All diseases

OMIM ID
607485
OMIM term:
FRONTOTEMPORAL LOBAR DEGENERATION WITH TDP43 INCLUSIONS, GRN-RELATED
Alternative terms:
FTLD-TDP, GRN-RELATED
FRONTOTEMPORAL DEMENTIA WITH TDP43 INCLUSIONS, GRN-RELATED
FRONTOTEMPORAL LOBAR DEGENERATION WITH UBIQUITIN-POSITIVE INCLUSIONS; FTLDU
FRONTOTEMPORAL DEMENTIA, UBIQUITIN-POSITIVE; FTDU
DEMENTIA, HEREDITARY DYSPHASIC DISINHIBITION; HDDD APHASIA, PRIMARY PROGRESSIVE, INCLUDED; PPA, INCLUDED
(∗) Location:
17q21.31  
(†) Associated OMIM genes:
GRN  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/6ubli8q6