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Encounter for nonprocreative screening for genetic disease carrier status

ICD10CM code

Medical Policies and Guidelines for Encounter for nonprocreative screening for genetic disease carrier status

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Similar Codes


ICD10CM codes

Z13.71 - Encounter for nonprocreative screening for genetic disease carrier status
Z31.440 - Encounter of male for testing for genetic disease carrier status for procreative management
Z31.430 - Encounter of female for testing for genetic disease carrier status for procreative management
Z13.79 - Encounter for other screening for genetic and chromosomal anomalies
Z71.83 - Encounter for nonprocreative genetic counseling
Z13.7 - Encounter for screening for genetic and chromosomal anomalies
Z36.8A - Encounter for antenatal screening for other genetic defects
Z31.5 - Encounter for procreative genetic counseling
Z31.43 - Encounter for genetic testing of female for procreative management
Z31.44 - Encounter for genetic testing of male for procreative management

HCPCS codes

D0190 - Screening of a patient
T1023 - Screening to determine the appropriateness of consideration of an individual for participation in a
G9920 - Screening performed and negative
G9921 - No screening performed, partial screening performed or positive screen without recommendations and r
G8401 - Clinician documented that patient was not an eligible candidate for screening
H1000 - Prenatal care, at-risk assessment
G9919 - Screening performed and positive and provision of recommendations
G9228 - Chlamydia, gonorrhea and syphilis screening results documented (report when results are present for
G9618 - Documentation of screening for uterine malignancy or those that had an ultrasound and/or endometrial
G0121 - Colorectal cancer screening; colonoscopy on individual not meeting criteria for high risk

CPT4 codes

81425 - Genome (eg, unexplained constitutional or heritable disorder or syndrome); sequence analysis
0060U - Twin zygosity, genomic targeted sequence analysis of chromosome 2, using circulating cell-free fetal
4293F - Patient screened for high-risk sexual behavior (HIV)
81412 - Ashkenazi Jewish associated disorders (eg, Bloom syndrome, Canavan disease, cystic fibrosis, familia
81422 - Fetal chromosomal microdeletion(s) genomic sequence analysis (eg, DiGeorge syndrome, Cri-du-chat syn
81432 - Hereditary breast cancer-related disorders (eg, hereditary breast cancer, hereditary ovarian cancer,
81416 - Exome (eg, unexplained constitutional or heritable disorder or syndrome); sequence analysis, each co
96040 - Medical genetics and genetic counseling services, each 30 minutes face-to-face with patient/family
81507 - Fetal aneuploidy (trisomy 21, 18, and 13) DNA sequence analysis of selected regions using maternal p
81415 - Exome (eg, unexplained constitutional or heritable disorder or syndrome); sequence analysis