Disease Directory White sponge nevus
Rare Disease

White sponge nevus

Type

Disease

Gene

KRT4, KRT13

About White sponge nevus

White sponge nevus is a rare disease catalogued by Orphanet (ORPHA:171723). It is associated with the KRT4, KRT13 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 White sponge nevus trials.

Search ClinicalTrials.gov for "White sponge nevus" or filter by Orphanet code ORPHA:171723 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:171723)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

Search NORD ↗

Find recruiting White sponge nevus trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for White sponge nevus. Updated daily.