ORPHA:699780
Juvenile CLN3 disease
Also called Juvenile neuronal ceroid lipofuscinosis type 3
- Body system
- Inborn errors of metabolism
- Inheritance pattern
- Autosomal recessive
- Typical age of onset
- Not documented in Orphadata
- Estimated prevalence
- Not documented in Orphadata
- Rarity class
- Not documented in Orphadata
ORPHA:699780 is classified under "Inborn errors of metabolism" in the Orphanet nomenclature.