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LAB TOOLS


 
RESULT
Found 93 matches for: Genetics
ORDER CODE TEST NAME
{11053R} {Porphobilinogen (PBG) Deaminase, Erythrocyte }
{11115R} {Bloom Mutation Analysis}
{11116R} {Fanconi Mutation Analysis}
{11117R} {Y Chromosome Microdeletion}
{11119R} {7-Dehydrocholesterol}
{11318R} {Glutaric Acidemia Type 1 DNA}
{11320R} {SCN1A DNA Sequencing Test}
{11328R} {Mitochondrial DNA Screening Panel}
{11330R} {Creatine/Guanidinoacetate Analysis, Plasma}
{11332R} {Creatine/Guanidinoacetate Analysis, Urine}
{11334R} {Urinary Polyols}
{11355R} {Chitotriosidase Assay}
{11357R} {Familial Mediterranean Fever}
{11359R} {Mutation Specific Testing}
{11361R} {Cowden Syndrome (PTEN)}
{11365R} {Familial Hibernian Fever}
{11367R} {Sotos syndrome (NSD1)}
{11371R} {SLOS Prenatal Diagnosis}
{11373R} {Fibrillin-1 Mutation assay}
{11375R} {COL1A1/COL1A2 Mutation assay}
{11377R} {Lysosomal Diseases Panel}
{11430R} {5-Methyltetrahydrofolate}
{11443R} {NF-1 DNA Testing Comprehensive}
{11514R} {Pompe Disease Full Sequence Analysis}
{11515R} {PKU (PAH) Sequencing}
{11517R} {Primary Ciliary Dyskinesia Panel}
{11520R} {Galactosemia (Gal-1-P), RBC}
{11535R} {POLG-Related Disorders Sequencing}
{11536R} {TK2-Related Mitochondrial DNA}
{11537R} {Mitochondrial DNA Depletion/Deletions}
{11538R} {Mitochondrial Complex IV DNA}
{11539R} {MCAD Deficiency Sequencing}
{11540R} {OTC Sequencing}
{11544R} {Angelman Syndrome UBE3A Sequencing}
{11545R} {Myotonic Dystrophy (DMPK)}
{11546R} {Mitochondrial Respiratory Chain Enzymes}
{11552R} {Glutaric Acid, Serum, Quantitative}
{11554R} {S-Sulfocysteine, Urine}
{11555R} {Maple Syrup Urine Disease}
{11570R} {Spinal Muscular Atrophy Carrier}
{11572R} {Tay-Sachs Enzyme (Leukocytes)}
{11574R} {Costello Syndrome (HRAS)}
{11576R} {Cobalamin C Deficiency (MMACHC)}
{11577R} {Alagille (JAG1) Mutation}
{11578R} {Cardiofaciocutaneous Syndrome (BRAF)}
{11579R} {Noonan Syndrome (PTPN11) }
{11580R} {Charge (CHD7) Sequencing}
{11581R} {Holoprosencephaly Sequencing}
{11582R} {Methylmalonic Acidemia Sequencing}
{11583R} {Niemann-Pick Type C, Full Gene Analysis}
{11584R} {Rett (MECP2) Sequencing, Deletion/Duplication}
{11586R} {Hunter/Iduronate Sulfatase, Enzyme Testing}
{11589R} {Stickler Syndrome Sequencing}
{11590R} {Free Fatty Acids}
{11597R} {Niemann-Pick C Protein analysis, Fibroblasts}
{11607R} {Coenzyme Q10, Reduced and Total, Plasma}
{11608R} {Marfan (FBN1) Sequencing}
{11609R} {Neurotransmitters, CSF}
{11611R} {Neuronal Ceroid Lipofuscinosis, PPT}
{11612R} {Neuronal Ceroid Lipofuscinosis, TPP}
{11614R} {PKU Diet Monitoring}
{11615R} {Sodium Benzoate Level}
{11616R} {Intracellular Cystine Assay, WBC}
{11989R} {Long QT Syndrome}
{12080R} {Canavan Disease Mutation Analysis}
{12082R} {GSD1A Mutation Analysis}
{12084R} {MLIV Mutation Analysis}
{12086R} {Niemann-Pick Disease Type A Mutation Analysis}
{12088R} {Tay-Sachs Disease Mutation Analysis}
{12776R} {Tay-Sachs Disease Enzyme Analysis (Hexosaminidase A)}
{13000R} {Aminolevulinic Acid (ALA), Urine}
{ACHER} {Acetylcholinesterase}
{AFAFPN} {Amniotic Fluid Alpha-Fetoprotein}
{ARSAL} {Arylsulfatase A, Leukocytes}
{CRTINE} {Creatine, Serum/Plasma}
{G1P} {Galactose-1-Phosphate}
{KENDNA} {Kennedy's Disease DNA}
{OSIPE} {Osteogenesis Imperfecta Evaluation}
{PORS} {Porphyrins, Serum}
{THIOMT} {Thiopurine Metabolites}
{YCDTN} {Carbohydrate Deficient Transferrin for Congenital Disorders of Glycosylation, Serum}
{YCPYRU} {Pyruvic Acid, CSF}
{YFACE} {Fatty Acid Profile, Essential (C12-C22)}
{YFATAC} {Fatty Acid Oxidation Probe Assay, Fibroblast}
{YFRUCM} {Fructosamine}
{YLCFA} {Fatty Acid Profile, Peroxisomal (C22-C26)}
{YNPICK} {Niemann-Pick, Types A & B}
{YPYRU} {Pyruvic Acid}
{YTSDM} {Tay-Sachs Disease, Mutation Analysis}
{YUACYL} {Acylglycines, Quantitative}
{YUALA} {Aminolevulinic Acid, Urine}
{YUHOMO} {Homocystein, Total, Urine}
{YUPPP} {Purine and Pyrimidine Panel}
 
 

PEDIATRIC DRAW INFORMATION

Pediatric Blood Culture Volumes

Pediatric Minimum Draw Volumes

Requirement for Virology PCR Tests

 

HLA DONOR TESTING

HLA Test Compendium

 

Downtime Donor Requisition

 

Testing for Viral Hemorrhagic Fever/Ebola

 

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are based on
AMA guidelines and
are for informational
purpose only.CPT
coding is the sole
responsibility of the
billing party. Please
direct any questions
regarding coding to
the payer being billed.

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