ORPHA:228343
CLN4 disease
Also called NCL4, Neuronal ceroid lipofuscinosis type 4
- Body system
- Inborn errors of metabolism
- Inheritance pattern
- Not documented in Orphadata
- Typical age of onset
- Adult
- Estimated prevalence
- <1 / 1 000 000 (Worldwide)
- Rarity class
- <1 / 1 000 000
ORPHA:228343 is classified under "Inborn errors of metabolism" in the Orphanet nomenclature.