Disease #00002

Official abbreviation FTD
Name Frontotemporal dementia
OMIM ID -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 11 genes APP, C9orf72, CHMP2B, FUS, GRN, MAPT, PSEN1, PSEN2, TARDBP, TBK1, VCP
Associated tissues -
Disease features -
Remarks -

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