All diseases

OMIM ID
176500
OMIM term:
CEREBRAL AMYLOID ANGIOPATHY, ITM2B-RELATED, 1
Alternative terms:
DEMENTIA, FAMILIAL BRITISH; FBD
PRESENILE DEMENTIA WITH SPASTIC ATAXIA
CEREBRAL AMYLOID ANGIOPATHY, BRITISH TYPE
(∗) Location:
13q14.2  
(†) Associated OMIM genes:
ITM2B  
(‡) Associated MGI genes:
Itm2b  

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