Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0280475
Disease: Childhood Oligodendroglioma
Childhood Oligodendroglioma
0.400 GeneticVariation disease BEFREE The oligodendroglioma model presented here is a valuable model for further functional elucidation of the effects of IDH1 mutations on tumor metabolism and may aid in the rational development of novel therapeutic strategies for the large subgroup of gliomas carrying IDH1 mutations. 24252742 2013
CUI: C0280475
Disease: Childhood Oligodendroglioma
Childhood Oligodendroglioma
0.400 GeneticVariation disease BEFREE The EMP3 and MGMT promoter methylation was more frequent in OII than in GBM patients, and the IDH1 mutation was absent in GBM. 22992787 2012
CUI: C0280475
Disease: Childhood Oligodendroglioma
Childhood Oligodendroglioma
0.400 GeneticVariation disease BEFREE 36 (57%) had oligodendroglioma and 27 astrocytoma.IDH-1 mutation was present in 53 (84%). 30292978 2018
CUI: C0280475
Disease: Childhood Oligodendroglioma
Childhood Oligodendroglioma
0.400 GeneticVariation disease BEFREE The DSC-MRI procedure may provide insight into the IDH1/2 mutation and ATRX expression status and MGMT methylation profile of diffuse glioma; however, taking integrated oligodendroglioma into account limits the diagnostic performance of rCBV in non-invasively predicting the molecular subtype. 29468261 2019
CUI: C0280475
Disease: Childhood Oligodendroglioma
Childhood Oligodendroglioma
0.400 GeneticVariation disease BEFREE Triple-positive (IDH1 and TERT mutation with 1p19q codeletion) glioma tended to be oligodendroglioma present with much better clinical outcome compared to TERT mutation only group who is glioblastoma inclined (median overall survival 39 months VS 18 months). 28915860 2017
CUI: C0280475
Disease: Childhood Oligodendroglioma
Childhood Oligodendroglioma
0.400 Biomarker disease BEFREE Patient KK was a 68-yr-old female who was found to have a large, left-sided insular mass that was shown to be an oligodendroglioma WHO grade II, positive for codeletion 1p/19q and IDH1 mutant on biopsy. 31058967 2020