HNSHA due to hexokinase deficiency   42484009

SNOMED CT code


SNOMED code42484009
nameHNSHA due to hexokinase deficiency
statusactive
date introduced2002-01-31
fully specified name(s)Hereditary nonspherocytic hemolytic anemia due to hexokinase deficiency (disorder)
synonyms
  • Hereditary nonspherocytic hemolytic anemia (HNSHA) due to hexokinase deficiency
  • Hereditary nonspherocytic haemolytic anaemia (HNSHA) due to hexokinase deficiency
  • Hereditary nonspherocytic hemolytic anemia due to hexokinase deficiency
  • Hereditary nonspherocytic haemolytic anaemia due to hexokinase deficiency
  • Hexokinase deficiency anaemia
  • HNSHA due to hexokinase deficiency
  • Hexokinase deficiency anemia
attributes - group3
Has interpretationPresent   52101004
InterpretsHemolysis   404227002
attributes - group6
Due toDeficiency of hexokinase   124297004
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 - group5
Finding siteErythrocyte   41898006
attributes - group4
OccurrenceCongenital   255399007
parents
  • Anemia due to enzyme deficiency   111577008
  • Autosomal hereditary disorder   1899006
  • Hemolytic anemia due to hexokinase deficiency   191177007
  • Erythrocyte enzyme deficiency   234401000
  • Hereditary nonspherocytic hemolytic anemia   301317008
  • Congenital anemia   63565007
  • Inborn error of metabolism   86095007
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 hexokinase deficiency   42484009

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Autosomal hereditary disorder   1899006
            HNSHA due to hexokinase deficiency   42484009

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
            Hemolytic anemia due to hexokinase deficiency   191177007
              HNSHA due to hexokinase deficiency   42484009

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 hexokinase deficiency   42484009

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 hexokinase deficiency   42484009

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Congenital anemia   63565007
          HNSHA due to hexokinase deficiency   42484009

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Inborn error of metabolism   86095007
          HNSHA due to hexokinase deficiency   42484009

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