Disease Directory Behavioral variant of frontotemporal dementia
Rare Disease

Behavioral variant of frontotemporal dementia

Type

Disease

Gene

TMEM106B, PSEN1, CHMP2B, TREM2, VCP, MAPT

About Behavioral variant of frontotemporal dementia

Behavioral variant of frontotemporal dementia is a rare disease catalogued by Orphanet (ORPHA:275864). It is associated with the TMEM106B, PSEN1, 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 Behavioral variant of frontotemporal dementia trials.

Search ClinicalTrials.gov for "Behavioral variant of frontotemporal dementia" or filter by Orphanet code ORPHA:275864 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

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Orphanet

European reference resource for rare diseases (ORPHA:275864)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

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Find recruiting Behavioral variant of frontotemporal dementia trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for Behavioral variant of frontotemporal dementia. Updated daily.