About Methylmalonic acidemia with homocystinuria, type cblC
Methylmalonic acidemia with homocystinuria, type cblC is a rare disease catalogued by Orphanet (ORPHA:79282). It is associated with the MMACHC 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 Methylmalonic acidemia with homocystinuria, type cblC trials.
Search ClinicalTrials.gov for "Methylmalonic acidemia with homocystinuria, type cblC" or filter by Orphanet code ORPHA:79282 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
Find recruiting Methylmalonic acidemia with homocystinuria, type cblC trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Methylmalonic acidemia with homocystinuria, type cblC. Updated daily.