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Results: 1 to 16 of 16

Tests names and labsConditionsGenes, analytes, and microbesMethods

AvaGen Test for Keratoconus Risk Factors and Corneal Dystrophies

Avellino Lab USA, Inc.
United States
171
  • E Sequence analysis of select exons

Invitae Corneal Dystrophies Panel

Invitae
United States
6533
  • D Deletion/duplication analysis

Meesmann corneal dystrophy, 122100, Autosomal dominant (Meesmann corneal dystrophy) (KRT12 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

Meesmann corneal dystrophy, 122100, Autosomal dominant; MECD (Meesmann corneal dystrophy) (KRT3 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

MitoMet®Plus aCGH Analysis

Baylor Genetics
United States
842637
  • D Deletion/duplication analysis

Corneal dystrophy panel. NGS panel of 27 genes.

Genologica Medica
Spain
4427
  • C Sequence analysis of the entire coding region

KRT12

Institute for Human Genetics University Medical Center Freiburg
Germany
11
  • C Sequence analysis of the entire coding region

Corneal Dystrophy NGS Panel

Fulgent Genetics
United States
4724
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Corneal Dystrophy , Panel Massive Sequencing (NGS) 18 Genes

Reference Laboratory Genetics
Spain
2718
  • C Sequence analysis of the entire coding region

Meesmann Corneal Distrophy , Sequencing KRT12 Gene

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

Meesmann Corneal Distrophy , Sequencing KRT3 Gene

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

Single gene testing KRT12

CeGaT GmbH
Germany
11
  • C Sequence analysis of the entire coding region

KRT3 Single Gene

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

KRT12 Single Gene

Fulgent Genetics
United States
11
  • 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

Comprehensive Eye Disorders NGS Panel

Fulgent Genetics
United States
1018459
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 16 of 16

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.