The ICD-10 code for Thalassemia is D56, which falls under the category of "Other Hemoglobinopathies." Thalassemia is a genetic blood disorder that affects the production of hemoglobin. In ICD-9, Thalassemia is classified under code 282.49, which is categorized as "Other Hemoglobinopathies." Thalassemia is characterized by abnormal red blood cell production and can lead to anemia and other complications.
Thalassemia is a group of inherited blood disorders characterized by abnormal production of hemoglobin, the protein responsible for carrying oxygen in red blood cells. There are several types of thalassemia, including alpha-thalassemia and beta-thalassemia, each with different subtypes. To classify and code thalassemia diagnoses, medical professionals use the International Classification of Diseases (ICD) coding system.
The ICD-10 code for thalassemia varies depending on the specific type and subtype. For example, the ICD-10 code for beta-thalassemia major is D56.1. This code specifically identifies the severe form of beta-thalassemia, which requires regular blood transfusions for survival. On the other hand, alpha-thalassemia has different codes depending on the number of affected genes and severity.
In contrast, the previous version of the coding system, ICD-9, had a different set of codes for thalassemia. The ICD-9 code for beta-thalassemia major was 282.49, while alpha-thalassemia had various codes ranging from 282.41 to 282.43, depending on the number of affected genes.
These codes are essential for medical professionals, researchers, and healthcare systems to accurately document and track thalassemia cases. They enable better understanding of the prevalence, impact, and management of thalassemia, ultimately aiding in the development of effective treatment strategies and improved patient care.