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Maternal care for (suspected) chromosomal abnormality in fetus, fetus 1

ICD10CM code

Medical Policies and Guidelines for Maternal care for (suspected) chromosomal abnormality in fetus, fetus 1

Related policies from health plans

Genetic Testing for Reproductive Carrier Screening and Prenatal Diagnosis - (0514)

Similar Codes


ICD10CM codes

O35.1XX1 - Maternal care for (suspected) chromosomal abnormality in fetus, fetus 1
O35.1 - Maternal care for (suspected) chromosomal abnormality in fetus
O35.1XX2 - Maternal care for (suspected) chromosomal abnormality in fetus, fetus 2
O35.1XX9 - Maternal care for (suspected) chromosomal abnormality in fetus, other fetus
O35.1XX4 - Maternal care for (suspected) chromosomal abnormality in fetus, fetus 4
O35.1XX3 - Maternal care for (suspected) chromosomal abnormality in fetus, fetus 3
O35.1XX5 - Maternal care for (suspected) chromosomal abnormality in fetus, fetus 5
O35.9XX1 - Maternal care for (suspected) fetal abnormality and damage, unspecified, fetus 1
O35.8XX1 - Maternal care for other (suspected) fetal abnormality and damage, fetus 1
O35.1XX0 - Maternal care for (suspected) chromosomal abnormality in fetus, not applicable or unspecified

HCPCS codes

H1000 - Prenatal care, at-risk assessment
S2260 - Induced abortion, 17 to 24 weeks
D0190 - Screening of a patient
D0191 - Assessment of a patient
G9618 - Documentation of screening for uterine malignancy or those that had an ultrasound and/or endometrial
Q4151 - Amnioband or guardian, per square centimeter
G0101 - Cervical or vaginal cancer screening; pelvic and clinical breast examination
G9597 - Pediatric patient with minor blunt head trauma not classified as low risk according to the pecarn pr
D9450 - CASE PRESENTATION
G8972 - One or more high risk factors for thromboembolism or more than one moderate risk factor for thromboe

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
88267 - Chromosome analysis, amniotic fluid or chorionic villus, count 15 cells, 1 karyotype, with banding
81420 - Fetal chromosomal aneuploidy (eg, trisomy 21, monosomy X) genomic sequence analysis panel, circulati
81511 - Fetal congenital abnormalities, biochemical assays of four analytes (AFP, uE3, hCG [any form], DIA)
81422 - Fetal chromosomal microdeletion(s) genomic sequence analysis (eg, DiGeorge syndrome, Cri-du-chat syn
99460 - Initial hospital or birthing center care, per day, for evaluation and management of normal newborn i
81507 - Fetal aneuploidy (trisomy 21, 18, and 13) DNA sequence analysis of selected regions using maternal p
0060U - Twin zygosity, genomic targeted sequence analysis of chromosome 2, using circulating cell-free fetal
99462 - Subsequent hospital care, per day, for evaluation and management of normal newborn