ORPHA:216

Neuronal ceroid lipofuscinosis

Also called CLN disease, NCL, NCL disease

Body system

Inborn errors of metabolism

Inheritance pattern

Autosomal dominant, Autosomal recessive

Typical age of onset

All ages

Estimated prevalence

Unknown (Worldwide)

Rarity class

Unknown

ORPHA:216 is classified under "Inborn errors of metabolism" in the Orphanet nomenclature.