Search results for sox2

334 hits were found for sox2

# Family MCID Name MIFTS Score
1
c MCR241 Microphthalmia, Syndromic 3 42 13.005
2
MCR013 Microphthalmia 61 4.116
3
P CLR023 Colorectal Cancer 99 3.362
4
P GST053 Gastric Cancer 84 3.113
5
EMB004 Embryonal Carcinoma 58 3.113
6
P LNG032 Lung Cancer 98 3.097
7
P BRS047 Breast Cancer 97 3.005
8
P OVR042 Ovarian Cancer 90 2.655
9
ESP021 Esophageal Cancer 91 2.644
10
P PRS040 Prostate Cancer 98 2.599
11
ESP020 Esophageal Atresia 56 2.586
12
P SNS001 Sensorineural Hearing Loss 61 2.559
13
ADN011 Adenoid Cystic Carcinoma 71 2.544
14
P SLV026 Salivary Gland Carcinoma 61 2.492
15
GLB015 Glioblastoma Multiforme 75 2.377
16
P TRT010 Teratoma 52 2.266
17
LNG039 Lung Squamous Cell Carcinoma 66 2.257
18
SMN007 Seminoma 45 2.184
19
P MDL005 Medulloblastoma 78 2.159
20
P NRB001 Neuroblastoma 72 2.117
21
P NSP012 Nasopharyngeal Carcinoma 67 2.117
22
SPT006 Septooptic Dysplasia 64 2.101
23
P HYP083 Hypopituitarism 53 2.101
24
TNG009 Tongue Squamous Cell Carcinoma 44 2.101
25
BRN028 Brain Cancer 74 2.084
26
GST040 Gastric Adenocarcinoma 71 2.084
27
P CTR002 Cataract 61 2.084
28
c AMY091 Amyotrophic Lateral Sclerosis 1 90 2.064
29
EWN003 Ewing Sarcoma 69 2.064
30
CRV038 Cervical Squamous Cell Carcinoma 59 2.064
32
c BSL007 Basal Cell Carcinoma 69 2.042
33
NTM002 Nut Midline Carcinoma 44 2.042
34
BSL006 Basaloid Squamous Cell Carcinoma 43 2.042
35
P PRK057 Parkinson Disease, Late-Onset 77 2.017
36
CRN036 Craniopharyngioma 66 2.017
37
P CRN015 Cornelia De Lange Syndrome 63 2.017
38
PTR032 Peters-Plus Syndrome 63 2.017
39
P GLY013 Glycogen Storage Disease 60 2.017
40
P TYR004 Tyrosinemia 58 2.017
41
P ORL007 Oral Cavity Cancer 57 2.017
42
OCL009 Ocular Cancer 55 2.017
43
LMB002 Lambert-Eaton Myasthenic Syndrome 55 2.017
44
FRY006 Fryns Microphthalmia Syndrome 55 1.910
46
P LNG064 Lung Cancer Susceptibility 3 78 1.681
47
CLB010 Coloboma of Macula 53 1.615
48
SPP011 Suppression of Tumorigenicity 12 60 1.486
49
c LKM061 Leukemia, Acute Myeloid 83 1.460
50
CHR103 Charge Syndrome 66 1.460
51
P ANR048 Aniridia 1 63 1.460
52
GLS001 Gliosarcoma 54 1.460
53
SCH018 Schizencephaly 52 1.460
54
GRM005 Germ Cell Cancer 48 1.460
55
ERM002 Ear Malformation 39 1.460
56
CLN009 Colon Squamous Cell Carcinoma 39 1.460
57
LWG005 Low-Grade Astrocytoma 38 1.460
58
P RTN008 Retinitis Pigmentosa 78 1.426
59
c NRP054 Neuropathy, Hereditary Sensory and Autonomic, Type Iii 67 1.426
60
c LNG044 Long Qt Syndrome 1 66 1.426
61
P KLL001 Kallmann Syndrome 64 1.426
62
P PLZ001 Pelizaeus-Merzbacher Disease 62 1.426
63
MSC190 Muscular Disease 52 1.426
64
c CNT033 Central Nervous System Cancer 47 1.426
65
c PRK052 Parkinson Disease 17 42 1.426
66
P MCR137 Microphthalmia, Isolated 2 42 1.426
67
c MLG081 Malignant Teratoma 42 1.426
68
c SPS210 Spastic Paraplegia 76, Autosomal Recessive 41 1.426
69
c MCR114 Microphthalmia, Isolated 3 39 1.426
70
OVR050 Ovarian Embryonal Carcinoma 36 1.426
71
HLZ001 Holzgreve Syndrome 35 1.426
72
INF039 Infratentorial Cancer 34 1.426
73
c INF161 Inflammatory Bowel Disease 28 32 1.426
74
GRM001 Germ Cell and Embryonal Cancer 30 1.426
75
GLB011 Glioblastoma Classical Subtype 23 1.426
76
P CNT039 Central Nervous System Immature Teratoma 17 1.426
77
SQM006 Squamous Cell Carcinoma 60 0.300
78
P ADN016 Adenocarcinoma 64 0.208
79
P GLM045 Glioma 63 0.204
80
GLL048 Glial Tumor 46 0.204
81
c SML038 Small Cell Cancer of the Lung 66 0.173
82
OBS525 Obsolete: Squamous Cell Carcinoma of Head and Neck 57 0.147
83
ORL015 Oral Squamous Cell Carcinoma 43 0.147
84
ORL011 Oral Cancer 60 0.129
85
HYP080 Hypogonadism 50 0.129
86
HYP064 Hypogonadotropism 41 0.129
87
SVR004 Severe Combined Immunodeficiency 74 0.122
88
P HYP730 Hypogonadotropic Hypogonadism 53 0.122
89
P PNC035 Pancreatic Cancer 85 0.115
90
CRV035 Cervical Cancer 76 0.115
91
MLN008 Melanoma 69 0.115
92
OST159 Osteogenic Sarcoma 67 0.115
93
P HPT023 Hepatocellular Carcinoma 100 0.108
94
P BLD134 Bladder Cancer 79 0.108
95
CHR074 Choriocarcinoma 47 0.108
96
c CRV002 Cervix Uteri Carcinoma in Situ 44 0.100
97
CRV045 Cervical Intraepithelial Neoplasia 39 0.100
98
P RTN024 Retinoblastoma 73 0.091
99
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.091
100
c FML008 Familial Retinoblastoma 53 0.091
101
P INS002 in Situ Carcinoma 52 0.091
102
PTT037 Pituitary Tumors 45 0.091
103
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 65 0.082
104
BRR014 Barrett Esophagus 65 0.082
105
SPN186 Spinal Cord Injury 61 0.082
106
THY029 Thyroid Carcinoma 60 0.082
107
ADN018 Adenoma 59 0.082
108
P EST001 Estrogen-Receptor Positive Breast Cancer 50 0.082
109
TRT001 Teratocarcinoma 46 0.082
110
PTT001 Pituitary Hypoplasia 34 0.082
111
CHL065 Cholangiocarcinoma 68 0.071
112
P SKN015 Skin Carcinoma 67 0.071
113
THY121 Thyroid Gland Anaplastic Carcinoma 64 0.071
114
P RHB003 Rhabdomyosarcoma 63 0.071
115
CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 60 0.071
116
HLC007 Helicobacter Pylori Infection 59 0.071
117
PPL022 Papilloma 55 0.071
118
P TCD001 Tic Disorder 54 0.071
119
P RCT021 Rectum Cancer 53 0.071
120
TRM010 Traumatic Brain Injury 53 0.071
121
INT079 Intrahepatic Cholangiocarcinoma 50 0.071
122
P AST007 Astrocytoma 50 0.071
123
HLX001 Helix Syndrome 48 0.071
124
AML029 Ameloblastoma 48 0.071
125
LRY018 Laryngeal Squamous Cell Carcinoma 44 0.071
126
c PCH010 Pachyonychia Congenita 3 44 0.071
127
SQM002 Squamous Cell Papilloma 43 0.071
128
P END039 Endodermal Sinus Tumor 42 0.071
129
TST018 Testicular Yolk Sac Tumor 39 0.071
130
GRM010 Germ Cells Tumors 34 0.071
131
END057 Endometrial Cancer 75 0.058
132
c MNN043 Meningioma, Familial 75 0.058
133
P OLG002 Oligodendroglioma 67 0.058
134
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.058
135
P THY023 Thymoma 65 0.058
136
P ART005 Arteriovenous Malformation 65 0.058
137
MNN042 Meningioma, Radiation-Induced 62 0.058
138
P ESP024 Esophagitis 62 0.058
139
P TST021 Testicular Germ Cell Tumor 61 0.058
140
DPH001 Diphtheria 60 0.058
141
HYP266 Hypoxia 57 0.058
142
TRN018 Transitional Cell Carcinoma 57 0.058
143
SKN022 Skin Squamous Cell Carcinoma 56 0.058
144
P LTR001 Lateral Sclerosis 54 0.058
145
PTT009 Pituitary Gland Disease 54 0.058
146
c MCR113 Microvascular Complications of Diabetes 3 53 0.058
147
P SML001 Small Cell Carcinoma 53 0.058
148
c THY107 Thymoma, Familial 53 0.058
149
P HYP040 Hypospadias 51 0.058
150
BRN071 Brain Injury 50 0.058
151
P ANT088 Anterior Segment Dysgenesis 49 0.058
152
c MCR120 Microvascular Complications of Diabetes 7 47 0.058
153
SPN021 Spinal Meningioma 47 0.058
154
P TCL004 T-Cell Leukemia 47 0.058
155
P TST026 Testicular Germ Cell Cancer 44 0.058
156
ATX038 Ataxia and Polyneuropathy, Adult-Onset 44 0.058
157
GRW007 Growth Hormone Deficiency 43 0.058
158
c MCR130 Microvascular Complications of Diabetes 6 41 0.058
159
c MCR133 Microvascular Complications of Diabetes 4 41 0.058
160
PLY100 Polyploidy 40 0.058
161
ARC025 Arachnoid Cysts, Intracranial 39 0.058
162
OVR094 Ovarian Epithelial Cancer 38 0.058
163
SCR001 Secretory Meningioma 38 0.058
164
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.058
165
P ALZ034 Alzheimer Disease 89 0.041
166
NRL016 Neural Tube Defects 83 0.041
167
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.041
168
DFC004 Deficiency Anemia 75 0.041
169
ULC004 Ulcerative Colitis 73 0.041
170
P FML011 Familial Adenomatous Polyposis 72 0.041
171
P EPL164 Epilepsy 72 0.041
172
P HYP086 Hypothyroidism 69 0.041
173
P HLP001 Holoprosencephaly 69 0.041
174
P CRN037 Craniosynostosis 68 0.041
175
PNC129 Pancreatic Adenocarcinoma 68 0.041
176
P LKM002 Leukemia 67 0.041
177
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 67 0.041
178
UND005 Undifferentiated Pleomorphic Sarcoma 67 0.041
179
SRC014 Sarcoma 66 0.041
180
DRM014 Dermatofibrosarcoma Protuberans 66 0.041
181
c RHB024 Rhabdomyosarcoma 2 66 0.041
182
P DYS154 Dystonia 65 0.041
183
GST092 Gastroesophageal Reflux 65 0.041
184
P CLD001 Cleidocranial Dysplasia 65 0.041
185
CLF027 Cleft Palate, Isolated 65 0.041
186
CLN015 Colon Adenocarcinoma 64 0.041
187
IDP011 Idiopathic Interstitial Pneumonia 64 0.041
188
PTT046 Pituitary Hormone Deficiency, Combined, 2 64 0.041
189
CLT003 Colitis 63 0.041
190
c WLM018 Wilms Tumor 5 62 0.041
191
P PLM036 Pulmonary Fibrosis 62 0.041
192
P HMN010 Hemangioma 62 0.041
193
P END044 Endometriosis 61 0.041
194
P ANP001 Anaplastic Large Cell Lymphoma 61 0.041
195
LNG099 Lung Disease 61 0.041
196
ATM095 Autoimmune Disease 61 0.041
197
P MYL006 Myeloid Leukemia 60 0.041
198
INS001 Insulinoma 60 0.041
199
RTN017 Retinal Detachment 60 0.041
200
ART141 Arteriovenous Malformations of the Brain 60 0.041
201
P BND020 Bone Disease 60 0.041
202
CRY035 Cryptorchidism, Unilateral or Bilateral 59 0.041
203
DCT002 Ductal Carcinoma in Situ 59 0.041
204
c HYD046 Hydatidiform Mole, Recurrent, 1 59 0.041
205
P HMN036 Hemangiopericytoma, Malignant 59 0.041
206
IRN001 Iron Deficiency Anemia 59 0.041
207
P SZR006 Seizure Disorder 59 0.041
208
EYD002 Eye Disease 59 0.041
209
BRS051 Breast Disease 58 0.041
210
ANG020 Angiosarcoma 58 0.041
211
P BCL017 B-Cell Lymphoma 58 0.041
212
END030 End Stage Renal Failure 58 0.041
213
THY022 Thymic Carcinoma 58 0.041
214
P INF032 Infertility 58 0.041
215
IRN002 Iron Metabolism Disease 58 0.041
216
c MST023 Mesothelioma, Malignant 57 0.041
217
PPL058 Papilloma of Choroid Plexus 57 0.041
218
VSL002 Visual Epilepsy 57 0.041
219
SRC027 Sarcoma, Synovial 57 0.041
220
PRS047 Prostatitis 57 0.041
221
P FBR017 Fibrosarcoma 57 0.041
222
AGN016 Aging 56 0.041
223
P MLN007 Male Infertility 56 0.041
224
c THY109 Thyroid Cancer, Nonmedullary, 1 55 0.041
225
P MYP006 Myopia 55 0.041
226
P PTT006 Pituitary Adenoma 55 0.041
227
P MCR010 Microcephaly 55 0.041
228
c OPT053 Optic Atrophy 1 54 0.041
229
ANS023 Anus, Imperforate 54 0.041
230
P LRY044 Larynx Cancer 54 0.041
231
P PRV002 Periventricular Nodular Heterotopia 54 0.041
232
CLR030 Clear Cell Renal Cell Carcinoma 54 0.041
233
P RTN016 Retinal Degeneration 54 0.041
234
TRC109 Tracheoesophageal Fistula with or Without Esophageal Atresia 54 0.041
235
P TRM003 Tremor 54 0.041
236
DMY004 Demyelinating Disease 52 0.041
237
ABL002 Ablepharon-Macrostomia Syndrome 52 0.041
238
PRS045 Prostatic Hypertrophy 52 0.041
239
PLM014 Pleomorphic Adenoma 52 0.041
240
THY124 Thyroid Gland Papillary Carcinoma 52 0.041
241
INV006 Inverted Papilloma 52 0.041
242
PRV004 Periventricular Leukomalacia 52 0.041
243
OVR059 Ovary Adenocarcinoma 52 0.041
244
FND002 Fundus Dystrophy 52 0.041
245
CYS014 Cystadenocarcinoma 52 0.041
246
PRS021 Prostatic Adenoma 51 0.041
247
P FBR031 Febrile Seizures 51 0.041
248
P CPL006 Capillary Hemangioma 51 0.041
249
SPP010 Suppressor of Tumorigenicity 3 51 0.041
250
ADR049 Adrenal Hypoplasia, Congenital 51 0.041
251
P TMP001 Temporal Lobe Epilepsy 51 0.041
252
SPN035 Spindle Cell Sarcoma 51 0.041
253
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.041
254
CLR003 Clear Cell Adenocarcinoma 51 0.041
255
FSC004 Fasciitis 50 0.041
256
P OVR082 Overgrowth Syndrome 50 0.041
257
CVR006 Cavernous Hemangioma 50 0.041
258
47X002 47,xyy 49 0.041
259
LRN003 Learning Disability 49 0.041
260
PRS129 Prostatic Hyperplasia, Benign 49 0.041
261
c SCH079 Schizophrenia 1 48 0.041
262
CRC014 Carcinoid Tumors, Intestinal 48 0.041
263
MNC006 Monoclonal Gammopathy of Uncertain Significance 48 0.041
264
OPT070 Optic Nerve Hypoplasia, Bilateral 48 0.041
265
NRN001 Neuroendocrine Carcinoma 47 0.041
266
c INH030 Inherited Retinal Disorder 47 0.041
267
c LRG017 Large Intestine Cancer 47 0.041
268
PPL018 Papillary Adenocarcinoma 47 0.041
269
TST014 Testicular Cancer 47 0.041
270
GST010 Gestational Trophoblastic Neoplasm 46 0.041
271
HYP231 Hypothalamic Hamartomas 46 0.041
272
P CHR573 Choroid Plexus Cancer 46 0.041
273
CLB026 Colobomatous Microphthalmia 46 0.041
274
P BNG032 Benign Mesothelioma 45 0.041
275
c SPR009 Sporadic Breast Cancer 45 0.041
276
c MLG068 Malignant Glioma 45 0.041
277
VLV044 Vulvar Intraepithelial Neoplasia 44 0.041
278
CYT002 Cytokine Deficiency 44 0.041
279
RFR003 Refractive Error 44 0.041
280
CRR002 Currarino Syndrome 43 0.041
281
GND001 Gonadoblastoma 43 0.041
282
CYS009 Cystadenoma 43 0.041
283
ANP009 Anaplastic Oligodendroglioma 43 0.041
284
SPR008 Supratentorial Primitive Neuroectodermal Tumor 43 0.041
285
APL023 Aplasia Cutis Congenita, Nonsyndromic 42 0.041
286
P LTH003 Lethal Congenital Contracture Syndrome 42 0.041
287
LCH016 Lichen Sclerosus Et Atrophicus 42 0.041
288
CTN004 Cutaneous Fibrous Histiocytoma 41 0.041
289
MCN008 Mucinous Cystadenocarcinoma 41 0.041
290
ESP025 Esophagus Adenocarcinoma 41 0.041
291
P ALK015 Alk-Positive Anaplastic Large Cell Lymphoma 40 0.041
292
CMB021 Combined Pituitary Hormone Deficiency 40 0.041
293
AML004 Ameloblastic Carcinoma 40 0.041
294
LKP003 Leukoplakia 40 0.041
295
PRM329 Premature Aging 39 0.041
296
ORL012 Oral Leukoplakia 39 0.041
297
SKN020 Skin Papilloma 39 0.041
298
SPS019 Spastic Paraparesis 39 0.041
299
AMP013 Ampulla of Vater Cancer 39 0.041
300
SKN023 Skin Tag 38 0.041
301
HPT070 Hepatosplenic T-Cell Lymphoma 38 0.041
302
FRS019 Farsightedness 38 0.041
303
MCK029 Meckel Diverticulum 38 0.041
304
PSD016 Pseudosarcomatous Fibromatosis 37 0.041
305
P ADT009 Auditory Neuropathy Spectrum Disorder 36 0.041
306
AMP009 Ampulla of Vater Adenocarcinoma 35 0.041
307
HRS011 Horseshoe Kidney 35 0.041
308
PPL052 Papillomatosis, Confluent and Reticulated 34 0.041
309
HMN016 Hemangioendothelioma 34 0.041
310
GGN002 Gigantism 34 0.041
311
P SCL047 Sclerocornea 33 0.041
312
OVR109 Ovarian Germ Cell Teratoma 32 0.041
313
TRC035 Tracheal Agenesis 32 0.041
314
ODN006 Odontoma 31 0.041
315
PLM009 Pleomorphic Adenoma Carcinoma 31 0.041
316
CRB208 Cerebral Malformation 31 0.041
317
TTH030 Teeth, Supernumerary 30 0.041
318
TRT017 Teratoma, Ovarian 29 0.041
319
SNN002 Sinonasal Undifferentiated Carcinoma 29 0.041
320
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 28 0.041
321
CLB009 Coloboma of Iris 28 0.041
322
ATY002 Atypical Choroid Plexus Papilloma 27 0.041
323
HTT002 Hutterite Cerebroosteonephrodysplasia Syndrome 27 0.041
324
PDT043 Pediatric Acute-Onset Neuropsychiatric Syndrome 26 0.041
325
MLG164 Malignant Epithelial Tumor of Ovary 26 0.041
326
ORB007 Orbital Cyst 23 0.041
327
c CLD019 Cleidocranial Dysplasia Spectrum Disorder 21 0.041
328
c MYS019 Miyoshi Muscular Dystrophy 2 21 0.041
329
P PRM252 Preimplantation Embryonic Lethality 1 21 0.041
330
VNS002 Venous Hemangioma 20 0.041
331
SYN112 Syndromic Microphthalmia-Anophthalmia-Coloboma 19 0.041
332
P ANT080 Antigen Defined by Monoclonal Antibody Aj9 18 0.041
334
ERL051 Early Response to Neural Induction Gene 10 0.041
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