Arginase Deficiency/Argininemia is a rare genetic disorder that affects the urea cycle, leading to the accumulation of arginine in the blood. The ICD-10 code for this condition is E72.21. In the previous ICD-9 coding system, it was classified under 270.6. Arginase Deficiency/Argininemia can cause symptoms like intellectual disability, developmental delay, and seizures. Early diagnosis and management are crucial to prevent complications and improve outcomes.
Arginase Deficiency, also known as Argininemia, is a rare genetic disorder that affects the urea cycle, which is responsible for removing ammonia from the body. This condition is caused by a mutation in the ARG1 gene, leading to a deficiency of the enzyme arginase. As a result, the body is unable to break down the amino acid arginine properly.
In the International Classification of Diseases, Tenth Revision (ICD-10), Arginase Deficiency/Argininemia is classified under the code E72.22. This code falls under the broader category of "Disorders of urea cycle metabolism" (E72.2). It specifically denotes the deficiency of arginase enzyme and its impact on arginine metabolism.
On the other hand, in the previous revision, the Ninth Revision (ICD-9), Arginase Deficiency/Argininemia is represented by the code 270.6. This code falls under the category of "Other disorders of amino-acid metabolism" (270), which encompasses various genetic disorders affecting amino acid metabolism.
It is important to note that ICD-10 provides a more detailed and specific classification system compared to ICD-9. The transition from ICD-9 to ICD-10 allows for better accuracy and improved coding of various medical conditions, including rare genetic disorders like Arginase Deficiency/Argininemia.
Seeking proper diagnosis and medical management is crucial for individuals with Arginase Deficiency/Argininemia. Consulting with healthcare professionals who specialize in metabolic disorders can provide appropriate guidance and support for affected individuals and their families.