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Summary Literature (0)
MIM:607485 - FRONTOTEMPORAL DEMENTIA 2; FTD2

Xenbase Genes: grn

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011842 - GRN-related frontotemporal lobar degeneration with Tdp43 inclusions
MONDO:0015059 - orbitosphenoid endochondral element
MONDO:0017276 - frontotemporal dementia

Disease Ontology (DO):
DOID:0060672 - Grn-related frontotemporal lobar degeneration with Tdp43 inclusions