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Z13.7
Encounter for screening for genetic and chromosomal anomalies
ICD10CM code
Similar Codes
ICD10CM codes
Z13.7
- Encounter for screening for genetic and chromosomal anomalies
Z13.79
- Encounter for other 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
Z36.3
- Encounter for antenatal screening for malformations
Z13.71
- Encounter for nonprocreative screening for genetic disease carrier status
Z13
- Encounter for screening for other diseases and disorders
Z13.4
- Encounter for screening for certain developmental disorders in childhood
Z13.8
- Encounter for screening for other specified diseases and disorders
Z36.83
- Encounter for fetal screening for congenital cardiac abnormalities
HCPCS codes
D0190
- Screening of a patient
T1023
- Screening to determine the appropriateness of consideration of an individual for participation in a
G9618
- Documentation of screening for uterine malignancy or those that had an ultrasound and/or endometrial
H1000
- Prenatal care, at-risk assessment
G0101
- Cervical or vaginal cancer screening; pelvic and clinical breast examination
G9318
- Imaging study named according to standardized nomenclature
G9919
- Screening performed and positive and provision of recommendations
G9920
- Screening performed and negative
H0002
- Behavioral health screening to determine eligibility for admission to treatment program
C8937
- Computer-aided detection, including computer algorithm analysis of breast mri image data for lesion
CPT4 codes
81420
- Fetal chromosomal aneuploidy (eg, trisomy 21, monosomy X) genomic sequence analysis panel, circulati
81425
- Genome (eg, unexplained constitutional or heritable disorder or syndrome); sequence analysis
81422
- Fetal chromosomal microdeletion(s) genomic sequence analysis (eg, DiGeorge syndrome, Cri-du-chat syn
81277
- Cytogenomic neoplasia (genome-wide) microarray analysis, interrogation of genomic regions for copy n
88289
- Chromosome analysis; additional high resolution study
88273
- Molecular cytogenetics; chromosomal in situ hybridization, analyze 10-30 cells (eg, for microdeletio
0060U
- Twin zygosity, genomic targeted sequence analysis of chromosome 2, using circulating cell-free fetal
81229
- Cytogenomic constitutional (genome-wide) microarray analysis; interrogation of genomic regions for c
88280
- Chromosome analysis; additional karyotypes, each study
81507
- Fetal aneuploidy (trisomy 21, 18, and 13) DNA sequence analysis of selected regions using maternal p