middle age onset Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A type of adult onset with onset of symptoms at the age of 40 to 60 years. (Human Phenotype Ontology, HP_0003596)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0003596
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Genes

2 genes associated with the middle age onset phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
PSEN2 presenilin 2
SNCA synuclein, alpha (non A4 component of amyloid precursor)