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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