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O28.2
Abnormal cytological finding on antenatal screening of mother
ICD10CM code
Similar Codes
ICD10CM codes
O28.2
- Abnormal cytological finding on antenatal screening of mother
O28.5
- Abnormal chromosomal and genetic finding on antenatal screening of mother
O28
- Abnormal findings on antenatal screening of mother
O28.4
- Abnormal radiological finding on antenatal screening of mother
O28.0
- Abnormal hematological finding on antenatal screening of mother
O28.8
- Other abnormal findings on antenatal screening of mother
O28.9
- Unspecified abnormal findings on antenatal screening of mother
O28.1
- Abnormal biochemical finding on antenatal screening of mother
O28.3
- Abnormal ultrasonic finding on antenatal screening of mother
R87.61
- Abnormal cytological findings in specimens from cervix uteri
HCPCS codes
G0143
- Screening cytopathology, cervical or vaginal (any reporting system), collected in preservative fluid
G0124
- Screening cytopathology, cervical or vaginal (any reporting system), collected in preservative fluid
G0141
- Screening cytopathology smears, cervical or vaginal, performed by automated system, with manual resc
G9618
- Documentation of screening for uterine malignancy or those that had an ultrasound and/or endometrial
G0123
- Screening cytopathology, cervical or vaginal (any reporting system), collected in preservative fluid
G0144
- Screening cytopathology, cervical or vaginal (any reporting system), collected in preservative fluid
G0145
- Screening cytopathology, cervical or vaginal (any reporting system), collected in preservative fluid
D0190
- Screening of a patient
H1000
- Prenatal care, at-risk assessment
P3001
- Screening papanicolaou smear, cervical or vaginal, up to three smears, requiring interpretation by p
CPT4 codes
81508
- Fetal congenital abnormalities, biochemical assays of two proteins (PAPP-A, hCG [any form]), utilizi
81512
- Fetal congenital abnormalities, biochemical assays of five analytes (AFP, uE3, total hCG, hyperglyco
81511
- Fetal congenital abnormalities, biochemical assays of four analytes (AFP, uE3, hCG [any form], DIA)
88267
- Chromosome analysis, amniotic fluid or chorionic villus, count 15 cells, 1 karyotype, with banding
0060U
- Twin zygosity, genomic targeted sequence analysis of chromosome 2, using circulating cell-free fetal
81507
- Fetal aneuploidy (trisomy 21, 18, and 13) DNA sequence analysis of selected regions using maternal p
88160
- Cytopathology, smears, any other source; screening and interpretation
88235
- Tissue culture for non-neoplastic disorders; amniotic fluid or chorionic villus cells
81420
- Fetal chromosomal aneuploidy (eg, trisomy 21, monosomy X) genomic sequence analysis panel, circulati
88143
- Cytopathology, cervical or vaginal (any reporting system), collected in preservative fluid, automate