For Endocrinologists · cleared or approved by the U.S. Food and Drug Administration. The FDA has...
Transcript of For Endocrinologists · cleared or approved by the U.S. Food and Drug Administration. The FDA has...
Endocrinology Test List
For Endocrinologists
Endocrinology Test List
Extensive CapabilitiesManaging patients with endocrine disorders is complex. Having access to the right test for the right patient is key. With a legacy of expertise in endocrine laboratory diagnostics, Quest Diagnostics offers an extensive menu of laboratory tests across the spectrum of endocrine disorders.
This test list highlights the extensive menu of laboratory diagnostic tests we offer, including highly specialized tests and those performed using highly specific and sensitive mass spectrometry detection. It is conveniently organized by glandular function or common endocrine disorder, making it easy for you to identify the tests you need to care for the patients you treat.
Abbreviations and FootnotesNDM, neonatal diabetes mellitus; MODY, maturity-onset diabetes of the young; CH, congenital hyperinsulinism; MSUD, maple syrup urine disease; IHH, idiopathic hypogonadotropic hypogonadism; BBS, Bardet-Biedl syndrome; OI, osteogenesis imperfecta; PKD, polycystic kidney disease; OPPG, osteoporosis-pseudoglioma syndrome; CPHD, combined pituitary hormone deficiency; GHD, growth hormone deficiency.
The tests highlighted in green are performed using highly specific and sensitive mass spectrometry detection. Panels that include a test(s) performed using mass spectrometry are highlighted in yellow. For tests highlighted in blue, refer to the Athena Diagnostics website (athenadiagnostics.com/content/test-catalog) for test information. These tests are performed by Athena Diagnostics.
† Multiple test codes are available. Refer to the Quest Diagnostics Nichols Institute Directory of Services or the online Test Center (QuestDiagnostics.com) for test information.
1 This test was developed and its performance characteristics have been determined by Quest Diagnostics Nichols Institute. Performance characteristics refer to the analytical performance of the test.
2 This test was developed and its performance characteristics have been determined by Athena Diagnostics. Performance characteristics refer to the analytical performance of the test.
3 This test was developed and its performance characteristics have been determined by Quest Diagnostics Nichols Institute. It has not been cleared or approved by the U.S. Food and Drug Administration. The FDA has determined that such clearance or approval is not necessary. Performance characteristics refer to the analytical performance of the test.
4 This test was performed using a kit that has not been cleared or approved by the FDA. The analytical performance characteristics of this test have been determined by Quest Diagnostics Nichols Institute. This test should not be used for diagnosis without confirmation by other medically established means.
Reflex tests are performed at an additional charge.
The following tests that are included in panels may be ordered separately: albumin, alkaline phosphatase, ALT, AST, bilirubin (direct and total), creatinine (serum and urine), electrolyte panel, hemoglobin, hepatic function panel, iron, phosphate, potassium, and total protein.
Comprehensive CareQuest Diagnostics Nichols Institute has been pioneering state-of-the-art endocrine testing for over four decades. Our commitment to innovative diagnostics and our dedication to quality and service means we deliver solutions that enable you to make informed clinical decisions for comprehensive patient management. We strive to remain at the forefront of innovation in endocrine testing so you can deliver the highest level of patient care.
Adrenal Medullary Function/Catecholamines
39627(X) Catecholamines, Fractionated, 24-Hour Urine
314(X) Catecholamines, Fractionated, Plasma
5244 Catecholamines, Fractionated, Random Urine
16381 Catecholamines, Fractionated, Supine, Plasma
16382 Catecholamines, Fractionated, Upright, Plasma
39626(X) Catecholamines, Fractionated, and VMA, 24-Hour Urine
16379 Chromogranin A, Electrochemiluminescence1
39527(X) Homovanillic Acid, 24-Hour Urine
6346 Homovanillic Acid, Random Urine
19548 Metanephrines, Fractionated, Free, LC/MS/MS, Plasma
14962(X) Metanephrines, Fractionated, LC/MS/MS, 24-Hour Urine
14961(X) Metanephrines, Fractionated, LC/MS/MS, Random Urine
889 Pheochromocytoma Evaluation2
Detects mutations in RET, SDHB, and VHL.
39517(X) VMA (Vanillylmandelic Acid), 24-Hour Urine
1710 VMA (Vanillylmandelic Acid), Random Urine
Adrenocortical Function See below for congenital adrenal hyperplasia.
815 ABCD1 (Adrenoleukodystrophy) DNA Sequencing Test2
211 ACTH, Plasma
4645 Adrenal Antibody Screen with Reflex to Titer
19552(X) 229 Aldosterone, 24-Hour Urine
17181 Aldosterone, LC/MS/MS
† Aldosterone/Cortisol Ratio
† Aldosterone/Cortisol Ratio, Adrenal Vein Sampling
16845 Aldosterone/Plasma Renin Activity Ratio, LC/MS/MS
5276(X) 3α-Androstanediol Glucuronide (3-Alpha Diol G)
17182 Androstenedione, LC/MS/MS
6547(X) Corticosterone, LC/MS/MS
37371 Cortisol Binding Globulin (Transcortin)
37355(X) Cortisol, Free and Cortisone, 24-Hour Urine
37077(X) Cortisol, Free and Total, LC/MS/MS
36423(X) Cortisol, Free, LC/MS/MS
11280(X) Cortisol, Free, LC/MS/MS, 24-Hour Urine
90582 Cortisol, Free, LC/MS/MS, Second Void Urine
19897(X) Cortisol, LC/MS/MS, Saliva
11281(X) Cortisol, Total, LC/MS/MS
37554(X) Cortisone, 24-Hour Urine
37098(X) Cortisone, Serum3
90973 Deoxycorticosterone
30543 11-Deoxycortisol, LC/MS/MS, Serum
29391(X) Dexamethasone
19894 DHEA (Dehydroepiandrosterone), Unconjugated, LC/MS/MS
38954 DHEA (Dehydroepiandrosterone), Urine
402 DHEA Sulfate
36168 Dihydrotestosterone, Free, Serum1
90567 Dihydrotestosterone, LC/MS/MS1
36707(X) Hirsutism Panel 2Includes androstenedione, DHEA sulfate, and free and total testosterone.
15202 17-Hydroxycorticosteroids with Creatinine, 24-Hour Urine
11178(X) 18-Hydroxycortisol, Free, 24-Hour Urine
38071(X) 6 Beta-Hydroxycortisol, 24-Hour Urine
37916(X) 21-Hydroxylase Antibody
8352 17-Hydroxypregnenolone, LC/MS/MS
17180 17-Hydroxyprogesterone, LC/MS/MS
17654(X) 17-Hydroxyprogesterone, Neonatal/Infant
15201(X) 17-Ketosteroids with Creatinine, 24-Hour Urine
70184(X) 17-Ketosteroids, Fractionated, Pediatrics, Urine
4932(X) 17-Ketosteroids, Fractionated, Urine
814 NR0B1 (Adrenal Hypoplasia Congenita) DNA Sequencing Test2
16846 Plasma Renin Activity, LC/MS/MS
738 Pregnanetriol, Urine
31493(X) Pregnenolone, LC/MS/MS
816Primary Adrenal Insufficiency Evaluation2 Detects mutations (including point mutations, deletions, insertions, and rearrangements) in ABCD1, AIRE, and NR0B1.
17183 Progesterone, LC/MS/MS
30740 Sex Hormone Binding Globulin
14966 Testosterone, Free, Bioavailable, and Total, LC/MS/MS
36170 Testosterone, Free (Dialysis) and Total (LC/MS/MS)
37073 Testosterone, Total and Free and Sex Hormone Binding Globulin
15983 Testosterone, Total, LC/MS/MS
39613(X) Tetrahydroaldosterone, Urine
8181 Hemoglobin A1c with Calculated Mean Plasma Glucose (MPG)
16802 Hemoglobin A1c with eAG
16715 Hemoglobin A1c with Reflex to GlycoMark®
802 HNF4A (MODY1) DNA Sequencing and Deletion Test2
37054(Z) β-Hydroxybutyrate
36177(X) IA-2 Antibody
36590 IGF Binding Protein-1 (IGFBP-1)1
853 INS (NDM) DNA Sequencing Test2
561 Insulin
36178 Insulin Autoantibody
36700 Insulin, Free (Bioactive)
91083 Insulin, LC/MS/MS
834 IPF1 (MODY4) DNA Sequencing Test2
841 IPF1 (NDM) DNA Sequencing Test2
36741 Islet Cell Antibody Screen with Reflex to Titer2
843 KCNJ11 (NDM) DNA Sequencing Test2
91398Metabolic Syndrome and Glucose Control Including InsulinIncludes cholesterol, total and HDL; glucose; insulin, LC/MS/MS; triglycerides; and calculated components.
15281 Microalbumin, 24-Hour Urine (with Creatinine)
4555 Microalbumin, 24-Hour Urine (without Creatinine)
6517 Microalbumin, Random Urine (with Creatinine)
17674 Microalbumin, Random Urine (without Creatinine)
885Monogenic Diabetes (MODY) Evaluation2
Includes sequencing and deletion detection in GCK, HNF4A, TCF1, and TCF2 and sequencing of IPF1.
882 Neonatal Diabetes Mellitus Evaluation2
Detects mutations in ABCC8, GCK, INS, IPF1, and KCNJ11.
678 Osmolality, Random Urine
677 Osmolality, Serum
760(X) Proinsulin4
34480 Somatostatin1
804 TCF1 (MODY3) DNA Sequencing and Deletion Test2
805 TCF2 (MODY5) DNA Sequencing and Deletion Test2
Dynamic Testing
17832(X) Aldosterone, Response to ACTH Stimulation, LC/MS/MS
19511(X) Androstenedione Response to ACTH Stimulation, LC/MS/MS
10068(X) Catecholamines, Total, Suppression by Clonidine, Plasma
16434 Cortisol, Free, Response to ACTH Stimulation
38149(X) Cortisol Response to ACTH Stimulation, Serum
† C-Peptide Response to Glucose
14747(X) C-Peptide Stimulation by Glucagon
† Growth Hormone, Multiple Specimens
17682(X) 17-Hydroxyprogesterone Response to ACTH Stimulation
† Insulin Response to Glucose
† Proinsulin Response to Glucose4
Endocrine Autoimmunity
4645 Adrenal Antibody with Reflex to Titer
812Autoimmune Polyglandular Syndrome (AIRE) Evaluation2
Detects point mutations, deletions, insertions, and rearrangements in AIRE.
15114 Gastric Parietal Cell Antibody, ELISA
34878 Glutamic Acid Decarboxylase-65 Antibody
37072(X) Growth Hormone Antibody3
37916(X) 21-Hydroxylase Antibody
36177(X) IA-2 Antibody
36178 Insulin Autoantibody
36741 Islet Cell Antibody Screen with Reflex to Titer3
36578 PTH Antibody1
36574 T3 (Triiodothyronine) Antibody1
36576 T4 (Thyroxine) Antibody1
5738 TBII (Thyrotropin-Binding Inhibitory Immunoglobulin)
267 Thyroglobulin Antibody
7260(X) Thyroid Peroxidase and Thyroglobulin Antibodies
5081 Thyroid Peroxidase Antibody (Anti-TPO)
36577 TSH Antibody1
30551 TSI (Thyroid Stimulating Immunoglobulin)
Endocrine Genetics
827 ABCC8 (CH) DNA Sequence Test2
815 ABCD1 (Adrenoleukodystrophy) DNA Sequencing Test2
711 ACTN4 DNA Sequencing Test2
14531 Acylcarnitine, Plasma
29881 Amino Acid Analysis, LC/MS, CSF
767(X) Amino Acid Analysis, LC/MS, Plasma
36183 Amino Acid Analysis, LC/MS, Urine
19779(X) Amino Acid Analysis for MSUD, LC/MS, Plasma
Test Code Test Name
Congenital Adrenal Hyperplasia (CAH)
14755(X) CAH (21-Hydroxylase Deficiency) Common Mutations1
Detects 11 CYP21A2 gene mutations and the 30kb deletion.
16072(X) CAH (21-Hydroxylase Deficiency) Rare Mutations1
Includes sequencing of the entire CYP21A2 gene.
15269(X)CAH Panel 1 (21-OH vs 11-βOH)Includes 17-hydroxyprogesterone/11-deoxycortisol ratio, 11-deoxycortisol/cortisol ratio, androstenedione, and total testosterone.
15273(X)CAH Panel 3 (aldosterone synthase deficiency)Includes 17-OH progesterone/11-deoxycortisol ratio, and 18-hydroxycorticosterone/aldosterone ratio.
15274(X)CAH Panel 4 (17-OH deficiency in females)Includes progesterone/17-hydroxyprogesterone ratio, corticosterone, cortisol, aldosterone, and estradiol.
15276(X) CAH Panel 6 (StAR deficiency)Includes cortisol, pregnenolone, DHEA, and aldosterone.
16978CAH Panel 6C (Full Screen)Includes androstenedione, cortisol, 11-deoxycortisol, DHEA, 17-hydroxypregnenolone, 17-hydroxyprogesterone, progesterone, and total testosterone.
15277(X) CAH Panel 7 (steroid replacement therapy monitoring)Includes androstenedione, total testosterone, 17-hydroxyprogesterone.
15279(X)CAH Panel 8 (17-OH deficiency in males)Includes progesterone/17-hydroxyprogesterone ratio, corticosterone, cortisol, aldosterone, and total testosterone.
15280(X)CAH Panel 9 (3β-HSD deficiency)Includes 17-hydroxypregnenolone/17-hydroxyprogesterone ratio, DHEA/androstenedione ratio, and cortisol.
10046(X)
CAH Panel 11, Neonatal Random UrineIncludes 17-OH pregnanolone; 15, 17-(OH)2-pregnanolone; 16-OH DHEA; pregnanetriol; tetrahydro 11-deoxycortisol; pregnanetriolone; 16-OH pregnenolone; pregnenetriol; tetrahydrocortisone; 6-OH tetrahydro 11-deoxycortisol; tetrahydro 11-dehydrocorticosterone; A-cortolone; B-cortolone; and 6-OH tetrahydro 11-dehydrocorticosterone.
879Congenital Adrenal Hyperplasia (CAH) Evaluation2
Includes sequencing and deletion detection in CYP21A2 and sequencing of CYP11B1.
875 CYP11B1 (CAH) DNA Sequencing Test2
877 CYP17A1 DNA Sequencing Test2
880CYP21A2 (CAH) DNA Evaluation2
Includes sequencing of the entire CYP21A2 gene, as well as detection of the common 30kb deletion.
30543 11-Deoxycortisol, LC/MS/MS, Serum
878 HSD3B2 DNA Sequencing Test2
17180 17-Hydroxyprogesterone, LC/MS/MS
17654(X) 17-Hydroxyprogesterone, Neonatal/Infant
874Lipoid CAH (StAR) Evaluation2
Detects mutations (including point mutations, deletions, insertions, and rearrangements) in StAR.
738 Pregnanetriol, Urine
90397Steroid Panel, 21-Hydroxylase Deficiency/ Stress DifferentiationIncludes 17-hydroxyprogesterone, androstenedione, and cortisol.
90392
Steroid Panel, ComprehensiveIncludes androstenedione, corticosterone, cortisol, cortisone, deoxycorticosterone, 11-deoxycortisol, DHEA, 18-hydroxycorticosterone, 17-hydroxypregnenolone, 17-hydroxyprogesterone, pregnenolone, progesterone, and total testosterone.
90398Steroid Panel, Congenital Adrenal Hyperplasia (CAH)Includes androstenedione, cortisol, deoxycorticosterone, 11-deoxycortisol, DHEA, 17-hydroxypregnenolone, 17-hydroxyprogesterone, progesterone, and total testosterone.
90426Steroid Panel, PCOS/CAH DifferentiationIncludes androstenedione, 11-deoxycortisol, DHEA, 17-hydroxyprogesterone, and free and total testosterone.
Diabetes Mellitus, Types 1 and 2
876 ABCC8 (NDM) DNA Sequencing Test2
15060(X) Adiponectin4
837 CEL (MODY8) Mutation Analysis2
372 C-Peptide
4643(X) C-Peptide, 24-Hour Urine
91713(X)
Diabetes, Advancing Chronic Kidney Disease Management PanelIncludes electrolyte panel; microalbumin, random urine with creatinine; creatinine, serum; hemoglobin; PTH, intact and calcium; phosphate (as phosphorus); QuestAssureD™ 25-hydroxyvitamin D (D2, D3), LC/MS/MS.
91712(X)Diabetes, Newly Diagnosed and Monitoring PanelIncludes glucose; hemoglobin A1c; lipid panel; hepatic function panel; microalbumin, random urine with creatinine; creatinine, serum.
91920Diabetes Risk Assessment Panel Includes lipid panel (cholesterol, HDL, cholesterol/HDL ratio, LDL-calculated, and triglycerides) with reflex to direct LDL, glucose, and hemoglobin A1c.
8340 Fructosamine
10584(X) GAD65, IA-2, and Insulin Autoantibody
803 GCK (MODY2) DNA Sequencing and Deletion Test2
842 GCK (NDM) DNA Sequencing Test2
519 Glucagon1
† Glucose
34878 Glutamic Acid Decarboxylase-65 Antibody
5032(X) Glycated Albumin
29488(X) Glycohemoglobin, Total
19599 GlycoMark®
496 Hemoglobin A1c
Quest Diagnostics – Endocrinology Test List
Liquid Chromatography Tandem Mass Spectrometry (LC/MS/MS) Athena Diagnostics test Panel includes LC/MS/MS test(s)
462Anosmic Kallmann/IHH Evaluation2
Detects mutations in FGF8, FGFR1, GnRHR, KAL1, KISS1R, PROK2, and PROKR2.
893 ApoB Mutation Analysis2
852 AQP2 (Nephrogenic Diabetes Insipidus) DNA Sequencing Test2
812Autoimmune Polyglandular Syndrome (AIRE) Evaluation2
Detects point mutations, deletions, insertions, and rearrangements in AIRE.
887 Bardet-Biedl Syndrome Evaluation2
Detects mutations in BBS1, BBS2, and BBS10.
871 BBS1 (BBS) DNA Sequencing Test2
872 BBS2 (BBS) DNA Sequencing Test2
886 BBS10 (BBS) DNA Sequencing Test2
14755(X) CAH (21-Hydroxylase Deficiency) Common Mutations1
Detects 11 CYP21A2 gene mutations and the 30kb deletion.
16072(X) CAH (21-Hydroxylase Deficiency) Rare Mutations1
Includes sequencing of the entire CYP21A2 gene.
90649 Cardio IQ™ ApoE Genotype1
70107(X) Carnitine, LC/MS/MS
15948(X) Carnitine, LC/MS/MS and Acylcarnitine
825 CASR DNA Sequencing Test2
461 CHD7 DNA Sequencing Test2
16478 Chromosomal Microarray, Postnatal, ClariSure® Oligo-SNP1
14596(X) Chromosome Analysis, Blood
14595(X) Chromosome Analysis, High Resolution
14597(X) Chromosome Analysis, Mosaicism
16843 Chromosome Analysis, Neonatal Blood
14593(X) Chromosome Analysis, Tissue
861 COL1A1 (OI) DNA Sequencing Test2
862 COL1A2 (OI) DNA Sequencing Test2
865 Combined Pituitary Hormone Deficiency Evaluation2
Detects mutations in POU1F1 and PROP1.
679Complete Kallmann/IHH Evaluation2
Detects mutations in CHD7, FGF8, FGFR1, GnRHR, GnRH1, KAL1, KISS1R, PROK2, PROKR2, and TACR3.
761 Complete PKD Evaluation2
Detects mutations and deletions in PKD1 and PKD2.
774 CYP11B1 DNA Sequencing Test2
779 CYP11B1/2 DNA Chimeric Gene Fusion Test2
880CYP21A2 (CAH) DNA Evaluation2
Includes sequencing of the entire CYP21A2 gene, as well as detection of the common 30kb deletion.
10917(X) Cystic Fibrosis Complete Rare Mutation Analysis, Entire Gene Sequence1
16080(X) Cystic Fibrosis Gene Deletion or Duplication3
10913(X) Cystic Fibrosis Rare Mutation Analysis, One Exon3
10915(X) Cystic Fibrosis Rare Mutation Analysis, Two Exon3
10458(X) Cystic Fibrosis Screen1
10947(X) Cystine, 24-Hour Urine
401(X) Cystine, Quantitative, Random Urine
884 Early Onset Obesity Evaluation2
Detects mutations in LEPR and MC4R.
883 Early Onset Obesity (LEPR) DNA Sequencing Test2
640 Early Onset Obesity (MC4R) DNA Sequencing Test2
Detects mutations in MC4R.
881 Endocrine Hypertension (HSD11B2) Evaluation
829 Familial Hypocalciuric Hypercalcemia (CASR) DNA Sequencing Test
195 FGF8 DNA Sequencing Test2
856 FGF23 (Hypophosphatemic Rickets) DNA Sequencing Test2
196 FGFR1 DNA Sequencing Test2
14608(X) FISH, Angelman3
37343(X) FISH, Chromosome-Specific Probe (specify probe & chromosome number)3
14610(X) FISH, DiGeorge, Velocardiofacial (VCFS)3
14615(X) FISH, Kallmann3
36053 FISH, Neonatal Screen3
14605(X) FISH, Prader Willi3
14606(X) FISH, SRY/X Centromere3
14609(X) FISH, Williams3
14613(X) FISH, Wolf-Hirschhorn3
14607(X) FISH, X-Linked Ichthyosis Steroid Sulfatase Deficiency3
823 GCK (CH) DNA Sequencing Test2
866 GH1 (GHD) DNA Sequencing Test2
867 GHR DNA Sequencing Test2
868 GHRHR (GHD) DNA Sequencing Test2
822 GLUD1 (CH) DNA Sequencing Test2
90915 Glycogen Storage Disease Type 1a Mutation Analysis (Ashkenazi Jewish)3
343 GnRH1 DNA Sequencing Test2
279 GnRHR DNA Sequencing Test2
848Growth Hormone Deficiency Evaluation2
Includes sequencing and deletion detection in SHOX and sequencing of GH1 and GHRHR.
775 HSD11B2 DNA Sequencing Test2
895 Hypercholesterolemia Evaluation2
Detects mutations in LDLR and disease-associated regions of ApoB.
857 Hypophosphatemic Rickets Evaluation2
Detects mutations in FGF23 and PHEX2.
716 INF2 (FSGS) DNA Sequencing Test2
717Inherited Focal and Segmental Glomerulosclerosis (FSGS) Evaluation2
Detects mutations in ACTN4, INF2, NPHS2, and TRPC6.
173 KAL1 DNA Sequencing Test2
826 KCNJ11 (CH) DNA Sequencing Test2
364 KISS1R DNA Sequencing Test2
664 KRAS DNA Sequencing Test2
658 KRAS/RAF1/SOS1 DNA Sequencing Evaluation2
714 LAMB2 DNA Sequencing Test2
894 LDLR (Hypercholesterolemia) DNA Sequencing Test2
747 Liddle's Syndrome Evaluation2
Detects mutations in SCNN1B and SCNN1G.
821 LRP5 Idiopathic Osteoporosis (IOP) DNA Sequencing Test2
811 LRP5 (OPPG) DNA Sequencing Test2
17625(X) Male Infertility Genetic Analysis
817 Male Precocious Puberty (LHCGR) DNA Sequencing Test2
818 MEN1 (MEN1) DNA Sequencing Test2
813 MEN2 (RET) DNA Sequencing Test2
91002 Methylmalonic Acid, GC/MS/MS
91032 Methylmalonic Acid, GC/MS/MS, Urine
749 Monogenic Hypertension Evaluation2
Detects mutations in CYP11B1, HSD11B2, SCNN1B, and SCNN1G.
851 Nephrogenic Diabetes Insipidus (AVPR2) DNA Sequencing Test2
854 Nephrogenic Diabetes Insipidus Evaluation2
Includes DNA sequencing of AQP2 and AVPR2.
721 Nephrotic Syndrome Evaluation2
Detects sequence variations in LAMB2, NPHS1, NPHS2, and WT1.
882 Neonatal Diabetes Mellitus Evaluation2
Detects mutations in ABCC8, GCK, INS, IPF1, and KCNJ11.
647 Neurofibromatosis Type 1 Deletion Test2
Detects deletions in NF1.
646 Neurofibromatosis Type 1 DNA Sequencing Test2
Detects mutations in NF1.
648 Neurofibromatosis Type 1 (NF1) Evaluation2
Detects deletions and mutations in NF1.
846 Noonan Syndrome (PTPN11) DNA Sequencing Test2
667Normosmic Kallmann/IHH Evaluation2
Detects mutations in FGFR1, GnRH1, GnRHR, KISS1R, PROK2, PROKR2, and TACR3.
710 NPHS2 (Podocin) Sequencing Analysis2
90404 Organic Acids, Qualitative, Urine
90561 Organic Acids, Full Panel, Quantitative, Urine
860 Osteogenesis Imperfecta Evaluation2
Detects mutations in COL1A1 and COL1A2.
37356 Phenylalanine
26336(X) Phenylalanine and Tyrosine
889 Pheochromocytoma Evaluation2
Detects mutations in VHL, RET and SDHB.
718 PLCE1 DNA Sequencing Test2
864 POU1F1 (CPHD) DNA Sequencing Test2
863 PROP1 (CPHD) DNA Sequencing Test2
855 PHEX (Hypophosphatemic Rickets) DNA Sequencing Test2
11369 Prader-Willi/Angelman Syndrome, DNA Methylation Analysis3
175 PROK2 DNA Sequencing Test2
180 PROKR2 DNA Sequencing Test2
748 Pseudohypoaldosteronism Type 1 Evaluation2
Detects mutations in SCNN1A, SCNN1B, and SCNN1G.
663 RAF1 DNA Sequencing Test2
772 SCNN1A DNA Sequencing Test2
745 SCNN1B DNA Sequencing Test2
888 SDHB DNA Sequencing Test2
91566 SHOX (GHD) DNA Sequencing and Deletion Test3
662 SOS1 DNA Sequencing Test2
358 TACR3 DNA Sequencing Test2
712 TRPC6 DNA Sequencing Test2
959 Tryptophan, LC/MS
902 Tyrosine
858 Von Hippel-Lindau Syndrome (VHL) Evaluation2
713 WT1 DNA Sequencing Test2
16313 XSense®, Fragile X with Reflex1
Endocrine Hypertension
17181 Aldosterone, LC/MS/MS
16845 Aldosterone/Plasma Renin Activity Ratio, LC/MS/MS
36718 Angiotensin II
39627(X) Catecholamines, Fractionated, 24-Hour Urine
11281(X) Cortisol, Total, LC/MS/MS
774 CYP11B1 DNA Sequencing Test2
779 CYP11B1/2 DNA Chimeric Gene Fusion Test2
881 Endocrine Hypertension (HSD11B2) Evaluation2
775 HSD11B2 DNA Sequencing Test2
11178(X) 18-Hydroxycortisol, Free, 24-Hour Urine
747 Liddle's Syndrome Evaluation2
Detects mutations in SCNN1B and SCNN1G.
14962(X) Metanephrines, Fractionated, LC/MS/MS, 24-Hour Urine
749 Monogenic Hypertension Evaluation2
Detects mutations in CYP11B1, HSD11B2, SCNN1B, and SCNN1G.
10520Pheochromocytoma EvaluationIncludes total catecholamines, catecholamine/creatinine ratio, total metanephrines, metanephrine/creatinine ratio, and creatinine (24-hour urine).
748 Pseudohypoaldosteronism Type 1 Evaluation2
Detects mutations in SCNN1A, SCNN1B, and SCNN1G.
772 SCNN1A DNA Sequencing Test2
745 SCNN1B DNA Sequencing Test2
Fluid, Electrolytes, and Renal Function
711 ACTN4 DNA Sequencing Test
19552(X) 229 Aldosterone, 24-Hour Urine
17181 Aldosterone, LC/MS/MS
† Aldosterone/Cortisol Ratio
† Aldosterone/Cortisol Ratio, Adrenal Vein Sampling
16845 Aldosterone/Plasma Renin Activity Ratio, LC/MS/MS
36718 Angiotensin II
852 AQP2 (Nephrogenic Diabetes Insipidus) DNA Sequencing Test2
252(X) Arginine Vasopressin (AVP, Antidiuretic Hormone, ADH)3
761 Complete PKD Evaluation2
Detects mutations and deletions in PKD1 and PKD2.
6547(X) Corticosterone, LC/MS/MS
37371 Cortisol Binding Globulin (Transcortin)
36423(X) Cortisol, Free, LC/MS/MS
11280(X) Cortisol, Free, LC/MS/MS, 24-Hour Urine
90582 Cortisol, Free, LC/MS/MS, Second Void Urine
37355(X) Cortisol, Free and Cortisone, 24-Hour Urine
37077(X) Cortisol, Free and Total, LC/MS/MS
19897(X) Cortisol, LC/MS/MS, Saliva
11281(X) Cortisol, Total, LC/MS/MS
37554(X) Cortisone, 24-Hour Urine
37098(X) Cortisone, Serum3
10570(X) Cystatin C
90973 Deoxycorticosterone, LC/MS/MS
11178(X) 18-Hydroxycortisol, Free, 24-Hour Urine
716 INF2 (FSGS) DNA Sequencing Test2
715Inherited Focal and Segmental Glomerulosclerosis (FSGS) Evaluation2
Detects mutations in ACTN4, NPHS2, and TRPC6.
717Inherited Focal and Segmental Glomerulosclerosis (FSGS) Evaluation2
Detects mutations in ACTN4, INF2, NPHS2, and TRPC6.
714 LAMB2 DNA Sequencing Test2
15281 Microalbumin, 24-Hour Urine (with Creatinine)
4555 Microalbumin, 24-Hour Urine (without Creatinine)
6517 Microalbumin, Random Urine (with Creatinine)
17674 Microalbumin, Random Urine (without Creatinine)
851 Nephrogenic Diabetes Insipidus (AVPR2) DNA Sequencing Test2
854 Nephrogenic Diabetes Insipidus Evaluation2
Includes DNA sequencing of AQP2, and AVPR2.
721 Nephrotic Syndrome Evaluation2
Detects sequence variations in LAMB2, NPHS1, NPHS2, and WT1.
710 NPHS2 (Podocin) Sequencing Analysis
678 Osmolality, Random Urine
677 Osmolality, Serum
16846 Plasma Renin Activity, LC/MS/MS
718 PLCE1 DNA Sequencing Test2
712 TRPC6 DNA Sequencing Test2
713 WT1 DNA Sequencing Test2
Gonadal Function
8658(X) Alpha Subunit3
5276(X) 3α-Androstanediol Glucuronide (3-Alpha Diol G)
17182 Androstenedione, LC/MS/MS
462Anosmic Kallmann/IHH Evaluation2
Detects mutations in FGF8, FGFR1, GnRHR, KAL1, KISS1R, PROK2, and PROKR2.
16842(X) Anti-Müllerian Hormone AssessR™1
679Complete Kallmann/IHH Evaluation2
Detects mutations in CHD7, FGF8, FGFR1, GnRHR, GnRH1, KAL1, KISS1R, PROK2, PROKR2, and TACR3.
19894 DHEA (Dehydroepiandrosterone), Unconjugated, LC/MS/MS
38954 DHEA (Dehydroepiandrosterone), Urine
402 DHEA Sulfate
90567 Dihydrotestosterone, LC/MS/MS1
36168 Dihydrotestosterone, Free, Serum1
36169 Estradiol, Free, LC/MS/MS
30289 Estradiol, Ultrasensitive, LC/MS/MS
439 Estrogen, Total, Serum
36742 Estrogens, Fractionated, LC/MS/MS
23244 Estrone, LC/MS/MS
37104(X) Estrone Sulfate
470 FSH (Follicle Stimulating Hormone)
36087 FSH (Follicle Stimulating Hormone), Pediatrics1
7137 FSH and LH
36176 FSH and LH, Pediatrics1
8396 hCG, Total, Quantitative
19720 hCG, Total, with HAMA Treatment
36707(X) Hirsutism Panel 2Includes androstenedione, DHEA sulfate, and free and total testosterone.
8352 17-Hydroxypregnenolone, LC/MS/MS
17180 17-Hydroxyprogesterone, LC/MS/MS
17654(X) 17-Hydroxyprogesterone, Neonatal/Infant
11303 Hyperglycosylated hCG (h-hCG)
34472 Inhibin A
34445 Inhibin B1
15201(X) 17-Ketosteroids with Creatinine, 24-Hour Urine
70184(X) 17-Ketosteroids, Fractionated, Pediatrics, Urine
4932(X) 17-Ketosteroids, Fractionated, Urine
615 LH
36086 LH, Pediatrics1
17625(X) Male Infertility Genetic Analysis
817 Male Precocious Puberty (LHCGR) DNA Sequencing Test2
667Normosmic Kallmann/IHH Evaluation2
Detects mutations in FGFR1, GnRH1, GnRHR, KISS1R, PROK2, PROKR2, and TACR3.
10328 Ovarian Antibody Screen with Reflex to Titer
31493(X) Pregnenolone, LC/MS/MS
17183 Progesterone, LC/MS/MS
746 Prolactin
40049 Prolactin, Dilution Study
16122 Prolactin, Total and Monomeric
30740 Sex Hormone Binding Globulin
90426Steroid Panel, PCOS/CAH DifferentiationIncludes androstenedione, 11-deoxycortisol, DHEA, 17-hydroxyprogesterone, and free and total testosterone.
90424 Steroid Panel, Polycystic Ovary Syndrome (PCOS)Includes androstenedione, DHEA, and total and free testosterone.
90433Steroid Panel, Premature AdrenarcheIncludes androstenedione, DHEA, 17-hydroxypregnenolone, 17-hydroxyprogesterone, and total testosterone.
14966 Testosterone, Free, Bioavailable, and Total, LC/MS/MS
15983 Testosterone, Total, LC/MS/MS
19958 Testosterone, Total (Males), Immunoassay
37073 Testosterone, Total and Free and Sex Hormone Binding Globulin
Growth and Growth Hormone
865 Combined Pituitary Hormone Deficiency Evaluation2
Detects mutations in POU1F1 and PROP1.
866 GH1 (GHD) DNA Sequencing Test2
867 GHR DNA Sequencing Test2
868 GHRHR (GHD) DNA Sequencing Test2
521 Growth Hormone (GH)
37072(X) Growth Hormone Antibody3
848Growth Hormone Deficiency EvaluationIncludes sequencing and deletion detection in SHOX and sequencing of GH1 and GHRHR.
† Growth Hormone, Multiple Specimens
16293 IGF-I, LC/MS1
36590 IGF Binding Protein-1 (IGFBP-1)1
37102(X) IGF Binding Protein-2 (IGFBP-2)1
34458 IGF Binding Protein-3 (IGFBP-3)
658 KRAS/RAF1/SOS1 DNA Sequencing Evaluation2
846 Noonan Syndrome (PTPN11) DNA Sequencing Test2
864 POU1F1 (CPHD) DNA Sequencing Test2
746 Prolactin
863 PROP1 (CPHD) DNA Sequencing Test2
91566 SHOX (GHD) DNA Sequencing and Deletion
662 SOS1 DNA Sequencing Test2
35167 T4, Free, Direct Dialysis
866 T4, Free (Non-dialysis)
17733 T4, Total (Thyroxine)
Hypothalamic and Pituitary Function
211 ACTH, Plasma
8658(X) Alpha Subunit1
252(X) Arginine Vasopressin (AVP, Antidiuretic Hormone, ADH)3
865 Combined Pituitary Hormone Deficiency Evaluation2
Detects mutations in POU1F1 and PROP1.
470 FSH (Follicle Stimulating Hormone)
36087 FSH (Follicle Stimulating Hormone), Pediatrics1
7137 FSH and LH
36176 FSH and LH, Pediatrics1
866 GH1 (GHD) DNA Sequencing Test2
521 Growth Hormone (GH)
37072(X) Growth Hormone Antibody3
615 LH
36086 LH, Pediatrics1
864 POU1F1 (CPHD) DNA Sequencing Test2
746 Prolactin
40049 Prolactin, Dilution Study
16122 Prolactin, Total and Monomeric
863 PROP1 (CPHD) DNA Sequencing Test2
34480 Somatostatin1
899 TSH
36577 TSH Antibody1
19537 TSH with HAMA Treatment
Lipid Disorders
15060(X) Adiponectin4
893 ApoB Mutation Analysis2
5223(X) Apolipoprotein A1
5224(X) Apolipoprotein B
7018(X)Apolipoprotein EvaluationIncludes apolipoprotein A1, apolipoprotein B, and apolipoprotein B/A1 ratio.
887 Bardet-Biedl Syndrome Evaluation2
Detects mutations in BBS1, BBS2, and BBS10.
886 BBS10 (BBS) DNA Sequencing Test2
90649 Cardio IQ™ ApoE Genotype1
91604 Cardio IQ™ Lipoprotein Fractionation, Ion Mobility
334(X) Cholesterol, Total
8293(X) Direct LDL
884 Early Onset Obesity Evaluation2
Detects mutations in LEPR and MC4R.
883 Early Onset Obesity (LEPR) DNA Sequencing Test2
640 Early Onset Obesity (MC4R) DNA Sequencing Test2
Detects mutations in MC4R.
90393 Fat Malabsorption (Response to Vitamin D2 Supplement)
608(X) HDL Cholesterol
35932(X) HDL Cholesterol Subclasses
31789 Homocysteine (Cardiovascular)
895 Hypercholesterolemia Evaluation2
Detects mutations in LDLR and disease-associated regions of ApoB.
894 LDLR (Hypercholesterolemia) DNA Sequencing Test2
90367 Leptin1
7600(X)Lipid PanelIncludes HDL and total cholesterol, triglycerides, and calculated components (LDL-cholesterol, cholesterol:HDL-cholesterol ratio, and non-HDL cholesterol).
14852(X)Lipid Panel w/Reflex to Direct LDLIncludes cholesterol, HDL, cholesterol/HDL ratio, LDL (calculated), and triglycerides.
34604(X) Lipoprotein(a)
449(X) Nonesterified Fatty Acids (Free Fatty Acids)
91001 Omega-3 and -6 Fatty Acids, Plasma
717 Phospholipids4
896 Triglycerides
90559 Very Long Chain Fatty Acids
Metabolic (Including Diabetes Mellitus) and Gastrointestinal Disorders
876 ABCC8 (NDM) DNA Sequencing Test2
15060(X) Adiponectin4
887 Bardet-Biedl Syndrome Evaluation2
Detects mutations in BBS1, BBS2, and BBS10.
886 BBS10 (BBS) DNA Sequencing Test2
825 CASR DNA Sequencing Test2
837 CEL (MODY8) Mutation Analysis2
372 C-Peptide
4643(X) C-Peptide, 24-Hour Urine
91713(X)
Diabetes, Advancing Chronic Kidney Disease Management PanelIncludes electrolyte panel; microalbumin, random urine with creatinine; creatinine, serum; hemoglobin; PTH, intact and calcium; phosphate (as phosphorus); QuestAssureD™ 25-hydroxyvitamin D (D2, D3), LC/MS/MS.
91712(X)Diabetes, Newly Diagnosed and Monitoring PanelIncludes glucose; hemoglobin A1c; lipid panel; hepatic function panel; microalbumin, random urine with creatinine; creatinine, serum.
884 Early Onset Obesity Evaluation2
Detects mutations in LEPR and MC4R.
883 Early Onset Obesity (LEPR) DNA Sequencing Test2
640 Early Onset Obesity (MC4R) DNA Sequencing Test2
Detects mutations in MC4R.
90393 Fat Malabsorption (Response to Vitamin D2 Supplement)
8340 Fructosamine
10584(X) GAD65, IA-2, and Insulin Autoantibody
478(X) Gastrin
803 GCK (MODY2) DNA Sequencing and Deletion Test2
842 GCK (NDM) DNA Sequencing Test2
519 Glucagon1
† Glucose
34878 Glutamic Acid Decarboxylase-65 Antibody
5032(X) Glycated Albumin
90915 Glycogen Storage Disease Type 1a Mutation Analysis (Ashkenazi Jewish)1
29488(X) Glycohemoglobin, Total
19599 GlycoMark®
496 Hemoglobin A1c
8181 Hemoglobin A1c with Calculated Mean Plasma Glucose (MPG)
16802 Hemoglobin A1c with eAG
16715 Hemoglobin A1c with Reflex to GlycoMark®
39625(X) 5-HIAA (5-Hydroxyindoleacetic Acid), 24-Hour Urine, with Creatinine
523(X) 5-HIAA (5-Hydroxyindoleacetic Acid), 24-Hour Urine, without Creatinine
1648(X) 5-HIAA (5-Hydroxyindoleacetic Acid), Random Urine
802 HNF4A (MODY1) DNA Sequencing and Deletion Test2
37054(Z) β-Hydroxybutyrate
36177(X) IA-2 Antibody
36590 IGF Binding Protein-1 (IGFBP-1)1
37102(X) IGF Binding Protein-2 (IGFBP-2)1
34458 IGF Binding Protein-3 (IGFBP-3)
16293 IGF-I, LC/MS1
853 INS (NDM) DNA Sequencing Test2
561 Insulin
36178 Insulin Autoantibody
36700 Insulin, Free (Bioactive)
91083 Insulin, LC/MS/MS1
834 IPF1 (MODY4) DNA Sequencing Test2
841 IPF1 (NDM) DNA Sequencing Test2
36741 Islet Cell Antibody Screen with Reflex to Titer2
843 KCNJ11 (NDM) DNA Sequencing Test2
90367 Leptin3
91398Metabolic Syndrome and Glucose Control Including InsulinIncludes cholesterol, total and HDL; glucose; insulin, LC/MS/MS; triglycerides; and calculated components.
15281 Microalbumin, 24-Hour Urine (with Creatinine)
4555 Microalbumin, 24-Hour Urine (without Creatinine)
6517 Microalbumin, Random Urine (with Creatinine)
17674 Microalbumin, Random Urine (without Creatinine)
885Monogenic Diabetes (MODY) Evaluation2
Includes sequencing and deletion detection in GCK, HNF4A, TCF1, and TCF2 and sequencing of IPF1.
882 Neonatal Diabetes Mellitus Evaluation2
Detects mutations in ABCC8, GCK, INS, IPF1, and KCNJ11.
449(X) Nonesterified Fatty Acids (Free Fatty Acids)
678 Osmolality, Random Urine
677 Osmolality, Serum
4789(X) Pancreatic Polypeptide3
760(X) Proinsulin4
17306 QuestAssureD™ 25-Hydroxyvitamin D (D2, D3), LC/MS/MS
91935 QuestAssureD™ for Infants, 25-Hydroxyvitamin D, LC/MS/MS
16761 QuestAssureD™ 25-Hydroxy and 1,25-Dihydroxyvitamin D, LC/MS/MS
34480 Somatostatin1
818(X) Serotonin, Blood
804 TCF1 (MODY3) DNA Sequencing and Deletion Test2
805 TCF2 (MODY5) DNA Sequencing and Deletion Test2
920(X) Vasoactive Intestinal Polypeptide (VIP)1
90559 Very Long Chain Fatty Acids
16558 Vitamin D, 1,25-Dihydroxy, LC/MS/MS
Multiple Endocrine Neoplasia
211 ACTH, Plasma
30742(X) Calcitonin
303 Calcium
1635(X) Calcium, 24-Hour Urine (with Creatinine)
306 Calcium, Ionized
11216(X) Calcium, Pediatric Urine (with Creatinine)
1633(X) Calcium, Random Urine (with Creatinine)
39627(X) Catecholamines, Fractionated, 24-Hour Urine
314(X) Catecholamines, Fractionated, Plasma
5244 Catecholamines, Fractionated, Random Urine
16381 Catecholamines, Fractionated, Supine, Plasma
16382 Catecholamines, Fractionated, Upright, Plasma
39626(X) Catecholamines, Fractionated, and VMA, 24-Hour Urine
16379 Chromogranin A, Electrochemiluminescence1
372 C-Peptide
4643(X) C-Peptide, 24-Hour Urine
478(X) Gastrin
519 Glucagon1
521 Growth Hormone (GH)
39625(X) 5-HIAA (5-Hydroxyindoleacetic Acid), 24-Hour Urine
1648(X) 5-HIAA (5-Hydroxyindoleacetic Acid), Random Urine
39527(X) Homovanillic Acid, 24-Hour Urine
6346 Homovanillic Acid, Random Urine
561 Insulin
36700 Insulin, Free (Bioactive)
91083 Insulin, LC/MS/MS1
36587(X) MEN2 and FMTC Mutations, Exons 10, 11, 13-161
14962(X) Metanephrines, Fractionated, LC/MS/MS, 24-Hour Urine
19548 Metanephrines, Fractionated, Free, LC/MS/MS, Plasma
14961(X) Metanephrines, Fractionated, LC/MS/MS, Random Urine
4789(X) Pancreatic Polypeptide3
889 Pheochromocytoma Evaluation2
Detects mutations in RET, SDHB, and VHL.
760(X) Proinsulin4
746 Prolactin
40049 Prolactin, Dilution Study
16122 Prolactin, Total and Monomeric
36736 PTH, Intact (ICMA) and Ionized Calcium
8837 PTH, Intact and Calcium
16560 PTH, Intact, Fine Needle Aspirate
34478(X) PTH-Related Protein (PTH-RP)1
818(X) Serotonin, Blood
29851 Serotonin, Serum
920(X) Vasoactive Intestinal Polypeptide (VIP)1
39517(X) VMA, 24-Hour Urine
1710 VMA (Vanillylmandelic Acid), Random Urine
Neuroendocrine Markers
16379 Chromogranin A, Electrochemiluminescence1
39625(X) 5-HIAA (5-Hydroxyindoleacetic Acid), 24-Hour Urine
1648(X) 5-HIAA (5-Hydroxyindoleacetic Acid), Random Urine
39527(X) Homovanillic Acid, 24-Hour Urine
6346 Homovanillic Acid, Random Urine
39517(X) VMA, 24-Hour Urine
1710 VMA (Vanillylmandelic Acid), Random Urine
920(X) Vasoactive Intestinal Polypeptide (VIP)1
34480 Somatostatin1
Obesity and Post-Obesity Surgery
15060(X) Adiponectin4
887 Bardet-Biedl Syndrome Evaluation2
Detects mutations in BBS1, BBS2, and BBS10.
886 BBS10 (BBS) DNA Sequencing Test2
90649 Cardio IQ™ ApoE Genotype1
91604 Cardio IQ™ Lipoprotein Fractionation, Ion Mobility
884 Early Onset Obesity Evaluation2
Detects mutations in LEPR and MC4R.
883 Early Onset Obesity (LEPR) DNA Sequencing Test2
640 Early Onset Obesity (MC4R) DNA Sequencing Test2
Detects mutations in MC4R.
457 Ferritin
467(X) Folate, RBC
466 Folate, Serum
7573 Iron, Total and Total Iron binding Capacity
90367 Leptin1
7600(X)Lipid PanelIncludes HDL and total cholesterol, and triglycerides; calculated components include LDL-cholesterol, chol/HDL ratio, and non-HDL cholesterol.
34604(X) Lipoprotein(a)
17306 QuestAssureD™ 25-Hydroxyvitamin D (D2, D3), LC/MS/MS
90353 Vitamin B1 (Thiamine), LC/MS/MS
Parathyroid and Mineral Metabolism
29498 Alkaline Phosphatase, Bone Specific
231 Alkaline Phosphatase Isoenzymes
812Autoimmune Polyglandular Syndrome (AIRE) Evaluation2
Detects point mutations, deletions, insertions, and rearrangements in AIRE.
30742(X) Calcitonin
36167(X) Collagen Cross-Linked N-Telopeptide (NTx), 2-Hour Urine or Second AM Void
36421 Collagen Cross-Linked N-Telopeptide (NTx), 24-Hour Urine
17406 Collagen Type I C-Telopeptide (CTx)
829 Familial Hypocalciuric Hypercalcemia (CASR) DNA Sequencing Test2
91001 Omega-3 and -6 Fatty Acids, Plasma
16322 Osteocalcin, N-MID
16609 Procollagen Type I Intact N Terminal Propeptide
36578 PTH Antibody1
36736 PTH, Intact (ICMA) and Ionized Calcium
8837 PTH, Intact and Calcium
16560 PTH, Intact, Fine Needle Aspirate
34478(X) PTH-Related Protein (PTH-RP)4
17306 QuestAssureD™ 25-Hydroxyvitamin D (D2, D3), LC/MS/MS
91935 QuestAssureD™ for Infants, 25-Hydroxyvitamin D, LC/MS/MS
16761 QuestAssureD™ 25-Hydroxy and 1,25-Dihydroxyvitamin D, LC/MS/MS
16558 Vitamin D, 1,25-Dihydroxy, LC/MS/MS
Pituitary Tumors
211 ACTH, Plasma
8658(X) Alpha Subunit1
252(X) Arginine Vasopressin (AVP, Antidiuretic Hormone, ADH)3
16379 Chromogranin A, Electrochemiluminescence1
37077(X) Cortisol, Free and Total, LC/MS/MS
36423(X) Cortisol, Free, LC/MS/MS
11280(X) Cortisol, Free, LC/MS/MS, 24-Hour Urine
90582 Cortisol, Free, LC/MS/MS, Second Void Urine
19897(X) Cortisol, LC/MS/MS, Saliva
11281(X) Cortisol, Total, LC/MS/MS
470 FSH (Follicle Stimulating Hormone)
36087 FSH (Follicle Stimulating Hormone), Pediatrics1
14570 FSH (Follicle Stimulating Hormone), Timed (5 Samples), Pediatrics1
7137 FSH and LH
36176 FSH and LH, Pediatrics1
521 Growth Hormone (GH)
37072(X) Growth Hormone Antibody3
34458 IGF Binding Protein-3 (IGFBP-3)
16293 IGF-I, LC/MS1
615 LH
36086 LH, Pediatrics1
746 Prolactin
40049 Prolactin, Dilution Study
16122 Prolactin, Total and Monomeric
34480 Somatostatin1
899 TSH
36577 TSH Antibody1
19537 TSH with HAMA Treatment
Resistance to Thyroid Hormone
8658(X) Alpha Subunit1
16053(X) Resistance to Thyroid Hormone (RTH) Mutation Analysis1
36598 T3, Free, Tracer Dialysis
859 T3, Total
36574 T3 (Triiodothyronine) Antibody
36576 T4 (Thyroxine) Antibody1
35167 T4, Free, Direct Dialysis
866 T4, Free (Non-dialysis)
17733 T4, Total (Thyroxine)
5738 TBII (Thyrotropin-Binding Inhibitory Immunoglobulin)
870 TBG (Thyroxine Binding Globulin)
15102(X)Thyroid Cascading ReflexInitial TSH results will determine further reflex orders of Free T4, TPO antibodies, and Free T3.
899 TSH
36577 TSH Antibody1
90896 TSH, Pregnancy
19537 TSH with HAMA Treatment
36127(X) TSH with Reflex to Free T4
30551 TSI (Thyroid Stimulating Immunoglobulin)
Selective Sampling-Petrosal Sinus and Adrenal Vein Sampling
211 ACTH, Plasma
18821 Aldosterone/Cortisol Ratio, 2 Sites
18822 Aldosterone/Cortisol Ratio, 3 Sites
18823 Aldosterone/Cortisol Ratio, 4 Sites
18825 Aldosterone/Cortisol Ratio, 5 Sites
18826 Aldosterone/Cortisol Ratio, 6 Sites
18827 Aldosterone/Cortisol Ratio, 7 Sites
18824 Aldosterone/Cortisol Ratio, 8 Sites
19573(X) Aldosterone/Cortisol Ratio, Adrenal Vein Sampling
18818 Aldosterone/Cortisol Ratio, Adrenal Vein Sampling 3 Sites
18819 Aldosterone/Cortisol Ratio, Adrenal Vein Sampling 5 Sites
Thyroid Cancer
90477 BRAF Mutation Analysis, Papillary Thyroid Cancer1
30742(X) Calcitonin
978(X) Carcinoembryonic Antigen (CEA)
15018 CEA with HAMA Treatment
90474 PAX8/PPAR[gamma] Translocation, Thyroid Cancer1
90479 RAS Mutation Analysis, Thyroid Cancer1
90473 RET/PTC Rearrangement, Thyroid Cancer1
267 Thyroglobulin Antibody
30278 Thyroglobulin PanelIncludes thyroglobulin and thyroglobulin antibody.
19584Thyroglobulin Panel with HAMA TreatmentIncludes thyroglobulin, pre and post HAMA precipitation, and thyroglobulin antibody.
16559 Thyroglobulin, Fine Needle Aspirate
90814Thyroid Cancer Monitoring1
Includes a thyroglobulin antibody test. If positive, reflexes to thyroglobulin measurement using LC/MS/MS. If negative, reflexes to thyroglobulin measurement using a highly sensitive immunoassay.
90469 Thyroid Cancer Mutation Panel (BRAF, RAS, RET/PTC, PAX8/PPAR)1
90819 Thyroid FNA Cytomorphology Evaluation
90818 Thyroid FNA Cytomorphology with Molecular Reflex
Thyroid Function See above for thyroid cancer.
30742(X) Calcitonin
16053(X) Resistance to Thyroid Hormone (RTH) Mutation Analysis1
90963 T3, Reverse, LC/MS/MS
36574 T3 (Triiodothyronine) Antibody1
34429 T3, Free, Non-Dialysis
36598 T3, Free, Tracer Dialysis
859 T3, Total
17732(X) T3, Uptake
36576 T4, (Thyroxine) Antibody1
35167 T4, Free, Direct Dialysis
866 T4, Free (Non-dialysis)
17733 T4, Total (Thyroxine)
870 TBG (Thyroxine Binding Globulin)
5738 TBII (Thyrotropin-Binding Inhibitory Immunoglobulin)
267 Thyroglobulin Antibody
30278 Thyroglobulin PanelIncludes thyroglobulin and thyroglobulin antibody.
19584Thyroglobulin Panel with HAMA TreatmentIncludes thyroglobulin, pre and post HAMA precipitation, and thyroglobulin antibody.
15102(X)Thyroid Cascading ReflexInitial TSH results will determine further reflex orders of Free T4, TPO antibodies, and Free T3.
7260(X) Thyroid Peroxidase and Thyroglobulin Antibodies
5081 Thyroid Peroxidase Antibody (Anti-TPO)
899 TSH
36577 TSH Antibody1
90896 TSH, Pregnancy
19537 TSH with HAMA Treatment
36127(X) TSH with Reflex to Free T4
30551 TSI (Thyroid Stimulating Immunoglobulin)
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