ICD10 code of Apert Syndrome and ICD9 code

Apert Syndrome is a rare genetic disorder characterized by abnormal growth of the skull and facial bones, leading to distinct physical features and potential complications. The International Classification of Diseases, 10th Revision (ICD-10) provides a specific code for Apert Syndrome, which is Q87.0. This code falls under Chapter XVII: Congenital Malformations, Deformations, and Chromosomal Abnormalities, and specifically relates to "Other specified congenital malformation syndromes affecting multiple systems."

On the other hand, the International Classification of Diseases, 9th Revision (ICD-9) is an older coding system that has been replaced by ICD-10. The corresponding ICD-9 code for Apert Syndrome is 755.55. This code was classified under the category "Other craniofacial anomalies."

It is crucial to accurately assign these codes in medical records and billing processes to ensure proper identification, tracking, and management of various conditions. These codes help healthcare providers, researchers, and insurance companies understand the prevalence, impact, and treatment patterns associated with specific disorders like Apert Syndrome.

Apert Syndrome affects multiple systems in the body, including the skull, face, hands, and feet. It can lead to various complications such as breathing difficulties, vision and hearing impairments, dental problems, and developmental delays. Early intervention and multidisciplinary care involving specialists from different medical fields are essential to address these challenges and optimize the quality of life for individuals with Apert Syndrome.

In conclusion, the ICD-10 code for Apert Syndrome is Q87.0, while the corresponding ICD-9 code is 755.55. These codes facilitate standardized documentation and classification of Apert Syndrome, enabling effective communication and analysis of medical information across healthcare systems.

by Diseasemaps