ORPHA:308442
Vitamin B12-responsive methylmalonic acidemia, type cblDv2
Also called Vitamin B12-responsive methylmalonic aciduria, type cblDv2
- Body system
- Inborn errors of metabolism
- Inheritance pattern
- Autosomal recessive
- Typical age of onset
- Not documented in Orphadata
- Estimated prevalence
- Not documented in Orphadata
- Rarity class
- Not documented in Orphadata
ORPHA:308442 is classified under "Inborn errors of metabolism" in the Orphanet nomenclature.