ORPHA:353308

Pyruvate carboxylase deficiency, infantile type

Also called Pyruvate carboxylase deficiency type A

Body system

Inborn errors of metabolism

Inheritance pattern

Autosomal recessive

Typical age of onset

Infancy

Estimated prevalence

Unknown (Worldwide)

Rarity class

Unknown

ORPHA:353308 is classified under "Inborn errors of metabolism" in the Orphanet nomenclature.