|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|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)|
|Downloads & Tools|
2 genes associated with the cerebral amyloid angiopathy phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.