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Maternal care for (suspected) chromosomal abnormality in fetus, fetus 4

ICD10CM code

Similar Codes


ICD10CM codes

O35.1XX4 - Maternal care for (suspected) chromosomal abnormality in fetus, fetus 4
O35.1XX5 - Maternal care for (suspected) chromosomal abnormality in fetus, fetus 5
O35.1XX3 - Maternal care for (suspected) chromosomal abnormality in fetus, fetus 3
O35.1XX2 - Maternal care for (suspected) chromosomal abnormality in fetus, fetus 2
O35.1XX1 - Maternal care for (suspected) chromosomal abnormality in fetus, fetus 1
O35.1 - Maternal care for (suspected) chromosomal abnormality in fetus
O35.9XX4 - Maternal care for (suspected) fetal abnormality and damage, unspecified, fetus 4
O35.8XX4 - Maternal care for other (suspected) fetal abnormality and damage, fetus 4
O35.1XX9 - Maternal care for (suspected) chromosomal abnormality in fetus, other fetus
O35.2XX4 - Maternal care for (suspected) hereditary disease in fetus, fetus 4

HCPCS codes

H1000 - Prenatal care, at-risk assessment
S2260 - Induced abortion, 17 to 24 weeks
Q4151 - Amnioband or guardian, per square centimeter
D9450 - CASE PRESENTATION
D0190 - Screening of a patient
G0204 - Diagnostic mammography, including computer-aided detection (cad) when performed; bilateral
G9618 - Documentation of screening for uterine malignancy or those that had an ultrasound and/or endometrial
S2411 - Fetoscopic laser therapy for treatment of twin-to-twin transfusion syndrome
G9597 - Pediatric patient with minor blunt head trauma not classified as low risk according to the pecarn pr
Q4137 - Amnioexcel, amnioexcel plus or biodexcel, per square centimeter

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)
36460 - Transfusion, intrauterine, fetal
81422 - Fetal chromosomal microdeletion(s) genomic sequence analysis (eg, DiGeorge syndrome, Cri-du-chat syn
99462 - Subsequent hospital care, per day, for evaluation and management of normal newborn
88267 - Chromosome analysis, amniotic fluid or chorionic villus, count 15 cells, 1 karyotype, with banding
59899 - Unlisted procedure, maternity care and delivery
81420 - Fetal chromosomal aneuploidy (eg, trisomy 21, monosomy X) genomic sequence analysis panel, circulati
99460 - Initial hospital or birthing center care, per day, for evaluation and management of normal newborn i