substantia nigra gliosis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description The presence of gliosis in the substantia nigra. (Human Phenotype Ontology, HP_0011960)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0011960
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Genes

2 genes associated with the substantia nigra gliosis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
LRRK2 leucine-rich repeat kinase 2
PARK2 parkin RBR E3 ubiquitin protein ligase