About: ITM2B-related cerebral amyloid angiopathy 1

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

Attributes	Values
type	Class
subClassOf	autosomal dominant disease cerebral amyloid angiopathy nodeID://b50939635
label	ITM2B-related cerebral amyloid angiopathy 1
described by	https://demo.openlinksw.com/about/id/entity/http/purl.obolibrary.org/obo/doid.owl
id	DOID:0070029
database_cross_reference	GARD:8344 OMIM:176500
has_exact_synonym	Cerebral Amyloid Angiopathy, British Type (en) FBD (en) Familial British Dementia (en) Presenile Dementia with Spastic Ataxia (en)
has_obo_namespace	disease_ontology
http://purl.obolib...g/obo/IAO_0000115	A cerebral amyloid angiopathy characterized by onset in the 4th to 6th decade of life, progressive mental deterioration, spasticity, muscular rigidity but no tremors, spontaneous movements or sensory changes that has_material_basis_in an autosomal dominant mutation of ITM2B on chromosome 13q14.2.
is topic of	Human Disease Ontology
is annotatedSource of	nodeID://b50939636

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