ORPHA:228337
CLN10 disease
Also called NCL10, Neuronal ceroid lipofuscinosis type 10
- Body system
- Inborn errors of metabolism
- Inheritance pattern
- Autosomal recessive
- Typical age of onset
- Adult, Antenatal, Infancy
- Estimated prevalence
- <1 / 1 000 000 (Worldwide)
- Rarity class
- <1 / 1 000 000
ORPHA:228337 is classified under "Inborn errors of metabolism" in the Orphanet nomenclature.