has material basis in germline mutation in ITM2B cerebral amyloid angiopathy ADan amyloidosis https://www.malacards.org/card/cerebral_amyloid_angiopathy_itm2b_related_2 Orphanet:97346 icd11.foundation:2086401830 FDD cerebral amyloid angiopathy, ITM2B-related, type 2 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. GARD:0009169 dementia, familial Danish familial Danish dementia HOOE cerebral amyloid angiopathy, ITM2B-RELATED, 2 cerebellar ataxia, cataract, deafness, and dementia or psychosis cerebellar ataxia, cataract, deafness, and dementia Or psychosis Heredopathia Ophthalmootoencephalica MESH:C538209 DOID:0070030 MONDO:0007297 UMLS:C1861735 familial dementia, Danish type ITM2B-related cerebral amyloid angiopathy 2 icd11.foundation:54507082 MEDGEN:396208 OMIM:117300 ITM2B amyloidosis