Disease Directory Semantic dementia
Rare Disease

Semantic dementia

Type

Disease

Gene

PSEN1, TMEM106B, CHMP2B, TREM2, MAPT, GRN

About Semantic dementia

Semantic dementia is a rare disease catalogued by Orphanet (ORPHA:100069). It is associated with the PSEN1, TMEM106B, CHMP2B genes. Search below for active recruiting clinical trials from ClinicalTrials.gov, or visit the Orphanet expert page for specialist centres, natural history studies, and patient registries.

Clinical Trial Eligibility Tips

What to know before applying to Semantic dementia trials.

Search ClinicalTrials.gov for "Semantic dementia" or filter by Orphanet code ORPHA:100069 to find disease-specific studies.

Ask your specialist to refer you to a Centre of Expertise — Orphanet lists all accredited centres for this condition worldwide.

Natural history studies and patient registries often enrol before drug trials open — contact the Orphanet patient community first.

Patient Resources

Patient Organization

Orphanet

Visit website ↗

Orphanet

European reference resource for rare diseases (ORPHA:100069)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

Search NORD ↗

Find recruiting Semantic dementia trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for Semantic dementia. Updated daily.