Search results for tbp

593 hits were found for tbp

# Family MCID Name MIFTS Score
1
c SPN296 Spinocerebellar Ataxia 17 47 45.980
2
P PRK057 Parkinson Disease, Late-Onset 79 29.070
3
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 17.807
4
P RTN024 Retinoblastoma 72 16.135
5
P HRP006 Herpes Simplex 65 15.705
6
P HNT016 Huntington Disease 73 15.250
7
P SCH015 Schizophrenia 74 12.201
8
c HRD026 Hereditary Ataxia 46 12.201
9
DNT005 Dentatorubral-Pallidoluysian Atrophy 59 11.548
10
P MCH002 Machado-Joseph Disease 63 11.091
11
IMM167 Immune Deficiency Disease 77 10.949
12
P RTN016 Retinal Degeneration 52 10.785
13
P DYS154 Dystonia 64 10.357
14
P FRD001 Friedreich Ataxia 62 9.973
15
c SPN293 Spinocerebellar Ataxia 12 45 9.938
16
FCL022 Focal Dystonia 41 9.892
17
CHR105 Choreoacanthocytosis 55 9.781
18
P RST001 Restless Legs Syndrome 52 9.781
19
TBR008 Tuberculous Peritonitis 35 8.458
20
CHR073 Choreatic Disease 53 8.403
21
c HNT004 Huntington Disease-Like 2 51 8.286
22
c HNT010 Huntington Disease-Like 1 55 7.866
23
PLR001 Pleural Tuberculosis 49 7.836
24
P MVM001 Movement Disease 61 7.284
25
c SPN294 Spinocerebellar Ataxia 1 53 7.249
26
c SPN309 Spinocerebellar Ataxia 6 58 7.073
27
ABD004 Abdominal Tuberculosis 39 7.073
28
SPN404 Spinal and Bulbar Muscular Atrophy, X-Linked 1 61 7.027
29
P RTN008 Retinitis Pigmentosa 79 7.027
30
CRB027 Cerebellar Disease 47 7.027
31
TNB001 Tinea Barbae 27 6.916
32
DSS008 Disease of Mental Health 74 6.916
33
TBR009 Tuberculous Empyema 23 6.916
34
DYS064 Dystonia 3, Torsion, X-Linked 45 6.916
35
GST051 Gastrointestinal Tuberculosis 36 6.916
36
PRC005 Pericardial Tuberculosis 33 6.916
37
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 4.393
38
HLX001 Helix Syndrome 47 2.580
39
EMB004 Embryonal Carcinoma 55 2.020
40
c TYP009 Type 2 Diabetes Mellitus 92 1.908
41
P BRS047 Breast Cancer 97 1.671
42
P MSC003 Muscular Atrophy 52 1.667
43
PRT036 Peritonitis 65 1.646
44
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 1.643
45
c LKM005 Leukemia, T-Cell, Chronic 33 1.643
46
TMT002 Temtamy Preaxial Brachydactyly Syndrome 54 1.622
47
P THL005 Thalassemia 56 1.546
48
P OVR042 Ovarian Cancer 88 1.520
49
HMN044 Human Immunodeficiency Virus Type 1 76 1.508
50
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 40 1.486
51
STM007 Stomatitis 52 1.470
52
VCC001 Vaccinia 49 1.383
53
ADN018 Adenoma 58 1.371
54
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 1.346
55
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 1.346
56
RCK004 Rickets 65 1.336
57
c HPT073 Hepatitis C Virus 71 1.267
58
P NRF002 Neurofibromatosis 60 1.250
59
P SZR006 Seizure Disorder 69 1.243
60
P END044 Endometriosis 62 1.190
61
ISC004 Ischemia 61 1.179
62
RYS001 Reye Syndrome 49 1.179
63
c DNT047 Dentinogenesis Imperfecta Type 2 35 1.179
64
48X005 48,xyyy 39 1.119
65
c BLD140 Blood Group, I System 47 1.115
66
KRT002 Keratomalacia 54 1.115
67
NNL006 Non-Alcoholic Steatohepatitis 54 1.106
68
P PTT006 Pituitary Adenoma 55 1.106
69
c HMP004 Hemophilia B 68 1.079
70
THR016 Thrombophlebitis 50 1.079
71
P HMP007 Hemophilia 52 1.079
72
P ADL017 Adult T-Cell Leukemia 54 1.065
73
RPD005 Rapidly Involuting Congenital Hemangioma 48 1.065
74
P MLN008 Melanoma 75 1.021
75
c AMY091 Amyotrophic Lateral Sclerosis 1 88 1.020
76
P LTR001 Lateral Sclerosis 58 1.020
77
PLR008 Pleurisy 49 1.015
78
ONC007 Oncocytoma 49 1.004
79
P MCR010 Microcephaly 59 0.987
80
P DMN002 Dementia 65 0.987
81
P MNN013 Meningitis 65 0.987
82
c SCL052 Scleroderma, Familial Progressive 60 0.969
83
CNN005 Connective Tissue Disease 66 0.969
84
CHR074 Choriocarcinoma 46 0.969
85
CYT002 Cytokine Deficiency 43 0.969
86
P HYP838 Hyperlipidemia, Familial Combined, 3 61 0.950
87
HRY003 Hairy Cell Leukemia 61 0.950
88
P LKM002 Leukemia 66 0.950
89
c NRD008 Neurodegeneration with Brain Iron Accumulation 3 54 0.930
90
GLC003 Glucose Intolerance 53 0.930
91
P BLN001 Blount's Disease 36 0.930
92
SPN186 Spinal Cord Injury 61 0.930
93
c SYS001 Systemic Lupus Erythematosus 86 0.908
94
PTT037 Pituitary Tumors 44 0.908
95
FNC007 Functioning Pituitary Adenoma 42 0.908
96
P LPS004 Lupus Erythematosus 61 0.908
97
P MYT002 Myotonic Dystrophy 51 0.908
98
NNF007 Non-Functioning Pituitary Adenoma 39 0.908
99
P FRG001 Fragile X Syndrome 70 0.884
100
ANT024 Anthrax Disease 58 0.884
101
ETN001 Eating Disorder 59 0.884
102
ARG004 Argyria 26 0.884
103
P NSP012 Nasopharyngeal Carcinoma 60 0.858
104
AMB001 Amebiasis 56 0.858
105
c SPR162 Spermatogenic Failure 50 42 0.828
106
AZS001 Azoospermia 45 0.828
107
c LKM061 Leukemia, Acute Myeloid 83 0.828
108
P MYL006 Myeloid Leukemia 60 0.828
109
VRL011 Viral Infectious Disease 60 0.828
110
SVR001 Severe Acute Respiratory Syndrome 68 0.793
111
P CRB088 Cerebral Atrophy 33 0.793
112
P PNC035 Pancreatic Cancer 86 0.772
113
PRC013 Pericarditis 53 0.751
114
P FML011 Familial Adenomatous Polyposis 71 0.747
115
GLN002 Glanders 38 0.747
116
PLG002 Plague 58 0.747
117
HYP056 Hypoglycemia 65 0.743
118
PLM001 Pulmonary Tuberculosis 69 0.718
119
P LNG032 Lung Cancer 98 0.709
120
47X002 47,xyy 48 0.700
121
HMP009 Haemophilus Influenzae 41 0.682
122
P DBT009 Diabetes Mellitus 67 0.637
123
c SML038 Small Cell Cancer of the Lung 69 0.616
124
LMB062 Limb Ischemia 55 0.606
125
P PRK039 Parkinsonism 55 0.575
126
HYP266 Hypoxia 56 0.575
127
HRW001 Hair Whorl 35 0.565
128
PRP027 Peripheral Vascular Disease 71 0.554
129
TCK004 Tick Infestation 29 0.554
130
CLL010 Cellular Ependymoma 58 0.551
131
LYM017 Lyme Disease 63 0.542
132
P MYC084 Mycobacterium Tuberculosis 1 68 0.531
133
THL004 Theileriasis 26 0.519
134
P ADN016 Adenocarcinoma 63 0.507
135
CRB037 Cerebral Palsy 67 0.507
136
c TBR025 Tuberous Sclerosis 1 84 0.495
137
P TBR001 Tuberous Sclerosis 69 0.483
138
BNR002 Bone Resorption Disease 47 0.470
139
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.470
140
LVR012 Liver Cirrhosis 62 0.456
141
PPL022 Papilloma 53 0.443
142
SQM002 Squamous Cell Papilloma 45 0.443
143
TRC037 Tracheobronchomalacia 23 0.443
144
CYS001 Cystic Fibrosis 77 0.429
145
P BLD134 Bladder Cancer 79 0.414
146
P NRB001 Neuroblastoma 66 0.414
147
P ALZ034 Alzheimer Disease 87 0.399
148
P URN019 Urinary Tract Infection 49 0.399
149
SQM006 Squamous Cell Carcinoma 59 0.399
150
P THR014 Thrombocytopenia 66 0.399
151
CNS002 Constrictive Pericarditis 39 0.399
152
CHC001 Chickenpox 56 0.399
153
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.384
154
CLT003 Colitis 63 0.384
155
GLB002 Glioblastoma 67 0.384
156
P SBS003 Substance Abuse 54 0.384
157
P HYD006 Hydrocephalus 63 0.384
158
P LVR013 Liver Disease 68 0.384
159
P SKN015 Skin Carcinoma 71 0.384
160
P GST053 Gastric Cancer 82 0.367
161
NNL005 Non-Alcoholic Fatty Liver Disease 63 0.367
162
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 0.367
163
P HYP750 Hypertriglyceridemia, Familial 62 0.367
164
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 0.367
165
SPS004 Spastic Quadriplegia 39 0.367
166
HYP060 Hyperinsulinism 53 0.367
167
EHR002 Ehrlichiosis 39 0.367
168
SQM013 Squamous Cell Carcinoma, Head and Neck 75 0.367
169
TBR011 Tuberculous Meningitis 48 0.367
170
SKN019 Skin Melanoma 70 0.367
171
FTT001 Fatty Liver Disease 61 0.367
172
INH017 Inherited Congenital Spastic Tetraplegia 23 0.367
173
TNG007 Tongue Carcinoma 55 0.350
174
TCK001 Tick-Borne Encephalitis 59 0.350
175
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 0.350
176
TXC005 Toxic Shock Syndrome 62 0.350
177
GLM045 Glioma 62 0.350
178
GLL048 Glial Tumor 52 0.350
179
P CRB059 Cerebellar Degeneration 36 0.350
180
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 0.332
181
P EXN002 Exanthem 58 0.332
182
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 0.332
183
LYM027 Lymphopenia 56 0.332
184
P PRN023 Prion Disease 60 0.332
185
P MYC033 Myoclonus 46 0.332
186
BBS001 Babesiosis 49 0.332
187
ULC004 Ulcerative Colitis 74 0.332
188
HMR014 Hemorrhagic Shock and Encephalopathy Syndrome 19 0.332
189
NSS002 Neisseria Meningitidis Infection 47 0.332
190
MNN020 Meningococcal Infection 45 0.332
191
P ERY048 Erythrocytosis, Familial, 2 56 0.313
192
P TMR010 Tumor Predisposition Syndrome 69 0.313
193
DSS032 Disease by Infectious Agent 55 0.313
194
c PRC016 Pre-Eclampsia 64 0.313
195
MNN032 Meningococcal Meningitis 52 0.313
196
VNH007 Von Hippel-Lindau Syndrome 73 0.313
197
HPT067 Hepatocellular Adenoma 42 0.313
198
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 70 0.313
199
ALP103 Alpha-1-Antitrypsin Deficiency 67 0.313
200
P PRT096 Peritoneal Mesothelioma 49 0.313
201
P ART021 Arteriosclerosis 53 0.313
202
P BNG032 Benign Mesothelioma 53 0.313
203
ALV003 Alveoli Adenoma 20 0.313
204
c MLG002 Malignant Peritoneal Mesothelioma 42 0.313
205
INH023 Inherited Cancer-Predisposing Syndrome 53 0.313
206
LYM133 Lymphoma, Hodgkin, Classic 74 0.293
207
P PLM037 Pulmonary Hypertension 69 0.293
208
P LCT002 Lactose Intolerance 52 0.293
209
P OST002 Osteoporosis 77 0.293
210
P MLT020 Multiple Sclerosis 79 0.293
211
P SLP006 Sleep Apnea 69 0.293
212
P LYM118 Lymphoma 69 0.293
213
GLC086 Glucocorticoid-Induced Osteoporosis 43 0.293
214
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 0.293
215
KPS004 Kaposi Sarcoma 76 0.293
216
CRD132 Cardiac Conduction Defect 59 0.293
217
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.293
218
P VSC007 Vascular Disease 62 0.293
219
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.293
220
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.293
221
SDD001 Sudden Infant Death Syndrome 60 0.293
222
P HYP076 Hyperthyroidism 53 0.293
223
MYL069 Myeloma, Multiple 77 0.271
224
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 46 0.271
225
MLD018 Mild Cognitive Impairment 48 0.271
226
MCR013 Microphthalmia 60 0.271
227
URL001 Urolithiasis 45 0.271
228
P EPD083 Epidermodysplasia Verruciformis 1 57 0.271
229
P CLR023 Colorectal Cancer 100 0.271
230
CRT072 Creutzfeldt-Jakob Disease 67 0.271
231
c BTT014 Beta-Thalassemia 72 0.271
232
P RSP003 Respiratory Failure 74 0.271
233
P HPT023 Hepatocellular Carcinoma 95 0.271
234
MLT157 Multiple System Atrophy 1 69 0.271
235
P EPL164 Epilepsy 70 0.271
236
c VRL010 Viral Hepatitis 52 0.271
237
BTT017 Beta-Thalassemia Major 53 0.271
238
ACT098 Acute Erythroid Leukemia 55 0.271
239
P INF032 Infertility 60 0.271
240
ADR008 Adrenal Adenoma 55 0.271
241
SPT005 Spotted Fever 49 0.271
242
P HYP069 Hyperparathyroidism 62 0.271
243
MTH009 Mouth Disease 57 0.271
244
SKN016 Skin Disease 62 0.271
245
HYP066 Hyperglycemia 60 0.271
246
SPS057 Spasticity 43 0.271
247
APP008 Appendicitis 62 0.271
248
CRV035 Cervical Cancer 72 0.248
249
c SPN283 Spinocerebellar Ataxia 37 35 0.248
250
P INF037 Inflammatory Bowel Disease 53 0.248
251
HMN002 Human Granulocytic Anaplasmosis 31 0.248
252
BCT022 Bacterial Infectious Disease 56 0.248
253
OCL051 Ocular Tuberculosis 29 0.248
254
P SPN301 Spinocerebellar Ataxia 2 59 0.248
255
c ATS007 Autism Spectrum Disorder 72 0.248
256
MTB004 Metabolic Acidosis 48 0.248
257
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 0.248
258
ATM095 Autoimmune Disease 61 0.248
259
c PLM127 Pulmonary Hypertension, Primary, 3 34 0.248
260
P PRG013 Paraganglioma 57 0.248
261
P UVT001 Uveitis 57 0.248
262
CMP010 Complex Regional Pain Syndrome 59 0.248
263
c ACT027 Acute Pancreatitis 60 0.248
264
P PNC044 Pancreatitis 61 0.248
265
c HPT016 Hepatitis B 62 0.248
266
KRT009 Keratosis 52 0.248
267
c INT064 Intermediate Uveitis 54 0.248
268
FCL012 Facial Paralysis 49 0.248
269
P PNV001 Panuveitis 48 0.248
270
HMP001 Hemopericardium 47 0.248
271
PRT038 Protein-Energy Malnutrition 53 0.248
272
P PRC012 Pericardial Effusion 50 0.248
273
P TMP001 Temporal Lobe Epilepsy 49 0.248
274
PNN001 Panniculitis 52 0.248
275
OVR094 Ovarian Epithelial Cancer 39 0.248
276
P TRM003 Tremor 50 0.248
277
P LCH002 Lichen Planus 55 0.248
278
P KDN018 Kidney Disease 72 0.248
279
c BCT007 Bacterial Meningitis 55 0.248
280
TBL029 Tubulin, Beta 28 0.221
281
FRN006 Frontotemporal Dementia 68 0.221
282
DYS002 Dysplastic Nevus Syndrome 54 0.221
283
ALC007 Alcohol Dependence 65 0.221
284
P KLZ004 Kala-Azar 1 41 0.221
285
CLF027 Cleft Palate, Isolated 64 0.221
286
c TBR026 Tuberous Sclerosis 2 71 0.221
287
TNP004 Tn Polyagglutination Syndrome 42 0.221
288
EWN003 Ewing Sarcoma 70 0.221
289
P GLM040 Glioma Susceptibility 1 70 0.221
290
P ATS364 Autism 72 0.221
291
EXT033 Extrapulmonary Tuberculosis 45 0.221
292
c SCN036 Secondary Progressive Multiple Sclerosis 55 0.221
293
RNL011 Renal Osteodystrophy 48 0.221
294
MLG169 Malignant Astrocytoma 57 0.221
295
IMP005 Impotence 52 0.221
296
P GRV001 Graves' Disease 54 0.221
297
ATN004 Autonomic Neuropathy 42 0.221
298
P SYP003 Syphilis 59 0.221
299
c SCN007 Secondary Hyperparathyroidism 51 0.221
300
HYP798 Hypophosphatemic Rickets, X-Linked Recessive 60 0.221
301
c CHR684 Chronic Kidney Disease 74 0.221
302
DYS073 Dysphagia 53 0.221
303
P HYP265 Hypotonia 42 0.221
304
VSC003 Visceral Leishmaniasis 54 0.221
305
CLF001 Cleft Lip 54 0.221
306
CLR030 Clear Cell Renal Cell Carcinoma 54 0.221
307
LSH001 Leishmaniasis 63 0.221
308
CRT015 Carotid Artery Occlusion 45 0.221
309
P NRP001 Neuropathy 59 0.221
310
GNT003 Genital Herpes 54 0.221
311
CNG120 Congenital Pseudoarthrosis 15 0.221
312
GNT189 Genetic Prion Disease 19 0.221
313
GRN005 Granuloma Inguinale 31 0.221
314
CLF056 Cleft Lip with or Without Cleft Palate 43 0.221
315
CNG284 Congenital Pseudoarthrosis of the Tibia 17 0.221
316
P PRS040 Prostate Cancer 95 0.192
317
CHR072 Chordoma 57 0.192
318
SCC001 Succinic Semialdehyde Dehydrogenase Deficiency 59 0.192
319
TRC038 Tracheobronchomegaly 27 0.192
320
WST001 West Syndrome 64 0.192
321
P SNS001 Sensorineural Hearing Loss 59 0.192
322
PNG002 Pain Agnosia 51 0.192
323
P CRD119 Cardiac Arrest 68 0.192
324
c FBR080 Fibromatosis, Gingival, 4 15 0.192
325
P MLN066 Melanoma, Cutaneous Malignant 1 66 0.192
326
c SPN291 Spinocerebellar Ataxia 7 50 0.192
327
c RTN129 Retinitis Pigmentosa 49 38 0.192
328
SRC014 Sarcoma 64 0.192
329
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 0.192
330
P CCK001 Cockayne Syndrome 68 0.192
331
ACQ007 Acquired Immunodeficiency Syndrome 58 0.192
332
URT010 Ureteral Obstruction 45 0.192
333
BLT006 Bilateral Breast Cancer 49 0.192
334
URM002 Uremia 47 0.192
335
c HPT001 Hepatitis C 61 0.192
336
P KDN017 Kidney Cancer 60 0.192
337
RLP003 Relapsing Fever 50 0.192
338
PRS047 Prostatitis 58 0.192
339
P CYS018 Cystitis 59 0.192
340
P RHN004 Rhinitis 57 0.192
341
CNS004 Constipation 56 0.192
342
P LPS002 Liposarcoma 64 0.192
343
GST040 Gastric Adenocarcinoma 66 0.192
344
P CHR345 Chronic Pain 50 0.192
345
SPN035 Spindle Cell Sarcoma 51 0.192
346
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.192
347
c HNT013 Huntington Disease-Like Syndrome 18 0.192
348
ANX004 Anoxia 40 0.192
349
P BRN022 Bronchiectasis 59 0.192
350
PTH003 Pathologic Nystagmus 52 0.192
351
ART008 Arteriosclerosis Obliterans 40 0.192
352
HDN002 Head Injury 44 0.192
353
P FBR031 Febrile Seizures 52 0.192
354
BP1002 Bap1 Tumor Predisposition Syndrome 42 0.192
355
P ENC004 Encephalitis 61 0.192
356
MD2001 Med23 18 0.192
357
MNR004 Mounier-Kuhn Syndrome 23 0.192
358
c HMN021 Human T-Cell Leukemia Virus Type 1 46 0.192
359
PRX097 Paroxysmal Dystonia 32 0.192
360
P OVR082 Overgrowth Syndrome 42 0.192
361
THY029 Thyroid Carcinoma 54 0.192
362
c CCK007 Cockayne Syndrome B 56 0.157
363
OBS037 Obesity-Hypoventilation Syndrome 44 0.157
364
OCL069 Ocular Motor Apraxia 57 0.157
365
AGN016 Aging 54 0.157
366
XRD010 Xeroderma Pigmentosum, Variant Type 72 0.157
367
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 0.157
368
c THY109 Thyroid Cancer, Nonmedullary, 1 55 0.157
369
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.157
370
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 0.157
371
ADR016 Adrenal Cortical Carcinoma 61 0.157
372
P PLY041 Polymyositis 59 0.157
373
MDD018 Middle East Respiratory Syndrome 44 0.157
374
P DRM010 Dermatomyositis 61 0.157
375
CRP032 Corpus Callosum, Agenesis of 49 0.157
376
ORL015 Oral Squamous Cell Carcinoma 43 0.157
377
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.157
378
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 0.157
379
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 0.157
380
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 0.157
381
MLR004 Malaria 78 0.157
382
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.157
383
NND010 Nondisjunction 34 0.157
384
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.157
385
BNB002 Bainbridge-Ropers Syndrome 45 0.157
386
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.157
387
HRN029 Hearing Loss, Noise-Induced 37 0.157
388
c CRN216 Craniosynostosis 5 21 0.157
389
c BRD016 Bardet-Biedl Syndrome 4 44 0.157
390
ADR054 Adrenocortical Carcinoma, Hereditary 47 0.157
391
HTC003 Hutchinson-Gilford Progeria Syndrome 65 0.157
392
P LKM071 Leukemia, Chronic Lymphocytic 74 0.157
393
STT001 Status Epilepticus 58 0.157
394
P ALC033 Alcohol Use Disorder 67 0.157
395
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.157
396
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.157
397
P HRD011 Hereditary Spherocytosis 63 0.157
398
LPD008 Lipid Metabolism Disorder 61 0.157
399
HMG005 Hemoglobinopathy 55 0.157
400
BRN024 Bronchitis 67 0.157
401
PLM031 Poliomyelitis 62 0.157
402
c ATM011 Autoimmune Hepatitis 62 0.157
403
P ADN017 Adenofibroma 33 0.157
404
P CRD246 Cardiovascular System Disease 55 0.157
405
HPT019 Hepatic Encephalopathy 59 0.157
406
P HYP086 Hypothyroidism 69 0.157
407
c PRM005 Primary Hyperparathyroidism 59 0.157
408
P MLN007 Male Infertility 56 0.157
409
P OTS001 Otosclerosis 49 0.157
410
P RHB003 Rhabdomyosarcoma 66 0.157
411
P FBR017 Fibrosarcoma 55 0.157
412
P ART023 Arthropathy 60 0.157
413
ADR004 Adrenal Cortical Adenocarcinoma 38 0.157
414
ANP005 Anaplastic Astrocytoma 59 0.157
415
OST159 Osteogenic Sarcoma 66 0.157
416
MDS022 Mediastinitis 47 0.157
417
CRB090 Cerebral Hypoxia 42 0.157
418
DNT001 Dental Fluorosis 42 0.157
419
CHL149 Childhood Acute Myeloid Leukemia 42 0.157
420
HYP082 Hypopharynx Cancer 47 0.157
421
BRN071 Brain Injury 50 0.157
422
LNG099 Lung Disease 62 0.157
423
CRH001 Crohn's Disease 80 0.157
424
DFF016 Diffuse Astrocytoma 48 0.157
425
CRL001 Cerulean Cataract 26 0.157
426
TRM010 Traumatic Brain Injury 50 0.157
427
ILS001 Ileus 49 0.157
428
CHL061 Childhood Leukemia 47 0.157
429
PRT029 Parathyroid Adenoma 51 0.157
430
SGC002 Sgce Myoclonus-Dystonia 23 0.157
431
ALL006 Allergic Asthma 56 0.157
432
CTN020 Cutaneous Sclerosis 16 0.157
433
LRN003 Learning Disability 49 0.157
434
OCL006 Ocular Hypertension 53 0.157
435
PSD088 Pseudobulbar Affect 33 0.157
436
FCL090 Facial Cleft 30 0.157
437
TCL024 T-Cell Non-Hodgkin Lymphoma 39 0.157
438
PRR019 Perioral Myoclonia with Absences 27 0.157
439
c STC015 Stickler Syndrome, Type I 51 0.111
440
c EPS035 Episodic Ataxia, Type 2 63 0.111
441
P SRC025 Sarcoidosis 1 70 0.111
442
P CRY007 Cryoglobulinemia, Familial Mixed 49 0.111
443
P MJR007 Major Affective Disorder 1 42 0.111
444
P CHN012 Chondrosarcoma 56 0.111
445
PRS129 Prostatic Hyperplasia, Benign 48 0.111
446
c NML003 Nemaline Myopathy 2 51 0.111
447
P AST005 Asthma 76 0.111
448
ABT001 Abetalipoproteinemia 68 0.111
449
MYP106 Myopathy, Myosin Storage, Autosomal Recessive 33 0.111
450
INS024 Insulin-Like Growth Factor I 77 0.111
451
WLS001 Wilson Disease 70 0.111
452
c CRD185 Ceroid Lipofuscinosis, Neuronal, 6 54 0.111
454
HMC014 Homocysteinemia 52 0.111
455
c MCR133 Microvascular Complications of Diabetes 4 41 0.111
456
c MCR115 Microvascular Complications of Diabetes 5 65 0.111
457
HTS002 Heat-Shock Rna 1 9 0.111
458
c SPN308 Spinocerebellar Ataxia 28 46 0.111
459
ACT119 Acute Promyelocytic Leukemia 62 0.111
460
CRB147 Cerebellofaciodental Syndrome 34 0.111
461
c MYS082 Myasthenic Syndrome, Congenital, 25, Presynaptic 27 0.111
462
c SPS233 Spastic Ataxia 9, Autosomal Recessive 21 0.111
463
PRT251 Proteinuria, Chronic Benign 58 0.111
464
ATS010 Autosomal Recessive Disease 42 0.111
465
P GRF003 Graft-Versus-Host Disease 71 0.111
466
c SPS101 Spastic Paraplegia 56, Autosomal Recessive 42 0.111
467
c PRM108 Primary Progressive Multiple Sclerosis 51 0.111
468
c CRB221 Cerebellar Ataxia Type 48 22 0.111
469
NRR001 Neuroretinitis 42 0.111
470
P OPN001 Open-Angle Glaucoma 55 0.111
471
P LKD001 Leukodystrophy 58 0.111
472
P CRB045 Cerebellar Hypoplasia 40 0.111
473
SLP001 Sleeping Sickness 56 0.111
474
PRM013 Premature Menopause 57 0.111
475
c MGR028 Migraine with or Without Aura 1 64 0.111
476
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 0.111
477
c ATR087 Atrial Standstill 1 74 0.111
478
c SPN225 Spondyloarthropathy 1 70 0.111
479
TMT003 Temtamy Syndrome 37 0.111
480
P KRB001 Krabbe Disease 69 0.111
481
P HYP760 Hypothyroidism, Congenital, Nongoitrous, 2 54 0.111
482
BRN032 Brain Glioma 45 0.111
483
RNL077 Renal Fibrosis 46 0.111
484
P SYN012 Synpolydactyly 38 0.111
485
P PNT019 Pontocerebellar Hypoplasia 45 0.111
486
c DVL067 Developmental and Epileptic Encephalopathy 42 34 0.111
487
c SPN427 Spinocerebellar Ataxia 48 30 0.111
488
END057 Endometrial Cancer 71 0.111
489
P MYC007 Myocardial Infarction 69 0.111
490
c CRD179 Ceroid Lipofuscinosis, Neuronal, 7 49 0.111
491
ALL003 Allergic Rhinitis 66 0.111
492
c NMN016 Niemann-Pick Disease, Type B 56 0.111
493
INT323 Intraocular Pressure Quantitative Trait Locus 63 0.111
494
P ATT013 Attention Deficit-Hyperactivity Disorder 66 0.111
495
c HYP595 Hypertension, Essential 84 0.111
496
CHR630 Chorea, Benign Hereditary 42 0.111
497
PPL052 Papillomatosis, Confluent and Reticulated 34 0.111
498
c CWD006 Cowden Syndrome 1 79 0.111
499
c MCR113 Microvascular Complications of Diabetes 3 52 0.111
500
P HMN032 Human Herpesvirus 8 47 0.111
501
c MCR130 Microvascular Complications of Diabetes 6 41 0.111
502
c MCR120 Microvascular Complications of Diabetes 7 47 0.111
503
c MJR024 Major Affective Disorder 9 40 0.111
504
c LBR008 Leber Congenital Amaurosis 13 41 0.111
505
c SPN311 Spinocerebellar Ataxia 13 48 0.111
506
c SPN312 Spinocerebellar Ataxia 14 45 0.111
507
MST021 Meester-Loeys Syndrome 38 0.111
508
CHN056 Chondrosarcoma, Extraskeletal Myxoid 42 0.111
509
FRG010 Fragile X Tremor/ataxia Syndrome 43 0.111
510
SRC027 Sarcoma, Synovial 58 0.111
511
c MJR022 Major Affective Disorder 8 37 0.111
512
c GLC092 Glaucoma, Primary Open Angle 61 0.111
513
HSH003 Hashimoto Thyroiditis 60 0.111
514
P NRD007 Neurodegeneration with Brain Iron Accumulation 51 0.111
515
c ATS383 Autosomal Dominant Non-Syndromic Intellectual Disability 1 36 0.111
516
c GRN065 Granulomatous Disease, Chronic, Autosomal Recessive, 5 23 0.111
517
c ACT073 Acute Leukemia 59 0.111
518
P PLY019 Polyneuropathy 53 0.111
519
P MYP006 Myopia 55 0.111
520
MST005 Mastitis 52 0.111
521
CHL014 Cholera 62 0.111
522
BRS099 Breast Ductal Carcinoma 61 0.111
523
PRS021 Prostatic Adenoma 43 0.111
524
CRY004 Cryoglobulinemia 47 0.111
525
P ANT006 Antiphospholipid Syndrome 55 0.111
526
P MYX008 Myxoid Chondrosarcoma 28 0.111
527
SPN051 Spondylitis 51 0.111
528
c ESS001 Essential Tremor 56 0.111
529
THY030 Thyroid Gland Disease 50 0.111
530
PRS045 Prostatic Hypertrophy 52 0.111
531
DNT012 Dental Caries 53 0.111
532
c HPT015 Hepatitis D 49 0.111
533
P HPT021 Hepatitis 68 0.111
534
CCC001 Coccidioidomycosis 58 0.111
535
LYM021 Lymphadenitis 56 0.111
536
c DLT002 Dilated Cardiomyopathy 79 0.111
537
RFT001 Rift Valley Fever 50 0.111
538
P HYP024 Hypoparathyroidism 55 0.111
539
DSS009 Disseminated Intravascular Coagulation 56 0.111
540
INF009 Inflammatory Spondylopathy 30 0.111
541
CRM001 Crimean-Congo Hemorrhagic Fever 51 0.111
542
ALL029 Allergic Disease 61 0.111
543
MNC001 Monocular Esotropia 30 0.111
544
ART016 Aortic Aneurysm 69 0.111
545
LNG039 Lung Squamous Cell Carcinoma 57 0.111
546
c GLY006 Glycogen Storage Disease Viii 34 0.111
547
CLN015 Colon Adenocarcinoma 64 0.111
548
RTN023 Retinitis 45 0.111
549
P BPL003 Bipolar Disorder 56 0.111
550
TLR001 Tularemia 56 0.111
551
DMY004 Demyelinating Disease 50 0.111
552
P GLL018 Gallbladder Cancer 53 0.111
553
GLY099 Glycogen Storage Disease Ixa1 35 0.111
554
c RTN041 Retinitis Pigmentosa 11 43 0.111
555
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 0.111
556
c NMN013 Niemann-Pick Disease, Type a 63 0.111
557
c SPS128 Spastic Paraplegia 7, Autosomal Recessive 58 0.111
558
UTR043 Uterine Sarcoma 40 0.111
559
ANR040 Aneurysm 60 0.111
560
c MNT226 Mental Retardation, Autosomal Dominant 31 35 0.111
561
P CLS010 Cluster Headache 42 0.111
562
c CNG216 Congenital Hydrocephalus 50 0.111
563
ATN005 Autonomic Dysfunction 45 0.111
564
BCK006 Back Pain 43 0.111
565
P THY032 Thyroiditis 56 0.111
566
c RNG022 Ring Chromosome 6 28 0.111
567
TRC096 Trichothiodystrophy 56 0.111
568
CRV002 Cervix Uteri Carcinoma in Situ 48 0.111
569
DYS030 Dysferlinopathy 38 0.111
570
P CNG024 Congenital Nystagmus 35 0.111
571
CRC021 Carcinosarcoma 62 0.111
572
P EXT030 Extraosseous Chondrosarcoma 31 0.111
573
P HDC001 Headache 56 0.111
574
P RBL001 Rubella 58 0.111
575
MLT076 Multiple System Atrophy with Orthostatic Hypotension 9 0.111
576
CRV045 Cervical Intraepithelial Neoplasia 38 0.111
577
CHR257 Chromosome 6q Deletion 14 0.111
578
P AMY004 Amyloidosis 69 0.111
579
P PRD008 Periodontitis 64 0.111
580
P AXN001 Axonal Neuropathy 33 0.111
581
PLC008 Placenta Disease 49 0.111
582
c BCT013 Bacterial Pneumonia 47 0.111
583
P FML187 Familial Hypertension 34 0.111
584
ORL011 Oral Cancer 60 0.111
585
EST005 Esotropia 42 0.111
586
RCR030 Recurrent Idiopathic Neuroretinitis 11 0.111
587
c ACT135 Acute Graft Versus Host Disease 51 0.111
588
ADG002 Audiogenic Seizures 25 0.111
589
QLT008 Qualitative or Quantitative Defects of Dysferlin 30 0.111
590
P RNG032 Ring Chromosome 39 0.111
591
P AVS003 Avascular Necrosis 41 0.111
592
GLY065 Glycogen Storage Disease Due to Liver Phosphorylase Kinase Deficiency 41 0.111
593
6QT002 6q Terminal Deletion Syndrome 22 0.111
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