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Results: 21 to 40 of 80

Tests names and labsConditionsGenes, analytes, and microbesMethods

Adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency, 201910, Autosomal recessive (Congenital adrenal hyperplasia) (CYP21A2 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

Invitae Broad Carrier Screen without X-linked Disorders

Invitae
United States
19598
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Broad Carrier Screen

Invitae
United States
224112
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Comprehensive Carrier Screen

Invitae
United States
886547
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

21-Hydroxylase-Deficient Congenital Adrenal Hyperplasia

Myriad Genetics, Inc.
United States
21
  • T Targeted variant analysis

Congenital Adrenal Hyperplasia (CAH) Panel

PreventionGenetics
United States
87
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

qCarrier Plus

Quantitative Genomic Medicine Laboratories, SL
Spain
328300
  • C Sequence analysis of the entire coding region

Congenital Adrenal Hyperplasia (CAH) via the CYP21A2 Gene

PreventionGenetics
United States
11
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

CAH (21-Hydroxylase Deficiency) Gene Sequencing

Quest Diagnostics Nichols Institute San Juan Capistrano
United States
11
  • T Targeted variant analysis

CAH (21-Hydroxylase Deficiency) Common Mutations

Quest Diagnostics Nichols Institute San Juan Capistrano
United States
11
  • T Targeted variant analysis

M Beacon Focus B; 14 Genes

Fulgent Genetics
United States
1714
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CYP21A2

Institute of Human Genetics Medical University Innsbruck
Austria
11
  • S Mutation scanning of the entire coding region

Inherited Metabolic Disorders Panel

Dhiti Omics Technologies Private Ltd
India
376317
  • C Sequence analysis of the entire coding region

Congenital adrenal hyperplasia panel. 9-gene NGS panel.

Genologica Medica
Spain
149
  • C Sequence analysis of the entire coding region

Genital Abnormalities / Sex Development Disorders Panel

Genologica Medica
Spain
9549
  • C Sequence analysis of the entire coding region

Adrenal hyperplasia: Full gene sequencing panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
44
  • C Sequence analysis of the entire coding region

Congenital Adrenal Hyperplasia (CYP21A2 Gene)

Duzen Laboratories Duzen BBAGUAS
Turkey
21
  • T Targeted variant analysis

CYP21A2 deletion/duplication analysis

Duzen Laboratories Duzen BBAGUAS
Turkey
21
  • D Deletion/duplication analysis

Adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency

Bioarray
Spain
11
  • D Deletion/duplication analysis

Adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency

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

Results: 21 to 40 of 80

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.