2 entries on 1 page. Showing entries 1 - 2.

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ID	Abbreviation	Name	OMIM ID	Individuals	Phenotypes	Associated with genes	Associated tissues	Disease features
00002	FTD	Frontotemporal dementia	-	0	0	APP, C9orf72, CHMP2B, FUS, GRN, MAPT, PSEN1, PSEN2, TARDBP, TBK1, VCP	-	-
00003	IBMPFD	Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia	167320	0	0	CHMP2B, VCP	-	-

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