|Dataset||HPO Gene-Disease Associations|
|Category||disease or phenotype associations|
|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)|
|Downloads & Tools|
7 genes associated with the frontotemporal dementia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.