Mondo Disease Ontology - cerebral amyloid angiopathy - Classes | NCBO BioPortal

Mondo Disease Ontology

Last uploaded: February 4, 2025

Id	http://purl.obolibrary.org/obo/MONDO_0005620 http://purl.obolibrary.org/obo/MONDO_0005620
Preferred Name	cerebral amyloid angiopathy
Definitions	Hereditary cerebral hemorrhage with amyloidosis (HCHWA) describes a group of rare familial central nervous system disorders characterized by amyloid deposition in the cerebral blood vessels leading to hemorrhagic and non-hemorrhagic strokes, focal neurological deficits, and progressive cognitive decline eventually leading to dementia.
Synonyms	CAA, familial cerebral amyloid angiopathy, familial cerebral amyloid angiopathy, genetic HCHWA hereditary cerebral hemorrhage with amyloidosis - Dutch type dutch hereditary cerebral amyloid angiopathy hereditary cerebral haemorrhage with amyloidosis - Dutch type
Type	http://www.w3.org/2002/07/owl#Class

definition	Hereditary cerebral hemorrhage with amyloidosis (HCHWA) describes a group of rare familial central nervous system disorders characterized by amyloid deposition in the cerebral blood vessels leading to hemorrhagic and non-hemorrhagic strokes, focal neurological deficits, and progressive cognitive decline eventually leading to dementia.
label	cerebral amyloid angiopathy
prefLabel	cerebral amyloid angiopathy
database_cross_reference	Orphanet:85458 GARD:10266 ICD9:277.39 MESH:D016657 EFO:0006790 SCTID:230724001 MEDGEN:267610 ICD10CM:I68.0 ICD10EXP:I68.0* ICD10EXP:E85.4+ NCIT:C84625 DOID:9246 UMLS:C1510489 See more See less
notation	MONDO:0005620
in_subset	http://purl.obolibrary.org/obo/mondo/mondo-simple#otar http://purl.obolibrary.org/obo/mondo/mondo-simple#orphanet_rare http://purl.obolibrary.org/obo/mondo/mondo-simple#rare http://purl.obolibrary.org/obo/mondo/mondo-simple#ordo_disorder http://purl.obolibrary.org/obo/mondo/mondo-simple#gard_rare http://purl.obolibrary.org/obo/mondo/mondo-simple#nord_rare See more See less
has_related_synonym	CAA, familial cerebral amyloid angiopathy, familial cerebral amyloid angiopathy, genetic
id	MONDO:0005620
skos_exactMatch	http://purl.obolibrary.org/obo/NCIT_C84625 http://identifiers.org/snomedct/230724001 http://purl.obolibrary.org/obo/EFO_0006790 http://purl.obolibrary.org/obo/DOID_9246 http://purl.bioontology.org/ontology/ICD10CM/I68.0 http://identifiers.org/medgen/267610 http://identifiers.org/mesh/D016657 http://purl.obolibrary.org/obo/Orphanet_85458 http://linkedlifedata.com/resource/umls/id/C1510489 See more See less
subClassOf	http://purl.obolibrary.org/obo/MONDO_0018634 http://purl.obolibrary.org/obo/MONDO_0011057 http://purl.obolibrary.org/obo/MONDO_0100545
type	http://www.w3.org/2002/07/owl#Class
has_exact_synonym	HCHWA hereditary cerebral hemorrhage with amyloidosis - Dutch type dutch hereditary cerebral amyloid angiopathy hereditary cerebral haemorrhage with amyloidosis - Dutch type
treeView	http://purl.obolibrary.org/obo/MONDO_0018634 http://purl.obolibrary.org/obo/MONDO_0011057 http://purl.obolibrary.org/obo/MONDO_0100545

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