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Test Catalog
MPAGP - Overview: Methylmalonic Aciduria-Propionic Aciduria Combined Gene Panel, Varies
Follow up for abnormal biochemical results suggestive of methylmalonic acidemia or propionic acidemia Establishing a molecular diagnosis for patients with methylmalonic acidemia or propionic acidemia Identifying variants within genes...
HFAOP - Overview: Fatty Acid Oxidation Gene Panel, Varies
Follow up for abnormal biochemical results suggestive of a fatty acid oxidation disorder Establishing a molecular diagnosis for patients with a fatty acid oxidation disorder Identifying variants within genes known to be associated with a...
GSDGP - Overview: Glycogen Storage Disease Gene Panel, Varies
Follow up of abnormal biochemical results consistent with glycogen storage disease (GSD) Establishing a molecular diagnosis for patients with GSD Identifying variants within genes known to be associated with GSD allowing for predictive...
ATAXP - Overview: Inherited Ataxia Gene Panel, Varies
Establishing a molecular diagnosis for patients with ataxia Identifying variants within genes known to be associated with ataxia, allowing for predictive testing of at-risk family members
LLTOT - Overview: Leukemia and Lymphoma Immunophenotyping, Technical Only, Tissue
Evaluation of tissues for potential involvement by: -Chronic lymphoproliferative disorders -Malignant lymphomas -Acute lymphoblastic leukemia -Acute myelogenous leukemia
LLPT - Overview: Leukemia/Lymphoma Immunophenotyping, Flow Cytometry, Tissue
Evaluation of tissues for potential involvement by: -Chronic lymphoproliferative disorders -Malignant lymphomas -Acute lymphoblastic leukemia -Acute myelogenous leukemia
PEPAN - Overview: Comprehensive Peripheral Neuropathy Gene Panel, Varies
Establishing a molecular diagnosis for patients with peripheral neuropathy Identifying variants within genes known to be associated with peripheral neuropathy, allowing for predictive testing of at-risk family members
CDGGP - Overview: Congenital Disorders of Glycosylation Gene Panel, Varies
Establishing a molecular diagnosis for patients with congenital disorders of glycosylation Identifying variants within genes known to be associated with congenital disorders of glycosylation, allowing for predictive testing of at-risk...
GNTHR - Overview: Thrombosis Disorders, Comprehensive Gene Panel, Next-Generation Sequencing, Varies
Evaluating hereditary thrombosis in patients with a personal or family history suggestive of a hereditary thrombosis disorder Confirming a hereditary thrombosis disorder diagnosis with the identification of a known or suspected pathogenic...
NTC3Z - Overview: NOTCH3 Gene, Full Gene Analysis, Varies
Establishing a molecular diagnosis in individuals with features of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) and NOTCH3-related disorders Identifying disease-causing variants...
EPPAN - Overview: Comprehensive Epilepsy With or Without Encephalopathy Gene Panel, Varies
Establishing a diagnosis of an epilepsy or seizure disorder associated with known causal genes Identifying disease-causing variants within genes known to be associated with inherited epilepsy or seizure disorders, allowing for predictive...
ALAGP - Overview: Alagille Syndrome Gene Panel, Varies
Providing a genetic evaluation for patients with a personal or family history suggestive of Alagille syndrome Establishing a diagnosis of Alagille syndrome
NCLGP - Overview: Neuronal Ceroid Lipofuscinosis (Batten Disease) Gene Panel, Varies
Follow up for abnormal biochemical or electron microscopy results suspicious for neuronal ceroid lipofuscinoses (NCL) Establishing a molecular diagnosis for patients with NCL Identifying variations within genes known to be associated with...
DHCRZ - Overview: Smith Lemli Opitz Syndrome, DHCR7 Gene, Full Gene Analysis, Varies
Follow up for abnormal biochemical results suggestive of Smith-Lemli-Opitz syndrome Establishing a molecular diagnosis for patients with Smith-Lemli-Opitz syndrome Identifying alterations within DHCR7 allowing for predictive testing of...
SOD1Z - Overview: SOD1 Gene, Full Gene Analysis, Varies
Establishing a molecular diagnosis for patients with amyotrophic lateral sclerosis (ALS) Identifying variants within SOD1 known to be associated with ALS, allowing for predictive testing of at-risk family members
MEV1 - Overview: Methemoglobinemia Evaluation, Blood
Diagnosis of methemoglobinemia and sulfhemoglobinemia and possible hereditary (congenital) causes Differentiation of methemoglobinemia and sulfhemoglobinemia from other causes of cyanosis (eg, congenital heart disease)
NF1Z - Overview: Neurofibromatosis Type 1, NF1, Full Gene Analysis, Varies
Evaluating patients with a personal or family history suggestive of neurofibromatosis type 1 (NF1) Establishing a diagnosis of a NF1 allowing for targeted cancer surveillance based on associated risks Identifying genetic variants...
FMARX - Overview: THC, MS, WB/SP Rfx
THC, MS, WB/SP Rfx
LSDGP - Overview: Lysosomal Storage Disease Gene Panel, Varies
Follow up for abnormal biochemical results and confirmation of suspected lysosomal storage disease (LSD) Establishing a molecular diagnosis for patients with LSD Identifying variants within genes known to be associated with LSD, allowing...
FCDUB - Overview: Barbiturates, Umbilical Cord Tissue
Barbiturates, Umbilical Cord Tissue
FCDU3 - Overview: Acetyl Fentanyl, Umbilical Cord Tissue
Acetyl Fentanyl, Umbilical Cord Tissue
FCDUE - Overview: Gabapentin, Umbilical Cord Tissue
Gabapentin, Umbilical Cord Tissue
FCDUA - Overview: Phencyclidine, Umbilical Cord Tissue
Phencyclidine, Umbilical Cord Tissue
FCDUD - Overview: Zolpidem, Umbilical Cord Tissue
Zolpidem, Umbilical Cord Tissue
FCDU5 - Overview: Amphetamines, Umbilical Cord Tissue
Amphetamines, Umbilical Cord Tissue
CLIR - Overview: CLIR Supplemental Report
CLIR Supplemental Report
FCDU4 - Overview: Novel Psychoactives, Umbilical Cord Tissue
Novel Psychoactives, Umbilical Cord Tissue
FCDU8 - Overview: Dextro/Levo Methorphan, Umbilical Cord Tissue
Dextro/Levo Methorphan, Umbilical Cord Tissue
FCDU6 - Overview: Cocaine and Metabolites, Umbilical Cord Tissue
Cocaine and Metabolites, Umbilical Cord Tissue
FCDU7 - Overview: Cannabinoids, Umbilical Cord Tissue
Cannabinoids, Umbilical Cord Tissue
FCDU9 - Overview: Muscle Relaxants, Umbilical Cord Tissue
Muscle Relaxants, Umbilical Cord Tissue
XSRM - Overview: Additional Sample for Reflex Oligoclonal Banding, Serum
Additional Sample for Reflex Oligoclonal Banding, Serum
FCDU2 - Overview: Benzodiazepines, Umbilical Cord Tissue
Benzodiazepines, Umbilical Cord Tissue
INTC1 - Overview: Fasting (8 Hours or more)
Fasting (8 Hours or more)
Whole Blood
FCDU1 - Overview: Opiates, Umbilical Cord Tissue
Opiates, Umbilical Cord Tissue
ZW10 - Overview: Miscellaneous Chemistry Testing, Varies
Miscellaneous Chemistry Testing, Varies
CMPRE - Overview: Family Member Comparator Specimen for Exome Sequencing, Varies
Submitting a biological family member's specimen to be used as a comparator for affected patients (probands) undergoing whole exome sequencing
EEEVI - Overview: Red Blood Cell (RBC) Enzyme Interpretation
Interpretation of results for the red blood cell enzyme evaluation Identifying defects of red cell enzyme metabolism Evaluating patients with Coombs-negative hemolytic anemia
MEV0 - Overview: Methemoglobin Summary Interpretation
Incorporating and summarizing subsequent results into an overall interpretation for the MEV1 / Methemoglobinemia Evaluation, Blood
SGUR - Overview: Specific Gravity, Random, Urine
As a partial assessment of the kidney's ability to concentrate urine
EXHD - Overview: Hematologic Disorders, DNA Extract and Hold, Varies
Reserving DNA on any specimen for which molecular analysis requiring DNA may be necessary at a future date, ensuring that adequate material for testing is available
CARNP - Overview: Carbapenemase Detection-Carba NP Test, Varies
Confirming carbapenemase production from pure isolates of Enterobacterales or Pseudomonas aeruginosa
Interpretation for the evaluation of stiff-person spectrum disorders including the classical or focal forms, such as stiff-limb or stiff-trunk, and progressive encephalomyelitis with rigidity and myoclonus, using serum specimens
CJDEI - Overview: Creutzfeldt-Jakob Disease Evaluation Interpretation, Spinal Fluid
Interpretation of the Creutzfeldt-Jakob Disease Evaluation
MOBRD - Overview: Mail Out Research, Blood
Mail Out Research, Blood
SLSUR - Overview: Consult Slide Surcharge (Bill Only)
Consult Slide Surcharge (Bill Only)
LCCA - Overview: Identification, Candida auris, Rapid PCR (Bill Only)
Identification, Candida auris, Rapid PCR (Bill Only)
G162 - Overview: CGO Custom Gene Panel (LPGD) (Bill Only)
CGO Custom Gene Panel (LPGD) (Bill Only)
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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....
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....
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...
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...