Glutaryl-CoA dehydrogenase deficiency, also known as glutaric aciduria type 1, is a rare genetic disorder that affects the body's ability to break down certain amino acids. This condition is caused by a deficiency of the enzyme glutaryl-CoA dehydrogenase, which is responsible for the metabolism of glutaric acid.
In terms of medical coding, the International Classification of Diseases, 10th Revision (ICD-10) provides specific codes for this condition. The ICD-10 code for Glutaryl-CoA dehydrogenase deficiency is E71.310. This code falls under the category of "Disorders of branched-chain amino-acid metabolism and fatty-acid metabolism" in the ICD-10 coding system.
On the other hand, the International Classification of Diseases, 9th Revision (ICD-9) was used prior to the implementation of ICD-10. The ICD-9 code for Glutaryl-CoA dehydrogenase deficiency is 270.3. This code is classified under the section "Other disorders of amino-acid metabolism" in the ICD-9 coding system.
It is important to note that ICD-10 codes are more specific and detailed compared to ICD-9 codes. The transition from ICD-9 to ICD-10 allows for more accurate and comprehensive coding of medical conditions, enabling healthcare professionals to better track and analyze diseases and conditions.
In conclusion, the ICD-10 code for Glutaryl-CoA dehydrogenase deficiency is E71.310, while the ICD-9 code is 270.3. These codes are used to classify and document this rare genetic disorder in medical records and billing systems.