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Results: 1 to 20 of 20

Tests names and labsConditionsGenes, analytes, and microbesMethods

Hemochromatosis (HFE gene)

Molecular Genetics and Cytogenetics, Clinical Laboratory Service RED DE SALUD UC CHRISTUS
Chile
11
  • T Targeted variant analysis

NGS Panel for Hemochromatosis and Hyperferritinemia /Hypoferritinemia Panel

BloodGenetics
Spain
1111
  • C Sequence analysis of the entire coding region

Hyperferritinemia Panel

Molecular Genetics Laboratory London Health Sciences Centre
Canada
1515
  • D Deletion/duplication analysis
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

Hereditary Hemochromatosis HFE Test

Mayo Clinic Laboratories Mayo Clinic
United States
11
  • T Targeted variant analysis

Hereditary Hemochromatosis DNA Mutation Analysis

Quest Diagnostics Nichols Institute San Juan Capistrano
United States
11
  • T Targeted variant analysis

HFE-Associated Hereditary Hemochromatosis: targeted gene sequencing

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
11
  • T Targeted variant analysis

Hereditary Hemochromatosis: H63D and C302Y mutation study

Institute of Human Genetics Foundation for Research in Genetics and Endocrinology
India
11
  • T Targeted variant analysis

Hereditary Hemochromatosis via the HFE 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

Hemochromatosis Panel

Mendelics
Brazil
16
  • C Sequence analysis of the entire coding region

Hereditary Hemochromatosis

Genetics Center
United States
11
  • T Targeted variant analysis

Hemochromatosis HFE, TRF2, FPN1

GENOTYPOS MSA
Greece
13
  • T Targeted variant analysis

Foresight

Myriad Genetics, Inc.
United States
112110
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Hemochromatosis: Full gene sequencing panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
76
  • C Sequence analysis of the entire coding region

Hereditary hemochromatosis (HFE2, HAMP, TFR2, SLC40A1, FTH1)

Center for Human Genetics Cliniques Universitaires Saint Luc
Belgium
15
  • S Mutation scanning of the entire coding region

Hemochromatosis

CHEO Genetics Diagnostic Laboratory Children's Hospital of Eastern Ontario
Canada
11
  • T Targeted variant analysis

TFR2-Related Hereditary Hemochromatosis: gene sequencing

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
11
  • C Sequence analysis of the entire coding region

HEMOCHROMATOSIS TYPE 4

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

Hereditary Hemochromatosis Panel

Blueprint Genetics
Finland
75
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Metabolism Panel

Blueprint Genetics
Finland
14434
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hereditary Hemochromatosis

Molecular Genetics Diagnostic Laboratory Detroit Medical Center University Laboratories
United States
21
  • T Targeted variant analysis

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.