primary progressive aphasia Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description Primary progressive aphasia (PPA) is a neurodegenerative disorder, characterized by a primary dissolution of language, with relative sparing of other mental faculties for at least the first 2 years of illness. PPA is recognized as the language variant in the frontotemporal dementia (FTD; see this term) spectrum of disorders. PPA can be classified into 3 subtypes based on specific speech and language features: semantic dementia (SD), progressive non-fluent aphasia (PNFA) and logopenic progressive aphasia (lv-PPA) (see these terms). (Orphanet Rare Disease Ontology, Orphanet_95432)
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1 genes associated with the disease primary progressive aphasia in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
MAPT microtubule-associated protein tau