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Lab test catalogue
Browse or search our laboratory test catalogue for more information on the tests and diagnostic services offered by the Department of Paediatric Laboratory Medicine (DPLM) at SickKids.
Our goal is to make the process of finding and ordering a test as simple as possible. Tests are categorized by lab discipline. Within each test specific page are the specimen requirements, ordering information, interpretation details and appropriate requisitions.
Using the search box at the top of the page, you are able to search by entering:
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Clinical Biochemistry - General
- 25-Hydroxyvitamin D
- Alpha-1-Acid glycoprotein (AAG), plasma or serum
- Alpha-1-Antitrypsin (AAT), plasma or serum
- Alpha-Fetoprotein (AFP)
- Anti-TPO Antibody, plasma or serum
- Beta-Hydroxybutyrate, CSF
- Beta-Hydroxybutyrate, serum (or plasma)
- C3-Complement, plasma or serum
- C4-Complement, plasma or serum
- Ceruloplasmin, plasma or serum
- Chloride, sweat
- Chylomicrons, fluid
- Cortisol, serum or plasma
- Dehydroepiandrosterone Sulphate (DHEA-S), plasma or serum
- Fatty Acids, Free, serum
- Fecal Calprotectin, Stool
- Fecal Elastase, stool
- Ferritin, serum or plasma
- Folate, erythrocytes
- Folate, serum
- Follicle Stimulating Hormone (FSH), serum or plasma
- Free T4, serum
- Gentamicin, plasma or serum
- Glucose-6-Phosphate Dehydrogenase (G6PD), erythrocytes
- Growth Hormone
- Haemoglobin, plasma
- Haptoglobin, plasma or serum
- Homocysteine, plasma or serum
- Insulin, serum or plasma
- Insulin-like Growth Factor 1 (IGF-1)
- Intralipid, plasma or serum
- Lipase, plasma or serum
- Lithium, serum
- Luteinizing Hormone (LH), serum and plasma
- NT-proBNP, blood
- Osmolality, fluid
- Osmolality, plasma or serum
- Osmolality, urine
- Pancreatic Amylase, serum or plasma
- Parathyroid Hormone (PTH)
- Procainamide and N-Acetylprocainamide , Serum
- Procalcitonin, blood
- Prolactin, serum and plasma
- Salicylate, plasma or serum
- Soluble Transferrin Receptor (sTfR), plasma or serum
- Testosterone, serum
- Thyroid-Stimulating Hormone (TSH), serum or plasma
- Tobramycin, plasma or serum
- Total Renin
- Triiodothyronine, Total, serum and plasma
- Vancomycin, plasma or serum
- Vitamin B12, serum or plasma
- Vitamin D, 1, 25 Dihydroxy, plasma or serum
Clinical Biochemistry - Immunology
- Anti-Endomysial Antibody IgA
- Anti-Glomerular Basement Membrane
- Anti-Liver Kidney Microsomal Antibody
- Anti-Mitochondrial Antibody
- Anti-Neutrophil Cytoplasmic Antibody (ANCA)
- Anti-Parietal Cell Antibody
- Anti-Pneumococcal capsular polysaccharide Ab, IgG, serum
- Anti-Smooth Muscle Antibody
- CD163
- CXCL9/MIG
- IFN-gamma
- Interleukin 1 beta
- Interleukin 10
- Interleukin 18
- Interleukin 6
- Soluble IL-2 Receptor (CD25)
- TNF-alpha
Clinical Biochemistry - Metabolic Diseases
- Acylcarnitines
- Amino Acids, Blood
- Amino Acids, CSF
- Amino Acids, Urine
- Biotinidase
- Breath Hydrogen
- Carnitine
- Carnitine, urine
- Congenital Disorder of Glycosylation Transferrin
- Creatine Disorders Panel, urine
- Dinitrophenylhydrazine, urine
- Galactosemia Screen
- Glycolipids TLC, urine
- Hyperoxaluria Panel (Currently not available)
- Lysosomal Enzymes
- Maple Syrup Urine Syndrome (DBS)
- Methylmalonic Acid
- Mitochondrial Diseases
- Mucopolysaccharides Screen, urine
- Mucopolysaccharides-TLC, urine (Currently not available)
- Nitroprusside, urine
- Oligosaccharides, urine
- Organic Acids, Urine
- Orotic Acid, Urine
- Oxalate
- Phenylalanine/Tyrosine (DBS)
- Sialic Acid, Urine
- Succinylacetone, Urine
- Sulfatides, Urine
- Sulfocysteine, urine
- Tay-Sachs Disease Carrier Test (Enzyme Analysis)
Clinical Biochemistry - Special
- 11-Deoxycortisol
- 21-OH Progesterone
- Alpha-Fetoprotein (AFP), CSF
- Androstenedione
- Corticosterone
- Cortisol by LC-MS/MS
- Estradiol (High Sensitivity)
- Homovanillic Acid (HVA), urine
- Progesterone
- Progesterone (17-Hydroxy)
- Testosterone by LC-MS/MS
- Vanillylmandelic Acid (VMA), Spot or random, urine
- Vanillylmandelic Acid (VMA), Timed, urine
- Vitamin A
- Vitamin E
Clinical Biochemistry - TDM & Toxicology
- Acetaminophen, plasma or serum
- Amikacin, plasma or serum
- Broad Spectrum Drug Screen, plasma or serum
- Broad Spectrum Drug Screen, urine
- Cannabinoid Metabolite, urine
- Carbamazepine, plasma or serum
- Carbamazepine-10,11-Epoxide
- Digoxin, plasma or serum
- Ethosuximide
- Formic Acid
- Gentamicin, plasma or serum
- Lamotrigine
- Methotrexate, plasma or serum
- Phenobarbital, plasma or serum
- Phenytoin, plasma or serum
- Primidone
- Sedatives-Barbiturates-Hypnotics Screen, plasma or serum
- Valproate, plasma or serum
- Voriconazole, plasma
Genome Diagnostics - Clinical Fibroblast Service
Genome Diagnostics - Cytogenetics
- Ataxia Telangiectasia /Nijmegen Breakage Syndrome
- Bloom Syndrome
- Fanconi Anemia (DEB, MMC)
- Fluorescence in situ Hybridization (FISH) - Blood
- Fluorescence in situ Hybridization (FISH) - Bone Marrow Aspirate/Unstimulated Peripheral Blood
- Fluorescence in situ Hybridization (FISH) - Tissue
- Fluorescence in situ Hybridization (FISH) - Tumour (Fresh/FFPE)
- Genomic SNP Microarray - Blood
- Genomic SNP Microarray -Tissue
- Karyotype, GTG-banding - Blood
- Karyotype, GTG-banding - Bone Marrow Aspirate
- Karyotype, GTG-banding -Tissue
- Karyotype, GTG-banding -Tumour
- SNP microarray – OncoScan – FFPE tumour tissue
Genome Diagnostics - Molecular Genetics
- 22q11.2 Deletion Syndrome
- Achondroplasia / Hypochondroplasia
- Angelman Syndrome
- Ashkenazi Jewish Screening Panel
- Atypical Hemolytic Uremic Syndrome and Membranoproliferative Glomerulonephritis Panel: Sequencing
- Autoinflammatory Disease Panel: Recurrent Fever Syndrome
- Autoinflammatory Disease: Aicardi-Goutieres Syndrome (AGS) panel
- Autoinflammatory Disease: Hemophagocytic Lymphohistiocytosis (HLH) panel
- Autoinflammatory Diseases (AID) panel
- Becker Muscular Dystrophy
- Beckwith-Wiedemann Syndrome
- Bloom Syndrome: BLM Recurrent Mutations
- Bone Marrow Transplant Testing (BMT)
- Canavan Disease
- Congenital Muscular Dystrophies Panel: Sequencing
- Connective Tissue Disease: Bone Involvement Panel
- Connective Tissue Disease: Ehlers-Danlos Syndrome Panel
- Connective Tissue Disease: Osteogenesis Imperfecta Panel
- Connective Tissue Disease: Osteopetrosis and disorders of increased bone density Panel
- Craniosynostosis Molecular Analysis
- Cystic Fibrosis
- DNA Banking
- Dopamine Beta-Hydroxylase Deficiency: DBH Sequencing
- Duchenne Muscular Dystrophy
- Fabry Disease
- Familial Dysautonomia
- Fanconi Anemia Group C: FANCC Recurrent Mutations
- Focal Segmental Glomerulosclerosis Panel
- Fragile X Syndrome
- FRAXE
- Hereditary Hearing Loss: Common and Non-Syndromic Hearing Loss Panel
- Hereditary Hearing Loss: Stickler Syndrome
- Hereditary Hearing Loss: Syndromic Hearing Loss - Treacher Collins syndrome, Waardenburg syndrome, Norrie syndrome, Alport syndrome
- Hereditary Hearing Loss: Usher Syndrome
- Hereditary Hemorrhagic Telangiectasia: ACVRL1, ENG
- Hereditary Hemorrhagic Telangiectasia: SMAD4 Sequencing
- Hereditary Spastic Paraplegia: Autosomal Dominant
- Hereditary Spastic Paraplegia: Autosomal Recessive
- Hereditary Spastic Paraplegia: X-Linked
- Hunter Disease
- Identity Testing - MCC Studies, Zygosity
- Li Fraumeni
- Mucolipidosis Type 4: MCOLN1 Recurrent Mutations
- Neurofibromatosis Type 1/Legius Syndrome
- Neuronal Ceroid Lipofuscinoses
- Niemann Pick Disease Type A and B: SMPD1 Recurrent Mutations
- Noonan Syndrome and RASopathies
- Prader-Willi Syndrome
- Rhabdoid Tumour Predisposition Syndrome
- Russell Silver Syndrome
- Shwachman-Diamond Syndrome
- Simpson-Golabi-Behmel Syndrome: GPC3 Sequencing, GPC3 and GPC4 Deletion/Duplication Analysis
- Spinal and Bulbar Muscular Atrophy (SBMA)
- Spinal Muscular Atrophy
- Thanatophoric Dysplasia (Type I & II)
- Trismus-Pseudocamptodactyly Syndrome: MYH8 Sequencing
- X-Inactivation Analysis
Haematopathology
- APT Test
- Autoimmune Lymphoproliferative Syndrome (ALPS)
- B cell subsets
- CD34 Enumeration, Apheresis
- CD34 Enumeration, Bone Marrow
- CD34 Enumeration, Peripheral Blood
- CD45 RA/RO
- Hereditary Spherocytosis Screening
- Lymphocyte Proliferation, PHA
- Lymphocyte subsets Enumeration (TBNK), Peripheral Blood
- Minimal Residual Disease (MRD) Day 29
- Minimal Residual Disease (MRD) Day 8
- Neutrophil Oxidative Burst Index (NOBI)
- NK Degranulation Assay
- Perforin Protein Expression
- Platelet-Membrane Glycoprotein Expression
- Recent Thymic Emigrants
- Regulatory T Cells
- T Cell Subsets, CD3/CD4/CD8
- TCRV Beta
Microbiology - Molecular
- Adenovirus PCR - Autopsy/Biopsy
- Adenovirus PCR - BAL (Broncho-Alveolar Lavage)
- Adenovirus PCR - Blood
- Adenovirus PCR - Corneal Scrape
- Adenovirus PCR - Eye
- Adenovirus PCR - Fluid-Pleural
- Adenovirus PCR - Urine
- Aspergillus PCR
- Bacterial 16S rDNA Detection from Clinical Specimens by Conventional Polymerase Chain Reaction (PCR)
- Bacterial meningitis PCR
- Bartonella Group PCR - Blood
- Bartonella Group PCR - CSF
- Bartonella Group PCR - Lymph Node
- BK Virus Quantitative PCR
- BK virus semi-quantitative PCR
- Bordetella pertussis DNA Detection by PCR
- CMV, EBV, HHV 6 by PCR - Autopsy/Biopsy
- CMV, EBV, HHV 6 by PCR - Blood
- CMV, EBV, HHV 6 by PCR - Body Fluid
- CMV, EBV, HHV 6 by PCR - CSF
- EBV Quantitative PCR
- Enterovirus by RT PCR - Blood
- Enterovirus by RT PCR - CSF
- Fungal PCR
- HHV 6A & HHV 6B by PCR
- HHV 7 by PCR
- HSV 1 & 2, VZV by PCR - Autopsy/Biopsy
- HSV 1 & 2, VZV by PCR - Blood
- HSV 1 & 2, VZV by PCR - Body Fluid
- HSV 1 & 2, VZV by PCR - CSF
- Human Herpes Group (HSV 1 & 2, VZV) by PCR - Lesion Scraping
- Human Herpes Group (HSV 1& 2, VZV) by PCR - Oral
- Human Herpes virus 8 by PCR - Biopsy
- JC virus PCR
- Kingella kingae PCR - Biopsy
- Kingella kingae PCR - Joint/Synovial Fluid
- Mycoplasma pneumoniae & Chlamydophila pneumoniae DNA Detection by PCR
- Parechovirus by RT-PCR - Blood
- Parechovirus by RT-PCR - CSF
- Parvovirus B19 by PCR
- Pneumocystis PCR
- Quantitative PCR for CMV
- Respiratory Viruses Multiplex PCR
- Ureaplasma parvum/urealyticum by PCR
- West Nile Virus PCR - CSF
- West Nile Virus PCR - Plasma/Serum
Customer Service
Toll Free: 1-855-381-3212
Local: 416-813-7200
Browse tests by laboratory
Customer Service
Toll Free: 1-855-381-3212
Local: 416-813-7200