Pyruvate Carboxylase Deficiency is a rare genetic disorder that affects the body's ability to convert certain nutrients into energy. The ICD-10 code for this condition is E74.4. In the previous coding system, the ICD-9 code used for Pyruvate Carboxylase Deficiency was 277.6. These codes are important for accurate medical record keeping and billing purposes.
Pyruvate carboxylase deficiency is a rare metabolic disorder characterized by the impaired function of the enzyme pyruvate carboxylase. This enzyme plays a crucial role in the production of glucose and several other important substances within the body.
The ICD-10 code for pyruvate carboxylase deficiency is E74.4. This code falls under the category of "Other disorders of carbohydrate metabolism," specifically within the subcategory of "Disorders of pyruvate metabolism and gluconeogenesis." The ICD-10 code system is used by healthcare professionals to classify and code diagnoses, allowing for standardized documentation and billing.
In contrast, the ICD-9 code for pyruvate carboxylase deficiency is 270.3. This code is categorized as "Disorders of amino-acid transport and metabolism" within the ICD-9 coding system. It is important to note that the ICD-9 system has been replaced by ICD-10 in most countries, as the latter provides a more detailed and comprehensive classification of diseases and conditions.
Diagnosis coding using ICD-10 helps healthcare providers accurately identify and track specific conditions, facilitating appropriate treatment and research. By utilizing these codes, medical professionals can ensure effective communication, data analysis, and reimbursement processes.
It is important to consult with a healthcare professional or medical coding specialist for accurate coding and documentation of any specific medical condition, as they possess the expertise to navigate the intricacies of the coding system.