Search Results:
Matching test names:
- C Diff (See: C. difficile Toxin B PCR with reflex to C. difficile Antigen and Toxins A/B EIA)
- C Peptide (See: C-Peptide)
- C Peptide (See: C-Peptide in a Series)
- C Reactive Protein High Sensitivity (See: CRP Cardiac Risk)
- C Telopeptide Beta Crosslinked (See: C-Telopeptide, Beta-Cross-Linked, Serum)
- C XC Ligand 9 (See: CXCL9 Cytokine)
- C. difficile Antigen and Toxins A/B by Enzyme Immunoassay
- C. difficile Toxin B PCR with reflex to C. difficile Antigen and Toxins A/B EIA
- C/c Genotyping, Prenatal
- C1 Esterase Inhibitor
- C1 Esterase Inhibitor, Functional
- C1 Function Assay to National Jewish Health
- C1 Inactivation (See: C1 Esterase Inhibitor, Functional)
- C1 Inhibitor (See: Autoantibody to C1-Inhibitor)
- C12-C22, Fatty Acid Profile (See: Fatty Acid Profile, Essential, Serum)
- C1-Esterase Inhibitor Level to National Jewish Health
- C1-Esterase Inhibitor Level, Plasma
- C1F
- C1q (See: Complement Component 1q)
- C1Q Binding Assay (See: Immune Complex Panel)
- C1Q Function Assay
- C1Q Function Assay to National Jewish Health
- C1QAB
- C1q-binding and C3d (See: Circulating Immune Complexes)
- C1QF
- C1r Level to National Jewish Health
- C1RL
- C1s Level to National Jewish Health
- C1SL
- C2 (See: Complement Component C2)
- C2 Function Assay to National Jewish Health
- C2 Level to National Jewish Health
- C2F
- C2L
- C3 (See: Complement C3)
- C3
- C3 Function Assay to National Jewish Health
- C3 Glomerulopathy Complement Panel
- C3 Level to National Jewish Health
- C3 Nephritic Factor
- C3a Level to National Jewish Health
- C3AR
- C3F
- C3G Functional Panel
- C3GN (See: C3G Functional Panel)
- C4 Acylcarnitine, Quantitative, Urine
- C4 Function Assay
- C4 Function Assay to National Jewish Health
- C4 Level
- C4 Level to National Jewish Health
- C4A (See: Complement Component 4A)
- C4AR
- C4F
- C4NJ
- C4U
- C5 (See: Complement Component 5)
- C5 Function Assay
- C5 Function Assay to National Jewish Health
- C5 Level to National Jewish Health
- C5-9 Deficiency Screen
- C5-9 Deficiency Screen to National Jewish Health
- C5ades Arg Level
- C5ades Arg Level to National Jewish Health
- C5AL
- C5-DC Acylcarnitine, Quantitative, Urine
- C5DCU
- C5F
- C5F
- C5L
- C5-OH Acylcarnitine, Quantitative, Urine
- C5OHU
- C6 Function Assay to National Jewish Health
- C6 Level
- C6F
- C6F
- C6L
- C7 Function Assay
- C7 Level
- C7 Level to National Jewish Health
- C7F
- C7F
- C7L
- C8 Function Assay
- C8 Function Assay to National Jewish Health
- C8 Level to National Jewish Health
- C8-C26, Fatty Acid Profile (See: Fatty Acid Profile, Comprehensive (C8-C26))
- C8F
- C8F
- C8L
- C9 Function Assay to National Jewish Health
- C9 Level to National Jewish Health
- C9F
- C9F
- C9L
- C9O72D
- C9O72F
- C9ORF72 (FTD) DNA Test
- C9ORF72 DNA Test
- CA 125
- CA 153 (See: Cancer Antigen 15-3)
- CA 15-3 (See: Cancer Antigen 15-3)
- CA 19-9, Tumor Marker (See: Cancer Antigen-GI (CA 19-9))
- CA 27.29 (See: Cancer Antigen 15-3)
- CA 27.29, Breast Tumor Marker
- CA 2729 (See: CA27.29 Breast Tumor Marker)
- CA125
- CA-125
- CA153 (See: Cancer Antigen 15-3)
- CA15-3 (See: Cancer Antigen 15-3)
- CA2 (See: Osteopetrosis Gene Sequencing)
- CA27.29 Breast Tumor Marker
- CA2729 (See: CA27.29 Breast Tumor Marker)
- CAA
- CAA1
- CAA25
- CACNA1S (See: Myotonia Evaluation)
- CADASIL Evaluation
- CADM 140 (See: MDA5 Antibody)
- Cadmium, Blood
- Cadmium, Urine
- CADU
- Caffeine
- CAH Panel 6C (Full Screen)
- CAH (21-Hydroxylase Deficiency) Common Mutations
- CAH (21-Hydroxylase Deficiency) Common Mutations - LG4650
- CAH (21-Hydroxylase Deficiency) Gene Sequencing
- CAH (21-Hydroxylase Deficiency) Rare Mutations - LG4651
- CAH 21 Hydroxylase Deficiency (See: Hydroxylase Gene (CYP21A2) Full Gene Analysis)
- CAH 21-Hydroxylase Deficiency Monitoring Profile
- CAH Panel (See: Steroid Panel, Comprehensive, Pediatric Endocrinology)
- CAH Panel (See: REORDER AS MMMISC for Test ID: ZW131. CAH 21-Hydroxylase Deficiency Monitoring Profile)
- CAH Panel 1 (21-Hydroxylase vs 11Beta-Hydroxylase Deficiency
- CAH Panel 1 (21-Hydroxylase vs 11Beta-Hydroxylase Deficiency15269 - LG5475
- CAH Pediatric Profile (See: Steroid Panel, Comprehensive, Pediatric Endocrinology)
- CAH21
- CAH-21 Hydroxylase Gene (CYP21A2) Full Gene Analysis (See: Hydroxylase Gene (CYP21A2) Full Gene Analysis)
- CAH6C
- Calamari (See: Allergen: Food, Squid)
- Calan (See: Verapamil)
- Calcitonin
- Calcitonin Fine Needle Aspirate or Biopsy, Lymph Node
- Calcitriol (See: 1,25 Dihydroxy Vitamin D, Pediatric Only)
- Calcium
- Calcium Channel Binding Antibody (See: Paraneoplastic Autoantibody Evaluation Cascade, Serum)
- Calcium, Ionized
- Calcium, Ionized, Prisma
- Calcium, Ionized, Serum/Plasma
- Calcium, Random Urine
- Calcium, Timed Urine
- Calculus (See: Stone Analysis)
- California Virus (LaCrosse) Encephalitis Antibody Panel, IgG and IgM, CSF
- California Virus (LaCrosse) Encephalitis Antibody Panel, IgG and IgM, CSF - LG6029
- Calprotectin (See: S100A8/A9 Protein)
- Calprotectin, Feces
- CALR (See: Next Generation Sequencing Oncology Tumor Testing)
- CALR (See: Myeloproliferative Neoplasms Focused NGS Panel)
- CALR (See: Myeloproliferative Neoplasms Expanded NGS Panel)
- Calreticulin (See: Next Generation Sequencing Oncology Tumor Testing)
- Campomelic Dysplasia (See: SOX9 Gene Analysis)
- Campylobacter (See: Enteric Pathogen and Virus Panel by Nucleic Acid)
- Campylobacter (See: GI Pathogen Panel, PCR, Feces - Research Only)
- Campylobacter jejuni Antibody IgG
- Campylobacter jejuni Antibody IgG - LG6086
- Can f1, Can f2, Can f3, Can f5 (See: Allergen: Dog Components, IgE)
- Canavan Disease Gene Analysis
- cANCA (See: Anti-Neutrophil Cytoplasmic Antibody (ANCA), IgG by IFA with Reflex to Titer)
- Cancer Antigen 15-3
- Cancer Antigen 27.29 (CA 27.29) (See: CA27.29 Breast Tumor Marker)
- Cancer Antigen-GI (CA 19-9)
- Cancer Custom (See: Hereditary Cancer Testing to Ambry)
- Cancer Neoplastic (See: Chromosome Analysis, Blood, Leukemia)
- Cancer, Bone Marrow (See: Chromosome Analysis, Bone Marrow, Diagnosis/Relapse)
- CancerNext (See: Hereditary Cancer Testing to Ambry)
- CancerNext Expanded (See: Hereditary Cancer Testing to Ambry)
- CancerTYPE ID
- Candida Ab (See: Candida albicans Antibodies IgA, IgG and IgM by ELISA)
- Candida albicans Antibodies IgA, IgG and IgM by ELISA
- Candida Antibody by ID
- Candida auris Screening, PCR to MDH
- Cannabinoids (THC) Confirmation Quantitative, Urine, Normalized to Creatinine
- Cannabinoids, Urine, Qualitative
- Capillary Blood Gas with Oxyhemoglobin
- Capillary Malformation-Arteriovenous Malformation (See: RASA1 Gene Analysis)
- Capsicum annuum (See: Allergen: Food, Pepper C. annuum, IgE)
- Carbamazepine and Carbamazepine-10,11 Epoxide
- Carbamazepine Epoxide and Total
- Carbamazepine Sensitivity (See: HLA Single Antigen Type Allele, Donor or Recipient)
- Carbamazepine Total
- Carbamoyl Phosphate Synthetase (See: Hyperammonemia Gene Sequencing)
- Carbamoyl Phosphate Synthetase, Liver
- Carbamyl Phosphate Synthetase, Liver - LG841
- Carbapenem Resistance (See: Carbapenem-Resistant Bacteria Culture)
- Carbapenem Resistant Enterobacteriaceae (See: Carbapenem-Resistant Bacteria Culture)
- Carbapenem Resistant PCR (See: Carbapenemase Gene Detection, PCR - Rectal Swab)
- Carbapenemase (See: Carbapenem-Resistant Bacteria Culture)
- Carbapenemase Gene Detection, PCR - Rectal Swab
- Carbapenem-Resistant Bacteria Culture
- Carbapenem-Resistant Organism Culture
- Carba-R (See: Carbapenemase Gene Detection, PCR - Rectal Swab)
- Carbatrol (See: Carbamazepine Epoxide and Total)
- Carbohydrate Deficient Glycoprotein Syndrome (See: Carbohydrate Deficient Transferrin (CDT), for Congenital Disorders of Glycosylation, Pediatric, Serum)
- Carbohydrate Deficient Transferrin (CDT), Adult
- Carbohydrate Deficient Transferrin (CDT), for Congenital Disorders of Glycosylation, Pediatric, Serum
- Carbohydrate Deficient Transferrin (CDT), for Congenital Disorders of Glycosylation, Pedriatric, Serum
- Carbon Dioxide (See: CO2, Total, Serum/Plasma)
- Carbon Dioxide (See: CO2, Total, Whole Blood)
- Carbon Monoxide
- Carboxyhemoglobin (See: Carbon Monoxide)
- Carboxylases Enzyme Assay
- Carboxylases Enzyme Assay - LG4644
- Carboxy-THC (See: Cannabinoids (THC) Confirmation Quantitative, Urine, Normalized to Creatinine)
- Carboxy-THC Confirmation, Qualitative, Urine
- Carcinoembryonic Antigen
- Carcinoembryonic Antigen (CEA)
- Cardiac Enzyme (See: Troponin T High Sensitivity - CSC Mpls, East, Grand Itasca, Lakes, Northland, Range, Ridges, Southdale, St. John's, West)
- Cardiolipin Antibodies, IgG and IgM
- Cardiolipin Antibody, IgA
- Cardiolipin Panel: IgA, IgG and IgM
- Cardiomyopathy Gene Analysis
- Cardiomyopathy, Dilated (See: Cardiomyopathy Gene Analysis)
- CARIS
- Carisoprodol and Meprobamate
- Carnitine Deficiency Gene Analysis
- Carnitine Palmitoyl Transferase Deficiency (See: Carnitine Deficiency Gene Analysis)
- Carnitine Palmitoyltransferase II CPTII enzyme
- Carnitine Palmitoyltransferase II CPTII enzyme - LG6135
- Carnitine, Free and Total (Includes Carnitine, Esterified)
- Carnitine, Plasma
- Carnitine, Quantitative, Urine
- Carnosine (See: Amino Acids, Timed Urine)
- Carnosine (See: Amino Acids, Plasma)
- Carnosine (See: Amino Acids, CSF)
- Carnosine (See: Amino Acids, Random Urine)
- CARNU
- Carotene
- Carrier Screening (See: Spinal Muscular Atrophy (SMA) Prenatal Screen Copy Number Analysis)
- Carrier Testing, Recessive Conditions (See: Invitae Carrier Screening)
- Cashew (See: Allergen: Adult Food Profile)
- Cashew Nut Component (See: Allergen: Cashew Component, Storage Protein, IgE)
- CASIEN
- CASPR2 Antibody
- CASPR2 Autoantibody
- CASPR2 Autoantibody - LG5427
- Cat Dander (See: Allergy Pediatric March Profile IgE)
- Cat Epithelium and Dander (See: Allergen: Inhalants, Environmental Profile 10)
- Cat Scratch Fever Serology (See: Bartonella henselae (Cat Scratch) Antibodies, IgG and IgM By IFA)
- Cat Serum Albumin (See: Allergen: Cat Components, IgE)
- Catapres (See: Clonidine)
- Catecholamines Fractionated, Plasma (Epinephrine, Norepinephrine and Dopamine)
- Catecholamines Fractionated, Urine Free
- Catecholamines, Free (See: Catecholamines Fractionated, Plasma (Epinephrine, Norepinephrine and Dopamine))
- Catecholamines, Free (See: Catecholamines, Plasma (Epinephrine & Norepinephrine))
- Catecholamines, Plasma (Epinephrine & Norepinephrine)
- Catecholamines, Plasma (Epinephrine & Norepinephrine) - LG3584
- Catheter Tip (See: Aerobic Bacterial Culture Routine)
- Catheterized Urine (See: Cytology, Urinary Tract)
- Cathinone and Methcathinone, Urine
- CATLN
- Cattle Epithelium (See: Allergen: Epidermal and Animal Proteins, Cow Hair and Dander)
- CAV3 (See: Long QT Syndrome Gene Analysis)
- Caveolin 3 Sequencing (See: Limb Girdle Muscular Dystrophy Evaluation)
- Cayenne Pepper (See: Allergen: Food, Pepper C. annuum, IgE)
- CBASIC (See: Basic Metabolic Panel)
- CBC with Platelets
- CBC With Platelets and Differential
- CBC with Platelets with Reflex to Iron Studies
- CBG (See: Capillary Blood Gas with Oxyhemoglobin)
- CBL (See: ABO, Rh, and DAT, Cord Blood)
- CBL (See: Next Generation Sequencing Oncology Tumor Testing)
- CBL (See: Myelodysplastic Syndrome Focused NGS Panel)
- CBL (See: Lymphoid Malignancy Comprehensive NGS Panel)
- CBL (See: Myeloid Malignancy Comprehensive NGS Panel)
- CBS Genotype (833 & 919) (See: Cystathionine B-Synthase, Genotype (833 & 919))
- CBSGEN
- CCM2 (See: Familial Cerebral Cavernous Malformations)
- CCOMP (See: Comprehensive Metabolic Panel)
- CCP Antibody (See: Cyclic Citrullinated Peptide Antibody, IgG)
- CCSF body fluid (See: Granulocyte Colony Stimulating Factor, Body Fluid or CSF)
- CD107a Mobilization
- CD107a Mobilization - Draw sample after 10 am
- CD11a (See: Leukocyte Adhesion Deficiency Panel)
- CD11b (See: Leukocyte Adhesion Deficiency Panel)
- CD15s (See: Leukocyte Adhesion Deficiency Panel)
- CD18 (See: Leukocyte Adhesion Deficiency Panel)
- CD19 B Cell Monitoring, Percent and Absolute Count
- CD19 Count (See: CD19 B Cell Monitoring, Percent and Absolute Count)
- CD19 for Rituxin Monitoring (See: CD19 B Cell Monitoring, Percent and Absolute Count)
- CD20 on B Cells, Blood
- CD34 (Hematopoietic Progenitor Stem Cell Assay)
- CD34 Absolute Count
- CD34 and CD3 Absolute Count
- CD34 Hematopoietic Stem Cell Count (See: CD34 Absolute Count)
- CD4 Count (See: T Helper/Inducer: T Suppressor/Cytotoxic Lymphocyte Ratio)
- CD4 Count (See: T Helper/Inducer:T Suppressor Cytotoxic Lymphocyte Ratio, B Cell and Natural Killer Cells)
- CD4 Plus T-Cell Recent Thymic Emigrants (RTE)
- CD4 RTE, Flow Cytometry (See: CD4 Plus T-Cell Recent Thymic Emigrants (RTE))
- CD4 T-Cell Recent Thymic Emigrants (RTE)
- CD4:CD8 Lymphocyte Ratio (See: T Helper/Inducer: T Suppressor/Cytotoxic Lymphocyte Ratio)
- CD4:CD8 Lymphocyte Ratio (See: T Helper/Inducer:T Suppressor Cytotoxic Lymphocyte Ratio, B Cell and Natural Killer Cells)
- CD40 Ligand (CD154)
- CD40 Ligand (CD154) ICOS Expression
- CD49d (See: Leukemia Lymphoma Evaluation Non CSF)
- CD52 (CAMPATH-1) by Immunohistochemistry, Tissue or Cells
- CD52 (CAMPATH-1) by Immunohistochemistry, Tissue or Cells - LG5087
- CD57 + NK Cells, Peripheral Blood by Flow Cytometry
- CD59 (MIRL) (See: High Sensitivity Paroxysmal Nocturnal Hemoglobinuria Assay by Flow Cytometry)
- CDAU (See: Drug Confirmatory Panel, Urine with Creatinine)
- CDG (See: Carbohydrate Deficient Transferrin (CDT), for Congenital Disorders of Glycosylation, Pediatric, Serum)
- CDG (See: Chronic Granulomatous Gene Analysis)
- Cdiff (See: C. difficile Toxin B PCR with reflex to C. difficile Antigen and Toxins A/B EIA)
- Cdiff Toxin (See: C. difficile Toxin B PCR with reflex to C. difficile Antigen and Toxins A/B EIA)
- CDK12 (See: Next Generation Sequencing Oncology Tumor Testing)
- CDKL5 (See: Rett Syndrome Gene Analysis)
- CDKN1B (See: Multiple Endocrine Neoplasia Gene Analysis)
- CDKN2A (See: Next Generation Sequencing Oncology Tumor Testing)
- CDKN2B (See: Next Generation Sequencing Oncology Tumor Testing)
- CDON (See: Holoprosencephly Gene Evaluation)
- CDTA
- CEBPA (See: Next Generation Sequencing Oncology Tumor Testing)
- CEBPA (See: Acute Myeloid Leukemia (AML) Focused NGS Panel, Blood or Bone Marrow)
- CEBPA (See: Acute Myeloid Leukemia (AML) Molecular Follow-Up, Blood or Bone Marrow Panel)
- CEBPA (See: Acute Myeloid Leukemia (AML) Expanded NGS Panel, Blood or Bone Marrow)
- Cece (See: Allergen: Chick Pea, IgE)
- Ceci (See: Allergen: Chick Pea, IgE)
- Celexa (See: Citalopram and Metabolite)
- Celiac (See: IgA)
- Celiac (See: HLA DQB1 for Celiac Disease)
- Celiac (Gluten) Antibody Panel
- Celiac Disease (See: Deamidated Gliadin Antibodies, IgA and IgG)
- Celiac Disease (See: Endomysial Antibody, IgA by IFA)
- Celiac Disease (See: Tissue Transglutaminase Antibody, IgA)
- Celiac Disease (See: Tissue Transglutaminase Antibodies, IgA and IgG)
- Celiac Disease Panel
- Cell Count and Differential, CSF
- Cell Count with Differential Fluid (See: Joint Fluid Exam)
- CELL CULT AF (See: Culture, Amniotic Fluid)
- Cell Culture for Sendout Testing (See: Culture, Amniotic Fluid)
- Cell Cycle Analysis (See: DNA Cell Cycle Analysis Ploidy and S-Phase)
- Cellcept (See: Mycophenolic Acid and Mycophenolic Acid Glucuronide)
- Cellcept (See: Mycophenolic Acid, Free Area Under the Curve Study)
- Celontin (See: Methsuximide as Desmethylmethsuximide)
- CELP (See: Multiple Sclerosis Panel)
- Central Nervous System (CNS) (See: Glioma Panel Focused NGS)
- Central Nervous System (CNS) (See: Glioma Expanded NGS Panel)
- Centromere Antibody, IgG
- Centromere B (See: Centromere Antibody, IgG)
- CEP290 (See: Bardet-Biedl Syndrome Gene Analysis)
- Cephalosporium Acremonium (See: Allergen: Cephalosporium)
- Ceramide Trihexoside (See: Plasma GL3)
- Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (See: CADASIL Evaluation)
- Cerebrooccular Dysplasia (See: Walker Warburg Syndrome Gene Analysis)
- Cerebrospinal Fluid Detection in Body Fluid (See: Beta-2 Transferrin)
- Cerebrospinal Fluid, Analysis (See: Cell Count and Differential, CSF)
- Cerebrospinal Fluid, Cytology (See: Cytology, CSF)
- Cerebrospinal Fluid, Protein (See: Protein, Total, CSF)
- Cerezyme (See: Imiglucerase Antibody)
- Certican (See: Everolimus)
- Certolizumab
- Ceruloplasmin
- Cervical Cancer (See: HPV High Risk DNA Cervical)
- Cervical Smear (See: Cytology, Screening Thin Layer Cervical-Vaginal Pap Test With Guided Screening)
- Cervical Smear (See: Cytology, Diagnostic Thin Layer Cervical-Vaginal Pap Test With Guided Screening)
- Cervical Smear (See: Cytology, Screening Thin Layer Cervical-Vaginal Pap Test, Grand Itasca)
- CF Amplified (See: Cystic Fibrosis, Full Mutation)
- CF70 (See: Cystic Fibrosis Mutation Analysis)
- CFC (See: Respiratory Aerobic Bacterial Culture)
- CFC1 (See: Holoprosencephly Gene Evaluation)
- CF-Delta F508 (See: Cystic Fibrosis Mutation Analysis)
- CFFTR (See: Pancreatic Panel, Hereditary)
- CFRESPCX (See: Respiratory Aerobic Bacterial Culture)
- CFRESPCXSTN (See: Respiratory Aerobic Bacterial Culture)
- CFTR Amplified Testing Cystic Fibrosis 1006
- CFTR Amplified Testing Cystic Fibrosis 1006 - LG6119
- CFTR Deletion/Duplication Analysis
- CFTR Deletion/Duplication Analysis - LG6124
- CFTR Intron 8 Poly T Analysis
- CFTR Intron 8 Poly T Analysis - LG5594
- CFTR Poly T Reflex Analysis to TG Repeat
- CFTR Poly T Reflex Analysis to TG Repeat - LG6125
- CG4 (See: Abbott i-Stat CG4 + Arterial - Point of Care Testing (POCT))
- CG4 (See: Abbott i-Stat CG4 + Venous - Point of Care Testing (POCT))
- CGH
- CGH (See: Constitutional Chromosomal Microarray (Copy Number))
- CGH FOL
- CGH for COUS (See: Constitutional Limited Chromosomal Microarray for Parental Follow-Up (Copy Number) (No Charge))
- CGH for COUS (See: Constitutional Limited Chromosomal Microarray (Copy number only) (Charged))
- CGH for Follow-Up (See: Constitutional Limited Chromosomal Microarray (Copy number only) (Charged))
- CGH for Parental Follow-Up (See: Constitutional Limited Chromosomal Microarray for Parental Follow-Up (Copy Number) (No Charge))
- CGH LTDHR (See: Constitutional Chromosomal Microarray (Copy Number) with Limited G-band Analysis)
- CGH ONC (See: Oncology Chromosomal Microarray (Copy Number/SNP))
- CGH SNP
- CGH SNP LHR (See: Constitutional Chromosomal Microarray (Copy Number/SNP) with Limited G-band Analysis)
- CGH w/Ltd blood high res (See: Constitutional Chromosomal Microarray (Copy Number) with Limited G-band Analysis)
- CGH with Limited Blood High Resolution Chromosomes
- CGH with Limited Blood High Resolution Chromosomes (See: Constitutional Chromosomal Microarray (Copy Number) with Limited G-band Analysis)
- CGH with SNP (See: Constitutional or Products of Conception (POC) Chromosomal Microarray (Copy Number/SNP))
- CGH with SNP Array for Oncology (See: Oncology Chromosomal Microarray (Copy Number/SNP))
- CGH with SNP with G-Band (See: Constitutional Chromosomal Microarray (Copy Number/SNP) with Limited G-band Analysis)
- CGH, Chromosomes (See: Constitutional Chromosomal Microarray (Copy Number) with Limited G-band Analysis)
- CH50
- CH50T (See: Complement Activity Total (CH50))
- Chagas (See: Trypanosoma cruzi Antibody, IgG)
- Chagas Testing (See: Trypanosoma Cruzi - BMT Only)
- Charcot Marie Tooth (CMT) Evaluation
- Charcot-Marie Tooth Disease, Type 1C (CMT1C) (See: LITAF/SIMPLE DNA Sequencing)
- Charcot-Marie-Tooth Disease (See: Charcot Marie Tooth (CMT) Evaluation)
- Charcot-Marie-Tooth Disease, Type 2E (CMT2E) (See: Neurofilament Light (NFL) DNA Sequencing)
- Charcot-Marie-Tooth Disease, Type 4A (CMT4A), CMT2K (CMT Type 2K) (See: GDAP1 DNA Sequencing)
- Charcot-Marie-Tooth Type 1 (See: Charcot Marie Tooth (CMT) Evaluation)
- Charcot-Marie-Tooth Type 2 (See: Charcot Marie Tooth (CMT) Evaluation)
- Charcot-Marie-Tooth Type 4 (See: Charcot Marie Tooth (CMT) Evaluation)
- Charcot-Marie-Tooth, Type 2A (See: MFN2 DNA Sequencing)
- Charge Syndrome Gene Analysis
- charged limited CGH (See: Constitutional Limited Chromosomal Microarray (Copy number only) (Charged))
- CHCD71
- CHD7 (See: Holoprosencephly Gene Evaluation)
- CHD7 Duplication and Deletion (See: Charge Syndrome Gene Analysis)
- CHD7 Gene Sequencing (See: Charge Syndrome Gene Analysis)
- Cheese Pumpkin (See: Allergen: Food, Summer Squash)
- CHEK1 (See: Next Generation Sequencing Oncology Tumor Testing)
- CHEK2 (See: Next Generation Sequencing Oncology Tumor Testing)
- Chem 10
- CHEM 8 (See: Basic Metabolic Panel)
- Chemical Screen Reflex to Microscopic (See: Urinalysis Macroscopic Reflex to Microscopic)
- Chemical Screen, Reflex to Microscopic, Reflex to Culture (See: Urinalysis Macroscopic Reflex to Microscopic and Culture)
- Chemokine (C-X-C motif) Ligand 9 (See: CXCL9 Cytokine)
- Chenodeoxycholic Acid (See: Bile Acids, Fractionated and Total)
- Chickenpox Titer (See: Varicella Zoster Virus Antibody, IgG)
- Chikungunya Antibodies, IgG and IgM
- Chikungunya by PCR
- Children's Oncology Group (COG) Flow Cytometry Blood
- Children's Oncology Group (COG) Flow Cytometry Bone Marrow
- Chimerism CD19 B Cell Subset
- Chimerism CD56 (NK Cells) Subset
- Chimerism CD71 Cell Subset, Blood
- Chimerism Informatives (Recipient & Donor)
- Chimerism Whole Blood and Bone Marrow
- Chitotriosidase
- Chlamydia Antibody Panel, IgG and IgM by IFA
- Chlamydia Antibody Panel, IgG by IFA
- Chlamydia Antibody Panel, IgM
- Chlamydia Antibody Panel, IgM by IFA
- Chlamydia Culture
- Chlamydia pneumonaiae by PCR, BAL Only
- Chlamydia pneumoniae (See: Respiratory Panel PCR)
- Chlamydia pneumoniae by PCR, BAL Only
- Chlamydia Trachomatis (See: Chlamydia Culture)
- Chlamydia trachomatis (See: G/C Chlamydia by PCR, Range and Grand Itasca Only)
- Chlamydia trachomatis (CT) and Neisseria gonorrhoeae (NG) by PCR to HCMC, Genital/Vaginal - Safe Child Only
- Chlamydia trachomatis (CT) and Neisseria gonorrhoeae (NG) by PCR to HCMC, Rectal - Safe Child Only
- Chlamydia trachomatis (CT) and Neisseria gonorrhoeae (NG) by PCR to HCMC, Throat - Safe Child Only
- Chlamydia trachomatis (CT) and Neisseria gonorrhoeae (NG) by PCR to HCMC, Urine - Safe Child Only
- Chlamydia Trachomatis by PCR
- Chlamydia trachomatis, Peritoneal Fluid by Gen-Probe
- Chlamydia Trachomatis/Neisseria Gonorrhoeae by PCR (See: Chlamydia/Gonorrhea by PCR)
- Chlamydia/Gono Amplified (See: Chlamydia Trachomatis by PCR)
- Chlamydia/Gono Amplified (See: Neisseria gonorrhoeae PCR)
- Chlamydia/Gono Amplified (See: Chlamydia/Gonorrhea by PCR)
- Chlamydia/Gonorrhea by PCR
- Chloral Hydrate
- Chloral Hydrate, Serum/Plasma
- Chloride (See: Electrolyte Panel)
- Chloride
- Chloride, Fecal (See: Electrolytes, Fecal)
- Chloride, Random Urine
- Chloride, Timed Urine
- Chloride, Whole Blood
- Chlorpheniramine (See: Antihistamines, ToxAssure(R) , Urine)
- Chlorpheniramine
- Chlorpheniramine, Urine
- Chlorpromazine
- Chlortrimeton (See: Antihistamines, ToxAssure(R) , Urine)
- CHLPRZ
- Cholestasis Gene Sequencing
- Cholesterol (See: Lipid Panel)
- Cholesterol
- Cholesterol (See: Lipid Panel Reflex to Direct LDL)
- Cholesterol Desmolase Deficiency (See: Lipoid Congenital Adrenal Hyperplasia)
- Cholesterol Ester Storage Disease (See: Acid Lipase)
- Cholesterol HDL and non-HDL Panel
- Cholesterol Panel
- Cholesterol, Fluid
- Cholic Acid (See: Bile Acids, Fractionated and Total)
- Cholinesterase, Plasma (See: Pseudocholinesterase/Dibucaine Inhibition)
- Cholinesterase, Serum or Plasma (See: Pseudocholinesterase, Total)
- Chorionic Gonadotropin (See: HCG Tumor Marker, Serum)
- Chorionic Gonadotropin (See: hCG, Serum/Plasma, Quantitative (Pregnancy Test) (plus Beta Subunit at Roche sites only)
- Chorionic Gonadotropin, Urine Qualitative (See: hCG, Urine, Qualitative (Pregnancy Test))
- Chorionic Villus, by FISH
- CHRFLD
- Christmas Factor (See: Factor 9 Activity)
- CHROM NB (See: Chromosome Analysis, Newborn (up to 21 days old))
- Chromatin Antibody, IgG
- Chromatin DNL (See: Chromatin Antibody, IgG)
- Chromium and Cobalt, Metal-on-Metal (MoM) Implants, Serum or Plasma
- Chromium and Cobalt, Metal-on-Metal (MoM) Implants, Whole Blood
- Chromium, Joint Fluid
- Chromium, Serum
- Chromium, Urine
- CHROMO AM (See: Chromosome Analysis, Amniotic Fluid)
- CHROMO BLHR (See: Chromosome Analysis, Blood, High Resolution)
- CHROMO BM
- CHROMO BM (See: Chromosome Analysis, Bone Marrow, Diagnosis/Relapse)
- CHROMO BREAK (See: Chromosome Analysis, Blood, Breakage Syndromes)
- CHROMO MT (See: Chromosome Analysis, Malignant Tissue)
- CHROMO SCE (See: Chromosome Analysis, Blood, Sister Chromatid Exchange)
- CHROMO SEX (See: Chromosome Analysis, Blood, Sex Chromosome)
- CHROMO SK (See: Chromosome Analysis, Skin/Products of Conception)
- Chromogranin A
- Chromosomal Microarray (CMA), Congenital, Constitutional (See: Constitutional Chromosomal Microarray (Copy Number) with Limited G-band Analysis)
- chromosome analysis (See: Chromosome Karyotyping (Parental) )
- Chromosome Analysis, Amniotic Fluid
- Chromosome Analysis, Blood, Breakage Syndromes
- Chromosome Analysis, Blood, Fanconi Mutagen Sensitivity
- Chromosome Analysis, Blood, Fanconi Mutagen Sensitivity Study
- Chromosome Analysis, Blood, High Resolution
- Chromosome Analysis, Blood, Leukemia
- Chromosome Analysis, Blood, Newborn Study - Up to 21 days old
- Chromosome Analysis, Blood, Sex Chromosome
- Chromosome Analysis, Blood, Sex Chromosome Study
- Chromosome Analysis, Blood, Sister Chromatid Exchange
- Chromosome Analysis, Bone Marrow, Diagnosis/Relapse
- Chromosome Analysis, Chorionic Villi
- Chromosome Analysis, Malignant Tissue
- Chromosome Analysis, Newborn (up to 21 days old)
- Chromosome Analysis, Skin/Products of Conception
- Chromosome Analysis, Skin/Products of Conception, Metaphase Band
- Chromosome Analysis. Blood
- Chromosome Blood Newborn (See: Chromosome Analysis, Newborn (up to 21 days old))
- Chromosome FISH, Amniotic Fluid with Reflex to Chromosome Analysis or Genomic Microarray
- Chromosome FISH, Chorionic Villus with Reflex to Chromosome Analysis or Genomic Microarray
- Chromosome Karyotyping (Parental)
- chromosomes (See: Chromosome Karyotyping (Parental) )
- CHROMU
- Chronic Granulomatous Gene Analysis
- Chronic Hepatitis B Panel
- Chronic Infantile Neurologic Cutaneous and Articular (CINCA) Syndrome (See: Periodic Fever Gene Analysis)
- Chronic Leukemia Immunophenotyping (See: Leukemia Lymphoma Evaluation Non CSF)
- Chronic Lymphocytic Leukemia (See: Leukemia Lymphoma Evaluation Non CSF)
- Chronic Lymphocytic Leukemia Focused NGS Panel
- Chronic Myeloid Leukemia (See: Lymphoid Malignancy Comprehensive NGS Panel)
- Chronic Myeloid Leukemia (See: Myeloid Malignancy Comprehensive NGS Panel)
- Chronic Myeloid Leukemia (Blast Crisis) (See: Leukemia Lymphoma Evaluation Non CSF)
- Chronic Urticaria (CU) Index Panel
- Chronic Urticaria (CU) Index Panel - LG6313
- CHST14 (See: Ehlers-Danlos Syndrome)
- Chylomicron Screen, Body Fluid
- CIC
- Cicer Arietinus, F309, Chickpea (See: Allergen: Chick Pea, IgE)
- Ciliary Dyskinesia, Primary (See: Kartagener's Syndrome Evaluation)
- Cimzia (See: Certolizumab)
- Cipro (See: Ciprofloxacin)
- Ciprofloxacin
- Ciprofloxacin - LG3872
- Circuit Ionized Calcium (See: Calcium, Ionized, PRISMA)
- Circulating Immune Complexes
- Circulating Immune Complexes to National Jewish Health
- Circulation Anticoagulant (See: Lupus Anticoagulant Panel)
- CITAC
- CITALO
- Citalopram
- Citalopram and Metabolite
- Citrate (See: Citric Acid, Serum or Plasma)
- Citrate, Urine
- Citric Acid
- Citric Acid, Serum or Plasma
- Citric Acid, Urine (See: Citrate, Urine)
- Citrulline (See: Amino Acids, Timed Urine)
- Citrulline (See: Amino Acids, Plasma)
- Citrulline (See: Amino Acids, CSF)
- Citrulline (See: Amino Acids, Random Urine)
- Citrullinemia, Gene Analysis
- CK MB (See: Creatine Kinase, MB)
- CK Total
- C-Kit (See: Kit Mutation Detection, Mastocytosis)
- CKMB (See: Creatine Kinase, MB)
- Cladosporium herbarum (See: Allergy Pediatric March Profile IgE)
- Clam, Lobster, Salmon, Scallop, Shrimp, Tuna (See: Allergen: Seafood IgE Panel)
- Clarinex (See: Loratadine and Metabolites)
- Claritin (See: Loratadine and Metabolites)
- Class I Allele Typing (See: HLA Single Antigen Type Allele, Donor or Recipient)
- Class I/II Antigen Typing (See: HLA Class I Deceased Donor)
- Class I/II Antigen Typing (See: HLA Typing DP Deceased Donor)
- Class I/II Antigen Typing (See: HLA Typing Class II Deceased Donor)
- Clastogen Exposure (See: Chromosome Analysis, Blood, Breakage Syndromes)
- CLCN1 (See: Myotonia Evaluation)
- CLCN7 (See: Osteopetrosis Gene Sequencing)
- CLDN1 (See: Ichthyosis Gene Analysis)
- CLIC2 (See: X-Linked Intellectual Disability Gene Analysis)
- CLL (See: Chronic Lymphocytic Leukemia Focused NGS Panel)
- CLL (See: Diffuse Large B Cell Lymphoma (DLBCL) NGS Panel)
- CLL Immunophenotyping (See: Leukemia Lymphoma Evaluation Non CSF)
- CLLBLD
- Clobazam Level, Quantitative
- Clomipramine and Desmethylclomipramine
- CLON
- Clonazepam (See: Drug Confirmatory Panel, Urine with Creatinine)
- Clonazepam and Metabolite
- Clonidine
- ClonoSeq MRD Detection
- Clopidogrel (See: Platelet Function P2Y12 (Verify Now))
- CLOR
- Clorazepate
- Clostridioides (Clostridium) difficile Culture
- Clostridioides difficile (See: C. difficile Toxin B PCR with reflex to C. difficile Antigen and Toxins A/B EIA)
- Clostridium difficile (See: C. difficile Toxin B PCR with reflex to C. difficile Antigen and Toxins A/B EIA)
- Clostridium difficile Culture
- Clostridium difficile Toxin B PCR
- Clozapine and Metabolites Quantitative
- Clozaril (See: Clozapine and Metabolites Quantitative)
- CLUE Test (See: Wet Prep)
- Clupea Harengus, F205, Sardines (See: Allergen: Herring, IgE)
- CMA (Chromosomal Microarray), Congenital, Constitutional (See: Constitutional Chromosomal Microarray (Copy Number/SNP) with Limited G-band Analysis)
- CMA Chromosomal Microarray, Congenital, Constitutional (See: Constitutional Chromosomal Microarray (Copy Number))
- CMAVM (See: RASA1 Gene Analysis)
- CMFA (See: Cystic Fibrosis Mutation Analysis)
- CML (See: Lymphoid Malignancy Comprehensive NGS Panel)
- CML (See: Myeloid Malignancy Comprehensive NGS Panel)
- CML-BC Immunophenotyping (See: Leukemia Lymphoma Evaluation Non CSF)
- CMP (See: Comprehensive Metabolic Panel)
- CMT Evaluation (See: Charcot Marie Tooth (CMT) Evaluation)
- CMT2A (See: MFN2 DNA Sequencing)
- CMV (See: Cytomegalovirus Antiviral Drug Resistance)
- CMV (See: Cytomegalovirus by Qualitative PCR)
- CMV (See: Viral Culture, Respiratory)
- CMV (See: Cytomegalovirus Resistance, Letermovir)
- CMV Antibody Titer (See: Cytomegalovirus Antibody, IgG)
- CMV Antibody, IgG (See: Cytomegalovirus Antibody, IgG)
- CMV Antibody, IgM (See: Cytomegalovirus (CMV) Antibody, IgM)
- CMV DNA by PCR (See: Cytomegalovirus DNA by PCR, Quantitative, Plasma, Urine and Bronchial Lavage)
- CMV IgG Avidity (See: Cytomegalovirus IgG Avidity)
- CMV PCR (See: Cytomegalovirus DNA by PCR, Quantitative, Plasma, Urine and Bronchial Lavage)
- CMV T Cell (See: CMV T-Cell Immunity Panel)
- CMV T-Cell Immunity Panel
- CMV Viral Load (See: Cytomegalovirus DNA by PCR, Quantitative, Plasma, Urine and Bronchial Lavage)
- CNS Demyelinating Disease Evaluation, Serum
- CNV (See: Hereditary Pressure Palsy Neuropathy)
- CNV (See: Gaucher Disease Mutation Analysis)
- CNV (See: Next Generation Sequencing)
- CNV (See: Osteopetrosis Gene Sequencing)
- CNV (See: Hereditary Hemorrhagic Telangiectasia (ACVR1 and ENG) Sequencing and Deletion/Duplication)
- CNV (See: ALDOB Gene Sequencing)
- CNV (See: Chronic Granulomatous Gene Analysis)
- CNV (See: Ichthyosis Gene Analysis)
- CNV (See: Epidermolysis Bullosa Gene Analysis)
- CNV (See: Holoprosencephly Gene Evaluation)
- CNV (See: PHOX2B Gene Sequencing)
- Co (See: Chromium and Cobalt, Metal-on-Metal (MoM) Implants, Serum or Plasma)
- Co (See: Chromium and Cobalt, Metal-on-Metal (MoM) Implants, Whole Blood )
- CO Hb (See: Carbon Monoxide)
- CO2 (See: Electrolyte Panel)
- CO2, Total, Serum/Plasma
- CO2, Total, Whole Blood
- COAGUCHEK
- CoaguChek PT/INR Point of Care Testing (POCT)
- Cobalamin C Disease (See: Methylmalonic Acidemia Gene Analysis)
- Cobalt, Joint Fluid
- Cobalt, Serum/Plasma
- Cocaethylene (cocaine metabolite) (See: Drug Confirmatory Panel, Urine with Creatinine)
- Cocaine Confirmation, Quantitative, Urine
- Cocaine Metabolite, Urine, Qualitative
- Coccidiodomycosis (See: Coccidioides Quantitative Antigen by EIA, Non-Blood)
- Coccidioides Antibody by CF
- Coccidioides Quantitative Antigen by EIA, Blood
- Coccidioides Quantitative Antigen by EIA, Non-Blood
- Coccidioides Quatitative Antigen by EIA, Non-Blood
- Coccidioidomycosis (See: Coccidioides Quantitative Antigen by EIA, Blood)
- Cockroach (See: Allergy Pediatric March Profile IgE)
- COCOU
- Cod (See: Allergy Pediatric March Profile IgE)
- Cod (See: Allergen: Adult Food Profile)
- Codeine (See: Opiates Confirmation, Quantitative, Urine)
- Codeine (See: Drug Confirmatory Panel, Urine with Creatinine)
- Codeine and Morphine Confirmation, Serum
- CODMOR
- Coeliac Disease (See: Endomysial Antibody, IgA by IFA)
- Coeliac Disease, Malabsorption (See: Deamidated Gliadin Antibodies, IgA and IgG)
- Coeliac Disease, Malabsorption (See: Tissue Transglutaminase Antibody, IgA)
- COENZ Q 10 (See: Coenzyme Q10, Total)
- Coenzyme Q10 Deficiency Gene Analysis
- Coenzyme Q10, Total
- Coffee spp, F221 (See: Allergen: Coffee, IgE)
- Coffin-Siris Syndrome Gene Analysis
- COGBM
- COGBM
- Cogentin (See: Benztropine)
- COL11A1 (See: Sticklers Syndrome Evaluation)
- COL11A2 (See: Sticklers Syndrome Evaluation)
- COL1A1 (See: Osteogenesis Imperfecta Gene Analysis)
- COL1A1 (See: Ehlers-Danlos Syndrome)
- COL1A1 (See: Sticklers Syndrome Evaluation)
- COL1A2 (See: Osteogenesis Imperfecta Gene Analysis)
- COL1A2 (See: Ehlers-Danlos Syndrome)
- COL3A Gene Analysis (See: Ehlers-Danlos Syndrome Type IV Deletion/Duplication Fibroblasts, Amniocytes or CVS )
- COL3A1 (See: Ehlers-Danlos Syndrome)
- COL5A1 (See: Ehlers-Danlos Syndrome)
- COL5A2 (See: Ehlers-Danlos Syndrome)
- COL6A1 (See: Congenital Muscular Dystrophy Gene Analysis)
- COL6A2 (See: Congenital Muscular Dystrophy Gene Analysis)
- COL6A3 (See: Congenital Muscular Dystrophy Gene Analysis)
- COL7A1 (See: Epidermolysis Bullosa Gene Analysis)
- COL9A1 (See: Sticklers Syndrome Evaluation)
- Cold Agglutinins
- COLEXPNGS
- COLFOC
- COLHER
- Collagen C Telopeptide (See: C-Telopeptide, Beta-Cross-Linked, Serum)
- Collagen Genes 1 & 2 (See: Osteogenesis Imperfecta Gene Analysis)
- Collagen Type I-C Telopeptide (See: C-Telopeptide, Beta-Cross-Linked, Serum)
- Collagen Type II Antibodies, Serum
- Collagen Type II Antibodies, Serum - LG5119
- Collagen VII Antibodies, IgG
- Collagen VII Antibodies, IgG - LG5413
- Colon Cancer Gene Testing (See: Lynch Syndrome)
- Colon Cancer Screen (See: Fecal Colorectal Cancer Screen (FIT))
- Colon Hereditary Gene Analysis Deletion and Duplication
- COLONEXT
- ColoNext (See: Hereditary Cancer Testing to Ambry)
- COLONEXT - LG6025
- Colorectal Cancer Panel (See: Next Generation Sequencing Oncology Tumor Testing)
- Colorectal Cancer Panel
- Colorectal Cancer:BRAF, KRAS, NRAS, PIK3CA, PTEN (See: Colorectal Focused NGS Panel)
- Colorectal Expanded NGS Panel
- Colorectal Focused NGS Panel
- COMDA (See: Drug Confirmatory Panel, Urine with Creatinine)
- Common Melon (See: Allergen: Cantaloupe, IgE)
- Common Sagebrush (See: Allergen: Sagebrush/Wormwood, IgE)
- Common Trisomy FISH Panel (See: Chorionic Villus, by FISH)
- Common Trisomy FISH Panel (See: Chromosome FISH, Chorionic Villus with Reflex to Chromosome Analysis or Genomic Microarray)
- Common Trisomy Panel (See: Chromosome FISH, Amniotic Fluid with Reflex to Chromosome Analysis or Genomic Microarray)
- Common Wormwood (See: Allergen: Sagebrush/Wormwood, IgE)
- COMP-4A (See: Complement Component 4A)
- Comparative Genomic Hubridization (CGH) with Single Nucleotide Polymorphism (SNP Array) with Limited G-Bands
- Comparative Genomic Hybridization (See: Constitutional Chromosomal Microarray (Copy Number))
- Comparative Genomic Hybridization - Recommended
- Comparative Genomic Hybridization (CGH) for Parental Follow-Up
- Comparative Genomic Hybridization (CGH) with Sigle Nucleotide Polymorphism (SNP Array) with Limited G-bands (See: Constitutional Chromosomal Microarray (Copy Number/SNP) with Limited G-band Analysis)
- Comparative Genomic Hybridization (CGH) with Single Nucleotide Polymorphism (SNP Array)
- Comparative Genomic Hybridization (CGH) with Single Nucleotide Polymorphism (SNP array) (See: Constitutional or Products of Conception (POC) Chromosomal Microarray (Copy Number/SNP))
- Comparative Genomic Hybridization (CGH) with Single Nucleotide Polymorphism (SNP Array) for Oncology (See: Oncology Chromosomal Microarray (Copy Number/SNP))
- Comparative Genomic Hybridization (CGH) with Single Nucleotide Polymorphism (SNP Array) for Oncology Samples
- Comparison Sample (See: Exome Family Member)
- Complement 1 Esterase Inhibitor, Functional (See: C1 Esterase Inhibitor, Functional)
- Complement 1 Esterase Inhibitor, Quantitation (See: C1 Esterase Inhibitor)
- Complement Activity Enzyme Immunoassay, Total (See: Complement Activity Total (CH50))
- Complement Activity Total (CH50)
- Complement B,C/B,A (See: Complement C3)
- Complement Bb Level
- Complement C1 Function Assay
- Complement C1q (See: Complement Component 1q)
- Complement C1r Level
- Complement C1s Level
- Complement C2 Function Assay
- Complement C2 Level
- Complement C3
- Complement C3a Level
- Complement C4
- Complement C5 Level by RID
- Complement C6 Function Assay
- Complement C7 Function Assay
- Complement C8 Level
- Complement C9 Function Assay
- Complement CH50, Total
- Complement Component 1q
- Complement Component 4A
- Complement Component 5
- Complement Component C2
- Complement Component C3 (See: Complement C3)
- Complement Component C4 (See: Complement C4)
- Complement Factor B Function (See: Factor B Function Assay to National Jewish Health)
- Complement Factor D Function (See: Factor D Function Assay to National Jewish Health)
- Complement Factor H (B1H)
- Complement Factor H Level (B1H)
- Complement Factor I
- Complement Kidney Genes (See: Genetic Renal Panel to MORL)
- Complement Nephropathy Gene Analysis
- Complement Nephropathy Gene Analysis (See: Genetic Renal Panel to MORL)
- Complete Alport Syndrome Evaluation
- Complete AML (See: Acute Myeloid Leukemia Panel)
- Complete AML Neoplasm Panel (See: Acute Myeloid Leukemia Panel)
- Complete Motor Neuropathy Profile (See: Motor Neuropathy Profile Complete)
- Complete Myeloproliferative Neoplasm Panel (See: Myeloproliferative Neoplasms Panel - blood or bone marrow only.)
- Complete Myeloproliferative Panel (See: Myeloproliferative Neoplasms Panel - blood or bone marrow only.)
- Complete Tuberous Sclerosis Evaluation
- Compliance Barbiturates Confirmation, Urine
- Compliance Drug Screen (See: Drug Screen, Comprehensive with Reported Medications, Whole Blood)
- Compliance Drug Screen (See: Drug Confirmatory Panel, Urine with Creatinine)
- Compound F (See: Cortisol)
- Comprehensive BRAC Analysis (See: BRCA1 and BRCA2 Hereditary Gene Analysis Deletion and Duplication)
- Comprehensive Congenital Adrenal Hyperplasia Steroid Panel (See: Steroid Panel, Comprehensive, Pediatric Endocrinology)
- Comprehensive Drug Analysis, Urine
- Comprehensive Metabolic Panel
- Comprehensive mtDNA Analysis Massively Parallel Sequencing
- Cone-Rod Dystrophy DNA Sequencing
- Confocal Microscopy (See: Epidermal Nerve Fiber)
- Congenital Adrenal Hyperplasia (See: Newborn Screening)
- Congenital Adrenal Hyperplasia (See: REORDER AS MMMISC for Test ID: ZW131. CAH 21-Hydroxylase Deficiency Monitoring Profile)
- Congenital Adrenal Hyperplasia Screening (See: CAH Panel 6C (Full Screen))
- Congenital Hyperinsulinism (See: Familial Hyperinsulinemia Gene Analysis)
- Congenital Muscular Dystrophy Gene Analysis
- Congenital Myopathy Gene Analysis
- Congenital Myxedema (See: Neuropathy Gene Analysis)
- Congenital TTP (See: ADAMTS 13 Gene Analysis)
- Congential Cytomegalovirus (cCMV) (See: Newborn Screening)
- Conjugated (See: Bilirubin, Direct and Total)
- Connexin 26 (See: Non-Syndromic Hearing Loss)
- Connexin32 (See: Charcot Marie Tooth (CMT) Evaluation)
- Constitutional Chromosomal Microarray (Copy Number)
- Constitutional Chromosomal Microarray (Copy Number) with Limited G-band Analysis
- Constitutional Chromosomal Microarray (Copy Number/SNP) with Limited G-band Analysis
- Constitutional Limited Chromosomal Microarray (Copy number only) (Charged)
- Constitutional Limited Chromosomal Microarray for Parental Follow-Up (Copy Number) (No Charge)
- Constitutional or Products of Conception (POC) Chromosomal Microarray (Copy Number/SNP)
- Constitutional, Congenital (See: Chromosome Analysis, Blood, High Resolution)
- Constitutional, Congenital (See: Chromosome Analysis, Newborn (up to 21 days old))
- Constitutional, Congenital (See: Chromosome Analysis, Blood, Sex Chromosome)
- Consult, Eye Tissue Basic (See: Eye Tissue Examination, Basic, Consultation)
- Contact Lens (See: Aerobic Bacterial Culture Routine)
- Contactin and Neurofascin
- Coombs Test (See: Direct Antiglobulin Test, Adult)
- Coombs' Test, Direct (See: Direct Antiglobulin Test, Neonate)
- COPATH
- Copper, Liver Tissue
- Copper, RBC
- Copper, RBC - LG6074
- Copper, Serum
- Copper, Serum or Plasma
- Copper, Urine
- Copy Number Variation (See: Hereditary Pressure Palsy Neuropathy)
- Copy Number variation (See: Gaucher Disease Mutation Analysis)
- Copy Number Variation (See: Next Generation Sequencing)
- Copy Number Variation (See: Osteopetrosis Gene Sequencing)
- Copy Number Variation (See: Hereditary Hemorrhagic Telangiectasia (ACVR1 and ENG) Sequencing and Deletion/Duplication)
- Copy Number Variation (See: ALDOB Gene Sequencing)
- Copy Number Variation (See: Chronic Granulomatous Gene Analysis)
- Copy Number Variation (See: Ichthyosis Gene Analysis)
- Copy Number Variation (See: Epidermolysis Bullosa Gene Analysis)
- Copy Number Variation (See: Holoprosencephly Gene Evaluation)
- Copy Number Variation (See: PHOX2B Gene Sequencing)
- COQ2 (See: Coenzyme Q10 Deficiency Gene Analysis)
- COQ6 (See: Coenzyme Q10 Deficiency Gene Analysis)
- COQ9 (See: Coenzyme Q10 Deficiency Gene Analysis)
- Cord Blood Gas (See: Blood Gas, Cord Blood)
- Cord Blood Gas (See: Blood Gas, Arterial Cord)
- Cord Blood Gas (See: Blood Gas, Venous Cord)
- Cord Blood Study (See: ABO, Rh, and DAT, Cord Blood)
- Cord Drug Screen (See: Drug Detection Panel (includes Marijuana), Umbilical Cord Tissue)
- Cord Drug Screen (See: Ethyl Glucuronide, Umbilical Cord Tissue, Qualitative)
- CORD SCRG
- Cord Tissue Collection (See: Cord Tissue Storage)
- Cord Tissue Storage
- Cord, pH
- Cordarone (See: Amiodarone and Metabolite)
- Corgard (See: Nadolol)
- Cornelia de Lange Syndrome Gene Sequencing
- Coronavirus (See: Respiratory Panel PCR)
- Coronavirus (2019-nCoV) (See: SARS-COV2 RT-PCR)
- CORT30 (LAB3405)
- CORT60 (LAB3406)
- CORTB (LAB3407)
- Cortical Dysplasia-Focal Epilepsy (See: Epilepsy Gene Analysis)
- Corticotropin (See: Adrenal Corticotropin)
- Corticotropin Timed Study (See: Adrenal Corticotropin, Timed Study)
- Cortisol
- Cortisol (See: Adrenal Corticotropin (ACTH) Stimulation Study, Baseline, Post 30 and Post 60 Minutes)
- Cortisol, Salivary
- Cortisol, Urine, Free by LC-MS/MS
- Cortisol/Cortisone, Free Urine
- Cortodoxone (See: 11-Deoxycortisol, Quantitative by HPLC-MS/MS, Serum or Plasma)
- Cortodoxone (See: 11-Deoxycortisol, Pediatric)
- Corylus Avellana Native (nCor a) 9 Ab IgE, f440 (See: Hazelnut Components, Allergy Panel)
- Corylus Avellana Recombinanat (rCor a) 1 IgE, f 428 (See: Hazelnut Components, Allergy Panel)
- Corylus Avellana Recombinant (rCor a) 8 Ab, IgE, f425 (See: Hazelnut Components, Allergy Panel)
- Corynebacterium diphtheriae Culture
- Cosyntropin (ACTH) Stimulation Panel (See: Adrenal Corticotropin (ACTH) Stimulation Study, Baseline, Post 30 and Post 60 Minutes)
- Cosyntropin Stimulation Study, 30 Minutes
- Coumadin (See: Warfarin, Serum or Plasma)
- Counsyl Family Prep Screen
- Counsyl Family Prep Screen (See: Foresight Carrier Screen)
- Counsyl Informed Pregnancy Screen
- Counsyl Inherited Cancer Screen
- COV19 (See: SARS-COV2 RT-PCR)
- Covid (See: SARS-COV2 RT-PCR)
- COVID Antibody (See: SARS-CoV-2 Nucleocapsid Total Antibody)
- COVID-19 (See: Influenza A/B, RSV, & SARS-CoV2 PCR)
- COVID-19 Nucleocapsid Aby (See: SARS-CoV-2 Nucleocapsid Total Antibody)
- Covid-19 Spike RBD Antibody, Semi-Quantitative (See: SARS-CoV2 Spike Antibody, Semi-Quantitative)
- COVTA
- Cow Hair and Dander (See: Allergen: Epidermal and Animal Proteins, Cow Hair and Dander)
- COX A AB, LHE LAB1333 (See: Coxsackie A Antibodies (Serotypes 2, 4, 7, 9, 10 and 16) Serum)
- Cox Deficiency (See: Mitochrondrial Complex IV Deficiency)
- Coxiella burnetii (Q Fever) Phase I and II by IFA
- Coxiella burnetii Qualitative, Real Time PCR
- Coxiella burnetii Qualitative, Real Time PCR - LG5039
- Coxsackie A Antibodies (Serotypes 2, 4, 7, 9, 10 and 16) Serum
- Coxsackie A9 Virus Antibody
- Coxsackie B Virus Antibodies
- CPAN (See: Pancreatic Panel, Hereditary)
- CPEPT (See: C-Peptide)
- C-Peptide
- C-Peptide
- C-Peptide in a Series
- CPK (See: CK Total)
- CPK-MB (See: Creatine Kinase, MB)
- CPRC (See: CRP Cardiac Risk)
- CPS1 (See: Hyperammonemia Gene Sequencing)
- CPT1A (See: Carnitine Deficiency Gene Analysis)
- CPT2 (See: Carnitine Deficiency Gene Analysis)
- Cr (See: Chromium and Cobalt, Metal-on-Metal (MoM) Implants, Serum or Plasma)
- Cr (See: Chromium and Cobalt, Metal-on-Metal (MoM) Implants, Whole Blood )
- Crack (See: Cocaine Metabolite, Urine, Qualitative)
- Crack (See: Cocaine Confirmation, Quantitative, Urine)
- CRDTHC (See: Drug Detection Panel (includes Marijuana), Umbilical Cord Tissue)
- CRE PCR (See: Carbapenemase Gene Detection, PCR - Rectal Swab)
- C-Reactive Protein (See: CRP Inflammation)
- Creatine Kinase Isoenzymes
- Creatine Kinase, MB
- Creatine Kinase, Total (See: CK Total)
- Creatine, Urine
- Creatinine
- Creatinine Clearance
- Creatinine, Fluid
- Creatinine, Random Urine
- Creatinine, Timed Urine
- CREBBP (See: Rubinstein-Taybi Syndrome Gene Analysis)
- CREBBP (See: Holoprosencephly Gene Evaluation)
- CREBBP (See: Next Generation Sequencing Oncology Tumor Testing)
- CRENAL (See: Renal Panel)
- Crigler-Najjar Syndrome, Type I, Type II (See: UDP-Glucuronsyl Transferase 1A1 (UGT1A1) Full Gene Sequencing Hyperbilirubinemia)
- Crigler-Najjar Syndrome, Type I, Type II (See: UDP-Glucuronsyl Transferase 1A1 (UGT1A1) Gene, Known Mutation)
- CRNPRG
- CRO PCR (See: Carbapenemase Gene Detection, PCR - Rectal Swab)
- Crohn's Prognostic
- Crosslinked N-telopeptide of Type 1 Collagen (See: N-Telopeptide, Cross-Linked, Urine)
- Crossmatch (See: ABO/RH Type and Screen, Adult)
- CRP Cardiac Risk
- CRP Cardiac Risk
- CRP Inflammation
- CRP Inflammation
- CRTAP (See: Osteogenesis Imperfecta Gene Analysis)
- CRYAB (See: Cardiomyopathy Gene Analysis)
- CRYAG (See: Cryptosporidium and Giardia Antigens)
- Cryofibrinogen, Plasma, Qualitative
- Cryoglobulin Identification
- Cryoglobulin, Quantitative
- Cryoglobulin, Quantitative with Reflex to Identification
- Cryptiter (See: Cryptococcal Antigen)
- Cryptococcal Antigen
- Cryptosporidium and Giardia Antigens
- Cryptosporidium in Stool Stain
- CRYSP (See: Cryptosporidium in Stool Stain)
- CRYST (See: Joint Fluid Exam)
- Crystal Analysis, Synovial Fluid
- Crystal Examination (See: Crystal Analysis, Synovial Fluid)
- Crystal Examination (See: Joint Fluid Exam)
- CSA (See: Cyclosporine)
- CSF (See: Cytology, CSF)
- CSF
- CSF (See: Aerobic Bacterial Culture Routine)
- CSF Cell Count and Differential (See: Cell Count and Differential, CSF)
- CSF3R (See: Next Generation Sequencing Oncology Tumor Testing)
- CSLICS
- CSRP3 (See: Cardiomyopathy Gene Analysis)
- CSTA (See: Ichthyosis Gene Analysis)
- CT IgG, IgM Ab (See: Chlamydia Antibody Panel, IgG and IgM by IFA)
- C-Telopeptide, Beta-Cross-Linked, Serum
- CTH (See: Plasma GL3)
- CTL Function (See: Cytotoxic T-Lymphocyte)
- CTLF
- CTNNB1 (See: Next Generation Sequencing Oncology Tumor Testing)
- CTRC (See: Pancreatic Panel, Hereditary)
- Cubanelle Pepper (See: Allergen: Food, Pepper C. annuum, IgE)
- Cucurbita Pepo Seeds, F226 (See: Allergen: Pumpkin Seed, IgE)
- CUL4B (See: X-Linked Intellectual Disability Gene Analysis)
- Culture (See: Aerobic Bacterial Culture Routine)
- Culture Fungal (See: Fungal Culture or Yeast Culture Routine)
- Culture Only Skin/Tissue (Cytogenetics)
- Culture, Amniotic Fluid
- Culture, Amniotic Fluid/Chorionic Villi
- Culture, Blood (See: Blood Culture Special Organism)
- Cumin Seed (See: Allergen: Food, Anise, IgE)
- Curled Dock (See: Allergen: Yellow Dock, IgE)
- Curly Dock (See: Allergen: Yellow Dock, IgE)
- CustomNext Cancer
- CustomNext Cancer (See: Hereditary Cancer Testing to Ambry)
- CustomNext-Cancer (See: CustomNext Cancer)
- Cutaneous Immunofluorescence Antibodies (IgG), Serum
- Cutaneous Immunofluorescence Antibodies (IgG), Serum - LG5432
- CVS (See: Chromosome FISH, Chorionic Villus with Reflex to Chromosome Analysis or Genomic Microarray)
- CVS FISH (See: Chorionic Villus, by FISH)
- CX (See: Beta Strep Group A Culture (Throat, Rectal, Vaginal))
- CX (See: Fungal Culture or Yeast Culture Routine)
- CX, Culture Chlamydia (See: Chlamydia Culture)
- CXBladder Detect
- CXBladder Monitor
- CXBladder Triage
- CXCL9 Cytokine
- CXCR4 (See: Next Generation Sequencing Oncology Tumor Testing)
- Cyamopsis Tetragonoloba, F246, Food Emulsifier, Thickener (See: Allergen: Guar Gum, IgE)
- Cyanide
- Cyanide as Thiocyanate, Urine
- Cyanide, Whole Blood
- CYBA (See: Chronic Granulomatous Gene Analysis)
- CYBB (See: Chronic Granulomatous Gene Analysis)
- CYCLB
- Cyclic AMP, Urine
- Cyclic AMP, Urine - LG1244
- Cyclic Citrullinated Peptide Antibody, IgG
- Cyclic Neutropenia (CN) (See: Periodic Fever Gene Analysis)
- Cyclobenzaprine
- Cyclospora (See: Cryptosporidium in Stool Stain)
- Cyclosporine
- Cyclosporine A (See: Cyclosporine)
- Cyclosporine Area Under the Curve
- Cyclosporine AUC (See: Cyclosporine Area Under the Curve)
- Cylex (See: ImmuKnow 9000)
- CYP11B1 (See: Disorders of Sexual Development Gene Analysis)
- CYP17A1 (See: Disorders of Sexual Development Gene Analysis)
- CYP19A1 (See: Disorders of Sexual Development Gene Analysis)
- CYP1A2 Genotype (See: Cytochrome P450 1A2 Genotype Sequencing)
- CYP21A2 (See: Hydroxylase Gene (CYP21A2) Full Gene Analysis)
- CYP21A2 Common Mutation Panel (See: CAH (21-Hydroxylase Deficiency) Common Mutations)
- CYP21A2 Gene (See: CAH (21-Hydroxylase Deficiency) Gene Sequencing)
- CYP27B1 Gene Sequencing (See: Hypophosphatemic Rickets Evaluation)
- CYP2R1 Gene Sequencing (See: Hypophosphatemic Rickets Evaluation)
- CYP3A4 (See: Cytochrome P450 3A4 Genotype)
- CYP4F22 (See: Ichthyosis Gene Analysis)
- Cypress (See: Allergen: Cedar, IgE)
- Cypress Arizona (See: Allergen: Tree, Japanese Cedar)
- CYPZ
- Cyst (See: Aerobic Bacterial Culture Routine)
- Cyst Fluid Cytology (See: Cytology, Cyst Fluid)
- Cystathionine (See: Amino Acids, Timed Urine)
- Cystathionine (See: Amino Acids, Plasma)
- Cystathionine (See: Amino Acids, CSF)
- Cystathionine (See: Amino Acids, Random Urine)
- Cystathionine B-Synthase, Genotype (833 & 919)
- Cystatin C (See: Cystatin C eGFR)
- Cystatin C eGFR
- Cystatin-C with CKD-EPI Calculation (See: Cystatin C eGFR)
- Cystic Fibrosis - Delta F508 (See: Cystic Fibrosis Mutation Analysis)
- Cystic Fibrosis (CFTR) 165 Pathogenic Variants
- Cystic Fibrosis Deletion/Duplication (See: CFTR Deletion/Duplication Analysis)
- Cystic Fibrosis Mutation Analysis
- Cystic Fibrosis Poly T (See: CFTR Poly T Reflex Analysis to TG Repeat)
- Cystic Fibrosis Respiratory Culture (See: Respiratory Culture, Cystic Fibrosis)
- Cystic Fibrosis Screening (See: Cystic Fibrosis (CFTR) 165 Pathogenic Variants)
- Cystic Fibrosis Specific 2 mutations
- Cystic Fibrosis Specific 2 mutations - LG6134
- Cystic Fibrosis Sweat Test (See: Sweat Chloride)
- Cystic Fibrosis, Full Mutation
- Cystic Fibrosis, Full Mutation, 1000 (See: Cystic Fibrosis, Full Mutation)
- Cysticercosis Antibody, IgG, by ELISA (CSF)
- Cystine, Leukocyte - Collect Mon-Thurs only. Must be delivered to UMMC Labs by 1500.
- Cystine, Leukocyte - Special Handling Required
- Cystoisopora (See: Cryptosporidium in Stool Stain)
- Cytochemistry Leukocyte (See: Toluidine Blue Stain)
- Cytochemistry Leukocyte (See: Periodic Acid Schiff Stain)
- Cytochemistry Leukocyte (See: Esterase, Alpha Naphthyl Butyrate (Esterase, Nonspecific) Stain)
- Cytochemistry Leukocyte (See: Peroxidase Stain, Blood/Bone Marrow)
- Cytochrome C Oxidase Deficiency (See: Mitochrondrial Complex IV Deficiency)
- Cytochrome P450 1A2 Genotype Sequencing
- Cytochrome P450 2C19 Genotype
- Cytochrome P450 2C19 Genotype, Blood
- Cytochrome P450 2C9 Genotype
- Cytochrome P450 2C9 Genotype by Sequence Analysis (See: Cytochrome P450 2C9 Genotype)
- Cytochrome P450 2C9 Genotype by Sequence Analysis, Blood
- Cytochrome P450 2D6 (CYP2D6)
- Cytochrome P450 2D6 (CYP2D6) Comprehensive Cascade
- Cytochrome P450 3A4 Genotype
- Cytochrome P450 3A4B Genotype, Blood
- Cytogenomic SNP Microarray, Fetal
- Cytokine Inflammation 4-Plex
- Cytokine Panel (See: Cytokine Storm 4-Plex)
- Cytokine Storm 4-Plex
- Cytokines (See: Interleukin-1 Alpha)
- Cytokines (See: Interleukin-1 Beta)
- Cytokines (See: Interleukin-3)
- Cytokines (See: Interleukin-4)
- Cytokines (See: Interleukin-6)
- Cytokines (See: Tumor Necrosis Factor - Alpha)
- Cytokines (See: Granulocyte Colony Stimulating Factor)
- Cytokines (See: Granulocyte Macrophage Colony Stimulating Factor, Blood)
- Cytokines (See: Interferon, Gamma)
- Cytokines (See: Tumor Necrosis Factor - Receptor I)
- Cytokines (See: Tumor Necrosis Factor - Receptor II)
- Cytokines (See: Transforming Growth Factor beta 1 (TGF-b1) - Whitley only)
- Cytokines (See: Osteopontin, Plasma)
- Cytokines (See: Prostaglandin D2 Synthase (PGD2S) - Whitley only)
- Cytokines (See: Prostaglandin D2 (PGD2) - Whitley only)
- Cytokines (See: Prostaglandin D Synthase (PGDS))
- Cytokines (See: Granulocyte Colony Stimulating Factor, Body Fluid or CSF)
- Cytokines (See: Granulocyte Macrophage Colony Stimulating Factor, Body Fluid or CSF)
- Cytokines (See: Interferon, Gamma, Body Fluid or CSF)
- Cytokines (See: Interleukin-1 Alpha, Body Fluid and CSF)
- Cytokines (See: Interleukin-1 Beta, Body Fluid and CSF)
- Cytokines (See: Interleukin-6, Body Fluid or CSF)
- Cytokines (See: Tumor Necrosis Factor-Alpha, Body Fluid or CSF)
- Cytokines (See: Osteopontin, Body Fluid or CSF)
- Cytology Breast (See: Cytology, Breast Nipple Secretion)
- Cytology, Anal Pap Test
- Cytology, Body Fluid
- Cytology, Breast Nipple Secretion
- Cytology, CSF
- Cytology, Cyst Fluid
- Cytology, Diagnostic Thin Layer Cervical Vaginal Pap Test, Grand Itasca
- Cytology, Diagnostic Thin Layer Cervical-Vaginal Pap Test With Guided Screening
- Cytology, Fat
- Cytology, Fine Needle Aspirate
- Cytology, Gastrointestinal Tract
- Cytology, Hemosiderin/Pulmonary
- Cytology, Pancreas (See: Cytology, Fine Needle Aspirate)
- Cytology, Pulmonary
- Cytology, Screening Thin Layer Cervical-Vaginal Pap Test With Guided Screening
- Cytology, Screening Thin Layer Cervical-Vaginal Pap Test, Grand Itasca
- Cytology, Urinary Tract
- Cytology, Vitreous Fluid
- Cytomegalovirus (See: Viral Culture, Respiratory)
- Cytomegalovirus (CMV) Antibody, IgM
- Cytomegalovirus (CMV) IGG and IGM Antibody, CSF
- Cytomegalovirus (CMV), Quantitative by PCR, Non Blood
- Cytomegalovirus Antibody, IgG
- Cytomegalovirus Antibody, IgG Avidity (See: Cytomegalovirus IgG Avidity)
- Cytomegalovirus Antiviral Drug Resistance
- Cytomegalovirus by Qualitative PCR
- Cytomegalovirus DNA by PCR, Quantitative, Plasma, Urine and Bronchial Lavage
- Cytomegalovirus IgG Avidity
- Cytomegalovirus Resistance, Letermovir
- Cytomegaovirus (See: Meningitis/Encephalitis Panel, Qualitative PCR, CSF)
- Cytotoxic T Lymphocyte (See: Cytotoxic T-Lymphocyte)
- Cytotoxic T-Lymphocyte
- Cytovene (See: Ganciclovir)