For your dog breed
Optimal Selection™ Canine test includes:
- Over 200 disorders
- Over 40 traits tests
- A genetic diversity score
- A printable report
You can find the most relevant tests included for your breed below:
Airedale Terrier |
Hemophilia B (Discovered in the Airedale Terrier), Factor VII Deficiency, Protein Losing Nephropathy, Lung Developmental Disease (Discovered in the Airedale Terrier) |
Alaskan Husky |
Alaskan Husky Encephalopathy, Degenerative Myelopathy |
Alaskan Klee Kai |
Factor VII Deficiency |
Alaskan Malamute |
Cone Degeneration (Discovered in the Alaskan Malamute), Early-Onset Progressive Polyneuropathy (Discovered in the Alaskan Malamute), Primary Ciliary Dyskinesia (Discovered in the Alaskan Malamute) |
Alpine Dachsbracke |
Neuronal Ceroid Lipofuscinosis 8 (Discovered in the Alpine Dachsbracke) |
American Eskimo Dog |
Degenerative Myelopathy, Progressive Rod Cone Degeneration (prcd-PRA) |
American Hairless Rat Terrier |
Primary Lens Luxation, Progressive Rod Cone Degeneration (prcd-PRA) |
American Staffordshire Terrier |
Hyperuricosuria, Cone-Rod Dystrophy 1, Canine Multifocal Retinopathy 1, Cone-Rod Dystrophy 2, Osteochondromatosis (Discovered in the American Staffordshire Terrier) |
Australian Cattle Dog |
Myotonia Congenita, MDR1 Medication Sensitivity, Cystinuria Type II-A, Primary Lens Luxation, Neuronal Ceroid Lipofuscinosis 12 (Discovered in the Australian Cattle Dog), Progressive Rod Cone Degeneration (prcd-PRA) |
Australian Shepherd |
MDR1 Medication Sensitivity, Hyperuricosuria, Cone Degeneration (Discovered in the Alaskan Malamute), Neuronal Ceroid Lipofuscinosis 8 (Discovered in the Australian Shepherd), Degenerative Myelopathy, Canine Multifocal Retinopathy 1, Progressive Rod Cone Degeneration (prcd-PRA), Collie Eye Anomaly (CEA) |
Australian Stumpy Tail Cattle Dog |
Myotonia Congenita, Cystinuria Type II-A, Progressive Rod Cone Degeneration (prcd-PRA) |
Barbet |
Progressive Rod Cone Degeneration (prcd-PRA) |
Basenji |
Fanconi Syndrome, Progressive Retinal Atrophy (Discovered in the Basenji), Pyruvate Kinase Deficiency (Discovered in the Basenji) |
Basset Fauve de Bretagne |
Primary Open Angle Glaucoma (Discovered in Basset Fauve de Bretagne) |
Basset Griffon Vendeen (Petit) |
Primary Open Angle Glaucoma (Discovered in Petit Basset Griffon Vendeen) |
Basset Hound |
X-Linked Severe Combined Immunodeficiency (Discovered in the Basset Hound) |
Beagle |
Pyruvate Kinase Deficiency (Discovered in the Beagle), Osteogenesis Imperfecta (Discovered in the Beagle), Neonatal Cerebellar Cortical Degeneration, Intestinal Cobalamin Malabsorption (Discovered in the Beagle), Musladin-Lueke Syndrome, Hypocatalasia, Factor VII Deficiency |
Bearded Collie |
Collie Eye Anomaly (CEA) |
Belgian Malinois |
Spongy Degeneration with Cerebellar Ataxia (Discovered in Belgian Malinois - SDCA1), Spongy Degeneration with Cerebellar Ataxia (Discovered in Belgian Malinois - SDCA2) |
Belgian Sheepdog |
Spongy Degeneration with Cerebellar Ataxia (Discovered in Belgian Malinois - SDCA1) |
Bernese Mountain Dog |
Degenerative Myelopathy, von Willebrand's Disease, type 1 |
Biewer Terrier |
Progressive Rod Cone Degeneration (prcd-PRA) |
Black Russian Terrier |
Hyperuricosuria, Juvenile Laryngeal Paralysis and Polyneuropathy, Progressive Rod Cone Degeneration (prcd-PRA) |
Bloodhound |
Degenerative Myelopathy |
Boerboel |
Hyperuricosuria, Canine Multifocal Retinopathy 1 |
Bolognese |
Progressive Rod Cone Degeneration (prcd-PRA) |
Border Collie |
MDR1 Medication Sensitivity, Intestinal Cobalamin Malabsorption (Discovered in the Border Collie), Sensory Neuropathy, Dental Hypomineralization, Trapped Neutrophil Syndrome, Goniodysgenesis and Glaucoma (Discovered in the Border Collie), Collie Eye Anomaly (CEA), Early Adult Onset Deafness For Border Collies only (Linkage test) |
Border Terrier |
Shaking Puppy Syndrome (Discovered in the Border Terrier) |
Borzoi |
Degenerative Myelopathy |
Bouvier Des Flanders |
Exercise-Induced Collapse |
Boxer |
Hemophilia A (Discovered in the Boxer), Degenerative Myelopathy |
Boykin Spaniel |
Exercise-Induced Collapse, Collie Eye Anomaly (CEA) |
Briard |
Congenital Stationary Night Blindness (CSNB) |
Brittany |
Complement 3 Deficiency |
Bull Terrier (Miniature) |
Polycystic Kidney Disease, Primary Lens Luxation, Lethal Acrodermatitis (Discovered in the Bull Terrier) |
Bull Terrier (Standard) |
Polycystic Kidney Disease, Primary Lens Luxation, Lethal Acrodermatitis (Discovered in the Bull Terrier) |
Bulldog (American) |
Ichthyosis (Discovered in the American Bulldog), Hyperuricosuria, Nemaline Myopathy, Canine Multifocal Retinopathy 1 |
Bulldog (Standard) |
Hyperuricosuria, Canine Multifocal Retinopathy 1 |
Bullmastiff |
Dominant Progressive Retinal Atrophy, Canine Multifocal Retinopathy 1 |
Cairn Terrier |
Macrothrombocytopenia, Pyruvate Kinase Deficiency (Discovered in the West Highland White Terrier), Craniomandibular Osteopathy, Globoid Cell Leukodystrophy (Discovered in Terriers) |
Cane Corso |
Canine Multifocal Retinopathy 1 |
Cardigan Welsh Corgi |
X-Linked Severe Combined Immunodeficiency (Discovered in the Cardigan Welsh Corgi), Degenerative Myelopathy, Rod-Cone Dysplasia 3 |
Cavalier King Charles Spaniel |
Muscular Dystrophy (Discovered in the Cavalier King Charles Spaniel), Xanthinuria (Discovered in the Cavalier King Charles Spaniel), Degenerative Myelopathy, Episodic falling syndrome (EFS) |
Central Asian Ovcharka |
Dystrophic Epidermolysis Bullosa (Discovered in the Central Asian Ovcharka) |
Chesapeake Bay Retriever |
Degenerative Myelopathy, Exercise-Induced Collapse, Progressive Rod Cone Degeneration (prcd-PRA) |
Chihuahua |
Neuronal Ceroid Lipofuscinosis 7, Progressive Rod Cone Degeneration (prcd-PRA) |
Chinese Crested |
Neuronal Ceroid Lipofuscinosis 7, Primary Lens Luxation, Progressive Rod Cone Degeneration (prcd-PRA) |
Chinese Foo Dog |
Primary Lens Luxation |
Chinese Shar-Pei |
Primary Open Angle Glaucoma and Lens Luxation (Discovered in Chinese Shar-Pei) |
Chinook |
MDR1 Medication Sensitivity, Chondrodysplasia |
Chow Chow |
Hereditary Elliptocytosis |
Clumber Spaniel |
Pyruvate Dehydrogenase Phosphatase 1 Deficiency, Exercise-Induced Collapse |
Cocker Spaniel |
Phosphofructokinase Deficiency, Exercise-Induced Collapse, Progressive Rod Cone Degeneration (prcd-PRA) |
Collie |
MDR1 Medication Sensitivity, Degenerative Myelopathy, Collie Eye Anomaly (CEA) |
Continental Toy Spaniel |
Progressive Retinal Atrophy (Discovered in the Papillon and Phalène), von Willebrand's Disease, type 1 |
Coton de Tulear |
Bandera's Neonatal Ataxia, von Willebrand's Disease, type 1, Canine Multifocal Retinopathy 2, Progressive Rod Cone Degeneration (prcd-PRA) |
Curly Coated Retriever |
Glycogen Storage Disease Type IIIa, (GSD IIIa), Exercise-Induced Collapse |
Dachshund (Longhaired) |
Neuronal Ceroid Lipofuscinosis 1, Osteogenesis Imperfecta (Discovered in the Dachshund), Narcolepsy (Discovered in the Dachshund), Mucopolysaccharidosis Type IIIA (Discovered in the Dachshund) |
Dachshund (Miniature Longhaired) |
Neuronal Ceroid Lipofuscinosis 1, Osteogenesis Imperfecta (Discovered in the Dachshund), Narcolepsy (Discovered in the Dachshund), Mucopolysaccharidosis Type IIIA (Discovered in the Dachshund) |
Dachshund (Miniature Shorthaired) |
Neuronal Ceroid Lipofuscinosis 1, Osteogenesis Imperfecta (Discovered in the Dachshund), Narcolepsy (Discovered in the Dachshund), Mucopolysaccharidosis Type IIIA (Discovered in the Dachshund) |
Dachshund (Miniature Wirehaired) |
Neuronal Ceroid Lipofuscinosis 1, Osteogenesis Imperfecta (Discovered in the Dachshund), Cone-Rod Dystrophy, Narcolepsy (Discovered in the Dachshund), Mucopolysaccharidosis Type IIIA (Discovered in the Dachshund) |
Dachshund (Shorthaired) |
Neuronal Ceroid Lipofuscinosis 1, Osteogenesis Imperfecta (Discovered in the Dachshund), Narcolepsy (Discovered in the Dachshund), Mucopolysaccharidosis Type IIIA (Discovered in the Dachshund) |
Dachshund (Wirehaired) |
Neuronal Ceroid Lipofuscinosis 1, Osteogenesis Imperfecta (Discovered in the Dachshund), Cone-Rod Dystrophy, Narcolepsy (Discovered in the Dachshund), Mucopolysaccharidosis Type IIIA (Discovered in the Dachshund) |
Dalmatian |
Acute Respiratory Distress Syndrome, Hyperuricosuria |
Danish Swedish Farmdog |
MDR1 Medication Sensitivity, Primary Lens Luxation |
Dobermann Pinscher |
von Willebrand's Disease, type 1, Deafness and Vestibular Dysfunction (Discovered in Doberman Pinscher) |
Dogue de Bordeaux |
Focal Non-Epidermolytic Palmoplantar Keratoderma, Canine Multifocal Retinopathy 1 |
Drentse Patrijshond |
von Willebrand's Disease, type 1 |
Dutch Shepherd Dog |
Spongy Degeneration with Cerebellar Ataxia (Discovered in Belgian Malinois - SDCA2) |
English Cocker Spaniel |
Phosphofructokinase Deficiency, Xanthinuria (Discovered in the Cavalier King Charles Spaniel), Acral Mutilation Syndrome, Exercise-Induced Collapse, Progressive Rod Cone Degeneration (prcd-PRA) |
English Setter |
Neuronal Ceroid Lipofuscinosis 8 (Discovered in the English Setter) |
English Shepherd |
MDR1 Medication Sensitivity, Progressive Rod Cone Degeneration (prcd-PRA), Collie Eye Anomaly (CEA) |
English Springer Spaniel |
Phosphofructokinase Deficiency, Degenerative Myelopathy, QT Syndrome, Acral Mutilation Syndrome, X-Linked Tremors |
English Toy Spaniel |
Muscular Dystrophy (Discovered in the Cavalier King Charles Spaniel) |
Entlebucher Mountain Dog |
Progressive Rod Cone Degeneration (prcd-PRA) |
Eurasier |
Cerebellar Hypoplasia |
Field Spaniel |
Progressive Rod Cone Degeneration (prcd-PRA) |
Finnish Hound |
Factor VII Deficiency, Progressive Early-Onset Cerebellar Ataxia |
Finnish Lapphund |
Canine Multifocal Retinopathy 3, Progressive Rod Cone Degeneration (prcd-PRA) |
Flat Coated Retriever |
POMC |
Fox Terrier (Smooth) |
Spinocerebellar Ataxia with Myokymia and/or Seizures |
Fox Terrier (Toy) |
Spinocerebellar Ataxia with Myokymia and/or Seizures, Congenital Hypothyroidism (Discovered in the Toy Fox and Rat Terrier), Primary Lens Luxation |
Fox Terrier (Wire) |
Van den Ende-Gupta Syndrome, Degenerative Myelopathy, Primary Lens Luxation |
French Bulldog |
Canine Multifocal Retinopathy 1 |
French Spaniel |
Acral Mutilation Syndrome |
Frisian Water Dog |
Severe Combined Immunodeficiency (Discovered in Frisian Water Dogs) |
German Hunting Terrier |
Primary Lens Luxation |
German Pinscher |
von Willebrand's Disease, type 1 |
German Shepherd Dog |
MDR1 Medication Sensitivity, Hyperuricosuria, Mucopolysaccharidosis Type VII (Discovered in the German Shepherd Dog), Hemophilia A (Discovered in the German Shepherd Dog - Variant 2), Cone Degeneration (Discovered in the German Shepherd Dog), Degenerative Myelopathy, Hemophilia A (Discovered in the German Shepherd Dog - Variant 1), X-Linked Ectodermal Dysplasia, Renal Cystadenocarcinoma and Nodular Dermatofibrosis, Canine Scott Syndrome, Canine Leukocyte Adhesion Deficiency (CLAD), type III |
German Shorthaired Pointer |
Cone Degeneration (Discovered in the German Shorthaired Pointer), von Willebrand's Disease, type 2, Neuronal Ceroid Lipofuscinosis 8 (Discovered in the Australian Shepherd), Acral Mutilation Syndrome |
German Spitz |
Hyperuricosuria |
German Wirehaired Pointer |
von Willebrand's Disease, type 2, Exercise-Induced Collapse |
Golden Retriever |
Muscular Dystrophy (Discovered in the Golden Retriever), Dystrophic Epidermolysis Bullosa (Discovered in the Golden Retriever), Degenerative Myelopathy, Sensory Ataxic Neuropathy, Progressive Retinal Atrophy (Discovered in the Golden Retriever - GR-PRA1 variant), Congenital Myasthenic Syndrome (Discovered in the Golden Retriever), Progressive Rod Cone Degeneration (prcd-PRA) |
Gordon Setter |
Cerebellar Ataxia |
Great Dane |
Centronuclear Myopathy (Discovered in the Great Dane), Ichthyosis (Discovered in the Great Dane) |
Great Pyrenees |
Glanzmann Thrombasthenia Type I (Discovered in Great Pyrenees), Canine Multifocal Retinopathy 1 |
Greater Swiss Mountain Dog |
P2RY12-associated Bleeding Disorder |
Greyhound |
Early-Onset Progressive Polyneuropathy (Discovered in the Greyhound), Hereditary Nasal Parakeratosis (Discovered in the Greyhound) |
Havanese |
Hemophilia A (Discovered in the Havanese) |
Hokkaido Inu |
Collie Eye Anomaly (CEA) |
Irish Red and White Setter |
Rod-Cone Dysplasia 1, von Willebrand's Disease, type 1 |
Irish Setter |
Rod-Cone Dysplasia 1, Globoid Cell Leukodystrophy (Discovered in the Irish Setter) |
Irish Terrier |
Hereditary Footpad Hyperkeratosis |
Irish Wolfhound |
Hyperekplexia or Startle Disease |
Italian Greyhound |
Amelogenesis Imperfecta, Progressive Retinal Atrophy 1 (Discovered in the Italian Greyhound) |
Japanese Chin |
GM2 Gangliosidosis (Discovered in the Japanese Chin), Progressive Rod Cone Degeneration (prcd-PRA) |
Japanese Shiba Inu |
GM1 Gangliosidosis (Discovered in the Shiba) |
Karelian Bear Dog |
Chondrodysplasia, Hypophosphatasia, Progressive Rod Cone Degeneration (prcd-PRA) |
Kerry Blue Terrier |
Degenerative Myelopathy, Factor XI Deficiency, von Willebrand's Disease, type 1 |
Komondor |
Intestinal Cobalamin Malabsorption (Discovered in the Komondor) |
Kooikerhondje |
von Willebrand's Disease, type 3 (Discovered in the Kooiker Hound) |
Kromfohrlander |
Hyperuricosuria, von Willebrand's Disease, type 1, Hereditary Footpad Hyperkeratosis |
Kuvasz |
Progressive Rod Cone Degeneration (prcd-PRA) |
Labrador Retriever |
Hyperuricosuria, Congenital Myasthenic Syndrome (Discovered in the Labrador Retriever), Alexander Disease, Skeletal Dysplasia 2, Narcolepsy (Discovered in the Labrador Retriever), Hereditary Elliptocytosis, Centronuclear Myopathy (Discovered in the Labrador Retriever), X-Linked Myotubular Myopathy, Exercise-Induced Collapse, Myotonia Congenita (Discovered in the Labrador Retriever), Stargardt Disease (Discovered in the Labrador Retriever), Progressive Rod Cone Degeneration (prcd-PRA), POMC, HNPK |
Lagotto Romagnolo |
Lagotto Storage Disease, Hyperuricosuria, Benign Familial Juvenile Epilepsy, Progressive Rod Cone Degeneration (prcd-PRA) |
Lakeland Terrier |
Primary Lens Luxation |
Lancashire Heeler |
Primary Lens Luxation, Progressive Rod Cone Degeneration (prcd-PRA), Collie Eye Anomaly (CEA) |
Landseer |
Cystinuria Type I-A, Muscular Dystrophy (Discovered in the Landseer) |
Lapponian Herder |
Canine Multifocal Retinopathy 3, Progressive Rod Cone Degeneration (prcd-PRA) |
Lhasa Apso |
Hemophilia B (Discovered in the Lhasa Apso), Progressive Retinal Atrophy (Discovered in the Lhasa Apso) |
Lucas Terrier |
Primary Lens Luxation |
Maltese |
Glycogen Storage Disease Type Ia |
Manchester Terrier |
von Willebrand's Disease, type 1 |
Manchester Terrier (Toy) |
Xanthinuria (Discovered in the Toy Manchester Terrier), von Willebrand's Disease, type 1, Progressive Rod Cone Degeneration (prcd-PRA) |
Markiesje |
Progressive Rod Cone Degeneration (prcd-PRA) |
Mastiff |
Dominant Progressive Retinal Atrophy, Canine Multifocal Retinopathy 1 |
McNab |
MDR1 Medication Sensitivity |
Mi-ki |
Progressive Rod Cone Degeneration (prcd-PRA) |
Miniature American Shepherd |
MDR1 Medication Sensitivity, Hyperuricosuria, Cone Degeneration (Discovered in the Alaskan Malamute), Canine Multifocal Retinopathy 1, Progressive Rod Cone Degeneration (prcd-PRA), Collie Eye Anomaly (CEA) |
Munsterlander (Large) |
Hyperuricosuria |
New Zealand Huntaway |
Mucopolysaccharidosis Type IIIA (Discovered in the New Zealand Huntaway) |
Newfoundland |
Cystinuria Type I-A |
Nordic Spitz |
Progressive Early-Onset Cerebellar Ataxia, Progressive Rod Cone Degeneration (prcd-PRA) |
Norfolk Terrier |
Epidermolytic Hyperkeratosis, Macrothrombocytopenia, Muscular Dystrophy (Discovered in the Norfolk Terrier) |
Norwegian Buhund |
Hereditary Ataxia (Discovered in the Norwegian Buhund) |
Norwegian Elkhound |
Chondrodysplasia, Early Retinal Degeneration (Discovered in the Norwegian Elkhound), Progressive Rod Cone Degeneration (prcd-PRA) |
Norwich Terrier |
Primary Lens Luxation, Cystic Renal Dysplasia and Hepatic Fibrosis |
Nova Scotia Duck Tolling Retriever |
Cleft Lip & Palate with Syndactyly, Cleft Palate, Progressive Rod Cone Degeneration (prcd-PRA), Collie Eye Anomaly (CEA) |
Old Danish Pointer |
Congenital Myasthenic Syndrome (Discovered in the Old Danish Pointer) |
Old English Sheepdog |
Cerebellar Ataxia, MDR1 Medication Sensitivity, Hemophilia A (Discovered in Old English Sheepdog), Exercise-Induced Collapse, Primary Ciliary Dyskinesia |
Papillon |
Progressive Retinal Atrophy (Discovered in the Papillon and Phalène), von Willebrand's Disease, type 1, Neuroaxonal Dystrophy (Discovered in the Papillon) |
Parson Russell Terrier |
Spinocerebellar Ataxia with Myokymia and/or Seizures, Hyperuricosuria, Spinocerebellar Ataxia (Late-Onset Ataxia), Severe Combined Immunodeficiency, Primary Lens Luxation, Enamel Hypoplasia (Discovered in the Parson Russell Terrier), Juvenile Encephalopathy (Discovered in the Parson Russell Terrier) |
Patterdale Terrier |
Primary Lens Luxation |
Pembroke Welsh Corgi |
Degenerative Myelopathy, Rod-Cone Dysplasia 3, von Willebrand's Disease, type 1, Exercise-Induced Collapse |
Plott |
Progressive Rod Cone Degeneration (prcd-PRA) |
Pointer |
Acral Mutilation Syndrome |
Pomeranian |
Hyperuricosuria, Hereditary Vitamin D-Resistant Rickets Type II, Progressive Rod Cone Degeneration (prcd-PRA) |
Poodle (Medium) |
Osteochondrodysplasia, von Willebrand's Disease, type 1, Progressive Rod Cone Degeneration (prcd-PRA) |
Poodle (Miniature) |
Osteochondrodysplasia, von Willebrand's Disease, type 1, Progressive Rod Cone Degeneration (prcd-PRA) |
Poodle (Standard) |
Neonatal Encephalopathy with Seizures, Degenerative Myelopathy, von Willebrand's Disease, type 1, Progressive Rod Cone Degeneration (prcd-PRA) |
Poodle (Toy) |
Osteochondrodysplasia, von Willebrand's Disease, type 1, GM2 Gangliosidosis (Discovered in the Toy Poodle), Progressive Rod Cone Degeneration (prcd-PRA) |
Portuguese Podengo Medio |
Progressive Rod Cone Degeneration (prcd-PRA) |
Portuguese Podengo Pequenos |
Progressive Rod Cone Degeneration (prcd-PRA) |
Portuguese Water Dog |
Early-onset PRA (Discovered in the Portuguese Water Dog), GM1 Gangliosidosis (Discovered in the Portuguese Water Dog), Progressive Rod Cone Degeneration (prcd-PRA) |
Presa Canario |
Canine Multifocal Retinopathy 1 |
Pug |
Degenerative Myelopathy, May-Hegglin Anomaly, Pyruvate Kinase Deficiency (Discovered in the Pug) |
Puli |
Progressive Rod Cone Degeneration (prcd-PRA) |
Pumi |
Primary Lens Luxation |
Rat Terrier |
Congenital Hypothyroidism (Discovered in the Toy Fox and Rat Terrier), Primary Lens Luxation, Progressive Rod Cone Degeneration (prcd-PRA) |
Rhodesian Ridgeback |
Juvenile Myoclonic Epilepsy, Degenerative Myelopathy |
Rottweiler |
Juvenile Laryngeal Paralysis and Polyneuropathy, Myotubular Myopathy, Neuroaxonal Dystrophy (Discovered in the Rottweiler) |
Russell Terrier |
Lamellar Ichthyosis, Spinocerebellar Ataxia with Myokymia and/or Seizures, Hyperuricosuria, Spinocerebellar Ataxia (Late-Onset Ataxia), Congenital Myasthenic Syndrome (Discovered in the Jack Russell Terrier), Severe Combined Immunodeficiency, Primary Lens Luxation, Progressive Rod Cone Degeneration (prcd-PRA) |
Russian Tsvetnaya Bolonka |
Progressive Rod Cone Degeneration (prcd-PRA) |
Saluki |
Neuronal Ceroid Lipofuscinosis 8 (Discovered in the Saluki) |
Samoyed |
X-Linked Progressive Retinal Atrophy 1, X-Linked Hereditary Nephropathy (Discovered in the Samoyed) |
Schapendoes |
Hyperuricosuria, Generalized Progressive Retinal Atrophy (Discovered in the Schapendoes) |
Schipperke |
Progressive Rod Cone Degeneration (prcd-PRA) |
Schnauzer (Giant) |
Hyperuricosuria, Dilated Cardiomyopathy (Discovered in the Schnauzer), Fetal Onset Neuroaxonal Dystrophy, Factor VII Deficiency, Progressive Rod Cone Degeneration (prcd-PRA) |
Schnauzer (Miniature) |
Persistent Müllerian Duct Syndrome, X-Linked Progressive Retinal Atrophy 2, Spondylocostal Dysostosis, Myotonia Congenita (Discovered in the Miniature Schnauzer), Demyelinating Neuropathy |
Schnauzer (Standard) |
Dilated Cardiomyopathy (Discovered in the Schnauzer) |
Scottish Deerhound |
Factor VII Deficiency |
Scottish Terrier |
Craniomandibular Osteopathy, von Willebrand's Disease, type 3 (Discovered in the Scottish Terrier), Ligneous Membranitis |
Sealyham Terrier |
Primary Lens Luxation |
Serbian Hound |
Progressive Rod Cone Degeneration (prcd-PRA) |
Shetland Sheepdog |
MDR1 Medication Sensitivity, Progressive Retinal Atrophy (Discovered in the Shetland Sheepdog - CNGA1 variant), von Willebrand's Disease, type 3 (Discovered in the Shetland Sheepdog), Progressive Retinal Atrophy (Discovered in the Shetland Sheepdog - BBS2 variant), Collie Eye Anomaly (CEA) |
Shih Tzu |
Prekallikrein Deficiency, Congenital Dyshormonogenic Hypothyroidism with Goiter (Discovered in the Shih Tzu) |
Siberian Husky |
X-Linked Progressive Retinal Atrophy 1 |
Silken Windhound |
MDR1 Medication Sensitivity, Collie Eye Anomaly (CEA) |
Silky Terrier |
Progressive Rod Cone Degeneration (prcd-PRA) |
Sloughi |
Rod-Cone Dysplasia 1a |
Soft Coated Wheaten Terrier |
Degenerative Myelopathy, Paroxysmal Dyskinesia, Protein Losing Nephropathy, Microphthalmia (Discovered in the Soft-Coated Wheaten Terrier) |
Spanish Water Dog |
Hyperuricosuria, Neuroaxonal Dystrophy, Progressive Rod Cone Degeneration (prcd-PRA) |
Stabyhoun |
Cerebral Dysfunction, von Willebrand's Disease, type 1 |
Staffordshire Bull Terrier |
L-2-Hydroxyglutaric Aciduria |
Sussex Spaniel |
Pyruvate Dehydrogenase Phosphatase 1 Deficiency |
Swedish Elkhound |
Progressive Rod Cone Degeneration (prcd-PRA) |
Swedish Lapphund |
Progressive Rod Cone Degeneration (prcd-PRA) |
Swedish Vallhund |
Progressive Retinal Atrophy (Discovered in the Swedish Vallhund) |
Teddy Roosevelt Terrier |
Primary Lens Luxation |
Tenterfield Terrier |
Spinocerebellar Ataxia with Myokymia and/or Seizures, Congenital Hypothyroidism (Discovered in the Tenterfield Terrier), Primary Lens Luxation |
Terrier Brazileiro |
Mucopolysaccharidosis Type VII (Discovered in the Brazilian Terrier) |
Tibetan Spaniel |
Progressive Retinal Atrophy Type III |
Tibetan Terrier |
Progressive Retinal Atrophy Type III, Primary Lens Luxation, Progressive Rod Cone Degeneration (prcd-PRA) |
Vizsla |
Cerebellar Cortical Degeneration, Exercise-Induced Collapse |
Volpino Italiano |
Primary Lens Luxation |
Weimaraner |
Hypomyelination, Hyperuricosuria |
Welsh Springer Spaniel |
Factor VII Deficiency |
Welsh Terrier |
Primary Lens Luxation |
West Highland White Terrier |
Pyruvate Kinase Deficiency (Discovered in the West Highland White Terrier), Craniomandibular Osteopathy, Globoid Cell Leukodystrophy (Discovered in Terriers), L-2-Hydroxyglutaric Aciduria (Discovered in the Westie) |
Whippet |
Phosphofructokinase Deficiency, Muscular Hypertrophy (Double Muscling), Collie Eye Anomaly (CEA) |
White Swiss Shepherd |
MDR1 Medication Sensitivity |
Wirehaired Vizsla |
Hyperuricosuria, Cerebellar Cortical Degeneration, Exercise-Induced Collapse |
Xoloitzcuintli |
Progressive Rod Cone Degeneration (prcd-PRA) |
Yorkshire Terrier |
Primary Lens Luxation, Progressive Rod Cone Degeneration (prcd-PRA) |