ICD10 code of Smith-Lemli-Opitz Syndrome and ICD9 code

Smith-Lemli-Opitz Syndrome (SLOS) is a rare genetic disorder characterized by impaired cholesterol synthesis. It is caused by mutations in the DHCR7 gene, which leads to reduced levels of the enzyme 7-dehydrocholesterol reductase. This enzyme is crucial for the production of cholesterol, a vital component for various physiological processes.

In terms of coding, the International Classification of Diseases, 10th Revision (ICD-10) provides a specific code for Smith-Lemli-Opitz Syndrome. The ICD-10 code for SLOS is Q87.1. This code falls under the category of "Other congenital malformation syndromes predominantly associated with short stature." Q87.1 is further classified as a "Congenital malformation syndromes predominantly associated with short stature."

On the other hand, the International Classification of Diseases, 9th Revision (ICD-9) does not have a specific code for Smith-Lemli-Opitz Syndrome. As ICD-9 lacks the specificity required to accurately represent this disorder, it may have been classified under a broader category or grouped with similar conditions.

It is important to note that the transition from ICD-9 to ICD-10 occurred in October 2015, and healthcare providers now primarily use ICD-10 codes for diagnostic purposes. The ICD-10 code Q87.1 for Smith-Lemli-Opitz Syndrome allows healthcare professionals to accurately identify and document this genetic disorder in medical records, facilitating effective communication, research, and appropriate management of affected individuals.

by Diseasemaps