Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0027831
Disease: Neurofibromatosis 1
Neurofibromatosis 1
0.040 GeneticVariation disease BEFREE Gliomas in people with NF1 show alterations in the RAS/MAPK pathway, generally in the absence of BRAF alterations (common to sporadic pilocytic astrocytomas) or IDH or histone H3 mutations (common to diffuse gliomas subsets). 30963251 2020
CUI: C0027831
Disease: Neurofibromatosis 1
Neurofibromatosis 1
0.040 GeneticVariation disease BEFREE None of the NF1 glioblastomas harbored isocitrate dehydrogenase 1 (IDH1) gene mutation, v-RAF murine sarcoma viral oncogene homolog B1 (BRAF) gene mutation, and telomerase reverse transcriptase (TERT) gene promoter mutation. 29138945 2018
CUI: C0027831
Disease: Neurofibromatosis 1
Neurofibromatosis 1
0.040 GeneticVariation disease BEFREE The present study suggests that adult cGBM differ from their supra-tentorial counterpart and constitute a heterogeneous group of IDH wild-type gliomas with at least two subgroups, one associated with H3K27M mutations and the other with neurofibromatosis type I. 29196927 2018
CUI: C0027831
Disease: Neurofibromatosis 1
Neurofibromatosis 1
0.040 AlteredExpression disease BEFREE Thus, optic nerve gliomas demonstrated molecular alterations typical of pilocytic astrocytomas, including the universal presence of either BRAF duplication or NF1 association and common mitogen-activated protein kinase pathway activation but very rare mutant IDH1 expression. 22892521 2012