Our pregnancy and prenatal test offerings include tests to determine the risk for heritable genetic disease, screen for and diagnose chromosomal abnormalities, and monitor the health of both fetus and mother throughout pregnancy. We also offer diagnostic testing for at-risk pregnancies through our cytogenetic and molecular genetics labs, as well as testing to determine the underlying cause of infertility or pregnancy loss. Visit ARUP Consult, our free laboratory test selection tool, for educational content about Pregnancy and Prenatal Laboratory Testing.
Carrier Screening
Our carrier screening tests assess the risk for particular disorders in your patients’ offspring, informing reproductive choices. This testing can be performed before or during pregnancy to ensure appropriate intervention and improve outcomes.
When it comes to choosing the right test, you are not alone. Our genetic counselors are available to guide you through the test selection, coordination, and reporting processes.
Learn more about testing recommendations for carrier screening by visiting our ARUP Consult Carrier Screening for Genetic Disorders topic.
Test Number |
Test Name |
3000258 |
Genetic Carrier Screen, (CF, FXS, and SMA) with Reflex to Methylation |
2013661 |
Cystic Fibrosis (CFTR) 165 Pathogenic Variants |
2013436 |
Spinal Muscular Atrophy (SMA) Copy Number Analysis |
2009033 |
Fragile X (FMR1) with Reflex to Methylation Analysis |
0051415 |
Ashkenazi Jewish Diseases, 16 Genes |
0051428 |
Tay-Sachs Disease (HEXA), 7 Variants |
2014680 |
Expanded Carrier Screen by Next Generation Sequencing |
2014677 |
Expanded Carrier Screen by Next Generation Sequencing with Fragile X |
Prenatal Screening and Diagnosis
Routine Prenatal Screening
Routine prenatal screening tests to assess the health of mother and fetus can be performed in-house at your local hospital or sent to ARUP, depending on your needs.
Need help standardizing these tests in your own lab? Our healthcare consultants have extensive experience in developing order sets and analyzing utilization patterns for more efficient, cost-effective care. Click here to learn more.
Prenatal Reflexive Panel and Components
Test Number |
Test Name |
0095044 |
Prenatal Reflexive Panel |
0050471 |
Rapid Plasma Reagin (RPR) with Reflex to Titer |
0050771 |
Rubella Antibody, IgG |
0010014 |
ABO-Rh Prenatal |
0010020 |
Antibody Screen RBC with Reflex to Identification |
2007573 |
Hepatitis B Virus Surface Antigen with Reflex to Confirmation, Prenatal |
Other Routine Tests
Test Number |
Test Name |
2006848 |
Acetylcholinesterase and Fetal Hemoglobin, Amniotic Fluid |
0082024 |
Fetal Fibronectin |
Infectious Disease
Infectious diseases can have serious consequences during pregnancy, and timely diagnosis is critical. We not only offer recommended routine screening tests, but we also offer testing for numerous other diseases that may adversely affect pregnancy outcomes.
Cytomegalovirus
Test Number |
Test Name |
2011813 |
Cytomegalovirus Antibody, IgG Avidity |
0060040 |
Cytomegalovirus by Qualitative PCR |
3005895 |
Cytomegalovirus by Quantitative NAAT, Plasma |
2008555 |
Cytomegalovirus by Qualitative PCR, Saliva |
0065004 |
Cytomegalovirus Rapid Culture |
Group B Streptococcus
Test Number |
Test Name |
0060705 |
Streptococcus Group B by PCR |
Hepatitis B Virus
Test Number |
Test Name |
2007573 |
Hepatitis B Virus Surface Antigen with Reflex to Confirmation, Prenatal |
2007575 |
Hepatitis B Virus Surface Antigen Confirmation, Prenatal |
Parvovirus
Test Number |
Test Name |
0060043 |
Parvovirus B19 by Qualitative PCR |
Toxoplasmosis
Test Number |
Test Name |
0050557 |
Toxoplasma gondii Antibody, IgM |
0050770 |
Toxoplasma gondii Antibody, IgG |
0050521 |
Toxoplasma gondii Antibodies, IgG and IgM |
0055591 |
Toxoplasma gondii by PCR |
Chromosomal Abnormalities and Neural Tube Defects
Prenatal testing includes both screening and diagnostic testing. A number of factors are involved in selecting the most appropriate prenatal test. Refer to our First and Second Trimester Maternal Serum Screening Options table for helpful information.
For more information about testing recommendations, see the ARUP Consult Prenatal Screening and Diagnosis for Chromosomal Abnormalities and Neural Tube Defects topic.
Screening: Maternal Serum
Test Number |
Test Name |
3000143 |
Maternal Serum Screen, Alpha Fetoprotein, hCG, Estriol, and Inhibin A (Quad) |
3000144 |
Maternal Serum Screen, Alpha Fetoprotein |
3000145 |
Maternal Serum Screen, First Trimester, hCG, PAPP-A, NT |
3000146 |
Maternal Screening, Sequential, Specimen #1, hCG, PAPP-A, NT |
3000147 |
Maternal Serum Screening, Integrated, Specimen #1, PAPP-A, NT |
3000148 |
Maternal Screening, Sequential, Specimen #2, Alpha Fetoprotein, hCG, Estriol, and Inhibin A |
3000149 |
Maternal Serum Screening, Integrated, Specimen #2, Alpha Fetoprotein, hCG, Estriol, and Inhibin A |
0070051 |
Estriol, Serum |
Screening: Non-Invasive Prenatal Testing (NIPT)
Test Number |
Test Name |
3003043 |
Non-Invasive Prenatal Aneuploidy Screen by Cell-Free DNA Sequencing |
Diagnosis
Test Number |
Test Name |
2002293 |
Chromosome Analysis, Amniotic Fluid |
2008367 |
Chromosome Analysis, Amniotic Fluid, with Reflex to Genomic Microarray |
2011130 |
Chromosome FISH, Amniotic Fluid with Reflex to Chromosome Analysis or Genomic Microarray |
2002291 |
Chromosome Analysis, Chorionic Villus |
2011131 |
Chromosome FISH, Chorionic Villus with Reflex to Chromosome Analysis or Genomic Microarray |
0040203 |
Chorionic Villus, FISH [13, 18, 21, X, and Y—CVS] |
2002297 |
Chromosome FISH, Prenatal [13, 18, 21, X, and Y—Amniotic Fluid] |
2002366 |
Cytogenomic SNP Microarray - Fetal |
Hematologic Conditions
Many serious hematologic disorders, including hemolytic disease of the fetus and newborn and hemolytic anemias, may affect the fetus during development and after birth. Laboratory testing for these conditions includes routine blood work, as well as specialized testing for red blood cell antigens.
Free educational resources to aid in test selection are available through ARUP Consult. See the ARUP Consult Hemolytic Disease of the Fetus and Newborn and Hemolytic Anemias topics for more information.
Test Number |
Test Name |
2001743 |
Fetal Hemoglobin Determination for Fetomaternal Hemorrhage |
3002003 |
RhE/e (RHCE) Antigen Genotyping |
3002002 |
RhC/c (RHCE) Antigen Genotyping |
0051368 |
RhD Gene (RHD) Copy Number |
3002001 |
Kell K/k (KEL) Antigen Genotyping |
3000193 |
Platelet Antigen Genotyping Panel |
3001053 |
Red Blood Cell Antigen Genotyping |
2005792 |
Hemoglobin Evaluation Reflexive Cascade |
Pregnancy Loss and Infertility
Laboratory testing for pregnancy loss and infertility may help affected couples make reproductive choices. ARUP offers genetic testing for pregnancy loss, as well as a variety of tests to evaluate the underlying cause of infertility.
Learn more about testing recommendations for infertility by visiting the ARUP Consult Infertility topic.
Pregnancy Loss
Test Number |
Test Name |
2002288 |
Chromosome Analysis, Products of Conception |
2005762 |
Chromosome Analysis, Products of Conception, with Reflex to Genomic Microarray |
2005633 |
Genomic SNP Microarray, Products of Conception |
3004273 |
Cytogenomic Molecular Inversion Probe Array FFPE Tissue - Products of Conception |
Infertility
Test Number |
Test Name |
2008509 |
Progesterone Quantitative by HPLC-MS/MS, Serum or Plasma |
0092332 |
17-Hydroxyprogesterone Quantitative by HPLC-MS/MS, Serum or Plasma |
2002656 |
Anti-Mullerian Hormone |
0070055 |
Follicle Stimulating Hormone, Serum |
0070045 |
Estradiol, Adult Premenopausal Female, Serum or Plasma |
0070115 |
Prolactin |
0020765 |
Macroprolactin |
2006108 |
Thyroid Stimulating Hormone with reflex to Free Thyroxine |
0081059 |
Testosterone, Free (Adult Females, Children, or Individuals on Testosterone-Suppressing Hormone Therapy) |
0070193 |
Luteinizing Hormone and Follicle Stimulating Hormone |