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Providing a comprehensive genetic evaluation for patients with a personal or family history suggestive of Epstein-Barr virus (EBV) susceptibility or a heritable predisposition to lymphoproliferative disease Establishing a diagnosis of a...
IMSNP - Overview: Inherited Motor and Sensory Neuropathy Gene Panel, Varies
Establishing a molecular diagnosis for patients with hereditary motor and sensory neuropathy (HMSN) or Charcot-Marie-Tooth (CMT) disease Identifying variants within genes known to be associated with HMSN or CMT disease, allowing for...
GNPRC - Overview: Protein C Deficiency, PROC Gene, Next-Generation Sequencing, Varies
Evaluating protein C deficiency in patients with a personal or family history suggestive of this hereditary thrombophilia Confirming a diagnosis of autosomal dominant protein C deficiency with the identification of a known or suspected...
GNPRS - Overview: Protein S Deficiency, PROS1 Gene, Next-Generation Sequencing, Varies
Evaluating protein S deficiency in patients with a personal or family history suggestive of this hereditary thrombophilia Confirming a diagnosis of autosomal dominant protein S deficiency with the identification of a known or suspected...
HEXBZ - Overview: Sandhoff Disease, HEXB Gene, Full Gene Analysis, Varies
Follow up for abnormal biochemical results suggestive of Sandhoff disease Establishing a molecular diagnosis for patients with Sandhoff disease Identifying variants within genes known to be associated with Sandhoff disease, allowing for...
RPB - Overview: Respiratory Panel, PCR, Varies
Rapid detection of respiratory infections caused by the following: -Adenovirus -Coronavirus serotypes HKU1, NL63, 229E, OC43 -SARS-CoV-2 -Human metapneumovirus -Human rhinovirus/enterovirus -Influenza A subtypes H1, H1-2009, H3, influenza A...
PHEPU - Overview: Previous Viral Hepatitis (Unknown Type), Serum
Determining if an individual has been infected following exposure to an unknown type of viral hepatitis virus Obtaining baseline serologic markers of an individual exposed to a source with an unknown type of hepatitis Determining...
GNF11 - Overview: Hemophilia C (Factor XI Deficiency), F11 Gene, Next-Generation Sequencing, Varies
Evaluating factor XI deficiency (FXID) in patients with a personal or family history suggestive of FXID Confirming an FXID diagnosis with the identification of known or suspected disease-causing alterations in the F11 gene Determining...
GNANG - Overview: Hereditary Angioedema Focused Gene Panel, Next-Generation Sequencing, Varies
Evaluating hereditary angioedema (HAE) with normal C1 inhibitor (C1INH) in patients with a suggestive personal or family history Confirming a diagnosis of HAE with normal C1INH with the identification of a known or suspected...
NSRGG - Overview: Noonan Syndrome and Related Conditions Gene Panel, Varies
Providing a genetic evaluation for patients with a personal or family history suggestive of Noonan syndrome, Noonan syndrome with multiple lentigines, Noonan syndrome with loose anagen hair, cardiofaciocutaneous syndrome, Costello syndrome,...
UCDP - Overview: Urea Cycle Disorders Gene Panel, Varies
Follow up for abnormal biochemical results suggestive of a urea cycle disorder (UCD) Establishing a molecular diagnosis for patients with a UCD Identifying variants within genes known to be associated with UCD, allowing for predictive...
THEV1 - Overview: Thalassemia and Hemoglobinopathy Evaluation, Blood and Serum
Evaluation of microcytosis Extensive and economical diagnosis and classification of hemoglobinopathies or thalassemia, including complex disorders Diagnosis of hereditary persistence of hemoglobin
GNF13 - Overview: Factor XIII Deficiency, F13A1 and F13B Genes, Next-Generation Sequencing, Varies
Evaluating factor XIII deficiency (FXIIID) in patients with a personal or family history suggestive of FXIIID Confirming an FXIIID diagnosis with the identification of known or suspected disease-causing alterations in the F13A1 or F13B...
CMITO - Overview: Combined Mitochondrial Full Genome and Nuclear Gene Panel, Varies
Diagnosing mitochondrial disease that results from variants in either nuclear-encoded genes or the mitochondrial genome A second-tier test for patients in whom previous targeted gene variant analyses for specific mitochondrial...
Evaluating congenital fibrinogen disorders (CFD) in patients with a personal or family history suggestive of a fibrinogen disorder Confirming a CFD diagnosis with the identification of known or suspected disease-causing alterations in the...
GNHMA - Overview: Hemophilia A, F8 Gene, Next-Generation Sequencing, Varies
Confirming a clinical diagnosis of hemophilia A in affected male patients with the identification of a disease-causing variant in the F8 gene Determining the disease-causing alteration within the F8 gene to delineate the underlying...
GNVWD - Overview: von Willebrand Disease, VWF and GP1BA Genes, Next-Generation Sequencing, Varies
Evaluating von Willebrand disease and platelet-type von Willebrand disease in patients with a personal or family history suggestive of von Willebrand disease Confirming von Willebrand disease or platelet-type von Willebrand disease...
CYPZ - Overview: 21-Hydroxylase Gene, CYP21A2, Full Gene Analysis, Varies
Carrier screening and diagnosis of 21-hydroxylase deficient congenital adrenal hyperplasia (CAH) in individuals with a personal or family history of 21-hydroxylase deficiency, or as follow-up to positive CAH newborn screens and/or...
ZW347 - Overview: Miscellaneous Blueprint Genetics Inc.
Miscellaneous Blueprint Genetics Inc.
ZW346 - Overview: Miscellaneous Cleveland Clinic
Miscellaneous Cleveland Clinic
ZW321 - Overview: Miscellaneous Next Molecular Analytics
Miscellaneous Next Molecular Analytics
ZW234 - Overview: Miscellaneous University of Alabama at Birmingham
Miscellaneous University of Alabama at Birmingham
ZW299 - Overview: Miscellaneous Childrens Hospital Los Angeles
Miscellaneous Childrens Hospital Los Angeles
ZW288 - Overview: Miscellaneous UF Health Pathology Laboratories
Miscellaneous UF Health Pathology Laboratories
ZW298 - Overview: Miscellaneous IntrinsicDx
Miscellaneous IntrinsicDx
ZW99 - Overview: Miscellaneous Univ of AL-Metabolic Disease Lab
Miscellaneous Univ of AL-Metabolic Disease Lab
ZW305 - Overview: Misc Washington University Neuromuscular Clinical Lab
Misc Washington University Neuromuscular Clinical Lab
FAMBS - Overview: Amphotericin B Susceptibility Testing
Amphotericin B Susceptibility Testing
FCFS - Overview: Caspofungin Susceptibility Testing
Caspofungin Susceptibility Testing
FLUCS - Overview: Fluconazole (Diflucan) Susceptibility Testing
Fluconazole (Diflucan) Susceptibility Testing
FISST - Overview: Isavuconazole Susceptibility Testing
Isavuconazole Susceptibility Testing
FITZS - Overview: Itraconazole Susceptibility Testing
Itraconazole Susceptibility Testing
ZW333 - Overview: Miscellaneous Nationwide Children's Hospital
Miscellaneous Nationwide Children's Hospital
ZW334 - Overview: Miscellaneous Variantyx, Inc.
Miscellaneous Variantyx, Inc.
ZW63 - Overview: Miscellaneous Esoterix Genetic Laboratories, LLC - MA
Miscellaneous Esoterix Genetic Laboratories, LLC - MA
ZW61 - Overview: Miscellaneous University of Minnesota Outreach Laboratory
Miscellaneous University of Minnesota Outreach Laboratory
ZW68 - Overview: Miscellaneous Greenwood Genetic Ctr
Miscellaneous Greenwood Genetic Ctr
ZW69 - Overview: Miscellaneous Eurofins Viracor
Miscellaneous Eurofins Viracor
ZW342 - Overview: Miscellaneous MDX Health Inc.
Miscellaneous MDX Health Inc.
ZW224 - Overview: Miscellaneous Revvity Omics
Miscellaneous Revvity Omics
ZW227 - Overview: Miscellaneous National B Virus Resource Laboratory
Miscellaneous National B Virus Resource Laboratory
ZW335 - Overview: Miscellaneous New York Blood Center
Miscellaneous New York Blood Center
ZW239 - Overview: Miscellaneous Cincinnati Children's Hospital Medical Center-Hematology/Oncology
Miscellaneous Cincinnati Children's Hospital Medical Center-Hematology/Oncology
ZW238 - Overview: Miscellaneous University of Southern California Endocrine Laboratories
Miscellaneous University of Southern California Endocrine Laboratories
ZW206 - Overview: Misc. Seattle Children's Hospital Laboratories
Misc. Seattle Children's Hospital Laboratories
ZW168 - Overview: Miscellaneous GeneDx, Inc. Testing
Miscellaneous GeneDx, Inc. Testing
ZW166 - Overview: Miscellaneous Cincinnati Childs Hosp Center
Miscellaneous Cincinnati Childs Hosp Center
ZW193 - Overview: Miscellaneous HNL Genomics
Miscellaneous HNL Genomics
ZW124 - Overview: Miscellaneous Sequenom
Miscellaneous Sequenom
ZW71 - Overview: Miscellaneous Inter Science Institute
Miscellaneous Inter Science Institute
Site Search
Primary ciliary dyskinesia - Insights
Learn more about Mayo Clinic Laboratories’ robust approach to testing for primary ciliary dyskinesia, a rare genetic condition that can lead to chronic otosinopulmonary disease and infertility in men....
https://www.mayocliniclabs.com/it-mmfiles/cpt-code-changes.xlsx
note, CPT Code changes listed on this document are effective January 1st, 2025.*** ***Updates and other changes may occur, and be reflected on this document, leading up to 2025*** ***CPT Code Updates...
CPT Codes and LOINC Update: September 2019 - Insights
View a full list of new CPT codes, Test Classification Updates, LOINC Codes, and Z-Codes posted to mayocliniclabs.com during the month of September 2019....
MCL Primary Ciliary Dyskinesia Genetic Testing Patient Information MC1235297
MCL Primary Ciliary Dyskinesia Genetic Testing Patient Information Complete print Reset Form Primary Ciliary Dyskinesia Genetic Testing Patient Information Instructions Accurate interpretation reporting...
New communication process for CPT Code changes - Insights
Mayo Clinic Laboratories (MCL) is pleased to announce an essential update to our CPT code communication process and website layout. This change is designed to bring timely notifications for accurate billing...