Cerebral Amyloid Angiopathy Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
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://ctdbase.org/detail.go?type=disease&acc=MESH:D016657
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Genes

2 genes/proteins associated with the disease Cerebral Amyloid Angiopathy from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
APP amyloid beta (A4) precursor protein 2.88009
APOE apolipoprotein E 2.88009