cerebral amyloid angiopathy Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An amyloidosis where amyloid protein progressively deposits in cerebral blood vessel walls with subsequent degenerative vascular changes that usually result in spontaneous cerebral hemorrhage, ischemic lesions and progressive dementia. (Human Disease Ontology, DOID_9246)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0011970
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Genes

2 genes associated with the cerebral amyloid angiopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
APP amyloid beta (A4) precursor protein
PSEN2 presenilin 2