O35.11X2
ICD-10-CMMaternal care for (suspected) chromosomal abnormality in fetus, Trisomy 13, fetus 2
This code signifies ongoing maternal medical management and surveillance due to a confirmed or suspected diagnosis of Trisomy 13 (Patau syndrome) in the second fetus of a multiple gestation pregnancy. This condition is a severe chromosomal disorder characterized by the presence of an extra copy of chromosome 13, leading to significant developmental abnormalities.
Use this code when the mother is receiving specialized care, monitoring, or counseling because a prenatal diagnostic test (e.g., amniocentesis, CVS, NIPT with confirmatory testing) has identified or strongly suggested Trisomy 13 in fetus 2. Documentation should clearly state the suspected or confirmed chromosomal abnormality and specify "fetus 2" in a multiple gestation.
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