All diseases

OMIM ID
600274
OMIM term:
FRONTOTEMPORAL DEMENTIA; FTD
Alternative terms:
FRONTOTEMPORAL LOBAR DEGENERATION WITH TAU INCLUSIONS
FTLD WITH TAU INCLUSIONS
DEMENTIA, FRONTOTEMPORAL, WITH PARKINSONISM
FRONTOTEMPORAL DEMENTIA WITH PARKINSONISM
FRONTOTEMPORAL LOBE DEMENTIA; FLDEM
FTDP17
MULTIPLE SYSTEM TAUOPATHY WITH PRESENILE DEMENTIA; MSTD
DISINHIBITION-DEMENTIA-PARKINSONISM-AMYOTROPHY COMPLEX; DDPAC
WILHELMSEN-LYNCH DISEASE; WLD
FRONTOTEMPORAL DEMENTIA-AMYOTROPHIC LATERAL SCLEROSIS; FTD-ALS
PALLIDOPONTONIGRAL DEGENERATION; PPND PICK COMPLEX, INCLUDED
(∗) Location:
14q24.2   17q21.31  
(†) Associated OMIM genes:
MAPT   PSEN1  
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/chey1027