Dyggve Melchior Clausen Syndrome is a rare genetic disorder characterized by skeletal abnormalities, intellectual disability, and developmental delays. The ICD10 code for this syndrome is Q87.1. Unfortunately, there is no specific ICD9 code for Dyggve Melchior Clausen Syndrome as ICD9 does not provide a direct equivalent for this condition. It is important to consult with a healthcare professional for accurate diagnosis and coding.
Dyggve Melchior Clausen Syndrome (DMC) is a rare genetic disorder characterized by progressive skeletal abnormalities and intellectual disability. It is inherited in an autosomal recessive manner, meaning that both parents must carry a mutated gene for the syndrome to manifest in their child.
Unfortunately, I cannot provide the specific ICD-10 or ICD-9 codes as I am unable to access real-time medical databases. However, I can provide you with general information about the coding system. The International Classification of Diseases (ICD) is a standardized system used by medical professionals to classify and code diagnoses and procedures. The ICD-10 codes are alphanumeric codes that are more detailed and specific compared to the older ICD-9 codes.
Dyggve Melchior Clausen Syndrome would be classified under the ICD-10 code range Q87.8, which includes other specified congenital malformation syndromes predominantly affecting multiple systems. The exact code within this range would provide more specific information about the syndrome and associated features.
In the previous ICD-9 coding system, Dyggve Melchior Clausen Syndrome would have been classified under the code 759.89, which is used for other and unspecified congenital anomalies. However, it is important to note that the ICD-9 codes are no longer in use, as they have been replaced by the more comprehensive ICD-10 codes.
It is always recommended to consult with a medical professional or refer to the official coding manuals for accurate and up-to-date coding information.