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Results: 1 to 20 of 29

Tests names and labsConditionsGenes, analytes, and microbesMethods

PRKN - MLPA

Centogene AG - the Rare Disease Company
Germany
31
  • D Deletion/duplication analysis

PRKN - NGS including CNV analysis

Centogene AG - the Rare Disease Company
Germany
31
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Hereditary Parkinson Disease and Parkinsonism Panel

Labcorp Genetics (formerly Invitae) LabCorp
United States
4426
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Parkinson disease, juvenile, type 2, 600116, Autosomal recessive; PARK2 (Young-onset Parkinson disease) (PRKN 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

Parkinson Disease and Parkinsonism Panel

PreventionGenetics, part of Exact Sciences
United States
6870
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Parkinson Disease Panel

PreventionGenetics, part of Exact Sciences
United States
2724
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Invitae Dystonia Comprehensive Panel

Labcorp Genetics (formerly Invitae) LabCorp
United States
6138
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Parkinson's Disease, Juvenile via the PRKN/PARK2 Gene

PreventionGenetics, part of Exact Sciences
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Parkinson's disease panel. NGS panel of 22 genes.

Genologica Medica
Spain
4522
  • C Sequence analysis of the entire coding region

Parkinson deletion/duplication analysis

Duzen Laboratories Duzen BBAGUAS
Turkey
88
  • D Deletion/duplication analysis

Parkinson Juvenil, PARK2

Duzen Laboratories Duzen BBAGUAS
Turkey
11
  • C Sequence analysis of the entire coding region

Dystonia and Parkinsonism Panel

GeneDx
United States
2073
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

PRKN

Institute for Human Genetics University Medical Center Freiburg
Germany
31
  • C Sequence analysis of the entire coding region

Parkinson Disease: Full gene sequencing panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
2024
  • C Sequence analysis of the entire coding region

PARKINSON, RECESSIVE JUVENILE (PARK2)

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

Parkinson Disease

Asper Biogene Asper Biogene LLC
Estonia
4230
  • C Sequence analysis of the entire coding region

Dystonia

Asper Biogene Asper Biogene LLC
Estonia
3940
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Parkinson disease type 2

Bioarray
Spain
11
  • D Deletion/duplication analysis

Single gene testing PANK2

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

Parkinson Syndrome, autosomal recessive Panel

CeGaT GmbH
Germany
911
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 29

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.