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Results: 1 to 15 of 15

Tests names and labsConditionsGenes, analytes, and microbesMethods

KCNJ18 Gene Thyrotoxic periodic paralysis type 2 NGS Genetic DNA Test

DNA Labs India
India
11
  • S Mutation scanning of the entire coding region

UCHL1 Gene PARK5 Parkinson NGS Genetic DNA Test

DNA Labs India
India
11
  • S Mutation scanning of the entire coding region

Thyrotoxic periodic paralysis, susceptibility to, 2, 613239, Isolated cases; TTPP2 (Thyrotoxic periodic paralysis) (KCNJ18 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

GeneSeq® Neuro: Hypokalemic and Hyperkalemic Periodic Paralysis Panel

MNG Laboratories (Medical Neurogenetics, LLC.)
United States
65
  • C Sequence analysis of the entire coding region

Non-dystrophic myotonias and periodic paralysis (WES based NGS panel of 13 genes, including CNV analysis)

CGC Genetics Unilabs
Portugal
113
  • C Sequence analysis of the entire coding region

Thyrotoxic periodic paralysis type 2 (sequence analysis of KCNJ18 gene)

CGC Genetics Unilabs
Portugal
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

Thyrotoxic periodic paralysis: Full gene sequencing panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
22
  • C Sequence analysis of the entire coding region

KCNJ18 Single Gene

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

Hypokalemic Periodic Paralysis: gene sequencing panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
13
  • C Sequence analysis of the entire coding region

PERIODIC PARALYSIS, HYPOKALEMIC

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

PERIODIC PARALYSIS, THYROTOXIC

Laboratorio de Genetica Clinica SL
Spain
22
  • C Sequence analysis of the entire coding region

KCNJ18 Sequencing

Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center
United States
11
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Bartter Syndrome incl. differential diagnosis Panel

CeGaT GmbH
Germany
106
  • 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

Results: 1 to 15 of 15

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.