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Encounter for other screening for genetic and chromosomal anomalies

ICD10CM code

Medical Policies and Guidelines for Encounter for other screening for genetic and chromosomal anomalies

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Similar Codes


ICD10CM codes

Z13.79 - Encounter for other screening for genetic and chromosomal anomalies
Z13.7 - Encounter for screening for genetic and chromosomal anomalies
Z36.0 - Encounter for antenatal screening for chromosomal anomalies
Z36.8A - Encounter for antenatal screening for other genetic defects
Z13.89 - Encounter for screening for other disorder
Z13.8 - Encounter for screening for other specified diseases and disorders
Z13 - Encounter for screening for other diseases and disorders
Z13.71 - Encounter for nonprocreative screening for genetic disease carrier status
Z36.8 - Encounter for other antenatal screening
Z36.3 - Encounter for antenatal screening for malformations

HCPCS codes

D0190 - Screening of a patient
T1023 - Screening to determine the appropriateness of consideration of an individual for participation in a
H1000 - Prenatal care, at-risk assessment
G9618 - Documentation of screening for uterine malignancy or those that had an ultrasound and/or endometrial
G0434 - Drug screen, other than chromatographic; any number of drug classes, by clia waived test or moderate
G9921 - No screening performed, partial screening performed or positive screen without recommendations and r
G0101 - Cervical or vaginal cancer screening; pelvic and clinical breast examination
G9318 - Imaging study named according to standardized nomenclature
G9920 - Screening performed and negative
H0002 - Behavioral health screening to determine eligibility for admission to treatment program

CPT4 codes

88289 - Chromosome analysis; additional high resolution study
81425 - Genome (eg, unexplained constitutional or heritable disorder or syndrome); sequence analysis
81420 - Fetal chromosomal aneuploidy (eg, trisomy 21, monosomy X) genomic sequence analysis panel, circulati
81422 - Fetal chromosomal microdeletion(s) genomic sequence analysis (eg, DiGeorge syndrome, Cri-du-chat syn
88280 - Chromosome analysis; additional karyotypes, each study
81277 - Cytogenomic neoplasia (genome-wide) microarray analysis, interrogation of genomic regions for copy n
88273 - Molecular cytogenetics; chromosomal in situ hybridization, analyze 10-30 cells (eg, for microdeletio
81229 - Cytogenomic constitutional (genome-wide) microarray analysis; interrogation of genomic regions for c
0060U - Twin zygosity, genomic targeted sequence analysis of chromosome 2, using circulating cell-free fetal
93303 - Transthoracic echocardiography for congenital cardiac anomalies; complete