Laboratory Test Directory

Search Our Test Directory

Test Name A to Z

Guide Name Test Name Updated Synonyms Test Code
Culture- Acid Fast Bacillus, Tissue/Fluid AFB Culture, Tissue/Fluid
Acid Fast Bacillus Culture, Tissue / Fluid, AFB Culture, Tissue, Tissue, AFB Culture, Fluid, AFB Culture, AFB Culture, Fluid, Culture, Tissue (AFB), Culture, Fluid (AFB), Mycobacterium , Mycobacteria
Culture- Bacterial, MRSA Screen Culture, MRSA Screen
Culture, MRSA Screen, Methicillin Resistant Staphylococcus aureus Screen, Bacterial Culture
Cytochemical Stains ( ANBE, MPO) Special Stains
ANBE, MPO, Myeloperoxidase, ANBE with Fluoride, Cytochemical Stains
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
Familial Mutation Analysis Familial Mutation Analysis
Familial gene sequencing, Familial variant analysis, Single site mutation testing, Single-site mutation testing, Mutation confirmation, Confirmatory mutation testing, Known mutation testing, Targeted mutation testing, Targeted variant analysis, Targeted germline mutation testing, Single mutation testing, Targeted Sanger sequencing
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
FBN1 Gene Sequencing FBN1 Gene Sequencing
FBN1 mutation analysis, FBN1 sequence analysis, Fibrillin, Marfan syndrome, MASS syndrome, Familial ectopia lentis
FISH Analysis FISH Analysis Only
Metaphase FISH, Constitutional FISH, Microdeletion syndrome, Microduplication syndrome, DiGeorge / Velocardiofacial syndrome (22q11.2), 22q11.2 deletion, Angelman syndrome (15q11.2-13), Prader-Willi syndrome (15q11.2-13), Cri-du-chat (5p-) syndrome (5p15.2), Wolf-Hirschhorn (4p-) syndrome (4p16.3), Williams syndrome (7q11.23), Smith-Magenis syndrome (17p11.2), Kallmann syndrome (Xp22.3), Miller-Dieker syndrome (17p13.3), Steroid sulfatase deficiency (STS) (Xp22.3), X-linked ichthyosis STS deletion, XIST deletion (Xq13.2), SRY detection (Yp11.3), Phelan-McDermid syndrome (22q13.3), Custom FISH analysis, Specialized FISH analysis, FISH for chromosome rearrangement, Chromosome translocation FISH, Chromosome inversion FISH, Marker chromosome FISH, Chromosome insertion FISH, Centromere FISH, Telomere FISH, Microdeletion FISH analysis
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
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
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
Human Metapneumovirus by PCR Qualitative Human Metapneumovirus PCR,Qual
Human Metapneumovirus PCR, Metapneumovirus PCR, hMPV by PCR
IDUA Gene Sequencing IDUA Gene Sequencing
Hurler syndrome, Hurler-Scheie syndrome, Scheie syndrome, Mucopolysaccharidosis type I, Mucopolysaccharidosis type 1, IDUA deficiency, Alpha-L-iduronidase deficiency, IDUA mutation detection, IDUA sequence analysis, IDUA sequencing, MPS I, MPS-I, MPS 1, MPS1, MPS-1
Imipramine and Desipramine Imipramine and Desipramine
Desipramine (including Imipramine), Imipramine and Desipramine, Tofranil, Imavate, Presamine, Antideprin, Deprenyl, Deprimin, Deprinol, Eupramin, Janimine, Melepramin, Norpramin, Novo-Parmine, TCA, Surplix, Tricyclic Antidepressants , Impril, Irmin
Immunofixation Electrophoresis IFE Quantitation, Serum
Serum Protein Electrophoresis, Immunoelectrophoresis, Monoclonal Protein Detection Quantitation and Char, IFE, MGUS study, Monoclonal Protein Study, Mutiple Myeloma Study, Protein ELP, SPEP, MGUS study
KMT2D (MLL2) Gene Sequencing KMT2D (MLL2) Gene Sequencing
KMT2D, MLL2, Kabuki syndrome
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
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
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
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)
About Lab Services
Nationwide Children's Laboratory Services strives to strengthen and expand our role as one of the country’s leading pediatric reference laboratories. Learn more.

Order Supplies

Nationwide Children's Laboratory Services will provide your office with supplies for the collection of specimens (blood, body fluids, tissue) that you send to us. Please complete this form to order the supplies you need. 

Laboratory Services
Convenient Locations

We're in your neighborhood!

Our convenient Laboratory Service Centers allows testing, diagnosis and treatment for children and families to be right where you need it most - in your community. 

View all 17 Ohio locations