Laboratory Test Directory

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Test Name A to Z

Guide Name Test Name Updated Synonyms Test Code
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
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