Frontotemporal Dementia Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
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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4 genes/proteins associated with the disease Frontotemporal Dementia from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
MAPT microtubule-associated protein tau 2.88009
CHMP2B charged multivesicular body protein 2B 2.88009
PSEN1 presenilin 1 2.88009
GRN granulin 2.88009