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Results: 121 to 140 of 145

Tests names and labsConditionsGenes, analytes, and microbesMethods

ACADM

MGZ Medical Genetics Center
Germany
11
  • C Sequence analysis of the entire coding region

Metabolic Myopathy / Fatty Acid Oxidation Disorder / Myalgia / Rhabdomyolysis

MGZ Medical Genetics Center
Germany
528
  • C Sequence analysis of the entire coding region

ACADM Deletion/duplication analysis

Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center
United States
11
  • D Deletion/duplication analysis

ACADM Single Gene

Fulgent Genetics
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Fatty Acid Oxidation Deficiency NGS Panel

Fulgent Genetics
United States
2322
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Clinical Exome

Fulgent Genetics
United States
51294672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Nuclear-Mito NGS Panel

Fulgent Genetics
United States
1103676
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Myopathy-Rhabdomyolysis NGS Panel

Fulgent Genetics
United States
3729
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Organic Acids, Comprehensive, Quantitative, Urine

Quest Diagnostics Nichols Institute San Juan Capistrano
United States
3857
  • A Analyte

Acylcarnitine, Plasma

Quest Diagnostics Nichols Institute San Juan Capistrano
United States
2622
  • A Analyte

Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency: ACADM Sequencing

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Medium Chain Acyl-CoA Dehydrogenase (ACADM) 2 Mutations

ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories
United States
11
  • T Targeted variant analysis

Metaboseq Gene Sequencing Panel

Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center
United States
5755
  • C Sequence analysis of the entire coding region

Medium Chain Acyl-Coenzyme A Dehydrogenase Deficiency

Clinical Biochemical Genetics Diagnostic Laboratory University Of Miami Miller School Of Medicine
United States
18
  • A Analyte

Medium-Chain Acyl-CoA Dehydrogenase Deficiency (MCADD)

Laboratory of Human Genetics GENOMED Health Care Center
Poland
11
  • X Mutation scanning of select exons

Medium Chain Acyl-Coenzyme A Dehydrogenase Deficiency (ACADM)

MVZ Dr. Eberhard & Partner Dortmund
Germany
11
  • T Targeted variant analysis

Medium Chain Acyl-Coenzyme A Dehydrogenase Deficiency - ACADM

Centre for Inherited Metabolic Diseases Karolinska University Hospital
Sweden
11
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Medium Chain Acyl-Coenzyme A Dehydrogenase Deficiency

Dep. of Paediatrics and Inherited Metabolic Disorders General University Hospital in Prague and First Faculty of Medicine, Charles University in Prague
Czech Republic
11
  • A Analyte
  • C Sequence analysis of the entire coding region

Medium-chain acyl-CoA dehydrogenase deficiency

Genetics Laboratory University of Oklahoma Health Sciences Center
United States
11
  • C Sequence analysis of the entire coding region

ACADM Sequencing

Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center
United States
11
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Results: 121 to 140 of 145

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.