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Results: 21 to 40 of 41

Tests names and labsConditionsGenes, analytes, and microbesMethods

PSEUDOHYPERALDOSTERONISM TYPE 1 (LIDDLE SYNDROME)

Laboratorio de Genetica Clinica SL
Spain
12
  • C Sequence analysis of the entire coding region

LIDDLE SYNDROME (PSEUDOALDOSTERONISM)

Laboratorio de Genetica Clinica SL
Spain
12
  • C Sequence analysis of the entire coding region

Comprehensive Pulmonary-Vascular Panel

Genomic Diagnostic Laboratory, Division of Genomic Diagnostics Children's Hospital of Philadelphia
United States
10086
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Liddle Syndrome Panel

Blueprint Genetics
Finland
12
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Ciliopathies

Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University
United States
4493
  • C Sequence analysis of the entire coding region

Liddle syndrome

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

Liddle syndrome

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

Single gene testing SCNN1G

CeGaT GmbH
Germany
31
  • C Sequence analysis of the entire coding region

Single gene testing SCNN1B

CeGaT GmbH
Germany
31
  • C Sequence analysis of the entire coding region

SCNN1B Single Gene

Fulgent Genetics
United States
31
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

SCNN1G Single Gene

Fulgent Genetics
United States
31
  • 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

Liddle's Syndrome Evaluation

Athena Diagnostics
United States
22
  • C Sequence analysis of the entire coding region

Monogenic Hypertension Evaluation

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

SCNN1B DNA Sequencing Test

Athena Diagnostics
United States
21
  • C Sequence analysis of the entire coding region

SCNN1G DNA Sequencing Test

Athena Diagnostics
United States
21
  • C Sequence analysis of the entire coding region

Pseudohypoaldosteronism Type 1 Evaluation (SCNN1A, SCNN1B, SCNN1G)

Athena Diagnostics
United States
23
  • 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

Lung Disorders NGS Panel

Fulgent Genetics
United States
7651
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Bronchiectasis NGS Panel

Fulgent Genetics
United States
2016
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 21 to 40 of 41

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.