Répertoire des cliniques de génétique en Ontario

Des services de génétique clinique sont offerts dans des sites hospitaliers à travers l’Ontario. Ce répertoire  liste les emplacements des cliniques de génétique, leurs services et les populations servies.

Ce répertoire dresse la liste des cliniques de génétique qui offrent l’un des services suivants :

  • Tests et conseils génétiques financés par Santé Ontario
  • Soins de suivi spécialisés pour les personnes ayant des troubles génétiques confirmés

Les cliniques peuvent être exclues du répertoire si elles n’acceptent pas de nouveaux aiguillages.

Comment utiliser le répertoire

Pour affiner la liste des cliniques, commencez par filtrer par Services offerts :

  • Pour les personnes qui pourraient avoir un trouble génétique et qui ont besoin de services de test ou de diagnostic, choisissez Tests et conseils génétiques.
  • Pour les personnes qui ont un trouble génétique confirmé et qui ont besoin de soins de suivi spécialisés, choisissez Soins continus.

Vous pouvez également filtrer les résultats par lieu, accès sans recommandation, population desservie et domaines de soins de diagnostic ou de test.

Pour de plus amples renseignements

Communiquez directement avec les cliniques pour obtenir des renseignements spécifiques à la clinique tels que :

  • les formulaires d’aiguillage
  • les troubles spécifiques observés
  • les services linguistiques fournis

Si vous êtes un patient et que vous avez des questions concernant un trouble précis, veuillez en discuter avec votre professionnel de la santé.

Si vous avez des questions ou des commentaires concernant l’utilisation de ce répertoire, veuillez communiquer avec nous à l’aide du formulaire figurant sur la page Programme provincial de génétique.

Affichage des résultats

Filtres

Filtres

Services Provided

Soins continus
Tests et conseils génétiques

Accepts self referral

Non
Oui

Emplacement

North York
Kitchener
Scarborough
Windsor
Mississauga
Kingston
North Bay Sault Ste. Marie Sudbury Timmins
Orillia
Peterborough
Oshawa
Richmond Hill
Hamilton
London
Thunder Bay
Ottawa
Toronto

Areas of care

Génétique prénatale
Génétique métabolique
Génétique pour la reproduction
Cardiogénétique
Génétique oncologique
Génétique pédiatrique
Neurogénétique
Génétique générale
Génétique oculaire
Affichage 10 de 84 résultats

Aorta Clinic, St Michael’s Hospital

Services Provided:
Soins continus
Accepts self referral:
Non
Emplacement:
Toronto
Areas of care:
Cardiogénétique
Mots-clés:

actin alpha 2 (ACTA2) aortic disease aortopathy bicuspid aortic valve (BAV) familial thoracic aortic aneurysms dissections (FTAAD) Loeys-Dietz syndrome (LDS) Marfan syndrome mitral valve prolapse (MVP) vascular dissection vascular Ehlers-Danlos syndrome (vEDS)

Aortopathy Clinic, Toronto General Hospital

Services Provided:
Tests et conseils génétiques
Accepts self referral:
Non
Emplacement:
Toronto
Areas of care:
Cardiogénétique
Mots-clés:

aortic aneurysm aortic disease aortic dissection aortopathy bicuspid aortopathy bicuspid valve-associated aortopathy cardiogenetics thoracic aortic aneurysm (TAA)

Bhalwani Familial Cancer Clinic, Princess Margaret Cancer Centre

Services Provided:
Tests et conseils génétiques
Accepts self referral:
Non
Emplacement:
Toronto
Areas of care:
Génétique oncologique
Mots-clés:

breast cancer cancer endocrine cancer kidney cancer lung cancer lymphoma melanoma ovarian cancer prostate cancer renal cell carcinoma leukemia bone marrow failure myelodysplastic syndrome adrenocortical carcinoma hematologic malignancy brain cancer bone cancer fallopian tube cancer mesothelioma sarcoma thyroid cancer hemangioblastoma pheochromocytoma paraganglioma retinoblastoma gastrointestinal stromal tumour neuroendocrine tumour pituitary tumour wilms tumour endometrial cancer parathyroid tumour

Bone Health-Osteology Clinic, CHEO

Services Provided:
Soins continus
Accepts self referral:
Non
Emplacement:
Ottawa
Areas of care:
Mots-clés:

unexplained bone fragility primary bone fragility osteogenesis imperfecta (OI) syndromic bone fragility connective tissue disorders Ehlers-Danlos syndrome (EDS) Marfan syndrome Loeys-Dietz syndrome (LDS) skeletal dysplasias fibrous dysplasia hypophosphatasia achondroplasia Calcium and phosphate metabolism disorders rickets ectopic mineralization disorders tumoral calcinosis Ollier’s disease fibrodysplasia ossificans progressive (FOP) high bone mass conditions sclerosing bone disorders osteopetrosis

CHEO Genetics Clinic (Regional Genetics Program)

Services Provided:
Tests et conseils génétiques
Accepts self referral:
Non
Emplacement:
Ottawa
Areas of care:
Génétique oncologique, Cardiogénétique, Génétique générale, Neurogénétique, Génétique oculaire, Génétique prénatale
Mots-clés:

adult genetics cancer cardiogenetics general genetics maternal health neurogenetics ocular genetics pediatric genetics preconception prenatal genetics

CHEO Tuberous Sclerosis Clinic

Services Provided:
Soins continus
Accepts self referral:
Non
Emplacement:
Ottawa
Areas of care:
Génétique oncologique, Neurogénétique
Mots-clés:

tuberous sclerosis complex (TSC)

Cancer Genetics Clinic Victoria Hospital, London Health Sciences Centre

Services Provided:
Tests et conseils génétiques, Soins continus
Accepts self referral:
Non
Emplacement:
London
Areas of care:
Génétique oncologique
Mots-clés:

breast cancer cancer colon cancer colorectal cancer endocrine cancer kidney cancer lung cancer lymphoma melanoma ovarian cancer prostate cancer renal cell cancer skin cancer pancreatic sarcoma brain endometrial paraganglioma/pheochromocytoma gastric leukemia

Cancer Genetics Clinic, Waterloo Regional Health Network Cancer Centre

Services Provided:
Tests et conseils génétiques
Accepts self referral:
Non
Emplacement:
Kitchener
Areas of care:
Génétique oncologique
Mots-clés:

brain cancer, BRCA1, BRCA2, breast cancer, cancer, colon cancer, colorectal cancer, endocrine cancer, endometrial cancer, gastric cancer, hereditary cancer, kidney cancer, lung cancer, lynch syndrome, melanoma, ovarian cancer, pancreatic cancer, pheochromocytoma/paraganglioma, polyposis, prostate cancer, renal cell cancer, skin cancer, stomach cancer, thyroid cancer

Cardiac Arrhythmia Clinic, Hamilton Health Sciences

Services Provided:
Soins continus
Accepts self referral:
Non
Emplacement:
Hamilton
Areas of care:
Cardiogénétique
Mots-clés:

arrhythmia arrhythmogenic right ventricular cardiomyopathy (ARVC) atrial fibrillation Brugada syndrome cardiac disorders cardiogenetics cardiomyopathy catecholaminergic polymorphic ventricular tachycardia (CPVT) dilated cardiomyopathy (DCM) familial hypercholesterolemia (FH) hypertrophic cardiomyopathy (HCM) long QT syndrome (LQTS) short QT syndrome (SQTS) sudden cardiac arrest sudden cardiac death

Cardiology Clinic Children’s Hospital of Western Ontario, London Health Sciences Centre

Services Provided:
Soins continus
Accepts self referral:
Non
Emplacement:
London
Areas of care:
Cardiogénétique
Mots-clés:

arrhythmia atrial fibrillation Brugada syndrome cardiac disorders cardiogenetics cardiomyopathy catecholaminergic polymorphic ventricular tachycardia (CPVT) congenital heart disease coronary artery disease hypertrophic cardiomyopathy (HCM) long QT syndrome (LQTS) short QT syndrome (SQTS)

Cardiology Clinic The Hospital for Sick Children

Services Provided:
Soins continus
Accepts self referral:
Non
Emplacement:
Toronto
Areas of care:
Cardiogénétique
Mots-clés:

arrhythmia atrial fibrillation Brugada syndrome cardiac disorders cardiogenetics cardiomyopathy catecholaminergic polymorphic ventricular tachycardia (CPVT) congenital heart disease coronary artery disease familial hypercholesterolemia (FH) hypertrophic cardiomyopathy (HCM) long QT syndrome (LQTS) short QT syndrome (SQTS)

Cardiology Clinic, CHEO

Services Provided:
Soins continus
Accepts self referral:
Non
Emplacement:
Ottawa
Areas of care:
Cardiogénétique
Mots-clés:

arrhythmia atrial fibrillation Brugada syndrome cardiac disorders cardiogenetics cardiomyopathy catecholaminergic polymorphic ventricular tachycardia (CPVT) congenital heart disease coronary artery disease hypertrophic cardiomyopathy (HCM) inherited cardiac conditions long QT syndrome (LQTS) short QT syndrome (SQTS)

Clinical Genetics, Lakeridge Health Oshawa

Services Provided:
Tests et conseils génétiques
Accepts self referral:
Non
Emplacement:
Oshawa
Areas of care:
Génétique oncologique, Génétique générale, Génétique pédiatrique, Génétique prénatale, Génétique pour la reproduction
Mots-clés:

adult genetics cancer cardiogenetics general genetics maternal health neurogenetics pediatric genetics preconception pregnancy prenatal genetics

Clinical Genetics, North York General Hospital

Services Provided:
Tests et conseils génétiques
Accepts self referral:
Non
Emplacement:
North York
Areas of care:
Génétique oncologique, Cardiogénétique, Génétique générale, Neurogénétique, Génétique pédiatrique, Génétique prénatale
Mots-clés:

adult genetics cancer cardiogenetics general genetics maternal health neurogenetics pediatric genetics preconception pregnancy prenatal genetics

Clinical Genetics, Trillium Health Partners

Services Provided:
Tests et conseils génétiques
Accepts self referral:
Non
Emplacement:
Mississauga
Areas of care:
Génétique oncologique, Cardiogénétique, Génétique générale, Neurogénétique, Génétique pédiatrique, Génétique prénatale
Mots-clés:

adult genetics cancer cardiogenetics general genetics maternal health neurogenetics pediatric genetics preconception pregnancy prenatal genetics

Dalglish Family 22q Clinic, Toronto General Hospital

Services Provided:
Soins continus
Accepts self referral:
Non
Emplacement:
Toronto
Areas of care:
Web Site URL:
Mots-clés:

22q 22q11 deletion syndrome 22q11.2 deletion syndrome DiGeorge syndrome 22q11.2DS Velocardiofacial syndrome VCFS 22q11.2DupS 22q11.2 duplication syndrome 22q11 duplication syndrome

Dr. Lysa Boissé Lomax, Hôtel Dieu Hospital

Services Provided:
Soins continus
Accepts self referral:
Non
Emplacement:
Kingston
Areas of care:
Génétique oncologique, Neurogénétique
Mots-clés:

tuberous sclerosis complex (TSC)

Fred A. Litwin Family Centre, University Health Network

Services Provided:
Tests et conseils génétiques, Soins continus
Accepts self referral:
Non
Emplacement:
Toronto
Areas of care:
Cardiogénétique, Génétique générale, Génétique métabolique, Neurogénétique, Génétique oculaire
Mots-clés:

adult genetics aortopathy arrhythmia biochemical genetics cardiogenetics cardiomyopathy channelopathy connective tissue disorders endocrine disorders Fabry disease familial hypercholesterolemia (FH) Gaucher disease general genetics hypertrophic cardiomyopathy (HCM) kidney disorders metabolic genetics neurogenetics ocular genetics phenylketonuria (PKU) retinal disorders genetic syndromes genetic causes of hearing loss skeletal system syndromes urogenital syndromes mitochondrial disorders psychiatric genetics multiple congenital anomalies

Heart Lung and Vascular Program, St. Michael's Hospital

Services Provided:
Soins continus
Accepts self referral:
Non
Emplacement:
Toronto
Areas of care:
Cardiogénétique
Mots-clés:

aortic aneurysm, aortic conditions, aortopathy, arrhythmia, Brugada syndrome, cardiogenetics, cardiomyopathy, cystic fibrosis (CF), catecholaminergic polymorphic ventricular tachycardia (CPVT), dilated cardiomyopathy (DCM), hypertrophic cardiomyopathy (HCM), hereditary hemorrhagic telangiectasia (HHT), Loeys-Dietz syndrome (LDS), long QT syndrome (LQTS), Marfan syndrome, primary ciliary dyskinesia (PCD), sudden cardiac death, vascular dissection, respiratory

Inherited Arrhythmia Clinic, St Michael’s Hospital

Services Provided:
Soins continus
Accepts self referral:
Non
Emplacement:
Toronto
Areas of care:
Cardiogénétique
Mots-clés:

arrhythmia atrial fibrillation Brugada syndrome cardiac disorders cardiogenetics cardiomyopathy catecholaminergic polymorphic ventricular tachycardia (CPVT) coronary artery disease hypertrophic cardiomyopathy (HCM) long QT syndrome (LQTS) short QT Syndrome (SQTS) arrhythmogenic cardiomyopathy (ACM) arrhythmogenic right ventricular cardiomyopathy (ARVC) arrhythmogenic right ventricular dysplasia (ARVD) sudden cardiac arrest sudden cardiac death

Inherited Heart Rhythm Clinic, London Health Sciences Centre

Services Provided:
Soins continus
Accepts self referral:
Non
Emplacement:
London
Areas of care:
Cardiogénétique
Mots-clés:

arrhythmia atrial fibrillation Brugada syndrome cardiac disorders cardiogenetics cardiomyopathy catecholaminergic polymorphic ventricular tachycardia (CPVT) congenital heart disease coronary artery disease hypertrophic cardiomyopathy (HCM) long QT syndrome (LQTS) short QT syndrome (SQTS)

McMaster TSC Clinic

Services Provided:
Soins continus
Accepts self referral:
Non
Emplacement:
Hamilton
Areas of care:
Génétique oncologique, Neurogénétique
Mots-clés:

tuberous sclerosis complex (TSC)

Medical Genetics Program of Southwestern Ontario, Victoria Hospital, London Health Sciences Centre

Services Provided:
Tests et conseils génétiques, Soins continus
Accepts self referral:
Non
Emplacement:
London
Areas of care:
Génétique générale, Génétique métabolique, Neurogénétique, Génétique pédiatrique, Génétique prénatale
Mots-clés:

cancer cardiogenetics general genetics metabolic genetics Newborn Screen Ontario (NSO) prenatal genetics

Metabolics Clinic, CHEO

Services Provided:
Tests et conseils génétiques, Soins continus
Accepts self referral:
Non
Emplacement:
Ottawa
Areas of care:
Génétique métabolique
Mots-clés:

amino acid disorder (ASD) autism spectrum disorder carbohydrate metabolism disorders cardiogenetics connective tissue disorders fatty acid oxidation disorders (FAODs) global developmental delay (GDD) intellectual disability lysosomal storage disorders metabolic genetics mitochondrial disorders neurodevelopmental disorders neurological disorders organic acid disorder peroxisomal disorder seizures

Neuromuscular & Neurometabolic Clinic, Hamilton Health Sciences

Services Provided:
Tests et conseils génétiques
Accepts self referral:
Non
Emplacement:
Hamilton
Areas of care:
Génétique métabolique, Neurogénétique
Mots-clés:

ataxia fatty acid oxidation disorders (FAODs) hereditary spastic paraplegia (HSP) mitochondrial disease muscular dystrophy neurogenetic disorders neurometabolic disorders neuromuscular disorders rhabdomyolysis spinal muscular atrophy (pediatric)

Neuromuscular Clinic, CHEO

Services Provided:
Soins continus
Accepts self referral:
Non
Emplacement:
Ottawa
Areas of care:
Neurogénétique
Mots-clés:

Becker muscular dystrophy Bethlem myopathy Charcot-Marie-Tooth disease congenital myopathy Duchenne muscular dystrophy Emery-Dreifuss muscular dystrophy facioscapulohumeral muscular dystrophy muscular dystrophy myotonic dystrophy (DM1 and DM2) myotubular myopathy nemaline myopathy neuromuscular disorders neuropathy spinal muscular atrophy

Northeastern Ontario Medical Genetics Program, Health Sciences North

Services Provided:
Tests et conseils génétiques
Accepts self referral:
Non
Emplacement:
North Bay Sault Ste. Marie Sudbury Timmins
Areas of care:
Génétique oncologique, Cardiogénétique, Génétique générale, Neurogénétique, Génétique oculaire, Génétique pédiatrique, Génétique prénatale
Mots-clés:

adult genetics cancer cardiogenetics general genetics neurogenetics ocular genetics pediatric genetics prenatal genetics adult genetics cancer cardiogenetics general genetics neurogenetics ocular genetics pediatric genetics prenatal genetics Sault Ste. Marie North Bay Timmins Northern Ontario Genetics Northeastern Ontario genetics

SickKids Clinical and Metabolic Genetics Clinic, Hospital for Sick Children

Services Provided:
Tests et conseils génétiques
Accepts self referral:
Non
Emplacement:
Toronto
Areas of care:
Génétique oncologique, Cardiogénétique, Génétique générale, Génétique métabolique, Neurogénétique, Génétique pédiatrique
Mots-clés:

amino acid disorder autism spectrum disorder connective tissue disorders fatty acid disorder global developmental delay hereditary heart diseases hereditary kidney diseases hereditary metabolic disorders inborn errors of metabolism inherited metabolic diseases inherited metabolic disorders inherited neurological disorders intellectual disability lysosomal storage metabolic disease mitochondria disorders neurodevelopmental disorders neurological dysfunction peroxisomal disorder organic acid disorder seizures sugar disorders

Zane Cohen Centre for Digestive Diseases, Mount Sinai Hospital

Services Provided:
Tests et conseils génétiques
Accepts self referral:
Oui
Emplacement:
Toronto
Areas of care:
Génétique oncologique
Mots-clés:

constitutional mismatch repair deficiency (CMMRD) colorectal cancer endometrial cancer familial adenomatous polyposis (FAP) gastric cancer gastrointestinal cancer hereditary diffuse gastric cancer syndrome (HDGC) hereditary hemorrhagic telangiectasia (HHT) hereditary nonpolyposis colorectal cancer (HNPCC) juvenile polyposis (JP) Lynch syndrome (LS) MUTYH (or MYH)-associated polyposis (MAP) pancreatic cancer Peutz-Jeghers syndrome (PJS) serrated polyposis syndrome (SPS)

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Dernière Mise à Jour: 09 mars 2026