Clinical and research tests for C3887494 - Genetic Testing Registry (GTR) - NCBI

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Tests names and labs	Conditions	Genes, analytes, and microbes	Methods
EDAR - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany	3	1	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	8	9	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	8	9	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	8	9	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Ectodermal dysplasia 10B, hypohidrotic/hair/tooth type, autosomal recessive, 224900, Autosomal recessive; ECTD10B (Hypohidrotic ectodermal dysplasia) (EDAR gene) (Sequence Analysis-All Coding Exons) (Prenatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey	1	1	C Sequence analysis of the entire coding region
Ectodermal dysplasia 10B, hypohidrotic/hair/tooth type, autosomal recessive, 224900, Autosomal recessive; ECTD10B (Hypohidrotic ectodermal dysplasia) (EDAR gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey	1	1	C Sequence analysis of the entire coding region
Ectodermal dysplasia NGS panel HNL Genomics Connective Tissue Gene Tests United States	8	9	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	8	9	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	8	9	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	15	9	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Invitae Ectodermal Dysplasia and Related Disorders Panel Labcorp Genetics (formerly Invitae) LabCorp United States	148	73	D Deletion/duplication analysis
Ectodermal Dysplasia Panel PreventionGenetics, part of Exact Sciences United States	11	6	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	2	1	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	3	1	D Deletion/duplication analysis
Ectodermal dysplasia panel. 23-gene NGS panel. Genologica Medica Spain	60	23	C Sequence analysis of the entire coding region
Ectodermal dysplasia: Full gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada	13	11	C Sequence analysis of the entire coding region
Autosomal recessive hypohidrotic ectodermal dysplasia syndrome Labor Dr. Wisplinghoff Germany	1	1	C Sequence analysis of the entire coding region
Autosomal recessive hypohidrotic ectodermal dysplasia syndrome Labor Dr. Wisplinghoff Germany	1	1	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	3	1	C Sequence analysis of the entire coding region
Hypohidrotic autosomal recessive ectodermal dysplasia Bioarray Spain	1	1	C Sequence analysis of the entire coding region

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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.