ADan amyloidosis

MONDO:0007297

A 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

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