D58.2

Applicable To

• Abnormal hemoglobin NOS

• Congenital Heinz body anemia

• Hb-C disease

• Hb-D disease

• Hb-E disease

• Hemoglobinopathy NOS

• Unstable hemoglobin hemolytic disease

Approximate Synonyms

• Abnormal hgb, alpha variant

• Abnormal hgb, alpha variant homozygous

• Abnormal hgb, beta variant

• Abnormal hgb, delta variant

• Abnormal hgb, delta variant homozygous

• Abnormal hgb, gamma variant

• Abnormal hgb, unidentified variant

• Abnormal presence of hemoglobin, alpha variant

• Abnormal presence of hemoglobin, alpha variant, homozygous

• Abnormal presence of hemoglobin, beta variant

• Abnormal presence of hemoglobin, delta variant

• Abnormal presence of hemoglobin, delta variant, homozygous

• Abnormal presence of hemoglobin, gamma variant

• Abnormal presence of hemoglobin, unidentified variant

• Hemoglobin c disease

• Hemoglobin c trait

• Hemoglobin d disease

• Hemoglobin d trait

• Hemoglobin e disease

• Hemoglobin e trait

• Hemoglobinopathy

• Hemoglobinopathy, hereditary

• Hereditary hemoglobinopathy

Clinical Information

• A blood disorder characterized by the appearance of sickle-shaped red blood cells and anemia. This disorder is caused by a specific mutation in the beta-globin hbb gene, whereby a lysine is substituted for a glutamic acid at the sixth amino acid in the protein.

• A disease characterized by compensated hemolysis with a normal hemoglobin level or a mild to moderate anemia. There may be intermittent abdominal discomfort, splenomegaly, and slight jaundice.

• A group of inherited disorders characterized by structural alterations within the hemoglobin molecule.

• An inherited disorder characterized by structural alterations of a globin chain within the hemoglobin molecule.

• Group of inherited disorders characterized by structural alterations within the hemoglobin molecule.

• Hemoglobins characterized by structural alterations within the molecule. The alteration can be either absence, addition or substitution of one or more amino acids in the globin part of the molecule at selected positions in the polypeptide chains.

Details

• D58.2 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.

• The 2023 edition of ICD-10-CM D58.2 became effective on October 1, 2022.

• This is the American ICD-10-CM version of D58.2 – other international versions of ICD-10 D58.2 may differ.