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

Glucose-6-phosphate dehydrogenase deficiency anemia   62403005

SNOMED CT code


SNOMED code62403005
nameGlucose-6-phosphate dehydrogenase deficiency anemia
statusactive
date introduced2002-01-31
fully specified name(s)Glucose-6-phosphate dehydrogenase deficiency anemia (disorder)
synonyms
  • Glucose-6-phosphate dehydrogenase deficiency anemia
  • G-6-PD deficiency anemia
  • Glucose-6-phosphate dehydrogenase deficiency
  • G6PD deficiency anemia
  • G-6-PD deficiency anaemia
  • G6PD deficiency anaemia
  • Glucose-6-phosphate dehydrogenase deficiency anaemia
attributes - group3
Has interpretationPresent   52101004
InterpretsHemolysis   404227002
attributes - group6
Due toDeficiency of glucose-6-phosphate dehydrogenase   124134002
attributes - group1
Has interpretationBelow reference range   281300000
InterpretsRed blood cell count   14089001
attributes - group4
OccurrenceCongenital   255399007
parents
children
  • G-6-PD class I variant anemia   22933009
  • G-6-PD class II variant anemia   34852006
  • G-6-PD class III variant anemia   24661004
  • G-6-PD class IV variant anemia   82003006
  • G-6-PD class V variant anemia   80963002
  • G-6-PD variant enzyme deficiency anemia   86859003
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
              Glucose-6-phosphate dehydrogenase deficiency anemia   62403005

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Genetic disease   782964007
        Hereditary disease   32895009
          Sex-linked hereditary disorder   82852009
            X-linked hereditary disease   128430005
              Glucose-6-phosphate dehydrogenase deficiency anemia   62403005

SNOMED CT Concept   138875005
  Clinical finding   404684003
    Disease   64572001
      Congenital disease   66091009
        Inborn error of metabolism   86095007
          Glucose-6-phosphate dehydrogenase deficiency anemia   62403005

ancestors
sorted most to least specific
cpt crosswalks

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