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O35.2XX2
Maternal care for (suspected) hereditary disease in fetus, fetus 2
ICD10CM code
Medical Policies and Guidelines for Maternal care for (suspected) hereditary disease in fetus, fetus 2
Related policies from health plans
CIGNA
Genetic Testing for Reproductive Carrier Screening and Prenatal Diagnosis - (0514)
Similar Codes
ICD10CM codes
O35.2XX2
- Maternal care for (suspected) hereditary disease in fetus, fetus 2
O35.2XX1
- Maternal care for (suspected) hereditary disease in fetus, fetus 1
O35.2XX3
- Maternal care for (suspected) hereditary disease in fetus, fetus 3
O35.2XX4
- Maternal care for (suspected) hereditary disease in fetus, fetus 4
O35.2XX5
- Maternal care for (suspected) hereditary disease in fetus, fetus 5
O35.2
- Maternal care for (suspected) hereditary disease in fetus
O35.2XX9
- Maternal care for (suspected) hereditary disease in fetus, other fetus
O35.1XX2
- Maternal care for (suspected) chromosomal abnormality in fetus, fetus 2
O35.2XX0
- Maternal care for (suspected) hereditary disease in fetus, not applicable or unspecified
O35.8XX2
- Maternal care for other (suspected) fetal abnormality and damage, fetus 2
HCPCS codes
H1000
- Prenatal care, at-risk assessment
S2260
- Induced abortion, 17 to 24 weeks
S2411
- Fetoscopic laser therapy for treatment of twin-to-twin transfusion syndrome
G9012
- Other specified case management service not elsewhere classified
D1120
- PROPHYLAXIS-CHILD
G8972
- One or more high risk factors for thromboembolism or more than one moderate risk factor for thromboe
D0190
- Screening of a patient
G9357
- Post-partum screenings, evaluations and education performed
A0433
- Advanced life support, level 2 (als 2)
S9435
- Medical foods for inborn errors of metabolism
CPT4 codes
0060U
- Twin zygosity, genomic targeted sequence analysis of chromosome 2, using circulating cell-free fetal
81508
- Fetal congenital abnormalities, biochemical assays of two proteins (PAPP-A, hCG [any form]), utilizi
36460
- Transfusion, intrauterine, fetal
99462
- Subsequent hospital care, per day, for evaluation and management of normal newborn
81512
- Fetal congenital abnormalities, biochemical assays of five analytes (AFP, uE3, total hCG, hyperglyco
99460
- Initial hospital or birthing center care, per day, for evaluation and management of normal newborn i
0502F
- Subsequent prenatal care visit (Prenatal) [Excludes: patients who are seen for a condition unrelated
88235
- Tissue culture for non-neoplastic disorders; amniotic fluid or chorionic villus cells
81507
- Fetal aneuploidy (trisomy 21, 18, and 13) DNA sequence analysis of selected regions using maternal p
85460
- Hemoglobin or RBCs, fetal, for fetomaternal hemorrhage; differential lysis (Kleihauer-Betke)