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ADan amyloidosis
MONDO:0007297A cerebral amyloid angiopathy characterized by ataxia, intention tremor, psychosis and dementia that has material basis in an autosomal dominant mutation of ITM2B on chromosome 13q14.2.
Also known as: FDD, HOOE, Heredopathia Ophthalmootoencephalica, cerebellar ataxia, cataract, deafness, and dementia Or psychosis, cerebral amyloid angiopathy, ITM2B-related, type 2, familial Danish dementia, familial dementia, Danish type, ITM2B-related cerebral amyloid angiopathy 2
13 clinical trials for this condition and its sub-types, 0 tagged with ADan amyloidosis itself.
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