Search results for tgfb1

703 hits were found for tgfb1

# Family MCID Name MIFTS Score
1
P CMR001 Camurati-Engelmann Disease 59 49.079
2
CYS001 Cystic Fibrosis 78 31.733
3
INF173 Inflammatory Bowel Disease, Immunodeficiency, and Encephalopathy 21 30.706
4
P ENC018 Encephalopathy 62 21.297
5
P BRS047 Breast Cancer 98 18.043
6
c INF063 Inflammatory Bowel Disease 25, Autosomal Recessive 44 17.217
7
P CLR023 Colorectal Cancer 100 17.122
8
P PNC035 Pancreatic Cancer 86 17.040
9
P GST053 Gastric Cancer 83 17.019
10
P HPT023 Hepatocellular Carcinoma 96 14.571
11
P INF037 Inflammatory Bowel Disease 53 14.541
12
P LNG032 Lung Cancer 98 13.951
13
P ADN016 Adenocarcinoma 63 13.792
14
END057 Endometrial Cancer 72 13.482
15
OST012 Osteoarthritis 77 13.333
16
P PRS040 Prostate Cancer 95 12.985
17
P OTS001 Otosclerosis 49 12.984
18
P AST005 Asthma 76 12.792
19
P OVR042 Ovarian Cancer 88 12.644
20
LVR012 Liver Cirrhosis 63 12.514
21
ATM095 Autoimmune Disease 61 12.453
22
P PLM036 Pulmonary Fibrosis 66 11.989
23
P KDN018 Kidney Disease 72 11.978
24
P OST002 Osteoporosis 76 11.896
25
LNG099 Lung Disease 62 11.844
26
P HRT032 Heart Disease 81 11.798
27
c SYS001 Systemic Lupus Erythematosus 87 11.734
28
P ART022 Arthritis 71 11.568
29
P MYL006 Myeloid Leukemia 61 11.372
30
c CHR684 Chronic Kidney Disease 69 11.342
31
P MYP006 Myopia 56 11.295
32
MLR004 Malaria 80 11.115
33
c HPT016 Hepatitis B 62 11.115
34
P RHM011 Rheumatoid Arthritis 82 11.107
35
RNL077 Renal Fibrosis 46 10.998
36
P HRD008 Hereditary Hemorrhagic Telangiectasia 65 10.814
37
LSH001 Leishmaniasis 64 10.728
38
P LVR013 Liver Disease 69 10.542
39
P GLM007 Glomerulonephritis 60 10.531
40
P MYC007 Myocardial Infarction 70 10.454
41
PLM129 Pulmonary Disease, Chronic Obstructive 74 10.410
42
URT010 Ureteral Obstruction 45 10.328
43
P SYS005 Systemic Scleroderma 74 10.162
44
BLR001 Biliary Atresia 55 10.162
45
P SCL018 Scoliosis 57 10.079
46
CHG001 Chagas Disease 66 10.069
47
P HYP061 Hypertrophic Cardiomyopathy 69 10.069
48
GNG012 Gingival Overgrowth 49 10.069
49
P PLM037 Pulmonary Hypertension 72 9.965
50
c MCR113 Microvascular Complications of Diabetes 3 52 9.864
51
OBS082 Obstructive Nephropathy 41 9.848
52
END086 End Stage Renal Disease 52 9.792
53
c DLT002 Dilated Cardiomyopathy 78 9.709
54
P DRR001 Diarrhea 55 9.709
55
PLM134 Pulmonary Fibrosis, Idiopathic 76 9.683
56
MYL005 Myelofibrosis 71 9.528
57
INT066 Interstitial Lung Disease 60 9.528
58
HYP068 Hyperostosis 47 9.504
59
NNL006 Non-Alcoholic Steatohepatitis 54 9.475
60
P THR014 Thrombocytopenia 66 9.372
61
P SCL048 Sclerosteosis 58 9.146
62
PNC129 Pancreatic Adenocarcinoma 65 9.090
63
P FBR017 Fibrosarcoma 56 9.090
64
P FCL005 Focal Segmental Glomerulosclerosis 57 9.090
65
NPH010 Nephrosclerosis 50 9.090
66
P TXP001 Toxoplasmosis 60 9.090
67
P CRN025 Corneal Dystrophy 49 9.060
68
GRN055 Granular Corneal Dystrophy 37 8.863
69
c VRL010 Viral Hepatitis 53 8.841
70
MRF001 Marfan Syndrome 76 8.735
71
IGG001 Iga Glomerulonephritis 50 8.580
72
c HYP595 Hypertension, Essential 85 8.494
73
MCS002 Mucositis 56 8.494
74
SQM013 Squamous Cell Carcinoma, Head and Neck 73 8.401
75
P OPN001 Open-Angle Glaucoma 55 8.401
76
EXP004 Exophthalmos 51 8.401
77
PRT013 Portal Hypertension 59 8.401
78
RTN017 Retinal Detachment 60 8.297
79
P APL001 Aplastic Anemia 73 8.297
80
c ATS007 Autism Spectrum Disorder 72 8.297
81
c TYP009 Type 2 Diabetes Mellitus 92 8.297
82
P VSC007 Vascular Disease 63 8.297
83
P ALZ034 Alzheimer Disease 87 8.180
84
PYR010 Peyronie's Disease 50 8.180
85
HSH003 Hashimoto Thyroiditis 60 8.180
86
P MYP004 Myopathy 67 8.180
87
SLC006 Silicosis 56 8.180
88
HYP457 Hypertrophic Scars 42 8.041
89
P PLY014 Polycystic Kidney Disease 69 8.041
90
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 8.041
91
FCL012 Facial Paralysis 49 8.041
92
GST092 Gastroesophageal Reflux 61 7.860
93
P VNB005 Van Buchem Disease 58 7.860
94
ACT119 Acute Promyelocytic Leukemia 62 7.860
95
P PNM006 Pneumoconiosis 55 7.860
96
P RCS002 Recessive Dystrophic Epidermolysis Bullosa 62 7.860
97
c ATS347 Autosomal Dominant Polycystic Kidney Disease 66 7.860
98
P DBT009 Diabetes Mellitus 67 7.860
99
P BRS044 Breast Adenocarcinoma 58 7.860
100
BRN012 Bronchiolitis Obliterans 56 7.860
101
FRZ001 Frozen Shoulder 55 7.860
102
HYD002 Hydronephrosis 58 7.860
103
P ALP004 Alport Syndrome 69 7.860
104
PRT029 Parathyroid Adenoma 51 7.860
105
P MYM013 Moyamoya Disease 1 59 7.500
106
LYM004 Lymphoid Interstitial Pneumonia 49 7.422
107
THY121 Thyroid Gland Anaplastic Carcinoma 67 7.422
108
RHM028 Rheumatic Heart Disease 56 7.422
109
P CRP001 Carpal Tunnel Syndrome 66 7.422
110
BRS050 Breast Cyst 38 7.422
111
ACS001 Acoustic Neuroma 56 7.422
112
P GNG025 Gingival Fibromatosis 47 7.422
113
P LTT001 Lattice Corneal Dystrophy 31 7.422
114
CHR177 Chromophobe Renal Cell Carcinoma 54 7.422
115
P RPD001 Rapidly Progressive Glomerulonephritis 44 7.422
116
PRS047 Prostatitis 58 7.422
117
P CMM008 Communicating Hydrocephalus 45 7.422
118
HRT012 Heart Valve Disease 53 7.422
119
P CTR002 Cataract 60 7.422
120
c LCL006 Localized Scleroderma 65 7.422
121
PLR008 Pleurisy 50 7.422
122
NRT004 Neuritis 53 7.422
123
P ESS003 Essential Thrombocythemia 69 7.422
124
PRN021 Paranasal Sinus Disease 44 7.422
125
IDP011 Idiopathic Interstitial Pneumonia 59 7.422
126
NNS002 Nonspecific Interstitial Pneumonia 42 7.422
127
P HYD006 Hydrocephalus 61 7.422
128
BRC012 Brucellosis 66 7.422
129
BLL004 Bullous Keratopathy 48 7.422
130
TRC008 Trachoma 53 7.422
131
URN010 Urinary Tract Obstruction 55 7.422
132
ORL004 Oral Submucous Fibrosis 56 7.422
133
OST016 Osteochondrosis 52 7.422
134
BRS051 Breast Disease 58 7.422
135
P SCK002 Sick Sinus Syndrome 55 7.422
136
ANK001 Ankylosis 51 7.422
137
NRM004 Neuroma 49 7.422
138
ESN002 Eosinophilia-Myalgia Syndrome 40 7.422
139
DST006 Diastolic Heart Failure 45 7.422
140
c JVN038 Juvenile Myasthenia Gravis 30 6.886
141
NPH018 Nephrogenic Systemic Fibrosis 49 6.572
142
CYS042 Cystic Fibrosis and Congenital Absence of the Vas Deferens 14 6.123
143
P PYR039 Peyronie Disease 39 6.006
144
KLD004 Keloid Disorder 39 6.006
145
P CNG499 Congenital Anomalies of Kidney and Urinary Tract 2 52 5.867
146
ANT018 Anthracosis 51 5.686
147
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 5.620
148
CYT002 Cytokine Deficiency 43 5.307
149
MCK005 Mckusick-Kaufman Syndrome 61 5.248
150
PST062 Pustulosis Palmaris Et Plantaris 46 5.248
151
CHN053 Chondromyxoid Fibroma 39 5.248
152
OST115 Osteonecrosis of the Jaw 41 5.248
153
TBR011 Tuberculous Meningitis 48 5.248
154
ECT070 Ectodermal Dysplasia 1, Hypohidrotic, X-Linked 60 5.248
155
OCL020 Ocular Cicatricial Pemphigoid 52 5.248
156
P BCK002 Beckwith-Wiedemann Syndrome 62 5.248
157
FBR032 Fibromuscular Dysplasia 48 5.248
158
P URN019 Urinary Tract Infection 49 5.248
159
c ATS393 Autosomal Recessive Cutis Laxa Type I 46 5.248
160
STF002 Stiff Skin Syndrome 53 5.248
161
LKR002 Leukoregulin 28 5.248
162
P ECT062 Ectodermal Dysplasia 10b, Hypohidrotic/hair/tooth Type, Autosomal Recessive 69 5.248
163
c VSC019 Vesicoureteral Reflux 1 57 5.248
164
c FBR084 Fibromatosis, Gingival, 1 49 5.248
165
KND001 Kindler Syndrome 63 5.248
166
OST032 Osteofibrous Dysplasia 52 5.248
167
OLG020 Oligoarticular Juvenile Idiopathic Arthritis 45 5.248
168
P GLP001 Geleophysic Dysplasia 46 5.248
169
c CTR185 Cataract 30 31 5.248
170
PMP014 Pemphigoid 51 5.248
171
EPT025 Epithelial Basement Membrane Dystrophy 26 5.248
172
P FML284 Familial Vesicoureteral Reflux 31 5.248
173
EVN001 Evans' Syndrome 46 5.248
174
CHR576 Chronic Beryllium Disease 42 5.248
175
URT037 Urethral Stricture 42 5.248
176
DSS008 Disease of Mental Health 74 5.248
177
P CNG001 Congenital Myasthenic Syndrome 68 5.248
178
THR016 Thrombophlebitis 50 5.248
179
TRC005 Tracheal Stenosis 43 5.248
180
SBM003 Submandibular Gland Disease 23 5.248
181
P DMN001 Diamond-Blackfan Anemia 71 5.248
182
GRD001 Giardiasis 46 5.248
183
STR008 Strongyloidiasis 52 5.248
184
CHL013 Cholecystolithiasis 37 5.248
185
TBR006 Tuberculoid Leprosy 43 5.248
186
P LRY019 Laryngitis 53 5.248
187
URT031 Ureteral Disease 41 5.248
188
CLN003 Clonorchiasis 43 5.248
189
GNG011 Gingival Disease 54 5.248
190
PNL013 Penile Disease 38 5.248
191
DFF003 Diffuse Scleroderma 41 5.248
192
HRT015 Heritable Pulmonary Arterial Hypertension 46 5.248
193
PST041 Posterior Urethral Valves 41 5.248
194
P BRY005 Beryllium Disease 39 5.248
195
CHR276 Chronic Active Epstein-Barr Virus Infection 41 5.248
196
DFF021 Diffuse Mesangial Sclerosis 39 5.248
197
IDP064 Idiopathic Neutropenia 39 5.248
198
c MCR130 Microvascular Complications of Diabetes 6 41 4.615
199
c MCR120 Microvascular Complications of Diabetes 7 47 4.615
200
c MCR133 Microvascular Complications of Diabetes 4 41 4.615
201
SVR004 Severe Combined Immunodeficiency 72 3.782
202
P END044 Endometriosis 62 3.276
203
P MLT020 Multiple Sclerosis 79 3.184
204
c HPT001 Hepatitis C 62 3.079
205
GLB002 Glioblastoma 67 2.923
206
P INF032 Infertility 57 2.923
207
TLN003 Telangiectasis 51 2.806
208
ART140 Arteries, Anomalies of 53 2.797
209
LPP008 Lipoprotein Quantitative Trait Locus 65 2.797
210
c SPN225 Spondyloarthropathy 1 70 2.757
211
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 2.757
212
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 2.757
213
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 2.757
214
SPN051 Spondylitis 51 2.757
215
INF009 Inflammatory Spondylopathy 30 2.757
216
FTT001 Fatty Liver Disease 62 2.605
217
PNC041 Pancreatic Ductal Adenocarcinoma 51 2.605
218
SQM006 Squamous Cell Carcinoma 60 2.571
219
ATH013 Atherosclerosis Susceptibility 63 2.551
220
IDP070 Idiopathic Scoliosis 42 2.551
221
PRS129 Prostatic Hyperplasia, Benign 49 2.523
222
P RHB003 Rhabdomyosarcoma 66 2.523
223
ADN018 Adenoma 59 2.523
224
CRV035 Cervical Cancer 73 2.495
225
PRT251 Proteinuria, Chronic Benign 57 2.495
226
NNL005 Non-Alcoholic Fatty Liver Disease 63 2.473
227
P GRF003 Graft-Versus-Host Disease 71 2.378
228
c HPT073 Hepatitis C Virus 71 2.370
229
SXL003 Sexual Disorder 49 2.316
230
PRS021 Prostatic Adenoma 43 2.316
231
IMP005 Impotence 52 2.316
232
PRS045 Prostatic Hypertrophy 53 2.316
233
P SCH015 Schizophrenia 74 2.316
234
CRH001 Crohn's Disease 80 2.316
235
RNL114 Renal Cell Carcinoma, Nonpapillary 80 2.261
236
P LNG064 Lung Cancer Susceptibility 3 70 2.261
237
IGR001 Ige Responsiveness, Atopic 59 2.252
238
P MYS003 Myasthenia Gravis 68 2.218
239
P SCL057 Scoliosis, Isolated 1 40 2.203
240
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 2.203
241
DSS032 Disease by Infectious Agent 55 2.184
242
ANR040 Aneurysm 61 2.184
243
ALL003 Allergic Rhinitis 67 2.113
244
P DVL012 Developmental Dysplasia of the Hip 1 46 2.113
245
c PRC016 Pre-Eclampsia 65 2.113
246
P RHN004 Rhinitis 57 2.113
247
P PRD008 Periodontitis 64 2.082
248
c SML038 Small Cell Cancer of the Lung 69 2.038
249
ULC004 Ulcerative Colitis 74 2.017
250
P THY032 Thyroiditis 57 2.017
251
CMB007 Combined Immunodeficiency 57 2.017
252
CLF027 Cleft Palate, Isolated 64 1.959
253
P BLD134 Bladder Cancer 79 1.958
254
P NSP012 Nasopharyngeal Carcinoma 61 1.950
255
P CRN300 Coronary Heart Disease 1 73 1.950
256
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 1.950
257
GTR002 Goiter 53 1.950
258
CLR108 Colorectal Adenoma 64 1.879
259
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 1.879
260
INT030 Intracranial Aneurysm 55 1.872
261
CLT003 Colitis 63 1.804
262
ORL015 Oral Squamous Cell Carcinoma 43 1.804
263
PRS042 Prostate Disease 42 1.804
264
CLR030 Clear Cell Renal Cell Carcinoma 54 1.804
265
ALL029 Allergic Disease 59 1.804
266
P LKM002 Leukemia 67 1.804
267
P HPT021 Hepatitis 69 1.804
268
c ACT135 Acute Graft Versus Host Disease 51 1.804
269
INT067 Interstitial Nephritis 46 1.779
270
ALL006 Allergic Asthma 56 1.779
272
P SPP010 Suppressor of Tumorigenicity 3 51 1.724
273
P ECL001 Eclampsia 52 1.724
274
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 60 1.724
275
P RCT021 Rectum Cancer 54 1.724
276
P MLN008 Melanoma 76 1.650
277
P LPR021 Leprosy 3 71 1.638
278
P KLZ004 Kala-Azar 1 41 1.638
279
DFC004 Deficiency Anemia 74 1.638
280
P EST001 Estrogen-Receptor Positive Breast Cancer 49 1.638
281
RCK004 Rickets 68 1.638
282
HNS001 Hansen's Disease 32 1.638
283
AGN016 Aging 54 1.615
284
CRV002 Cervix Uteri Carcinoma in Situ 47 1.544
285
HYP066 Hyperglycemia 61 1.544
286
P ESP024 Esophagitis 60 1.544
287
PTT037 Pituitary Tumors 44 1.544
288
CRV045 Cervical Intraepithelial Neoplasia 39 1.544
289
c ATM011 Autoimmune Hepatitis 63 1.516
290
CMR006 Camurati-Engelmann Disease, Type 2 21 1.508
291
P LPS004 Lupus Erythematosus 61 1.452
292
PLY150 Polykaryocytosis Inducer 29 1.441
293
c MYP018 Myopia 6 27 1.441
294
DWN001 Down Syndrome 70 1.441
295
VSC003 Visceral Leishmaniasis 55 1.441
296
P CYS018 Cystitis 59 1.441
297
GST040 Gastric Adenocarcinoma 67 1.441
298
PPT005 Peptic Ulcer Disease 58 1.441
299
P DDN001 Duodenal Ulcer 53 1.441
300
ART017 Aortic Disease 49 1.441
301
PRC003 Proctitis 49 1.441
302
CHR178 Chromosomal Triplication 34 1.441
303
DFF005 Diffuse Large B-Cell Lymphoma 54 1.367
304
RBB001 Ribbing Disease 20 1.326
305
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 1.324
306
P ATX030 Ataxia-Telangiectasia 80 1.324
307
c HPT003 Hepatitis a 63 1.324
308
OCC016 Occupational Asthma 33 1.324
309
c ACT073 Acute Leukemia 58 1.324
310
ACT250 Acute Megakaryocytic Leukemia 60 1.324
311
P SNS001 Sensorineural Hearing Loss 59 1.324
312
RLP002 Relapsing-Remitting Multiple Sclerosis 56 1.324
313
TRN018 Transitional Cell Carcinoma 56 1.324
314
P KDN017 Kidney Cancer 61 1.324
315
GST045 Gastroenteritis 58 1.324
316
HYP080 Hypogonadism 50 1.324
317
c ATR087 Atrial Standstill 1 74 1.313
318
ART016 Aortic Aneurysm 68 1.313
319
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 1.238
320
INT323 Intraocular Pressure Quantitative Trait Locus 64 1.238
321
GLL048 Glial Tumor 52 1.238
322
P TRT010 Teratoma 51 1.238
323
HYP266 Hypoxia 57 1.238
324
GLM045 Glioma 63 1.238
325
CLF001 Cleft Lip 53 1.238
326
KRN002 Kearns-Sayre Syndrome 63 1.185
327
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 80 1.185
328
SCK003 Sickle Cell Anemia 74 1.185
329
P MJR001 Major Depressive Disorder 68 1.185
330
P ALC033 Alcohol Use Disorder 61 1.185
331
MNT002 Mental Depression 57 1.185
332
ILS001 Ileus 50 1.185
333
P HYP078 Hypertrophy of Breast 41 1.185
334
DPR016 Depression 65 1.185
335
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 1.158
336
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 1.158
337
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 1.158
338
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 1.158
339
c MCR115 Microvascular Complications of Diabetes 5 65 1.158
340
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 1.158
341
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 1.158
342
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 1.158
343
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 1.158
344
OST159 Osteogenic Sarcoma 66 1.158
345
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 1.158
346
DRM006 Dermatitis 62 1.158
347
CHL068 Cholestasis 61 1.158
348
P OVR082 Overgrowth Syndrome 49 1.072
349
c GLL024 Gallbladder Disease 1 52 1.072
350
STR067 Stroke, Ischemic 80 1.072
351
c AMY091 Amyotrophic Lateral Sclerosis 1 88 1.072
352
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 1.072
353
P MDL005 Medulloblastoma 75 1.072
354
P NRB001 Neuroblastoma 66 1.072
355
AMB001 Amebiasis 57 1.072
356
P PTT006 Pituitary Adenoma 55 1.072
357
SKL002 Skeletal Muscle Neoplasm 25 1.072
358
P LTR001 Lateral Sclerosis 58 1.072
359
END011 Endometriosis of Ovary 39 1.072
360
P GLL018 Gallbladder Cancer 53 1.072
361
VNH007 Von Hippel-Lindau Syndrome 73 1.003
362
P LYS001 Loeys-Dietz Syndrome 65 1.003
363
P FLL037 Follicular Lymphoma 74 1.003
364
P HYP098 Hypereosinophilic Syndrome 66 1.003
365
CLF056 Cleft Lip with or Without Cleft Palate 42 1.003
366
HML018 Homologous Wasting Disease 21 1.003
367
c SCL052 Scleroderma, Familial Progressive 61 0.979
368
P DRM053 Dermatitis, Atopic 65 0.979
369
P ATR011 Atrial Fibrillation 66 0.979
370
BNR002 Bone Resorption Disease 47 0.979
371
P LYM118 Lymphoma 67 0.979
372
P GLM040 Glioma Susceptibility 1 71 0.979
373
MMM006 Mammographic Density 39 0.979
374
CHL065 Cholangiocarcinoma 58 0.979
375
PLM001 Pulmonary Tuberculosis 69 0.979
376
FDL002 Food Allergy 47 0.979
377
MLG169 Malignant Astrocytoma 57 0.979
378
P BND020 Bone Disease 59 0.979
379
THY020 Thyroid Hyalinizing Trabecular Adenoma 20 0.979
380
INT079 Intrahepatic Cholangiocarcinoma 51 0.979
381
P PNC044 Pancreatitis 61 0.979
382
ISC004 Ischemia 61 0.979
383
LPD008 Lipid Metabolism Disorder 62 0.979
384
ALL014 Allergic Encephalomyelitis 34 0.979
385
CRN141 Corneal Dystrophy, Reis-Bucklers Type 36 0.889
386
P ATS364 Autism 69 0.875
387
c ART138 Aortic Aneurysm, Familial Abdominal, 1 61 0.875
388
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 0.875
389
c MGR028 Migraine with or Without Aura 1 64 0.875
390
TND004 Tendinopathy 45 0.875
391
MYL009 Myelodysplastic Syndrome 67 0.875
392
TND005 Tendinitis 54 0.875
393
c LKM061 Leukemia, Acute Myeloid 83 0.875
394
c ART101 Aortic Valve Disease 2 66 0.875
395
TTT001 Tatton-Brown-Rahman Syndrome 46 0.875
396
c GLC092 Glaucoma, Primary Open Angle 62 0.875
397
MNN043 Meningioma, Familial 79 0.875
398
THY029 Thyroid Carcinoma 51 0.875
399
RPD005 Rapidly Involuting Congenital Hemangioma 46 0.875
400
P BCL017 B-Cell Lymphoma 59 0.875
401
NRM001 Neuromyelitis Optica 61 0.875
402
PLS011 Plasmacytoma 56 0.875
403
LNG039 Lung Squamous Cell Carcinoma 57 0.875
404
SMN007 Seminoma 42 0.875
405
SCR001 Secretory Meningioma 40 0.875
406
LYM002 Lymphoplasmacyte-Rich Meningioma 35 0.875
408
P MGR003 Migraine with Aura 52 0.875
409
P MGR001 Migraine Without Aura 49 0.875
410
CNN003 Conn's Syndrome 79 0.875
411
P EYD002 Eye Disease 57 0.875
412
MDD003 Middle Cerebral Artery Infarction 37 0.875
413
P ART005 Arteriovenous Malformation 65 0.875
414
SPN021 Spinal Meningioma 50 0.875
415
P BNC003 Bone Cancer 58 0.875
416
BRN071 Brain Injury 50 0.875
417
OVR094 Ovarian Epithelial Cancer 39 0.875
418
PRM243 Primary Bone Cancer 22 0.875
419
P THL005 Thalassemia 56 0.758
420
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.758
421
P TST021 Testicular Germ Cell Tumor 61 0.758
422
c THY107 Thymoma, Familial 42 0.758
423
c PLM164 Pulmonary Hypertension, Primary, 1 76 0.758
424
P ZNC008 Zinc Finger Protein 1 23 0.758
425
CHR005 Chorioamnionitis 50 0.758
427
c BRN108 Branchiootic Syndrome 1 62 0.758
428
C1Q001 C1q Deficiency 40 0.758
429
c THY109 Thyroid Cancer, Nonmedullary, 1 55 0.758
430
c HYP836 Hypercholesterolemia, Familial, 1 73 0.758
431
DCT002 Ductal Carcinoma in Situ 58 0.758
432
CLR109 Colorectal Adenocarcinoma 50 0.758
433
BCT022 Bacterial Infectious Disease 56 0.758
434
CHL149 Childhood Acute Myeloid Leukemia 43 0.758
435
TRM010 Traumatic Brain Injury 51 0.758
436
URM002 Uremia 47 0.758
437
CRC021 Carcinosarcoma 64 0.758
438
DGN001 Degenerative Disc Disease 49 0.758
439
P ATR005 Atrophic Gastritis 50 0.758
440
P ALP008 Alopecia 54 0.758
441
SVR001 Severe Acute Respiratory Syndrome 67 0.758
442
P GST044 Gastritis 55 0.758
443
PLR007 Pleural Empyema 51 0.758
444
P ART023 Arthropathy 61 0.758
445
FLL031 Follicular Adenoma 40 0.758
446
PRT036 Peritonitis 65 0.758
447
P HYP086 Hypothyroidism 69 0.758
448
MST005 Mastitis 53 0.758
449
P PLY011 Polycystic Ovary Syndrome 57 0.758
450
UTR024 Uterine Carcinosarcoma 59 0.758
451
CLN019 Colonic Disease 47 0.758
452
P PNM007 Pneumonia 67 0.758
453
GNG013 Gingivitis 59 0.758
454
P THY023 Thymoma 64 0.758
455
BRN002 Bronchiolitis 57 0.758
456
P INS002 in Situ Carcinoma 53 0.758
457
VSC002 Vascular Dementia 60 0.758
458
GRM010 Germ Cells Tumors 33 0.758
459
c NNS007 Nonsyndromic Deafness 33 0.758
460
48X005 48,xyyy 39 0.758
461
BRN056 Bronchopulmonary Dysplasia 56 0.758
462
PLM052 Pulmonary Arteriovenous Malformation 40 0.758
463
CHR072 Chordoma 57 0.696
464
QLT002 Qualitative or Quantitative Defects of Dystrophin 19 0.619
465
PRM334 Primary Bone Dysplasia with Increased Bone Density 15 0.619
466
P VTR007 Vitreoretinopathy 46 0.619
467
c ART115 Aortic Valve Disease 1 74 0.619
468
ADN027 Adenomyosis 57 0.619
469
OST022 Osteopathia Striata with Cranial Sclerosis 54 0.619
470
CRD132 Cardiac Conduction Defect 60 0.619
471
MSC157 Muscular Dystrophy, Duchenne Type 79 0.619
472
c NPH049 Nephrotic Syndrome, Type 2 51 0.619
473
c TLN011 Telangiectasia, Hereditary Hemorrhagic, Type 2 45 0.619
474
c DRM040 Dermatitis Herpetiformis, Familial 35 0.619
475
c BNM016 Bone Mineral Density Quantitative Trait Locus 1 24 0.619
476
P MLN069 Melanoma, Uveal 61 0.619
477
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.619
478
ANG054 Angina Pectoris 66 0.619
479
CKT002 Cakut 47 0.619
480
ART074 Aortic Dissection 53 0.619
481
IMM003 Immunoglobulin Alpha Deficiency 44 0.619
482
P CRB188 Cerebral Arteriopathy, Autosomal Recessive, with Subcortical Infarcts and Leukoencephalopathy 38 0.619
483
HLC007 Helicobacter Pylori Infection 67 0.619
484
CYS047 Cystic Fibrosis, Modifier of, 1 15 0.619
485
ACR041 Acromelic Frontonasal Dysostosis 53 0.619
486
c PCH010 Pachyonychia Congenita 3 43 0.619
487
P ESP035 Esophagitis, Eosinophilic, 1 58 0.619
488
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.619
489
ENT011 Enterocolitis 55 0.619
490
c NPH055 Nephrotic Syndrome, Type 1 52 0.619
491
P RTN024 Retinoblastoma 73 0.619
492
PLM151 Pulmonary Arteriovenous Fistulas 35 0.619
493
ESP021 Esophageal Cancer 83 0.619
494
PNG002 Pain Agnosia 51 0.619
495
LMY002 Leiomyoma 51 0.619
496
CTN007 Cutaneous Leishmaniasis 62 0.619
497
c ACT075 Acute Myocardial Infarction 56 0.619
498
ART010 Arteriolosclerosis 37 0.619
499
INT007 Intermediate Coronary Syndrome 54 0.619
500
SKN019 Skin Melanoma 71 0.619
501
P PSR002 Psoriasis 63 0.619
502
P CHL066 Cholangitis 52 0.619
503
CHR074 Choriocarcinoma 46 0.619
504
ACT162 Acute Sensory Ataxic Neuropathy 24 0.619
505
P MSC005 Muscular Dystrophy 67 0.619
506
P OPT006 Optic Nerve Disease 58 0.619
507
P CND004 Candidiasis 58 0.619
508
THL004 Theileriasis 31 0.619
509
SPN035 Spindle Cell Sarcoma 54 0.619
510
P INF038 Influenza 68 0.619
511
PST011 Pustulosis of Palm and Sole 52 0.619
512
P DRM007 Dermatitis Herpetiformis 54 0.619
513
HLX001 Helix Syndrome 48 0.619
514
BRN028 Brain Cancer 74 0.619
515
P MLN007 Male Infertility 56 0.619
516
P GRV001 Graves' Disease 55 0.619
517
CRT013 Carotid Stenosis 51 0.619
518
TST015 Testicular Disease 42 0.619
519
HMG005 Hemoglobinopathy 56 0.619
520
GST033 Gestational Diabetes 61 0.619
521
SRC014 Sarcoma 65 0.619
522
P RSP003 Respiratory Failure 74 0.619
523
TTN003 Tetanus 65 0.619
524
MNN009 Meningoencephalitis 48 0.619
525
CNG034 Congestive Heart Failure 69 0.619
526
P PRN023 Prion Disease 60 0.619
527
CRB039 Cerebrovascular Disease 66 0.619
528
THY030 Thyroid Gland Disease 50 0.619
529
P OVR049 Ovarian Disease 52 0.619
530
DYS032 Dystrophinopathies 47 0.619
531
SPL018 Splenomegaly 49 0.619
532
P SCK005 Sickle Cell Disease 56 0.619
533
P CHR345 Chronic Pain 50 0.619
534
UTR043 Uterine Sarcoma 40 0.619
535
NNT049 Nontuberculous Mycobacterial Lung Disease 46 0.619
536
ASC010 Ascaris Lumbricoides Infection 49 0.566
537
P LKM062 Leukemia, Acute Lymphoblastic 69 0.566
538
LYM133 Lymphoma, Hodgkin, Classic 74 0.438
539
c SBC035 Subacute Cutaneous Lupus Erythematosus 34 0.438
540
IMM204 Immuno-Osseous Dysplasia 19 0.438
541
DSC009 Discoid Lupus Erythematosus 43 0.438
542
P HRD217 Hereditary Optic Neuropathy 36 0.438
543
SPN186 Spinal Cord Injury 61 0.438
545
OBS067 Obesity Due to Melanocortin 4 Receptor Deficiency 36 0.438
546
SPS019 Spastic Paraparesis 38 0.438
547
NDL020 Nodal Marginal Zone B-Cell Lymphoma 29 0.438
548
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 0.438
549
SPP011 Suppression of Tumorigenicity 12 61 0.438
550
INS024 Insulin-Like Growth Factor I 78 0.438
551
ASP026 Asplenia, Isolated Congenital 43 0.438
552
P RTN008 Retinitis Pigmentosa 80 0.438
553
P ART067 Aortic Aneurysm, Familial Thoracic 1 61 0.438
554
PSR001 Psoriatic Arthritis 62 0.438
555
c PRG019 Paragangliomas 2 30 0.438
556
OSS014 Ossification of the Posterior Longitudinal Ligament of Spine 48 0.438
557
CHR222 Chromosome 1p36 Deletion Syndrome 45 0.438
558
P MYC084 Mycobacterium Tuberculosis 1 68 0.438
559
c OPT053 Optic Atrophy 1 62 0.438
560
PRX015 Paroxysmal Extreme Pain Disorder 56 0.438
561
ALC007 Alcohol Dependence 66 0.438
562
c OTS005 Otosclerosis 1 25 0.438
563
P PLY168 Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease 65 0.438
564
c FNC027 Fanconi Anemia, Complementation Group a 81 0.438
565
SCH016 Schimke Immunoosseous Dysplasia 53 0.438
566
c LKM063 Leukemia, Chronic Myeloid 71 0.438
567
CHR100 Chronic Ulcer of Skin 57 0.438
568
ADR016 Adrenal Cortical Carcinoma 62 0.438
569
P SLP006 Sleep Apnea 69 0.438
570
P FML011 Familial Adenomatous Polyposis 71 0.438
571
MRG003 Marginal Zone B-Cell Lymphoma 52 0.438
572
MSC007 Muscle Hypertrophy 64 0.438
573
BRR014 Barrett Esophagus 66 0.438
574
RNL025 Renal Hypoplasia 41 0.438
575
NDL024 Nodal Marginal Zone Lymphoma 37 0.438
576
HMN047 Human Cytomegalovirus Infection 57 0.438
577
P CTN015 Cutaneous T Cell Lymphoma 48 0.438
578
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 61 0.438
579
CRP032 Corpus Callosum, Agenesis of 49 0.438
580
P CRN013 Craniodiaphyseal Dysplasia 43 0.438
581
c EPD076 Epidermolysis Bullosa Dystrophica, Autosomal Recessive 52 0.438
582
P CRB048 Cerebral Cavernous Malformations 63 0.438
583
LMY014 Leiomyoma, Uterine 56 0.438
584
c CRB191 Cerebral Cavernous Malformations 2 45 0.438
585
c CRB094 Cerebral Cavernous Malformations 3 41 0.438
586
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 63 0.438
587
c OTS006 Otosclerosis 2 16 0.438
588
P MCR129 Microvascular Complications of Diabetes 1 68 0.438
589
LYM143 Lymphoma, Non-Hodgkin, Familial 75 0.438
590
GLC105 Glucocorticoid Deficiency 4 with or Without Mineralocorticoid Deficiency 33 0.438
591
c OTS012 Otosclerosis 10 16 0.438
592
c OTS011 Otosclerosis 8 15 0.438
593
P ASP006 Aspergillosis 72 0.438
594
P SMK004 Smoking As a Quantitative Trait Locus 3 44 0.438
595
c SCH079 Schizophrenia 1 44 0.438
596
c ALB021 Albinism, Oculocutaneous, Type Ii 59 0.438
597
PRT082 Preterm Premature Rupture of the Membranes 57 0.438
598
ADR054 Adrenocortical Carcinoma, Hereditary 47 0.438
599
c OTS009 Otosclerosis 5 12 0.438
600
c LNG109 Lung Cancer Susceptibility 1 26 0.438
601
P HYP058 Hypervitaminosis a 47 0.438
602
VRC005 Varicose Veins 60 0.438
603
DNY001 Denys-Drash Syndrome 57 0.438
604
MYL069 Myeloma, Multiple 77 0.438
605
c THY102 Thyroid Cancer, Nonmedullary, 2 55 0.438
606
TBC004 Tobacco Addiction 63 0.438
607
P HNT016 Huntington Disease 73 0.438
608
P HYP828 Hyper-Ige Recurrent Infection Syndrome 1, Autosomal Dominant 57 0.438
609
THY111 Thyroid Carcinoma, Familial Medullary 67 0.438
610
MYL057 Myelopathy, Htlv-1-Associated 38 0.438
611
PMP006 Pemphigus Vulgaris, Familial 58 0.438
612
P HRS035 Hirschsprung Disease 1 66 0.438
613
HRW001 Hair Whorl 35 0.438
614
MLD001 Melioidosis 67 0.438
615
c NMN014 Niemann-Pick Disease, Type C2 49 0.438
616
AML029 Ameloblastoma 47 0.438
617
NRR001 Neuroretinitis 42 0.438
618
P PLY041 Polymyositis 59 0.438
619
P AMY004 Amyloidosis 70 0.438
620
EPD018 Epididymo-Orchitis 31 0.438
621
P MSC003 Muscular Atrophy 52 0.438
622
AVN001 Avian Influenza 61 0.438
623
MLR003 Melorheostosis 48 0.438
624
SCR011 Scrapie 39 0.438
625
P EPD009 Epidermolysis Bullosa Dystrophica 66 0.438
626
RTN023 Retinitis 46 0.438
627
DRM011 Dermatophytosis 52 0.438
628
P PMP001 Pemphigus 55 0.438
629
c CHR036 Chronic Cholangitis 25 0.438
630
HPT022 Hepatoblastoma 54 0.438
631
HGH041 High-Grade Astrocytoma 36 0.438
632
P PLM034 Pulmonary Emphysema 58 0.438
633
CRV025 Cervical Incompetence 35 0.438
634
47X002 47,xyy 48 0.438
635
HRT011 Heart Septal Defect 49 0.438
636
ADR004 Adrenal Cortical Adenocarcinoma 38 0.438
637
SKN022 Skin Squamous Cell Carcinoma 54 0.438
638
TRT001 Teratocarcinoma 42 0.438
639
P MST009 Mastocytosis 64 0.438
640
THY125 Thyroid Gland Medullary Carcinoma 48 0.438
641
THY123 Thyroid Gland Follicular Carcinoma 55 0.438
642
P ACN011 Acne 57 0.438
643
MYF001 Myofibroma 42 0.438
644
MNC006 Monoclonal Gammopathy of Uncertain Significance 47 0.438
645
TNC002 Tinea Capitis 42 0.438
646
P MMB011 Membranous Nephropathy 50 0.438
647
P KRT007 Keratoconus 50 0.438
648
CRB004 Cerebral Artery Occlusion 45 0.438
649
P DRM010 Dermatomyositis 61 0.438
650
c MCR112 Microvascular Complications of Diabetes 2 42 0.438
651
c FTL070 Fetal Akinesia Deformation Sequence 2 36 0.438
652
P CTN003 Cutaneous Lupus Erythematosus 52 0.438
653
OST003 Osteonecrosis 61 0.438
654
CRB008 Cerebral Atherosclerosis 46 0.438
655
GT001 Gout 64 0.438
656
PLC002 Plica Syndrome 35 0.438
657
NRG002 Neurogenic Bladder 55 0.438
658
LWC001 Low Compliance Bladder 45 0.438
659
SPN020 Spondylosis 46 0.438
660
PPL022 Papilloma 53 0.438
661
LRY018 Laryngeal Squamous Cell Carcinoma 44 0.438
662
SQM002 Squamous Cell Papilloma 46 0.438
663
c BSL007 Basal Cell Carcinoma 68 0.438
664
P SCL009 Sclerosing Cholangitis 48 0.438
665
RTN020 Retinal Vascular Disease 46 0.438
666
P NPH012 Nephrotic Syndrome 60 0.438
667
ORC001 Orchitis 44 0.438
668
TST014 Testicular Cancer 52 0.438
669
LPR001 Lepromatous Leprosy 49 0.438
670
MTR002 Mitral Valve Insufficiency 52 0.438
671
MCR013 Microphthalmia 60 0.438
672
FLL008 Folliculitis 46 0.438
673
HMN014 Human Immunodeficiency Virus Infectious Disease 54 0.438
674
GNG006 Gingival Hypertrophy 36 0.438
675
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 0.438
676
c SPR009 Sporadic Breast Cancer 42 0.438
677
P LRY044 Larynx Cancer 54 0.438
678
SYN007 Synovitis 55 0.438
679
P EPD016 Epidermolysis Bullosa 53 0.438
680
TRP002 Tropical Spastic Paraparesis 49 0.438
681
OLG001 Oligospermia 45 0.438
682
SHL001 Shoulder Impingement Syndrome 35 0.438
683
MNN017 Mononeuropathy 41 0.438
684
P ADL010 Adult Respiratory Distress Syndrome 71 0.438
685
CHL122 Cholesteatoma of Middle Ear 51 0.438
686
AZS001 Azoospermia 45 0.438
687
P LMY004 Leiomyosarcoma 62 0.438
688
NDL007 Nodular Goiter 48 0.438
689
SML011 Smoldering Myeloma 32 0.438
690
RFR003 Refractive Error 41 0.438
691
KDN013 Kidney Hypertrophy 34 0.438
692
c HRD039 Hereditary Amyloidosis 45 0.438
693
HTL001 Htlv-1 Associated Myelopathy/tropical Spastic Paraparesis 38 0.438
694
c LKM005 Leukemia, T-Cell, Chronic 34 0.438
695
RPT005 Repetitive Motion Disorders 16 0.438
696
CML001 Cumulative Trauma Disorders 18 0.438
697
BCK006 Back Pain 47 0.438
698
OVR077 Overuse Syndrome 16 0.438
700
CVR010 Cavernous Malformation 30 0.438
701
IDP023 Idiopathic Subglottic Tracheal Stenosis 13 0.438
702
P ORL007 Oral Cavity Cancer 51 0.438
703
PRN019 Perinatal Necrotizing Enterocolitis 60 0.438
Content
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