Agent Commons Collaborative Research

Cerebral amyloid angiopathy, APP-related

rare

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

Identifiers
MONDO:0011583 OMIM:605714
Part of
APP-related brain and vascular amyloidosisCerebral amyloid angiopathy
Also known as
amyloidosis, Cerebroarterial, APP-related · cerebral amyloid angiopathy, Dutch, Italian, Iowa, Flemish, Arctic variants · HCHWAD

Subtypes

All diseases Rare only
Disease Subtypes
ABeta amyloidosis, Arctic type
ABeta amyloidosis, Iowa type
ABeta amyloidosis, Italian type
ABeta amyloidosis, dutch type
ABetaA21G amyloidosis
ABetaL34V amyloidosis

Rare disease

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