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Results: 1 to 13 of 13

Tests names and labsConditionsGenes, analytes, and microbesMethods

LECITHIN:CHOLESTEROL ACYLTRANSFERASE DEFICIENCY - Norum disease, 245900, Autosomal recessive (LCAT deficiency) (LCAT 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

LECITHIN:CHOLESTEROL ACYLTRANSFERASE DEFICIENCY - Norum disease, 245900, Autosomal recessive (LCAT deficiency) (LCAT gene) (Sequence Analysis-All Coding Exons) (Prenatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Anterior Segment Dysgenesis Disorders Panel

PreventionGenetics, part of Exact Sciences
United States
272278
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Fish-Eye Disease and Norum Disease via the LCAT Gene

PreventionGenetics, part of Exact Sciences
United States
21
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

LCAT deficiency (sequence analysis of LCAT gene)

CGC Genetics Unilabs
Portugal
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

Fish-eye Disease (LCAT Single Gene Test)

Fulgent Genetics
United States
21
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Complete LCAT Deficiency (LCAT Single Gene Test)

Fulgent Genetics
United States
21
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Lecithin Cholesterol Acyltransferase Deficiency

Asper Biogene Asper Biogene LLC
Estonia
11
  • C Sequence analysis of the entire coding region

LECITHIN:CHOLESTEROL ACYLTRANSFERASE DEFICIENCY

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

LCAT Single Gene

Fulgent Genetics
United States
21
  • D Deletion/duplication analysis
  • 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

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 13 of 13

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.