WormBase Tree Display for DO_term: DOID:0070028
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DOID:0070028 | Name | APP-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 APP on chromosome 21q21.3. | ||||
Synonym | Exact | Amyloidosis, Cerebroarterial, App-Related | |||
Amyloidosis, Hereditary, With Cerebral Hemorrhage, Dutch Variant | |||||
Cerebral Amyloid Angiopathy, App-Related, Arctic Variant | |||||
Cerebral Amyloid Angiopathy, App-Related, Dutch Variant | |||||
Cerebral Amyloid Angiopathy, App-Related, Flemish Variant | |||||
Cerebral Amyloid Angiopathy, App-Related, Iowa Variant | |||||
Cerebral Amyloid Angiopathy, App-Related, Italian Variant | |||||
HCHWAD | |||||
Parent | Is_a | DOID:9246 | |||
DOID:0050736 | |||||
DB_info | Database | OMIM | disease | 605714 | |
Attribute_of | Gene_by_orthology | WBGene00000149 |