The ICD-10 code for Monosomy 6p25 is Q93.5, which falls under the category of "Chromosomal deletion syndromes." In the previous ICD-9 coding system, there was no specific code for Monosomy 6p25. It is important to consult a healthcare professional or medical coding specialist for accurate coding and further information.
Monosomy 6p25 is a chromosomal disorder characterized by the deletion or loss of genetic material from the short arm of chromosome 6 at position 25. This condition is quite rare and can lead to various developmental delays and physical abnormalities.
In terms of medical coding, the ICD-10 code for Monosomy 6p25 is Q93.89. The ICD-10 is the International Classification of Diseases, 10th Revision, which is a standardized system used to classify and code diagnoses, symptoms, and procedures in medical settings. The code Q93.89 specifically denotes "Other deletions of part of a chromosome," which encompasses Monosomy 6p25 among other similar chromosomal abnormalities.
On the other hand, the ICD-9 code for Monosomy 6p25 is 758.39. The ICD-9 is the previous version of the classification system, which has been replaced by ICD-10. The code 758.39 represents "Other deletions and partial deletions of autosomes, NEC" in the ICD-9 system.
It is important to note that accurate coding is crucial for medical documentation, billing, and research purposes. However, it is always recommended to consult with a healthcare professional or medical coder for precise coding information, as they possess the expertise to ensure accurate and up-to-date coding practices.
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