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Results: 1 to 15 of 15

Tests names and labsConditionsGenes, analytes, and microbesMethods

OSMR Gene Amyloidosis, primary localized cutaneous, type 1 NGS Genetic DNA Test

DNA Labs India
India
11
  • S Mutation scanning of the entire coding region

Amyloidosis, primary localized cutaneous, 1, 105250, Autosomal dominant; PLCA1 (Familial primary localized cutaneous amyloidosis) (OSMR 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

Hereditary amyloidosis (WES based NGS panel of 21 genes, including CNV analysis)

CGC Genetics Unilabs
Portugal
121
  • C Sequence analysis of the entire coding region

HEREDITARY AMYLOIDOSIS SYNDROME PANEL

Laboratorio de Genetica Clinica SL
Spain
122
  • E Sequence analysis of select exons

ICHTHYOSIFORM ERYTHRODERMA CONGENITAL EXOME PANEL

Laboratorio de Genetica Clinica SL
Spain
160
  • E Sequence analysis of select exons

ICTHYOSIS EXOME PANEL

Laboratorio de Genetica Clinica SL
Spain
160
  • E Sequence analysis of select exons

Familial Amyloidosis

Genologica Medica
Spain
4419
  • C Sequence analysis of the entire coding region

Genomic Unity® Custom Analysis

Variantyx, Inc.
United States
14054
  • D Deletion/duplication analysis
  • X Mutation scanning of select exons
  • C Sequence analysis of the entire coding region

Amyloid Related Disorders (NGS Panel and Copy Number Analysis)

MNG Laboratories (Medical Neurogenetics, LLC.)
United States
516
  • C Sequence analysis of the entire coding region

Retinal Dystrophy Xpanded Panel

GeneDx
United States
20856
  • C Sequence analysis of the entire coding region

Amyloidosis: Full gene sequencing panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
88
  • C Sequence analysis of the entire coding region

Familial Amyloidosis and Related Disorders , Panel Massive Sequencing (NGS) 8 Genes

Reference Laboratory Genetics
Spain
58
  • C Sequence analysis of the entire coding region

AMYLOIDOSIS

Laboratorio de Genetica Clinica SL
Spain
510
  • C Sequence analysis of the entire coding region

OSMR 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

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.