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

155 Results

Constitutional FISH: Prader Willi/Angelman Syndrome

Category: Chromosomal Anomalies
Subcategory: FISH: Angelman/Prader Willi Syndrome
Test Type: Cytogenetic

Constitutional FISH: Smith-Magenis Syndrome

Category: Chromosomal Anomalies
Subcategory: FISH: Smith-Magenis Syndrome
Test Type: Cytogenetic

Constitutional FISH test: 22q11.21 Deletion Syndrome

Category: Chromosomal Anomalies
Subcategory: FISH: 22q11.21 Deletion Syndrome
Test Type: Cytogenetic

Constitutional FISH Test: Wolf-Hirschhorn syndrome

Category: Chromosomal Anomalies
Subcategory: FISH: Wolf-Hirschhorn Syndrome
Test Type: Cytogenetic

Constitutional FISH: Williams Syndrome

Category: Chromosomal Anomalies
Subcategory: FISH: Williams Syndrome
Test Type: Cytogenetic

CPT1 deficiency

Category: Metabolic
Subcategory: Fatty Acid Oxidation Diseases
Test Type: Single Gene

CPT2 deficiency

Category: Metabolic
Subcategory: Fatty Acid Oxidation Diseases
Test Type: Single Gene

Fabry Disease

Category: Metabolic
Subcategory: Fabry Disease
Test Type: Single Gene

Fatty Acid Oxidation Diseases: Other

Category: Metabolic
Subcategory: Fatty Acid Oxidation Diseases
Test Type: Gene Panel

FISH: 22q11.21 Deletion Syndrome (DiGeorge)

Category: Chromosomal Anomalies
Subcategory: 22q11.21 Deletion Syndrome
Test Type: Cytogenetic