Home Contact Sitemap

PedAM

Pediatric Disease Annotations & Medicines



   oligodendroglioma
  

Disease ID 260
Disease oligodendroglioma
Definition
A relatively slow-growing glioma that is derived from oligodendrocytes and tends to occur in the cerebral hemispheres, thalamus, or lateral ventricle. They may present at any age, but are most frequent in the third to fifth decades, with an earlier incidence peak in the first decade. Histologically, these tumors are encapsulated, relatively avascular, and tend to form cysts and microcalcifications. Neoplastic cells tend to have small round nuclei surrounded by unstained nuclei. The tumors may vary from well-differentiated to highly anaplastic forms. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, p2052; Adams et al., Principles of Neurology, 6th ed, p655)
Synonym
oligodendrogliomas
Orphanet
DOID
UMLS
C0028945
MeSH
Comorbidity
UMLS | Disease | Sentences' Count(Total Sentences:13)
C0017636  |  glioblastoma  |  14
C0206716  |  ganglioglioma  |  3
C0017636  |  glioblastomas  |  3
C0334583  |  pilocytic astrocytoma  |  2
C0004114  |  astrocytoma  |  2
C0030312  |  pancytopenia  |  1
C0004114  |  astrocytomas  |  1
C0007102  |  colon cancer  |  1
C0011649  |  mature cystic teratoma  |  1
C0280793  |  oligoastrocytoma  |  1
C0020255  |  hydrocephalus  |  1
C0206719  |  central neurocytoma  |  1
C1368903  |  cystic teratoma  |  1
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:8)
IDH2  |  3418  |  CTD_human;ORPHANET
IDH1  |  3417  |  CTD_human
GDNF  |  2668  |  CTD_human
HEY1  |  23462  |  CTD_human
DTX1  |  1840  |  CTD_human
HES1  |  3280  |  CTD_human
POT1  |  25913  |  ORPHANET
TP73-AS1  |  57212  |  CTD_human
Inferring Gene
Entrez_id | Symbol | Resource(Total Genes:1)
1029  |  CDKN2A  |  infer
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:235)
137196  |  CCDC26  |  DISEASES
23152  |  CIC  |  DISEASES
55810  |  FOXJ2  |  DISEASES
8646  |  CHRD  |  DISEASES
10683  |  DLL3  |  DISEASES
151887  |  CCDC80  |  DISEASES
10454  |  TAB1  |  DISEASES
23064  |  SETX  |  DISEASES
708  |  C1QBP  |  DISEASES
595  |  CCND1  |  DISEASES
2735  |  GLI1  |  DISEASES
2026  |  ENO2  |  DISEASES
2822  |  GPLD1  |  DISEASES
3485  |  IGFBP2  |  DISEASES
7475  |  WNT6  |  DISEASES
2956  |  MSH6  |  DISEASES
54454  |  ATAD2B  |  DISEASES
22865  |  SLITRK3  |  DISEASES
8358  |  HIST1H3B  |  DISEASES
2354  |  FOSB  |  DISEASES
29997  |  GLTSCR2  |  DISEASES
23002  |  DAAM1  |  DISEASES
2952  |  GSTT1  |  DISEASES
3236  |  HOXD10  |  DISEASES
968  |  CD68  |  DISEASES
3270  |  HRC  |  DISEASES
55902  |  ACSS2  |  DISEASES
2670  |  GFAP  |  DISEASES
529  |  ATP6V1E1  |  DISEASES
3021  |  H3F3B  |  DISEASES
1116  |  CHI3L1  |  DISEASES
4853  |  NOTCH2  |  DISEASES
5156  |  PDGFRA  |  DISEASES
8728  |  ADAM19  |  DISEASES
4440  |  MSI1  |  DISEASES
1840  |  DTX1  |  DISEASES
1019  |  CDK4  |  DISEASES
29109  |  FHOD1  |  DISEASES
10154  |  PLXNC1  |  DISEASES
10010  |  TANK  |  DISEASES
3417  |  IDH1  |  DISEASES
2581  |  GALC  |  DISEASES
5159  |  PDGFRB  |  DISEASES
9480  |  ONECUT2  |  DISEASES
5862  |  RAB2A  |  DISEASES
1031  |  CDKN2C  |  DISEASES
443  |  ASPA  |  DISEASES
6855  |  SYP  |  DISEASES
30846  |  EHD2  |  DISEASES
822  |  CAPG  |  DISEASES
5593  |  PRKG2  |  DISEASES
5929  |  RBBP5  |  DISEASES
10926  |  DBF4  |  DISEASES
5395  |  PMS2  |  DISEASES
11010  |  GLIPR1  |  DISEASES
429  |  ASCL1  |  DISEASES
11057  |  ABHD2  |  DISEASES
7157  |  TP53  |  DISEASES
2014  |  EMP3  |  DISEASES
26018  |  LRIG1  |  DISEASES
4594  |  MUT  |  DISEASES
23500  |  DAAM2  |  DISEASES
1956  |  EGFR  |  DISEASES
4851  |  NOTCH1  |  DISEASES
64849  |  SLC13A3  |  DISEASES
6695  |  SPOCK1  |  DISEASES
55079  |  FEZF2  |  DISEASES
7071  |  KLF10  |  DISEASES
389  |  RHOC  |  DISEASES
26059  |  ERC2  |  DISEASES
114793  |  FMNL2  |  DISEASES
5909  |  RAP1GAP  |  DISEASES
79190  |  IRX6  |  DISEASES
6285  |  S100B  |  DISEASES
51127  |  TRIM17  |  DISEASES
27306  |  HPGDS  |  DISEASES
6259  |  RYK  |  DISEASES
10085  |  EDIL3  |  DISEASES
64321  |  SOX17  |  DISEASES
7373  |  COL14A1  |  DISEASES
9833  |  MELK  |  DISEASES
25924  |  MYRIP  |  DISEASES
4255  |  MGMT  |  DISEASES
81603  |  TRIM8  |  DISEASES
162979  |  ZNF296  |  DISEASES
6203  |  RPS9  |  DISEASES
4144  |  MAT2A  |  DISEASES
5354  |  PLP1  |  DISEASES
84275  |  SLC25A33  |  DISEASES
23261  |  CAMTA1  |  DISEASES
51029  |  DESI2  |  DISEASES
7015  |  TERT  |  DISEASES
3265  |  HRAS  |  DISEASES
947  |  CD34  |  DISEASES
27243  |  CHMP2A  |  DISEASES
7368  |  UGT8  |  DISEASES
5978  |  REST  |  DISEASES
8496  |  PPFIBP1  |  DISEASES
23075  |  SWAP70  |  DISEASES
55228  |  PNMAL1  |  DISEASES
56676  |  ASCL3  |  DISEASES
56776  |  FMN2  |  DISEASES
23019  |  CNOT1  |  DISEASES
1351  |  COX8A  |  DISEASES
1730  |  DIAPH2  |  DISEASES
3039  |  HBA1  |  DISEASES
11284  |  PNKP  |  DISEASES
55553  |  SOX6  |  DISEASES
5178  |  PEG3  |  DISEASES
121227  |  LRIG3  |  DISEASES
30845  |  EHD3  |  DISEASES
3231  |  HOXD1  |  DISEASES
752  |  FMNL1  |  DISEASES
8354  |  HIST1H3I  |  DISEASES
5155  |  PDGFB  |  DISEASES
10215  |  OLIG2  |  DISEASES
6938  |  TCF12  |  DISEASES
63827  |  BCAN  |  DISEASES
79191  |  IRX3  |  DISEASES
3418  |  IDH2  |  DISEASES
84619  |  ZGPAT  |  DISEASES
430  |  ASCL2  |  DISEASES
79582  |  SPAG16  |  DISEASES
5787  |  PTPRB  |  DISEASES
139065  |  SLITRK4  |  DISEASES
57142  |  RTN4  |  DISEASES
10608  |  MXD4  |  DISEASES
4004  |  LMO1  |  DISEASES
4862  |  NPAS2  |  DISEASES
7317  |  UBA1  |  DISEASES
5329  |  PLAUR  |  DISEASES
1809  |  DPYSL3  |  DISEASES
10252  |  SPRY1  |  DISEASES
20  |  ABCA2  |  DISEASES
7316  |  UBC  |  DISEASES
121549  |  ASCL4  |  DISEASES
58473  |  PLEKHB1  |  DISEASES
5154  |  PDGFA  |  DISEASES
4983  |  OPHN1  |  DISEASES
27030  |  MLH3  |  DISEASES
8350  |  HIST1H3A  |  DISEASES
4763  |  NF1  |  DISEASES
8356  |  HIST1H3J  |  DISEASES
1454  |  CSNK1E  |  DISEASES
55959  |  SULF2  |  DISEASES
4134  |  MAP4  |  DISEASES
4133  |  MAP2  |  DISEASES
8353  |  HIST1H3E  |  DISEASES
6663  |  SOX10  |  DISEASES
4916  |  NTRK3  |  DISEASES
2673  |  GFPT1  |  DISEASES
23187  |  PHLDB1  |  DISEASES
388677  |  NOTCH2NL  |  DISEASES
9444  |  QKI  |  DISEASES
9860  |  LRIG2  |  DISEASES
3020  |  H3F3A  |  DISEASES
4194  |  MDM4  |  DISEASES
3075  |  CFH  |  DISEASES
5451  |  POU2F1  |  DISEASES
10763  |  NES  |  DISEASES
57326  |  PBXIP1  |  DISEASES
6280  |  S100A9  |  DISEASES
284486  |  THEM5  |  DISEASES
8357  |  HIST1H3H  |  DISEASES
9118  |  INA  |  DISEASES
84631  |  SLITRK2  |  DISEASES
8880  |  FUBP1  |  DISEASES
9077  |  DIRAS3  |  DISEASES
2778  |  GNAS  |  DISEASES
8022  |  LHX3  |  DISEASES
57580  |  PREX1  |  DISEASES
5728  |  PTEN  |  DISEASES
7422  |  VEGFA  |  DISEASES
163732  |  CITED4  |  DISEASES
55859  |  BEX1  |  DISEASES
4337  |  MOCS1  |  DISEASES
546  |  ATRX  |  DISEASES
25932  |  CLIC4  |  DISEASES
6135  |  RPL11  |  DISEASES
199  |  AIF1  |  DISEASES
26050  |  SLITRK5  |  DISEASES
4821  |  NKX2-2  |  DISEASES
8351  |  HIST1H3D  |  DISEASES
55966  |  AJAP1  |  DISEASES
1677  |  DFFB  |  DISEASES
768  |  CA9  |  DISEASES
3400  |  ID4  |  DISEASES
5422  |  POLA1  |  DISEASES
54840  |  APTX  |  DISEASES
10396  |  ATP8A1  |  DISEASES
116448  |  OLIG1  |  DISEASES
4155  |  MBP  |  DISEASES
4336  |  MOBP  |  DISEASES
11009  |  IL24  |  DISEASES
2068  |  ERCC2  |  DISEASES
5803  |  PTPRZ1  |  DISEASES
1267  |  CNP  |  DISEASES
816  |  CAMK2B  |  DISEASES
29998  |  GLTSCR1  |  DISEASES
815  |  CAMK2A  |  DISEASES
1729  |  DIAPH1  |  DISEASES
84189  |  SLITRK6  |  DISEASES
9699  |  RIMS2  |  DISEASES
377007  |  KLHL30  |  DISEASES
9048  |  ARTN  |  DISEASES
64098  |  PARVG  |  DISEASES
146713  |  RBFOX3  |  DISEASES
1029  |  CDKN2A  |  DISEASES
23040  |  MYT1L  |  DISEASES
392862  |  GRID2IP  |  DISEASES
8848  |  TSC22D1  |  DISEASES
8605  |  PLA2G4C  |  DISEASES
5424  |  POLD1  |  DISEASES
389549  |  FEZF1  |  DISEASES
8842  |  PROM1  |  DISEASES
57670  |  KIAA1549  |  DISEASES
6565  |  SLC15A2  |  DISEASES
22862  |  FNDC3A  |  DISEASES
4193  |  MDM2  |  DISEASES
85476  |  GFM1  |  DISEASES
55799  |  CACNA2D3  |  DISEASES
55534  |  MAML3  |  DISEASES
9353  |  SLIT2  |  DISEASES
6586  |  SLIT3  |  DISEASES
917  |  CD3G  |  DISEASES
4857  |  NOVA1  |  DISEASES
8352  |  HIST1H3C  |  DISEASES
8355  |  HIST1H3G  |  DISEASES
84707  |  BEX2  |  DISEASES
8968  |  HIST1H3F  |  DISEASES
6141  |  RPL18  |  DISEASES
23186  |  RCOR1  |  DISEASES
9141  |  PDCD5  |  DISEASES
8153  |  RND2  |  DISEASES
647219  |  ASCL5  |  DISEASES
Locus
Symbol | Locus(Total Locus:2)
IDH2  |  15q26.1
POT1  |  7q31.33
Disease ID 260
Disease oligodendroglioma
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype
HPO | Name | Sentences' Count(Total Phenotypes:8)
HP:0100843  |  Glioblastoma  |  14
HP:0002664  |  Neoplasia  |  9
HP:0009592  |  Astrocytoma  |  2
HP:0009733  |  Glioma  |  2
HP:0001876  |  Low blood cell count  |  1
HP:0030692  |  Brain tumor  |  1
HP:0000238  |  Nonsyndromal hydrocephalus  |  1
HP:0003003  |  Colon cancer  |  1
Disease ID 260
Disease oligodendroglioma
Manually Symptom
UMLS  | Name(Total Manually Symptoms:3)
C1608408  |  malignant transformation
C1417325  |  multiple sclerosis
C0036572  |  seizures
Text Mined Symptom(Waiting for update.)
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:13)
snpId pubmedId geneId geneSymbol diseaseId sourceId sentence score Year geneSymbol_dbSNP CHROMOSOME POS REF ALT
rs1042522183932247157TP53umls:C0028945BeFreeAiming to study the role of TP53 Pro47Ser and Arg72Pro on glioma susceptibility and oncologic prognosis of patients, we investigated the genotype distribution of these SNPs in 94 gliomas (81 astrocytomas, 8 ependymomas and 5 oligodendrogliomas) and in 100 healthy subjects by the polymerase chain reaction-restriction fragment length polymorphism approach.0.0208786182008TP53177676154GT,C
rs11133391241357909575CLOCKumls:C0028945BeFreeThe variant allele for CLOCK rs11133391 under a recessive model increased risk of oligodendroglioma (OR 2.41; 95 % CI 1.31-4.42; p = 0.005), though not other glioma subtypes (p for heterogeneity = 0.0033).0.0002714422013CLOCK455501788TC
rs11540654183932247157TP53umls:C0028945BeFreeAiming to study the role of TP53 Pro47Ser and Arg72Pro on glioma susceptibility and oncologic prognosis of patients, we investigated the genotype distribution of these SNPs in 94 gliomas (81 astrocytomas, 8 ependymomas and 5 oligodendrogliomas) and in 100 healthy subjects by the polymerase chain reaction-restriction fragment length polymorphism approach.0.0208786182008TP53177676040CT,G,A
rs118101777252772073418IDH2umls:C0028945BeFreeThe majority of oligodendrogliomas (ODGs) exhibit combined losses of chromosomes 1p and 19q and mutations of isocitrate dehydrogenase (IDH1-R132H or IDH2-R172K).0.2458957762015IDH21590087472CT
rs118101777252772073417IDH1umls:C0028945BeFreeThe majority of oligodendrogliomas (ODGs) exhibit combined losses of chromosomes 1p and 19q and mutations of isocitrate dehydrogenase (IDH1-R132H or IDH2-R172K).0.1387830282015IDH21590087472CT
rs121913500239341753417IDH1umls:C0028945BeFreeWe evaluated nuclear cMYC protein levels and IDH1 (R132H) by immunohistochemistry in patients with oligodendroglioma/oligoastrocytomas (n = 20), astrocytomas (grade II) (n = 19), anaplastic astrocytomas (n = 21) or glioblastomas (n = 111).0.1387830282013IDH12208248388CT
rs121913500252772073417IDH1umls:C0028945BeFreeThe majority of oligodendrogliomas (ODGs) exhibit combined losses of chromosomes 1p and 19q and mutations of isocitrate dehydrogenase (IDH1-R132H or IDH2-R172K).0.1387830282015IDH12208248388CT
rs121913500252772073418IDH2umls:C0028945BeFreeThe majority of oligodendrogliomas (ODGs) exhibit combined losses of chromosomes 1p and 19q and mutations of isocitrate dehydrogenase (IDH1-R132H or IDH2-R172K).0.2458957762015IDH12208248388CT
rs121913500223857873417IDH1umls:C0028945BeFreeThe 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.0.1387830282012IDH12208248388CT
rs121913500235272653417IDH1umls:C0028945BeFreeThis glioma xenograft is the first to display a pure oligodendroglioma histology and expression of R132H.0.1387830282013IDH12208248388CT
rs121913503252772073418IDH2umls:C0028945BeFreeThe majority of oligodendrogliomas (ODGs) exhibit combined losses of chromosomes 1p and 19q and mutations of isocitrate dehydrogenase (IDH1-R132H or IDH2-R172K).0.2458957762015IDH21590088606CT
rs121913503252772073417IDH1umls:C0028945BeFreeThe majority of oligodendrogliomas (ODGs) exhibit combined losses of chromosomes 1p and 19q and mutations of isocitrate dehydrogenase (IDH1-R132H or IDH2-R172K).0.1387830282015IDH21590088606CT
rs1800371183932247157TP53umls:C0028945BeFreeAiming to study the role of TP53 Pro47Ser and Arg72Pro on glioma susceptibility and oncologic prognosis of patients, we investigated the genotype distribution of these SNPs in 94 gliomas (81 astrocytomas, 8 ependymomas and 5 oligodendrogliomas) and in 100 healthy subjects by the polymerase chain reaction-restriction fragment length polymorphism approach.0.0208786182008TP53177676230GA
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:0)
(Waiting for update.)
Chemical(Total Drugs:4)
CUI ChemicalName ChemicalID CasRN DiseaseName DiseaseID DirectEvidence PubMedIDs
C0028945carmustineD002330154-93-8oligodendrogliomaMESH:D009837therapeutic15332326
C0028945temozolomideC04724685622-93-1oligodendrogliomaMESH:D009837therapeutic20842591
C0028945thiotepaD01385252-24-4oligodendrogliomaMESH:D009837therapeutic11303620
C0028945vincristineD014750-oligodendrogliomaMESH:D009837therapeutic15015656
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:D009837temodartemozolomide5MGCAPSULE;ORALPrescriptionABYesNo
MESH:D009837temodartemozolomide100MG/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:D00983711/3/2003temodartemozolomideRecurrent 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:D00983711/3/2003temodartemozolomideRecurrent 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'