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Results: 1 to 20 of 23

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

CentoNeuro Panel

Centogene AG - the Rare Disease Company
Germany
18861858
  • 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

Huntington disease-like 1, 603218, Autosomal dominant (Huntington disease-like 1) (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

Huntington disease-like 1 (HDL1, detection of expansion on PRNP gene)

CGC Genetics Unilabs
Portugal
11
  • T Targeted variant analysis

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

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

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

Huntington disease-like 1

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

Choreatic Movement Disorders Panel

CeGaT GmbH
Germany
1621
  • C Sequence analysis of the entire coding region

PRNP

MGZ Medical Genetics Center
Germany
61
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

PRNP Single Gene

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

Results: 1 to 20 of 23

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.