Disease Directory Combined oxidative phosphorylation defect type 30
Rare Disease

Combined oxidative phosphorylation defect type 30

Type

Disease

Gene

TRMT10C

About Combined oxidative phosphorylation defect type 30

Combined oxidative phosphorylation defect type 30 is a rare disease catalogued by Orphanet (ORPHA:478042). It is associated with the TRMT10C 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 Combined oxidative phosphorylation defect type 30 trials.

Search ClinicalTrials.gov for "Combined oxidative phosphorylation defect type 30" or filter by Orphanet code ORPHA:478042 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:478042)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

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Find recruiting Combined oxidative phosphorylation defect type 30 trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for Combined oxidative phosphorylation defect type 30. Updated daily.