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ICD10 code of Catel Manzke Syndrome and ICD9 code

What is the ICD10 code for Catel Manzke Syndrome? And the ICD9 code for Catel Manzke Syndrome?

ICD9 and ICD10 codes of Catel Manzke Syndrome

Catel Manzke Syndrome is a rare genetic disorder characterized by craniofacial abnormalities, skeletal malformations, and intellectual disability. Unfortunately, there is no specific ICD-10 code assigned for this syndrome. In the ICD-9 coding system, it is classified under 756.0 for "Anomalies of skull and face bones" and 759.89 for "Other specified congenital anomalies." It is important to consult with a healthcare professional for accurate diagnosis and coding information.
Catel Manzke Syndrome (CMS) is a rare genetic disorder characterized by various skeletal and craniofacial abnormalities. Although I cannot diagnose or provide medical advice, I can provide you with information about the ICD-10 and ICD-9 codes associated with this condition.

In the International Classification of Diseases, 10th Revision (ICD-10), Catel Manzke Syndrome is classified under Q87.1. This code falls under the category of "Other specified congenital malformation syndromes affecting multiple systems." The ICD-10 code Q87.1 is used to identify and track cases of CMS in medical records and statistical data.

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the other hand, the International Classification of Diseases, 9th Revision (ICD-9) is an older coding system that has been replaced by ICD-10. While ICD-9 codes are no longer used for current medical coding, they were widely utilized before the transition to ICD-10. Unfortunately, ICD-9 does not have a specific code for Catel Manzke Syndrome. It is important to note that ICD-9 codes are no longer updated or maintained, so healthcare providers now primarily use the ICD-10 coding system.

Remember, it is crucial to consult with a qualified healthcare professional or geneticist who can provide accurate diagnosis, information, and guidance regarding Catel Manzke Syndrome or any other medical condition.
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