O35.15X9
ICD-10-CMMaternal care for (suspected) chromosomal abnormality in fetus, sex chromosome abnormality, other fetus
This code signifies that a pregnant patient is receiving medical management due to a suspected or confirmed sex chromosome abnormality in one of the fetuses, when the pregnancy involves multiple gestations and the specific fetus affected is not otherwise specified. This includes conditions like Turner syndrome (XO), Klinefelter syndrome (XXY), or other aneuploidies involving the X or Y chromosomes. The maternal care is focused on monitoring the pregnancy and planning for potential fetal outcomes related to this genetic condition.
Apply this code when documentation indicates maternal care for a fetus with a suspected or diagnosed sex chromosome abnormality in a multiple gestation pregnancy, and the specific fetus is not identified (e.g., "fetus 2" or "fetus A"). This typically follows abnormal prenatal screening results (e.g., NIPT, quad screen) or diagnostic testing (e.g., amniocentesis, CVS) confirming or highly suggesting a sex chromosome anomaly. Documentation should clearly state the type of abnormality (sex chromosome) and the multiple gestation context.
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