Laboratory Test Directory

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Test Name A to Z

Guide Name Test Name Updated Synonyms Test Code
Allergen, Food, Blueberry IgE Allergen, Food, Blueberry IgE
Lowbush Blueberry, Highbush Blueberry, Whinberry, Whortleberry, ImmunoCAP(R) f288 , Bilberry, European Blueberry, Vaccinium myrtillis, V. angustifolium, V. corymbosum
XBLUEB
Allergen, Food, Lentil IgE Allergen, Lentil IgE
Cicer lens , ImmunoCAP® f235 , Lens culinaris , Lentilla lens , Lens esculenta
XLENT
Allergen, Rye Grass IgE Allergen, Rye Grass IgE
Annual Ryegrass, Ray-Grass, ImmunoCAP® g5 , Lolium perenne , Rye Grass , Perennial Rye Grass
XRYEG
Amino Acid Quantitative, Serum Amino Acid Quant, Serum
Amino Acid Quantitative, Serum, Phosphoserine, Taurine, Phosphoethanolamine, Aspartic Acid, Hydroxyproline, Threonine, Serine, Asparagine, Glutamic Acid, Glutamine, Sarcosine, Proline, Glycine, Alanine, Citrulline, Valine, Methionine, Cystine, Isoleucine, Leucine, Tyrosine, Cystathionine, Phenylalanine, Homocystine, Tryptophan, Ornithine, Lysine, 1-Methylhistidine, Histidine, 3-Methylhistidine, Anserine, Carnosine, Arginine, Alloisoleucine
QAAS
Amino Acid Quantitative, Urine Amino Acid Quant, Urine
Phosphoserine, Taurine, Phosphoethanolamine, Aspartic Acid, Hydroxyproline, Threonine, Serine, Asparagine, Glutamic Acid, Glutamine, Sarcosine, Proline, Glycine, Alanine, Citrulline, Valine, Methionine, Cystine, Isoleucine, Leucine, Tyrosine, Cystathionine, Phenylalanine, Homocystine, Ornithine, Lysine, 1-Methylhistidine, Histidine, , 3-Methylhistidine, Anserine, Carnosine, Arginine, Alloisoleucine,
QAAUP
Amitriptyline and Nortriptyline, Serum Amitriptyline and Nortriptyline, Serum
Elavil, Amitriptyline, Pamelor, Nortriptyline, Tricyclic Antidepressants (TCA), TCA (Tricyclic Antidepressants), Allegron and Nortrilen (Nortriptyline), Tryptanol, Endep, Elatrol, Tryptizol, Trepiline, Laroxyl, Saroten, Triptyl, Redomex , Sensoval, Aventyl, Pamelor, Norpress, Allegron, Nortrilen
XAMTRP
ANO5 Gene Sequencing ANO5 Gene Sequencing
LGMD2L, Anoctamin 5, Limb-girdle muscular dystrophy type 2L, LGMD, LGMD type 2L, Miyoshi muscular dystrophy 3, Limb girdle muscular dystrophy, ANO5 sequence analysis, ANO5 mutation analysis
ANO5
Anti-Factor Xa-Low Molecular Weight Heparin Assay Anti-Factor Xa-LMWH Assay
Xa, Heparin, Low Molecular Weight, Factor Xa (Anti-), Low Molecular Weight Heparin, Anti-Factor Xa Low Molecular Weight Heparin, Lovenox (enoxaparin)
AFXA
Antigen Stimulation (Proliferation) Antigen Stimulation
Antigen Stimulation, Blast Transformation, Lymphoblastic Transformation, Antigens, Lymphocyte Antigen Proliferation, Candida Antigen, Tetanus Antigen
XATS
Apolipoprotein B Apolipoprotein B
APO-B100, Low Density Lipoprotein B, BHL Apliopoprotein , Apo B, APO-B, APOB, ApoB/apoB, BHL, Apliopoprotein B, Low Density Lipoprotein, B, Plasma Apo B
XAPB
Arbovirus Antibody IgG Titer, (Acute) Arbovirus Ab, Acute Titer
Eastern Arbovirus Antibody (Acute), California Arbovirus Antibody (Acute), Lacrosse Arbovirus Antibody (Acute), St. Louis Arbovirus Antibody (Acute), Western Arbovirus Antibody (Acute), Eastern Equine Arbovirus Antibody (Acute), Western Equine Arbovirus Antibody (Acute)
ARBA
Arbovirus Antibody IgG Titer, (Convalescent) Arbovirus Ab,Convalescent Titer
Eastern Arbovirus Antibody (Convalescent), Arbovirus Antibody IgG, (Convalescent), LaCrosse Arbovirus Antibody (Convalescent), St. Louis Arbovirus Antibody (Convalescent), Western Arbovirus Antibody (Convalescent), Eastern Equine Arbovirus Antibody (Convalescent), Western Equine Arbovirus Antibody (Convalescent)
ARBC
Bone Marrow Immunophenotype Leukocyte Immunophenotype
Bone marrow immunophenotype, Leukocyte immunophenotype, Immunophenotype Bone Marrow, Lymphoma, Leukemia, IBM
FLOWSP
Bone Marrow Pathology Bone Marrow Pathology
Bone marrow aspiration, Bone Marrow Pathology, Leukemia(Bone Marrow Pathology), Metastasis (Bone Marrow Pathology), Metatstatic (Bone Marrow Pathology)
AP7
BRAF V600 Mutation Analysis BRAF V600 Mutation Analysis
BRAF V600 variant detection, BRAF codon 600 mutation, BRAF exon 15 targeted sequencing, BRAF V600E mutation detection, BRAF V600K mutation detection, BRAF V600R mutation detection, BRAF V600 cancer testing, BRAF V600 tumor testing, BRAF V600 somatic testing, Low grade pediatric glioma, Ganglioglioma, Pleiomorphic xanthoastrocytoma (PXA), Diffusely infiltrative astrocytoma, Melanoma, Hairly cell leukemia, Papillary thyroid carcinoma, Thyroid cancer, Colon cancer, Ovarian cancer, Endometrial cancer, BRAF V600E, c.1799T>A, p.Val600Glu mutation
BRAFV600
CAPN3 (Calpain) Gene Sequencing CAPN3 (Calpain) Gene Sequencing
Calpainopathy, CAPN3, Calpain mutation analysis, LGMD, LGMD type 2A, LGMD2A, Limb-girdle muscular dystrophy type 2A, Limb girdle muscular dystrophy, CAPN3 sequence analysis
CAL
Carnitine Profile, Urine Carnitine Profile, Urine
L-Carnitine Urine, Soft-CARNU, Carnitine Free & Total Urine, Urinary Carnitine Quantitative, Carnitine, Urine
XCARPU
Caveolin 3 (CAV3) Gene Sequencing Caveolin 3 (CAV3) Gene Sequencing
CAV3, Caveolin-3, LGMD1C, Caveolin 3, Limb-girdle muscular dystrophy type 1C, LGMD, Limb girdle muscular dystrophy, CAV3-related rippling muscule disease, CAV3-related isolated hyperCKemia, CAV3-related hypertrophic cardiomyopathy, CAV3-related distal myopathy, CAV3 sequence analysis
CAV3
D Lactate, Plasma D Lactate, Plasma
D-lactate, D lactate, Lactate (D) Plasma, 8878 Mayo test code
XDLAC
Digoxin Digoxin
Lanoxin
XDIG
DNAJB6 Gene Sequencing DNAJB6 Gene Sequencing
DNAJB6 mutation analysis, DNAJB6 sequence analysis, LGMD, LGMD1E, LGMD type 1E, Limb-girdle muscular dystrophy type 1E, Limb girdle muscular dystrophy
DNAJB6
Double Stranded DNA Antibody, (Crithidia) Titer Crithidia (IFA) Titer
Double Stranded DNA antibody, ds DNA Antibody, (Crithidia), Crithidia, Systemic lupus erythematosus, Lupus, SLE, Autoimmune
CRTH
Dysferlin (DYSF) Gene Sequencing Dysferlin (DYSF) Gene Sequencing
Dysferlinopathy, DYSF mutation analysis, DYSF sequence analysis, LGMD, LGMD2B, LGMD type 2B, Limb-girdle muscular dystrophy type 2B, Limb girdle muscular dystrophy, Miyoshi distal myopathy
DYS
Electrolytes Electrolytes
Electrolytes, Carbon Dioxide (Electrolytes), Chloride (Electrolytes), Cl (Electrolytes), CO2 (Electrolytes), K (Electrolytes), Lytes, Na (Electrolytes), Potassium (Electrolytes), Sodium (Electrolytes)
LYT
Electron Microscopy Studies Electron Microscopy Studies
Electron microscopy studies, Biopsy (Electron Microscopy), Brain biopsy (Electron Microscopy), Cilia biopsy (Electron Microscopy), EM (Electron Microscopy Studies), Kidney biopsy (Electron Microscopy), Liver biopsy (Electron Microscopy), Lymph node biopsy (Electron Microscopy)
AP27
Electron Study of Lymphocytes for Suspected Storage Disorder EM of lymphocytes
Electron microscopy (of lymphocytes), Electron study of lymphocytes for suspected storage disorders, EM (for Suspected Storage Disorders), Lymphocytes (Electron Microscopy), Storage disorders (Electron microscopy)
AP6
Fatty Acid Profile, Essential, Serum Fatty Acid Profile, Essential, Serum
C12-C22, Fatty Acid Profile, Essential, Essential Fatty Acids, Long-Chain Fatty Acids (LCFA), Omega 3, Omega 6, Omega 7, Omega 9, Omega fatty acids, Soft-FAPEP, Polyunsaturated Fatty Acids, Lauric Acid, Myristic Acid, Hexadecenoic Acid, Palmitoleic Acid, Palmitic Acid, Gamma-Linolenic Acid, Alpha-Linolenic Acid, Linoleic Acid, Oleic Acid, Vaccenic Acid, Stearic Acid, Eicosapentaenoic Acid, Arachidonic Acid, Mead Acid, Homo-Gamma-Linolenic Acid, Arachidic Acid, Docosahexaenoic Acid, Docosapentaenoic Acid, Docosatetraenoic Acid, Docosenoic Acid, Nervonic Acid, Total Lipid Fatty
XFAPEP
Fatty Acids, Long Chain Fatty Acids, Long Chain
Long Chain Fatty Acids, Very Long Chain Fatty Acids, Phytanic acids, X-linked Adrenoleukodystrophy, Zellweger Spectrum Disease
XFAT
Fine Needle Aspirations Pathology Fine Needle Aspirations
Cytology (Fine Needle Aspiration), Diagnostic biopsies, Biopsy (Fine Needle Aspiration), Fine needle aspirations pathology, FNA, Lymph node biopsy, cell block
AP4
FKRP (Fukutin-Related Protein) Gene Sequencing FKRP (Fukutin-Related Protein) Gene Sequencing
Fukutin-related protein, LGMD, LGMD2I, LGMD type 2I, Limb-girdle muscular dystrophy type 2I, Limb girdle muscular dystrophy, Congenital muscular dystrophy type 1C, Merosin-deficient congenital muscular dystrophy, Merosin-deficient CMD type 1C (MDC1C), Muscle-eye-brain disease, Muscular dystrophy-dystroglycanopathy (MDDG), MDDG type C5, MDDG type A5, MDDG type B5
FKRP
FSH / LH Series - GNRH Stimulation FSH LH Stim
Follicle Stimulating Hormone - GNRH Stimulation, FSH / LH Series - GNRH Stimulation, GNRH Stimulation, Gonadotropin Releasing Hormone Stimulaiton, LH Series, Luteinizing Hormone - GNRH Stimulation
FLST
Heavy Metals Panel 3, Blood Heavy Metals, Blood
Arsenic, Blood (Heavy Metals Screen), Heavy Metals, Blood, Mercury, Blood (Heavy Metals), Lead , Element testing, As, Hg, Pb
XMETAL
Hematologic Cancer Fusion Analysis Hematologic Cancer Fusion Analysis
Heme fusion detection, Leukemia fusion, Leukemia translocation, Leukemia rearrangement, Lymphoma fusion , Lymphoma translocation, Lymphoma rearrangement, Myeloma fusion , Myeloma translocation, Myeloma rearrangement, Blood cancer fusion detection, Heme cancer fusion panel, Tumor profiling, Tumor somatic profiling, Tumor molecular profiling, Tumor fusion profiling, Somatic fusion detection, RNA fusion detection, Cancer gene fusion detection, Pan-heme fusion detection, Pan heme fusion panel, Hematologic fusion panel, Archer FusionPlex NGS Assay, Philadelphia chromosome-like ALL, Ph-like ALL, Ph like ALL, B-ALL fusion
HEMFUSN
Hepatic Function Panel Hepatic Function Panel
Hepatic Function Panel, LFT, Liver Function tests
HFP
Hepatic Function Panel (Newborn) Newborn Hepatic Function Panel
Albumin, ALP, ALT, Aspartate amino transferase, Hepatic Function Panel (Newborn), Liver Function Panel, Protein, Total, Alanine aminotransferase
NHFP
Immunohistochemistry and Special Stains Immunohistochemistry and Special Stains
immunoperoxidase, tumor markers, lymphoid markers, immunophenotyping, IHC, Special stains
AP28
Interleukin 28B Associated Variants, IL28B, 2 SNPs IL28B Assoc Variants 2SNP
IL28B Assoc Variants 2SNP, Interleukin 28B, IL-28B , Interleukin 28B Polymorphism , Lambda Interferon Genotyping , Ribavirin Genotyping - IL28B, Hepatitis C Virus Genotyping, IL28B.12979860, Interleukin 28B Polymorphism
XIL28B
Keppra (Levetiracetam) Keppra (Levetiracetam)
Keppra (Levetiracetam), Levetiracetam, anti-epileptic
XKEP
Lactate Lactate
LA, Lactate, Lactic Acid, plasma lactate
LACT
Lactate Dehydrogenase LDH
Lactate Dehydrogenase, LD, LDH
LDH
Lactate Dehydrogenase, Fluid Lactate Dehydrogenase, Fluid
Lactate Dehydrogenase, Fluid, LD, Fluid, LDH, Fluid
LDHF
Lactate, CSF Lactate, CSF
CSF, Lactate, Cerebrospinal Fluid, Lactate, Lactate, CSF, Lactic Acid, CSF
LACC
LAMA2 (Merosin) Gene Sequencing LAMA2 (Merosin) Gene Sequencing
MDC1A, LAMA-2 related congenital muscular dystrophy, Merosin-deficient congenital muscular dystrophy 1A, Limb-girdle muscular dystrophy, Limb girdle muscular dystrophy, LGMD, Laminin alpha-2 deficient CMD, Early-onset LAMA2 deficiency, Late-onset LAMA2 deficiency
MERGS
Lamotrigine Lamotrigine
Lamictal
XLAMO
Lead with Zinc Protoporphyrin Lead with XZZP
Pb (Lead with Zinc Protoporphryn), Zinc Protoporphyrin , ZnPP , Porphyrins, ZPP, ZPP/Heme Ratio, Lead, Pb
PBXZP
Lead, Filter Card Filter Paper Lead
PBFP
Lead, Only Lead, Only
Pb (Lead), Lead Screen, PB only
PBO
Lead, Urine Lead, Urine
Lead, Urine, Pb, Urine, Element testing
XLEADU
Legionella Antigen, Urine Legionella Antigen Urine
Legionella Antigen, Urine, Legionella Urinary Antigen, Legionella Serogroup 1 Urinary Antigen
XLEGI
Leukocyte Adhesion Panel Leukocyte Adhesion Panel
LAD, Leukocyte Adhesion Panel, Leukocyte Function Panel, Leukocyte Function Assay, Neutrophil Adhesion Mrkrs: CD18/11b, Neutrophil Adhesion
LADP
Lipase Lipase
Lip, Lipase
LIPA
Lipase, Fluid Lipase, Fluid
Lipase Fluid
LIPF
Lipid Profile Lipid Profile
Cholesterol (Lipid Profile), HDL, High Density Lipoprotein, LDL, Lipid Profile, Low Density Lipoprotein, Triglyceride, Very Low Density Lipoprotein, VLDL
LIPP
Lipoprotein (a) Lipoprotein, a
lp (a), Lp(a) apoprotein
XLIPOA
Lithium Lithium
Li
LI
Liver Kidney Microsomal Antibody Liver Kidney Microsomal Ab
Kidney Microsomal Antibody, Liver Kidney Microsomal Antibody, Liver Microsomal Antibody, LKM, Microsomal Antibody, Liver and Kidney, P450 2D6 Antibody, IgG, Liver-Kidney Microsome - 1 Antibody, IgG, Anti-P450 2D6 Antibody, AntiP450 2D6 Antibody, IgG, LKM-1 Antibody, IgG, LKM-1 IgG, LKM1 IgG, LMK1
XLKMA
LMNA (Lamin A/C) Gene Sequencing LMNA (Lamin A/C) Gene Sequencing
Laminopathy, LMNA mutation analysis, LMNA sequence analysis, LMNA-related disorders, LGMD, LGMD1B, LGMD type 1B, Limb-girdle muscular dystrophy type 1B, Dilated cardiomyopathy 1A, LMNA-related Emery-Dreifuss muscular dystrophy, Hutchinson-Gilford progeria syndrome, Familial partial lipodystrophy type 2, Charcot-Marie-Tooth disease type 2B1 (recessive) , Lethal restrictive dermopathy (recessive), Limb girdle muscular dystrophy
LAC
Lupus Anticoagulant Workup Lupus Anticoagulant Workup
LAW, Lupus Anticoagulant Workup
LAW
Luteinizing Hormone, 3rd generation LH
LH, Luteinizing Hormone, 3rd generation LH
LH
Lyme Disease Antibodies with Immunoblot Reflex Lyme Serology
Lyme disease, Borrelia burgdorferi Antibody, Lyme disease antibody
LYMAB
Lymph Node Immunophenotype Immunophenotype, Lymph Node
Tissue Immunophenotype, Lymph Node Immunophenotype, Lymphoma, Leukemia, ILN
FLOWSP
Lymph Node Pathology Lymph Node Pathology
Hodgkin's Lymphoma, Lymph Node Pathology, Lymphadenopathy, Lymphoma, Non-Hodgkin's Lymphoma
AP19
Lymphocyte Subset (T, B, NK Cells) Quantitation by Flow, Blood Lymphocyte Subset (T, B, NK Cells) Quantitation by Flow, Blood
IPB, AIDS (Acquired Immune Deficiency Syndrome), B Cell, CD3 count, Flow Cytometry, CD19 count, Flow Cytometery, CD4 count, Flow Cytometry, CD56 count, Flow Cytometry, CD8 count Flow Cytometry, Flow Cytometry, T and B Cells, Helper Suppressor Ratio, Immune Competence, Immune Status, Flow Cytometry, Immunodeficiency Panel, Flow Cytometry, Immunophenotyping CD4 Count, Flow Cytometry, Lymphocyte Surface Marker Assay, Quantitative CD4 and CD8, Suppressor Helper Ratio, T and B Cells, T Cell, T Helper/T Suppressor Ratio, T4/T8 Helper Suppressor Ratio, T and B Lymphocyte surface Marker, Lymphocyte Enumeration, Lymphocyte Subset Enumeration, Severe Combined Immunodeficiency, SCID, NK, Natural Killer Cells, NK cell quantitation, Total NK Cells, QN Lymphocyte Subsets
TBNK
Lysosomal Enzyme Screen Lysosomal Enzyme Screen
Lysosomal enzyme screen, Lysosomal storage disease screen, Lysosomal storage disease enzyme panel, Krabbe disease, Mucopolysaccharidosis (MPS I, IIIB, IVB, VI, VII), Gaucher disease, Pompe disease, Fabry disease, Hurler-Scheie syndromes, Sanfilippo syndrome, Lysosomal diseases panel, Niemann-Pick disease
XLYSO
Lysosomal Krabbe Screen Lysosomal Krabbe Screen
4MU-Beta-D-galactoside, Beta galactosidase, GM1 gangliosidosis, Galactosylceramide, Galactocerebrosidase, Krabbe disease, Lysosomal storage disease
XLKRA
Lysosomal MPS Screen Lysosomal MPS Screen
Lysosomal enzyme screen, Lysosomal storage disease, Mucopolysaccharidosis, GM1 gangliosidoses , Beta-glucuronidase deficiency, Beta galactosidase, 4MU-Beta-D-galactoside, 4MU-a-L-iduronide, a-L-iduronidase, Mucopolysaccharidosis (MPS I, IIIB, IVB, VI, VII), Hurler-Scheie syndromes (MPS I), Hurler Scheie syndromes (MPS I)
XLMPS
Lysozyme, Serum Lysozyme, Serum
Muramidase serum, Serum lysozyme
XLYSOZ
Mitochondrial DNA Screen (Point Mutations & Deletions) Mitochondrial DNA Screen
LHON, MELAS, NARP, MERRF, mtDNA Deletion Syndromes, Leber Hereditary Optic Neuropathy
XMDS
Mitogen Stimulation Mitogen Stimulation
Lymphoblastic Transformation, Mitogens, Mitogen Stimulation, Lymphocyte Mitogen Proliferation, Mitogen Proliferation, PHA, Con A, ConA, PWM
XMTS
Mucopolysaccharides (MPS) Screen, Urine, to MAYO Mucopolysaccharides (MPS) Screen, Urine, to MAYO
Mucopolysaccharides Screen (MPS)U, Arylsulfatase B Deficiency, Berry Spot, Beta-Galactosidase Deficiency, Beta-Glucoronidase Deficiency, Chondroitin Sulfate, Dermatan Sulfate, GAGS (Glycosaminoglycans, Galactose-6-Sulfatase Deficiency, Heparan Sulfate, Hunter Syndrome, Hurler Syndrome, Hurler/Scheie Syndrome, Iduronate Sulfatase Deficiency, Iduronidase Deficiency, Keratan Sulfate, Lysosomal Storage Disease, Maroteaux Lamy Syndrome, Maroteaux-Lamy Syndrome, Morquio A or B, MPS I OR II OR III OR IVA OR IVB OR VI OR VII, Mucopolysaccharides, Multiple Sulfatase Deficiency, Sanfilippo Syndrome, Scheie Syndrome, MSD (Maple Syrup Disease), Lysosomal Storage, Sly Syndrome
XMPSSC
Mucopolysaccharides (MPS), Quantitative, Urine Mucopolysaccharides
Arylsulfatase B Deficiency, Beta-Galactosidase Deficiency, Beta-Glucoronidase Deficiency, Chondroitin Sulfate, Dermatan Sulfate, GAGS (Glycosaminoglycans), Galactose-6-Sulfatase Deficiency, Heparan Sulfate, Hunter Syndrome, Hurler Syndrome, Hurler/Scheie Syndrome, Iduronate Sulfatase Deficiency, Iduronidase Deficiency, Keratan Sulfate, Lysosomal Storage, Lysosomal Storage Disease, Maroteaux Lamy Syndrome, Morquio A, Morquio B, MPS I, MPS II, MPS III, MPS IVA, MPS IVB, MPS VI, MPS VII, Mucopolysaccharides, Multiple Sulfatase Deficiency, Sanfilippo Syndrome, Scheie Syndrome, Sly Syndrome, Berry Spot, MSD (Maple Syrup Disease), MPSQN Mayo Test Code, Urine GAG
XMUCQN
Myotilin (MYOT) Gene Sequencing Myotilin (MYOT) Gene Sequencing
Myotilinopathy, Myotilin-related myopathy, Myofibrillar myopathy, LGMD, LGMD1A, LGMD type 1A, Limb-girdle muscular dystrophy type 1A, Limb girdle muscular dystrophy, MYOT mutation analysis, MYOT sequence analysis
MYO
NGS Periodic Fever Syndromes Panel NGS Periodic Fever Syndromes Panel
Familial Mediterranean fever, Familial Hibernian fever, TNF receptor associated periodic syndrome (TRAPS) , Mevalonate kinase deficiency, Hyper-IgD syndrome, Mevalonic aciduria, Muckle-Wells syndrome, Familial cold autoinflammatory syndrome, Neonatal onset multisystem inflammatory disease, NOMID, Chronic infantile neurologic cutaneous & articular, CINCA syndrome, Cyclic neutropenia, Severe congenital neutropenia, Pyogenic arthritis, pyoderma gangrenosum, and acne, PAPA syndrome, Majeed syndrome, MEFV, TNFRSF1A, MVK, NLRP3, CIAS1, ELANE, ELA2, PSTPIP1, LPIN2, NLRP12
NGSPFS
NGS RASopathy Panel (Noonan Spectrum Disorders NGS Panel) NGS RASopathy Panel (Noonan Spectrum Disorders)
Noonan spectrum disorders Next-Gen gene panel, Noonan syndrome gene panel, Noonan-related genes, RASopathies panel, Costello syndrome, Cardio-facio-cutaneous (CFC) syndrome, LEOPARD syndrome, PTPN11, SOS1, RAF1, KRAS, NRAS, SHOC2, BRAF, MAP2K1 (MEK1), MAP2K2 (MEK2), HRAS, CBL, RIT1, NF1, SPRED1, Cardiofaciocutaneous syndrome, Noonan spectrum Next-Gen sequencing panel, Noonan NextGen panel
NGSRP
NOTCH1 Gene Sequencing NOTCH1 Gene Sequencing
Left ventricular outflow tract obstruction, LVOTO, Left heart disease, Adams-Oliver syndrome type 5, Aortic valve disease, NOTCH1 mutation analysis, NOTCH1 sequence analysis, NOTCH1 sequencing
NOTCH1
Ova and Parasite Examination Ova and Parasite Examination
O and P, Stool, Ova-Parasite Examination, Stool, Cystoisospora (Isospora), Cyclospora, Schistosomiasis, Schistosoma, Larvae of Parasitic Helminths (Worm)
OVAP
Platelet Aggregation Platelet Aggregation
Platelet Aggregation, Plt Agg, Platelet Agg, Platelet Aggregation with ATP Release, Platelet Aggregation with Luminescence, Lumi Agg, PLTA, Lumi Platelet Aggregation
PLTAB
PTPN11 Gene Sequencing PTPN11 Gene Sequencing
Noonan syndrome, LEOPARD syndrome, PTPN11 mutation analysis, PTPN11 sequence analysis, Noonan spectrum disorder, RASopathy
PTPN11
RAF1 Gene Sequencing RAF1 Gene Sequencing
Noonan syndrome, LEOPARD syndrome, RAF1 mutation analysis, RAF1 sequence analysis, Noonan spectrum disorder
RAF1
SGCA (Alpha-Sarcoglycan) Gene Sequencing SGCA (Alpha-Sarcoglycan) Gene Sequencing
Sarcoglycanopathy, Alphasarcoglycan, Limb-girdle muscular dystrophy type 2D, LGMD, LGMD2D, LGMD type 2D, SGCA sequence analysis, SGCA mutation analysis, Alpha-sarcoglycan mutation analysis, Alpha sarcoglycan, Limb girdle muscular dystrophy
ASG
SGCB (Beta-Sarcoglycan) Gene Sequencing SGCB (Beta-Sarcoglycan) Gene Sequencing
Sarcoglycanopathy, Sarcoglycan, Betasarcoglycan, LGMD, Limb-girdle muscular dystrophy type 2E, LGMD2E, LGMD type 2E, SGCB sequence analysis, SGCB mutation analysis, Beta-sarcoglycan mutation analysis, Beta sarcoglycan, Limb girdle muscular dystrophy
BSG
SGCD (Delta-Sarcoglycan) Gene Sequencing SGCD (Delta-Sarcoglycan) Gene Sequencing
Deltasarcoglycan, Sarcoglycan, LGMD, LGMD2F, Delta-sarcoglycan mutation analysis, Limb-girdle muscular dystrophy type 2F, Limb girdle muscular dystrophy, SGCD-related dilated cardiomyopathy, Dilated cardiomyopathy 1L (SGCD), LGMD type 2F, SGCD sequence analysis, SGCD mutation analysis, Delta sarcoglycan
DSG
SGCG (Gamma-Sarcoglycan) Gene Sequencing SGCG (Gamma-Sarcoglycan) Gene Sequencing
Sarcoglycanopathy, LGMD, LGMD2C, LGMD type 2C, Gammasarcoglycan, Sarcoglycan, Gamma-sarcoglycan mutation analysis, Limb-girdle muscular dystrophy type 2C, Limb girdle muscular dystrophy, SGCG sequence analysis, Gamma sarcoglycan, SGCG mutation analysis
GSG
Staclot LA StaClot LA
Lupus Anticoagulant (Staclot LA), SLA, Staclot LA, Battery member of Lupus Anticoagulant Workup, Hexagonal Phase Phosphatidylethanolamine
SLA
Targeted Oncology Microarray Analysis Targeted Oncology Microarray Analysis
LOH, SNP micorarray, cancer microarray, cancer array, cancer SNP microarray, Wilms tumor microarray, Neuroblastoma microarray, Neuroblastoma segmental aneuploidy, Neuroblastoma segmental loss of heterozygosity, Neuroblastoma loss of heterozygosity 1p and 11q, Wilms Tumor loss of heterozygosity 1p and 16q, genome oncology array, cancer oncology genome array, Wilms tumor segmental loss of heterozygosity, cancer genome microarray, Neuroblastoma LOH, Tumor SNP array, Wilms Tumor LOH, Tumor SNP microarray, Wilms tumor 1q gain, NBL segmental aberrations, Cancer chromosomal microarray, oncology chromosomal microarray, oncology microarray, oncology snp microarray, oncology genome array, Cancer genome array, Neuroblastoma array, Wilms tumor array, cancer oncology microarray, Neoplastic SNP microarray, Neoplastic array, neoplastic genome array
TONCMA
Thyrotropin Receptor Antibody, Serum Thyrotropin Receptor Antibody, Serum
Antibodies to TSH receptor, Inhibitory Immunoglobulin, Long-Acting Thyroid Stimulator (LATS), TBII (TSH-Binding Inhibiting Immunoglobulin), Thyroid-Stimulating Hormone Receptor (TSH Receptor, TRAb (Thyrotropin Receptor Antibody), TSH (Thyroid-Stimulating Hormone) Receptor Binding, TSH Binding Inhibition Index, TSH Receptor (Thyroid-Stimulating Hormone Receptor, TSH-Binding Inhibiting Immunoglobulin (TBII), Graves Disease, TSH Receptor Antibody , Thyroid Stimulating Hormone Receptor, TRAB , TRAb/TBII
XTHYRO
TP53 Gene Sequencing TP53 Gene Sequencing
Li-Fraumeni syndrome, Li-Fraumeni-like syndrome, TP53 mutation analysis, TP53 sequence analysis, p53 gene sequencing
TP53GS
Transplant, Lymphocyte Subset (T, B, NK Cells), Quantitation by Flow, Blood Transplant, Lymphocyte Subset (T, B, NK Cells), Quantitation by Flow, Blood
TIPB, AIDS (Acquired Immune Deficiency Syndrome), B Cell, CD19 count, Flow Cytometery, CD3 count, Flow Cytometry, CD4 count, Flow Cytometry, CD56 count, Flow Cytometry, CD8 count Flow Cytometry, Flow Cytometry, T and B Cells, Helper Suppressor Ratio, Immune Competence, Immune Status, Flow Cytometry, Immunodeficiency Panel, Flow Cytometry, Immunophenotyping CD4 Count, Flow Cytometry, Lymphocyte Surface Marker Assay, Quantitative CD4 and CD8, Suppressor Helper Ratio, T and B Cells, T Cell, T Helper/T Suppressor Ratio, T4/T8 Helper Suppressor Ratio, T and B Lymphocyte surface Marker, Lymphocyte Enumeration, Lymphocyte Subset Enumeration, Severe Combined Immunodeficiency, SCID, NK, Natural Killer Cells, NK cell quantitation, Total NK Cells, QN Lymphocyte Subsets, Peripheral Blood Transplant
TBNKTX
Transplantation Pathology Transplantation Pathology
Heart Transplant Pathology, Kidney Transplant Pathology, Liver Transplant Pathology, Lung Transplant Pathology, Transplantation Pathology
AP20
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