Laboratory Test Directory

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Test Name A to Z

Guide Name Test Name Updated Synonyms Test Code
Infliximab or Biosimilar Activity and Neutralizing Antibody Infliximab Act & Neutraliz AB
Human Anti-Chimeric Antibody , Remicade , Infliximab/HACA Measurement, Infliximab Activity, Anti-INF-alpha Drug, TNFa antibody , Anser IFX, Inflectra, IFX and IFX-dybb Act & Neut AB
XINFLX
Insulin Antibodies, Serum Insulin Antibodies, Serum
Anti-Insulin, Human Insulin, INAB (Insulin Antibodies), Insulin Ab, Insulin Antibody, IAA , Insulin Autoantibody
XINAB
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
Jo-1 Antibody JO-1 IgG Autoantibodies
JO-1 IgG Autoantibodies, Histidyl-transferase RNA synthetase, Jo-1 Antibody, Histadyl
XJO1A
Lipid Profile Lipid Profile
Cholesterol (Lipid Profile), HDL, High Density Lipoprotein, LDL, Lipid Profile, Low Density Lipoprotein, Triglyceride, Very Low Density Lipoprotein, VLDL
LIPP
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
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 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
Mercury, Whole Blood Mercury, Blood
Hg, Blood, Mercury, Blood, HGB, Element testing, Hg WB
XMER
Mononucleosis Screen Mono Screen
Heterophile Antibody, Mononucleosis Screen, EBV screen, EBV Ig M
MONOS
MTHFR Polymorphism Analysis (C677T & A1298C) - NOT ORDERABLE MTHFR Polymorphism Analysis (C677T & A1298C) - NOT ORDERABLE
Methylenetetrahydrofolate reductase, Methylene tetrahydrofolate reductase, MTHFR common variants detection, MTHFR mutation analysis, MTHFR C677T variant, MTHFR c.665C>T, MTHFR A1298C variant, MTHFR c.1286A>C, Hyperhomocysteinemia
NOT ORDERABLE
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
Natural Killer Assay (NK Function) NK Function
NK Function, Natural Killer Function, Natural Killer Cell, Natural Killer, Natural Killer Assay, HLH: NK Function
XNKF
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
Oxalate, Urine Oxalates, Urine
Oxalates, Urine, Hyperoxaluria
XOXAB
Parvovirus B 19 Antibody, IgM Parvovirus B19 Antibody, IgM
B19, Erythrovirus B19 IgM, Human Parvovirus B19 IgM, Fifth Disease
XPARM
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