Cerebral amyloid angiopathy, APP-related
MONDO:0011583A 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
15 clinical trials for this condition and its sub-types.
Follow this condition — get notified about new trials