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Search all medical codes
O35.2XX0
Maternal care for (suspected) hereditary disease in fetus, not applicable or unspecified
ICD10CM code
Medical Policies and Guidelines for Maternal care for (suspected) hereditary disease in fetus, not applicable or unspecified
Related policies from health plans
ANTHEM-BLUECROSS-CA
Chromosomal Microarray Analysis (CMA) for Development Delay, Autism Spectrum
CIGNA
Genetic Testing for Reproductive Carrier Screening and Prenatal Diagnosis - (0514)
ANTHEM-BLUECROSS-CT
CG-GENE-10 Chromosomal Microarray Analysis (CMA) for Developmental Delay, Autism Spectrum Disorder, Intellectual Disability and Congenital Anomalies
Similar Codes
ICD10CM codes
O35.2XX0
- Maternal care for (suspected) hereditary disease in fetus, not applicable or unspecified
O35.2
- Maternal care for (suspected) hereditary disease in fetus
O35.2XX9
- Maternal care for (suspected) hereditary disease in fetus, other fetus
O35.2XX1
- Maternal care for (suspected) hereditary disease in fetus, fetus 1
O35.2XX2
- Maternal care for (suspected) hereditary disease in fetus, fetus 2
O35.2XX4
- Maternal care for (suspected) hereditary disease in fetus, fetus 4
O35.1XX0
- Maternal care for (suspected) chromosomal abnormality in fetus, not applicable or unspecified
O35.2XX3
- Maternal care for (suspected) hereditary disease in fetus, fetus 3
O35.2XX5
- Maternal care for (suspected) hereditary disease in fetus, fetus 5
O35.8XX0
- Maternal care for other (suspected) fetal abnormality and damage, not applicable or unspecified
HCPCS codes
H1000
- Prenatal care, at-risk assessment
G9012
- Other specified case management service not elsewhere classified
G9918
- Functional status not performed, reason not otherwise specified
G9597
- Pediatric patient with minor blunt head trauma not classified as low risk according to the pecarn pr
C1889
- Implantable/insertable device, not otherwise classified
S2260
- Induced abortion, 17 to 24 weeks
G9925
- Safety concerns screening not provided, reason not otherwise specified
D0190
- Screening of a patient
G8972
- One or more high risk factors for thromboembolism or more than one moderate risk factor for thromboe
S9435
- Medical foods for inborn errors of metabolism
CPT4 codes
81508
- Fetal congenital abnormalities, biochemical assays of two proteins (PAPP-A, hCG [any form]), utilizi
0060U
- Twin zygosity, genomic targeted sequence analysis of chromosome 2, using circulating cell-free fetal
59899
- Unlisted procedure, maternity care and delivery
36460
- Transfusion, intrauterine, fetal
88235
- Tissue culture for non-neoplastic disorders; amniotic fluid or chorionic villus cells
81425
- Genome (eg, unexplained constitutional or heritable disorder or syndrome); sequence analysis
81512
- Fetal congenital abnormalities, biochemical assays of five analytes (AFP, uE3, total hCG, hyperglyco
0502F
- Subsequent prenatal care visit (Prenatal) [Excludes: patients who are seen for a condition unrelated
99462
- Subsequent hospital care, per day, for evaluation and management of normal newborn
59100
- Hysterotomy, abdominal (eg, for hydatidiform mole, abortion)
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