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Z13.79
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
Related policies from health plans
CIGNA
Transvaginal Ultrasound, Non-Obstetrical - (0398)
SUNFLOWER
Concert Genetic Oncology: Algorithmic Testing (PDF)
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