Breed |
Available Tests |
Airedale Terrier
|
-
Coagulation Factor VII Deficiency
-
Degenerative Myelopathy (Common Variant)
-
Hyperuricosuria
-
Protein Losing Nephropathy
|
Alaskan Husky
|
-
Alaskan Husky Encephalopathy
-
Cone Degeneration
-
Cone Degeneration (German Shorthaired Pointer Type)
-
GM1 Gangliosidosis (Alaskan Husky Type)
-
Polyneuropathy with Ocular Abnormalities and Neuronal Vacuolation
|
Alaskan Malamute
|
-
Alaskan Malamute Polyneuropathy
-
Cone Degeneration
-
Degenerative Myelopathy (Common Variant)
-
Primary Ciliary Dyskinesia (Alaskan Malamute Type)
|
Alaskan Sled Dog
|
-
Cone Degeneration
-
Cone Degeneration (German Shorthaired Pointer Type)
|
American Bulldog
|
-
Degenerative Myelopathy (Common Variant)
-
Hyperuricosuria
-
Ichthyosis (American Bulldog Type)
-
Multifocal Retinopathy 1
-
Neuronal Ceroid Lipofuscinosis 10
|
American Eskimo Dog
|
-
Degenerative Myelopathy (Common Variant)
-
Primary Lens Luxation
-
Progressive Retinal Atrophy, Progressive Rod-Cone Degeneration
-
Thrombopathia (American Eskimo Dog Type)
|
American Foxhound
|
-
Catalase Deficiency
-
Coagulation Factor VII Deficiency
-
Degenerative Myelopathy (Common Variant)
|
American Hairless Terrier
|
-
Congenital Hypothyroidism with Goiter (Terrier Type)
-
Degenerative Myelopathy (Common Variant)
-
Primary Lens Luxation
-
Progressive Retinal Atrophy, Progressive Rod-Cone Degeneration
|
Australian Kelpie
|
-
Collie Eye Anomaly
-
Degenerative Myelopathy (Common Variant)
-
Intestinal Lipid Malabsorption
|
Barbet
|
-
Progressive Retinal Atrophy, Progressive Rod-Cone Degeneration
-
Von Willebrand Disease I
|
Basenji
|
-
Fanconi Syndrome
-
Progressive Retinal Atrophy (Basenji Type)
-
Pyruvate Kinase Deficiency (Basenji Type)
-
Spinocerebellar Ataxia (Terrier Type)
|
Bernese Mountain Dog
|
-
Degenerative Myelopathy (Bernese Mountain Dog Variant)
-
Degenerative Myelopathy (Common Variant)
-
Von Willebrand Disease I
|
Bichon Frise
|
-
Chondrodystrophy (CDDY and IVDD Risk) with or without Chondrodysplasia (CDPA)
-
Degenerative Myelopathy (Common Variant)
|
Black Russian Terrier
|
-
Hyperuricosuria
-
Juvenile Laryngeal Paralysis and Polyneuropathy (Black Russian Terrier Type)
|
Boston Terrier
|
-
Degenerative Myelopathy (Common Variant)
-
Hereditary Cataracts
-
Mucopolysaccharidosis I (Boston Terrier Type)
|
Boxer
|
-
Degenerative Myelopathy (Common Variant)
-
Hemophilia A (Boxer Type)
|
Brazilian Terrier
|
-
Mucopolysaccharidosis VII (Brazilian Terrier Type)
-
Multifocal Retinopathy 1
-
Von Willebrand Disease I
|
Brittany
|
-
Chondrodystrophy (CDDY and IVDD Risk) with or without Chondrodysplasia (CDPA)
-
Complement 3 Deficiency
|
Bull Terrier
|
-
Lethal Acrodermatitis
-
Neuronal Ceroid Lipofuscinosis 4A
-
Primary Lens Luxation
|
Bulldog
|
-
Cystinuria Type 3 (Bulldog Type Risk Factor, Variants 2 and 3)
-
Degenerative Myelopathy (Common Variant)
-
Hyperuricosuria
-
Multifocal Retinopathy 1
|
Bullmastiff
|
-
Degenerative Myelopathy (Common Variant)
-
Multifocal Retinopathy 1
-
Progressive Retinal Atrophy (Bullmastiff/Mastiff Type)
|
Cane Corso
|
-
Multifocal Retinopathy 1
-
Neuronal Ceroid Lipofuscinosis 1 (Cane Corso Type)
|
Catahoula Leopard Dog
|
-
Chondrodystrophy (CDDY and IVDD Risk) with or without Chondrodysplasia (CDPA)
-
Degenerative Myelopathy (Common Variant)
|
Chesapeake Bay Retriever
|
-
Chondrodystrophy (CDDY and IVDD Risk) with or without Chondrodysplasia (CDPA)
-
Degenerative Myelopathy (Common Variant)
-
Ectodermal Dysplasia (Chesapeake Bay Retriever Type)
-
Exercise-Induced Collapse
-
Progressive Retinal Atrophy, Progressive Rod-Cone Degeneration
|
Chinese Shar-Pei
|
-
Primary Open Angle Glaucoma and Primary Lens Luxation (Shar Pei Type)
-
Shar-Pei Autoinflammatory Disease
|
Chinook
|
-
Chondrodysplasia (Karelian Bear Dog and Norwegian Elkhound Type)
-
Multidrug Resistance 1
|
Chow Chow
|
-
Degenerative Myelopathy (Common Variant)
-
Elliptocytosis
|
Clumber Spaniel
|
-
Chondrodystrophy (CDDY and IVDD Risk) with or without Chondrodysplasia (CDPA)
-
Degenerative Myelopathy (Common Variant)
-
Exercise-Induced Collapse
-
Pyruvate Dehydrogenase Deficiency
|
Curly-Coated Retriever
|
-
Exercise-Induced Collapse
-
Glycogen Storage Disease IIIa
-
Progressive Retinal Atrophy, Cone-Rod Dystrophy 4
|
Czechoslovakian Wolfdog
|
-
Degenerative Myelopathy (Common Variant)
-
Pituitary Dwarfism (Shepherd Type)
|
Dalmatian
|
-
Acute Respiratory Distress Syndrome
-
Degenerative Myelopathy (Common Variant)
-
Hyperuricosuria
|
Danish-Swedish Farmdog
|
-
Hyperuricosuria
-
Multidrug Resistance 1
-
Primary Lens Luxation
-
Protein Losing Nephropathy
|
Decker Terrier
|
-
Congenital Hypothyroidism with Goiter (Terrier Type)
-
Degenerative Myelopathy (Common Variant)
|
Deutsch-Drahthaar
|
-
Coagulation Factor VII Deficiency
-
Degenerative Myelopathy (Common Variant)
-
Exercise-Induced Collapse
-
Von Willebrand Disease II
|
Drentsche Patrijshond
|
-
Hyperuricosuria
-
Von Willebrand Disease I
|
Dutch Partridge Dog
|
-
Hyperuricosuria
-
Von Willebrand Disease I
|
Dutch Shepherd
|
-
Degenerative Myelopathy (Common Variant)
-
Inflammatory Myopathy (Shepherd Type)
-
Von Willebrand Disease I
|
English Setter
|
-
Neuronal Ceroid Lipofuscinosis 8 (Setter Type)
-
Progressive Retinal Atrophy, Rod-Cone Dysplasia 4
|
English Shepherd
|
-
Collie Eye Anomaly
-
Degenerative Myelopathy (Common Variant)
-
Hyperuricosuria
-
Multidrug Resistance 1
-
Progressive Retinal Atrophy, Progressive Rod-Cone Degeneration
|
English Toy Spaniel
|
-
Chondrodystrophy (CDDY and IVDD Risk) with or without Chondrodysplasia (CDPA)
-
Degenerative Myelopathy (Common Variant)
|
Finnish Hound
|
-
Cerebellar Ataxia (Finnish Hound Type)
-
Coagulation Factor VII Deficiency
|
Fox Terrier
|
-
Congenital Hypothyroidism with Goiter (Terrier Type)
-
Degenerative Myelopathy (Common Variant)
-
Primary Lens Luxation
-
Spinocerebellar Ataxia (Terrier Type)
|
German Hunting Terrier
|
-
Hyperuricosuria
-
Primary Lens Luxation
|
German Pinscher
|
-
Degenerative Myelopathy (Common Variant)
-
Von Willebrand Disease I
|
German Wirehaired Pointer
|
-
Coagulation Factor VII Deficiency
-
Degenerative Myelopathy (Common Variant)
-
Exercise-Induced Collapse
-
Von Willebrand Disease II
|
Gordon Setter
|
-
Cerebellar Degeneration
-
Degenerative Myelopathy (Common Variant)
-
Neuronal Ceroid Lipofuscinosis 8 (Setter Type)
-
Progressive Retinal Atrophy, Rod-Cone Dysplasia 4
|
Great Dane
|
-
Ichthyosis (Great Dane Type)
-
Inherited Myopathy of Great Danes
-
Leukoencephalomyelopathy
|
Great Pyrenees
|
-
Degenerative Myelopathy (Common Variant)
-
Glanzmann's Thrombasthenia (Great Pyrenees Type)
-
Multifocal Retinopathy 1
|
Greater Swiss Mountain Dog
|
-
Hyperuricosuria
-
P2RY12 Receptor Platelet Disorder
|
Greyhound
|
-
Degenerative Myelopathy (Common Variant)
-
Greyhound Polyneuropathy
-
Hereditary Nasal Parakeratosis (Greyhound Type)
|
Havanese
|
-
Chondrodystrophy (CDDY and IVDD Risk) with or without Chondrodysplasia (CDPA)
-
Multifocal Retinopathy 1
-
Von Willebrand Disease I
|
Irish Terrier
|
-
Darier Disease and Associated Infundibular Cyst Formation
-
Degenerative Myelopathy (Common Variant)
-
Hereditary Footpad Hyperkeratosis (Irish Terrier and Kromfohrländer type)
|
Irish Wolfhound
|
-
Degenerative Myelopathy (Common Variant)
-
Startle Disease
|
Jagdterrier
|
-
Hyperuricosuria
-
Primary Lens Luxation
|
Japanese Spitz
|
-
Coagulation Factor VII Deficiency
-
Progressive Retinal Atrophy, Rod-Cone Dysplasia 4
|
Karelian Bear Dog
|
-
Chondrodysplasia (Karelian Bear Dog and Norwegian Elkhound Type)
-
Progressive Retinal Atrophy, Progressive Rod-Cone Degeneration
|
Keeshond
|
-
Degenerative Myelopathy (Common Variant)
-
Progressive Retinal Atrophy (Giant Schnauzer Type)
|
Kerry Blue Terrier
|
-
Canine Multiple System Degeneration (Kerry Blue Terrier Type)
-
Degenerative Myelopathy (Common Variant)
-
Factor XI Deficiency
-
Von Willebrand Disease I
|
Kromfohrländer
|
-
Hereditary Footpad Hyperkeratosis (Irish Terrier and Kromfohrländer type)
-
Hyperuricosuria
-
Von Willebrand Disease I
|
Kuvasz
|
-
Degenerative Myelopathy (Common Variant)
-
Progressive Retinal Atrophy, Progressive Rod-Cone Degeneration
|
Lagotto Romagnolo
|
-
Benign Familial Juvenile Epilepsy
-
Hyperuricosuria
-
Lagotto Storage Disorder
-
Progressive Retinal Atrophy, Progressive Rod-Cone Degeneration
|
Lancashire Heeler
|
-
Collie Eye Anomaly
-
Craniomandibular Osteopathy
-
Degenerative Myelopathy (Common Variant)
-
Primary Lens Luxation
|
Landseer Newfoundland
|
-
Cystinuria (Newfoundland Type)
-
Degenerative Myelopathy (Common Variant)
-
Thrombopathia (Newfoundland Type)
|
Lapponian Herder
|
-
Degenerative Myelopathy (Common Variant)
-
Multifocal Retinopathy 3
-
Pompe Disease
-
Progressive Retinal Atrophy, Late-Onset (Lapponian Herder Type)
-
Progressive Retinal Atrophy, Progressive Rod-Cone Degeneration
|
Leonberger
|
-
Laryngeal Paralysis and Polyneuropathy (Leonberger Type 3)
-
Polyneuropathy (Leonberger Type 1)
-
Polyneuropathy (Leonberger Type 2)
|
Lhasa Apso
|
-
Hemophilia B (Lhasa Apso Type)
-
Oculocutaneous Albinism (Small Breed Type)
-
Progressive Retinal Atrophy, Golden Retriever 1
-
Progressive Retinal Atrophy, PRA4 (Lhasa Apso Type)
|
Longhaired Whippet
|
-
Collie Eye Anomaly
-
Glycogen Storage Disease VII, PFK Deficiency
-
Multidrug Resistance 1
-
Myostatin Deficiency (Whippet Type)
|
Lucas Terrier
|
-
Congenital Macrothrombocytopenia (Cairn and Norfolk Terrier Type)
-
Degenerative Myelopathy (Common Variant)
-
Epidermolytic Hyperkeratosis
-
Primary Lens Luxation
|
Maltese
|
-
Chondrodystrophy (CDDY and IVDD Risk) with or without Chondrodysplasia (CDPA)
-
Glycogen Storage Disease Ia
|
Mastiff
|
-
Cystinuria Type 3 (Bulldog Type Risk Factor, Variants 2 and 3)
-
Degenerative Myelopathy (Common Variant)
-
Hyperuricosuria
-
Multifocal Retinopathy 1
-
Progressive Retinal Atrophy (Bullmastiff/Mastiff Type)
|
Miniature Bull Terrier
|
-
Lethal Acrodermatitis
-
Primary Lens Luxation
|
Miniature Fox Terrier
|
-
Congenital Hypothyroidism with Goiter (Terrier Type)
-
Degenerative Myelopathy (Common Variant)
-
Primary Lens Luxation
-
Spinocerebellar Ataxia (Terrier Type)
|
Miniature Pinscher
|
-
Chondrodystrophy (CDDY and IVDD Risk) with or without Chondrodysplasia (CDPA)
-
Cystinuria (Miniature Pinscher Type)
|
Newfoundland
|
-
Cystinuria (Newfoundland Type)
-
Degenerative Myelopathy (Common Variant)
-
Lafora Disease
-
Thrombopathia (Newfoundland Type)
|
Norfolk Terrier
|
-
Congenital Macrothrombocytopenia (Cairn and Norfolk Terrier Type)
-
Degenerative Myelopathy (Common Variant)
-
Epidermolytic Hyperkeratosis
-
Primary Lens Luxation
|
Norwegian Elkhound
|
-
Chondrodysplasia (Karelian Bear Dog and Norwegian Elkhound Type)
-
Early Retinal Degeneration
-
Primary Open Angle Glaucoma (Norwegian Elkhound Type)
-
Progressive Retinal Atrophy, Progressive Rod-Cone Degeneration
|
Norwich Terrier
|
-
Degenerative Myelopathy (Common Variant)
-
Diffuse Cystic Renal Dysplasia and Hepatic Fibrosis
-
Primary Lens Luxation
|
Nova Scotia Duck Tolling Retriever
|
-
Chondrodystrophy (CDDY and IVDD Risk) with or without Chondrodysplasia (CDPA)
-
Cleft Palate and Syndactyly (Nova Scotia Duck Tolling Retriever Type)
-
Collie Eye Anomaly
-
Degenerative Myelopathy (Common Variant)
-
Progressive Retinal Atrophy, Progressive Rod-Cone Degeneration
|
Old Danish Pointer
|
-
Congenital Myasthenic Syndrome (Old Danish Pointer Type)
-
Progressive Retinal Atrophy, Rod-Cone Dysplasia 4
|
Patterdale Terrier
|
-
Degenerative Myelopathy (Common Variant)
-
Primary Lens Luxation
|
Pekingese
|
-
Chondrodystrophy (CDDY and IVDD Risk) with or without Chondrodysplasia (CDPA)
-
Oculocutaneous Albinism (Small Breed Type)
|
Phalene
|
-
Coagulation Factor VII Deficiency
-
Neuroaxonal Dystrophy (Papillon Type)
-
Progressive Retinal Atrophy, PRA1 (Papillon Type)
-
Von Willebrand Disease I
|
Plott
|
-
Degenerative Myelopathy (Common Variant)
-
Mucopolysaccharidosis I (Plott Hound Type)
|
Pointer
|
-
Acral Mutilation Syndrome
-
Degenerative Myelopathy (Common Variant)
|
Portuguese Podengo
|
-
Degenerative Myelopathy (Common Variant)
-
Primary Lens Luxation
|
Portuguese Podengo Pequeno
|
-
Degenerative Myelopathy (Common Variant)
-
Primary Lens Luxation
-
Progressive Retinal Atrophy, Cone-Rod Dystrophy 4
-
Progressive Retinal Atrophy, Progressive Rod-Cone Degeneration
|
Portuguese Water Dog
|
-
Chondrodystrophy (CDDY and IVDD Risk) with or without Chondrodysplasia (CDPA)
-
GM1 Gangliosidosis (Portuguese Water Dog Type)
-
Progressive Retinal Atrophy, Early-Onset (Portuguese Water Dog Type)
-
Progressive Retinal Atrophy, Progressive Rod-Cone Degeneration
|
Pug
|
-
Degenerative Myelopathy (Common Variant)
-
May-Hegglin Anomaly
-
Pyruvate Kinase Deficiency (Pug Type)
|
Puli
|
-
Degenerative Myelopathy (Common Variant)
-
Primary Lens Luxation
|
Pumi
|
-
Degenerative Myelopathy (Common Variant)
-
Primary Lens Luxation
|
Rat Terrier
|
-
Chondrodystrophy (CDDY and IVDD Risk) with or without Chondrodysplasia (CDPA)
-
Congenital Hypothyroidism with Goiter (Terrier Type)
-
Degenerative Myelopathy (Common Variant)
-
Primary Lens Luxation
-
Progressive Retinal Atrophy, Progressive Rod-Cone Degeneration
|
Redbone Coonhound
|
-
Coagulation Factor VII Deficiency
-
Degenerative Myelopathy (Common Variant)
|
Rhodesian Ridgeback
|
-
Degenerative Myelopathy (Common Variant)
-
Early Onset Adult Deafness (Rhodesian Ridgeback Type)
-
Hemophilia A (Rhodesian Ridgeback Type)
-
Hemophilia B (Rhodesian Ridgeback Type)
-
Juvenile Myoclonic Epilepsy (Rhodesian Ridgeback Type)
|
Russian Tsvetnaya Bolonka
|
-
Chondrodystrophy (CDDY and IVDD Risk) with or without Chondrodysplasia (CDPA)
-
Progressive Retinal Atrophy, Progressive Rod-Cone Degeneration
|
Saarloos Wolfdog
|
-
Degenerative Myelopathy (Common Variant)
-
Pituitary Dwarfism (Shepherd Type)
|
Saint Bernard
|
-
Degenerative Myelopathy (Common Variant)
-
Laryngeal Paralysis and Polyneuropathy (Leonberger Type 3)
-
Polyneuropathy (Leonberger Type 1)
|
Samoyed
|
-
Amelogenesis Imperfecta (Samoyed Type)
-
Degenerative Myelopathy (Common Variant)
-
Hereditary Nephritis (Samoyed Type)
-
Progressive Retinal Atrophy, X-Linked 1 (Husky Type)
-
Retinal Dysplasia/Oculoskeletal Dysplasia 2
|
Schipperke
|
-
Mucopolysaccharidosis IIIB (Schipperke Type)
-
Progressive Retinal Atrophy, Progressive Rod-Cone Degeneration
|
Scottish Terrier
|
-
Chondrodystrophy (CDDY and IVDD Risk) with or without Chondrodysplasia (CDPA)
-
Craniomandibular Osteopathy
-
Ligneous Membranitis
-
Von Willebrand Disease III (Scottish Terrier Type)
|
Sealyham Terrier
|
-
Chondrodystrophy (CDDY and IVDD Risk) with or without Chondrodysplasia (CDPA)
-
Coagulation Factor VII Deficiency
-
Degenerative Myelopathy (Common Variant)
-
Primary Lens Luxation
|
Shar-Pei
|
-
Primary Open Angle Glaucoma and Primary Lens Luxation (Shar Pei Type)
-
Shar-Pei Autoinflammatory Disease
|
Shiba Inu
|
-
GM1 Gangliosidosis (Shiba Inu Type)
-
GM2 Gangliosidosis (Shiba Inu Type)
|
Shih Tzu
|
-
Chondrodystrophy (CDDY and IVDD Risk) with or without Chondrodysplasia (CDPA)
-
Degenerative Myelopathy (Common Variant)
-
Prekallikrein Deficiency
|
Shorty Bull
|
-
Degenerative Myelopathy (Common Variant)
-
Hereditary Cataracts
-
L-2-Hydroxyglutaric Aciduria (Staffordshire Bull Terrier Type)
-
Multifocal Retinopathy 1
-
Progressive Retinal Atrophy, Cone-Rod Dystrophy 4
|
Siberian Husky
|
-
Cone Degeneration
-
Degenerative Myelopathy (Common Variant)
-
Progressive Retinal Atrophy, X-Linked 1 (Husky Type)
|
Silken Windhound
|
-
Collie Eye Anomaly
-
Degenerative Myelopathy (Common Variant)
-
Multidrug Resistance 1
|
Silky Terrier
|
-
Degenerative Myelopathy (Common Variant)
-
Progressive Retinal Atrophy, Progressive Rod-Cone Degeneration
|
Skye Terrier
|
-
Chondrodystrophy (CDDY and IVDD Risk) with or without Chondrodysplasia (CDPA)
-
Craniomandibular Osteopathy
|
Smooth Fox Terrier
|
-
Congenital Hypothyroidism with Goiter (Terrier Type)
-
Degenerative Myelopathy (Common Variant)
-
Primary Lens Luxation
-
Spinocerebellar Ataxia (Terrier Type)
|
Soft Coated Wheaten Terrier
|
-
Adult Paroxysmal Dyskinesia
-
Degenerative Myelopathy (Common Variant)
-
Microphthalmia (Soft Coated Wheaten Terrier Type)
-
Protein Losing Nephropathy
|
South African Boerboel
|
-
Hyperuricosuria
-
Multifocal Retinopathy 1
|
St. Bernard
|
-
Degenerative Myelopathy (Common Variant)
-
Laryngeal Paralysis and Polyneuropathy (Leonberger Type 3)
-
Polyneuropathy (Leonberger Type 1)
|
Stabyhoun
|
-
Degenerative Myelopathy (Common Variant)
-
Von Willebrand Disease I
|
Staffordshire Bull Terrier
|
-
Degenerative Myelopathy (Common Variant)
-
Hereditary Cataracts
-
L-2-Hydroxyglutaric Aciduria (Staffordshire Bull Terrier Type)
|
Standard Schnauzer
|
-
Degenerative Myelopathy (Common Variant)
-
Dilated Cardiomyopathy (Schnauzer Type)
-
Myotonia Congenita (Schnauzer Type)
-
Persistent Müllerian Duct Syndrome
|
Sussex Spaniel
|
-
Chondrodystrophy (CDDY and IVDD Risk) with or without Chondrodysplasia (CDPA)
-
Pyruvate Dehydrogenase Deficiency
|
Swedish Lapphund
|
-
Degenerative Myelopathy (Common Variant)
-
Multifocal Retinopathy 3
-
Pompe Disease
-
Progressive Retinal Atrophy, Progressive Rod-Cone Degeneration
|
Swedish Vallhund
|
-
Hyperuricosuria
-
Progressive Retinal Atrophy (Swedish Vallhund Type)
|
Teddy Roosevelt Terrier
|
-
Chondrodystrophy (CDDY and IVDD Risk) with or without Chondrodysplasia (CDPA)
-
Congenital Hypothyroidism with Goiter (Terrier Type)
-
Degenerative Myelopathy (Common Variant)
-
Primary Lens Luxation
|
Tenterfield Terrier
|
-
Degenerative Myelopathy (Common Variant)
-
Primary Lens Luxation
-
Spinocerebellar Ataxia (Terrier Type)
|
Toy Fox Terrier
|
-
Congenital Hypothyroidism with Goiter (Terrier Type)
-
Degenerative Myelopathy (Common Variant)
-
Primary Lens Luxation
-
Progressive Retinal Atrophy, Progressive Rod-Cone Degeneration
-
Spinocerebellar Ataxia (Terrier Type)
|
Vizsla
|
-
Cerebellar Cortical Degeneration
-
Exercise-Induced Collapse
-
Exfoliative Cutaneous Lupus Erythematosus (ECLE)
-
Hyperuricosuria
|
Wachtelhund
|
-
Degenerative Myelopathy (Common Variant)
-
Glycogen Storage Disease VII (Wachtelhund Type)
|
Weimaraner
|
-
Chondrodystrophy (CDDY and IVDD Risk) with or without Chondrodysplasia (CDPA)
-
Hyperuricosuria
-
Hypomyelination (Weimaraner Type)
-
Spinal Dysraphism
|
Welsh Springer Spaniel
|
-
Coagulation Factor VII Deficiency
-
Familial Nephropathy (Cocker Spaniel Type)
|
Welsh Terrier
|
-
Degenerative Myelopathy (Common Variant)
-
Primary Lens Luxation
|
West Highland White Terrier
|
-
Craniomandibular Osteopathy
-
Globoid Cell Leukodystrophy (Terrier Type)
-
Pyruvate Kinase Deficiency (Terrier Type)
-
Von Willebrand Disease I
|
Whippet
|
-
Degenerative Myelopathy (Common Variant)
-
Glycogen Storage Disease VII, PFK Deficiency
-
Myostatin Deficiency (Whippet Type)
|
Wirehaired Pointing Griffon
|
-
Degenerative Myelopathy (Common Variant)
-
Hereditary Cataracts (Wirehaired Pointing Griffon Type)
|
Wirehaired Vizsla
|
-
Cerebellar Cortical Degeneration
-
Exercise-Induced Collapse
-
Hyperuricosuria
|