Pierson syndrome   723449004

SNOMED CT code


SNOMED code723449004
namePierson syndrome
statusactive
date introduced2017-07-31
fully specified name(s)Pierson syndrome (disorder)
synonyms
  • Pierson syndrome
  • Microcoria and congenital nephrosis syndrome
attributes - group1
Associated morphologyMorphologically abnormal structure   49755003
OccurrenceCongenital   255399007
Finding siteEye structure   81745001
Pathological processPathological developmental process   308490002
attributes - group2
Pathological processPathological developmental process   308490002
OccurrenceCongenital   255399007
Finding siteGlomerulus structure   68288006
attributes - group4
InterpretsAlbumin measurement   26758005
Has interpretationBelow reference range   281300000
attributes - group3
InterpretsUrine protein measurement   57378007
Has interpretationAbove reference range   281302008
parents
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Eye / vision finding   118235002
      Visual system disorder   128127008
        Congenital anomaly of visual system   127329003
          Congenital anomaly of eye   19416009
            Pierson syndrome   723449004

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
                Steroid-resistant nephrotic syndrome   236381000
                  Pierson syndrome   723449004

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Developmental disorder   5294002
        Developmental hereditary disorder   363070008
          Pierson syndrome   723449004

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Eye / vision finding   118235002
      Visual system disorder   128127008
        Hereditary disorder of the visual system   363343008
          Pierson syndrome   723449004

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Viscus structure finding   406123005
      Abdominal organ finding   249561001
        Kidney finding   249578005
          Kidney disease   90708001
            Hereditary nephropathy   367591000119105
              Pierson syndrome   723449004

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Autosomal hereditary disorder   1899006
            Autosomal recessive hereditary disorder   85995004
              Pierson syndrome   723449004

ancestors
sorted most to least specific
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