Laboratory Test Directory

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Test Name A to Z

Guide Name Test Name Updated Synonyms Test Code
Mycoplasma Pneumoniae Antibody (IgG) Qualitative Mycoplasma Ab, IgG
Mycoplasma Pneumoniae Antibody (IgG), Qualitative Mycoplasma IgG
MIGG
Mycoplasma Pneumoniae Antibody (IgM) Qualitative Mycoplasma Ab, IgM
Mycoplasma Pneumoniae Antibody (IgM), Qualitative Mycoplasama IgM
MIGM
Mycoplasma pneumoniae by PCR, Qualitative Mycoplasma Pneumoniae by PCR
Mycoplasma pneumoniae by PCR, Mycoplasma PCR, M. pneumo PCR, walking pneumonia
MPNTT
Mycoplasma pneumoniae CSF by PCR, Qualitative M. pneumoniae CSF by PCR, Qual
MPN CSF by PCR, walking pneumonia
MPNCSF
Myelin Associated Glycoprotein (MAG) Antibody, IgM Myelin Associated Glycoprotein
MAG, Myelin Associated Glycoprotein (MAG) Antibody, IgM, Myelin Associated Glycoprotein Antibody, IgM
XMAG
Myelin Basic Protein Myelin Basic Protein
Myelin Basic Protein, MBP ARUP test code, 80515 ARUP ref lab code
XMBP
Myoglobin, Urine Myoglobin, Urine
Urine myoglobin, Myoglobin, Urine
XMYO
Myotilin (MYOT) Gene Sequencing Myotilin (MYOT) Gene Sequencing
Myotilinopathy, Myotilin-related myopathy, Myofibrillar myopathy, LGMD, LGMD1A, LGMD type 1A, Limb-girdle muscular dystrophy type 1A, Limb girdle muscular dystrophy, MYOT mutation analysis, MYOT sequence analysis
MYO
Myotonic Dystrophy (DM1) Comprehensive Analysis Myotonic Dystrophy
Myotonic Dystrophy, DMPK Gene, Myotonic Dystrophy, DM-1
XMYTOD
NGS Periodic Fever Syndromes Panel NGS Periodic Fever Syndromes Panel
Familial Mediterranean fever, Familial Hibernian fever, TNF receptor associated periodic syndrome (TRAPS) , Mevalonate kinase deficiency, Hyper-IgD syndrome, Mevalonic aciduria, Muckle-Wells syndrome, Familial cold autoinflammatory syndrome, Neonatal onset multisystem inflammatory disease, NOMID, Chronic infantile neurologic cutaneous & articular, CINCA syndrome, Cyclic neutropenia, Severe congenital neutropenia, Pyogenic arthritis, pyoderma gangrenosum, and acne, PAPA syndrome, Majeed syndrome, MEFV, TNFRSF1A, MVK, NLRP3, CIAS1, ELANE, ELA2, PSTPIP1, LPIN2, NLRP12
NGSPFS
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
Osmolality Osmolality
Measured osmolality
OSMO
Oxcarbazepine or Eslicarbazepine Metabolite (MHD) Eslicarb Metabolite (MHD)
Oxcarbazepine Metabolite, Trileptal, 10-Hydroxycarbazepine, 11-Dihydrocarbamazepine, MHC, MHD, 10-OH-Carbazepine (MHD), Eslicarbazepine, GP 47680, Metabolite of Oxcarbazepine, Monohydroxy Carbamazepine, Monohydroxy Carbamazepine (MHD), Oxcarbazepine
XOXCAR
Parasites, Blood Smear Blood smear for parasites
Malarial Smear, Parasites, Blood Smear, microfilaria , babesia , trypanosomes
MAL
Parental SNP Microarray Analysis (Chromosomal Microarray) Parental SNP Microarray
Parental follow-up microarray, Microarray analysis on parental sample, Parental microarray for known genomic loss/gain, Parental aCGH, Parental array, Parental CGH, Parental chromosomal microarray (CMA), Parental whole genome microarray, Parental CGH+SNP, Parental SNP array, Parental SNP chip
PSNPMA
POC (Products of Conception) / Tissue Microarray Analysis POC (Products of Conception) Microarray Analysis
POC microarray, POC array, POC oligonucleotide microarray, POC SNP microarray, POC array comparative genomic hybridization (aCGH), POC aCGH, Fetal tissue microarray, Placental microarray, Pregnancy loss microarray, Umbilical cord microarray, Tissue microarray, Miscarriage microarray
POCMA
POC Microarray with 5-Cell Chromosome Analysis POC Microarray with 5-Cell Chromosome Analysis
Products of Conception (POC) Microarray, POC Microarray with Abbreviated Karyotype, POC Microarray with 5-Cell Karyotype, POC Microarray with Limited Karyotype, Miscarriage Microarray, Pregnancy Loss Microarray
POCMA5C
POLG Gene Sequencing POLG Gene Sequencing
POLG1, POLGA, POLG alpha, MEMSA (myoclonic epilepsy, myopathy, ataxia), Alpers Huttenlocher syndrome , Childhood myocerebro-hepatopathy spectrum (MCHS), Ataxia neuropathy spectrum (ANS), Progressive external ophthalmoplegia (PEO), Valproic acid (VPA) induced liver failure, POLG mutation analysis, POLG sequence analysis, Mitochondrial DNA depletion syndrome 4A, Mitochondrial DNA depletion syndrome 4B
POLGSEQ
Post-Transplant Analysis, Bone Marrow Engraftment Bone Marrow Engraftment - Post Transplant
Molecular Post BMT, Chimerism study, Chimerism testing, Post transplant, Post BMT testing, Post-BMT recipient genotyping, Bone marrow transplant , Post BMT testing by DNA markers, Post-BMT DNA typing, Sorted cell chimerism by molecular DNA genotyping, HSCT post-transplant, Stem cell transplant
BMPT
Prothrombin Time Mixing Studies PT Mixing Studies
Mixing Studies, Prothrombin Time, Prothrombin Time, Mixing Studies, PT Mixing Studies
PTM
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