About: cerebral amyloid angiopathy

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An Entity of Type : owl:Class, within Data Space : linkeddata.uriburner.com:28898 associated with source document(s)

Xref MGI. OMIM mapping confirmed by DO. [SN].

Attributes	Values
type	Class
subClassOf	inherited metabolic disorder amyloidosis nodeID://b50956399 nodeID://b50956400 nodeID://b50956401
label	cerebral amyloid angiopathy
comment	Xref MGI. OMIM mapping confirmed by DO. [SN].
described by	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id	DOID:9246
database_cross_reference	MESH:D028243 ORDO:85458 SNOMEDCT_US_2021_09_01:45639009 UMLS_CUI:C0268393 UMLS_CUI:C1510489 UMLS_CUI:C1527338 UMLS_CUI:C1956349
has_exact_synonym	Cerebral Hemorrhage, Hereditary, with Amyloidosis (en) Hereditary Cerebral Hemorrhage with Amyloidosis (en)
has_obo_namespace	disease_ontology
in_subset	DO_rare_slim
http://purl.obolib...g/obo/IAO_0000115	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.
is subClassOf of	CST3-related cerebral amyloid angiopathy APP-related cerebral amyloid angiopathy ITM2B-related cerebral amyloid angiopathy 1 ITM2B-related cerebral amyloid angiopathy 2
is topic of	Human Disease Ontology
is annotatedSource of	nodeID://b50956402

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