frontotemporal dementia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A basal ganglia disease characterized by progressive neuronal loss predominantly involving the frontal and/or temporal lobes of the brain resulting in a gradual and progressive decline in behavior or language. (Human Disease Ontology, DOID_9255)
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7 genes associated with the frontotemporal dementia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
C9ORF72 chromosome 9 open reading frame 72
CHMP2B charged multivesicular body protein 2B
GRN granulin
MAPT microtubule-associated protein tau
PSEN1 presenilin 1
UBQLN2 ubiquilin 2
VCP valosin containing protein