Congenital nephrotic syndrome   48796009

SNOMED CT code


SNOMED code48796009
nameCongenital nephrotic syndrome
statusactive
date introduced2002-01-31
fully specified name(s)Congenital nephrotic syndrome (disorder)
synonyms
  • Congenital nephrotic syndrome
  • Familial nephrotic syndrome
attributes - group1
Pathological processPathological developmental process   308490002
Associated morphologyMorphologically abnormal structure   49755003
OccurrenceCongenital   255399007
Finding siteGlomerulus structure   68288006
attributes - group3
InterpretsAlbumin measurement   26758005
Has interpretationBelow reference range   281300000
attributes - group2
InterpretsUrine protein measurement   57378007
Has interpretationAbove reference range   281302008
parents
children
  • Congenital nephrotic syndrome NOS   197602005  removed: 2010-01-31
  • Familial mesangial sclerosis   236383002
  • Finnish congenital nephrotic syndrome   197601003
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

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Viscus structure finding   406123005
      Abdominal organ finding   249561001
        Kidney finding   249578005
          Kidney disease   90708001
            Hereditary nephropathy   367591000119105
              Congenital nephrotic syndrome   48796009

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Viscus structure finding   406123005
      Abdominal organ finding   249561001
        Kidney finding   249578005
          Kidney disease   90708001
            Congenital anomaly of the kidney   44513007
              Congenital nephrotic syndrome   48796009

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Urine finding   301830001
      Finding of urine substance level   785672002
        Urine substance level above reference range   1217345006
          Proteinuria   29738008
            Protein-losing nephropathy   370494002
              Nephrotic syndrome   52254009
                Congenital nephrotic syndrome   48796009

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Autosomal hereditary disorder   1899006
            Autosomal recessive hereditary disorder   85995004
              Congenital nephrotic syndrome   48796009

ancestors
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cpt crosswalks

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