For Endocrinologists

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


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




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



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


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)

http://www.questdiagnostics.com/testcenter/TestDetail.action?ntc=39627





http://www.athenadiagnostics.com/content/test-catalog/find-test/service-detail/q/id/1575












































































































































































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



887 Bardet-Biedl Syndrome Evaluation2

Detects mutations in BBS1, BBS2, and BBS10.

871 BBS1 (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.


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.



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


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



36718 Angiotensin II



774 CYP11B1 DNA Sequencing Test2

779 CYP11B1/2 DNA Chimeric Gene Fusion Test2

881 Endocrine Hypertension (HSD11B2) Evaluation2



747 Liddle's Syndrome Evaluation2

Detects mutations in SCNN1B and SCNN1G.


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


† Aldosterone/Cortisol Ratio

† Aldosterone/Cortisol Ratio, Adrenal Vein Sampling


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)




37355(X) Cortisol, Free and Cortisone, 24-Hour Urine




37554(X) Cortisone, 24-Hour Urine

37098(X) Cortisone, Serum3

10570(X) Cystatin C

90973 Deoxycorticosterone, LC/MS/MS


716 INF2 (FSGS) DNA Sequencing Test2


Detects mutations in ACTN4, NPHS2, and TRPC6.


Detects mutations in ACTN4, INF2, NPHS2, and TRPC6.

714 LAMB2 DNA Sequencing Test2





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



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



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




867 GHR DNA Sequencing Test2

868 GHRHR (GHD) DNA Sequencing Test2

521 Growth Hormone (GH)


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


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


746 Prolactin


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







7137 FSH and LH





615 LH



746 Prolactin




34480 Somatostatin1

899 TSH

36577 TSH Antibody1

19537 TSH with HAMA Treatment

Lipid Disorders


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.





91604 Cardio IQ™ Lipoprotein Fractionation, Ion Mobility

334(X) Cholesterol, Total

8293(X) Direct LDL






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





825 CASR DNA Sequencing Test2

837 CEL (MODY8) Mutation Analysis2

372 C-Peptide


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.






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


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



37102(X) IGF Binding Protein-2 (IGFBP-2)1


16293 IGF-I, LC/MS1

853 INS (NDM) DNA Sequencing Test2

561 Insulin



91083 Insulin, LC/MS/MS1

834 IPF1 (MODY4) DNA Sequencing Test2

841 IPF1 (NDM) DNA Sequencing Test2


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.





885Monogenic Diabetes (MODY) Evaluation2

Includes sequencing and deletion detection in GCK, HNF4A, TCF1, and TCF2 and sequencing of IPF1.



449(X) Nonesterified Fatty Acids (Free Fatty Acids)



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
























































































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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)


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


372 C-Peptide


478(X) Gastrin

519 Glucagon1


39625(X) 5-HIAA (5-Hydroxyindoleacetic Acid), 24-Hour Urine




561 Insulin


91083 Insulin, LC/MS/MS1

36587(X) MEN2 and FMTC Mutations, Exons 10, 11, 13-161


19548 Metanephrines, Fractionated, Free, LC/MS/MS, Plasma

14961(X) Metanephrines, Fractionated, LC/MS/MS, Random Urine

4789(X) Pancreatic Polypeptide3


Detects mutations in RET, SDHB, and VHL.

760(X) Proinsulin4

746 Prolactin



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


39517(X) VMA, 24-Hour Urine


Neuroendocrine Markers


39625(X) 5-HIAA (5-Hydroxyindoleacetic Acid), 24-Hour Urine




39517(X) VMA, 24-Hour Urine



34480 Somatostatin1

Obesity and Post-Obesity Surgery






91604 Cardio IQ™ Lipoprotein Fractionation, Ion Mobility






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)


90353 Vitamin B1 (Thiamine), LC/MS/MS

Parathyroid and Mineral Metabolism

29498 Alkaline Phosphatase, Bone Specific

231 Alkaline Phosphatase Isoenzymes



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


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












14570 FSH (Follicle Stimulating Hormone), Timed (5 Samples), Pediatrics1

7137 FSH and LH





16293 IGF-I, LC/MS1

615 LH


746 Prolactin



34480 Somatostatin1

899 TSH

36577 TSH Antibody1


Resistance to Thyroid Hormone


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





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


36127(X) TSH with Reflex to Free T4


Selective Sampling-Petrosal Sinus and Adrenal Vein Sampling

211 ACTH, Plasma

18821 Aldosterone/Cortisol Ratio, 2 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


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




870 TBG (Thyroxine Binding Globulin)



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


36127(X) TSH with Reflex to Free T4



































































































































































































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For Endocrinologists