Disease Directory Nance-Horan syndrome
Rare Disease

Nance-Horan syndrome

Type

Malformation syndrome

Gene

NHS

About Nance-Horan syndrome

Nance-Horan syndrome is a rare disease catalogued by Orphanet (ORPHA:627). It is associated with the NHS 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 Nance-Horan syndrome trials.

Search ClinicalTrials.gov for "Nance-Horan syndrome" or filter by Orphanet code ORPHA:627 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:627)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

Search NORD ↗

Find recruiting Nance-Horan syndrome trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for Nance-Horan syndrome. Updated daily.