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O35.2
Maternal care for (suspected) hereditary disease in fetus
ICD10CM code
Similar Codes
ICD10CM codes
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
O35.2XX0
- Maternal care for (suspected) hereditary disease 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
O35.1
- Maternal care for (suspected) chromosomal abnormality in fetus
O35.1XX9
- Maternal care for (suspected) chromosomal abnormality in fetus, other fetus
HCPCS codes
H1000
- Prenatal care, at-risk assessment
S2411
- Fetoscopic laser therapy for treatment of twin-to-twin transfusion syndrome
D0190
- Screening of a patient
S2260
- Induced abortion, 17 to 24 weeks
S9435
- Medical foods for inborn errors of metabolism
G9357
- Post-partum screenings, evaluations and education performed
D1120
- PROPHYLAXIS-CHILD
G9012
- Other specified case management service not elsewhere classified
Q4151
- Amnioband or guardian, per square centimeter
G9842
- Patient has metastatic disease at diagnosis
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
36460
- Transfusion, intrauterine, fetal
81512
- Fetal congenital abnormalities, biochemical assays of five analytes (AFP, uE3, total hCG, hyperglyco
81507
- Fetal aneuploidy (trisomy 21, 18, and 13) DNA sequence analysis of selected regions using maternal p
99462
- Subsequent hospital care, per day, for evaluation and management of normal newborn
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
85460
- Hemoglobin or RBCs, fetal, for fetomaternal hemorrhage; differential lysis (Kleihauer-Betke)
88235
- Tissue culture for non-neoplastic disorders; amniotic fluid or chorionic villus cells