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Results: 21 to 40 of 40

Tests names and labsConditionsGenes, analytes, and microbesMethods

Pseudohypoaldosterolism panel. NGS panel of 10 genes.

Genologica Medica
Spain
1510
  • C Sequence analysis of the entire coding region

Apparent mineralocorticoid excess: Full gene sequencing

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
11
  • C Sequence analysis of the entire coding region

11-beta-hydroxysteroid dehydrogenase

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

Genomic Unity® Custom Analysis

Variantyx, Inc.
United States
14054
  • D Deletion/duplication analysis
  • X Mutation scanning of select exons
  • C Sequence analysis of the entire coding region

Monogenic Hypertension Genetic Panel

MNG Laboratories (Medical Neurogenetics, LLC.)
United States
1611
  • C Sequence analysis of the entire coding region

Bartter Syndrome

Asper Biogene Asper Biogene LLC
Estonia
3524
  • C Sequence analysis of the entire coding region

Bartter Syndrome NGS Panel

Fulgent Genetics
United States
3927
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

11-BETA-HYDROXYSTEROID DEHYDROGENASE DEFICIENCY TYPE 2

Laboratorio de Genetica Clinica SL
Spain
11
  • C Sequence analysis of the entire coding region

Pseudohypoaldosteronism Panel

Blueprint Genetics
Finland
110
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Apparent mineralocorticoid excess

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

Apparent mineralocorticoid excess

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

Pseudohypoaldosteronism Panel

CeGaT GmbH
Germany
79
  • C Sequence analysis of the entire coding region

HSD11B2 Single Gene

Fulgent Genetics
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Pseudohypoaldosteronism Type 2 NGS Panel

Fulgent Genetics
United States
139
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Monogenic Hypertension Evaluation

Athena Diagnostics
United States
44
  • C Sequence analysis of the entire coding region

HSD11B2 DNA Sequencing Test

Athena Diagnostics
United States
11
  • C Sequence analysis of the entire coding region

Endocrine Hypertension (HSD11B2) Evaluation

Athena Diagnostics
United States
11
  • C Sequence analysis of the entire coding region

Clinical Exome

Fulgent Genetics
United States
51284672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Pseudoprimary hyperaldosteronism

Laboratory for Molecular Diagnostics Center for Nephrology and Metabolic Disorders
Germany
11
  • C Sequence analysis of the entire coding region

Apparent mineralocorticoid excess

Laboratory for Molecular Diagnostics Center for Nephrology and Metabolic Disorders
Germany
11
  • C Sequence analysis of the entire coding region

Results: 21 to 40 of 40

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.