Hyperprolinemia Type II is a metabolic disorder characterized by elevated levels of proline in the blood and urine. The ICD10 code for this condition is E72.4. Unfortunately, there is no specific ICD9 code for Hyperprolinemia Type II as it was replaced by the ICD10 coding system. It is important to consult with a healthcare professional for accurate diagnosis and appropriate management of this condition.
Hyperprolinemia Type II is a rare genetic disorder characterized by elevated levels of proline in the blood and urine. The condition is caused by a deficiency of the enzyme pyrroline-5-carboxylate dehydrogenase (P5CDH), which is involved in the breakdown of proline.
In terms of medical coding, the International Classification of Diseases, Tenth Revision (ICD-10) provides a specific code for Hyperprolinemia Type II. The ICD-10 code for this condition is E72.42. This code falls under the category of "Other disorders of amino-acid metabolism," which is located in Chapter IV (Endocrine, Nutritional, and Metabolic Diseases) of the ICD-10 coding system.
On the other hand, the International Classification of Diseases, Ninth Revision (ICD-9) is an older version of the coding system. For Hyperprolinemia Type II, the corresponding ICD-9 code is 270.8. This code is found under the category of "Other disorders of amino-acid metabolism" in Chapter 4 (Diseases Of The Blood And Blood-Forming Organs) of the ICD-9 coding system.
It is important to note that ICD-10 codes are now widely used, as ICD-9 codes have been largely phased out in many countries. These codes are essential for accurately documenting and tracking medical conditions, facilitating research, and ensuring appropriate reimbursement for healthcare services provided.