ORPHA:35706
Glutaric acidemia type 3
Also called Glutaric aciduria type 3, Glutaryl-CoA oxidase deficiency
- Body system
- Inborn errors of metabolism
- Inheritance pattern
- Autosomal recessive
- Typical age of onset
- All ages
- Estimated prevalence
- Unknown (Worldwide)
- Rarity class
- Unknown
ORPHA:35706 is classified under "Inborn errors of metabolism" in the Orphanet nomenclature.
Common signs
- Abnormality of circulating enzyme level
- Sacral dimple
- Lethargy
- Global developmental delay
- Specific learning disability
- Failure to thrive