Values current as of October 11, 2022

Mayo Test ID
2OHGP
3MGAP
ADPKP
AHUGP
ALAGP
ALPGP
ANPAT
APGP
BA190
BAP1Z
BCRAB
BHDZ
BHISC
BRGYP
CASRG
CDGGP
CDHZ
CGPH
CHLGP
CKDGP
CLADP
CLIR
CMPRE
CNSA
COMCP
CRCGP
CSFP
CYSGP
DHCRZ
ENDCP
EPPAN
F5M
FABAA
FARP
FARWB
FBAC
FCAHM
FCARP
FCLCN
FDGTX
FDM1
FDMZ
FETCE
FFMDS
FFTEN
FHER
FHLAA
FHLAB
FHLAC
FIBDD
FINA
FIXCF
FMARP
FMT21
FNEU
FNTSM
FONS
FPFUZ
FPGT
FPHIV
FPLAC
FRMTA
FSCN4
FSUAB
GA2P
GALZ
GSDGP
HBOCZ
HEXBZ
HFAOP
HHLP
HMEP
HPGLP
IN16Q
KETGP
LLTOF
LRCCZ
LSDGP
LYNCP
MCP2Z
MCSTP
MMAGP
MPAGP
MSUDP
NCLGP
NEPHP
NF1Z
NPM1Q
NTC3Z
PANCP
PCGP
PDGP
PFIB
PHEGP
PMLR
PRS8P
PTNZ
RBART
RENCP
RETZZ
RFSGS
RSCGP
STK1Z
T821Q
TCRB
THYRP
TSCP
TYRGP
UCDP
VHLZZ
WESDX
WESMT
WESR
WILMP
XCP
ZW1
ZW102
ZW105
ZW111
ZW112
ZW113
ZW117
ZW119
ZW121
ZW123
ZW124
ZW127
ZW128
ZW129
ZW130
ZW131
ZW139
ZW140
ZW143
ZW144
ZW146
ZW147
ZW149
ZW150
ZW152
ZW153
ZW155
ZW163
ZW166
ZW167
ZW168
ZW169
ZW171
ZW172
ZW173
ZW175
ZW179
ZW182
ZW185
ZW186
ZW187
ZW189
ZW190
ZW191
ZW193
ZW194
ZW196
ZW199
ZW2
ZW201
ZW204
ZW206
ZW207
ZW208
ZW210
ZW211
ZW214
ZW217
ZW218
ZW221
ZW224
ZW225
ZW227
ZW234
ZW235
ZW238
ZW239
ZW241
ZW242
ZW246
ZW266
ZW278
ZW279
ZW282
ZW288
ZW292
ZW293
ZW294
ZW298
ZW299
ZW3
ZW300
ZW305
ZW308
ZW328
ZW330
ZW333
ZW334
ZW335
ZW336
ZW340
ZW51
ZW53
ZW57
ZW58
ZW59
ZW61
ZW63
ZW68
ZW69
ZW70
ZW71
ZW73
ZW74
ZW76
ZW78
ZW79
ZW80
ZW83
ZW85
ZW86
ZW87
ZW91
ZW96
ZW99
s current as of October 11, 2022
Published Name
2-Hydroxyglutaric Aciduria Gene Panel, Varies
3-Methylglutaconic Aciduria Panel, Varies
Focused Autosomal Dominant Polycystic Kidney Disease Gene Panel, Varies
Atypical Hemolytic Uremic Syndrome (aHUS)/Thrombotic Microangiopathy (TMA) /Complement 3
Alagille Syndrome Gene Panel, Varies
Alport Syndrome Gene Panel, Varies
Anatomic Pathology Consultation, Wet Tissue
Acute Porphyria Gene Panel, Varies
BCR/ABL1, p190, mRNA Detection, Reverse Transcription-PCR (RT-PCR), Quantitative, Monitoring Assay,
BAP1-Tumor Predisposition Syndrome, BAP1 Full Gene Analysis, Varies
BCR/ABL1, p210, mRNA Detection, Reverse Transcription-PCR (RT-PCR), Quantitative, Monitoring Chronic
Birt-Hogg-Dube Syndrome, FLCN, Full Gene Analysis, Varies
Bone Histomorphometry, Gross Microscopic Exam
Hereditary Breast/Gynecologic Cancer Panel, Varies
CASR Full Gene Sequencing with Deletion/Duplication, Varies
Congenital Disorders of Glycosylation Gene Panel, Varies
Hereditary Diffuse Gastric Cancer Syndrome, CDH1, Full Gene Analysis, Varies
Custom Gene Panel, Hereditary, Next-Generation Sequencing, Varies
Cholestasis Gene Panel, Varies
Cystic Kidney Disease Gene Panel, Varies
Congenital Lactic Acidosis Panel, Varies
CLIR Supplemental Report
Family Member Comparator Specimen for Exome Sequencing, Varies
Central Nervous System Consultation, Autopsy, Varies
Hereditary Common Cancer Panel, Varies
Hereditary Gastrointestinal Cancer Panel, Varies
Carrier Screen, Focused Panel, Varies
Cystinuria Gene Panel, Varies
Smith Lemli Opitz Syndrome, DHCR7 Gene, Full Gene Analysis, Varies
Hereditary Endocrine Cancer Panel, Varies
Comprehensive Epilepsy With or Without Encephalopathy Gene Panel, Varies
5-Methyltetrahydrofolate
Anti-bestrophin Autoantibodies
Autoimmune Retinopathy Panel by Immunoblot (ARP)
Anti-retinal autoantibodies follow up, WB
Bile Acids, Urine
Chromosome Analysis, Hematologic Malignancy
Cancer-Associated Retinopathy Panel (CARP) by Immunoblot and IHC
CLCN1 DNA Sequencing Test
Digitoxin, Serum
DMPK DNA Test (DM1)
CNBP DNA Test (DM2)
Mitochondrial Respiratory Chain Enzyme Analysis (ETC) - Skin Fibroblasts
FISH, MDS/Myeloid Panel, -5/5q-, -7/7q-, +8,20q
Tetrahydrobiopterin and Neopterin Profile (BH4, N)
HER-2/neu, Quantitative, ELISA
HLA A High Resolution
HLA B High Resolution
HLA C High Resolution
PROMETHEUS IBD sgi Diagnostic
NAbFeron (IFNB-1) Neutralizing Antibody Test
Immunofixation, CSF
Melanoma Associated Retinopathy MAR Panel by Immunoblot and IHC
MaterniT21 Plus
Neurotransmitter Metabolites (5HIAA, HVA, 3OMD) (CSF)
Neurotransmitter Profile 3
Western blot for anti-optic nerve autoantibodies in the serum
Phenosense Entry HIV Drug Resistance Assay
Phenosense Combination HIV Drug Resistance Assay
Phenosense HIV Drug Resistance Replication Capacity
PROMETHEUS LactoTYPE
Recombx MaTa Autoantibody Test
SCN4A (Myotonia) DNA Sequencing Test
Sulfatide Autoantibody Test
Glutaric Aciduria Type II Gene Panel, Varies
Galactosemia, GALT Gene, Full Gene Analysis, Varies
Glycogen Storage Disease Gene Panel, Varies
BRCA1/BRCA2 Genes, Full Gene Analysis, Varies
Sandhoff Disease, HEXB Gene, Full Gene Analysis, Varies
Fatty Acid Oxidation Gene Panel, Varies
AudioloGene Hereditary Hearing Loss Panel, Varies
Hemiplegic Migraine With or Without Epilepsy Gene Panel, Varies
Hereditary Paraganglioma/Pheochromocytoma Panel, Varies
CBFB-MYH11 Inversion(16), Quantitative Detection and Minimal Disease Risk Monitoring, qRT-PCR, Varies
Ketone Disorders Gene Panel, Varies
Leukemia and Lymphoma Phenotyping, Technical Only, Varies
Hereditary Leiomyomatosis and Renal Cell Cancer Syndrome, FH, Full Gene Analysis, Varies
Lysosomal Storage Disease Gene Panel, Varies
Lynch Syndrome Panel, Varies
MECP2 Gene, Full Gene Analysis, Varies
MayoComplete Solid Tumor Panel, Next-Generation Sequencing, Tumor
Methylmalonic Aciduria Gene Panel, Varies
Methylmalonic Aciduria-Propionic Aciduria Combined Gene Panel, Varies
Maple Syrup Urine Disease Gene Panel, Varies
Neuronal Ceroid Lipofuscinosis (Batten Disease) Gene Panel, Varies
Comprehensive Nephrology Gene Panel, Varies
Neurofibromatosis Type 1, NF1, Full Gene Analysis, Varies
Nucleophosmin (NPM1) Mutation Analysis, Varies
NOTCH3 Gene, Full Gene Analysis, Varies
Hereditary Pancreatic Cancer Panel, Varies
Porphyria Comprehensive Gene Panel, Varies
Peroxisomal Disorder Gene Panel, Varies
Parafibromin, Immunostain, Technical Component Only
Phenylalanine Disorders Gene Panel, Varies
PML/RARA Quantitative, PCR, Varies
Hereditary Prostate Cancer Panel, Varies
PTEN Hamartoma Tumor Syndrome, PTEN Full Gene Analysis, Varies
Bartter Syndrome Gene Panel, Varies
Hereditary Renal Cancer Panel, Varies
Multiple Endocrine Neoplasia Type 2 Syndrome, RET, Full Gene Analysis, Varies
Focal Segmental Glomerulosclerosis (FSGS) and Nephrotic Syndrome Gene Panel, Varies
Nephrocalcinosis, Nephrolithiasis, and Renal Electrolyte Imbalance Gene Panel, Varies
Peutz-Jeghers Syndrome, STK11, Full Gene Analysis, Varies
RUNX1-RUNX1T1 Translocation (8;21), Minimal Residual Disease Monitoring, Quantitative, Varies
T-Cell Receptor V-Beta Repertoire Analysis, Spectratyping, Blood
Hereditary Thyroid Cancer Panel, Varies
Tuberous Sclerosis Gene Panel, Varies
Tyrosine Disorders Gene Panel, Varies
Urea Cycle Disorders Gene Panel, Varies
Von Hippel Lindau Syndrome, VHL, Full Gene Analysis, Varies
Whole Exome Sequencing for Hereditary Disorders , Varies
Whole Exome and Mitochondrial Genome Sequencing, Varies
Whole Exome Sequencing Reanalysis, Varies
Hereditary Wilms Tumor Panel, Varies
Hereditary Expanded Cancer Panel, Varies
Miscellaneous MML Referral Test 1
Miscellaneous U of TX San Ant Test
Misc Arkansas Children's Hospital Testing
Miscellaneous MiraVista Diagnostics
Miscellaneous Yale Univ Testing
Miscellaneous LabCorp-RTP,NC
Misc National Genetics Inst Testing
Misc University of Florida Testing
Miscellaneous Versiti Wisconsin, Inc.
Misc Ohio State Univ Ref Lab Test
Miscellaneous Sequenom
Miscellaneous Athena Testing
Miscellaneous University Hospital Clinical Lab Test
Miscellaneous Pacific Rim Pathology Medical Corp
Miscellaneous DIANON Systems
Miscellaneous Quest/Nichols Testing
Miscellaneous Child Hosp-Philadelphia
Miscellaneous Child Med Ctr Dallas
Miscellaneous IMMCO Diagnostics
Mass Gen DNA Diag Lab
Misc Prometheus Laboratories Test
Misc Johns Hopkins-DNA Analysis Lab
Misc Monogram Biosciences, Inc.
Misc Johns Hopkins-Molecular Microbiology
Misc Baylor Cytogenetics Laboratory
Misc Center for Human Genetics
Miscellaneous BioAgilytix Diagnostics
Miscellaneous Children's Hospital of Philadelphia (CHOP)
Miscellaneous CHMC - Setchell
Miscellaneous University of Virginia Health System
Miscellaneous GeneDx, Inc. Testing
Misc Univ of PA School of Medicine
Miscellaneous City of Hope Testing
Miscellaneous Center for Genetic Testing at St. Francis
Miscellaneous Joli Diagnsotics, Inc.
Miscellaneous Kennedy Krieger Institute
Misc Medical Neurogenetics, LLC
Miscellaneous Genova Diagnostics
Miscellaneous Ambry Genetics
Miscellaneous University of Chicago Genetics Sernices
Miscellaneous University of Iowa Diagnostic Labs
Miscellaneous Esoterix Genetic Laboratories, LLC - NY Testing
Miscellaneous Nemours Children's Health-Gastroenterology
Miscellaneous University of Texas Health Center at Tyler Microbiology
Miscellaneous Connective Tissue Gene Tests Lab (CTGT)
Miscellaneous Prevention Genetics Lab
Misc National Jewish Health Mycobacteriology Test
Miscellaneous Nemours Children's Health-Molecular
Miscellaneous MML Referral Test 2
Misc Baylor John Welsh Cardiovascular Diag Lab
Misc Cincinnati Childrens Hospital Medical Center
Misc Seattle Children's Hospital Laboratories
Miscellaneous MD Anderson Cancer Center
Miscellaneous Genetic Assays Inc.
Miscellaneous Univ of IA Molecular Otolaryngology
Miscellaneous OSUWMC Polaris Core Laboratory
Miscellaneous Ocular Immunology Laboratory OHSU
Miscellaneous University of Utah Genome Center
Miscellaneous Harvard Medical School
Miscellaneous Baylor Medical Genetics Laboratories
Miscellaneous PerkinElmer Genetics, Inc.
Miscellaneous Exagen Diagnostics
Miscellaneous National B Virus Resource Laboratory
Miscellaneous University of Alabama at Birmingham
Miscellaneous UCSF Medical Center
Miscellaneous University of Southern California Endocrine Laboratories
Miscellaneous Cincinnati Children's Hospital Medical Center-Hematology/Oncology
Miscellaneous Knight Diagnostic Laboratories
Miscellaneous ARUP Testing
Miscellaneous Childrens Hospital of Colorado Testing
Miscellaneous Machaon Diagnostics
Miscellaneous University of Washington Medical Center-Clinical Immunology Lab
Miscellaneous Cincinnati Children's Nephrology
Miscellaneous University of Washington Medical Center (UW Virology Dept of Lab Medicine)
Miscellaneous UF Health Medical Lab-Shands Hospital
Miscellaneous UNC Center for AIDS Research Clinical Pharmacology & Analytical Chemistry Laboratory
Miscellaneous UPMC Molecular and Genomic Pathology
Miscellaneous Asuragen Clinical Services
Miscellaneous IntrinsicDx
Miscellaneous Childrens Hospital Los Angeles
Miscellaneous MML Referral Test 3
Miscellaneous Karius Laboratory
Misc Washington University Neuromuscular Clinical Lab
Miscellaneous UCSF Clinical Laboratory, Molecular Pathology Division
Miscellaneous Imanis Life Sciences, LLC
Misc Texas Childrens Hospital, Cancer Genomics Lab
Miscellaneous Nationwide Children's Hospital
Miscellaneous Variantyx, Inc.
Miscellaneous New York Blood Center
Miscellaneous Amprion Inc.
Miscellaneous CareDx, Inc.
Miscellaneous Quest Testing
Miscellaneous Baylor Institute of Metabolic Disease
Miscellaneous Esoterix Coagulation
Miscellaneous Duke University
Misc Esoterix Endocrinology
Miscellaneous University of Minnesota Outreach Laboratory
Miscellaneous Esoterix Genetic Laboratories, LLC - MA
Miscellaneous Greenwood Genetic Ctr
Miscellaneous Eurofins Viracor Clinical Diag
Miscellaneous IMUGEN Inc Testing
Miscellaneous Inter Science Institute
Misc Johns Hopkins-DACI Ref Lab
Miscellaneous Kennedy Krieger Institute-Peroxisomal Diseases Laboratory
Miscellaneous LabCorp of America
Miscellaneous Medical Coll of WI
Miscellaneous Med Coll of WI
Miscellaneous Medtox Laboratories, Inc.
Miscellaneous Quest Diagnostics
Miscellaneous National Jewish Health
Miscellaneous NMS Testing
Miscellaneous Palo Alto Testing
Miscellaneous RFFIT Testing
Miscellaneous Quest Diagnostics Valencia
Miscellaneous Univ of AL Testing
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