Pallister Hall Syndrome is a rare genetic disorder characterized by a wide range of symptoms including extra fingers or toes, abnormal development of the hypothalamus, and various malformations in the body. The ICD10 code for Pallister Hall Syndrome is Q87.0. Unfortunately, there is no specific ICD9 code for this syndrome as it is not included in the ICD9 classification system.
Pallister Hall Syndrome is a rare genetic disorder characterized by a wide range of symptoms affecting multiple body systems. It is caused by mutations in the GLI3 gene, which plays a crucial role in embryonic development.
When it comes to medical coding, Pallister Hall Syndrome is classified under the International Classification of Diseases, 10th Revision (ICD-10). The ICD-10 code for Pallister Hall Syndrome is Q87.0. This code falls under the category of "Other congenital malformation syndromes predominantly associated with short stature" in the ICD-10 coding system.
As for the ICD-9 code, it is the previous version of the coding system and has been replaced by ICD-10. However, for reference purposes, the ICD-9 code for Pallister Hall Syndrome was 759.89. In the ICD-9 system, this code falls under the category of "Other congenital anomalies, not elsewhere classified."
It is important to note that medical coding is essential for accurate and standardized documentation of healthcare diagnoses. These codes allow healthcare providers, insurance companies, and researchers to efficiently analyze and track diseases, disorders, and conditions. Proper coding ensures effective communication and facilitates appropriate reimbursement for medical services rendered.
Please consult a healthcare professional or medical coding specialist for the most up-to-date and accurate coding information related to Pallister Hall Syndrome.