Infantile neuronal ceroid lipofuscinosis   58258004

SNOMED CT code


SNOMED code58258004
nameInfantile neuronal ceroid lipofuscinosis
statusactive
date introduced2002-01-31
fully specified name(s)Infantile neuronal ceroid lipofuscinosis (disorder)
synonyms
  • Hagberg-Santavouri type neuronal ceroid lipofuscinosis
  • Neuronal ceroid lipofuscinosis infantile Finnish type
  • Polyunsaturated fatty acid lipidosis
  • Haltia-Santavouri type neuronal ceroid lipofuscinosis
  • Infantile neuronal ceroid lipofuscinosis
  • Hagberg-Santavuori disease
  • Santavuori disease
  • Neuronal ceroid lipofuscinosis, infantile Finnish type
  • Polyunsaturated acid lipidosis
attributes - group1
Associated morphologyDegenerative abnormality   107669003
attributes - group2
OccurrenceCongenital   255399007
attributes - group3
Finding siteNervous system structure   25087005
parentsNeuronal ceroid lipofuscinosis   42012007
children
  • Late-infantile neuronal ceroid lipofuscinosis   14637005
  • Neuronal ceroid lipofuscinosis type 6A   1296784002
  • Progressive myoclonic epilepsy type 3   783064000
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Degenerative disorder   362975008
        Neuronal ceroid lipofuscinosis   42012007
          Infantile neuronal ceroid lipofuscinosis   58258004

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