Index Terms Starting With 'H' (Hemoglobin)

  • Hemoglobin - see also condition

    • abnormal (disease) - see Disease, hemoglobin
    • AS genotype D57.3
      ICD-10-CM Diagnosis Code D57.3

      Sickle-cell trait

        2016 2017 2018 2019 2020 2021 Billable/Specific Code
      Applicable To
      • Hb-S trait
      • Heterozygous hemoglobin S
    • Constant Spring D58.2
      ICD-10-CM Diagnosis Code D58.2

      Other hemoglobinopathies

        2016 2017 2018 2019 2020 2021 Billable/Specific Code
      Applicable To
      • Abnormal hemoglobin NOS
      • Congenital Heinz body anemia
      • Hb-C disease
      • Hb-D disease
      • Hb-E disease
      • Hemoglobinopathy NOS
      • Unstable hemoglobin hemolytic disease
      Type 1 Excludes
      • familial polycythemia (D75.0)
      • Hb-M disease (D74.0)
      • hemoglobin E-beta thalassemia (D56.5)
      • hereditary persistence of fetal hemoglobin [HPFH] (D56.4)
      • high-altitude polycythemia (D75.1)
      • methemoglobinemia (D74.-)
      • other hemoglobinopathies with thalassemia (D56.8)
    • E-beta thalassemia D56.5
      ICD-10-CM Diagnosis Code D56.5

      Hemoglobin E-beta thalassemia

        2016 2017 2018 2019 2020 2021 Billable/Specific Code
      Type 1 Excludes
      • beta thalassemia (D56.1)
      • beta thalassemia minor (D56.3)
      • beta thalassemia trait (D56.3)
      • delta-beta thalassemia (D56.2)
      • delta-beta thalassemia trait (D56.3)
      • hemoglobin E disease (D58.2)
      • other hemoglobinopathies (D58.2)
      • sickle-cell beta thalassemia (D57.4-)
    • fetal, hereditary persistence D56.4
      (HPFH)
      ICD-10-CM Diagnosis Code D56.4

      Hereditary persistence of fetal hemoglobin [HPFH]

        2016 2017 2018 2019 2020 2021 Billable/Specific Code
    • H Constant Spring D56.0
      ICD-10-CM Diagnosis Code D56.0

      Alpha thalassemia

        2016 2017 2018 2019 2020 2021 Billable/Specific Code
      Applicable To
      • Alpha thalassemia major
      • Hemoglobin H Constant Spring
      • Hemoglobin H disease
      • Hydrops fetalis due to alpha thalassemia
      • Severe alpha thalassemia
      • Triple gene defect alpha thalassemia
      Type 1 Excludes
      • alpha thalassemia trait or minor (D56.3)
      • asymptomatic alpha thalassemia (D56.3)
      • hydrops fetalis due to isoimmunization (P56.0)
      • hydrops fetalis not due to immune hemolysis (P83.2)
      Use Additional
      • code, if applicable, for hydrops fetalis due to alpha thalassemia (P56.99)
    • low NOS D64.9
      ICD-10-CM Diagnosis Code D64.9

      Anemia, unspecified

        2016 2017 2018 2019 2020 2021 Billable/Specific Code
    • S D57.3
      (Hb S)
      ICD-10-CM Diagnosis Code D57.3

      Sickle-cell trait

        2016 2017 2018 2019 2020 2021 Billable/Specific Code
      Applicable To
      • Hb-S trait
      • Heterozygous hemoglobin S