Disease Directory Vitamin B12-unresponsive methylmalonic acidemia type mut0
Metabolic

Vitamin B12-unresponsive methylmalonic acidemia type mut0

Type

Clinical subtype

Gene

MMUT

About Vitamin B12-unresponsive methylmalonic acidemia type mut0

Vitamin B12-unresponsive methylmalonic acidemia type mut0 is a rare disease catalogued by Orphanet (ORPHA:289916). It is associated with the MMUT 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 Vitamin B12-unresponsive methylmalonic acidemia type mut0 trials.

Search ClinicalTrials.gov for "Vitamin B12-unresponsive methylmalonic acidemia type mut0" or filter by Orphanet code ORPHA:289916 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:289916)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

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Find recruiting Vitamin B12-unresponsive methylmalonic acidemia type mut0 trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for Vitamin B12-unresponsive methylmalonic acidemia type mut0. Updated daily.