cerebral amyloid angiopathy Gene Set

Dataset OMIM 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://www.omim.org/entry/105150
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Genes

1 genes associated with the cerebral amyloid angiopathy phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
CST3 cystatin C