2017/18 ICD-10-CM Diagnosis Code D58.2

Other hemoglobinopathies

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
Type 1 Excludes Help
A type 1 excludes note is a pure excludes. It means "not coded here". A type 1 excludes note indicates that the code excluded should never be used at the same time as D58.2. A type 1 excludes note is for used for when two conditions cannot occur together, such as a congenital form versus an acquired form of the same condition.
  • familial polycythemia (
    ICD-10-CM Diagnosis Code D75.0

    Familial erythrocytosis

      2016 2017 2018 Billable/Specific Code
    Applicable To
    • Benign polycythemia
    • Familial polycythemia
    Type 1 Excludes
    • hereditary ovalocytosis (D58.1)
    D75.0
    )
  • Hb-M disease (
    ICD-10-CM Diagnosis Code D74.0

    Congenital methemoglobinemia

      2016 2017 2018 Billable/Specific Code
    Applicable To
    • Congenital NADH-methemoglobin reductase deficiency
    • Hemoglobin-M [Hb-M] disease
    • Methemoglobinemia, hereditary
    D74.0
    )
  • hemoglobin E-beta thalassemia (
    ICD-10-CM Diagnosis Code D56.5

    Hemoglobin E-beta thalassemia

      2016 2017 2018 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-)
    D56.5
    )
  • hereditary persistence of fetal hemoglobin [HPFH] (
    ICD-10-CM Diagnosis Code D56.4

    Hereditary persistence of fetal hemoglobin [HPFH]

      2016 2017 2018 Billable/Specific Code
    D56.4
    )
  • high-altitude polycythemia (
    ICD-10-CM Diagnosis Code D75.1

    Secondary polycythemia

      2016 2017 2018 Billable/Specific Code
    Applicable To
    • Acquired polycythemia
    • Emotional polycythemia
    • Erythrocytosis NOS
    • Hypoxemic polycythemia
    • Nephrogenous polycythemia
    • Polycythemia due to erythropoietin
    • Polycythemia due to fall in plasma volume
    • Polycythemia due to high altitude
    • Polycythemia due to stress
    • Polycythemia NOS
    • Relative polycythemia
    Type 1 Excludes
    • polycythemia neonatorum (P61.1)
    • polycythemia vera (D45)
    D75.1
    )
  • methemoglobinemia (
    ICD-10-CM Diagnosis Code D74
    • D74 Methemoglobinemia
      • D74.0 Congenital methemoglobinemia
      • D74.8 Other methemoglobinemias
      • D74.9 Methemoglobinemia, unspecified
    D74.-
    )
  • other hemoglobinopathies with thalassemia (
    ICD-10-CM Diagnosis Code D56.8

    Other thalassemias

      2016 2017 2018 Billable/Specific Code
    Applicable To
    • Dominant thalassemia
    • Hemoglobin C thalassemia
    • Mixed thalassemia
    • Thalassemia with other hemoglobinopathy
    Type 1 Excludes
    • hemoglobin C disease (D58.2)
    • hemoglobin E disease (D58.2)
    • other hemoglobinopathies (D58.2)
    • sickle-cell anemia (D57.-)
    • sickle-cell thalassemia (D57.4)
    D56.8
    )
The following code(s) above D58.2 contain annotation back-references
Annotation Back-References
In this context, annotation back-references refer to codes that contain:
  • Applicable To annotations, or
  • Code Also annotations, or
  • Code First annotations, or
  • Excludes1 annotations, or
  • Excludes2 annotations, or
  • Includes annotations, or
  • Note annotations, or
  • Use Additional annotations
that may be applicable to D58.2:
  • D50-D89
    2018 ICD-10-CM Range D50-D89

    Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism

    Type 2 Excludes
    • autoimmune disease (systemic) NOS (M35.9)
    • certain conditions originating in the perinatal period (P00-P96)
    • complications of pregnancy, childbirth and the puerperium (O00-O9A)
    • congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
    • endocrine, nutritional and metabolic diseases (E00-E88)
    • human immunodeficiency virus [HIV] disease (B20)
    • injury, poisoning and certain other consequences of external causes (S00-T88)
    • neoplasms (C00-D49)
    • symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)
    Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism
  • D58
    ICD-10-CM Diagnosis Code D58

    Other hereditary hemolytic anemias

      2016 2017 2018 Non-Billable/Non-Specific Code
    Type 1 Excludes
    • hemolytic anemia of the newborn (P55.-)
    Other hereditary hemolytic anemias
Approximate Synonyms Clinical Information ICD-10-CM D58.2 is grouped within Diagnostic Related Group(s) (MS-DRG v35.0):

Convert D58.2 to ICD-9-CM

Code History
Code annotations containing back-references to D58.2:

Diagnosis Index entries containing back-references to D58.2:

ICD-10-CM Codes Adjacent To D58.2
D57.419 …… unspecified
D57.8 Other sickle-cell disorders
D57.80 …… without crisis
D57.81 Other sickle-cell disorders with crisis
D57.811 Other sickle-cell disorders with acute chest syndrome
D57.812 Other sickle-cell disorders with splenic sequestration
D57.819 …… unspecified
D58 Other hereditary hemolytic anemias
D58.0 Hereditary spherocytosis
D58.1 Hereditary elliptocytosis
D58.2 Other hemoglobinopathies
D58.8 Other specified hereditary hemolytic anemias
D58.9 Hereditary hemolytic anemia, unspecified
D59 Acquired hemolytic anemia
D59.0 Drug-induced autoimmune hemolytic anemia
D59.1 Other autoimmune hemolytic anemias
D59.2 Drug-induced nonautoimmune hemolytic anemia
D59.3 Hemolytic-uremic syndrome
D59.4 Other nonautoimmune hemolytic anemias
D59.5 Paroxysmal nocturnal hemoglobinuria [Marchiafava-Micheli]
D59.6 Hemoglobinuria due to hemolysis from other external causes

Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.