Cerebral amyloid angiopathy, APP-related

MONDO:0011583

A cerebral amyloid angiopathy that has material basis in an autosomal dominant mutation of APP on chromosome 21q21.3.

Also known as: HCHWAD, amyloidosis, Cerebroarterial, APP-related, cerebral amyloid angiopathy, APP-related, cerebral amyloid angiopathy, Dutch, Italian, Iowa, Flemish, Arctic variants, APP-related cerebral amyloid angiopathy, amyloidosis, hereditary, with cerebral hemorrhage, Dutch variant, cerebral amyloid angiopathy, APP-related, Arctic variant, cerebral amyloid angiopathy, APP-related, Dutch variant

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