U.S. flag

An official website of the United States government

Filters

See more specimen types...

Other countries

Results: 1 to 20 of 26

Tests names and labsConditionsGenes, analytes, and microbesMethods

PRNP - Repeat expansion analysis

Centogene AG - the Rare Disease Company
Germany
61
  • T Targeted variant analysis

PRNP - NGS including CNV analysis

Centogene AG - the Rare Disease Company
Germany
61
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Hereditary Amyotrophic Lateral Sclerosis, Frontotemporal Dementia and Alzheimer Disease Panel 

Labcorp Genetics (formerly Invitae) LabCorp
United States
7233
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Creutzfeldt-Jakob disease, 123400, Autosomal dominant (Sporadic Creutzfeldt-Jakob disease) (PRNP 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

Creutzfeldt-Jakob disease, 123400, Autosomal dominant (Sporadic Creutzfeldt-Jakob disease) (PRNP 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

Creutzfeldt-Jakob disease, variant, resistance to, 123400, Autosomal dominant; CJD (Sporadic Creutzfeldt-Jakob disease) (HLA-DQB1 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

Creutzfeldt-Jakob disease, variant, resistance to, 123400, Autosomal dominant; CJD (Sporadic Creutzfeldt-Jakob disease) (HLA-DQB1 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

Alzheimer's panel

Genologica Medica
Spain
2510
  • C Sequence analysis of the entire coding region

Dementia panel. NGS panel of 21 genes.

Genologica Medica
Spain
4421
  • C Sequence analysis of the entire coding region

Familial Amyloidosis

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

Alzheimer's panel. NGS panel of 10 genes.

Genologica Medica
Spain
2510
  • C Sequence analysis of the entire coding region

Prion Disease Genetic Analysis

Duzen Laboratories Duzen BBAGUAS
Turkey
31
  • C Sequence analysis of the entire coding region

PRNP - Gene sequencing

Amsterdam UMC Genome Diagnostics Amsterdam University Medical Center
Netherlands
61
  • C Sequence analysis of the entire coding region

Prion Disease (PRNP Single Gene Test)

Fulgent Genetics
United States
61
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CREUZTFELDT-JACOB DISEASE

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

Invitae Hereditary Prion Disease Test

Labcorp Genetics (formerly Invitae) LabCorp
United States
71
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Creutzfeldt-Jakob disease

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

Single gene testing PRNP

CeGaT GmbH
Germany
51
  • C Sequence analysis of the entire coding region

Dementia all Panel

CeGaT GmbH
Germany
3236
  • C Sequence analysis of the entire coding region

Frontotemporal Dementia (FTD) Panel

CeGaT GmbH
Germany
2928
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 26

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.