SNOMED CT Concept  138875005

Clinical finding  404684003

Disease  64572001

Developmental disorder  5294002

Developmental hereditary disorder  363070008

Congenital nephrotic syndrome  48796009

Finnish congenital nephrotic syndrome   197601003

SNOMED CT code


SNOMED code197601003
nameFinnish congenital nephrotic syndrome
statusactive
date introduced2002-01-31
fully specified name(s)Finnish congenital nephrotic syndrome (disorder)
synonyms
  • Finnish congenital nephrotic syndrome
  • CNF - Finnish congenital nephrotic syndrome
  • Congenital Finnish nephrosis
attributes - group1
Associated morphologyMorphologically abnormal structure   49755003
OccurrenceCongenital   255399007
Pathological processPathological developmental process   308490002
Finding siteGlomerulus structure   68288006
attributes - group2
Has interpretationBelow reference range   281300000
InterpretsAlbumin measurement   26758005
attributes - group3
InterpretsUrine protein measurement   57378007
Has interpretationAbove reference range   281302008
parentsCongenital nephrotic syndrome   48796009
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Developmental hereditary disorder   363070008
          Congenital nephrotic syndrome   48796009
            Finnish congenital nephrotic syndrome   197601003

ancestors
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