Laboratory Test Directory

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Test Name A to Z

Guide Name Test Name Updated Synonyms Test Code
Drug Abuse Panel 10, Urine Drug Abuse Panel 10, Urine
XDOA10
Drug Toxicology Monitoring 1, with Confirmation, Oral Fluid Drug Toxicology Monitoring 1, with Confirmation, Oral Fluid
XORDG
Drugs of Abuse (6-Panel), Urine Drugs of Abuse, Urine
Drugs of Abuse (6-Panel)
DOA
Drugs of Abuse with THC Quant, Urine DOA with THC Quant, Urine
Drug , Drug of abuse with THC Quant, DOA with THC Quant, Drugs of Abuse with THC Quant
DOAT
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
Enterovirus D68 by PCR Enterovirus D68 by PCR
D68, EV68, EVD68
EVD68
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
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
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
FISHON
Glucose Glucose
Dextrose, Glucose
GLUC
Histone Antibody, IgG Histone Antibody, IgG
Histone Antibody IgG, Drug Induced SLE, Antihistone Ab, Anti-Histone Antibodies, AHA
XHIG
HIV-1 DNA by PCR HIV DNA by PCR Diagnostic
Human Immunodeficiency Virus PCR, HIV DNA by PCR Diagnostic, Diagnostic HIV PCR, HIV Provirus PCR, HIV by PCR Qualitative
HIVT
HLA DQ2/DQ8 HLA DQ2/DQ8
DQ2/DQ8, Celiac HLA DQ2/DQ8, HLA DQ2/DQ8, Celiac Genetics, Celiac Genetics (Celiac Gen)
XD2D8
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
XIMBU
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
Meconium Drug Test Meconium Drug Test
Meconium Drug Test, Drugs of Abuse Screen 10 panel Meconium, Drug Panel 10 meconium
XMECO
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
Myotonic Dystrophy (DM1) Comprehensive Analysis Myotonic Dystrophy
Myotonic Dystrophy, DMPK Gene, Myotonic Dystrophy, DM-1
XMYTOD
Neonatal Workup Neonatal Workup
Direct Coombs (Neonatal Workup), Neonatal Workup
NWU
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