The ICD10 code for PMM2-CDG is E77.8, which falls under the category of "Other disorders of glycoprotein metabolism." Unfortunately, there is no specific ICD9 code for PMM2-CDG as the ICD9 system does not have a direct equivalent for this condition. It is important to consult with a healthcare professional for accurate diagnosis and coding information.
PMM2-CDG, also known as congenital disorder of glycosylation type Ia, is a rare genetic disorder that affects the body's ability to produce certain proteins and sugars. When it comes to medical coding, the International Classification of Diseases, 10th Revision (ICD-10) is used to classify and code diseases and disorders. However, it is important to note that ICD-10 codes are not specific to individual genetic disorders but rather provide broader categories for classification.
In the case of PMM2-CDG, the appropriate ICD-10 code would be E77.0. This code falls under the category of "disorders of glycoprotein metabolism and other congenital disorders of glycosylation." It helps healthcare professionals accurately document and track cases of PMM2-CDG within their patient population.
As for the International Classification of Diseases, 9th Revision (ICD-9), it has been replaced by ICD-10 in most countries. Nevertheless, for historical purposes, the ICD-9 code for PMM2-CDG would be 271.8. This code falls under the category of "other disorders of carbohydrate transport and metabolism."
It is important to consult a healthcare professional or medical coding specialist for accurate coding and documentation purposes.