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Abnormal findings on antenatal screening of mother

ICD10CM code

Medical Policies and Guidelines for Abnormal findings on antenatal screening of mother

Related policies from health plans

Concert Genetic Testing: Non invasive Prenatal Screening (PDF)
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Concert Genetic Testing: Prenatal Diagnosis Pregnancy Loss (PDF)

Similar Codes


ICD10CM codes

O28 - Abnormal findings on antenatal screening of mother
O28.8 - Other abnormal findings on antenatal screening of mother
O28.9 - Unspecified abnormal findings on antenatal screening of mother
O28.4 - Abnormal radiological finding on antenatal screening of mother
O28.2 - Abnormal cytological finding on antenatal screening of mother
O28.0 - Abnormal hematological finding on antenatal screening of mother
O28.1 - Abnormal biochemical finding on antenatal screening of mother
O28.5 - Abnormal chromosomal and genetic finding on antenatal screening of mother
O28.3 - Abnormal ultrasonic finding on antenatal screening of mother
P09 - Abnormal findings on neonatal screening

HCPCS codes

H1000 - Prenatal care, at-risk assessment
D0190 - Screening of a patient
G9618 - Documentation of screening for uterine malignancy or those that had an ultrasound and/or endometrial
G9357 - Post-partum screenings, evaluations and education performed
G9920 - Screening performed and negative
G9919 - Screening performed and positive and provision of recommendations
G8806 - Performance of trans-abdominal or trans-vaginal ultrasound and pregnancy location documented
S3620 - Newborn metabolic screening panel, includes test kit, postage and the laboratory tests specified by
G8409 - Clinician documented that patient was not an eligible candidate for abi measurement measure
S2260 - Induced abortion, 17 to 24 weeks

CPT4 codes

81508 - Fetal congenital abnormalities, biochemical assays of two proteins (PAPP-A, hCG [any form]), utilizi
81512 - Fetal congenital abnormalities, biochemical assays of five analytes (AFP, uE3, total hCG, hyperglyco
81511 - Fetal congenital abnormalities, biochemical assays of four analytes (AFP, uE3, hCG [any form], DIA)
81507 - Fetal aneuploidy (trisomy 21, 18, and 13) DNA sequence analysis of selected regions using maternal p
0060U - Twin zygosity, genomic targeted sequence analysis of chromosome 2, using circulating cell-free fetal
59025 - Fetal non-stress test
59020 - Fetal contraction stress test
59000 - Amniocentesis; diagnostic
81420 - Fetal chromosomal aneuploidy (eg, trisomy 21, monosomy X) genomic sequence analysis panel, circulati
82106 - Alpha-fetoprotein (AFP); amniotic fluid