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Encounter for antenatal screening for chromosomal anomalies

ICD10CM code

Medical Policies and Guidelines for Encounter for antenatal screening for chromosomal anomalies

Related policies from health plans

Genetic Testing for Inherited Diseases
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Genetic Testing for Reproductive Carrier Screening and Prenatal Diagnosis - (0514)
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Prenatal Testing (CG043)
CG-GENE-13 Genetic Testing for Inherited Diseases
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Vitamin D Testing - (0526)
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RAD.00038 Use of 3-D, 4-D or 5-D Ultrasound in Maternity Care
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Concert Genetic Testing: Non invasive Prenatal Screening (PDF)

Similar Codes


ICD10CM codes

Z36.0 - Encounter for antenatal screening for chromosomal anomalies
Z13.7 - Encounter for screening for genetic and chromosomal anomalies
Z36.3 - Encounter for antenatal screening for malformations
Z13.79 - Encounter for other screening for genetic and chromosomal anomalies
Z36.8A - Encounter for antenatal screening for other genetic defects
Z36.8 - Encounter for other antenatal screening
Z36.9 - Encounter for antenatal screening, unspecified
Z36.89 - Encounter for other specified antenatal screening
Z36.81 - Encounter for antenatal screening for hydrops fetalis
Z36.4 - Encounter for antenatal screening for fetal growth retardation

HCPCS codes

D0190 - Screening of a patient
H1000 - Prenatal care, at-risk assessment
G9618 - Documentation of screening for uterine malignancy or those that had an ultrasound and/or endometrial
T1023 - Screening to determine the appropriateness of consideration of an individual for participation in a
G0101 - Cervical or vaginal cancer screening; pelvic and clinical breast examination
G9920 - Screening performed and negative
S2260 - Induced abortion, 17 to 24 weeks
S3620 - Newborn metabolic screening panel, includes test kit, postage and the laboratory tests specified by
G9919 - Screening performed and positive and provision of recommendations
G0143 - Screening cytopathology, cervical or vaginal (any reporting system), collected in preservative fluid

CPT4 codes

81420 - Fetal chromosomal aneuploidy (eg, trisomy 21, monosomy X) genomic sequence analysis panel, circulati
0060U - Twin zygosity, genomic targeted sequence analysis of chromosome 2, using circulating cell-free fetal
88267 - Chromosome analysis, amniotic fluid or chorionic villus, count 15 cells, 1 karyotype, with banding
81422 - Fetal chromosomal microdeletion(s) genomic sequence analysis (eg, DiGeorge syndrome, Cri-du-chat syn
81512 - Fetal congenital abnormalities, biochemical assays of five analytes (AFP, uE3, total hCG, hyperglyco
81507 - Fetal aneuploidy (trisomy 21, 18, and 13) DNA sequence analysis of selected regions using maternal p
81511 - Fetal congenital abnormalities, biochemical assays of four analytes (AFP, uE3, hCG [any form], DIA)
81508 - Fetal congenital abnormalities, biochemical assays of two proteins (PAPP-A, hCG [any form]), utilizi
88289 - Chromosome analysis; additional high resolution study
93530 - Right heart catheterization, for congenital cardiac anomalies