optic glioma Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A glioma originating in the optic nerve or optic chiasm. (Human Phenotype Ontology, HP_0009734)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0009734
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3 genes associated with the optic glioma phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
NF1 neurofibromin 1
TSC1 tuberous sclerosis 1
TSC2 tuberous sclerosis 2