A
-
- Hemophilia B (Discovered in the Airedale Terrier)
- Factor VII Deficiency
- Protein Losing Nephropathy
- Lung Developmental Disease (Discovered in the Airedale Terrier)
-
- Alaskan Husky Encephalopathy
- Degenerative Myelopathy
-
- Factor VII Deficiency
-
- Cone Degeneration (Discovered in the Alaskan Malamute)
- Early-Onset Progressive Polyneuropathy (Discovered in the Alaskan Malamute)
- Primary Ciliary Dyskinesia (Discovered in the Alaskan Malamute)
-
- Neuronal Ceroid Lipofuscinosis 8 (Discovered in the Alpine Dachsbracke)
- Chondrodystrophy (CDDY)*
- Intervertebral Disc Disease (IVDD) Risk*
-
- Degenerative Myelopathy
- Progressive Rod Cone Degeneration (prcd-PRA)
- Chondrodystrophy (CDDY)*
- Intervertebral Disc Disease (IVDD) Risk*
- Thrombopathia (Discovered in the Eskimo Spitz)*
-
- Hyperuricosuria, Cone-Rod Dystrophy 1
- Canine Multifocal Retinopathy 1
- Cone-Rod Dystrophy 2
- Osteochondromatosis (Discovered in the American Staffordshire Terrier)
- Chondrodystrophy (CDDY)*
- Intervertebral Disc Disease (IVDD) Risk*
- Hereditary Calcium Oxalate Urolithiasis
- Type 1*
-
- Chondrodystrophy (CDDY)*
- Intervertebral Disc Disease (IVDD) Risk*
-
- Disproportionate Dwarfism (Discovered in the Dogo Argentino)*
-
- 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)
- Junctional Epidermolysis Bullosa (Discovered in the Australian Cattle Dog Mix)*
-
- Intestinal Lipid Malabsorption (Discovered in the Australian Kelpie)*
-
- 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)
- Chondrodystrophy (CDDY)*
- Intervertebral Disc Disease (IVDD) Risk*
- Junctional Epidermolysis Bullosa (Discovered in the Australian Shepherd)*
-
Craniomandibular Osteopathy (Discovered in the Australian Terrier)*
-
- Myotonia Congenita
- Cystinuria Type II-A
- Progressive Rod Cone Degeneration (prcd-PRA)
B
-
- Progressive Rod Cone Degeneration (prcd-PRA)
- Chondrodystrophy (CDDY)*
- Intervertebral Disc Disease (IVDD) Risk*
-
- Fanconi Syndrome
- Progressive Retinal Atrophy (Discovered in the Basenji)
- Pyruvate Kinase Deficiency (Discovered in the Basenji)
-
- Primary Open Angle Glaucoma (Discovered in Basset Fauve de Bretagne)
-
- Primary Open Angle Glaucoma (Discovered in Petit Basset Griffon Vendeen)
-
- X-Linked Severe Combined Immunodeficiency (Discovered in the Basset Hound)
- Chondrodystrophy (CDDY)*
- Intervertebral Disc Disease (IVDD) Risk*
- Craniomandibular Osteopathy*
- (Discovered in the Basset Hound)*
- Dystrophic Epidermolysis Bullosa (Discovered in the Basset Hound)*
- Lafora Disease (Linkage Test)*
- Thrombopathia (Discovered in the Basset Hound)*
-
- Chondrodystrophy (CDDY)*
- Intervertebral Disc Disease (IVDD) Risk*
-
- 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
- Canine Congenital Stationary Night Blindness*
- Chondrodystrophy (CDDY)*
- Intervertebral Disc Disease (IVDD) Risk*
- Lafora Disease (Linkage Test)*
-
- Chondrodystrophy (CDDY)*
- Intervertebral Disc Disease (IVDD) Risk*
-
- Collie Eye Anomaly (CEA)
-
- Spongy Degeneration with Cerebellar Ataxia (Discovered in Belgian Malinois - SDCA1)
- Spongy Degeneration with Cerebellar Ataxia (Discovered in Belgian Malinois - SDCA2)
- Cardiomyopathy*
- Juvenile Mortality (Discovered in the Belgian Shepherd)*
- CNS Atrophy with Cerebellar Ataxia (Discovered in the Belgian Shepherd)*
- Hereditary Ataxia (Discovered in the Belgian Malinois)*
-
Spongy Degeneration with Cerebellar Ataxia (Discovered in Belgian Malinois - SDCA1), Cardiomyopathy*, Juvenile Mortality (Discovered in the Belgian Shepherd)*, CNS Atrophy with Cerebellar Ataxia (Discovered in the Belgian Shepherd)*
-
- Cardiomyopathy*
- Juvenile Mortality (Discovered in the Belgian Shepherd)*
-
- Chondrodystrophy (CDDY)*
- Intervertebral Disc Disease (IVDD) Risk*
-
- Chondrodystrophy (CDDY)*
- Intervertebral Disc Disease (IVDD) Risk*
-
- Degenerative Myelopathy
- von Willebrand's Disease
- type 1
-
- Progressive Rod Cone Degeneration (prcd-PRA)
-
- Hyperuricosuria, Juvenile Laryngeal Paralysis and Polyneuropathy
- Progressive Rod Cone Degeneration (prcd-PRA)
-
- Degenerative Myelopathy
-
- Hyperuricosuria
- Canine Multifocal Retinopathy 1
-
- Progressive Rod Cone Degeneration (prcd-PRA)
-
- MDR1 Medication Sensitivity
- Intestinal Cobalamin Malabsorption (Discovered in the Border Collie)
- Sensory Neuropathy
- Dental Hypomineralization
- Trapped Neutrophil Syndrome
- Collie Eye Anomaly (CEA)
- Early Adult Onset Deafness For Border Collies only (Linkage test)
- Hereditary Calcium Oxalate Urolithiasis Type 1*
- Neuronal Ceroid Lipofuscinosis 5 (Discovered in the Border Collie)*
-
- Shaking Puppy Syndrome (Discovered in the Border Terrier)
-
- Degenerative Myelopathy
-
- Hereditary Calcium Oxalate Urolithiasis Type 1*
- Limb-girdle Muscular Dystrophy (Discovered in the Boston Terrier)*
-
- Exercise-Induced Collapse
-
- Hemophilia A (Discovered in the Boxer)
- Degenerative Myelopathy
-
- Chondrodystrophy (CDDY)*
- Intervertebral Disc Disease (IVDD) Risk*v
-
Congenital Stationary Night Blindness (CSNB)
-
- Complement 3 Deficiency
-
- Laryngeal Paralysis (Discovered in the Bull Terrier
- Miniature Bull Terrier)*
-
Polycystic Kidney Disease, Primary Lens Luxation, Lethal Acrodermatitis (Discovered in the Bull Terrier), Laryngeal Paralysis (Discovered in the Bull Terrier, Miniature Bull Terrier)*
-
- Polycystic Kidney Disease
- Primary Lens Luxation
- Lethal Acrodermatitis (Discovered in the Bull Terrier)
- Chondrodystrophy (CDDY)*
- Intervertebral Disc Disease (IVDD) Risk*
- Laryngeal Paralysis (Discovered in the Bull Terrier
- Miniature Bull Terrier)*
-
- Ichthyosis (Discovered in the American Bulldog)
- Hyperuricosuria
- Nemaline Myopathy
- Canine Multifocal Retinopathy 1
-
- Hyperuricosuria
- Canine Multifocal Retinopathy 1
- Hereditary Calcium Oxalate Urolithiasis Type 1*
-
- Dominant Progressive Retinal Atrophy
- Canine Multifocal Retinopathy 1
- Hereditary Calcium Oxalate Urolithiasis Type 1*
C
-
- Macrothrombocytopenia
- Pyruvate Kinase Deficiency (Discovered in the West Highland White Terrier)
- Craniomandibular Osteopathy
- Globoid Cell Leukodystrophy (Discovered in Terriers)
-
- Canine Multifocal Retinopathy 1
- Dental-Skeletal-Retinal Anomaly (Discovered in the Cane Corso)*
-
- X-Linked Severe Combined Immunodeficiency (Discovered in the Cardigan Welsh Corgi)
- Degenerative Myelopathy
- Rod-Cone Dysplasia 3
- Chondrodystrophy (CDDY)*
- Intervertebral Disc Disease (IVDD) Risk*
-
- Chondrodystrophy (CDDY)*
- Intervertebral Disc Disease (IVDD) Risk*
-
- Muscular Dystrophy (Discovered in the Cavalier King Charles Spaniel)
- Xanthinuria (Discovered in the Cavalier King Charles Spaniel)
- Degenerative Myelopathy
- Episodic falling syndrome (EFS)
- Chondrodystrophy (CDDY)*
- Intervertebral Disc Disease (IVDD) Risk*
-
- Dystrophic Epidermolysis Bullosa (Discovered in the Central Asian Ovcharka)
-
- Degenerative Myelopathy
- Exercise-Induced Collapse
- Progressive Rod Cone Degeneration (prcd-PRA)
- Chondrodystrophy (CDDY)*
- Intervertebral Disc Disease (IVDD) Risk*
-
- Neuronal Ceroid Lipofuscinosis 7
- Progressive Rod Cone Degeneration (prcd-PRA)
- Chondrodystrophy (CDDY)*
- Intervertebral Disc Disease (IVDD) Risk*
-
- Neuronal Ceroid Lipofuscinosis 7
- Primary Lens Luxation
- Progressive Rod Cone Degeneration (prcd-PRA)
- Canine Multiple Systems Degeneration (Discovered in the Chinese Crested Dog)*
- Chondrodystrophy (CDDY)*
- Intervertebral Disc Disease (IVDD) Risk*
-
- Primary Lens Luxation
-
- Primary Open Angle Glaucoma and Lens Luxation (Discovered in Chinese Shar-Pei)
-
- MDR1 Medication Sensitivity, Chondrodysplasia
- Chondrodystrophy (CDDY)*
- Intervertebral Disc Disease (IVDD) Risk*
-
- Hereditary Elliptocytosis, Chondrodystrophy (CDDY)*
- Intervertebral Disc Disease (IVDD) Risk*
-
- Pyruvate Dehydrogenase Phosphatase 1 Deficiency
- Exercise-Induced Collapse, Chondrodystrophy (CDDY)*
- Intervertebral Disc Disease (IVDD) Risk*
-
- Phosphofructokinase Deficiency
- Exercise-Induced Collaps
- Progressive Rod Cone Degeneration (prcd-PRA)
- Bernard-Soulier Syndrome (Discovered in the Cocker Spaniel)*
- Chondrodystrophy (CDDY)*
- Intervertebral Disc Disease (IVDD) Risk*
-
- MDR1 Medication Sensitivity
- Degenerative Myelopathy
- Collie Eye Anomaly (CEA)
- Inflammatory Pulmonary Disease (Discovered in the Rough Collie)*
- Dermatomyositis
- PAN2 variant (locus A) (Discovered in the Shetland Sheepdog Collie)*
- ermatomyositis MAP3K7CL variant (locus B) (Discovered in the Shetland Sheepdog Collie)*
-
- Progressive Retinal Atrophy (Discovered in the Papillon and Phalène), von Willebrand's Disease, type 1
- Chondrodystrophy (CDDY)*, Intervertebral Disc Disease (IVDD) Risk*
-
- Bandera's Neonatal Ataxia, von Willebrand's Disease, type 1
- Canine Multifocal Retinopathy 2
- Progressive Rod Cone Degeneration (prcd-PRA)
- Chondrodystrophy (CDDY)*
- Intervertebral Disc Disease (IVDD) Risk*
-
- Glycogen Storage Disease Type IIIa
- (GSD IIIa)
- Exercise-Induced Collapse
D
-
- Chondrodystrophy (CDDY)*
- Intervertebral Disc Disease (IVDD) Risk*
-
- Neuronal Ceroid Lipofuscinosis 1
- Osteogenesis Imperfecta (Discovered in the Dachshund)
- Narcolepsy (Discovered in the Dachshund)
- Mucopolysaccharidosis Type IIIA (Discovered in the Dachshund)
- Chondrodystrophy (CDDY)*
- Intervertebral Disc Disease (IVDD) Risk*
-
- Neuronal Ceroid Lipofuscinosis 1
- Osteogenesis Imperfecta (Discovered in the Dachshund)
- Narcolepsy (Discovered in the Dachshund)
- Mucopolysaccharidosis Type IIIA (Discovered in the Dachshund)
- Chondrodystrophy (CDDY)*
- Intervertebral Disc Disease (IVDD) Risk*
- Coat Color Dilution*
- Neurological Defects (Discovered in the Miniature Dachshund)*
- Lafora Disease (Linkage Test)*
- Limb-girdle muscular dystrophy (Discovered in the Miniature Dachshund)*
- Progressive Retinal Atrophy (Discovered in the Miniature Long Haired Dachshund)*
-
- Neuronal Ceroid Lipofuscinosis 1
- Osteogenesis Imperfecta (Discovered in the Dachshund)
- Narcolepsy (Discovered in the Dachshund)
- Mucopolysaccharidosis Type IIIA (Discovered in the Dachshund)
- Chondrodystrophy (CDDY)*
- Intervertebral Disc Disease (IVDD) Risk*
- Coat Color Dilution*
- Neurological Defects (Discovered in the Miniature Dachshund)*
- Lafora Disease (Linkage Test)*
- Limb-girdle muscular dystrophy (Discovered in the Miniature Dachshund)*
-
- 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)
- Chondrodystrophy (CDDY)*
- Intervertebral Disc Disease (IVDD) Risk*
- Coat Color Dilution*
- Neurological Defects (Discovered in the Miniature Dachshund)*
- Lafora Disease (Linkage Test)*
- Limb-girdle muscular dystrophy (Discovered in the Miniature Dachshund)*
-
- Neuronal Ceroid Lipofuscinosis 1
- Osteogenesis Imperfecta (Discovered in the Dachshund)
- Narcolepsy (Discovered in the Dachshund)
- Mucopolysaccharidosis Type IIIA (Discovered in the Dachshund)
- Chondrodystrophy (CDDY)*
- Intervertebral Disc Disease (IVDD) Risk*
-
- 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)
- Chondrodystrophy (CDDY)*
- Intervertebral Disc Disease (IVDD) Risk*
-
- Acute Respiratory Distress Syndrome
- Hyperuricosuria
-
- Acute Respiratory Distress Syndrome
- Hyperuricosuria
- Chondrodystrophy (CDDY)*
- Intervertebral Disc Disease (IVDD) Risk*
-
- MDR1 Medication Sensitivity
- Primary Lens Luxation
- Chondrodystrophy (CDDY)*
- Intervertebral Disc Disease (IVDD) Risk*
-
- von Willebrand's Disease, type 1
- Deafness and Vestibular Dysfunction (Discovered in Doberman Pinscher)
- Bilateral Deafness*
- Vestibular Dysfunction (Discovered in Dobermann)*
- MYO7A gene variant*
- Dilated Cardiomyopathy (Discovered in the Doberman) (variants 1-4)
-
- Focal Non-Epidermolytic Palmoplantar Keratoderma
- Canine Multifocal Retinopathy 1
-
- von Willebrand's Disease, type 1
-
- Chondrodystrophy (CDDY)*
- Intervertebral Disc Disease (IVDD) Risk*
-
- Spongy Degeneration with Cerebellar Ataxia (Discovered in Belgian Malinois - SDCA2)
- Inflammatory Myopathy (Discovered in the Dutch Shepherd Dog)*
E
-
- Phosphofructokinase Deficiency
- Xanthinuria (Discovered in the Cavalier King Charles Spaniel)
- Acral Mutilation Syndrome
- Exercise-Induced Collapse
- Progressive Rod Cone Degeneration (prcd-PRA)
- Chondrodystrophy (CDDY)*
- Intervertebral Disc Disease (IVDD) Risk*
- Familial Nephropathy (FN)
- (Discovered in the English Cocker Spaniel)*
-
- Neuronal Ceroid Lipofuscinosis 8 (Discovered in the English Setter)
-
- MDR1 Medication Sensitivity
- Progressive Rod Cone Degeneration (prcd-PRA)
- Collie Eye Anomaly (CEA)
-
- Phosphofructokinase Deficiency
- Degenerative Myelopathy
- QT Syndrome
- Acral Mutilation Syndrome
- X-Linked Tremors
- Chondrodystrophy (CDDY)*
- Intervertebral Disc Disease (IVDD) Risk*
- Familial Nephropathy (FN)
- (Discovered in the English Cocker Spaniel)*
-
- Muscular Dystrophy (Discovered in the Cavalier King Charles Spaniel)
- Chondrodystrophy (CDDY)*
- Intervertebral Disc Disease (IVDD) Risk*
-
- Progressive Rod Cone Degeneration (prcd-PRA)
- Chondrodystrophy (CDDY)*
- Intervertebral Disc Disease (IVDD) Risk*
-
- Cerebellar Hypoplasia
F
-
- Progressive Rod Cone Degeneration (prcd-PRA)
- Chondrodystrophy (CDDY)*
- Intervertebral Disc Disease (IVDD) Risk*
-
- Factor VII Deficiency
- Progressive Early-Onset Cerebellar Ataxia
-
- Canine Multifocal Retinopathy 3
- Progressive Rod Cone Degeneration (prcd-PRA)
- Chondrodystrophy (CDDY)*
- Intervertebral Disc Disease (IVDD) Risk*
-
- POMC
-
- Spinocerebellar Ataxia with Myokymia and/or Seizures
-
- Spinocerebellar Ataxia with Myokymia and/or Seizures
- Congenital Hypothyroidism (Discovered in the Toy Fox and Rat Terrier)
- Primary Lens Luxation
-
- Van den Ende-Gupta Syndrome
- Degenerative Myelopathy
- Primary Lens Luxation
-
- Canine Multifocal Retinopathy 1
- Chondrodystrophy (CDDY)*
- Intervertebral Disc Disease (IVDD) Risk*
-
- Acral Mutilation Syndrome
-
- Severe Combined Immunodeficiency (Discovered in Frisian Water Dogs)
G
-
- Primary Lens Luxation
- Chondrodystrophy (CDDY)*
- Intervertebral Disc Disease (IVDD) Risk*
-
- Primary Lens Luxation
-
- von Willebrand's Disease, type 1
- Glycogen Storage Disease Type Ia (Discovered in the German Pinscher)*
-
- 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
-
- 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
-
- Hyperuricosuria
-
- von Willebrand's Disease, type 2
- Exercise-Induced Collapse
-
- 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)
- Congenital Eye Malformations (Discovered in the Golden Retriever)*
- Ichthyosis Type 2 (Discovered in the Golden Retriever)*
- Neuronal Ceroid Lipofuscinosis 5 (Discovered in the Golden Retriever)*
- Progressive Retinal Atrophy (GR-PRA2) (Discovered in the Golden Retriever)*
-
- Cerebellar Ataxia
-
- Centronuclear Myopathy (Discovered in the Great Dane)
- Ichthyosis (Discovered in the Great Dane)
-
- Glanzmann Thrombasthenia Type I (Discovered in Great Pyrenees)
- Canine Multifocal Retinopathy 1
-
- P2RY12-associated Bleeding Disorder
-
- Early-Onset Progressive Polyneuropathy (Discovered in the Greyhound)
- Hereditary Nasal Parakeratosis (Discovered in the Greyhound)
H
-
- Hemophilia A (Discovered in the Havanese)
- Chondrodystrophy (CDDY)*
- Intervertebral Disc Disease (IVDD) Risk*
- Hereditary Calcium Oxalate Urolithiasis, Type 1*
-
- Congenital Myasthenic Syndrome (Discovered in the Heideterrier)*
-
- Collie Eye Anomaly (CEA)
I
-
- Rod-Cone Dysplasia 1, von
- Willebrand's Disease, type 1
-
- Rod-Cone Dysplasia 1
- Globoid Cell Leukodystrophy (Discovered in the Irish Setter)
-
- Hereditary Footpad Hyperkeratosis
- Darier Disease (Discovered in the Irish Terrier)*
-
- Hyperekplexia or Startle Disease
-
- Amelogenesis Imperfecta, Progressive Retinal Atrophy 1 (Discovered in the Italian Greyhound)
- Congenital Muscular Dystrophy (Discovered in the Italian Greyhound)*
J
-
- GM2 Gangliosidosis (Discovered in the Japanese Chin)
- Progressive Rod Cone Degeneration (prcd-PRA), Chondrodystrophy (CDDY)*
- Intervertebral Disc Disease (IVDD) Risk*
-
- GM1 Gangliosidosis (Discovered in the Shiba)
K
-
- Chondrodysplasia
- Hypophosphatasia
- Progressive Rod Cone Degeneration (prcd-PRA)
- Pituitary Dwarfism (Discovered in the Karelian Bear Dog)*
-
- Degenerative Myelopathy
- Factor XI Deficiency, von
- Willebrand's Disease, type 1
-
- Intestinal Cobalamin Malabsorption (Discovered in the Komondor)
-
- von Willebrand's Disease, type 3 (Discovered in the Kooiker Hound), Chondrodystrophy (CDDY)*
- Intervertebral Disc Disease (IVDD) Risk*
-
- Hyperuricosuria, von
- Willebrand's Disease, type 1
- Hereditary Footpad Hyperkeratosis
-
- Progressive Rod Cone Degeneration (prcd-PRA)
L
-
- 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
- Congenital Cornification (Discovered in the Labrador Retriever)*
- Ehlers-Danlos syndrome (Discovered in the Labrador Retriever)*
- Hemophilia A (Discovered in the Labrador Retriever)*
- Muscular Dystrophy-Dystroglycanopathy (Discovered in the Labrador Retriever)*
-
- Lagotto Storage Disease
- Hyperuricosuria
- Benign Familial Juvenile Epilepsy
- Progressive Rod Cone Degeneration (prcd-PRA)
-
- Primary Lens Luxation
-
- Primary Lens Luxation
- Progressive Rod Cone Degeneration (prcd-PRA)
- Collie Eye Anomaly (CEA), Enamel Hypoplasia (Discovered in the Lancashire Heeler)*
-
- Cystinuria Type I-A, Muscular Dystrophy (Discovered in the Landseer)
-
- Canine Multifocal Retinopathy 3
- Progressive Rod Cone Degeneration (prcd-PRA)
- Progressive Retinal Atrophy (Discovered in the Lapponian Herder)*
-
- Hemophilia B (Discovered in the Lhasa Apso)
- Progressive Retinal Atrophy (Discovered in the Lhasa Apso), Chondrodystrophy (CDDY)*
- Intervertebral Disc Disease (IVDD) Risk*
-
- Chondrodystrophy (CDDY)*
- Intervertebral Disc Disease (IVDD) Risk*
-
- Primary Lens Luxation
M
-
- Glycogen Storage Disease Type Ia, Chondrodystrophy (CDDY)*
- Intervertebral Disc Disease (IVDD) Risk*
-
- von Willebrand's Disease, type 1
-
- Xanthinuria (Discovered in the Toy Manchester Terrier), von
- Willebrand's Disease, type 1
- Progressive Rod Cone Degeneration (prcd-PRA)
- Juvenile Dilated Cardiomyopathy (Discovered in the Toy Manchester Terrier)*
-
- Progressive Rod Cone Degeneration (prcd-PRA)
-
- Dominant Progressive Retinal Atrophy
- Canine Multifocal Retinopathy 1
-
- MDR1 Medication Sensitivity
-
- Progressive Rod Cone Degeneration (prcd-PRA), Chondrodystrophy (CDDY)*
- Intervertebral Disc Disease (IVDD) Risk*
-
- 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)
- Chondrodystrophy (CDDY)*
- Intervertebral Disc Disease (IVDD) Risk*
- Startle Disease (Discovered in the Miniature American Shepherd)*
-
- Chondrodystrophy (CDDY)*
- Intervertebral Disc Disease (IVDD) Risk*
- Mucopolysaccharidosis VI (Discovered in the Miniature Pinscher)*
-
- Hyperuricosuria
N
-
- Chondrodystrophy (CDDY)*
- Intervertebral Disc Disease (IVDD) Risk*
-
- Mucopolysaccharidosis Type IIIA (Discovered in the New Zealand Huntaway)
-
- Cystinuria Type I-A
-
- Progressive Early-Onset Cerebellar Ataxia
- Progressive Rod Cone Degeneration (prcd-PRA)
-
- Epidermolytic Hyperkeratosis
- Macrothrombocytopenia
- Muscular Dystrophy (Discovered in the Norfolk Terrier)
-
- Hereditary Ataxia (Discovered in the Norwegian Buhund)
-
- Chondrodysplasia
- Early Retinal Degeneration (Discovered in the Norwegian Elkhound)
- Progressive Rod Cone Degeneration (prcd-PRA)
-
- Primary Lens Luxation
- Cystic Renal Dysplasia and Hepatic Fibrosis
-
- Cleft Lip & Palate with Syndactyly, Cleft Palate
- Progressive Rod Cone Degeneration (prcd-PRA), Collie Eye Anomaly (CEA)
- Chondrodystrophy (CDDY)*, Intervertebral Disc Disease (IVDD) Risk*
-
- Hyperuricosuria
O
-
- GM2 Gangliosidosis (Discovered in the Japanese Chin)
- Progressive Rod Cone Degeneration (prcd-PRA), Chondrodystrophy (CDDY)*
- Intervertebral Disc Disease (IVDD) Risk*
-
- Cerebellar Ataxia, MDR1 Medication Sensitivity
- Hemophilia A (Discovered in Old English Sheepdog)
- Exercise-Induced Collapse
- Primary Ciliary Dyskinesia
P
-
- Progressive Retinal Atrophy (Discovered in the Papillon and Phalène), von Willebrand's Disease, type 1
- Neuroaxonal Dystrophy (Discovered in the Papillon)
- Chondrodystrophy (CDDY)*
- Intervertebral Disc Disease (IVDD) Risk*
-
- 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)
- Chondrodystrophy (CDDY)*, Intervertebral Disc Disease (IVDD) Risk*
-
- Primary Lens Luxation
-
- Chondrodystrophy (CDDY)*
- Intervertebral Disc Disease (IVDD) Risk*
-
- Degenerative Myelopathy
- Rod-Cone Dysplasia 3, von Willebrand's Disease, type 1
- Exercise-Induced Collapse, Chondrodystrophy (CDDY)*
- Intervertebral Disc Disease (IVDD) Risk*
-
- Progressive Rod Cone Degeneration (prcd-PRA)
-
- Acral Mutilation Syndrome
-
- Juvenile Cataract (Discovered in the Wirehaired Pointing Griffon)*
-
- Chondrodystrophy (CDDY)*
- Intervertebral Disc Disease (IVDD) Risk*
-
- Hyperuricosuria
- Hereditary Vitamin D-Resistant Rickets Type II
- Progressive Rod Cone Degeneration (prcd-PRA)
-
- Osteochondrodysplasia, von Willebrand's Disease, type 1
- Progressive Rod Cone Degeneration (prcd-PRA)
-
- Osteochondrodysplasia, von Willebrand's Disease, type 1
- Progressive Rod Cone Degeneration (prcd-PRA), Chondrodystrophy (CDDY)*
- Intervertebral Disc Disease (IVDD) Risk*
-
- Neonatal Encephalopathy with Seizures
- Degenerative Myelopathy, von Willebrand's Disease, type 1
- Progressive Rod Cone Degeneration (prcd-PRA)
-
- Osteochondrodysplasia, von Willebrand's Disease, type 1
- GM2 Gangliosidosis (Discovered in the Toy Poodle)
- Progressive Rod Cone Degeneration (prcd-PRA), Chondrodystrophy (CDDY)*
- Intervertebral Disc Disease (IVDD) Risk*
-
- Osteochondrodysplasia
- von Willebrand's Disease, type 1
- GM2 Gangliosidosis (Discovered in the Toy Poodle)
- Progressive Rod Cone Degeneration (prcd-PRA)
- Chondrodystrophy (CDDY)* and Intervertebral Disc Disease (IVDD) Risk*
-
- Progressive Rod Cone Degeneration (prcd-PRA)
-
- Progressive Rod Cone Degeneration (prcd-PRA)
-
- Early-onset PRA (Discovered in the Portuguese Water Dog)
- GM1 Gangliosidosis (Discovered in the Portuguese Water Dog)
- Progressive Rod Cone Degeneration (prcd-PRA)
- Chondrodystrophy (CDDY)*, Intervertebral Disc Disease (IVDD) Risk*
-
- Canine Multifocal Retinopathy 1
- Chondrodystrophy (CDDY)*
- Intervertebral Disc Disease (IVDD) Risk*
-
- Degenerative Myelopathy, May-Hegglin Anomaly
- Pyruvate Kinase Deficiency (Discovered in the Pug)
-
- Progressive Rod Cone Degeneration (prcd-PRA)
- Chondrodystrophy (CDDY)*
- Intervertebral Disc Disease (IVDD) Risk*
-
- Primary Lens Luxation
-
- Chondrodystrophy (CDDY)*
- Intervertebral Disc Disease (IVDD) Risk*
R
-
- Congenital Hypothyroidism (Discovered in the Toy Fox and Rat Terrier
- Primary Lens Luxation
- Progressive Rod Cone Degeneration (prcd-PRA)
-
- Juvenile Myoclonic Epilepsy
- Degenerative Myelopathy
- Early Onset Adult Deafness*
- (Discovered in the Rhodesian Ridgeback)*
-
- Juvenile Laryngeal Paralysis and Polyneuropathy
- Myotubular Myopathy
- Neuroaxonal Dystrophy (Discovered in the Rottweiler)
- Hereditary Calcium Oxalate Urolithiasis Type 1* Palmoplantar Hyperkeratosis (Discovered in the Rottweiler)*
- Sensorineural Deafness (Discovered in the Rottweiler)*
-
- 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)
-
- Progressive Rod Cone Degeneration (prcd-PRA)
- Chondrodystrophy (CDDY)*
- Intervertebral Disc Disease (IVDD) Risk*
S
-
- Neuronal Ceroid Lipofuscinosis 8 (Discovered in the Saluki)
- Succinic Semialdehyde Dehydrogenase Deficiency (Discovered in the Saluki)*
-
- X-Linked Progressive Retinal Atrophy 1
- X-Linked Hereditary Nephropathy (Discovered in the Samoyed)
-
- Hyperuricosuria, Generalized Progressive Retinal Atrophy (Discovered in the Schapendoes)
- Chondrodystrophy (CDDY)*
- Intervertebral Disc Disease (IVDD) Risk*
-
- Progressive Rod Cone Degeneration (prcd-PRA)
-
- Hyperuricosuria, Dilated Cardiomyopathy (Discovered in the Schnauzer)
- Fetal Onset Neuroaxonal Dystrophy
- Factor VII Deficiency
- Progressive Rod Cone Degeneration (prcd-PRA)
-
- Persistent Müllerian Duct Syndrome
- X-Linked Progressive Retinal Atrophy 2
- Spondylocostal Dysostosis, Myotonia Congenita (Discovered in the Miniature Schnauzer)
- Demyelinating Neuropathy, Chondrodystrophy (CDDY)*
- Intervertebral Disc Disease (IVDD) Risk*
-
- Dilated Cardiomyopathy (Discovered in the Schnauzer)
- Chondrodystrophy (CDDY)*
- Intervertebral Disc Disease (IVDD) Risk*
- Leukodystrophy (Discovered in the Standard Schnauzer)*
-
- Factor VII Deficiency
-
- Craniomandibular Osteopathy, von Willebrand's Disease, type 3 (Discovered in the Scottish Terrier)
- Ligneous Membranitis, Chondrodystrophy (CDDY)*
- Intervertebral Disc Disease (IVDD) Risk*
-
- Primary Lens Luxation, Chondrodystrophy (CDDY)*
- Intervertebral Disc Disease (IVDD) Risk*
-
- Progressive Rod Cone Degeneration (prcd-PRA)
-
- 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
- Dermatomyositis, PAN2 variant (locus A) (Discovered in the Shetland Sheepdog Collie*
- Dermatomyositis MAP3K7CL variant (locus B) (Discovered in the Shetland Sheepdog Collie)*
-
- Prekallikrein Deficiency
- Congenital Dyshormonogenic Hypothyroidism with Goiter (Discovered in the Shih Tzu)
- Chondrodystrophy (CDDY)*
- Intervertebral Disc Disease (IVDD) Risk*
-
- X-Linked Progressive Retinal Atrophy 1
-
- MDR1 Medication Sensitivity, Collie Eye Anomaly (CEA)
-
- Progressive Rod Cone Degeneration (prcd-PRA)
-
- Chondrodystrophy (CDDY)*
- Intervertebral Disc Disease (IVDD) Risk*
-
- Rod-Cone Dysplasia 1a
-
- Chondrodystrophy (CDDY)*
- Intervertebral Disc Disease (IVDD) Risk*
-
- Degenerative Myelopathy, Paroxysmal Dyskinesia
- Protein Losing Nephropathy
- Microphthalmia (Discovered in the Soft-Coated Wheaten Terrier)
-
- Chondrodystrophy (CDDY)*
- Intervertebral Disc Disease (IVDD) Risk*
- Early Onset Progressive Retinal Atrophy (Discovered in the Spanish Water Dog)*
-
- Cerebral Dysfunction, von Willebrand's Disease, type 1
- Chondrodystrophy (CDDY)*
- Intervertebral Disc Disease (IVDD) Risk*
-
- L-2-Hydroxyglutaric Aciduria, Congenital Muscular Dystrophy (Discovered in the Staffordshire Bull Terrier)*
- Hereditary Calcium Oxalate Urolithiasis, Type 1*
-
- Pyruvate Dehydrogenase Phosphatase 1 Deficiency
- Chondrodystrophy (CDDY)*
- Intervertebral Disc Disease (IVDD) Risk*
-
- Progressive Rod Cone Degeneration (prcd-PRA)
-
- Progressive Rod Cone Degeneration (prcd-PRA)
-
- Progressive Retinal Atrophy (Discovered in the Swedish Vallhund)
-
- Chondrodystrophy (CDDY)*
- Intervertebral Disc Disease (IVDD) Risk*
T
-
- Primary Lens Luxation
-
- Spinocerebellar Ataxia with Myokymia and/or Seizures
- Congenital Hypothyroidism (Discovered in the Tenterfield Terrier)
- Primary Lens Luxation
-
- Mucopolysaccharidosis Type VII (Discovered in the Brazilian Terrier)
-
- Progressive Retinal Atrophy Type III, Chondrodystrophy (CDDY)*
- Intervertebral Disc Disease (IVDD) Risk*
-
- Progressive Retinal Atrophy Type III, Primary Lens Luxation
- Progressive Rod Cone Degeneration (prcd-PRA)
- Chondrodystrophy (CDDY)*
- Intervertebral Disc Disease (IVDD) Risk*
V
-
- Cerebellar Cortical Degeneration
- Exercise-Induced Collapse
-
- Primary Lens Luxation
W
-
- Hypomyelination
- Hyperuricosuria
- Craniomandibular Osteopathy (Discovered in the Weimaraner)*
-
- Factor VII Deficiency
- Chondrodystrophy (CDDY)*
- Intervertebral Disc Disease (IVDD) Risk*
-
- Primary Lens Luxation
-
- 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)
-
- Phosphofructokinase Deficiency
- Muscular Hypertrophy (Double Muscling)
- Collie Eye Anomaly (CEA)
-
- MDR1 Medication Sensitivity
-
- Hyperuricosuria
- Cerebellar Cortical Degeneration
- Exercise-Induced Collapse
X
-
- Progressive Rod Cone Degeneration (prcd-PRA)