ABetaA21G amyloidosis

MONDO:0017948

Hereditary cerebral hemorrhage with amyloidosis (HCHWA), Flemish type is a form of HCHWA characterized by an age of onset of 45 years of age, progressive Alzheimer's disease-like dementia and lobar intracerebral hemorrhage in some patients.

Also known as: ABeta amyloidosis, Flemish type, ABetaA21G-related amyloidosis, HCHWA, Flemish type, cerebral amyloid angiopathy, APP-related, Flemish variant, hereditary cerebral haemorrhage with amyloidosis, Flemish type, hereditary cerebral hemorrhage with amyloidosis, Flemish type

13 clinical trials for this condition and its sub-types, 0 tagged with ABetaA21G amyloidosis itself.

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Where it sits in the disease tree

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Part of

↑ Cerebral amyloid angiopathy, APP-related (1)

Including sub-types (13) Tagged with ABetaA21G amyloidosis (0)

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