Laboratory Test Directory

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Test Name A to Z

Guide Name Test Name Updated Synonyms Test Code
Kingella kingae Joint Fluid PCR Qualitative K. kingae Joint Fluid PCR Qual
Kingella Joint Fluid PCR, Kingella Synovial Fluid PCR
KNGJF
KMT2D (MLL2) Gene Sequencing KMT2D (MLL2) Gene Sequencing
KMT2D, MLL2, Kabuki syndrome
KMT2DGS
KRAS Gene Sequencing KRAS Gene Sequencing
Noonan syndrome, Cardio-facio-cutaneous (CFC) syndrome, Costello syndrome, Noonan spectrum disorder, KRAS sequence analysis, KRAS mutation analysis, RASopathy
KRAS
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
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
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
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
Potassium Potassium
K, Potassium
K
Potassium, Fluid Potassium, Fluid
K, Fluid, Potassium Fluid
KF
Potassium, Urine Potassium, Urine
K, Urine, Potassium Urine
KU
Potassium, Urine Output Potassium, Urine Timed
K, Urine Output, Potassium, Urine Output, 24 hour Urine Potassium
KUT
PSAP Gene Sequencing, Krabbe Disease PSAP Gene Sequencing, Krabbe Disease
GALC deficiency, Galactocerebrosidase deficiency, Galactosylceramidase deficiency, Globoid cell leukodystrophy, Prosaposin, Saposin A, Saposin B, Saposin C, Saposin D, Sphingolipid activator protein 1 (SAP1), Sphingolipid activator protein 2 (SAP2), Combined SAP deficiency, Atypical Gaucher disease, Atypical Krabbe disease, SAP-b deficiency metachromatic leukodystrophy, PSAP full gene sequencing, PSAP Sanger sequencing, Krabbe disease
KDPSAPSEQ
Pyrroles, Urine Pyrroles, Urine
Mauve Factor, Kryptopyrroles, Urinary Pyrroles, Pyrroles Urine, pyrroluria
XPYR
Renal Pathology Renal Pathology
Biopsy (Kidney), Biopsy (Renal), Kidney Biopsy, Kidney Pathology, Pathology (Renal), Renal Biopsy, Renal Pathology
AP5
Spinal Muscular Atrophy, SMN1 Diagnostic Spinal Muscular Atrophy, Diagnostic
Spinal Muscular Atrophy DNA 1,2,3, SMA 123, Werdnig-Hoffman Disease, SMA type 1, Kugelberg-Welander (Type III), Proximal Spinal Muscular Atrophies, Spinal Muscular Atrophy, SMA Mutation, Spinal Muscular Atrophy Diagnostic (Prior Lab) , SMN1 Gene test, SMA Diagnostic, Spinal Muscular Atrophy (Homozygus deletion), SMN 2
XSMA
Targeted Tumor Variant Analysis Targeted Tumor Variant Analysis
Targeted tumor mutation analysis, Targeted cancer mutation confirmation, Known tumor mutation testing, Targeted somatic mutation testing, Single site tumor mutation analysis, Tumor mutation Sanger confirmation, Targeted tumor Sanger sequencing, Confirmatory tumor mutation testing, Targeted Sanger sequencing for tumor
TTVA
Transplantation Pathology Transplantation Pathology
Heart Transplant Pathology, Kidney Transplant Pathology, Liver Transplant Pathology, Lung Transplant Pathology, Transplantation Pathology
AP20
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