Search for "c"
| Test Name |
Synonyms |
| C DIFFICILE TOXINS A&B EIA |
C. diff., Clostridium difficile, |
| C1 ESTERASE FUNCTIONAL |
|
| C1 ESTERASE INHIBITOR QUANT |
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| C1Q BINDING IMMUNE COMPLEX |
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| C2 COMPLEMENT |
Complement component 2, |
| C3 |
B1C/l1, Complement C3, |
| C4 |
B1E, Complement C4, |
| CA 125 |
|
| CA 125,FL |
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| CA19 9 |
|
| CA27 29 |
|
| CADASIL EVALUATION |
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| CADMIUM,WB |
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| CAFFEINE |
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| CALCITONIN |
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| CALCIUM |
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| CALCIUM,FL |
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| CALCIUM,UR |
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| CAMPYLOBACTOR JEJUNI AB |
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| CANDIDA AB (ID) |
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| CANDIDA IGG,IGA,IGM |
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| CANNABINOIDS |
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| CARBAMAZEPINE |
TEGRETOL, |
| CARBAMAZEPINE EPOXIDE & TOTAL |
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| CARBAMAZEPINE,FREE & TOTAL |
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| CARBOHYDRATE DEFICIENT TRANSF |
Transferrin electrophoresis, |
| CARBOXY HGB |
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| CARBOXYLASES |
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| CARNITINE FREE & TOTAL |
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| CARNITINE TRANSPORT ASSAY |
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| CAROTENE, BETA |
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| CATECHOLAMINES FRACT URINE |
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| CATECHOLAMINES FRACTIONATED |
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| CBC,PLT/DIFF |
Complete Blood Count with Differential, |
| CBC/PLT |
Complete Blood Count, Hemogram, |
| CBC/PLT, CORD |
Fetal CBC, Umbilical Cord CBC and Platelet, |
| CCA DNA |
CONTRACTUAL CONGENETAL ARCHNODACTYLY, |
| CCHS DNA |
CONGENITAL CENTRAL HYPOVENTILATION SYNDROME, |
| CD34-STEM CELLS |
Stem Cell Absolute Counts, |
| CDH1 SEQUENCING |
|
| CDKL5 SEQUENCING |
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| CEA |
|
| CEA, FL |
|
| CELIAC SCREEN |
|
| CELL COUNTS, FL |
Body Fluid Analysis, Fluid Cell Counts, |
| CERULOPLASMIN |
Cerulo, |
| CF,RARE MUTATION 2 EXON |
|
| CFC,TEST 1,TIER 1 |
Cardio-Facio-Cutaneous Syndrome, Test 1, Tier 1, |
| CFC,TEST 1,TIER 2 |
Cardio-Facio-Cutaneous Test 1,Tier 2, |
| CFC,TEST 2 |
Cardio-Facio-Cutaneous Test 2, |
| CFTR (GENZYME) |
|
| CFTR INTRON 8 POLY T VARIANT (BAYLOR) |
|
| CH50 COMPLEMENT |
|
| CHAGAS IGG AB |
TRYPANOSOMA CRUZI IGG;, |
| CHARCOT MARIE TOOTH COMPLETE |
|
| CHARGE SYNDROME |
CHD7 GENE MUTATION, |
| CHEMICAL DEPEN SCRN 9,UR |
|
| CHEMICAL DEPEN SCRN,UR |
|
| CHIC2 FISH |
|
| CHIMERISM |
|
| CHLAMYDIA AB IGG&IGM PANEL |
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| CHLAMYDIA AB PANEL IGG |
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| CHLAMYDIA AB PANEL IGM |
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| CHLAMYDIA CULTURE |
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| CHLAMYDIA DNA PROBE |
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| CHLAMYDIA PLASMID DNA AMPLIFICATION |
Chlamydia amplification, Probetec Chlamydia, |
| CHLAMYDIA PNEUMONIAE DNA PCR |
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| CHLAMYDIA PSITTACI CULTURE |
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| CHLAMYDIA TRACHOMATIS CULTURE |
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| CHLORIDE |
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| CHLORIDE,FL |
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| CHLORIDE,UR |
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| CHLORPROMAZINE |
Thorazine, |
| CHOL/HDL RATIO |
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| CHOLESTEROL |
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| CHOLESTEROL,FL |
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| CHOLINESTERASE, RBC |
cholinesterase, whole blood, cholinesterase, whole blood, cholinesterase,whole blood, cholinesterase,whole blood, rbc cholinesterase, |
| CHROMATIN AB |
|
| CHROMIUM |
|
| CHROMOGRANIN A |
|
| Chromosome Analysis-Amniotic Fluid |
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| Chromosome Analysis-Blood |
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| Chromosome Analysis-Bone Marrow |
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| Chromosome Analysis-Products of Conception (POC) |
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| Chromosome Analysis-Solid Tumor |
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| CHROMSOME ANALYSIS (BAYLOR) |
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| CHROMSOME MICROARRAY ANALYSIS |
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| CHRONIC GRANULOMATOUS DISEASE DNA |
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| CITRIC ACID URINE |
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| CK |
|
| CK ISOENYZME |
CK-MB, CPK ISOENZYME, MASS MB, |
| CK,FL |
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| CL, WB |
|
| CLCN 1 DNA |
|
| CLCN7,KNOWN MUTATION |
OSTEOPEROSIS, AUTOSOMAL RECESSIVE (OPTB1), |
| CLCN7-AUTO RECESSIVE |
CLCN7, |
| CLN1 GENE SEQUENCING |
|
| CLN2 GENE SEQUENCING |
|
| CLN3 GENE |
Juvenile Batten disease, Mutation for Batten disease, |
| CLN3 GENE SEQUENCING |
|
| CLO3A DNA SEQUENCING |
EHLERS-DANLOS SYNDROME, |
| CLOMIPRAMINE & METABOLITE |
|
| CLONAZEPAM |
|
| CLONIDINE |
|
| CLOSTRIDIUM BOTULINUM CULTURE |
Botulism, CLOSTRIDIUM BOTULINUM CULTURE, |
| CLOSTRIDIUM DIFFICILE CYTOTOXIN AB |
|
| CLOSURE TIME(EPI) |
Platelet Function Screen, |
| CLOUSTON SYNDROME |
GJB6 GENE, |
| CLOZAPINE |
|
| CMT DEMYELINATING NEUROPATHY |
CHARCOT-MARIE-TOOTH, TYPES 1A, 1B, 1C, 1D, 1X, 4A, 4F, |
| CMT DOMINANT EVALUATION |
CHARCOT-MARIE-TOOTH DISEASE, TYPES 1A, 1B, 1D, 1X, 2E, |
| CMT PARTIAL,AXONAL |
ATHENA #392, |
| CMT PRENATAL |
|
| CMV ANTIGENEMIA |
|
| CMV DNA PCR,QNT |
|
| CMV GENOTYPING: DRUG RESISTANCE |
Cytomegalovirus drug resistance, |
| CO2 |
|
| CO2, FL |
|
| CO2,UR |
|
| COCAINE/METABOLITE,UR |
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| COCCIDIOIDES PANEL,CSF |
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| COCCIDOIDES AB |
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| COCKAYNE SYNDROME,TYPE A |
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| COCKAYNE SYNDROME,TYPE B |
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| COENZYME Q10 |
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| COFFIN-LOWRY SYN,TIER 1 |
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| COFFIN-LOWRY SYN,TIER 2 |
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| COLARIS,COMPREHENSIVE |
HNPCC, |
| COLD AGGLUTININS TITER |
Cold Agglutinin Antibodies, |
| COLLAGEN AB TYPE II |
|
| COLLAGEN SCREEN,OSTEOGENESIS IMPERFECTA |
OSTEOGENESIS IMPERFECTA, TYPES I,II,III, IV OR EHLERS-DANLOS SYNDROME, |
| COMPLETE HNPP EVALUATION |
CHAROT-MARIE-TOOTH, TYPE 1A, CMT1A, HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES, |
| COMPREHENSIVE METABOLIC PROF |
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| CONFIRM AMPHET |
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| CONFIRM BARBS |
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| CONFIRM BARBS |
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| CONFIRM BENZODIAZPNS |
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| CONFIRM COC/METAB |
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| CONFIRM MTD/MET |
EDDP, Methadone Metabolite Confirmation, |
| CONFIRM OPIATES |
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| CONFIRM OPIATES |
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| CONFIRM PCP |
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| CONFIRM PCP |
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| CONFIRM PRPXY |
Propoxyphene Confirmation, |
| CONFIRM THC |
Cannabinoids, Marijuana Metabolite Confirmation, THC Confirmation, |
| CONGENITAL & CYCLIC NEUTROPENIA |
ELA2 MUTATION, |
| CONGENITAL ADRENAL HYPERPLASIA - DNA |
CAH, |
| CONNEXIN 26 |
|
| CONNEXIN 26 KNOWN MUTATION,BOSTON |
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| CONNEXIN 30 |
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| CONNEXIN 30-BOSTON |
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| CONNEXIN 32 |
CHAROT-MARIE-TOOTH,TYPE 1X, |
| COPPER |
|
| COPPER URINE |
|
| COPPER,LIVER TISSUE |
|
| CORNELIA de LANGE DUP/DEL |
NIPBL gene dup/del, |
| CORNELIA DE LANGE SYNDROME |
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| CORTISOL |
|
| CORTISOL STIM TEST |
|
| CORTISOL,FREE URINE |
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| CORTISOL/DEXAMETHASONE SP |
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| COXSACKIE A VIRUS |
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| COXSACKIE B VIRUS AB |
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| C-PEPTIDE |
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| CPT II DEFICIENCY |
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| CREATINE |
|
| CREATININE |
|
| CREATININE CLEARANCE |
|
| CREATININE,FL |
|
| CREATININE,UR |
|
| CROUZON SYNDROME |
|
| CRYOGLOBULIN |
Cryocrit, Cryoprecipitins, |
| CRYOGLOBULIN PROFILE(CRYO+CRYOFB) |
|
| CRYOPRECIPITATE |
Pooled cryo, Pooled cryoprecipitate, |
| CRYPTOCOCCUS ANTIGEN |
Cryptococcus neoformans Ag, |
| CSA MONOCLONAL |
|
| CSF ANALYSIS |
CSF Cell Counts, |
| CSF CULTURE, BACTERIAL |
Cerobrospinal Fluid, Culture, CSF, Spinal Fluid, |
| CSF DIFFERENTIAL |
|
| CYANIDE,WB |
|
| CYCLIC AMP URINE |
|
| CYCLIC CITRULLINATED PEPTIDE AB |
|
| CYCLOSPORA/ISOSPORA MODIFIED KINYOUN STAIN |
Cryptosporidium Stain, Cyclospora Stain, Parasitology Stain by Modified Acid-Fast, |
| CYSTIC FIBROSIS 3199 DELETION |
|
| CYSTIC FIBROSIS DNA (BAYLOR) |
|
| CYSTIC FIBROSIS SEQUENCING |
CYSTIC FIBROSIS ENTIRE GENE SEQUENCING, |
| CYSTICERCOSIS IGG EIA |
|
| CYSTINE,CELLULAR |
cystinosis prep, |
| CYTOKERATIN AB |
soluble liver antigen Ab, |
| CYTOMEGALAVIRUS IGG&IGM |
CMV IgG/IgM, |
| CYTOMEGALOVIRUS IGG AB |
CMV IGG; , |
| CYTOMEGALOVIRUS IGM AB |
CMV IGM, |
|