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the other hand, the International Classification of Diseases, 9th Revision (ICD-9) is an older coding system that has been replaced by ICD-10.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 It is important to note that ICD-9 codes are no longer updated or maintained, so healthcare providers now primarily use the ICD-10 coding system.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.