Search results for KLF4

752 hits were found for KLF4

# Family MCID Name MIFTS Score
1
P CLR023 Colorectal Cancer 100 21.579
2
P GST053 Gastric Cancer 82 17.894
3
P PNC035 Pancreatic Cancer 87 16.734
4
ESP021 Esophageal Cancer 84 16.449
5
P BRS047 Breast Cancer 97 16.351
6
P CRB048 Cerebral Cavernous Malformations 63 13.331
7
P FML011 Familial Adenomatous Polyposis 70 12.672
8
MNN043 Meningioma, Familial 79 11.741
9
SCR001 Secretory Meningioma 40 11.741
10
SKN022 Skin Squamous Cell Carcinoma 53 11.683
11
BRK010 Burkitt Lymphoma 65 11.355
12
LPP008 Lipoprotein Quantitative Trait Locus 65 10.921
14
PNC013 Pancreatic Ductal Carcinoma 48 10.649
15
P ECT006 Ectodermal Dysplasia 62 10.624
16
P MDL005 Medulloblastoma 75 10.124
17
P PRK057 Parkinson Disease, Late-Onset 79 10.014
18
c LKM061 Leukemia, Acute Myeloid 83 9.493
19
P RTN008 Retinitis Pigmentosa 79 7.311
20
P PLZ001 Pelizaeus-Merzbacher Disease 65 7.125
21
c LNG044 Long Qt Syndrome 1 66 7.081
22
c EPL236 Epilepsy, Idiopathic Generalized 15 36 7.081
23
c INF161 Inflammatory Bowel Disease 28 38 7.081
24
GRM005 Germ Cell Cancer 46 7.081
25
c NRP054 Neuropathy, Hereditary Sensory and Autonomic, Type Iii 66 6.975
27
c SPR092 Spermatogenic Failure, Y-Linked, 1 30 6.975
28
DSS008 Disease of Mental Health 74 6.975
29
RSP023 Rasopathy 54 6.975
30
GRM001 Germ Cell and Embryonal Cancer 28 6.975
31
SKL030 Skull Base Cancer 25 6.975
32
NNN026 Noonan Syndrome with Multiple Lentigines 64 6.975
33
P SKL005 Skull Base Meningioma 27 6.975
34
FRN003 Frontal Convexity Meningioma 31 6.975
35
P HPT023 Hepatocellular Carcinoma 95 3.864
36
P PRS040 Prostate Cancer 95 3.585
37
P BLD134 Bladder Cancer 79 3.203
38
P LNG064 Lung Cancer Susceptibility 3 69 3.176
39
P TRT010 Teratoma 50 3.101
40
SQM006 Squamous Cell Carcinoma 59 3.017
41
P LNG032 Lung Cancer 98 2.811
42
P OVR042 Ovarian Cancer 88 2.724
43
GST040 Gastric Adenocarcinoma 66 2.430
44
P BCL017 B-Cell Lymphoma 57 2.412
45
P LYM118 Lymphoma 66 2.373
46
P NSP012 Nasopharyngeal Carcinoma 60 2.300
47
OST159 Osteogenic Sarcoma 66 2.223
48
GLB002 Glioblastoma 67 2.218
49
P MYL006 Myeloid Leukemia 60 2.209
50
PNC041 Pancreatic Ductal Adenocarcinoma 51 2.101
51
GLL048 Glial Tumor 51 2.094
52
GLM045 Glioma 62 2.078
53
END057 Endometrial Cancer 76 2.074
54
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 44 2.071
55
ATH013 Atherosclerosis Susceptibility 63 2.055
56
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 2.040
57
P NRB001 Neuroblastoma 66 1.966
58
P LKM002 Leukemia 65 1.961
59
SVR004 Severe Combined Immunodeficiency 70 1.946
60
P VSC007 Vascular Disease 62 1.926
61
P SKN015 Skin Carcinoma 71 1.891
62
LYM002 Lymphoplasmacyte-Rich Meningioma 35 1.877
63
INT395 Intracranial Meningioma 47 1.877
64
LYM133 Lymphoma, Hodgkin, Classic 69 1.845
65
c SML038 Small Cell Cancer of the Lung 68 1.840
66
ORL015 Oral Squamous Cell Carcinoma 43 1.801
67
DFF005 Diffuse Large B-Cell Lymphoma 55 1.751
68
CLT003 Colitis 63 1.744
69
P LKM062 Leukemia, Acute Lymphoblastic 69 1.733
70
ANR040 Aneurysm 60 1.706
71
ART016 Aortic Aneurysm 68 1.678
72
HYP266 Hypoxia 56 1.638
73
BRS099 Breast Ductal Carcinoma 61 1.616
74
ADN018 Adenoma 58 1.598
75
ISC004 Ischemia 61 1.587
76
c PLM164 Pulmonary Hypertension, Primary, 1 75 1.569
77
P ADN016 Adenocarcinoma 63 1.560
78
LYM143 Lymphoma, Non-Hodgkin, Familial 74 1.550
79
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 1.531
80
TCL027 T-Cell Acute Lymphoblastic Leukemia 52 1.501
81
HYP066 Hyperglycemia 60 1.491
82
BLD173 Bladder Small Cell Carcinoma 44 1.450
83
P PLM037 Pulmonary Hypertension 69 1.439
84
NNL005 Non-Alcoholic Fatty Liver Disease 63 1.416
85
P MLN008 Melanoma 75 1.404
86
CRB004 Cerebral Artery Occlusion 45 1.387
87
SPN186 Spinal Cord Injury 60 1.376
88
CMB007 Combined Immunodeficiency 56 1.367
89
PST011 Pustulosis of Palm and Sole 52 1.357
90
P PSR002 Psoriasis 63 1.357
91
ALL014 Allergic Encephalomyelitis 34 1.337
92
CRV035 Cervical Cancer 72 1.296
93
CLF001 Cleft Lip 54 1.285
94
P FLL037 Follicular Lymphoma 66 1.285
95
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 1.273
96
TRM010 Traumatic Brain Injury 50 1.262
97
P MYC007 Myocardial Infarction 69 1.238
98
P HRP006 Herpes Simplex 65 1.226
99
OVR094 Ovarian Epithelial Cancer 39 1.213
100
RNL077 Renal Fibrosis 46 1.212
101
GST103 Gastric Cancer, Hereditary Diffuse 68 1.204
102
BRR014 Barrett Esophagus 66 1.186
103
SKN016 Skin Disease 63 1.186
104
c LKM063 Leukemia, Chronic Myeloid 70 1.158
105
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 1.143
106
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 1.140
107
URT010 Ureteral Obstruction 44 1.130
108
THY029 Thyroid Carcinoma 55 1.130
109
c CRB094 Cerebral Cavernous Malformations 3 41 1.127
110
PRS021 Prostatic Adenoma 43 1.120
111
PRS045 Prostatic Hypertrophy 53 1.120
112
PRP027 Peripheral Vascular Disease 71 1.111
113
PRS129 Prostatic Hyperplasia, Benign 48 1.110
114
P INF037 Inflammatory Bowel Disease 53 1.100
115
PRT251 Proteinuria, Chronic Benign 58 1.090
116
KRT009 Keratosis 52 1.075
117
ART140 Arteries, Anomalies of 52 1.058
118
LNG039 Lung Squamous Cell Carcinoma 57 1.043
119
CLN015 Colon Adenocarcinoma 64 1.043
120
P VND007 Van Der Woude Syndrome 1 60 1.035
121
CLF027 Cleft Palate, Isolated 64 1.035
122
P ADL010 Adult Respiratory Distress Syndrome 70 1.035
123
CLF056 Cleft Lip with or Without Cleft Palate 43 1.035
124
CLF004 Cleft Lip/palate 56 1.035
125
P GLM007 Glomerulonephritis 59 1.035
126
BWN006 Bowen's Disease 32 1.035
127
P INS002 in Situ Carcinoma 52 1.023
128
NNL006 Non-Alcoholic Steatohepatitis 54 0.987
129
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 0.986
130
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 0.986
131
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.986
132
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.986
133
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.986
134
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 0.986
135
c BDY019 Body Mass Index Quantitative Trait Locus 18 46 0.986
136
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.986
137
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.986
138
c BSL007 Basal Cell Carcinoma 67 0.986
139
OST012 Osteoarthritis 77 0.986
140
P BCL004 B-Cell Non-Hodgkin Lymphoma 41 0.986
141
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.982
142
P TMR010 Tumor Predisposition Syndrome 69 0.971
143
ADN011 Adenoid Cystic Carcinoma 68 0.971
144
BRN015 Bronchiolo-Alveolar Adenocarcinoma 55 0.971
145
ADN089 Adenosquamous Lung Carcinoma 51 0.971
146
c PCH010 Pachyonychia Congenita 3 43 0.960
147
CYT002 Cytokine Deficiency 43 0.960
148
LPD008 Lipid Metabolism Disorder 61 0.959
149
c WLM013 Wilms Tumor 1 65 0.946
150
HLC007 Helicobacter Pylori Infection 67 0.946
151
THY128 Thyroid Tumor 33 0.946
152
DNT012 Dental Caries 53 0.946
153
ULC004 Ulcerative Colitis 74 0.946
154
c CHR684 Chronic Kidney Disease 73 0.946
155
P ALZ034 Alzheimer Disease 87 0.931
156
c ATR087 Atrial Standstill 1 74 0.931
157
ORL019 Oral Hairy Leukoplakia 39 0.916
158
CYS001 Cystic Fibrosis 77 0.916
159
STR067 Stroke, Ischemic 79 0.916
160
MSN001 Mesangial Proliferative Glomerulonephritis 44 0.916
161
47X002 47,xyy 47 0.916
162
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 0.916
163
LKP003 Leukoplakia 39 0.916
164
P INF032 Infertility 60 0.900
165
BRN056 Bronchopulmonary Dysplasia 57 0.900
166
ACT114 Acute Myeloblastic Leukemia Without Maturation 26 0.900
167
c CRB191 Cerebral Cavernous Malformations 2 45 0.884
168
ACC008 Accelerated Tumor Formation 20 0.884
169
BRN004 Brain Edema 54 0.884
170
LYM019 Lymphosarcoma 46 0.884
171
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 31 0.867
172
P RHM011 Rheumatoid Arthritis 81 0.856
173
c PLY162 Polyposis Syndrome, Hereditary Mixed, 1 59 0.852
174
c CLR087 Colorectal Cancer 12 34 0.852
175
SML009 Small Intestine Adenocarcinoma 57 0.852
176
ALL003 Allergic Rhinitis 66 0.849
177
c TYP009 Type 2 Diabetes Mellitus 91 0.849
178
c PRG094 Paragangliomas 5 29 0.849
179
PPL022 Papilloma 53 0.849
180
P PNM007 Pneumonia 64 0.849
181
TRN015 Transient Cerebral Ischemia 62 0.849
182
SQM002 Squamous Cell Papilloma 45 0.849
183
EXS001 Exostosis 49 0.849
184
P RHN004 Rhinitis 56 0.849
185
CRT013 Carotid Stenosis 51 0.849
186
TNG007 Tongue Carcinoma 55 0.849
187
P SLP005 Sleep Disorder 61 0.849
188
c SCL052 Scleroderma, Familial Progressive 60 0.829
189
P AST005 Asthma 75 0.829
190
PDT001 Pediatric Lymphoma 28 0.829
191
ALL006 Allergic Asthma 55 0.829
192
P MNC007 Monocytic Leukemia 48 0.829
193
FTT001 Fatty Liver Disease 61 0.829
194
MYL005 Myelofibrosis 70 0.811
195
MYL069 Myeloma, Multiple 76 0.808
196
P PHC003 Pheochromocytoma 70 0.808
197
ADR040 Adrenal Gland Pheochromocytoma 45 0.808
198
ESP027 Esophagus Squamous Cell Carcinoma 45 0.808
199
MLD006 Mal De Meleda 45 0.786
200
P MYC084 Mycobacterium Tuberculosis 1 68 0.786
201
P HNT016 Huntington Disease 73 0.786
202
P GLM040 Glioma Susceptibility 1 70 0.786
203
P ESP035 Esophagitis, Eosinophilic, 1 57 0.786
204
MLG169 Malignant Astrocytoma 57 0.786
205
ESP023 Esophageal Disease 52 0.786
206
P ESP024 Esophagitis 60 0.786
207
LRY018 Laryngeal Squamous Cell Carcinoma 47 0.786
208
LNG031 Lung Benign Neoplasm 51 0.786
209
CRB039 Cerebrovascular Disease 65 0.786
210
c PRS097 Prostate Cancer, Hereditary, 1 38 0.762
211
c PRS114 Prostate Cancer, Hereditary, 2 33 0.762
212
PLM173 Palmoplantar Hyperkeratosis with Squamous Cell Carcinoma of Skin and 46,xx Sex Reversal 34 0.762
213
c PRS070 Prostate Cancer, Hereditary, 12 22 0.762
214
c PRS071 Prostate Cancer, Hereditary, 13 25 0.762
215
c PRS117 Prostate Cancer, Hereditary, 11 24 0.762
216
PRS015 Prostate Signet Ring Cell Adenocarcinoma 25 0.762
217
PSD011 Pseudovascular Skin Squamous Cell Carcinoma 16 0.762
218
MLR004 Malaria 77 0.760
219
c MGR028 Migraine with or Without Aura 1 63 0.760
220
c ART067 Aortic Aneurysm, Familial Thoracic 1 61 0.760
221
CHL065 Cholangiocarcinoma 57 0.760
222
THR024 Thrombosis 56 0.760
223
P RCT021 Rectum Cancer 54 0.760
224
P LMY004 Leiomyosarcoma 62 0.760
225
P MLN007 Male Infertility 56 0.760
226
TRT001 Teratocarcinoma 41 0.760
227
INT079 Intrahepatic Cholangiocarcinoma 51 0.760
228
END062 Endometrial Hyperplasia 47 0.760
229
CLR030 Clear Cell Renal Cell Carcinoma 53 0.733
230
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 0.732
231
NRL016 Neural Tube Defects 80 0.732
232
LNG105 Lung Disease, Immunodeficiency, and Chromosome Breakage Syndrome 36 0.732
233
ANP005 Anaplastic Astrocytoma 59 0.732
234
HMS001 Hemosiderosis 48 0.732
235
PRP016 Paraplegia 52 0.732
236
P END044 Endometriosis 62 0.732
237
CRT015 Carotid Artery Occlusion 45 0.732
238
P RRH023 Rare Hereditary Hemochromatosis 52 0.732
239
MST020 Mast Cell Activation Syndrome 27 0.732
240
P CRN300 Coronary Heart Disease 1 73 0.698
241
c TBR025 Tuberous Sclerosis 1 84 0.698
242
P LKM071 Leukemia, Chronic Lymphocytic 74 0.698
243
ODN009 Odontoonychodermal Dysplasia 35 0.698
244
P ART021 Arteriosclerosis 53 0.698
245
P TBR001 Tuberous Sclerosis 69 0.698
246
c ACT073 Acute Leukemia 59 0.698
247
HPT022 Hepatoblastoma 54 0.698
248
END041 Endometrial Adenocarcinoma 63 0.660
249
c NRF023 Neurofibromatosis, Type Ii 70 0.654
250
TST014 Testicular Cancer 51 0.654
251
ANG020 Angiosarcoma 63 0.565
252
GLM044 Glomerular Disease 34 0.548
253
ORL011 Oral Cancer 60 0.542
254
SQM013 Squamous Cell Carcinoma, Head and Neck 75 0.539
255
OVR062 Ovary Serous Adenocarcinoma 25 0.539
256
PRM126 Primary Peritoneal Carcinoma 61 0.539
257
RPD005 Rapidly Involuting Congenital Hemangioma 48 0.487
258
LNG115 Lung Sarcomatoid Carcinoma 37 0.487
259
c MCR133 Microvascular Complications of Diabetes 4 41 0.463
260
c MCR113 Microvascular Complications of Diabetes 3 52 0.463
261
c MCR130 Microvascular Complications of Diabetes 6 41 0.463
262
c MCR120 Microvascular Complications of Diabetes 7 47 0.463
263
EPD052 Epidermolysis Bullosa Simplex Superficialis 17 0.451
264
P RNL017 Renal Oncocytoma 54 0.431
265
CHR177 Chromophobe Renal Cell Carcinoma 54 0.431
266
HPT070 Hepatosplenic T-Cell Lymphoma 35 0.431
267
P BDY004 Body Mass Index Quantitative Trait Locus 11 82 0.425
268
SMN007 Seminoma 42 0.425
269
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 0.412
270
P SPP010 Suppressor of Tumorigenicity 3 50 0.412
271
ATM095 Autoimmune Disease 61 0.412
272
P PLM036 Pulmonary Fibrosis 65 0.412
273
P ART022 Arthritis 70 0.412
274
P KDN017 Kidney Cancer 60 0.398
275
c PRG020 Paragangliomas 3 39 0.383
276
HMC014 Homocysteinemia 52 0.383
277
CLR108 Colorectal Adenoma 63 0.383
278
VNH007 Von Hippel-Lindau Syndrome 72 0.381
279
IRN008 Iron Overload in Africa 50 0.381
280
c CHL136 Cholestasis, Progressive Familial Intrahepatic, 2 57 0.381
281
c HPT073 Hepatitis C Virus 70 0.381
282
RJS001 Ruijs-Aalfs Syndrome 47 0.381
283
c PRG047 Progressive Familial Intrahepatic Cholestasis 64 0.381
284
ADL096 Adult Hepatocellular Carcinoma 60 0.381
285
HPT079 Hepatoid Adenocarcinoma 39 0.381
286
PDT042 Pediatric Hepatocellular Carcinoma 51 0.381
287
LVR002 Liver Angiosarcoma 42 0.381
288
MLT003 Multilocular Clear Cell Renal Cell Carcinoma 33 0.381
289
FBR086 Fibrolamellar Carcinoma 59 0.381
290
HPT011 Hepatocellular Clear Cell Carcinoma 46 0.381
291
MRK001 Merkel Cell Carcinoma 64 0.381
292
LNG012 Lung Occult Squamous Cell Carcinoma 20 0.381
293
LNG007 Lung Mixed Small Cell and Squamous Cell Carcinoma 20 0.381
294
NNN007 Non-Involuting Congenital Hemangioma 40 0.381
295
KPS002 Kaposiform Hemangioendothelioma 50 0.381
296
PTY007 Pityriasis Rotunda 27 0.381
297
MLT165 Multilocular Cystic Renal Neoplasm of Low Malignant Potential 28 0.381
298
EMB004 Embryonal Carcinoma 55 0.368
299
P HYD006 Hydrocephalus 62 0.368
300
PLM134 Pulmonary Fibrosis, Idiopathic 76 0.336
301
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.336
302
P LRY044 Larynx Cancer 53 0.336
303
RTN020 Retinal Vascular Disease 45 0.336
304
NRR001 Neuroretinitis 42 0.336
305
GLC003 Glucose Intolerance 53 0.336
306
RTN023 Retinitis 45 0.336
307
P KDN018 Kidney Disease 71 0.319
308
P MSC005 Muscular Dystrophy 66 0.319
309
c AMY091 Amyotrophic Lateral Sclerosis 1 87 0.301
310
P RPD001 Rapidly Progressive Glomerulonephritis 43 0.301
311
P LTR001 Lateral Sclerosis 57 0.301
312
PLM010 Pulmonary Edema 54 0.301
313
P FCL005 Focal Segmental Glomerulosclerosis 57 0.301
314
c ACT075 Acute Myocardial Infarction 55 0.301
315
P MYC008 Myocarditis 59 0.301
316
P MLT020 Multiple Sclerosis 79 0.281
317
MNT001 Mantle Cell Lymphoma 65 0.281
318
P LNG028 Long Qt Syndrome 63 0.281
319
P THL005 Thalassemia 56 0.281
320
HYP025 Hyperphosphatemia 47 0.260
321
KWS002 Kawasaki Disease 65 0.260
322
MRF001 Marfan Syndrome 76 0.260
323
P TCD001 Tic Disorder 50 0.260
324
BCT022 Bacterial Infectious Disease 55 0.260
325
MCN001 Mucinous Adenocarcinoma 49 0.260
326
HMG005 Hemoglobinopathy 55 0.260
327
APP009 Appendix Adenocarcinoma 47 0.260
328
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 0.260
329
P RTN016 Retinal Degeneration 52 0.260
330
CRH001 Crohn's Disease 80 0.260
331
P SCK005 Sickle Cell Disease 56 0.260
332
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 0.260
333
c LKM005 Leukemia, T-Cell, Chronic 33 0.260
334
DWN001 Down Syndrome 70 0.238
335
P RTN024 Retinoblastoma 72 0.238
336
MSC157 Muscular Dystrophy, Duchenne Type 78 0.238
337
ENT011 Enterocolitis 55 0.238
338
P CRN024 Corneal Disease 43 0.238
339
P ALP004 Alport Syndrome 69 0.238
340
TTH006 Tooth Disease 51 0.238
341
P GCH001 Gaucher's Disease 69 0.238
342
NRT004 Neuritis 53 0.238
343
SPN035 Spindle Cell Sarcoma 51 0.238
344
P CHR071 Charcot-Marie-Tooth Disease 64 0.238
345
TXC005 Toxic Shock Syndrome 61 0.238
346
SRC014 Sarcoma 64 0.238
347
P OPT009 Optic Neuritis 57 0.238
348
P RTN018 Retinal Disease 53 0.238
349
GBL002 Goblet Cell Carcinoid 32 0.238
350
CHR178 Chromosomal Triplication 33 0.238
352
BRN071 Brain Injury 50 0.238
353
CRB086 Cerebral Aneurysms 40 0.238
354
P APL001 Aplastic Anemia 72 0.213
355
ERY003 Erythema Multiforme 56 0.213
356
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 0.213
357
P MCH002 Machado-Joseph Disease 62 0.213
358
ADR007 Adrenoleukodystrophy 73 0.213
359
BRT054 Brittle Bone Disorder 74 0.213
360
P MCP040 Mucopolysaccharidosis-Plus Syndrome 70 0.213
362
SVR097 Severe Cutaneous Adverse Reaction 68 0.213
363
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 0.213
364
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.213
365
INT030 Intracranial Aneurysm 55 0.213
366
NRL005 Neurilemmoma 60 0.213
367
c MLG084 Malignant Fibrous Histiocytoma 62 0.213
368
P SPN046 Spinal Muscular Atrophy 62 0.213
369
P OVR049 Ovarian Disease 50 0.213
370
LYS002 Lysosomal Storage Disease 51 0.213
371
c MCP001 Mucopolysaccharidosis Iii 69 0.213
372
SCH014 Schistosomiasis 56 0.213
373
P MYT002 Myotonic Dystrophy 51 0.213
374
ADR022 Adrenomyeloneuropathy 38 0.213
375
P MSC003 Muscular Atrophy 52 0.213
376
DSR013 Disorders of Gnas Inactivation 15 0.213
377
SYN149 Syndromic Rod-Cone Dystrophy 21 0.213
378
c MNS014 Monosomy 22 34 0.213
379
ERY066 Erythema Multiforme Major 29 0.213
380
CVR010 Cavernous Malformation 29 0.213
381
c ATS007 Autism Spectrum Disorder 71 0.184
382
ACT119 Acute Promyelocytic Leukemia 62 0.184
383
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 59 0.184
384
DCT002 Ductal Carcinoma in Situ 58 0.184
385
P ATS364 Autism 72 0.184
386
PLY150 Polykaryocytosis Inducer 29 0.184
387
FCT001 Factor Viii Deficiency 61 0.184
388
c GLY008 Glycogen Storage Disease Ii 72 0.184
389
AST006 Astigmatism 46 0.184
390
AGN016 Aging 53 0.184
391
P USH001 Usher Syndrome 63 0.184
392
EWN003 Ewing Sarcoma 69 0.184
393
P TST021 Testicular Germ Cell Tumor 61 0.184
394
c HMP029 Hemophilia a 69 0.184
395
PCK003 Pick Disease of Brain 70 0.184
396
c NMN015 Niemann-Pick Disease, Type C1 68 0.184
397
P HMN036 Hemangiopericytoma, Malignant 56 0.184
398
RTN187 Retinitis Pigmentosa-Deafness Syndrome 48 0.184
399
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 0.184
400
P ADL017 Adult T-Cell Leukemia 53 0.184
401
P BND020 Bone Disease 60 0.184
402
LMB062 Limb Ischemia 55 0.184
403
P HMN010 Hemangioma 61 0.184
404
P FBR017 Fibrosarcoma 55 0.184
405
P EYD002 Eye Disease 57 0.184
406
CNG034 Congestive Heart Failure 69 0.184
407
P HPT021 Hepatitis 68 0.184
408
ACT098 Acute Erythroid Leukemia 55 0.184
409
P CPL006 Capillary Hemangioma 53 0.184
410
VNS002 Venous Hemangioma 18 0.184
411
CVR006 Cavernous Hemangioma 51 0.184
412
P GST044 Gastritis 55 0.184
413
P PNC044 Pancreatitis 61 0.184
414
c ACT027 Acute Pancreatitis 60 0.184
415
P NMN002 Niemann-Pick Disease 60 0.184
416
BLP005 Blepharitis 50 0.184
417
P PRD008 Periodontitis 63 0.184
418
MSL001 Measles 61 0.184
419
P LPS004 Lupus Erythematosus 61 0.184
420
P HMP007 Hemophilia 52 0.184
421
GRM010 Germ Cells Tumors 33 0.184
422
HMN016 Hemangioendothelioma 35 0.184
423
THR123 Thrombotic Microangiopathy 40 0.184
424
P ENC018 Encephalopathy 62 0.184
425
PRM329 Premature Aging 36 0.184
426
P SCL048 Sclerosteosis 58 0.150
427
P STR022 Stargardt Disease 61 0.150
428
P CRD119 Cardiac Arrest 68 0.150
429
MYL009 Myelodysplastic Syndrome 67 0.150
430
MNN042 Meningioma, Radiation-Induced 51 0.150
431
c HNT011 Huntington Disease-Like 3 33 0.150
432
PRP001 Propionic Acidemia 65 0.150
433
P SCH015 Schizophrenia 74 0.150
434
P JRV004 Jervell and Lange-Nielsen Syndrome 1 56 0.150
435
P CRG003 Crigler-Najjar Syndrome, Type I 64 0.150
436
c SYS001 Systemic Lupus Erythematosus 85 0.150
437
ONC005 Oncogene Bmyc 9 0.150
438
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 55 0.150
439
P ART028 Aortic Aneurysm, Familial Thoracic 4 61 0.150
440
P NJM001 Nijmegen Breakage Syndrome 75 0.150
441
c FNC027 Fanconi Anemia, Complementation Group a 80 0.150
442
P RTT002 Rett Syndrome 79 0.150
443
INS024 Insulin-Like Growth Factor I 77 0.150
444
P CHR625 Charcot-Marie-Tooth Disease, Demyelinating, Type 1b 57 0.150
445
DST033 Distichiasis 35 0.150
446
P DRM053 Dermatitis, Atopic 65 0.150
447
SRC027 Sarcoma, Synovial 58 0.150
448
ATS010 Autosomal Recessive Disease 42 0.150
449
INT323 Intraocular Pressure Quantitative Trait Locus 63 0.150
450
HLX001 Helix Syndrome 47 0.150
451
P GRF003 Graft-Versus-Host Disease 71 0.150
452
MRF007 Marfanoid Hypermobility Syndrome 49 0.150
453
c OPT053 Optic Atrophy 1 62 0.150
454
LYM029 Lymphedema-Distichiasis Syndrome 52 0.150
455
P MLN069 Melanoma, Uveal 59 0.150
456
P KLZ004 Kala-Azar 1 41 0.150
457
c HRD202 Hereditary Lymphedema I 54 0.150
458
P RSP003 Respiratory Failure 73 0.150
459
PRP080 Peripheral Artery Disease 54 0.150
460
P ESS003 Essential Thrombocythemia 68 0.150
461
P GLY013 Glycogen Storage Disease 59 0.150
462
XLN231 X-Linked Alport Syndrome 41 0.150
463
P SPS008 Spastic Ataxia 41 0.150
464
CNS002 Constrictive Pericarditis 39 0.150
465
THY020 Thyroid Hyalinizing Trabecular Adenoma 19 0.150
466
P ANT006 Antiphospholipid Syndrome 55 0.150
467
c HPT016 Hepatitis B 62 0.150
468
P SYS005 Systemic Scleroderma 73 0.150
469
HGH043 High Grade Glioma 46 0.150
470
P HYP061 Hypertrophic Cardiomyopathy 68 0.150
471
PRM236 Primary Biliary Cholangitis 62 0.150
472
ALC006 Alcoholic Hepatitis 61 0.150
473
c HPT003 Hepatitis a 63 0.150
474
c DLT002 Dilated Cardiomyopathy 79 0.150
475
c BNG093 Benign Teratoma 39 0.150
476
LYM022 Lymphangioma 54 0.150
477
AZS001 Azoospermia 45 0.150
478
PRC013 Pericarditis 53 0.150
479
CHR074 Choriocarcinoma 46 0.150
480
P FBR003 Fibrous Histiocytoma 43 0.150
481
LSH001 Leishmaniasis 63 0.150
482
VNZ002 Venezuelan Equine Encephalitis 45 0.150
483
P ENC004 Encephalitis 61 0.150
484
VSC003 Visceral Leishmaniasis 54 0.150
485
END086 End Stage Renal Disease 54 0.150
486
P CHL066 Cholangitis 51 0.150
488
c FML191 Familial Long Qt Syndrome 54 0.150
489
c ATS438 Autosomal Recessive Spastic Ataxia 24 0.150
490
P FML364 Familial Thoracic Aortic Aneurysm and Aortic Dissection 70 0.150
491
P TRM003 Tremor 50 0.150
492
CRV068 Cervical Polyp 27 0.106
493
MYL020 Myelomeningocele 51 0.106
494
MTR082 Maturity-Onset Diabetes of the Young, Type 8, with Exocrine Dysfunction 41 0.106
495
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 0.106
496
c MJR022 Major Affective Disorder 8 37 0.106
497
c NMN014 Niemann-Pick Disease, Type C2 49 0.106
498
BRN032 Brain Glioma 45 0.106
499
P ATR011 Atrial Fibrillation 66 0.106
500
c WLF009 Wolfram Syndrome 2 43 0.106
501
SPL004 Splenic Marginal Zone Lymphoma 50 0.106
502
SGW002 Segawa Syndrome, Autosomal Recessive 44 0.106
503
P MTR004 Maturity-Onset Diabetes of the Young 66 0.106
504
ILT001 Ileitis 49 0.106
505
ATR057 Atrioventricular Block 54 0.106
506
P EST001 Estrogen-Receptor Positive Breast Cancer 49 0.106
507
CMB008 Combined Oxidative Phosphorylation Deficiency 35 0.106
508
c CRD086 Cardiomyopathy, Familial Hypertrophic, 1 69 0.106
509
MCL075 Macular Dystrophy, Corneal 55 0.106
510
CHR072 Chordoma 56 0.106
511
c EPD076 Epidermolysis Bullosa Dystrophica, Autosomal Recessive 51 0.106
512
P BSL038 Basal Ganglia Calcification, Idiopathic, 1 51 0.106
513
CRB011 Cerebrotendinous Xanthomatosis 64 0.106
514
CRY035 Cryptorchidism, Unilateral or Bilateral 57 0.106
515
P OST002 Osteoporosis 76 0.106
516
PRX015 Paroxysmal Extreme Pain Disorder 56 0.106
517
P CRN052 Craniometaphyseal Dysplasia, Autosomal Dominant 61 0.106
518
DNT005 Dentatorubral-Pallidoluysian Atrophy 59 0.106
519
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.106
520
c MTR019 Maturity-Onset Diabetes of the Young, Type 2 53 0.106
521
P PLV020 Pelvic Organ Prolapse 57 0.106
522
c RTN150 Retinitis Pigmentosa 10 44 0.106
523
P HML033 Hemolytic Uremic Syndrome, Atypical 1 67 0.106
524
PPL049 Papillon-Lefevre Syndrome 65 0.106
525
P KRB001 Krabbe Disease 69 0.106
526
LGH007 Leigh Syndrome 70 0.106
527
P CLD001 Cleidocranial Dysplasia 64 0.106
528
c MLT156 Multiple Endocrine Neoplasia, Type I 71 0.106
529
CRD223 Cardiac Arrhythmia 63 0.106
530
CRD132 Cardiac Conduction Defect 59 0.106
531
P MPL001 Maple Syrup Urine Disease 69 0.106
532
c NML003 Nemaline Myopathy 2 51 0.106
533
TTH030 Teeth, Supernumerary 32 0.106
534
P BRN019 Bernard-Soulier Syndrome 61 0.106
535
c CRD187 Cardiomyopathy, Dilated, 3b 47 0.106
536
XNT003 Xanthomatosis 48 0.106
537
c MYT020 Myotonic Dystrophy 2 57 0.106
538
c BRN108 Branchiootic Syndrome 1 63 0.106
539
c MYP072 Myopathy, Myofibrillar, 1 55 0.106
540
SCK003 Sickle Cell Anemia 74 0.106
541
HTR014 Heterotaxy, Visceral, 1, X-Linked 40 0.106
542
DRV001 Dravet Syndrome 69 0.106
543
c INF138 Infantile Liver Failure Syndrome 2 29 0.106
544
c CRT089 Cortical Dysplasia, Complex, with Other Brain Malformations 10 39 0.106
545
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 61 0.106
546
c CNG012 Congenital Generalized Lipodystrophy 65 0.106
547
FML037 Female Breast Cancer 51 0.106
548
CNZ001 Coenzyme Q10 Deficiency Disease 41 0.106
549
c MJR024 Major Affective Disorder 9 40 0.106
550
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 0.106
551
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.106
552
BMB001 Bombay Phenotype 31 0.106
553
c SPS210 Spastic Paraplegia 76, Autosomal Recessive 38 0.106
554
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 0.106
555
PLY001 Polycythemia Vera 69 0.106
556
P TYS001 Tay-Sachs Disease 69 0.106
557
c THY107 Thymoma, Familial 42 0.106
558
MSC152 Muscular Dystrophy, Becker Type 69 0.106
559
BRT005 Barth Syndrome 55 0.106
560
P CHN012 Chondrosarcoma 56 0.106
561
DDN011 Duodenal Atresia 47 0.106
562
c BRD010 Bardet-Biedl Syndrome 1 64 0.106
563
KRT019 Keratitis, Hereditary 66 0.106
564
P HYP750 Hypertriglyceridemia, Familial 61 0.106
565
P TTR001 Tetralogy of Fallot 69 0.106
566
HTC003 Hutchinson-Gilford Progeria Syndrome 65 0.106
567
c THY109 Thyroid Cancer, Nonmedullary, 1 55 0.106
568
LMY014 Leiomyoma, Uterine 55 0.106
569
P MTC003 Metachromatic Leukodystrophy 71 0.106
570
c NPH019 Nephronophthisis 1 50 0.106
571
PHN003 Phenylketonuria 76 0.106
572
P SJG008 Sjogren Syndrome 60 0.106
573
DHY002 Dihydropyrimidine Dehydrogenase Deficiency 57 0.106
574
PND002 Pendred Syndrome 57 0.106
575
WRN001 Werner Syndrome 69 0.106
576
P WSK001 Wiskott-Aldrich Syndrome 72 0.106
577
FBR012 Fabry Disease 71 0.106
578
FRN006 Frontotemporal Dementia 68 0.106
579
c MCR115 Microvascular Complications of Diabetes 5 65 0.106
580
ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 35 0.106
581
c LNG050 Long Qt Syndrome 5 45 0.106
582
c FNC028 Fanconi Anemia, Complementation Group L 46 0.106
583
c FNC025 Fanconi Anemia, Complementation Group J 52 0.106
584
GST019 Gastrointestinal Stromal Tumor 78 0.106
585
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 0.106
586
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.106
587
c CNG385 Congenital Heart Defects, Multiple Types, 3 18 0.106
588
P DNG005 Dengue Virus 55 0.106
589
c INF064 Inflammatory Bowel Disease 28, Autosomal Recessive 30 0.106
590
CHR375 Chromosome 8p11 Myeloproliferative Syndrome 28 0.106
591
P MGL010 Megalencephalic Leukoencephalopathy with Subcortical Cysts 2a 39 0.106
592
c BTT014 Beta-Thalassemia 72 0.106
593
c LKM070 Leukemia, Acute Monocytic 56 0.106
594
CHR635 Chromosome 5q Deletion Syndrome 50 0.106
595
OCL020 Ocular Cicatricial Pemphigoid 52 0.106
596
c HYP836 Hypercholesterolemia, Familial, 1 73 0.106
597
DYS192 Dystonia, Dopa-Responsive 56 0.106
598
HRW001 Hair Whorl 35 0.106
599
c SPN309 Spinocerebellar Ataxia 6 58 0.106
600
P FRD001 Friedreich Ataxia 62 0.106
601
c FNC042 Fanconi Anemia, Complementation Group D2 54 0.106
602
c MTR020 Maturity-Onset Diabetes of the Young, Type 3 54 0.106
603
P EPL140 Epilepsy, Idiopathic Generalized 60 0.106
604
c RTN041 Retinitis Pigmentosa 11 43 0.106
605
c FML001 Familial Atrial Fibrillation 65 0.106
606
MSC190 Muscular Disease 36 0.106
607
P RCS002 Recessive Dystrophic Epidermolysis Bullosa 62 0.106
608
c ATS013 Autosomal Recessive Congenital Ichthyosis 66 0.106
609
P CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 64 0.106
610
P LYM033 Lymphoproliferative Syndrome 59 0.106
611
NTM002 Nut Midline Carcinoma 44 0.106
612
P PRK039 Parkinsonism 55 0.106
613
THY121 Thyroid Gland Anaplastic Carcinoma 66 0.106
614
c INF194 Infantile Liver Failure Syndrome 30 0.106
615
LWG006 Low Grade Glioma 41 0.106
616
MLD018 Mild Cognitive Impairment 48 0.106
617
DPH001 Diphtheria 59 0.106
618
CCT002 Cicatricial Pemphigoid 53 0.106
619
P MYF003 Myofibrillar Myopathy 50 0.106
620
P PLY014 Polycystic Kidney Disease 71 0.106
621
MRG003 Marginal Zone B-Cell Lymphoma 52 0.106
622
P WLF004 Wolfram Syndrome 61 0.106
623
P CYS018 Cystitis 58 0.106
624
HPT019 Hepatic Encephalopathy 59 0.106
625
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.106
626
BLD053 Blood Platelet Disease 51 0.106
627
MYL031 Myeloproliferative Neoplasm 66 0.106
628
THR004 Thrombocytosis 52 0.106
629
HYP068 Hyperostosis 47 0.106
630
SRS001 Serous Cystadenocarcinoma 51 0.106
631
SKN013 Skin Benign Neoplasm 49 0.106
632
P THY023 Thymoma 64 0.106
633
VCC001 Vaccinia 49 0.106
634
c HRD010 Hereditary Spastic Paraplegia 65 0.106
635
P EPD016 Epidermolysis Bullosa 53 0.106
636
P LPS002 Liposarcoma 64 0.106
637
P ATR010 Atrial Heart Septal Defect 58 0.106
638
P BRD002 Bardet-Biedl Syndrome 66 0.106
639
P OST001 Osteopetrosis 70 0.106
640
PHR002 Pharyngoconjunctival Fever 32 0.106
641
P ICH004 Ichthyosis 56 0.106
642
P DRR001 Diarrhea 55 0.106
643
HRT011 Heart Septal Defect 49 0.106
644
GLC106 Glucocorticoid Resistance, Generalized 47 0.106
645
c ATS018 Autosomal Recessive Alport Syndrome 43 0.106
646
EMB002 Embryoma 37 0.106
647
LVR012 Liver Cirrhosis 62 0.106
648
P EPD009 Epidermolysis Bullosa Dystrophica 66 0.106
649
DYS101 Dysgerminoma 43 0.106
650
MTR010 Mature Teratoma 40 0.106
651
P MLT074 Multiple Endocrine Neoplasia 58 0.106
652
P NML001 Nemaline Myopathy 49 0.106
653
P BPL003 Bipolar Disorder 56 0.106
654
P INT068 Intestinal Disease 53 0.106
655
P DYS154 Dystonia 64 0.106
656
P MTR014 Motor Neuron Disease 65 0.106
657
P INT143 Interstitial Cystitis 59 0.106
658
RTR008 Root Resorption 44 0.106
659
FST001 Foster-Kennedy Syndrome 39 0.106
660
P HRT032 Heart Disease 84 0.106
661
INF021 Infant Gynecomastia 30 0.106
662
P PLY011 Polycystic Ovary Syndrome 57 0.106
663
P MYP006 Myopia 55 0.106
664
BTT017 Beta-Thalassemia Major 54 0.106
665
P EPL164 Epilepsy 70 0.106
666
DRY001 Dry Eye Syndrome 49 0.106
667
P PLY019 Polyneuropathy 52 0.106
668
P CRN025 Corneal Dystrophy 49 0.106
669
P LVR013 Liver Disease 68 0.106
670
P MYP004 Myopathy 67 0.106
671
CRN036 Craniopharyngioma 63 0.106
672
PNC129 Pancreatic Adenocarcinoma 64 0.106
673
P PTT006 Pituitary Adenoma 55 0.106
674
CYS014 Cystadenocarcinoma 51 0.106
675
ANV001 Anovulation 46 0.106
676
GRM004 Germinoma 40 0.106
677
P EMR001 Emery-Dreifuss Muscular Dystrophy 62 0.106
678
DGN002 Degenerative Myopia 31 0.106
679
CLB002 Clubfoot 50 0.106
680
P LKD001 Leukodystrophy 58 0.106
681
MCR013 Microphthalmia 59 0.106
682
RTN003 Retinal Ischemia 48 0.106
683
RCK004 Rickets 64 0.106
684
P ART005 Arteriovenous Malformation 64 0.106
685
GYN001 Gynecomastia 48 0.106
686
LMY002 Leiomyoma 51 0.106
687
PMP014 Pemphigoid 48 0.106
688
PRM013 Premature Menopause 57 0.106
689
P MTH008 Methylmalonic Acidemia 52 0.106
690
P THR014 Thrombocytopenia 66 0.106
691
ALC009 Alcoholic Liver Cirrhosis 54 0.106
692
OLV001 Olivopontocerebellar Atrophy 50 0.106
693
P HML001 Hemolytic-Uremic Syndrome 52 0.106
694
P CRD246 Cardiovascular System Disease 55 0.106
695
P DMN002 Dementia 65 0.106
696
CRN027 Corneal Neovascularization 47 0.106
697
P KRT007 Keratoconus 49 0.106
698
P DRM010 Dermatomyositis 61 0.106
699
LYM009 Lymphocytic Choriomeningitis 46 0.106
700
HPT004 Hepatic Coma 43 0.106
701
TLN003 Telangiectasis 51 0.106
702
KRT001 Keratoconjunctivitis Sicca 49 0.106
703
GT001 Gout 63 0.106
704
BRN028 Brain Cancer 73 0.106
705
P CTR002 Cataract 59 0.106
706
P VSC011 Vasculitis 61 0.106
707
P NRF002 Neurofibromatosis 60 0.106
708
PSD016 Pseudosarcomatous Fibromatosis 37 0.106
709
LRN003 Learning Disability 49 0.106
710
OVR012 Ovarian Serous Cystadenocarcinoma 55 0.106
711
KLD004 Keloid Disorder 38 0.106
712
ISL099 Isolated Methylmalonic Acidemia 35 0.106
713
ACT200 Acute Monoblastic Leukemia 40 0.106
714
URC002 Urea Cycle Disorder 51 0.106
715
P TYR004 Tyrosinemia 49 0.106
716
P DBT009 Diabetes Mellitus 67 0.106
717
P ATR005 Atrophic Gastritis 50 0.106
718
FSC004 Fasciitis 49 0.106
719
c ATS347 Autosomal Dominant Polycystic Kidney Disease 64 0.106
720
DGN001 Degenerative Disc Disease 48 0.106
721
P PLY018 Polycythemia 56 0.106
722
LNG099 Lung Disease 62 0.106
723
FND002 Fundus Dystrophy 54 0.106
724
OLG006 Oligoastrocytoma 35 0.106
725
STM007 Stomatitis 52 0.106
726
ALB002 Albinism 46 0.106
727
P MTC069 Mitochondrial Disorders 57 0.106
728
48X005 48,xyyy 39 0.106
729
MLT028 Multiminicore Disease 44 0.106
730
PTT037 Pituitary Tumors 44 0.106
731
P SZR006 Seizure Disorder 69 0.106
732
BCK006 Back Pain 43 0.106
733
CYT019 Cytogenetically Normal Acute Myeloid Leukemia 30 0.106
734
P AMY004 Amyloidosis 69 0.106
735
KRT006 Keratoconjunctivitis 53 0.106
736
P ALP008 Alopecia 53 0.106
737
PDT025 Pediatric Multiple Sclerosis 35 0.106
738
c HRD039 Hereditary Amyloidosis 45 0.106
739
P MRC003 Mercury Poisoning 48 0.106
740
c CLD019 Cleidocranial Dysplasia Spectrum Disorder 20 0.106
741
LMB050 Limbal Stem Cell Deficiency 51 0.106
742
c INH030 Inherited Retinal Disorder 28 0.106
743
SFT003 Soft Tissue Sarcoma 43 0.106
744
P 8P1002 8p11 Myeloproliferative Syndrome 35 0.106
745
c INF185 Infantile Epilepsy Syndrome 30 0.106
746
ACT248 Acute Monoblastic/monocytic Leukemia 25 0.106
747
MNG006 Monogenic Diabetes 45 0.106
748
c CHR135 Charcot-Marie-Tooth Disease Type 2a 23 0.106
749
P HYP265 Hypotonia 42 0.106
750
P PRD021 Periodic Paralysis 42 0.106
751
c MTC199 Mitochondrial Disorder Due to a Defect in Mitochondrial Protein Synthesis 12 0.106
752
c ACT134 Acute Liver Failure 57 0.106
Content
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