SNOMED CT Concept  138875005

Clinical finding  404684003

Finding of blood, lymphatics and immune system  299691001

Disorder of cellular component of blood  414022008

Anemia  271737000

Anemia due to intrinsic red cell abnormality  323666000

Anemia due to membrane defect  111575000

Hereditary spherocytosis   55995005

SNOMED CT code


SNOMED code55995005
nameHereditary spherocytosis
statusactive
date introduced2002-01-31
fully specified name(s)Hereditary spherocytosis (disorder)
synonyms
  • HS - Hereditary spherocytosis
  • Congenital spherocytic haemolytic anaemia
  • Hereditary spherocytosis
  • Familial spherocytosis
  • Minkowsky-Chauffard syndrome
  • Congenital spherocytosis
  • Familial acholuric jaundice
  • Congenital spherocytic hemolytic anemia
attributes - group3
Has interpretationPresent   52101004
InterpretsHemolysis   404227002
attributes - group5
Associated morphologySpherocyte   259682008
attributes - group4
Finding siteErythrocyte   41898006
attributes - group1
Has interpretationBelow reference range   281300000
InterpretsRed blood cell count   14089001
attributes - group2
Has interpretationBelow reference range   281300000
InterpretsMeasurement of total hemoglobin concentration   441689006
parents
  • Anemia due to membrane defect   111575000
  • Autosomal hereditary disorder   1899006
  • Erythrocyte membrane abnormality   234409003
  • Hereditary hemolytic anemia   38911009
children
  • Hereditary spherocytosis due to beta spectrin defect   69981004
  • Hereditary spherocytosis due to deficiency of protein 4.2   33905008
  • Hereditary spherocytosis due to spectrin deficiency   25266006
hierarchies
a selection of possible paths
SNOMED CT Concept   138875005
  Clinical finding   404684003
    Finding of blood, lymphatics and immune system   299691001
      Disorder of cellular component of blood   414022008
        Anemia   271737000
          Anemia due to intrinsic red cell abnormality   323666000
            Anemia due to membrane defect   111575000
              Hereditary spherocytosis   55995005

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Autosomal hereditary disorder   1899006
            Hereditary spherocytosis   55995005

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of body system   362965005
        Red blood cell disorder   38292009
          Erythrocyte membrane abnormality   234409003
            Hereditary spherocytosis   55995005

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of body system   362965005
        Red blood cell disorder   38292009
          Hereditary red blood cell disorder   414394009
            Hereditary hemolytic anemia   38911009
              Hereditary spherocytosis   55995005

ancestors
sorted most to least specific
cpt crosswalks

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