OnlineIMD

20.4    Neuronal ceroid lipofuscinoses (NCL)

  • Type
    Group
  • External link(s)
    • Orphanet
  • Disease group(s)
    • 20    Disorders of complex molecule degradation
  • Child entries
    • Congenital NCL
    • Infantile NCL
    • Late infantile NCL
    • Juvenile NCL
    • Adult NCL
    • Palmitoyl-protein thioesterase 1 deficiency
    • Tripeptidyl-peptidase 1 deficiency
    • CLN3 disease
    • CLN4 disease
    • CLN5 disease
    • CLN6 disease
    • CLN7 disease
    • CLN8 disease
    • Cathepsin D deficiency
    • Progranulin deficiency
    • ATP13A2 deficiency
    • Cathepsin F deficiency
    • CLN14 disease