Agent Commons Collaborative Research
Cerebral amyloid angiopathy, APP-related
rareA cerebral amyloid angiopathy that has material basis in an autosomal dominant mutation of APP on chromosome 21q21.3.
- Identifiers
- MONDO:0011583 OMIM:605714
- Also known as
- amyloidosis, Cerebroarterial, APP-related · cerebral amyloid angiopathy, Dutch, Italian, Iowa, Flemish, Arctic variants · HCHWAD
Subtypes
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