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Pediatric Disease Annotations & Medicines



   astrocytoma
  

Disease ID 173
Disease astrocytoma
Definition
Neoplasms of the brain and spinal cord derived from glial cells which vary from histologically benign forms to highly anaplastic and malignant tumors. Fibrillary astrocytomas are the most common type and may be classified in order of increasing malignancy (grades I through IV). In the first two decades of life, astrocytomas tend to originate in the cerebellar hemispheres; in adults, they most frequently arise in the cerebrum and frequently undergo malignant transformation. (From Devita et al., Cancer: Principles and Practice of Oncology, 5th ed, pp2013-7; Holland et al., Cancer Medicine, 3d ed, p1082)
Synonym
[m]astrocytoma nos
astrocytic glioma
astrocytic gliomas
astrocytic neoplasm
astrocytic tumor
astrocytoma (disorder)
astrocytoma [disease/finding]
astrocytoma, no icd-o subtype
astrocytoma, no icd-o subtype (morphologic abnormality)
astrocytoma, no international classification of diseases for oncology subtype
astrocytoma, no international classification of diseases for oncology subtype (morphologic abnormality)
astrocytoma, nos
astrocytomas
astroglioma
astrogliomas
glioma, astrocytic
gliomas, astrocytic
Orphanet
DOID
UMLS
C0004114
MeSH
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:58)
C0041341  |  tuberous sclerosis  |  61
C0041341  |  tuberous sclerosis complex  |  34
C0017636  |  glioblastomas  |  8
C0017636  |  glioblastoma  |  8
C0014544  |  epilepsy  |  5
C0028945  |  oligodendroglioma  |  3
C0555198  |  malignant glioma  |  3
C0153633  |  malignant brain tumor  |  2
C0028738  |  nystagmus  |  2
C1519214  |  secondary glioblastoma  |  2
C1527311  |  brain edema  |  2
C0555198  |  malignant gliomas  |  2
C0151740  |  increased intracranial pressure  |  1
C0020255  |  hydrocephalus  |  1
C0334579  |  anaplastic astrocytomas  |  1
C0001430  |  adenoma  |  1
C0025286  |  meningiomas  |  1
C0026986  |  myelodysplastic syndrome  |  1
C0004134  |  ataxia  |  1
C0014038  |  encephalitis  |  1
C1266119  |  solitary fibrous tumor  |  1
C0334583  |  pilocytic astrocytoma  |  1
C0151740  |  raised intracranial pressure  |  1
C0039538  |  teratoma  |  1
C0334579  |  anaplastic astrocytoma  |  1
C0206664  |  teratocarcinoma  |  1
C0085113  |  neurofibromatosis  |  1
C0004114  |  astrocytoma  |  1
C0087086  |  thrombi  |  1
C0206734  |  hemangioblastoma  |  1
C0004352  |  autism  |  1
C0042165  |  anterior uveitis  |  1
C0153633  |  brain cancer  |  1
C0206716  |  gangliogliomas  |  1
C1368910  |  mature teratoma  |  1
C0028945  |  oligodendrogliomas  |  1
C1621958  |  glioblastoma multiforme  |  1
C0032000  |  pituitary adenoma  |  1
C0271051  |  macular edema  |  1
C0024454  |  maffucci syndrome  |  1
C0019348  |  herpes simplex  |  1
C0003857  |  arteriovenous malformation  |  1
C0028326  |  noonan syndrome  |  1
C0025149  |  medulloblastoma  |  1
C1266177  |  dysembryoplastic neuroepithelial tumor  |  1
C0035305  |  retinal detachment  |  1
C0002871  |  anemia  |  1
C0549423  |  obstructive hydrocephalus  |  1
C1956097  |  4p- syndrome  |  1
C0025149  |  medulloblastomas  |  1
C0334583  |  pilocytic astrocytomas  |  1
C0020676  |  hypothyroidism  |  1
C0025286  |  meningioma  |  1
C1096063  |  intractable epilepsy  |  1
C0006625  |  cachexia  |  1
C0018991  |  hemiplegia  |  1
C0079419  |  li-fraumeni syndrome  |  1
C0175702  |  williams syndrome  |  1
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:24)
TP53  |  7157  |  CLINVAR
PTPN11  |  5781  |  CTD_human
FGFR1  |  2260  |  CTD_human
NF1  |  4763  |  CTD_human
NOTCH2  |  4853  |  CTD_human
NOTCH1  |  4851  |  CTD_human
NTRK2  |  4915  |  CTD_human
MMP9  |  4318  |  CTD_human
ESR1  |  2099  |  CTD_human
DLL3  |  10683  |  CTD_human
NDRG1  |  10397  |  CTD_human
BRAF  |  673  |  CTD_human
KRAS  |  3845  |  CTD_human
AR  |  367  |  CTD_human
HIF1A  |  3091  |  CTD_human
ESR2  |  2100  |  CTD_human
HEY1  |  23462  |  CTD_human
HEY2  |  23493  |  CTD_human
NCOA3  |  8202  |  CTD_human
MMP3  |  4314  |  CTD_human
LATS1  |  9113  |  CTD_human
LATS2  |  26524  |  CTD_human
ACVR1  |  90  |  CTD_human
KIAA1549  |  57670  |  CTD_human
Inferring Gene
Entrez_id | Symbol | Resource(Total Genes:2)
3383  |  ICAM1  |  infer
5175  |  PECAM1  |  infer
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:857)
137196  |  CCDC26  |  DISEASES
972  |  CD74  |  DISEASES
2067  |  ERCC1  |  DISEASES
6591  |  SNAI2  |  DISEASES
1015  |  CDH17  |  DISEASES
6515  |  SLC2A3  |  DISEASES
51564  |  HDAC7  |  DISEASES
7132  |  TNFRSF1A  |  DISEASES
3566  |  IL4R  |  DISEASES
7145  |  TNS1  |  DISEASES
51605  |  TRMT6  |  DISEASES
10683  |  DLL3  |  DISEASES
132949  |  AASDH  |  DISEASES
7414  |  VCL  |  DISEASES
4282  |  MIF  |  DISEASES
5008  |  OSM  |  DISEASES
5594  |  MAPK1  |  DISEASES
10633  |  RASL10A  |  DISEASES
3162  |  HMOX1  |  DISEASES
23492  |  CBX7  |  DISEASES
55007  |  FAM118A  |  DISEASES
328  |  APEX1  |  DISEASES
4792  |  NFKBIA  |  DISEASES
5875  |  RABGGTA  |  DISEASES
6790  |  AURKA  |  DISEASES
79444  |  BIRC7  |  DISEASES
7076  |  TIMP1  |  DISEASES
4313  |  MMP2  |  DISEASES
4350  |  MPG  |  DISEASES
9100  |  USP10  |  DISEASES
7249  |  TSC2  |  DISEASES
1666  |  DECR1  |  DISEASES
8797  |  TNFRSF10A  |  DISEASES
6449  |  SGTA  |  DISEASES
79187  |  FSD1  |  DISEASES
7040  |  TGFB1  |  DISEASES
973  |  CD79A  |  DISEASES
3082  |  HGF  |  DISEASES
85865  |  GTPBP10  |  DISEASES
8976  |  WASL  |  DISEASES
5054  |  SERPINE1  |  DISEASES
165  |  AEBP1  |  DISEASES
7431  |  VIM  |  DISEASES
79176  |  FBXL15  |  DISEASES
4353  |  MPO  |  DISEASES
1440  |  CSF3  |  DISEASES
6198  |  RPS6KB1  |  DISEASES
40  |  ASIC2  |  DISEASES
6347  |  CCL2  |  DISEASES
1949  |  EFNB3  |  DISEASES
7448  |  VTN  |  DISEASES
3558  |  IL2  |  DISEASES
595  |  CCND1  |  DISEASES
329  |  BIRC2  |  DISEASES
41  |  ASIC1  |  DISEASES
2735  |  GLI1  |  DISEASES
3458  |  IFNG  |  DISEASES
57122  |  NUP107  |  DISEASES
2597  |  GAPDH  |  DISEASES
2026  |  ENO2  |  DISEASES
79923  |  NANOG  |  DISEASES
1432  |  MAPK14  |  DISEASES
59084  |  ENPP5  |  DISEASES
1839  |  HBEGF  |  DISEASES
6678  |  SPARC  |  DISEASES
3565  |  IL4  |  DISEASES
4292  |  MLH1  |  DISEASES
57415  |  C3orf14  |  DISEASES
9168  |  TMSB10  |  DISEASES
4436  |  MSH2  |  DISEASES
3485  |  IGFBP2  |  DISEASES
3398  |  ID2  |  DISEASES
5657  |  PRTN3  |  DISEASES
2956  |  MSH6  |  DISEASES
60672  |  MIIP  |  DISEASES
1509  |  CTSD  |  DISEASES
134637  |  ADAT2  |  DISEASES
9429  |  ABCG2  |  DISEASES
1958  |  EGR1  |  DISEASES
8743  |  TNFSF10  |  DISEASES
22865  |  SLITRK3  |  DISEASES
2322  |  FLT3  |  DISEASES
51116  |  MRPS2  |  DISEASES
3598  |  IL13RA2  |  DISEASES
5335  |  PLCG1  |  DISEASES
6615  |  SNAI1  |  DISEASES
8358  |  HIST1H3B  |  DISEASES
1026  |  CDKN1A  |  DISEASES
6659  |  SOX4  |  DISEASES
51299  |  NRN1  |  DISEASES
1948  |  EFNB2  |  DISEASES
652  |  BMP4  |  DISEASES
2354  |  FOSB  |  DISEASES
83596  |  BCL2L12  |  DISEASES
6779  |  STATH  |  DISEASES
821  |  CANX  |  DISEASES
8089  |  YEATS4  |  DISEASES
3315  |  HSPB1  |  DISEASES
65997  |  RASL11B  |  DISEASES
2952  |  GSTT1  |  DISEASES
3236  |  HOXD10  |  DISEASES
51421  |  AMOTL2  |  DISEASES
968  |  CD68  |  DISEASES
79148  |  MMP28  |  DISEASES
599  |  BCL2L2  |  DISEASES
27175  |  TUBG2  |  DISEASES
1463  |  NCAN  |  DISEASES
3270  |  HRC  |  DISEASES
50632  |  CALY  |  DISEASES
445  |  ASS1  |  DISEASES
10155  |  TRIM28  |  DISEASES
9113  |  LATS1  |  DISEASES
2670  |  GFAP  |  DISEASES
2521  |  FUS  |  DISEASES
85415  |  RHPN2  |  DISEASES
5989  |  RFX1  |  DISEASES
3021  |  H3F3B  |  DISEASES
182  |  JAG1  |  DISEASES
1116  |  CHI3L1  |  DISEASES
4608  |  MYBPH  |  DISEASES
55643  |  BTBD2  |  DISEASES
3845  |  KRAS  |  DISEASES
891  |  CCNB1  |  DISEASES
10752  |  CHL1  |  DISEASES
4853  |  NOTCH2  |  DISEASES
1794  |  DOCK2  |  DISEASES
1643  |  DDB2  |  DISEASES
5156  |  PDGFRA  |  DISEASES
301  |  ANXA1  |  DISEASES
8728  |  ADAM19  |  DISEASES
4440  |  MSI1  |  DISEASES
29923  |  HILPDA  |  DISEASES
1019  |  CDK4  |  DISEASES
2799  |  GNS  |  DISEASES
51719  |  CAB39  |  DISEASES
10643  |  IGF2BP3  |  DISEASES
3569  |  IL6  |  DISEASES
6426  |  SRSF1  |  DISEASES
10010  |  TANK  |  DISEASES
5168  |  ENPP2  |  DISEASES
5460  |  POU5F1  |  DISEASES
6386  |  SDCBP  |  DISEASES
4316  |  MMP7  |  DISEASES
7057  |  THBS1  |  DISEASES
9493  |  KIF23  |  DISEASES
3417  |  IDH1  |  DISEASES
4659  |  PPP1R12A  |  DISEASES
894  |  CCND2  |  DISEASES
23603  |  CORO1C  |  DISEASES
7450  |  VWF  |  DISEASES
5629  |  PROX1  |  DISEASES
5525  |  PPP2R5A  |  DISEASES
999  |  CDH1  |  DISEASES
5159  |  PDGFRB  |  DISEASES
23469  |  PHF3  |  DISEASES
27075  |  TSPAN13  |  DISEASES
27092  |  CACNG4  |  DISEASES
4087  |  SMAD2  |  DISEASES
81671  |  VMP1  |  DISEASES
1031  |  CDKN2C  |  DISEASES
5052  |  PRDX1  |  DISEASES
7077  |  TIMP2  |  DISEASES
23031  |  MAST3  |  DISEASES
57148  |  RALGAPB  |  DISEASES
3783  |  KCNN4  |  DISEASES
10552  |  ARPC1A  |  DISEASES
5595  |  MAPK3  |  DISEASES
6598  |  SMARCB1  |  DISEASES
6855  |  SYP  |  DISEASES
2033  |  EP300  |  DISEASES
51171  |  HSD17B14  |  DISEASES
3552  |  IL1A  |  DISEASES
3553  |  IL1B  |  DISEASES
330  |  BIRC3  |  DISEASES
64761  |  PARP12  |  DISEASES
90  |  ACVR1  |  DISEASES
2034  |  EPAS1  |  DISEASES
7301  |  TYRO3  |  DISEASES
10000  |  AKT3  |  DISEASES
3791  |  KDR  |  DISEASES
5290  |  PIK3CA  |  DISEASES
60482  |  SLC5A7  |  DISEASES
84083  |  ZRANB3  |  DISEASES
8942  |  KYNU  |  DISEASES
941  |  CD80  |  DISEASES
2247  |  FGF2  |  DISEASES
55247  |  NEIL3  |  DISEASES
7474  |  WNT5A  |  DISEASES
6774  |  STAT3  |  DISEASES
1788  |  DNMT3A  |  DISEASES
3383  |  ICAM1  |  DISEASES
3827  |  KNG1  |  DISEASES
1462  |  VCAN  |  DISEASES
80315  |  CPEB4  |  DISEASES
51176  |  LEF1  |  DISEASES
1950  |  EGF  |  DISEASES
8829  |  NRP1  |  DISEASES
7472  |  WNT2  |  DISEASES
25824  |  PRDX5  |  DISEASES
5243  |  ABCB1  |  DISEASES
1021  |  CDK6  |  DISEASES
29999  |  FSCN3  |  DISEASES
5395  |  PMS2  |  DISEASES
1616  |  DAXX  |  DISEASES
7078  |  TIMP3  |  DISEASES
11010  |  GLIPR1  |  DISEASES
429  |  ASCL1  |  DISEASES
1017  |  CDK2  |  DISEASES
2065  |  ERBB3  |  DISEASES
5925  |  RB1  |  DISEASES
7168  |  TPM1  |  DISEASES
3480  |  IGF1R  |  DISEASES
8826  |  IQGAP1  |  DISEASES
81631  |  MAP1LC3B  |  DISEASES
84643  |  KIF2B  |  DISEASES
1000  |  CDH2  |  DISEASES
2627  |  GATA6  |  DISEASES
7157  |  TP53  |  DISEASES
396  |  ARHGDIA  |  DISEASES
2064  |  ERBB2  |  DISEASES
207  |  AKT1  |  DISEASES
2014  |  EMP3  |  DISEASES
3756  |  KCNH1  |  DISEASES
388  |  RHOB  |  DISEASES
805  |  CALM2  |  DISEASES
5433  |  POLR2D  |  DISEASES
55502  |  HES6  |  DISEASES
26018  |  LRIG1  |  DISEASES
7220  |  TRPC1  |  DISEASES
6502  |  SKP2  |  DISEASES
5295  |  PIK3R1  |  DISEASES
1956  |  EGFR  |  DISEASES
8795  |  TNFRSF10B  |  DISEASES
1030  |  CDKN2B  |  DISEASES
4851  |  NOTCH1  |  DISEASES
6506  |  SLC1A2  |  DISEASES
472  |  ATM  |  DISEASES
27250  |  PDCD4  |  DISEASES
7424  |  VEGFC  |  DISEASES
1793  |  DOCK1  |  DISEASES
5805  |  PTS  |  DISEASES
341640  |  FREM2  |  DISEASES
23657  |  SLC7A11  |  DISEASES
4613  |  MYCN  |  DISEASES
127124  |  ATP6V1G3  |  DISEASES
83439  |  TCF7L1  |  DISEASES
6695  |  SPOCK1  |  DISEASES
2321  |  FLT1  |  DISEASES
2893  |  GRIA4  |  DISEASES
2697  |  GJA1  |  DISEASES
10309  |  CCNO  |  DISEASES
50853  |  VILL  |  DISEASES
7070  |  THY1  |  DISEASES
8714  |  ABCC3  |  DISEASES
8324  |  FZD7  |  DISEASES
1436  |  CSF1R  |  DISEASES
11197  |  WIF1  |  DISEASES
701  |  BUB1B  |  DISEASES
5468  |  PPARG  |  DISEASES
3815  |  KIT  |  DISEASES
9133  |  CCNB2  |  DISEASES
9162  |  DGKI  |  DISEASES
673  |  BRAF  |  DISEASES
3242  |  HPD  |  DISEASES
5291  |  PIK3CB  |  DISEASES
50848  |  F11R  |  DISEASES
25865  |  PRKD2  |  DISEASES
808  |  CALM3  |  DISEASES
1476  |  CSTB  |  DISEASES
6285  |  S100B  |  DISEASES
6271  |  S100A1  |  DISEASES
2264  |  FGFR4  |  DISEASES
9794  |  MAML1  |  DISEASES
114757  |  CYGB  |  DISEASES
6352  |  CCL5  |  DISEASES
6777  |  STAT5B  |  DISEASES
3071  |  NCKAP1L  |  DISEASES
51035  |  UBXN1  |  DISEASES
10630  |  PDPN  |  DISEASES
7412  |  VCAM1  |  DISEASES
2487  |  FRZB  |  DISEASES
27306  |  HPGDS  |  DISEASES
10461  |  MERTK  |  DISEASES
3490  |  IGFBP7  |  DISEASES
27148  |  STK36  |  DISEASES
213  |  ALB  |  DISEASES
51319  |  RSRC1  |  DISEASES
7871  |  SLMAP  |  DISEASES
6259  |  RYK  |  DISEASES
308  |  ANXA5  |  DISEASES
9607  |  CARTPT  |  DISEASES
1437  |  CSF2  |  DISEASES
3313  |  HSPA9  |  DISEASES
6469  |  SHH  |  DISEASES
107  |  ADCY1  |  DISEASES
216  |  ALDH1A1  |  DISEASES
9833  |  MELK  |  DISEASES
58157  |  NGB  |  DISEASES
7248  |  TSC1  |  DISEASES
57447  |  NDRG2  |  DISEASES
9317  |  PTER  |  DISEASES
55662  |  HIF1AN  |  DISEASES
3611  |  ILK  |  DISEASES
5347  |  PLK1  |  DISEASES
11318  |  GPR182  |  DISEASES
7529  |  YWHAB  |  DISEASES
2923  |  PDIA3  |  DISEASES
1398  |  CRK  |  DISEASES
6786  |  STIM1  |  DISEASES
558  |  AXL  |  DISEASES
3816  |  KLK1  |  DISEASES
79085  |  SLC25A23  |  DISEASES
51129  |  ANGPTL4  |  DISEASES
332  |  BIRC5  |  DISEASES
8772  |  FADD  |  DISEASES
55872  |  PBK  |  DISEASES
4255  |  MGMT  |  DISEASES
5604  |  MAP2K1  |  DISEASES
56890  |  MDM1  |  DISEASES
598  |  BCL2L1  |  DISEASES
3479  |  IGF1  |  DISEASES
2357  |  FPR1  |  DISEASES
162979  |  ZNF296  |  DISEASES
6203  |  RPS9  |  DISEASES
3308  |  HSPA4  |  DISEASES
170626  |  XAGE3  |  DISEASES
3688  |  ITGB1  |  DISEASES
8988  |  HSPB3  |  DISEASES
6869  |  TACR1  |  DISEASES
28511  |  NKIRAS2  |  DISEASES
1493  |  CTLA4  |  DISEASES
54676  |  GTPBP2  |  DISEASES
11031  |  RAB31  |  DISEASES
3596  |  IL13  |  DISEASES
26505  |  CNNM3  |  DISEASES
3627  |  CXCL10  |  DISEASES
10963  |  STIP1  |  DISEASES
2353  |  FOS  |  DISEASES
253782  |  CERS6  |  DISEASES
10465  |  PPIH  |  DISEASES
23627  |  PRND  |  DISEASES
56098  |  PCDHGC4  |  DISEASES
435  |  ASL  |  DISEASES
9451  |  EIF2AK3  |  DISEASES
10067  |  SCAMP3  |  DISEASES
4176  |  MCM7  |  DISEASES
54541  |  DDIT4  |  DISEASES
54205  |  CYCS  |  DISEASES
57124  |  CD248  |  DISEASES
4323  |  MMP14  |  DISEASES
9934  |  P2RY14  |  DISEASES
80777  |  CYB5B  |  DISEASES
660  |  BMX  |  DISEASES
5340  |  PLG  |  DISEASES
54715  |  RBFOX1  |  DISEASES
7015  |  TERT  |  DISEASES
1072  |  CFL1  |  DISEASES
3265  |  HRAS  |  DISEASES
947  |  CD34  |  DISEASES
10393  |  ANAPC10  |  DISEASES
8061  |  FOSL1  |  DISEASES
27243  |  CHMP2A  |  DISEASES
27165  |  GLS2  |  DISEASES
9688  |  NUP93  |  DISEASES
8463  |  TEAD2  |  DISEASES
836  |  CASP3  |  DISEASES
358  |  AQP1  |  DISEASES
2944  |  GSTM1  |  DISEASES
10432  |  RBM14  |  DISEASES
8837  |  CFLAR  |  DISEASES
1464  |  CSPG4  |  DISEASES
5591  |  PRKDC  |  DISEASES
4327  |  MMP19  |  DISEASES
8877  |  SPHK1  |  DISEASES
113026  |  PLCD3  |  DISEASES
4179  |  CD46  |  DISEASES
998  |  CDC42  |  DISEASES
285  |  ANGPT2  |  DISEASES
27122  |  DKK3  |  DISEASES
7298  |  TYMS  |  DISEASES
26251  |  KCNG2  |  DISEASES
25843  |  MOB4  |  DISEASES
3234  |  HOXD8  |  DISEASES
8560  |  DEGS1  |  DISEASES
4233  |  MET  |  DISEASES
63973  |  NEUROG2  |  DISEASES
2744  |  GLS  |  DISEASES
2997  |  GYS1  |  DISEASES
4684  |  NCAM1  |  DISEASES
818  |  CAMK2G  |  DISEASES
3183  |  HNRNPC  |  DISEASES
10397  |  NDRG1  |  DISEASES
2146  |  EZH2  |  DISEASES
5315  |  PKM  |  DISEASES
54822  |  TRPM7  |  DISEASES
80153  |  EDC3  |  DISEASES
23019  |  CNOT1  |  DISEASES
6863  |  TAC1  |  DISEASES
1351  |  COX8A  |  DISEASES
6867  |  TACC1  |  DISEASES
3039  |  HBA1  |  DISEASES
4312  |  MMP1  |  DISEASES
8706  |  B3GALNT1  |  DISEASES
6657  |  SOX2  |  DISEASES
57125  |  PLXDC1  |  DISEASES
56992  |  KIF15  |  DISEASES
977  |  CD151  |  DISEASES
3309  |  HSPA5  |  DISEASES
1555  |  CYP2B6  |  DISEASES
2932  |  GSK3B  |  DISEASES
3326  |  HSP90AB1  |  DISEASES
5499  |  PPP1CA  |  DISEASES
10460  |  TACC3  |  DISEASES
55515  |  ASIC4  |  DISEASES
51330  |  TNFRSF12A  |  DISEASES
121227  |  LRIG3  |  DISEASES
5034  |  P4HB  |  DISEASES
3714  |  JAG2  |  DISEASES
8784  |  TNFRSF18  |  DISEASES
8905  |  AP1S2  |  DISEASES
706  |  TSPO  |  DISEASES
5454  |  POU3F2  |  DISEASES
8354  |  HIST1H3I  |  DISEASES
842  |  CASP9  |  DISEASES
9021  |  SOCS3  |  DISEASES
5155  |  PDGFB  |  DISEASES
8519  |  IFITM1  |  DISEASES
10215  |  OLIG2  |  DISEASES
6938  |  TCF12  |  DISEASES
4601  |  MXI1  |  DISEASES
63827  |  BCAN  |  DISEASES
7490  |  WT1  |  DISEASES
2621  |  GAS6  |  DISEASES
3418  |  IDH2  |  DISEASES
1287  |  COL4A5  |  DISEASES
84619  |  ZGPAT  |  DISEASES
5727  |  PTCH1  |  DISEASES
4088  |  SMAD3  |  DISEASES
3916  |  LAMP1  |  DISEASES
6297  |  SALL2  |  DISEASES
682  |  BSG  |  DISEASES
6182  |  MRPL12  |  DISEASES
10057  |  ABCC5  |  DISEASES
284361  |  EMC10  |  DISEASES
10013  |  HDAC6  |  DISEASES
2152  |  F3  |  DISEASES
219699  |  UNC5B  |  DISEASES
5133  |  PDCD1  |  DISEASES
3320  |  HSP90AA1  |  DISEASES
957  |  ENTPD5  |  DISEASES
139065  |  SLITRK4  |  DISEASES
23336  |  SYNM  |  DISEASES
55596  |  ZCCHC8  |  DISEASES
1641  |  DCX  |  DISEASES
10608  |  MXD4  |  DISEASES
1576  |  CYP3A4  |  DISEASES
135138  |  PACRG  |  DISEASES
3091  |  HIF1A  |  DISEASES
92140  |  MTDH  |  DISEASES
23462  |  HEY1  |  DISEASES
64778  |  FNDC3B  |  DISEASES
2246  |  FGF1  |  DISEASES
23583  |  SMUG1  |  DISEASES
90627  |  STARD13  |  DISEASES
2290  |  FOXG1  |  DISEASES
857  |  CAV1  |  DISEASES
5329  |  PLAUR  |  DISEASES
2309  |  FOXO3  |  DISEASES
1978  |  EIF4EBP1  |  DISEASES
5781  |  PTPN11  |  DISEASES
59277  |  NTN4  |  DISEASES
5764  |  PTN  |  DISEASES
5747  |  PTK2  |  DISEASES
6776  |  STAT5A  |  DISEASES
9324  |  HMGN3  |  DISEASES
8717  |  TRADD  |  DISEASES
7518  |  XRCC4  |  DISEASES
1508  |  CTSB  |  DISEASES
2305  |  FOXM1  |  DISEASES
100134938  |  UPK3BL  |  DISEASES
9474  |  ATG5  |  DISEASES
3205  |  HOXA9  |  DISEASES
1003  |  CDH5  |  DISEASES
1499  |  CTNNB1  |  DISEASES
3005  |  H1F0  |  DISEASES
4771  |  NF2  |  DISEASES
7316  |  UBC  |  DISEASES
2738  |  GLI4  |  DISEASES
646643  |  SBK2  |  DISEASES
347  |  APOD  |  DISEASES
3516  |  RBPJ  |  DISEASES
57556  |  SEMA6A  |  DISEASES
302  |  ANXA2  |  DISEASES
58473  |  PLEKHB1  |  DISEASES
54963  |  UCKL1  |  DISEASES
10533  |  ATG7  |  DISEASES
5154  |  PDGFA  |  DISEASES
2335  |  FN1  |  DISEASES
80705  |  TSGA10  |  DISEASES
2202  |  EFEMP1  |  DISEASES
80781  |  COL18A1  |  DISEASES
331  |  XIAP  |  DISEASES
355  |  FAS  |  DISEASES
51155  |  HN1  |  DISEASES
120  |  ADD3  |  DISEASES
401409  |  RAB19  |  DISEASES
5789  |  PTPRD  |  DISEASES
11065  |  UBE2C  |  DISEASES
4100  |  MAGEA1  |  DISEASES
509  |  ATP5C1  |  DISEASES
3683  |  ITGAL  |  DISEASES
5725  |  PTBP1  |  DISEASES
23155  |  CLCC1  |  DISEASES
801  |  CALM1  |  DISEASES
11186  |  RASSF1  |  DISEASES
253260  |  RICTOR  |  DISEASES
60  |  ACTB  |  DISEASES
9961  |  MVP  |  DISEASES
8350  |  HIST1H3A  |  DISEASES
286319  |  TUSC1  |  DISEASES
6714  |  SRC  |  DISEASES
4763  |  NF1  |  DISEASES
1969  |  EPHA2  |  DISEASES
841  |  CASP8  |  DISEASES
2213  |  FCGR2B  |  DISEASES
9583  |  ENTPD4  |  DISEASES
2526  |  FUT4  |  DISEASES
1902  |  LPAR1  |  DISEASES
9332  |  CD163  |  DISEASES
56474  |  CTPS2  |  DISEASES
8356  |  HIST1H3J  |  DISEASES
2547  |  XRCC6  |  DISEASES
9220  |  TIAF1  |  DISEASES
1786  |  DNMT1  |  DISEASES
4192  |  MDK  |  DISEASES
55959  |  SULF2  |  DISEASES
7037  |  TFRC  |  DISEASES
2157  |  F8  |  DISEASES
4478  |  MSN  |  DISEASES
5599  |  MAPK8  |  DISEASES
4133  |  MAP2  |  DISEASES
8353  |  HIST1H3E  |  DISEASES
8682  |  PEA15  |  DISEASES
25999  |  CLIP3  |  DISEASES
6241  |  RRM2  |  DISEASES
6663  |  SOX10  |  DISEASES
10787  |  NCKAP1  |  DISEASES
2673  |  GFPT1  |  DISEASES
6772  |  STAT1  |  DISEASES
6935  |  ZEB1  |  DISEASES
23187  |  PHLDB1  |  DISEASES
22876  |  INPP5F  |  DISEASES
7150  |  TOP1  |  DISEASES
2475  |  MTOR  |  DISEASES
2736  |  GLI2  |  DISEASES
22904  |  SBNO2  |  DISEASES
919  |  CD247  |  DISEASES
800  |  CALD1  |  DISEASES
388677  |  NOTCH2NL  |  DISEASES
9444  |  QKI  |  DISEASES
8678  |  BECN1  |  DISEASES
1870  |  E2F2  |  DISEASES
961  |  CD47  |  DISEASES
729447  |  GAGE2A  |  DISEASES
64216  |  TFB2M  |  DISEASES
55127  |  HEATR1  |  DISEASES
2786  |  GNG4  |  DISEASES
142  |  PARP1  |  DISEASES
3020  |  H3F3A  |  DISEASES
7042  |  TGFB2  |  DISEASES
80342  |  TRAF3IP3  |  DISEASES
4194  |  MDM4  |  DISEASES
5287  |  PIK3C2B  |  DISEASES
79465  |  ULBP3  |  DISEASES
80328  |  ULBP2  |  DISEASES
5788  |  PTPRC  |  DISEASES
3075  |  CFH  |  DISEASES
5743  |  PTGS2  |  DISEASES
9857  |  CEP350  |  DISEASES
356  |  FASLG  |  DISEASES
1490  |  CTGF  |  DISEASES
912  |  CD1D  |  DISEASES
10763  |  NES  |  DISEASES
23493  |  HEY2  |  DISEASES
1942  |  EFNA1  |  DISEASES
2173  |  FABP7  |  DISEASES
387119  |  CEP85L  |  DISEASES
6098  |  ROS1  |  DISEASES
3632  |  INPP5A  |  DISEASES
664  |  BNIP3  |  DISEASES
6277  |  S100A6  |  DISEASES
56647  |  BCCIP  |  DISEASES
9184  |  BUB3  |  DISEASES
8394  |  PIP5K1A  |  DISEASES
1755  |  DMBT1  |  DISEASES
1520  |  CTSS  |  DISEASES
7101  |  NR2E1  |  DISEASES
4170  |  MCL1  |  DISEASES
8357  |  HIST1H3H  |  DISEASES
100288142  |  NBPF20  |  DISEASES
840  |  CASP7  |  DISEASES
4803  |  NGF  |  DISEASES
6566  |  SLC16A1  |  DISEASES
51684  |  SUFU  |  DISEASES
51750  |  RTEL1  |  DISEASES
81621  |  KAZALD1  |  DISEASES
4102  |  MAGEA3  |  DISEASES
2633  |  GBP1  |  DISEASES
84631  |  SLITRK2  |  DISEASES
4923  |  NTSR1  |  DISEASES
959  |  CD40LG  |  DISEASES
8880  |  FUBP1  |  DISEASES
5223  |  PGAM1  |  DISEASES
2778  |  GNAS  |  DISEASES
1791  |  DNTT  |  DISEASES
4774  |  NFIA  |  DISEASES
3725  |  JUN  |  DISEASES
9211  |  LGI1  |  DISEASES
3597  |  IL13RA1  |  DISEASES
9334  |  B4GALT5  |  DISEASES
79656  |  BEND5  |  DISEASES
8569  |  MKNK1  |  DISEASES
5728  |  PTEN  |  DISEASES
7422  |  VEGFA  |  DISEASES
6441  |  SFTPD  |  DISEASES
4318  |  MMP9  |  DISEASES
5631  |  PRPS1  |  DISEASES
7075  |  TIE1  |  DISEASES
4904  |  YBX1  |  DISEASES
5328  |  PLAU  |  DISEASES
2275  |  FHL3  |  DISEASES
139322  |  APOOL  |  DISEASES
2022  |  ENG  |  DISEASES
546  |  ATRX  |  DISEASES
2170  |  FABP3  |  DISEASES
9550  |  ATP6V1G1  |  DISEASES
1896  |  EDA  |  DISEASES
3399  |  ID3  |  DISEASES
9314  |  KLF4  |  DISEASES
55613  |  MTMR8  |  DISEASES
4855  |  NOTCH4  |  DISEASES
127733  |  UBXN10  |  DISEASES
3014  |  H2AFX  |  DISEASES
81569  |  ACTL8  |  DISEASES
9696  |  CROCC  |  DISEASES
728239  |  MAGED4  |  DISEASES
3621  |  ING1  |  DISEASES
199  |  AIF1  |  DISEASES
3397  |  ID1  |  DISEASES
50943  |  FOXP3  |  DISEASES
9656  |  MDC1  |  DISEASES
780  |  DDR1  |  DISEASES
648  |  BMI1  |  DISEASES
2550  |  GABBR1  |  DISEASES
687  |  KLF9  |  DISEASES
4821  |  NKX2-2  |  DISEASES
3604  |  TNFRSF9  |  DISEASES
8351  |  HIST1H3D  |  DISEASES
390992  |  HES3  |  DISEASES
10590  |  SCGN  |  DISEASES
8434  |  RECK  |  DISEASES
4609  |  MYC  |  DISEASES
26586  |  CKAP2  |  DISEASES
55966  |  AJAP1  |  DISEASES
7161  |  TP73  |  DISEASES
768  |  CA9  |  DISEASES
54880  |  BCOR  |  DISEASES
5420  |  PODXL  |  DISEASES
3400  |  ID4  |  DISEASES
5080  |  PAX6  |  DISEASES
28984  |  RGCC  |  DISEASES
1906  |  EDN1  |  DISEASES
9636  |  ISG15  |  DISEASES
10186  |  LHFP  |  DISEASES
161003  |  STOML3  |  DISEASES
23322  |  RPGRIP1L  |  DISEASES
7010  |  TEK  |  DISEASES
4507  |  MTAP  |  DISEASES
3456  |  IFNB1  |  DISEASES
6194  |  RPS6  |  DISEASES
54801  |  HAUS6  |  DISEASES
833  |  CARS  |  DISEASES
689  |  BTF3  |  DISEASES
6456  |  SH3GL2  |  DISEASES
665  |  BNIP3L  |  DISEASES
5884  |  RAD17  |  DISEASES
3486  |  IGFBP3  |  DISEASES
105  |  ADARB2  |  DISEASES
6150  |  MRPL23  |  DISEASES
29126  |  CD274  |  DISEASES
3717  |  JAK2  |  DISEASES
2574  |  GAGE2C  |  DISEASES
645037  |  GAGE2B  |  DISEASES
51378  |  ANGPT4  |  DISEASES
7158  |  TP53BP1  |  DISEASES
1010  |  CDH12  |  DISEASES
55504  |  TNFRSF19  |  DISEASES
116448  |  OLIG1  |  DISEASES
6624  |  FSCN1  |  DISEASES
11200  |  CHEK2  |  DISEASES
4155  |  MBP  |  DISEASES
5888  |  RAD51  |  DISEASES
361  |  AQP4  |  DISEASES
5799  |  PTPRN2  |  DISEASES
53353  |  LRP1B  |  DISEASES
115708  |  TRMT61A  |  DISEASES
23521  |  RPL13A  |  DISEASES
11009  |  IL24  |  DISEASES
2068  |  ERCC2  |  DISEASES
9208  |  LRRFIP1  |  DISEASES
208  |  AKT2  |  DISEASES
7520  |  XRCC5  |  DISEASES
2113  |  ETS1  |  DISEASES
10401  |  PIAS3  |  DISEASES
143187  |  VTI1A  |  DISEASES
80310  |  PDGFD  |  DISEASES
10018  |  BCL2L11  |  DISEASES
146956  |  EME1  |  DISEASES
5803  |  PTPRZ1  |  DISEASES
2596  |  GAP43  |  DISEASES
1267  |  CNP  |  DISEASES
3161  |  HMMR  |  DISEASES
11346  |  SYNPO  |  DISEASES
7756  |  ZNF207  |  DISEASES
9255  |  AIMP1  |  DISEASES
5530  |  PPP3CA  |  DISEASES
6696  |  SPP1  |  DISEASES
983  |  CDK1  |  DISEASES
6387  |  CXCL12  |  DISEASES
27327  |  TNRC6A  |  DISEASES
2737  |  GLI3  |  DISEASES
8537  |  BCAS1  |  DISEASES
6489  |  ST8SIA1  |  DISEASES
57584  |  ARHGAP21  |  DISEASES
1285  |  COL4A3  |  DISEASES
144195  |  SLC2A14  |  DISEASES
1286  |  COL4A4  |  DISEASES
6202  |  RPS8  |  DISEASES
2628  |  GATM  |  DISEASES
29998  |  GLTSCR1  |  DISEASES
51147  |  ING4  |  DISEASES
64223  |  MLST8  |  DISEASES
4357  |  MPST  |  DISEASES
65993  |  MRPS34  |  DISEASES
5609  |  MAP2K7  |  DISEASES
55508  |  SLC35E3  |  DISEASES
79659  |  DYNC2H1  |  DISEASES
56105  |  PCDHGA11  |  DISEASES
2950  |  GSTP1  |  DISEASES
6093  |  ROCK1  |  DISEASES
10410  |  IFITM3  |  DISEASES
1654  |  DDX3X  |  DISEASES
23028  |  KDM1A  |  DISEASES
8091  |  HMGA2  |  DISEASES
23466  |  CBX6  |  DISEASES
7122  |  CLDN5  |  DISEASES
51701  |  NLK  |  DISEASES
1994  |  ELAVL1  |  DISEASES
7018  |  TF  |  DISEASES
377007  |  KLHL30  |  DISEASES
7852  |  CXCR4  |  DISEASES
1385  |  CREB1  |  DISEASES
1111  |  CHEK1  |  DISEASES
9564  |  BCAR1  |  DISEASES
3481  |  IGF2  |  DISEASES
5537  |  PPP6C  |  DISEASES
3281  |  HSBP1  |  DISEASES
146713  |  RBFOX3  |  DISEASES
2260  |  FGFR1  |  DISEASES
3833  |  KIFC1  |  DISEASES
643376  |  BTBD18  |  DISEASES
1029  |  CDKN2A  |  DISEASES
26354  |  GNL3  |  DISEASES
23040  |  MYT1L  |  DISEASES
7155  |  TOP2B  |  DISEASES
22809  |  ATF5  |  DISEASES
8848  |  TSC22D1  |  DISEASES
257415  |  FAM133B  |  DISEASES
56616  |  DIABLO  |  DISEASES
960  |  CD44  |  DISEASES
7124  |  TNF  |  DISEASES
3491  |  CYR61  |  DISEASES
387  |  RHOA  |  DISEASES
7465  |  WEE1  |  DISEASES
6490  |  PMEL  |  DISEASES
9852  |  EPM2AIP1  |  DISEASES
9351  |  SLC9A3R2  |  DISEASES
1012  |  CDH13  |  DISEASES
1154  |  CISH  |  DISEASES
2263  |  FGFR2  |  DISEASES
9715  |  FAM131B  |  DISEASES
222255  |  ATXN7L1  |  DISEASES
7153  |  TOP2A  |  DISEASES
1028  |  CDKN1C  |  DISEASES
3586  |  IL10  |  DISEASES
3831  |  KLC1  |  DISEASES
54934  |  KANSL2  |  DISEASES
8842  |  PROM1  |  DISEASES
5270  |  SERPINE2  |  DISEASES
57670  |  KIAA1549  |  DISEASES
6513  |  SLC2A1  |  DISEASES
7045  |  TGFBI  |  DISEASES
4193  |  MDM2  |  DISEASES
57620  |  STIM2  |  DISEASES
55208  |  DCUN1D2  |  DISEASES
6168  |  RPL37A  |  DISEASES
55799  |  CACNA2D3  |  DISEASES
5478  |  PPIA  |  DISEASES
1316  |  KLF6  |  DISEASES
56034  |  PDGFC  |  DISEASES
51428  |  DDX41  |  DISEASES
221823  |  PRPS1L1  |  DISEASES
1977  |  EIF4E  |  DISEASES
2994  |  GYPB  |  DISEASES
284  |  ANGPT1  |  DISEASES
6224  |  RPS20  |  DISEASES
4603  |  MYBL1  |  DISEASES
6586  |  SLIT3  |  DISEASES
4147  |  MATN2  |  DISEASES
3620  |  IDO1  |  DISEASES
10480  |  EIF3M  |  DISEASES
4857  |  NOVA1  |  DISEASES
8352  |  HIST1H3C  |  DISEASES
8355  |  HIST1H3G  |  DISEASES
3684  |  ITGAM  |  DISEASES
4090  |  SMAD5  |  DISEASES
586  |  BCAT1  |  DISEASES
375612  |  LHFPL3  |  DISEASES
6999  |  TDO2  |  DISEASES
8968  |  HIST1H3F  |  DISEASES
3939  |  LDHA  |  DISEASES
1649  |  DDIT3  |  DISEASES
317  |  APAF1  |  DISEASES
116986  |  AGAP2  |  DISEASES
8742  |  TNFSF12  |  DISEASES
10381  |  TUBB3  |  DISEASES
3679  |  ITGA7  |  DISEASES
122830  |  NAA30  |  DISEASES
2108  |  ETFA  |  DISEASES
567  |  B2M  |  DISEASES
3316  |  HSPB2  |  DISEASES
64506  |  CPEB1  |  DISEASES
9212  |  AURKB  |  DISEASES
4782  |  NFIC  |  DISEASES
126520  |  PLK5  |  DISEASES
2323  |  FLT3LG  |  DISEASES
25804  |  LSM4  |  DISEASES
100129528  |  MUC8  |  DISEASES
728558  |  ENTPD1-AS1  |  DISEASES
100124700  |  HOTAIR  |  DISEASES
100133311  |  HOXA-AS3  |  DISEASES
104472848  |  IRAIN  |  DISEASES
338799  |  LINC01089  |  DISEASES
114044  |  MCM3AP-AS1  |  DISEASES
692196  |  SNORD76  |  DISEASES
57212  |  TP73-AS1  |  DISEASES
101929665  |  UBE2R2-AS1  |  DISEASES
Locus(Waiting for update.)
Disease ID 173
Disease astrocytoma
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:49)
HP:0002664  |  Neoplasia  |  45
HP:0100843  |  Glioblastoma  |  8
HP:0009733  |  Glioma  |  8
HP:0030692  |  Brain tumor  |  6
HP:0001250  |  Seizures  |  3
HP:0000969  |  Dropsy  |  2
HP:0000639  |  Nystagmus  |  2
HP:0002315  |  Headaches  |  2
HP:0040184  |  Oral hemorrhage  |  2
HP:0002181  |  Cerebral edema  |  2
HP:0000821  |  Underactive thyroid  |  1
HP:0011477  |  Upbeat nystagmus  |  1
HP:0012122  |  Anterior uveitis  |  1
HP:0000541  |  Detached retina  |  1
HP:0002346  |  Head tremor  |  1
HP:0002863  |  Myelodysplastic syndrome  |  1
HP:0002835  |  Aspiration  |  1
HP:0000238  |  Nonsyndromal hydrocephalus  |  1
HP:0001347  |  Hyperreflexia  |  1
HP:0001067  |  Neurofibromas  |  1
HP:0002893  |  Pituitary adenoma  |  1
HP:0001251  |  Ataxia  |  1
HP:0002888  |  Ependymoma  |  1
HP:0012302  |  Herpes simplex encephalitis  |  1
HP:0002383  |  Encephalitis  |  1
HP:0009792  |  Teratoma  |  1
HP:0001541  |  Ascites  |  1
HP:0002539  |  Cortical dysplasia  |  1
HP:0009713  |  Spinal hemangioblastoma  |  1
HP:0002301  |  Hemiplegia  |  1
HP:0002516  |  Intracranial pressure elevation  |  1
HP:0012174  |  Glioblastoma multiforme  |  1
HP:0001337  |  Tremor  |  1
HP:0004326  |  Cachexia  |  1
HP:0040049  |  Macular edema  |  1
HP:0000718  |  Aggressive behaviour  |  1
HP:0009592  |  Astrocytoma  |  1
HP:0012231  |  Exudative retinal detachment  |  1
HP:0010828  |  Hemifacial spasm  |  1
HP:0001269  |  Hemiparesis  |  1
HP:0012721  |  Venous malformations  |  1
HP:0100026  |  Arteriovenous malformation  |  1
HP:0002885  |  Medulloblastoma  |  1
HP:0007034  |  Generalized hyperreflexia  |  1
HP:0001903  |  Anemia  |  1
HP:0002273  |  Tetraparesis  |  1
HP:0000717  |  Autism  |  1
HP:0010797  |  Hemangioblastoma  |  1
HP:0002858  |  Mengiomia  |  1
Disease ID 173
Disease astrocytoma
Manually Symptom
UMLS  | Name(Total Manually Symptoms:12)
C2364133  |  infection
C2248595  |  dedifferentiation
C1608408  |  malignant transformation
C1527311  |  brain oedema
C1090821  |  sepsis
C0341687  |  nephrotic syndrome in amyloidosis
C0041341  |  tuberous sclerosis
C0024454  |  maffucci's syndrome
C0018989  |  hemiparesis
C0017638  |  glioma
C0002793  |  anaplastic change
C0002793  |  anaplasia
Text Mined Symptom
UMLS | Name | Sentences' Count(Total Symptoms:5)
C0041341  |  tuberous sclerosis  |  33
C0017638  |  glioma  |  5
C1608408  |  malignant transformation  |  4
C0009450  |  infection  |  1
C0018989  |  hemiparesis  |  1
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:40)
snpId pubmedId geneId geneSymbol diseaseId sourceId sentence score Year geneSymbol_dbSNP CHROMOSOME POS REF ALT
rs1046487026014354137196CCDC26umls:C0004114BeFreeIn addition, SNPs rs10464870 and rs891835 in CCDC26 were associated with an increased risk of non-astrocytoma tumor subtypes (p trend = 0.009, p trend = 0.007, respectively).0.0002714422015CCDC268129465577CT
rs11348802224132923673BRAFumls:C0004114BeFreeThe BT-40 low-grade childhood astrocytoma xenograft model expresses mutated BRAF(V600E) and is highly sensitive to the MEK inhibitor selumetinib (AZD6244).0.1316159192014BRAF7140753336AT,G,C
rs11348802222038996673BRAFumls:C0004114BeFreeWith regard to implications for therapy, our results support evaluation of BRAF(V600E)-specific inhibitors for treating BRAF(V600E) MA patients.0.1316159192011BRAF7140753336AT,G,C
rs113488022241329235609MAP2K7umls:C0004114BeFreeThe BT-40 low-grade childhood astrocytoma xenograft model expresses mutated BRAF(V600E) and is highly sensitive to the MEK inhibitor selumetinib (AZD6244).0.0010857672014BRAF7140753336AT,G,C
rs11348802222586120673BRAFumls:C0004114BeFreeOur findings indicate a rational therapeutic strategy for treating a subset of pediatric astrocytomas with BRAF(V600E) mutation and CDKN2A deficiency.0.1316159192012BRAF7140753336AT,G,C
rs113488022225861201029CDKN2Aumls:C0004114BeFreeOur findings indicate a rational therapeutic strategy for treating a subset of pediatric astrocytomas with BRAF(V600E) mutation and CDKN2A deficiency.0.015492052012BRAF7140753336AT,G,C
rs11810177725427834546ATRXumls:C0004114BeFreeATRX and IDH1-R132H immunohistochemistry with subsequent copy number analysis and IDH sequencing as a basis for an integrated diagnostic approach for adult astrocytoma, oligodendroglioma and glioblastoma.0.0019000932014IDH21590087472CT
rs118101777254278343418IDH2umls:C0004114BeFreeATRX and IDH1-R132H immunohistochemistry with subsequent copy number analysis and IDH sequencing as a basis for an integrated diagnostic approach for adult astrocytoma, oligodendroglioma and glioblastoma.0.0104343432014IDH21590087472CT
rs121909717193797942670GFAPumls:C0004114BeFreeThe process of inducing GFAP aggregates in astrocytoma-derived cells is different between R239C and R416W mutant GFAP. A time-lapse recording study.0.011410492009GFAP1744908075GT,A
rs121913499193404323417IDH1umls:C0004114BeFreeSelective acquisition of IDH1 R132C mutations in astrocytomas associated with Li-Fraumeni syndrome.0.0279361072009IDH12208248389GT,A
rs1219134991934043281890QTRT1umls:C0004114BeFreeWithout exception, all were R132C (CGT-->TGT), which in sporadic astrocytomas accounts for <5% of IDH1 mutations.0.0002714422009IDH12208248389GT,A
rs121913499193404329097USP14umls:C0004114BeFreeWithout exception, all were R132C (CGT-->TGT), which in sporadic astrocytomas accounts for <5% of IDH1 mutations.0.0002714422009IDH12208248389GT,A
rs121913499195543373417IDH1umls:C0004114BeFreeIDH1 mutations of the R132C type are strongly associated with astrocytoma, while IDH2 mutations predominantly occur in oligodendroglial tumors.0.0279361072009IDH12208248389GT,A
rs12191350024599602768CA9umls:C0004114BeFreeTo study the putative expression patterns and clinical significance of Hsp27, we assessed the associations between Hsp27, R132H mutation of Isocitrate dehydrogenase1 (IDH1-R132H), Hypoxia-inducible factor subunit alpha (HIF-1 alpha), Carbonic anhydrase IX (CA IX), and patient prognosis in astrocytic gliomas.0.0029957922015IDH12208248388CT
rs121913500239347693417IDH1umls:C0004114BeFreeAs the presence of the p.R132H mutation in the IDH1 gene seems to be a more powerful prognostic marker than O(6)-methylguanine-DNA methyltransferase promoter status, we evaluated the presence of IDH1 mutation in Polish patients with astrocytoma, glioblastoma, oligoastrocytoma, ganglioglioma, oligodendroglioma, and ependymoma.0.0279361072014IDH12208248388CT
rs121913500254278343418IDH2umls:C0004114BeFreeATRX and IDH1-R132H immunohistochemistry with subsequent copy number analysis and IDH sequencing as a basis for an integrated diagnostic approach for adult astrocytoma, oligodendroglioma and glioblastoma.0.0104343432014IDH12208248388CT
rs12191350025427834546ATRXumls:C0004114BeFreeATRX and IDH1-R132H immunohistochemistry with subsequent copy number analysis and IDH sequencing as a basis for an integrated diagnostic approach for adult astrocytoma, oligodendroglioma and glioblastoma.0.0019000932014IDH12208248388CT
rs121913500245996023417IDH1umls:C0004114BeFreeTo study the putative expression patterns and clinical significance of Hsp27, we assessed the associations between Hsp27, R132H mutation of Isocitrate dehydrogenase1 (IDH1-R132H), Hypoxia-inducible factor subunit alpha (HIF-1 alpha), Carbonic anhydrase IX (CA IX), and patient prognosis in astrocytic gliomas.0.0279361072015IDH12208248388CT
rs121913500245996023091HIF1Aumls:C0004114BeFreeTo study the putative expression patterns and clinical significance of Hsp27, we assessed the associations between Hsp27, R132H mutation of Isocitrate dehydrogenase1 (IDH1-R132H), Hypoxia-inducible factor subunit alpha (HIF-1 alpha), Carbonic anhydrase IX (CA IX), and patient prognosis in astrocytic gliomas.0.1246244432015IDH12208248388CT
rs121913500197985093417IDH1umls:C0004114BeFreeIDH1 R132H mutations occur in approximately 70% of astrocytomas and oligodendroglial tumors.0.0279361072009IDH12208248388CT
rs12191350024557705113451AZIN2umls:C0004114BeFreeFractional anisotropy and ADC from DTI can noninvasively detect IDH1 R132H mutation in astrogliomas.0.0002714422015IDH12208248388CT
rs12191350024557705339896GADL1umls:C0004114BeFreeFractional anisotropy and ADC from DTI can noninvasively detect IDH1 R132H mutation in astrogliomas.0.0002714422015IDH12208248388CT
rs121913500198183343417IDH1umls:C0004114BeFreeFurthermore, IMab-1 specifically stained the IDH1(R132H)-expressing cells in astrocytomas in immunohistochemistry, whereas it did not react with IDH1(R132H)-negative primary glioblastoma sections.0.0279361072009IDH12208248388CT
rs121913500223857873417IDH1umls:C0004114BeFreeThe mutation analysis performed on the latter case with DNA separately sampled from the oligodendroglioma- like area and the astrocytoma-like area detected IDH1 G395A in both areas.0.0279361072012IDH12208248388CT
rs121913500236199256774STAT3umls:C0004114BeFreeWe investigated the expression of Sox11 in 132 diffuse astrocytomas in relation to the regulator cell marker nestin, c-Met and IDH1-R132H, which have shown to be differentially expressed among the molecular subgroups of malignant gliomas, as well as to an inducer of astrocytic differentiation, that is, signal transducer and activator of transcription (p-STAT-3), clinicopathological features and survival.0.0013572092013IDH12208248388CT
rs1378529722325091426580BSCL2umls:C0004114BeFreeIn this study, we show that expression of seipin N-glycosylation mutant N88S led to decreased triglyceride (TG) content in astrocytoma and motor neuron cell lines.0.0002714422013BSCL2;HNRNPUL2-BSCL21162702499TC
rs1695211282132950GSTP1umls:C0004114BeFreeGSTP1 Ile105Val polymorphism in astrocytomas and glioblastomas.0.010368332010GSTP11167585218AG
rs180151618465141472ATMumls:C0004114BeFreeThree-hit hypothesis in astrocytoma: tracing the polymorphism D1853N in ATM gene through a pedigree of the proband affected with primary brain tumor.0.0005428842008ATM11108304735GA
rs22974402601435451750RTEL1umls:C0004114BeFreeMoreover, the stratified analyses showed a decreased risk of astrocytoma associated with RTEL1 rs6089953, rs6010620 and rs2297440 (p trend = 0.022, p trend = 0.042, p trend = 0.029, respectively) as well as an increased risk of this subtype associated with RTEL1 rs4809324 (p trend = 0.033).0.0005428842015RTEL1;RTEL1-TNFRSF6B2063680946TC
rs371409680NA7157TP53umls:C0004114CLINVARNA0.260462981NATP53177673772CT
rs48093242601435451750RTEL1umls:C0004114BeFreeMoreover, the stratified analyses showed a decreased risk of astrocytoma associated with RTEL1 rs6089953, rs6010620 and rs2297440 (p trend = 0.022, p trend = 0.042, p trend = 0.029, respectively) as well as an increased risk of this subtype associated with RTEL1 rs4809324 (p trend = 0.033).0.0005428842015RTEL1;RTEL1-TNFRSF6B2063686867TC
rs5498193060553383ICAM1umls:C0004114BeFreeICAM-1 (Lys469Glu) and PECAM-1 (Leu125Val) polymorphisms in diffuse astrocytomas.0.0067200332009ICAM1;ICAM4;LOC1053722721910285007AG
rs5498193060555175PECAM1umls:C0004114BeFreeICAM-1 (Lys469Glu) and PECAM-1 (Leu125Val) polymorphisms in diffuse astrocytomas.0.0029099162009ICAM1;ICAM4;LOC1053722721910285007AG
rs58064122227055852670GFAPumls:C0004114BeFreeOn the basis of the protective role shown by both these small heat shock proteins (sHSPs), and on the already well established neuroprotective effects of curcumin in several diseases, we have investigated the effects of this compound in an in vitro model of Alexander disease, consisting in U251-MG astrocytoma cells transiently transfected with a construct encoding for GFAP carrying the p.R239C mutation in frame with the reporter green fluorescent protein (GFP).0.011410492012GFAP1744913334GA
rs58064122193797942670GFAPumls:C0004114BeFreeThe process of inducing GFAP aggregates in astrocytoma-derived cells is different between R239C and R416W mutant GFAP. A time-lapse recording study.0.011410492009GFAP1744913334GA
rs60106202601435451750RTEL1umls:C0004114BeFreeMoreover, the stratified analyses showed a decreased risk of astrocytoma associated with RTEL1 rs6089953, rs6010620 and rs2297440 (p trend = 0.022, p trend = 0.042, p trend = 0.029, respectively) as well as an increased risk of this subtype associated with RTEL1 rs4809324 (p trend = 0.033).0.0005428842015RTEL1;RTEL1-TNFRSF6B2063678486AG
rs60899532601435451750RTEL1umls:C0004114BeFreeMoreover, the stratified analyses showed a decreased risk of astrocytoma associated with RTEL1 rs6089953, rs6010620 and rs2297440 (p trend = 0.022, p trend = 0.042, p trend = 0.029, respectively) as well as an increased risk of this subtype associated with RTEL1 rs4809324 (p trend = 0.033).0.0005428842015RTEL1;RTEL1-TNFRSF6B2063659655AG
rs668193060553383ICAM1umls:C0004114BeFreeICAM-1 (Lys469Glu) and PECAM-1 (Leu125Val) polymorphisms in diffuse astrocytomas.0.0067200332009NANANANANA
rs668193060555175PECAM1umls:C0004114BeFreeICAM-1 (Lys469Glu) and PECAM-1 (Leu125Val) polymorphisms in diffuse astrocytomas.0.0029099162009NANANANANA
rs89183526014354137196CCDC26umls:C0004114BeFreeIn addition, SNPs rs10464870 and rs891835 in CCDC26 were associated with an increased risk of non-astrocytoma tumor subtypes (p trend = 0.009, p trend = 0.007, respectively).0.0002714422015CCDC268129479506TG
GWASdb Annotation(Total Genotypes:0)
(Waiting for update.)
GWASdb Snp Trait(Total Genotypes:0)
(Waiting for update.)
Mapped by lexical matching(Total Items:0)
(Waiting for update.)
Mapped by homologous gene(Total Items:1)
HP ID HP Name MP ID MP Name Annotation
HP:0009733GliomaMP:0009625abnormal abdominal lymph node morphology;HP:0002181Cerebral edema
Chemical(Total Drugs:4)
CUI ChemicalName ChemicalID CasRN DiseaseName DiseaseID DirectEvidence PubMedIDs
C0004114carmustineD002330154-93-8astrocytomaMESH:D001254therapeutic11096723
C0004114cisplatinD00294515663-27-1astrocytomaMESH:D001254therapeutic16193384
C0004114temozolomideC04724685622-93-1astrocytomaMESH:D001254therapeutic15865885
C0004114vincristineD014750-astrocytomaMESH:D001254therapeutic1312230
FDA approved drug and dosage information(Total Drugs:2)
DiseaseID Drug_name active_ingredients strength Dosage Form/Route Marketing Status TE code RLD RS
MESH:D001254temodartemozolomide5MGCAPSULE;ORALPrescriptionABYesNo
MESH:D001254temodartemozolomide100MG/VIALPOWDER;INTRAVENOUSPrescriptionNoneYesYes
FDA labeling changes(Total Drugs:2)
DiseaseID Pediatric_Labeling_Date Trade_Name Generic_Name_or_Proper_Name Indications Studied Label Changes Summary Product Labeling BPCA(B) PREA(P) BPCA(B) and PREA(P) Pediatric Rule (R) Sponsor Pediatric Exclusivity Granted Date NNPS
MESH:D00125411/3/2003temodartemozolomideRecurrent CNS tumorsTemozolomide effectiveness in children has not been demonstrated New data from 2 open-label Phase 2 studies in pediatric patients 3-18 years of age. In one study there were 29 patients with recurrent brain stem glioma and 34 patients with recurrent high grade astrocyoma. In a second study there were 122 patients enrolled with various types of tumors; 113 CNS tumors and 9 non-CNS tumors. The temozolomide toxicity profile in children is similar to adultsLabelingB---Schering11/20/2002FALSE'
MESH:D00125411/3/2003temodartemozolomideRecurrent CNS tumorsTemozolomide effectiveness in children has not been demonstrated New data from 2 open-label Phase 2 studies in pediatric patients 3-18 years of age. In one study there were 29 patients with recurrent brain stem glioma and 34 patients with recurrent high grade astrocyoma. In a second study there were 122 patients enrolled with various types of tumors; 113 CNS tumors and 9 non-CNS tumors. The temozolomide toxicity profile in children is similar to adultsLabelingB---Schering11/20/2002FALSE'