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Results: 1 to 15 of 15

Tests names and labsConditionsGenes, analytes, and microbesMethods

Iron-refractory iron deficiency anemia, 206200, Autosomal recessive; IRIDA (IRIDA syndrome) (TMPRSS6 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

WES iron disorders

Translational Metabolic Laboratory Radboud University Medical Centre
Netherlands
2046
  • E Sequence analysis of select exons

panel microcytic anemia-due to iron disorder (SLC11A2, TMPRSS6, TF, CP)

Translational Metabolic Laboratory Radboud University Medical Centre
Netherlands
44
  • C Sequence analysis of the entire coding region

TMPRSS6 - iron-refractory iron deficiency anemia

Translational Metabolic Laboratory Radboud University Medical Centre
Netherlands
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Iron-Refractory Iron Deficiency Anemia (IRIDA) via the TMPRSS6 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

Iron-refractory Iron Deficiency Anemia (TMPRSS6 Single Gene Test)

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

IRIDA SYNDROME

Laboratorio de Genetica Clinica SL
Spain
11
  • C Sequence analysis of the entire coding region

Iron-Refractory Iron Deficiency Anemia, Sequencing TMPRSS6 Gene

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

GDF2 Single Gene

Fulgent Genetics
United States
331
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

IRIDA syndrome

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

TMPRSS6 Single Gene

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

Hereditary Hemorrhagic Telangiectasia NGS Panel

Fulgent Genetics
United States
415
  • 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

HBA1/HBA2 and HBB Mutation Analysis

Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center
United States
63
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Iron-Refractory Iron Deficiency Anemia

BloodGenetics
Spain
11
  • 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.