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O35.1XX1
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
CIGNA
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