The ICD-10 code for Cholesteryl Ester Storage Disease is E75.5, while the ICD-9 code is 272.7. Cholesteryl Ester Storage Disease is a rare genetic disorder characterized by the accumulation of cholesteryl esters in various tissues and organs. It can lead to hepatomegaly, splenomegaly, and cardiovascular complications. Proper diagnosis and management are crucial for individuals with this condition.
Cholesteryl Ester Storage Disease (CESD), also known as lysosomal acid lipase deficiency, is a rare genetic disorder characterized by the impaired breakdown of cholesteryl esters and triglycerides. This results in the accumulation of these lipids within various tissues and organs, leading to a wide range of symptoms.
In terms of medical coding, the International Classification of Diseases, 10th Revision (ICD-10) provides a specific code for Cholesteryl Ester Storage Disease. The ICD-10 code for CESD is E75.7. This code falls under the broader category of "other lipid storage disorders" (E75), which encompasses various inherited metabolic disorders related to lipid metabolism.
In contrast, the International Classification of Diseases, 9th Revision (ICD-9) does not have a specific code for Cholesteryl Ester Storage Disease. However, under the ICD-9 system, physicians might utilize a more general code to describe the symptoms or manifestations associated with CESD. For instance, codes such as 272.7 (other disorders of lipoid metabolism) or 272.8 (other disorders of lipoprotein metabolism) could potentially be used to indicate the presence of CESD.
It is important to note that medical coding is crucial for accurate documentation, billing, and research purposes. These codes assist healthcare providers, insurers, and researchers in identifying and classifying various conditions, including rare diseases like Cholesteryl Ester Storage Disease.