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Results: 1 to 20 of 26

Tests names and labsConditionsGenes and analytesMethods

Ectodermal dysplasia type 4, hair/nail type

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

Ectodermal dysplasia, ectrodactyly, and macular dystrophy

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

Skeletal Disorders and Joint Problems Sequencing Panel

PreventionGenetics
United States
327258
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

CDH3. Complete sequencing

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

Single gene testing CDH3

CeGaT GmbH
Germany
21
  • C Sequence analysis of the entire coding region

Ectodermal dysplasia-ectrodactyly-macular dystrophy syndrome (deletion/duplication analysis of CDH3 gene)

CGC Genetics
Portugal
11
  • D Deletion/duplication analysis

Ectodermal dysplasia-ectrodactyly-macular dystrophy syndrome (deletion/duplication analysis of CDH3 gene)

CGC Genetics
Portugal
11
  • D Deletion/duplication analysis

Ectrodactyly-Macular Dystrophy-Ectodermal Dysplasia (EEM Syndrome), Sequencing CDH3 Gene

Reference Laboratory Genetics
Spain
11
  • C Sequence analysis of the entire coding region

Eye diseases comprehensive panel

Asper Biogene Asper Biogene LLC
Estonia
351275
  • C Sequence analysis of the entire coding region

Ectodermal dysplasia

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
1612
  • C Sequence analysis of the entire coding region

STARGARDT SYNDROME

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
1213
  • C Sequence analysis of the entire coding region

Ectodermal dysplasia - ectrodactyly - macular dystrophy

Bioarray
Spain
11
  • C Sequence analysis of the entire coding region

Retina/Photoreceptor Dystrophy: Sequencing Panel

EGL Genetic Diagnostics Eurofins Clinical Diagnostics
United States
36120
  • C Sequence analysis of the entire coding region

Ectodermal dysplasia, ectrodactyly and macular dystrophy (sequence analysis of CDH3 gene)

CGC Genetics
Portugal
11
  • C Sequence analysis of the entire coding region

Retinal Dystrophy Panel

Molecular Vision Laboratory
United States
372287
  • C Sequence analysis of the entire coding region

Stargardt Disease and Macular Dystrophies Panel

CeGaT GmbH
Germany
1222
  • C Sequence analysis of the entire coding region

Ectodermal dysplasia (including hypotrichosis and hypoplastic hair) Panel

CeGaT GmbH
Germany
2955
  • C Sequence analysis of the entire coding region

Stargardt Panel

Molecular Vision Laboratory
United States
2813
  • C Sequence analysis of the entire coding region

CDH3

Fulgent Genetics
United States
21
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Skeletal Dysplasias NGS panel

Fulgent Genetics
United States
370161
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 26

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