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  • Did you mean vlcad (108)?

Results: 1 to 20 of 107

Tests names and labsConditionsGenes and analytesMethods

Very Long-Chain Acyl-CoA Dehydrogenase Deficiency (VLCADD): Gene Deletion/Duplication

EGL Genetic Diagnostics Eurofins Clinical Diagnostics
United States
11
  • D Deletion/duplication analysis

Very Long-Chain Acyl-CoA Dehydrogenase Deficiency (VLCADD): Full Gene Sequencing

EGL Genetic Diagnostics Eurofins Clinical Diagnostics
United States
11
  • C Sequence analysis of the entire coding region

Baby Genes Targeted Panel

Baby Genes Inc.
United States
8990
  • T Targeted variant analysis

Very Long Chain Acyl-CoA Dehydrogenase Deficiency via ACADVL Gene Sequencing with CNV Detection

PreventionGenetics
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

New Born testing (CentoICU)

Centogene AG - the Rare Disease Company
Germany
767514
  • C Sequence analysis of the entire coding region

CentoICU platinum plus

Centogene AG - the Rare Disease Company
Germany
768514
  • C Sequence analysis of the entire coding region

AllNeuro panel

Centogene AG - the Rare Disease Company
Germany
7861205
  • C Sequence analysis of the entire coding region

Very long chain acyl-CoA dehydrogenase deficiency

Fatty Acid Oxidation Laboratory Medical College of Wisconsin
United States
22
  • A Analyte

Long Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency

Fatty Acid Oxidation Laboratory Medical College of Wisconsin
United States
92
  • A Analyte

Very Long Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency, Full Gene Analysis

Mayo Clinic Genetic Testing Laboratories Mayo CLinic
United States
11
  • C Sequence analysis of the entire coding region

Acyl-CoA, very long-chain, dehydrogenase deficiency

Centogene AG - the Rare Disease Company
Germany
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

ACADVL - Very Long-Chain Acyl-CoA Dehydrogenase

Translational Metabolic Laboratory Radboud University Medical Centre
Netherlands
11
  • C Sequence analysis of the entire coding region

Very Long Chain Acyl-CoA Dehydrogenase Deficiency

Counsyl
United States
11
  • C Sequence analysis of the entire coding region

Disorders of Fatty Acid Oxidation Sequencing Panel with CNV Detection

PreventionGenetics
United States
2527
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Metabolic Myopathies, Rhabdomyolysis and Exercise Intolerance Sequencing Panel with CNV Detection

PreventionGenetics
United States
10683
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Hyperammonemia Sequencing Panel with CNV Detection

PreventionGenetics
United States
3837
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

qCarrier Plus

Quantitative Genomic Medicine Laboratories, SL
Spain
328300
  • C Sequence analysis of the entire coding region

ACADVL. Complete sequencing

Instituto de Medicina Genomica
Spain
11
  • C Sequence analysis of the entire coding region

ACADVL. MLPA testing

Instituto de Medicina Genomica
Spain
11
  • D Deletion/duplication analysis

Fatty Acid Oxidation Panel (MitomeNGS)

Baylor Miraca Genetics Laboratories
United States
1617
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 107

IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.

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