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Results: 1 to 20 of 29

Tests names and labsConditionsGenes, analytes, and microbesMethods

EDAR - NGS including CNV analysis

Centogene AG - the Rare Disease Company
Germany
31
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Ectodermal dysplasia Deletion / Duplication panel

HNL Genomics Connective Tissue Gene Tests
United States
89
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Ectodermal dysplasia NGS panel

HNL Genomics Connective Tissue Gene Tests
United States
89
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Ectodermal dysplasia Comprehensive panel

HNL Genomics Connective Tissue Gene Tests
United States
89
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominant, 129490, Autosomal dominant; ECTD10A (Hypohidrotic ectodermal dysplasia) (EDAR gene) (Sequence Analysis-All Coding Exons) (Prenatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominant, 129490, Autosomal dominant; ECTD10A (Hypohidrotic ectodermal dysplasia) (EDAR gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Ectodermal dysplasia NGS panel

HNL Genomics Connective Tissue Gene Tests
United States
89
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Ectodermal dysplasia Deletion / Duplication panel

HNL Genomics Connective Tissue Gene Tests
United States
89
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Ectodermal dysplasia Comprehensive panel

HNL Genomics Connective Tissue Gene Tests
United States
89
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Tooth Agenesis Panel

PreventionGenetics, part of Exact Sciences
United States
159
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Invitae Ectodermal Dysplasia and Related Disorders Panel

Invitae
United States
14873
  • D Deletion/duplication analysis

Ectodermal Dysplasia Panel

PreventionGenetics, part of Exact Sciences
United States
116
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Ectodermal Dysplasia via the EDAR Gene

PreventionGenetics, part of Exact Sciences
United States
21
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

EDAR MLPA

Institute for Human Genetics University Medical Center Freiburg
Germany
31
  • D Deletion/duplication analysis

Ectodermal dysplasia panel. 23-gene NGS panel.

Genologica Medica
Spain
6023
  • C Sequence analysis of the entire coding region

Ectodermal dysplasia: Full gene sequencing panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
1311
  • C Sequence analysis of the entire coding region

Autosomal dominant hypohidrotic ectodermal dysplasia

Labor Dr. Wisplinghoff
Germany
11
  • C Sequence analysis of the entire coding region

Autosomal dominant hypohidrotic ectodermal dysplasia

Labor Dr. Wisplinghoff
Germany
11
  • C Sequence analysis of the entire coding region

qGenEx Craniofacial Anomalies

Quantitative Genomic Medicine Laboratories, SL
Spain
135136
  • C Sequence analysis of the entire coding region

Ectodermal Dysplasia via the EDARADD Gene

Center for Comprehensive Genetic Services Shahid Beheshti University of Medical Sciences
Iran
31
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 29

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.