Laboratory Test Directory

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Test Name A to Z

Guide Name Test Name Updated Synonyms Test Code
25 Hydroxyvitamin D2 and D3, Serum 25 Hydroxyvitamin D2 and D3, Serum
25-Hydroxy D2, 25-Hydroxy D3, 25-Hydroxy Vitamin D, 25-Hydroxycholecalciferol, 25-Hydroxyergocalciferol, 25-OH Vitamin D, Calcidiol, D2, D3, Vitamin D Assay, Vit D 25-Hydroxy Fractionated
X25HDN
7-Dehydrocholesterol, Plasma 7 Dehydrocholesterol
7-Dehydrocholesterol Reductase Deficiency, 8-Dehydrocholesterol, RSH Syndrome, Smith Lemli Opitz (SLO), 7DHC , 7-DHC, Dehydrocholesterol 7, SLO , SLOS , Smith-Lemli-Opitz syndrome
XSLOB
Acetaminophen Acetaminophen
Tylenol, Datril, Paracetamol, APAP
ACET
Allergen, Dog Dander IgE Allergen: Dog dander IgE
Allergen Dog Dander, Dog Dander allergen, Allergen Environ: Dog Dander, Dog Epithelium
PEDD
Allergen, Food, Red Dye IgE Allergen, Food, Red Dye IgE
Carmine, Dactylopius coccus, Cochineal , Red Dye, Red 4
XRDYE
Allergen, Mite farinae IgE Allergen: Mite farinae IgE
Allergen Mite farinae, Mite farinae allergen, Dust mite farinae, Dermatophagoides farinae, House Dust Mite, Allergen Environ: Mite farinae
PEMFA
Allergen, Mite ptero. IgE Allergen: Mite ptero. IgE
Allergen Mite pteronyssinus, Dust mite pteronyssinus, Dermatophagoides pteronyssinus, Mite ptero. allergen, House Dust Mite, Allergen Environ: Mite ptero.
PEMPT
ALPS (Autoimmune Lymphoproliferative Syndrome) Panel ALPS Panel
B220, CD45B220, ALPS, DNTC, ALPS Panel by Flow, XALPS
ALPS
Aminolevulinic Acid (ALA), Urine Aminolevulinic Acid, Urine
ALA, Tyrosinemia (Hereditary) Metabolite Urine, Delta-ALA, 5-Aminolevulinic Acid , Delta-Aminolevulinic Acid
XALA
Anti-DNAse B Anti-DNAse B
DNAse B, Anti-DNAse B, GAS Enzymes, Group A Strep Enzymes (Anti-DNAse B), Strep Group A Enzymes
DNB
Arginine Vasopressin Hormone Anti-Diuretic Hormone
ADH, Anti-Diuretic Hormone, Vasopressin, AVH, AVP, Diabetes Insipidus, SIADH, Antidiuretic Hormone
XADH
B Cell ALL MRD Bone Marrow Testing BALL MRD Bone Marrow Testing
MRD, B-CELL ALL, DAY 29, End of Consolidation,
MRDBM
B-Cell ALL MRD, Peripheral Blood Day 8 BALL MRD, Periperhal Blood Day 8
MRD, DAY 8, B-CELL ALL, ALL
BALMRD
BRAF V600 Mutation Analysis BRAF V600 Mutation Analysis
BRAF V600 variant detection, BRAF codon 600 mutation, BRAF exon 15 targeted sequencing, BRAF V600E mutation detection, BRAF V600K mutation detection, BRAF V600R mutation detection, BRAF V600 cancer testing, BRAF V600 tumor testing, BRAF V600 somatic testing, Low grade pediatric glioma, Ganglioglioma, Pleiomorphic xanthoastrocytoma (PXA), Diffusely infiltrative astrocytoma, Melanoma, Hairly cell leukemia, Papillary thyroid carcinoma, Thyroid cancer, Colon cancer, Ovarian cancer, Endometrial cancer, BRAF V600E, c.1799T>A, p.Val600Glu mutation
BRAFV600
Catecholamine Fractionation, Free, 24 Hour, Urine Catecholamine Fractionation, Free, 24 Hour, Urine
Adrenaline, Catecholamine Fractionation, Urine, Catecholamines, 24-Hour Urine, Catecholamines, Total, Catecholamines, Urine, Dopamine, Epinephrine, Noradrenaline, Norepinephrine, Pressor Amines
XCATUM
Clomipramine and Metabolite Clomipramine and Metabolite
Anafranil, Desmethylclomipramine, Norclomipramine, Anafranil Level
XCLOMB
Connexin 26 Mutation Analysis (GJB2 Sequencing) Connexin 26
Connexin 26, CX26, GJB2 sequence analysis, Connexin 26 sequencing, Connexin 26 sequence analysis, Pre-lingual hearing loss, Non-syndromic hearing loss, Non-syndromic deafness, DFNB1A, DFNB1, DFNA3A, DFNA3
CONN
Connexin 30 Deletion Analysis (GJB6 Deletion Detection) Connexin 30
CX30, Non-syndromic hearing loss, Non-syndromic deafness, DFNA2, DFNB1B, DFNA3B, Connexin 30 deletion detection, Connexin 30 targeted deletion analysis, GJB6 targeted deletion analysis, GJB6 gene deletion
CONN30
D Lactate, Plasma D Lactate, Plasma
D-lactate, D lactate, Lactate (D) Plasma, 8878 Mayo test code
XDLAC
Deamidated Gliadin Peptide Antibody, IgA Deamidated Gliadin Peptide Antibody, IgA
Deamidated Gliadin IgA Peptide Antibody, celiac
DGLIAA
Deamidated Gliadin Peptide Antibody, IgG Deamidated Gliadin Peptide Antibody, IgG
Deamidated Gliadin IgG Peptide Antibody, celiac
DGLIAG
Dehydroepiandrosterone Dehydroepiandrosterone
Dehydroepiandrosterone (DHEA), DHEA
DHEA
Deoxycorticosterone Deoxycorticosterone
21-hydroxyprogesterone, 11-deoxycorticosterone
DOC
DHEA SO4 DHEA SO4
DHEA SO4, Dehydroepiandrosterone sulfate, DHEAS, DHEA Sulfate
DHS4
Diazepam and Nordiazepam Diazepam
Diazepam, Nordiazepam (Diazepam), Benzodiazepines, Clorazepate, Diastat, Diazemuls, Stesolid, T-Quil, Tranxene, Valium, Valrelease, Zetran
XDZB
Differential Count WBC Differential
Diff, Diff Count, WBC Differential, White Blood Cell Differential, Blood smear
DIFF
Digoxin Digoxin
Lanoxin
XDIG
Dihydrotestosterone Dihydrotestosterone (DHT)
Dihydrotestosterone, DHT, Androstaner-3-one, Hydroxy-5alpha
XDTEST
Dilute Russell Viper Venom Test Dil. Russells Viper Venom Test
Russell Viper Venom Time, Battery member of Lupus Anticoagulant Workup, Dilute Russell Viper Venom Time, DRVVT
DRVVT
Diphtheria & Tetanus Antibodies Diphtheria and Tetanus Ab
Diphtheria & Tetanus Antibodies, Tetanus & Diphtheria Antibodies
ADAT
Diphtheria Antibody Diphtheria Antibody
Diphtheria Antibody
DIPH
Direct Coombs Direct Coombs
DAT, Direct Antiglobulin Test, Direct Coombs, Coombs (Direct)
DAT
Direct Strep A Antigen Screen, throat Direct Group A Strep Test, throat
Direct Strep A Antigen Screen, Streptococous pyogenes (Antigen screen)
DSSCB
Disopyramide, Serum or Plasma Disopyramide, Serum or Plasma
Disopyramide, Norpace, Rythmodan, disopyramide phosphate, Norpace CR
XDISO
Disorders of N Glycosylation, Serum Disorders of N Glycosylation, Serum
Carbohydrate Deficient Glycoprotein Syndrome CDGS, CDG (Congenital Disorders of Glycosylation), N-linked Glycosylation Disorders, N-glycan, N-linked oligosaccharides, N glycosylation
XCDGN
DMD Gene Sequencing DMD Gene Sequencing
Dystrophin gene sequencing, Duchenne muscular dystrophy, Becker muscular dystrophy, Dilated cardiomyopathy 3B, DMD-associated cardiomyopathy, Dystrophinopathy, Dystrophinopathies
DMDGS
DNA Isolation and Storage DNA Isolation and Storage
DNA extraction, DNA storage, DNA for future testing, DNA isolation
DNASTOR
DNA Ploidy Analysis DNA Ploidy Analysis
DNA Ploidy Analysis, Ploidy Analysis, DNA, DNA Index
DNAP
DNAJB6 Gene Sequencing DNAJB6 Gene Sequencing
DNAJB6 mutation analysis, DNAJB6 sequence analysis, LGMD, LGMD1E, LGMD type 1E, Limb-girdle muscular dystrophy type 1E, Limb girdle muscular dystrophy
DNAJB6
Donor Stem Cell Panel w Chagas Donor Stem Cell Panel w Chagas
IDM, Immunodeficiency markers, Trypanosoma cruzi, Chagas
XDSPCH
Double Stranded DNA Antibody, (Crithidia) Titer Crithidia (IFA) Titer
Double Stranded DNA antibody, ds DNA Antibody, (Crithidia), Crithidia, Systemic lupus erythematosus, Lupus, SLE, Autoimmune
CRTH
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
NMO (Aquaporin 4) IgG FACS Assay, Serum Neuromyelitis Optica (NMO), Serum
NMO Antibodies, AQP4, Aquaporin, AQP, AQP4 ELISA, Devic's Antibody, Neuromyelitis Optica (NMO), NMO-IgG, Optic Neuritix Antibody, Optic-Spinal MS Antibody, Transverse Myelitis Antibody, Vision Loss Antibody, Neuromyelitis Optica Evaluation , Neuromyelitis Optica (NMO)/Aquaporin-4-IgG Cell-Bi, Aquaporin-4-IgG Cell-Binding Assay Serum, NMOSD
XNMOFS
Oxidative Burst Assay Oxidative Burst Assay
CGD Screen, Oxidative Burst Assay, Respiratory Burst, Chronic Granulomatous Disease, Substitute for NBT Test, DHR, OBA
DHRB
Phenytoin Phenytoin
Dilantin, Phosphenytoin, Fosphenytoin
DPH
Protein, Peritoneal Dialysate Protein, Peritoneal dialysate
Dialysate, Peritoneal, Protein, Peritoneal Dialysate, Protein
PRDIAL
Pseudocholinesterase, Dibucaine Inhibition Pseudocholinesterase, Dibucaine Inhibition
Dibucaine Number, Cholinesterase Inhibition by Dibucaine, Pseudocholinesterase Inhibition Dibucaine Number, Cholinesterase Serum, Butyrylcholinesterase
XPCHED
Purines and Pyrimidines Panel, Urine Purines and Pyrimidines Panel, Urine
5-hydroxymethyluracil, Adenine, Adenosine, Deoxyadenosine, Deoxyguanosine, Deoxyinosine, Guanosine, Hyperuricemias, Hypoxanthine, Inosine, Orotic Acid, Pyrimidine, Succinyladenosine, Thymidine, Thymine, Uracil, Uric Acid, Uridine, Xanthine, S-Sulfocysteine
XPUPYU
Quantitative D-dimer Quantitative D-dimer
Quantitative D-dimer, D-dimer Quantitative, Quant D-dimer, High Sensitivity D-dimer
QDDIM
Serum Drug Screen Serum/Blood Drug Screen
Drug screen, Blood drug screen, Toxocology Screen
XSDRG
SGCD (Delta-Sarcoglycan) Gene Sequencing SGCD (Delta-Sarcoglycan) Gene Sequencing
Deltasarcoglycan, Sarcoglycan, LGMD, LGMD2F, Delta-sarcoglycan mutation analysis, Limb-girdle muscular dystrophy type 2F, Limb girdle muscular dystrophy, SGCD-related dilated cardiomyopathy, Dilated cardiomyopathy 1L (SGCD), LGMD type 2F, SGCD sequence analysis, SGCD mutation analysis, Delta sarcoglycan
DSG
SLC26A4 (Pendrin) Gene Sequencing, Pendred Syndrome SLC26A4 (Pendrin) Gene Sequencing,Pendred Syndrome
Pendred syndrome, DFNB4, SLC26A4, Pendrin, congenital deafness, congenital sensorineural hearing loss
PEND
Soft Tissue Sarcoma Tumor Analysis by RT-PCR Soft Tissue Sarcoma Tumor Analysis by RT-PCR
RT-PCR Fusion Transcript Analysis - Pediatric Solid Tumors, ARMS, PNET, EWS-FLI-1 fusion, EWS-ERG fusion, PAX3-FOXO1 fusion, PAX7-FOXO1 fusion , SYT-SSX1/SSX2 fusion , EWS-WT1 fusion , ETV6-NTRK3 fusion , Sarcoma panel, Ewing sarcoma, Alveolar rhabdomyosarcoma, Synovial sarcoma, Desmoplastic small round cell tumor, DSRCT, Congenital fibrosarcoma, Cellular mesoblastic nephroma, Primitive neuroectodermal tumor, Soft tissue sarcoma fusion transcript detection, Pediatric solid tumor fusion transcript detection, Sarcoma RT-PCR
RTPCR
System Test System Test
Test, Display Test
BECTEST
Trazodone Trazodone
Trazodone, Desyrel, Molipaxin
XTRAS
Type and Coombs (Non-neonate) Type and Coombs, Non neonate
Type and DAT, Coombs, Direct Coombs
BTDBS
Urine Drug Screen Urine Drug Screen
Drug screen, Toxocology Screen
XUDRUG
Urine Drugs With Quant THC Urine Drugs With Quant THC
Drug screen, THC, Urine THC
XUDGT
Valproic Acid Valproic Acid
Depakane, Depakene, Depakote
VPA
Vitamin D-25 Hydroxy 25-OH Vitamin D
25-Hydroxy Vitamin D, Vitamin D-25OH, Vit D 25, Calcitriol, Calciferol, Calcifediol, Vitamin D, Ergocalciferol, D25-Hydroxy Vitamin, Vit D
VITD
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