frontotemporal dementia Gene Set

Dataset DISEASES Curated Gene-Disease Assocation Evidence Scores
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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Genes

2 genes involed in the disease frontotemporal dementia from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

Symbol Name
GRN granulin
MAPT microtubule-associated protein tau