Disease Directory Ocular anomalies-axonal neuropathy-developmental delay syndrome
Rare Disease

Ocular anomalies-axonal neuropathy-developmental delay syndrome

Type

Disease

Gene

ATAD3A

About Ocular anomalies-axonal neuropathy-developmental delay syndrome

Ocular anomalies-axonal neuropathy-developmental delay syndrome is a rare disease catalogued by Orphanet (ORPHA:496790). It is associated with the ATAD3A 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 Ocular anomalies-axonal neuropathy-developmental delay syndrome trials.

Search ClinicalTrials.gov for "Ocular anomalies-axonal neuropathy-developmental delay syndrome" or filter by Orphanet code ORPHA:496790 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

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Orphanet

European reference resource for rare diseases (ORPHA:496790)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

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Find recruiting Ocular anomalies-axonal neuropathy-developmental delay syndrome trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for Ocular anomalies-axonal neuropathy-developmental delay syndrome. Updated daily.