Ontario Genetic Test Directory

This directory lists diagnostic genetic tests available in Ontario for rare and inherited diseases, including molecular genetic, constitutional cytogenetic and pharmacogenetic tests.

This directory does not include:

Please contact your local genetics laboratory to confirm availability of testing, patient eligibility or sample requirements.

See Genetics Guidance for evidence-based clinical guidance on genetic testing in Ontario, and the Ontario Genetics Clinic Directory for a list of genetics clinics in Ontario.

The information in this directory is intended for informational purposes only and may not reflect all recent updates.

Displaying Results

148 Results

Neurofibromatosis type 1

Category: Cancer
Subcategory: Neurofibromatosis type 1
Test Type: Single Gene

Neurofibromatosis type 1

Category: Cancer
Subcategory: Neurofibromatosis type 1
Test Type: Single Gene

Nevoid Basal Cell Carcinoma Syndrome/ Gorlin Syndrome

Category: Cancer
Subcategory: Nevoid Basal Cell Carcinoma Syndrome (Gorlin Syndrome)
Test Type: Gene Panel

Nijmegen Breakage Syndrome

Category: Cancer
Subcategory: Nijmegen Breakage Syndrome
Test Type: Single Gene

Nijmegen Breakage Syndrome

Category: Cancer
Subcategory: Nijmegen Breakage Syndrome
Test Type: Single Gene

Oculopharyngeal muscular dystrophy (OPMD)

Category: Neurogenetics
Subcategory: Oculopharyngeal muscular dystrophy (OPMD)
Test Type: Single Gene

Pancreatic Adenocarcinoma

Category: Cancer
Subcategory: Hereditary Pancreatic Cancer (Adenocarcinoma)
Test Type: Gene Panel

Pediatric Cardiomyopathy and Arrythmia Panel

Category: Cardiogenetics
Subcategory: Cardiomyopathy and Arrhythmia
Test Type: Gene Panel

Pediatric Cardiomyopathy Panel

Category: Cardiogenetics
Subcategory: Cardiomyopathy
Test Type: Gene Panel

Pediatric Hypertrophic Cardiomyopathy Panel

Category: Cardiogenetics
Subcategory: Hypertrophic Cardiomyopathy
Test Type: Gene Panel