Laboratory Test Directory

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Test Name A to Z

Guide Name Test Name Updated Synonyms Test Code
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
Creatine Disorders Panel, Serum or Plasma Creatine Disorders Panel, Serum or Plasma
AGAT, Creatine, GAA & Creatine, GAMT, Guanidinoacetic Acid, GAAPR
XGAASP
Creatine Disorders Panel, Urine Creatine Disorders Panel, Urine
AGAT, GAA & Creatine, GAMT, Guanidinoacetic Acid & Creatine, GAAUP
XGAAUP
Culture- Bacterial, GC Screen only Culture, GC Screen
Bacterial Culture, GC Screen only, Genital, Bacterial Culture (Screen Only), Neisseria gonorrhoeae Screen Culture
GCSC
Culture- Bacterial, Group B Strep Screen Culture, Group B Strep Screen
Bacterial Culture, Group B Strep Screen, Streptococcus agalactiae, Bacterial Culture, Genital Culture for Group B Strep
GBSC
Culture- Bacterial, Throat Screen for Gp A Strep. Culture,Throat Gp A Strep only
Throat for Group A Strep Only, Culture Throat Screen for Group A Strep, Group A Strep Throat Screen Culture
THSC
Culture- Viral, General Virus Culture
Culture, General (Viral), General, Viral Culture, Herpes zoster, Varicella zoster
VIRC
Elafin, Plasma or Serum Elafin, Plasma or Serum
Elafin Plasma, Elafin Serum, Elavin for GvHD, Human Elafin, Graft vs Host Disease – part of the panel, GvHD – part of the panel, GVHD - part of the panel
XELAF
Factor II (Prothrombin) Mutation Factor II (Prothrombin) Mutation
Prothrombin (F2) Mutation , Factor 2 mutation analysis, F2 mutation analysis, Prothrombin (Factor II) mutation analysis, Prothrombin-related thrombophilia, 20210G>A mutation, G20210A mutation, Prothrombin (Factor 2) G20210A mutation PCR
F2MUT
Fasting Glucose Fasting Glucose Battery
Glucose
FGLUC
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
FSH / LH Series - GNRH Stimulation FSH LH Stim
Follicle Stimulating Hormone - GNRH Stimulation, FSH / LH Series - GNRH Stimulation, GNRH Stimulation, Gonadotropin Releasing Hormone Stimulaiton, LH Series, Luteinizing Hormone - GNRH Stimulation
FLST
Gabapentin Gabapentin
Gabarone, Neurontin, Gabapentin Free (Gabapentin
XGABA
Galactokinase, Blood Galactokinase, Blood
Galactokinase B, Galactokinase (RBC), Galactokinase Deficiency, Galactosemia, Galactokinase Blood
XGALKB
Galactose, Quantitative, Plasma Galactose, Quantitative, Plasma
GALP, Galactose Quantitative Plasma, Galactose Plasma, Galactokinase, Galactose, Galactosemia, Galactose QN P
XGALP
GALC Gene Common 30-kb Deletion, Krabbe Disease GALC Gene Common 30-kb Deletion, Krabbe Disease
GALC deficiency, Galactocerebrosidase deficiency, Galactosylceramidase deficiency, Globoid cell leukodystrophy, GALC gene common deletion detection by PCR, Krabbe disease common deletion detection, GALC exon 11-17 deletion detection
KDGALCCD
GALC Gene Deletion/Duplication Analysis, Krabbe Disease GALC Gene Deletion/Duplication, Krabbe Disease
GALC deficiency, Galactocerebrosidase deficiency, Galactosylceramidase deficiency, Globoid cell leukodystrophy, GALC gene comprehensive deletion/duplication test, GALC deletion/duplication analysis by MLPA, GALC gene MLPA analysis, GALC gene atypical deletion/duplication detection, GALC gene del/dup analysis, Krabbe disease
KDGALCDD
GALC Gene Sequencing, Krabbe Disease GALC Gene Sequencing, Krabbe Disease
GALC deficiency, Galactocerebrosidase deficiency, Galactosylceramidase deficiency, Globoid cell leukodystrophy, GALC Sanger sequencing, GALC sequence analysis, GALC full gene sequencing, Krabbe disease
KDGALCSEQ
GAN (Giant Axonal Neuropathy) Gene Sequencing Giant Axonal Neuropathy (GAN) Gene Sequencing
GAN, Giant axonal neuropathy, GAN mutation analysis, GAN sequence analysis
GAN
Ganglioside (GM1) Antibodies, IgG and IgM GM1 Antibody Panel
Ganglioside-monosialic acid, GM1 Antibody Panel, Anti-GM Antibodies, Anti-GM1 Antibody Panel, Ganglioside Antibodies, Ganglioside (GM1) Antibodies, IgG and IgM, Ganglioside Abs IgG and IgM, GM1 IgG IgM
XGM1
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