Disease Directory ABeta amyloidosis, Dutch type
Rare Disease

ABeta amyloidosis, Dutch type

Type

Clinical subtype

Gene

APP

About ABeta amyloidosis, Dutch type

ABeta amyloidosis, Dutch type is a rare disease catalogued by Orphanet (ORPHA:100006). It is associated with the APP gene. 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 ABeta amyloidosis, Dutch type trials.

Search ClinicalTrials.gov for "ABeta amyloidosis, Dutch type" or filter by Orphanet code ORPHA:100006 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:100006)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

Search NORD ↗

Find recruiting ABeta amyloidosis, Dutch type trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for ABeta amyloidosis, Dutch type. Updated daily.