U.S. flag

An official website of the United States government

Filters

See more specimen types...

Other countries

See more countries

Results: 1 to 20 of 57

Tests names and labsConditionsGenes, analytes, and microbesMethods

SOD1 Gene, Full Gene Analysis

Mayo Clinic Laboratories Mayo Clinic
United States
21
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Motor Neuron Disease Gene Panel

Mayo Clinic Laboratories Mayo Clinic
United States
234
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Amyotrophic lateral sclerosis and related disorders NGS panel

HNL Genomics Connective Tissue Gene Tests
United States
124
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Amyotrophic lateral sclerosis and related disorders Deletion/ Duplication panel

HNL Genomics Connective Tissue Gene Tests
United States
124
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Amyotrophic lateral sclerosis and related disorders Comprehensive panel

HNL Genomics Connective Tissue Gene Tests
United States
124
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Genomic Unity Motor Neuron Disorders Analysis (includes AR, C9ORF72 STR analysis)

Variantyx, Inc.
United States
14118
  • D Deletion/duplication analysis
  • X Mutation scanning of select exons
  • C Sequence analysis of the entire coding region

Amyotrophic lateral sclerosis and related disorders NGS panel

HNL Genomics Connective Tissue Gene Tests
United States
124
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Amyotrophic lateral sclerosis and related disorders Deletion/ Duplication panel

HNL Genomics Connective Tissue Gene Tests
United States
124
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Amyotrophic lateral sclerosis and related disorders Comprehensive panel

HNL Genomics Connective Tissue Gene Tests
United States
124
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

SOD1

Institute of Human Genetics Medical University Innsbruck
Austria
21
  • C Sequence analysis of the entire coding region

FUS

Institute of Human Genetics Medical University Innsbruck
Austria
21
  • C Sequence analysis of the entire coding region

Amyotrophic lateral sclerosis/motor neuron disease (WES based NGS panel of 30 genes, including CNV analysis)

CGC Genetics Unilabs
Portugal
130
  • C Sequence analysis of the entire coding region

Spastic Paraplegia and Amyotrophic Lateral Sclerosis Panel

Mendelics
Brazil
260
  • C Sequence analysis of the entire coding region

Amyotrophic lateral sclerosis

Bioarray
Spain
12
  • C Sequence analysis of the entire coding region

Amyotrophic lateral sclerosis

Bioarray
Spain
14
  • C Sequence analysis of the entire coding region

Amyotrophic lateral sclerosis

Bioarray
Spain
126
  • C Sequence analysis of the entire coding region

Amyotrophic lateral sclerosis

Bioarray
Spain
11
  • T Targeted variant analysis

Amyotrophic Lateral Sclerosis (ALS)

Genetiks Genetic Diagnosis Center Genetic Diseases Evaluation Center
Turkey
11
  • C Sequence analysis of the entire coding region

Xpanded Adult Movement Disorders Panel

GeneDx
United States
5473
  • C Sequence analysis of the entire coding region

Amyotrophic Lateral Sclerosis/ Frontotemporal Lobar Degeneration Panel

GeneDx
United States
224
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 57

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.