 12.914
669
EMB004 Embryonal Carcinoma 55 12.903
670
P CHN012 Chondrosarcoma 56 12.862
671
HRY003 Hairy Cell Leukemia 53 12.849
672
NRL005 Neurilemmoma 60 12.843
673
P MLT074 Multiple Endocrine Neoplasia 58 12.823
674
P MYS005 Myositis 55 12.822
675
RBS001 Rabies 57 12.803
676
CRD132 Cardiac Conduction Defect 59 12.797
677
c FML346 Familial Adenomatous Polyposis 1 65 12.796
678
P SYP003 Syphilis 59 12.795
679
GTR002 Goiter 52 12.781
680
AVN001 Avian Influenza 61 12.762
681
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 12.751
682
P HMN010 Hemangioma 61 12.736
683
P HML001 Hemolytic-Uremic Syndrome 52 12.736
684
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 12.680
685
MYL031 Myeloproliferative Neoplasm 66 12.668
686
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 12.641
687
P SNS001 Sensorineural Hearing Loss 60 12.631
688
BRC012 Brucellosis 66 12.616
689
PLS011 Plasmacytoma 56 12.609
690
NTR005 Nutritional Deficiency Disease 60 12.604
691
P MNC007 Monocytic Leukemia 48 12.601
692
c ATL015 Atelosteogenesis, Type Ii 40 12.597
693
INT066 Interstitial Lung Disease 60 12.593
694
P INT068 Intestinal Disease 53 12.578
695
c BTT014 Beta-Thalassemia 72 12.548
696
PRP080 Peripheral Artery Disease 54 12.542
697
URM002 Uremia 47 12.533
698
END040 Endogenous Depression 54 12.507
699
P ASP006 Aspergillosis 71 12.504
700
c ALP036 Alopecia, Androgenetic, 2 16 12.503
701
c ATM111 Autoimmune Hepatitis Type 2 28 12.497
702
HYP014 Hyperuricemia 51 12.488
703
P DRM010 Dermatomyositis 61 12.485
704
P MCR010 Microcephaly 59 12.423
705
P TXP001 Toxoplasmosis 59 12.414
706
P GLL018 Gallbladder Cancer 59 12.381
707
TCL027 T-Cell Acute Lymphoblastic Leukemia 52 12.357
708
LMB062 Limb Ischemia 55 12.321
709
c ART115 Aortic Valve Disease 1 72 12.305
710
BRN056 Bronchopulmonary Dysplasia 57 12.298
711
RHB001 Rhabdoid Cancer 68 12.278
712
PRP016 Paraplegia 52 12.259
713
PLY001 Polycythemia Vera 69 12.255
714
PSY004 Psychotic Disorder 66 12.232
715
CHR178 Chromosomal Triplication 33 12.232
716
DMY004 Demyelinating Disease 50 12.226
717
c FBR070 Febrile Seizures, Familial, 8 44 12.205
718
CNT047 Contact Dermatitis 56 12.186
719
GNT003 Genital Herpes 54 12.175
720
MYC006 Mycosis Fungoides 64 12.148
721
ETN001 Eating Disorder 59 12.118
722
P LNG028 Long Qt Syndrome 63 12.075
723
c GLC092 Glaucoma, Primary Open Angle 60 12.062
724
c ATS347 Autosomal Dominant Polycystic Kidney Disease 64 12.055
725
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 12.022
726
HRP004 Herpes Zoster 60 12.019
727
PLS009 Plasma Cell Neoplasm 64 12.001
728
SXL003 Sexual Disorder 49 11.983
729
P PTT006 Pituitary Adenoma 55 11.960
730
c CNG415 Congenital Disorder of Glycosylation, Type Ia 58 11.938
731
P LMY004 Leiomyosarcoma 62 11.921
732
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 11.913
733
RSP023 Rasopathy 54 11.902
734
THY111 Thyroid Carcinoma, Familial Medullary 67 11.886
735
OST017 Osteomyelitis 63 11.829
736
P PRN023 Prion Disease 60 11.822
737
c FNC027 Fanconi Anemia, Complementation Group a 80 11.817
738
DYS015 Dysentery 49 11.816
739
P LCH002 Lichen Planus 54 11.810
740
SPP011 Suppression of Tumorigenicity 12 61 11.764
741
c HMN021 Human T-Cell Leukemia Virus Type 1 46 11.744
742
INF034 Infective Endocarditis 53 11.715
743
P MTR014 Motor Neuron Disease 65 11.709
744
c WLM013 Wilms Tumor 1 65 11.687
745
WST005 West Nile Virus 55 11.668
746
INT002 Intermittent Claudication 61 11.660
747
NRN004 Neuroendocrine Tumor 55 11.656
748
THY030 Thyroid Gland Disease 50 11.620
749
MTB004 Metabolic Acidosis 48 11.596
750
VSC002 Vascular Dementia 59 11.583
751
P SYN012 Synpolydactyly 41 11.582
752
c MSC169 Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 1 61 11.580
753
MCR013 Microphthalmia 59 11.575
754
P MLN069 Melanoma, Uveal 59 11.566
755
c OVR114 Ovarian Cancer 1 60 11.563
756
PRD004 Prediabetes Syndrome 52 11.560
757
P TRT010 Teratoma 50 11.557
758
P OPT006 Optic Nerve Disease 57 11.550
759
GST050 Gastrointestinal System Disease 55 11.529
760
JPN002 Japanese Encephalitis 61 11.527
761
RTN020 Retinal Vascular Disease 45 11.523
762
P CRN276 Corneal Endothelial Dystrophy 52 11.516
763
NRT001 Neurotic Disorder 56 11.513
764
PST092 Posttransplant Acute Limbic Encephalitis 29 11.492
765
BRN002 Bronchiolitis 57 11.484
766
HDR007 Hidrotic Ectodermal Dysplasia 2 21 11.474
767
SBC016 Subacute Delirium 42 11.463
768
P PYL005 Pyelonephritis 56 11.443
769
c PLM127 Pulmonary Hypertension, Primary, 3 34 11.433
770
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 62 11.417
771
P CHR012 Chronic Granulomatous Disease 69 11.407
772
P PMP001 Pemphigus 54 11.388
773
PLC008 Placenta Disease 48 11.386
774
AMN003 Amnestic Disorder 53 11.369
775
BRR014 Barrett Esophagus 66 11.367
776
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 11.327
777
MLG079 Malignant Pleural Mesothelioma 42 11.296
778
DWR001 Dwarfism 44 11.268
779
PRN019 Perinatal Necrotizing Enterocolitis 60 11.241
780
ARG004 Argyria 26 11.231
781
SND001 Sandhoff Disease 66 11.227
782
APN008 Apnea, Obstructive Sleep 66 11.224
783
TRY001 Trypanosomiasis 50 11.194
784
P MVM001 Movement Disease 61 11.194
785
P ESS003 Essential Thrombocythemia 68 11.187
786
LWC001 Low Compliance Bladder 44 11.186
787
CRT013 Carotid Stenosis 51 11.180
788
LNG062 Longevity 2 11 11.177
789
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 11.166
790
P HMP002 Hemophagocytic Lymphohistiocytosis 60 11.161
791
NPH009 Nephrolithiasis 54 11.118
792
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 11.112
793
c INF071 Inflammatory Bowel Disease 1 65 11.108
794
MTH009 Mouth Disease 57 11.105
795
ANT024 Anthrax Disease 57 11.099
796
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 11.061
797
c CTR132 Cataract 3, Multiple Types 41 11.051
798
TBC004 Tobacco Addiction 63 11.038
799
P THR015 Thrombophilia 51 11.037
800
IGR001 Ige Responsiveness, Atopic 58 11.002
801
ANR007 Anorexia Nervosa 59 10.999
802
RNL065 Renal Cell Carcinoma, Papillary, 1 79 10.999
803
ABD017 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 46 10.976
804
SYN036 Syncope 44 10.971
805
c SLV029 Silver-Russell Syndrome 2 26 10.967
806
THR004 Thrombocytosis 52 10.967
807
XRD010 Xeroderma Pigmentosum, Variant Type 72 10.932
808
c SCN007 Secondary Hyperparathyroidism 50 10.925
809
P MYT002 Myotonic Dystrophy 51 10.918
810
P SCL009 Sclerosing Cholangitis 46 10.867
811
CHR066 Chronic Fatigue Syndrome 59 10.852
812
c HYD046 Hydatidiform Mole, Recurrent, 1 59 10.838
813
P FCL005 Focal Segmental Glomerulosclerosis 57 10.820
814
P MST009 Mastocytosis 64 10.816
815
LYM040 Lymphoblastic Lymphoma 53 10.795
816
P MMB011 Membranous Nephropathy 50 10.789
817
FDL002 Food Allergy 47 10.785
818
SCK003 Sickle Cell Anemia 74 10.782
819
KWS002 Kawasaki Disease 65 10.738
820
DBT084 Diabetes Mellitus, Ketosis-Prone 59 10.727
821
P RBL001 Rubella 58 10.721
822
HRT011 Heart Septal Defect 49 10.716
823
NRT004 Neuritis 53 10.716
824
THY125 Thyroid Gland Medullary Carcinoma 48 10.712
825
CMM005 Common Cold 55 10.699
826
AND005 Androgen Insensitivity Syndrome, Mild 21 10.686
827
APH002 Aphasia 55 10.682
828
P MCR258 Microcephalic Osteodysplastic Primordial Dwarfism, Type Ii 55 10.672
829
HML018 Homologous Wasting Disease 21 10.669
830
BLR008 Bilirubin Metabolic Disorder 57 10.652
831
c PRS136 Prostate Cancer, Hereditary, 6 33 10.650
832
MST004 Mast Cell Neoplasm 41 10.622
833
HST010 Histiocytosis 49 10.621
834
FRN006 Frontotemporal Dementia 68 10.587
835
EXT007 Extracutaneous Mastocytoma 38 10.585
836
TND005 Tendinitis 53 10.555
837
ATN004 Autonomic Neuropathy 42 10.546
838
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 10.532
839
DCT002 Ductal Carcinoma in Situ 58 10.519
840
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 10.512
841
P THR005 Thrombotic Thrombocytopenic Purpura 64 10.487
842
ATR057 Atrioventricular Block 54 10.486
843
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 10.471
844
MTR002 Mitral Valve Insufficiency 51 10.460
845
TRT001 Teratocarcinoma 41 10.445
846
HPT004 Hepatic Coma 43 10.440
847
CRT015 Carotid Artery Occlusion 45 10.433
848
FLR002 Filariasis 55 10.429
849
PNC001 Pancytopenia 52 10.414
850
P VNW001 Von Willebrand's Disease 64 10.410
851
SLP001 Sleeping Sickness 56 10.402
852
CRN030 Coronary Stenosis 50 10.394
853
ATN005 Autonomic Dysfunction 45 10.386
854
P LCT001 Lactic Acidosis 50 10.384
855
VGN023 Vaginitis 56 10.373
856
c DWL002 Dowling-Degos Disease 1 58 10.372
857
PLS007 Plasmodium Falciparum Malaria 52 10.364
858
END041 Endometrial Adenocarcinoma 63 10.359
859
FCL014 Focal Epilepsy 53 10.341
860
DNG002 Dengue Hemorrhagic Fever 59 10.340
861
P HYP265 Hypotonia 42 10.334
862
c GLL024 Gallbladder Disease 1 53 10.332
863
DRM011 Dermatophytosis 52 10.317
864
CLF027 Cleft Palate, Isolated 64 10.300
865
LYM017 Lyme Disease 63 10.289
866
c CHL119 Cholangitis, Primary Sclerosing 57 10.277
867
MCR385 Microcephaly, Epilepsy, and Diabetes Syndrome 2 15 10.249
868
MLC004 Mulchandani-Bhoj-Conlin Syndrome 51 10.232
869
c CHR417 Chronic Graft Versus Host Disease 55 10.224
870
c PRS130 Prostate Cancer, Hereditary, 8 32 10.223
871
c HYP724 Hyperlipoproteinemia, Type Iii 66 10.222
872
MCR004 Macroglobulinemia 48 10.219
873
P CHR071 Charcot-Marie-Tooth Disease 64 10.219
874
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 69 10.213
875
OBS002 Obsessive-Compulsive Disorder 67 10.204
876
P BNC003 Bone Cancer 58 10.190
877
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 60 10.176
878
c BCT007 Bacterial Meningitis 55 10.168
879
P DMN001 Diamond-Blackfan Anemia 73 10.159
880
BRS099 Breast Ductal Carcinoma 61 10.151
881
CRN237 Corneal Dystrophy, Avellino Type 41 10.129
882
TST014 Testicular Cancer 51 10.129
883
FCL081 Focal Cortical Dysplasia, Type Ii 60 10.109
884
ADN011 Adenoid Cystic Carcinoma 68 10.108
885
P LPS002 Liposarcoma 64 10.067
886
CRD223 Cardiac Arrhythmia 63 10.058
887
P PRM002 Primary Hyperoxaluria 65 10.055
888
HSH003 Hashimoto Thyroiditis 60 10.045
889
PLR008 Pleurisy 49 10.041
890
KRT006 Keratoconjunctivitis 53 10.034
891
DBT006 Diabetic Macular Edema 48 10.026
892
ILS001 Ileus 49 10.019
893
P ALP009 Alopecia Areata 59 10.011
895
c CNG112 Congenital Muscular Dystrophy Type 1a 32 10.004
896
FNG017 Fungal Infectious Disease 54 9.999
897
P ANG015 Angioedema 56 9.989
898
KLD004 Keloid Disorder 38 9.978
899
TNG007 Tongue Carcinoma 55 9.942
900
HPT019 Hepatic Encephalopathy 59 9.937
901
CRY035 Cryptorchidism, Unilateral or Bilateral 57 9.918
902
TYP007 Typhoid Fever 63 9.896
903
KHN001 Kuhnt-Junius Degeneration 48 9.890
904
LMY014 Leiomyoma, Uterine 55 9.871
905
LYM009 Lymphocytic Choriomeningitis 46 9.867
906
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 51 9.865
907
CMM004 Common Variable Immunodeficiency 71 9.860
908
CHR100 Chronic Ulcer of Skin 57 9.835
909
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 9.827
910
CRB090 Cerebral Hypoxia 42 9.824
911
CND006 Candida Glabrata 29 9.823
912
LNG108 Langerhans Cell Histiocytosis 57 9.818
913
c FML021 Familial Hypercholesterolemia 71 9.804
914
P SHR001 Short Bowel Syndrome 53 9.802
915
RST023 Resting Heart Rate, Variation in 40 9.792
916
ING001 Inguinal Hernia 59 9.777
917
SRC027 Sarcoma, Synovial 58 9.772
918
PCK003 Pick Disease of Brain 70 9.772
919
P PLY041 Polymyositis 58 9.763
920
P MTR004 Maturity-Onset Diabetes of the Young 66 9.750
921
TNS005 Tonsillitis 57 9.719
922
YLL002 Yellow Fever 61 9.715