Disease Directory Acrodermatitis enteropathica
Rare Disease

Acrodermatitis enteropathica

Type

Disease

Gene

SLC39A4

About Acrodermatitis enteropathica

Acrodermatitis enteropathica is a rare disease catalogued by Orphanet (ORPHA:37). It is associated with the SLC39A4 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 Acrodermatitis enteropathica trials.

Search ClinicalTrials.gov for "Acrodermatitis enteropathica" or filter by Orphanet code ORPHA:37 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:37)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

Search NORD ↗

Find recruiting Acrodermatitis enteropathica trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for Acrodermatitis enteropathica. Updated daily.