Short answer · Medically reviewed summary · Last updated: 2023-07-10
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.
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ICD10 code of Catel Manzke Syndrome and ICD9 code
ICD-10 and ICD-9 codes for Catel Manzke Syndrome, with classification details for clinicians, coders and patients.
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the other hand, the International Classification of Diseases, 9th Revision (ICD-9) is an older coding system that has been replaced by ICD-10.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 It is important to note that ICD-9 codes are no longer updated or maintained, so healthcare providers now primarily use the ICD-10 coding system.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.
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the other hand, the International Classification of Diseases, 9th Revision (ICD-9) is an older coding system that has been replaced by ICD-10.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.
Author: DiseaseMaps Editorial Team
Reviewed against authoritative medical sources (NIH GARD, Orphanet, OMIM)
Last updated: 2023-07-10
Medical disclaimer:
This information does not substitute professional medical advice. Always consult your doctor before making health decisions.
Source:
DiseaseMaps.org
