basal ganglia gliosis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description The presence of gliosis in the basal ganglia. (Human Phenotype Ontology, HP_0006999)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0006999
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Genes

3 genes associated with the basal ganglia gliosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
PRNP prion protein
SCO2 SCO2 cytochrome c oxidase assembly protein
VRK1 vaccinia related kinase 1