ZFIN Human Disease: CST3-related cerebral amyloid angiopathy

OBO ID: DOID:0070027

Term Name:	CST3-related cerebral amyloid angiopathy		Search Ontology:
Synonyms:	Amyloidosis VI Amyloidosis, Cerebroarterial, Icelandic Type Cerebral Hemorrhage, Hereditary, with Amyloidosis Cerebral Hemorrhage, Hereditary, with Amyloidosis, Icelandic Variant HCHWA Hereditary Cerebral Hemorrhage with Amyloidosis Hereditary Cerebral Hemorrhage with Amyloidosis, Icelandic Variant
Definition:	A cerebral amyloid angiopathy that has_material_basis_in an autosomal dominant mutation of the CST3 gene on chromosome 20p11.21. https://www.ncbi.nlm.nih.gov/pubmed/2900981
References:	OMIM:105150
Ontology:	Human Disease ( DOID:0070027 )

Relationships

is a type of:	autosomal dominant disease cerebral amyloid angiopathy autosomal dominant disease cerebral amyloid angiopathy Show first 5 Terms

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Alliance (1)

GENES INVOLVED

Human Gene	Zebrafish Ortholog	OMIM Term	OMIM Phenotype ID
CST3	cst3	Cerebral amyloid angiopathy	105150

ZEBRAFISH MODELS No data available

PHENOTYPE No data available

CITATIONS: None