Disease Directory Total early-onset cataract
Rare Disease

Total early-onset cataract

Type

Clinical subtype

Gene

CRYAA, CRYBB2, GJA8, HSF4, MIP, NHS

About Total early-onset cataract

Total early-onset cataract is a rare disease catalogued by Orphanet (ORPHA:98994). It is associated with the CRYAA, CRYBB2, GJA8 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 Total early-onset cataract trials.

Search ClinicalTrials.gov for "Total early-onset cataract" or filter by Orphanet code ORPHA:98994 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:98994)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

Search NORD ↗

Find recruiting Total early-onset cataract trials

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