Disease Directory Early-onset nuclear cataract
Rare Disease

Early-onset nuclear cataract

Type

Clinical subtype

Gene

WFS1, CRYAA, CRYAB, CRYBA1, CRYBB2, CRYBB3

About Early-onset nuclear cataract

Early-onset nuclear cataract is a rare disease catalogued by Orphanet (ORPHA:98991). It is associated with the WFS1, CRYAA, CRYAB 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 Early-onset nuclear cataract trials.

Search ClinicalTrials.gov for "Early-onset nuclear cataract" or filter by Orphanet code ORPHA:98991 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:98991)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

Search NORD ↗

Find recruiting Early-onset nuclear cataract trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for Early-onset nuclear cataract. Updated daily.