Orphanet: CLN2 disease
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CLN2 disease

ORPHA:228349

Classification level: Subtype of disorder
  • Synonym(s):
    • Classic late infantile NCL
    • Classic late infantile neuronal ceroid lipofuscinosis
  • Prevalence: -
  • Inheritance: Autosomal recessive 
  • Age of onset: Childhood
  • ICD-10: E75.4
  • OMIM: 204500
  • UMLS: C1876161
  • MeSH: -
  • GARD: 3045
  • MedDRA: -

Summary

This disease is described under Neuronal ceroid lipofuscinosis

  A summary on this disease is available in

Detailed information

Guidelines

Disease review articles

ERN : produced/endorsed by ERN(s)
FSMR : produced/endorsed by FSMR(s)

Additional information

Further information on this disease

Patient-centred resources for this disease

Research activities on this disease

Specialised Social Services

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