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Results: 1 to 20 of 20

Tests names and labsConditionsGenes, analytes, and microbesMethods

Renal Stone/Electrolyte Gene Panel

Mayo Clinic Laboratories Mayo Clinic
United States
8271
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Expanded Renal Disease Panel

Invitae
United States
693388
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CUL3 - NGS including CNV analysis

Centogene AG - the Rare Disease Company
Germany
21
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Autism Spectrum Disorders (ASD) Panel

PreventionGenetics, part of Exact Sciences
United States
224170
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Pseudohypoaldosteronism, type IIE, 614496, Autosomal dominant; PHA2E (Pseudohypoaldosteronism type 2) (CUL3 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

RenalZoom

Johns Hopkins Genomics DNA Diagnostic Laboratory Johns Hopkins Hospital
United States
527338
  • C Sequence analysis of the entire coding region

Pseudohypoaldosteronism Type II via the CUL3 Gene

PreventionGenetics, part of Exact Sciences
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Pseudohypoaldosteronism Type II Panel

PreventionGenetics, part of Exact Sciences
United States
44
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Pseudohypoaldosterolism panel. NGS panel of 10 genes.

Genologica Medica
Spain
1510
  • 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

Pseudohypoaldosteronism, type II: Full gene sequencing panel

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

Pseudohypoaldosteronism , Panel Massive Sequencing (NGS) 9 Genes

Reference Laboratory Genetics
Spain
79
  • C Sequence analysis of the entire coding region

PSEUDOHYPOALDOSTERONISM, TYPE 2 - GORDON SYNDROME (AUTOSOMAL DOMINANT)

Laboratorio de Genetica Clinica SL
Spain
44
  • C Sequence analysis of the entire coding region

CUL3 Gene Sequencing and Deletion/Duplication Analysis

DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Pseudohypoaldosteronism

Institute of Human Genetics Cologne University
Germany
88
  • C Sequence analysis of the entire coding region

Pseudohypoaldosteronism Panel

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

CUL3 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

Clinical Exome

Fulgent Genetics
United States
51294672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Pseudohypoaldosteronism, type IIE

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

Results: 1 to 20 of 20

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.