Disease Directory Limited systemic sclerosis
Rare Disease

Limited systemic sclerosis

Type

Clinical subtype

Gene

HLA-DRB1

About Limited systemic sclerosis

Limited systemic sclerosis is a rare disease catalogued by Orphanet (ORPHA:220407). It is associated with the HLA-DRB1 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 Limited systemic sclerosis trials.

Search ClinicalTrials.gov for "Limited systemic sclerosis" or filter by Orphanet code ORPHA:220407 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:220407)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

Search NORD ↗

Find recruiting Limited systemic sclerosis trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for Limited systemic sclerosis. Updated daily.