All diseases

OMIM ID
600795
OMIM term:
FRONTOTEMPORAL DEMENTIA, CHROMOSOME 3-LINKED; FTD3
Alternative terms:
DMT1; DEM
DEMENTIA, FAMILIAL NONSPECIFIC
(∗) Location:
3p11.2  
(†) Associated OMIM genes:
CHMP2B  
(‡) Associated MGI genes:

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