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ICD10 code of Trisomy 13 Syndrome / Patau Syndrome and ICD9 code
What is the ICD10 code for Trisomy 13 Syndrome / Patau Syndrome? And the ICD9 code for Trisomy 13 Syndrome / Patau Syndrome?
Trisomy 13 Syndrome, also known as Patau Syndrome, is a genetic disorder caused by the presence of an extra copy of chromosome 13. The ICD-10 code for Trisomy 13 Syndrome is Q91.3. In the ICD-9 code system, it is classified as 758.1. This condition is characterized by multiple physical abnormalities and intellectual disabilities. It is important to consult with a healthcare professional for accurate diagnosis and management of Trisomy 13 Syndrome.
Trisomy 13 Syndrome, also known as Patau Syndrome, is a chromosomal disorder caused by the presence of an extra copy of chromosome 13. It is characterized by a range of physical abnormalities and intellectual disabilities.
The ICD-10 code for Trisomy 13 Syndrome is Q91.3, which falls under the category of "Chromosomal anomalies, NEC" in the ICD-10 coding system. This code specifically represents the presence of an extra chromosome 13 in the individual's genetic makeup.
In the previous ICD-9 coding system, Trisomy 13 Syndrome was identified by the code 758.1, which falls under the category of "Other chromosomal anomalies." This code indicated the presence of an additional chromosome 13 in the individual's genetic material.
It is important to note that accurate coding is crucial for medical records, insurance claims, and statistical purposes. Proper coding allows healthcare professionals and researchers to track the prevalence, impact, and outcomes of specific conditions like Trisomy 13 Syndrome, aiding in the improvement of patient care and understanding of the disorder.
The ICD-10 code for Trisomy 13 Syndrome is Q91.3, which falls under the category of "Chromosomal anomalies, NEC" in the ICD-10 coding system. This code specifically represents the presence of an extra chromosome 13 in the individual's genetic makeup.
In the previous ICD-9 coding system, Trisomy 13 Syndrome was identified by the code 758.1, which falls under the category of "Other chromosomal anomalies." This code indicated the presence of an additional chromosome 13 in the individual's genetic material.
It is important to note that accurate coding is crucial for medical records, insurance claims, and statistical purposes. Proper coding allows healthcare professionals and researchers to track the prevalence, impact, and outcomes of specific conditions like Trisomy 13 Syndrome, aiding in the improvement of patient care and understanding of the disorder.
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