kodex

Kodex

D58.2

Other hemoglobinopathies

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Hierarchy

  • D50-D89 Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism (D50-D89)
    • D55-D59 Hemolytic anemias (D55-D59)
      • 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

Inclusion Terms

D58.2

  • Abnormal hemoglobin NOS
  • Congenital Heinz body anemia
  • Hb-C disease
  • Hb-D disease
  • Hb-E disease
  • Hemoglobinopathy NOS
  • Unstable hemoglobin hemolytic disease

Excludes 1

D58.2

  • familial polycythemia (D75.0)
    • D75.0 Familial erythrocytosis
  • Hb-M disease (D74.0)
    • D74.0 Congenital methemoglobinemia
  • D56.5 Hemoglobin E-beta thalassemia
  • D56.4 Hereditary persistence of fetal hemoglobin [HPFH]
  • high-altitude polycythemia (D75.1)
    • D75.1 Secondary polycythemia
  • D74 Methemoglobinemia
  • other hemoglobinopathies with thalassemia (D56.8)
    • D56.8 Other thalassemias

D58

  • hemolytic anemia of the newborn (P55.-)
    • P55 Hemolytic disease of newborn

Excludes 2

D50-D89

  • autoimmune disease (systemic) NOS (M35.9)
    • M35.9 Systemic involvement of connective tissue, unspecified
  • P00-P96 Certain conditions originating in the perinatal period (P00-P96)
  • complications of pregnancy, childbirth and the puerperium (O00-O9A)
    • O00-O9A Pregnancy, childbirth and the puerperium (O00-O9A)
  • Q00-Q99 Congenital malformations, deformations and chromosomal abnormalities (Q00-Q99)
  • endocrine, nutritional and metabolic diseases (E00-E88)
  • B20 Human immunodeficiency virus [HIV] disease
  • S00-T88 Injury, poisoning and certain other consequences of external causes (S00-T88)
  • C00-D49 Neoplasms (C00-D49)
  • symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)