frontotemporal cerebral atrophy Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Atrophy (wasting, decrease in size of cells or tissue) affecting the frontotemporal cerebrum. (Human Phenotype Ontology, HP_0006892)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0006892
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Genes

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

Symbol Name
PLA2G6 phospholipase A2, group VI (cytosolic, calcium-independent)