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Results: 1 to 14 of 14

Tests names and labsConditionsGenes and analytesMethods

Congenital Abnormalities of the Kidney and Urinary Tract (CAKUT) NextGen Sequencing (NGS) Panel

PreventionGenetics
United States
3342
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Medullary Cystic Kidney Disease type 2 and Familial Juvenile Hyperuricemic Nephropathy type 1 via the UMOD Gene

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

TruGenome Predisposition Screen (Whole Genome Sequencing)

Illumina Clinical Services Laboratory Illumina
United States
15411578
  • C Sequence analysis of the entire coding region

UMOD. Complete sequencing

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

UMOD. Sequencing of the exons 3 and 4

Instituto de Medicina Genomica
Spain
11
  • E Sequence analysis of select exons

Familial juvenile hyperuricemic nephropathy type 1

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

UMOD

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

Hereditary Interstitial Kidney Disease Assay

Athena Diagnostics Inc Quest Diagnostics
United States
31
  • E Sequence analysis of select exons

Ciliopathies: Sequencing and Deletion/Duplication Panel

Emory Genetics Laboratory Emory University
United States
165112
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hyperuricemic nephropathy, familial juvenile 1

MedGene
Slovakia
11
  • C Sequence analysis of the entire coding region

Ciliopathies NGS Panel

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
15895
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hyperuricemic nephropathy, familial juvenile 1

Praxis fuer Humangenetik Wien
Austria
11
  • C Sequence analysis of the entire coding region

Hyperuricemic nephropathy, Familial juvenile : UMOD gene screening (exons 3-7)

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
11
  • E Sequence analysis of select exons

Hyperuricemic nephropathy, familial juvenile 1

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

Results: 1 to 14 of 14

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