ORPHA:79310
Vitamin B12-responsive methylmalonic acidemia type cblA
Also called Vitamin B12-responsive methylmalonic aciduria type cblA
- Body system
- Inborn errors of metabolism
- Inheritance pattern
- Autosomal recessive
- Typical age of onset
- Childhood
- Estimated prevalence
- <1 / 1 000 000 (Worldwide)
- Rarity class
- <1 / 1 000 000
ORPHA:79310 is classified under "Inborn errors of metabolism" in the Orphanet nomenclature.