HNSHA due to triosephosphate isomerase deficiency   44641000

SNOMED CT code


SNOMED code44641000
nameHNSHA due to triosephosphate isomerase deficiency
statusactive
date introduced2002-01-31
fully specified name(s)Hereditary nonspherocytic hemolytic anemia due to triosephosphate isomerase deficiency (disorder)
synonyms
  • Hereditary nonspherocytic haemolytic anaemia (HNSHA) due to triosephosphate isomerase deficiency
  • Hereditary nonspherocytic hemolytic anemia (HNSHA) due to triosephosphate isomerase deficiency
  • Hereditary nonspherocytic hemolytic anemia due to triosephosphate isomerase deficiency
  • Hereditary nonspherocytic haemolytic anaemia due to triosephosphate isomerase deficiency
  • Triosephosphate deficiency anaemia
  • HNSHA due to triosephosphate isomerase deficiency
  • Triosephosphate deficiency anemia
attributes - group3
Has interpretationPresent   52101004
InterpretsHemolysis   404227002
attributes - group5
Due toTriose phosphate isomerase deficiency   234405009
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
attributes - group4
Finding siteErythrocyte   41898006
parents
  • Anemia due to enzyme deficiency   111577008
  • Autosomal dominant hereditary disorder   11164009
  • Erythrocyte enzyme deficiency   234401000
  • Hereditary nonspherocytic hemolytic anemia   301317008
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
        Hemolytic disorder   128086004
          Hemolytic anemia   61261009
            Anemia due to enzyme deficiency   111577008
              HNSHA due to triosephosphate isomerase deficiency   44641000

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Autosomal hereditary disorder   1899006
            Autosomal dominant hereditary disorder   11164009
              HNSHA due to triosephosphate isomerase deficiency   44641000

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Disorder of body system   362965005
        Red blood cell disorder   38292009
          Erythrocyte enzyme deficiency   234401000
            HNSHA due to triosephosphate isomerase deficiency   44641000

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 nonspherocytic hemolytic anemia   301317008
                HNSHA due to triosephosphate isomerase deficiency   44641000

ancestors
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