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Results: 1 to 20 of 45 (representing 21 labs)

Tests names and labsConditionsGenes and analytesMethods

Liddle syndrome

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

Liddle syndrome

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

SCNN1G. Complete sequencing

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

SCNN1B . Complete sequencing

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

Liddle syndrome and Autosomal Recessive Pseudohypoaldosteronism Type 1 via the SCNN1G Gene

PreventionGenetics
United States
21
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Liddle Syndrome and Autosomal Recessive Pseudohypoaldosteronism Type 1 via the SCNN1B Gene

PreventionGenetics
United States
21
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

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

Primary Ciliary Dyskinesia and Cystic Fibrosis Panel

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
4142
  • C Sequence analysis of the entire coding region

Comprehensive Pulmonary Panel

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
9293
  • C Sequence analysis of the entire coding region

Liddle Disease, Sequencing SCNN1B Gene

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

Liddle Disease, Sequencing SCNN1G Gene

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

Autosomal Dominant Pseudohypoaldosteronism Type 1 , Sequencing SCNN1G Gene

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

Ciliopathy Focus Panel

Courtagen Diagnostics Laboratory Courtagen Life Sciences
United States
219152
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Liddle syndrome

Institute of Human Genetics Cologne University
Germany
12
  • 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

BARTTER SYNDROME

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
2927
  • C Sequence analysis of the entire coding region

Liddle syndrome: SCNN1G gene sequence analysis

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
11
  • C Sequence analysis of the entire coding region

Liddle syndrome: SCNN1B gene sequence analysis

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
11
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 45

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.

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