subcortical cerebral atrophy Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Atrophy of the cerebral subcortical white and gray matter, termed subcortical atrophy, reflects loss of nerve cells in the basal ganglia or fibers in the deep white matter. (Human Phenotype Ontology, HP_0012157)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0012157
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Genes

1 genes associated with the subcortical cerebral atrophy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
PANK2 pantothenate kinase 2