Home Contact Sitemap

PedAM

Pediatric Disease Annotations & Medicines



   fibrillary astrocytoma
  

Disease ID 1325
Disease fibrillary astrocytoma
Definition
The most frequent histological variant of diffuse astrocytoma. It is predominantly composed of fibrillary neoplastic astrocytes. Nuclear atypia is a diagnostic criterion but mitotic activity, necrosis and microvascular proliferation are absent. The occasional or regional occurrence of gemistocytic neoplastic cells is compatible with the diagnosis of fibrillary astrocytoma. (WHO)
Synonym
astrocytoma, fibrillary
astrocytomas, fibrillary
fibrillary astrocytoma (morphologic abnormality)
fibrillary astrocytomas
fibrous astrocytoma
fibrous astrocytoma (morphologic abnormality)
Orphanet
DOID
UMLS
C0334582
Curated Gene
Entrez_id | Symbol | Resource(Total Genes:1)
IDH2  |  3418  |  ORPHANET
Inferring Gene(Waiting for update.)
Text Mined Gene
Entrez_id | Symbol | Score | Resource(Total Genes:105)
618  |  BCYRN1  |  DISEASES
7051  |  TGM1  |  DISEASES
4313  |  MMP2  |  DISEASES
4832  |  NME3  |  DISEASES
4833  |  NME4  |  DISEASES
165  |  AEBP1  |  DISEASES
595  |  CCND1  |  DISEASES
4172  |  MCM3  |  DISEASES
3488  |  IGFBP5  |  DISEASES
6909  |  TBX2  |  DISEASES
994  |  CDC25B  |  DISEASES
6237  |  RRAS  |  DISEASES
5880  |  RAC2  |  DISEASES
3741  |  KCNA5  |  DISEASES
2670  |  GFAP  |  DISEASES
3021  |  H3F3B  |  DISEASES
3832  |  KIF11  |  DISEASES
3417  |  IDH1  |  DISEASES
4659  |  PPP1R12A  |  DISEASES
5037  |  PEBP1  |  DISEASES
9368  |  SLC9A3R1  |  DISEASES
6855  |  SYP  |  DISEASES
4171  |  MCM2  |  DISEASES
7078  |  TIMP3  |  DISEASES
429  |  ASCL1  |  DISEASES
7157  |  TP53  |  DISEASES
3487  |  IGFBP4  |  DISEASES
55502  |  HES6  |  DISEASES
1956  |  EGFR  |  DISEASES
1030  |  CDKN2B  |  DISEASES
673  |  BRAF  |  DISEASES
10630  |  PDPN  |  DISEASES
11167  |  FSTL1  |  DISEASES
6853  |  SYN1  |  DISEASES
6997  |  TDGF1  |  DISEASES
79085  |  SLC25A23  |  DISEASES
4255  |  MGMT  |  DISEASES
6504  |  SLAMF1  |  DISEASES
23261  |  CAMTA1  |  DISEASES
57521  |  RPTOR  |  DISEASES
6620  |  SNCB  |  DISEASES
991  |  CDC20  |  DISEASES
25992  |  SNED1  |  DISEASES
7015  |  TERT  |  DISEASES
947  |  CD34  |  DISEASES
8061  |  FOSL1  |  DISEASES
8639  |  AOC3  |  DISEASES
274  |  BIN1  |  DISEASES
818  |  CAMK2G  |  DISEASES
7156  |  TOP3A  |  DISEASES
3039  |  HBA1  |  DISEASES
10215  |  OLIG2  |  DISEASES
83482  |  SCRT1  |  DISEASES
3418  |  IDH2  |  DISEASES
682  |  BSG  |  DISEASES
10608  |  MXD4  |  DISEASES
4602  |  MYB  |  DISEASES
5910  |  RAP1GDS1  |  DISEASES
5764  |  PTN  |  DISEASES
347  |  APOD  |  DISEASES
27030  |  MLH3  |  DISEASES
120  |  ADD3  |  DISEASES
253260  |  RICTOR  |  DISEASES
4763  |  NF1  |  DISEASES
404552  |  SCGB1D4  |  DISEASES
4133  |  MAP2  |  DISEASES
1284  |  COL4A2  |  DISEASES
8682  |  PEA15  |  DISEASES
388677  |  NOTCH2NL  |  DISEASES
9444  |  QKI  |  DISEASES
1291  |  COL6A1  |  DISEASES
961  |  CD47  |  DISEASES
2987  |  GUK1  |  DISEASES
3020  |  H3F3A  |  DISEASES
1063  |  CENPF  |  DISEASES
10763  |  NES  |  DISEASES
2173  |  FABP7  |  DISEASES
1755  |  DMBT1  |  DISEASES
6125  |  RPL5  |  DISEASES
5728  |  PTEN  |  DISEASES
546  |  ATRX  |  DISEASES
778  |  CACNA1F  |  DISEASES
10590  |  SCGN  |  DISEASES
5420  |  PODXL  |  DISEASES
2596  |  GAP43  |  DISEASES
2199  |  FBLN2  |  DISEASES
9699  |  RIMS2  |  DISEASES
151  |  ADRA2B  |  DISEASES
146713  |  RBFOX3  |  DISEASES
1029  |  CDKN2A  |  DISEASES
23040  |  MYT1L  |  DISEASES
7155  |  TOP2B  |  DISEASES
8848  |  TSC22D1  |  DISEASES
8605  |  PLA2G4C  |  DISEASES
9715  |  FAM131B  |  DISEASES
7153  |  TOP2A  |  DISEASES
55355  |  HJURP  |  DISEASES
5270  |  SERPINE2  |  DISEASES
57670  |  KIAA1549  |  DISEASES
6091  |  ROBO1  |  DISEASES
9353  |  SLIT2  |  DISEASES
4603  |  MYBL1  |  DISEASES
6586  |  SLIT3  |  DISEASES
23186  |  RCOR1  |  DISEASES
100133311  |  HOXA-AS3  |  DISEASES
Locus
Symbol | Locus(Total Locus:1)
IDH2  |  15q26.1
Disease ID 1325
Disease fibrillary astrocytoma
Integrated Phenotype(Waiting for update.)
Text Mined Phenotype(Waiting for update.)
Disease ID 1325
Disease fibrillary astrocytoma
Manually Symptom(Waiting for update.)
Text Mined Symptom(Waiting for update.)
Manually Genotype(Total Text Mining Genotypes:0)
(Waiting for update.)
All Snps(Total Genotypes:1)
snpId pubmedId geneId geneSymbol diseaseId sourceId sentence score Year geneSymbol_dbSNP CHROMOSOME POS REF ALT
rs113488022247677147157TP53umls:C0334582BeFreeA BRAF p.Thr599dup or p.V600E mutation was identified by Sanger sequencing in one and five gliomas, respectively, and a somatic TP53 mutation was identified in a fibrillary astrocytoma.0.0013572092014BRAF7140753336AT,G,C
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:0)
(Waiting for update.)
FDA approved drug and dosage information(Total Drugs:0)
(Waiting for update.)
FDA labeling changes(Total Drugs:0)
(Waiting for update.)