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Encounter for antenatal screening for other genetic defects

ICD10CM code

Medical Policies and Guidelines for Encounter for antenatal screening for other genetic defects

Related policies from health plans

Genetic Testing for Inherited Diseases
Genetic Testing for Inherited Diseases
Genetic Testing for Inherited Diseases
Genetic Testing for TP53 Mutations
CG-GENE-13 Genetic Testing for Inherited Diseases
CG-GENE-13 Genetic Testing for Inherited Diseases
CG-GENE-13 Genetic Testing for Inherited Diseases
CG-GENE-18 Genetic Testing for TP53 Mutations
Vitamin D Testing - (0526)
Vitamin D Testing - (0526)

Similar Codes


ICD10CM codes

Z36.8A - Encounter for antenatal screening for other genetic defects
Z36.8 - Encounter for other antenatal screening
Z36.89 - Encounter for other specified antenatal screening
Z36.0 - Encounter for antenatal screening for chromosomal anomalies
Z36.3 - Encounter for antenatal screening for malformations
Z36.9 - Encounter for antenatal screening, unspecified
Z13.79 - Encounter for other screening for genetic and chromosomal anomalies
Z36.2 - Encounter for other antenatal screening follow-up
Z36.4 - Encounter for antenatal screening for fetal growth retardation
Z13.7 - Encounter for screening for genetic and chromosomal anomalies

HCPCS codes

H1000 - Prenatal care, at-risk assessment
D0190 - Screening of a patient
S3620 - Newborn metabolic screening panel, includes test kit, postage and the laboratory tests specified by
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
T1023 - Screening to determine the appropriateness of consideration of an individual for participation in a
G9921 - No screening performed, partial screening performed or positive screen without recommendations and r
G0472 - Hepatitis c antibody screening, for individual at high risk and other covered indication(s)
G0434 - Drug screen, other than chromatographic; any number of drug classes, by clia waived test or moderate

CPT4 codes

81512 - Fetal congenital abnormalities, biochemical assays of five analytes (AFP, uE3, total hCG, hyperglyco
81508 - Fetal congenital abnormalities, biochemical assays of two proteins (PAPP-A, hCG [any form]), utilizi
0060U - Twin zygosity, genomic targeted sequence analysis of chromosome 2, using circulating cell-free fetal
81511 - Fetal congenital abnormalities, biochemical assays of four analytes (AFP, uE3, hCG [any form], DIA)
81422 - Fetal chromosomal microdeletion(s) genomic sequence analysis (eg, DiGeorge syndrome, Cri-du-chat syn
81507 - Fetal aneuploidy (trisomy 21, 18, and 13) DNA sequence analysis of selected regions using maternal p
81420 - Fetal chromosomal aneuploidy (eg, trisomy 21, monosomy X) genomic sequence analysis panel, circulati
93530 - Right heart catheterization, for congenital cardiac anomalies
81425 - Genome (eg, unexplained constitutional or heritable disorder or syndrome); sequence analysis
59000 - Amniocentesis; diagnostic