All diseases

OMIM ID
117300
OMIM term:
CEREBRAL AMYLOID ANGIOPATHY, ITM2B-RELATED, 2
Alternative terms:
DEMENTIA, FAMILIAL DANISH; FDD
FAMILIAL DANISH DEMENTIA
CEREBELLAR ATAXIA, CATARACT, DEAFNESS, AND DEMENTIA OR PSYCHOSIS
HEREDOPATHIA OPHTHALMOOTOENCEPHALICA; HOOE
(∗) Location:
13q14.2  
(†) Associated OMIM genes:
ITM2B  
(‡) Associated MGI genes:
Itm2b  

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