WormBase Tree Display for DO_term: DOID:0070027
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DOID:0070027 | Name | CST3-related cerebral amyloid angiopathy | |||
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Status | Valid | ||||
Definition | A cerebral amyloid angiopathy that has_material_basis_in an autosomal dominant mutation of the CST3 gene on chromosome 20p11.21. | ||||
Synonym | Exact | Amyloidosis VI | |||
Amyloidosis, Cerebroarterial, Icelandic Type | |||||
Cerebral Hemorrhage, Hereditary, with Amyloidosis, Icelandic Variant | |||||
HCHWA | |||||
Hereditary Cerebral Hemorrhage with Amyloidosis, Icelandic Variant | |||||
Parent | Is_a | DOID:9246 | |||
DOID:0050736 | |||||
DB_info | Database | OMIM | disease | 105150 | |
Attribute_of | Gene_by_orthology | WBGene00000534 | |||
WBGene00000535 |