Human Gene Set: HP_FRONTOTEMPORAL_DEMENTIA


Standard name HP_FRONTOTEMPORAL_DEMENTIA
Systematic name M35668
Brief description Frontotemporal dementia
Full description or abstract A dementia associated with degeneration of the frontotemporal lobe and clinically associated with personality and behavioral changes such as disinhibition, apathy, and lack of insight. The hallmark feature of frontotemporal dementia is the presentation with focal syndromes such as progressive language dysfunction, or aphasia, or behavioral changes characteristic of frontal lobe disorders. [https://orcid.org/0000-0002-0736-9199, PMID:24966676]
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0002145
Related gene sets  
External links https://hpo.jax.org/app/browse/term/HP:0002145
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Source species Homo sapiens
Contributed by Human Phenotype Ontology Group (The Jackson Laboratory (JAX))
Source platform or
identifier namespace		 Human_NCBI_Gene_ID
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Version history 2026.1.Hs: Updated to HPO Release 2026-01-08.


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