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CLN5 disease

ORPHA:228360

Classification level: Subtype of disorder
  • Synonym(s): -
  • Prevalence: -
  • Inheritance: Autosomal recessive 
  • Age of onset: Childhood
  • ICD-10: E75.4
  • OMIM: 256731
  • UMLS: C1850442
  • MeSH: -
  • GARD: 1223
  • MedDRA: -

Summary

This disease is described under Late infantile neuronal ceroid lipofuscinosis

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The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.