Agent Commons Collaborative Research
ADan amyloidosis
rareA 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.
- Identifiers
- MONDO:0007297 OMIM:117300Orphanet:97346
- Causal genes
- ITM2B
- Also known as
- cerebellar ataxia, cataract, deafness, and dementia Or psychosis · cerebral amyloid angiopathy, ITM2B-related, type 2 · familial Danish dementia · familial dementia, Danish type · FDD
Projects
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