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Results: 1 to 20 of 230

Tests names and labsConditionsGenes and analytesMethods

Macular degeneration, age-related: Full gene sequencing panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
1517
  • C Sequence analysis of the entire coding region

Macular Degeneration Related Disorders , Panel Massive Sequencing (NGS) 15 Genes

Reference Laboratory Genetics
Spain
1515
  • C Sequence analysis of the entire coding region

Macular Degeneration NGS Panel

Fulgent Genetics
United States
5319
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Clinical Exome

Fulgent Genetics
United States
51484673
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Macular degeneration, age-related type 3

Centogene AG - the Rare Disease Company
Germany
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

panel Age-related Macular Degeneration (CFH, CFI, CFB, C3)

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

Macular degeneration, age-related type 8, association with

Centogene AG - the Rare Disease Company
Germany
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Macular degeneration, age-related type 11

Centogene AG - the Rare Disease Company
Germany
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Macular degeneration, age-related, 2, 153800, Autosomal dominant; ARMD2 (Stargardt disease) (ABCA4 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Genetic Diagnosis and Research Centre
Turkey
11
  • C Sequence analysis of the entire coding region

Macular degeneration, age-related, 2, 153800, Autosomal dominant; ARMD2 (Stargardt disease) (MLPA)

Intergen Genetic Diagnosis and Research Centre
Turkey
11
  • D Deletion/duplication analysis

Stargardt, arRP, Age-Related Macular Degeneration, CORD3 - ABCA4 Sequencing

Children's Hospital Colorado Precision Diagnostics Laboratory Children's Hospital Colorado
United States
41
  • C Sequence analysis of the entire coding region

Macular degeneration, age-related type 6

Centogene AG - the Rare Disease Company
Germany
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CFB - age-related macular degeneration

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

Macular degeneration, age-related, 15, susceptibility to, 615591; ARMD15 (C9 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Genetic Diagnosis and Research Centre
Turkey
11
  • C Sequence analysis of the entire coding region

Macular degeneration, age-related, neovascular type, 610149 (HTRA1 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Genetic Diagnosis and Research Centre
Turkey
11
  • C Sequence analysis of the entire coding region

Macular degeneration, age-related, 14, reduced risk of, 615489 (CFB gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Genetic Diagnosis and Research Centre
Turkey
11
  • C Sequence analysis of the entire coding region

Macular degeneration, age-related, 14, reduced risk of, 615489; ARMD14 (Immunodeficiency due to a classical component pathway complement deficiency) (C2 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Genetic Diagnosis and Research Centre
Turkey
11
  • C Sequence analysis of the entire coding region

Macular degeneration, age-related, 3, 608895, Autosomal dominant (Hereditary sensorimotor neuropathy with hyperelastic skin) (FBLN5 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Genetic Diagnosis and Research Centre
Turkey
11
  • C Sequence analysis of the entire coding region

Neuropathy, hereditary, with or without age-related macular degeneration, 608895, Autosomal dominant; HNARMD (Hereditary sensorimotor neuropathy with hyperelastic skin) (FBLN5 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Genetic Diagnosis and Research Centre
Turkey
11
  • C Sequence analysis of the entire coding region

Age-related macular degeneration (ARMD)

Centogene AG - the Rare Disease Company
Germany
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 230

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.

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