ORPHA:79189
Peroxisome biogenesis disorder
Also called PBD-ZSD, Peroxisome biogenesis disorder spectrum, Peroxisome biogenesis disorder-Zellweger spectrum disorder
- Body system
- Inborn errors of metabolism
- Inheritance pattern
- Autosomal recessive
- Typical age of onset
- Infancy, Neonatal
- Estimated prevalence
- 1-9 / 100 000 (United States)
- Rarity class
- 1-9 / 100 000
ORPHA:79189 is classified under "Inborn errors of metabolism" in the Orphanet nomenclature.