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

14 clinical trials for this condition and its sub-types, 0 tagged with Cerebral amyloid angiopathy, APP-related itself.

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Where it sits in the disease tree

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Part of

↑ Cerebral amyloid angiopathy (17) ↑ APP-related brain and vascular amyloidosis (5)

Sub-types of Cerebral amyloid angiopathy, APP-related

ABeta amyloidosis, dutch type 1 trial
ABeta amyloidosis, Arctic type 0 trials
ABeta amyloidosis, Iowa type 0 trials
ABeta amyloidosis, Italian type 0 trials
ABetaA21G amyloidosis 0 trials
ABetaL34V amyloidosis 0 trials

Including sub-types (14) Tagged with Cerebral amyloid angiopathy, APP-related (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.