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O35.1XX3
Maternal care for (suspected) chromosomal abnormality in fetus, fetus 3
ICD10CM code
Similar Codes
ICD10CM codes
O35.1XX3
- Maternal care for (suspected) chromosomal abnormality in fetus, fetus 3
O35.1XX4
- Maternal care for (suspected) chromosomal abnormality in fetus, fetus 4
O35.1XX2
- Maternal care for (suspected) chromosomal abnormality in fetus, fetus 2
O35.1XX5
- Maternal care for (suspected) chromosomal abnormality in fetus, fetus 5
O35.1XX1
- Maternal care for (suspected) chromosomal abnormality in fetus, fetus 1
O35.9XX3
- Maternal care for (suspected) fetal abnormality and damage, unspecified, fetus 3
O35.1
- Maternal care for (suspected) chromosomal abnormality in fetus
O35.8XX3
- Maternal care for other (suspected) fetal abnormality and damage, fetus 3
O35.1XX9
- Maternal care for (suspected) chromosomal abnormality in fetus, other fetus
O35.2XX3
- Maternal care for (suspected) hereditary disease in fetus, fetus 3
HCPCS codes
H1000
- Prenatal care, at-risk assessment
S2260
- Induced abortion, 17 to 24 weeks
D0190
- Screening of a patient
G9618
- Documentation of screening for uterine malignancy or those that had an ultrasound and/or endometrial
G9597
- Pediatric patient with minor blunt head trauma not classified as low risk according to the pecarn pr
G9593
- Pediatric patient with minor blunt head trauma classified as low risk according to the pecarn predic
D9450
- CASE PRESENTATION
D0191
- Assessment of a patient
Q4151
- Amnioband or guardian, per square centimeter
G8806
- Performance of trans-abdominal or trans-vaginal ultrasound and pregnancy location documented
CPT4 codes
81512
- Fetal congenital abnormalities, biochemical assays of five analytes (AFP, uE3, total hCG, hyperglyco
81508
- Fetal congenital abnormalities, biochemical assays of two proteins (PAPP-A, hCG [any form]), utilizi
81420
- Fetal chromosomal aneuploidy (eg, trisomy 21, monosomy X) genomic sequence analysis panel, circulati
81507
- Fetal aneuploidy (trisomy 21, 18, and 13) DNA sequence analysis of selected regions using maternal p
81511
- Fetal congenital abnormalities, biochemical assays of four analytes (AFP, uE3, hCG [any form], DIA)
0060U
- Twin zygosity, genomic targeted sequence analysis of chromosome 2, using circulating cell-free fetal
88267
- Chromosome analysis, amniotic fluid or chorionic villus, count 15 cells, 1 karyotype, with banding
36460
- Transfusion, intrauterine, fetal
81422
- Fetal chromosomal microdeletion(s) genomic sequence analysis (eg, DiGeorge syndrome, Cri-du-chat syn
0503F
- Postpartum care visit (Prenatal)