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ICD10 code of Pfeiffer Syndrome and ICD9 code
What is the ICD10 code for Pfeiffer Syndrome? And the ICD9 code for Pfeiffer Syndrome?
Pfeiffer Syndrome is a rare genetic disorder characterized by craniosynostosis (premature fusion of skull bones) and abnormalities in the hands and feet. The ICD10 code for Pfeiffer Syndrome is Q87.0. In the previous ICD9 coding system, it was classified under 756.4. It is important to consult with a healthcare professional for accurate diagnosis and appropriate management of this condition.
Pfeiffer Syndrome is a rare genetic disorder characterized by craniosynostosis, meaning the premature fusion of certain bones in the skull, as well as abnormalities in the hands and feet. The ICD-10 code for Pfeiffer Syndrome is Q87.0. This code falls under the category of "Congenital malformation syndromes predominantly associated with short stature."
In contrast, the ICD-9 code for Pfeiffer Syndrome is 756.0. This code is classified under "Other congenital musculoskeletal anomalies," which includes various skeletal and musculoskeletal disorders present at birth.
It is essential to note that the ICD-9 code has been replaced by the ICD-10 code globally. The transition to ICD-10 allows for more specific and detailed coding, facilitating accurate diagnosis and treatment. Proper coding enables healthcare professionals to track and analyze the prevalence of specific conditions, improve patient care, and enhance research efforts in understanding rare disorders like Pfeiffer Syndrome.
In contrast, the ICD-9 code for Pfeiffer Syndrome is 756.0. This code is classified under "Other congenital musculoskeletal anomalies," which includes various skeletal and musculoskeletal disorders present at birth.
It is essential to note that the ICD-9 code has been replaced by the ICD-10 code globally. The transition to ICD-10 allows for more specific and detailed coding, facilitating accurate diagnosis and treatment. Proper coding enables healthcare professionals to track and analyze the prevalence of specific conditions, improve patient care, and enhance research efforts in understanding rare disorders like Pfeiffer Syndrome.
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