Blood and Clotting Coagulation factor VII deficiency Elliptocytosis Hemophilia A (German Shepherd Dog, type 2) Pyruvate kinase deficiency (Labrador Retriever type) Thrombopathia (American Eskimo Dog type) Von Willebrand disease I Von Willebrand disease II Hemophilia A (Boxer type) Hemophilia A (German Shepherd Dog, type 1) Leukocyte adhesion deficiency, type III Pyruvate kinase deficiency (Basenji type) Glycogen storage disease VII (Wachtelhund type) Hemophilia B (Cairn Terrier type) Pyruvate kinase deficiency (Beagle type) Pyruvate kinase deficiency (Pug type) Pyruvate kinase deficiency (Terrier type) Thrombopathia (Basset Hound type) Thrombopathia (Newfoundland type) Von Willebrand disease III (Kooikerhondje type) Von Willebrand disease III (Scottish Terrier type) Glanzmann's thrombasthenia (Great Pyrenees type) Glanzmann's thrombasthenia (Otterhound type) Hemophilia B (Lhasa Apso type) Hemophilia B (Rhodesian Ridgeback type) May-Hegglin anomaly P2RY12 receptor platelet disorder Prekallikrein deficiency
Cancer Renal cystadenocarcinoma and nodular dermatofibrosis Dental Amelogenesis imperfecta Drug Metabolism Multidrug resistance 1 At-Risk Eyes Collie eye anomaly Cone degeneration GM2 Gangliosidosis (Poodle type) Hereditary cataracts (Australian Shepherd type) Progressive retinal atrophy (Bullmastiff/Mastiff type) Progressive retinal atrophy, Cone-rod dystrophy 1 Progressive retinal atrophy, Cone-rod dystrophy 2 Progressive retinal atrophy, Golden Retriever 2 Progressive retinal atrophy, Progressive rod-cone degeneration Hereditary cataracts Multifocal retinopathy 1 Primary lens luxation Progressive retinal atrophy, Golden Retriever 1 Congenital stationary night blindness GM1 Gangliosidosis (Alaskan Husky type) Progressive retinal atrophy (Basenji type)
Progressive retinal atrophy (Irish Setter type) Cone degeneration (German Shorthaired Pointer type) Dry eye curly coat syndrome GM1 Gangliosidosis (Shiba Inu type) Multifocal retinopathy 2 Progressive retinal atrophy, generalized Progressive retinal atrophy, PRA1 (Papillon type) Progressive retinal atrophy, Rod-cone dysplasia 3 Early retinal degeneration GM1 Gangliosidosis (Portuguese Water Dog type) Multifocal retinopathy 3 Primary open angle glaucoma Progressive retinal atrophy (Sloughi type) Progressive retinal atrophy, Cone-rod dystrophy 3 Juvenile Laryngeal Paralysis and Polyneuropathy Heart Dilated cardiomyopathy Immune System Trapped neutrophil syndrome Cyclic neutropenia Leukocyte adhesion deficiency, type III Severe combined immunodeficiency disease (Terrier type) Severe combined immunodeficiency disease (Wetterhoun type) Complement 3 deficiency Primary ciliary dyskinesia Severe combined immunodeficiency disease, X-linked (Basset Hound type)
Severe combined immunodeficiency disease, X-linked (Corgi type) Liver/Gastrointestinal Gallbladder mucoceles Intestinal cobalamin malabsorption (Border Collie type) Glycogen storage disease IIIa Intestinal cobalamin malabsorption (Beagle type) Metabolic GM2 Gangliosidosis (Poodle type) Pyruvate kinase deficiency (Labrador Retriever type) Intestinal cobalamin malabsorption (Border Collie type) Mucopolysaccharidosis VII (Shepherd type) Neuronal ceroid lipofuscinosis 4A Neuronal ceroid lipofuscinosis 5 Neuronal ceroid lipofuscinosis 6 Neuronal ceroid lipofuscinosis 8 (Australian Shepherd type) Pyruvate kinase deficiency (Basenji type) Glycogen storage disease VII (Wachtelhund type) GM1 Gangliosidosis (Alaskan Husky type) Mucopolysaccharidosis IIIA (New Zealand Huntaway type) Neuronal ceroid lipofuscinosis 1 Neuronal ceroid lipofuscinosis 2 Pyruvate dehydrogenase deficiency Pyruvate kinase deficiency (Beagle type) Pyruvate kinase deficiency (Pug type) Pyruvate kinase deficiency (Terrier type) Adult-onset neuronal ceroid lipofuscinosis
Globoid cell leukodystrophy (Irish Setter type) Globoid cell leukodystrophy (Terrier type) Glycogen storage disease Ia Glycogen storage disease IIIa GM1 Gangliosidosis (Shiba Inu type) Mucopolysaccharidosis I Neuronal ceroid lipofuscinosis 10 Neuronal ceroid lipofuscinosis 8 (Setter type) Pompe disease GM1 Gangliosidosis (Portuguese Water Dog type) GM2 Gangliosidosis (Japanese Chin type) Intestinal cobalamin malabsorption (Beagle type) L-2-hydroxyglutaric aciduria (Staffordshire Bull Terrier type) Mucopolysaccharidosis IIIA (Dachshund type) Midline Defect Juvenile Laryngeal Paralysis and Polyneuropathy Musculoskeletal Degenerative myelopathy Exercise-induced collapse Myotubular myopathy 1 Osteochondrodysplasia Congenital myasthenic syndrome (Labrador Retriever type) Golden Retriever muscular dystrophy Mucopolysaccharidosis VII (Shepherd type) Osteogenesis imperfecta (Golden Retriever type) Skeletal dysplasia 2
Glycogen storage disease VII (Wachtelhund type) GM1 Gangliosidosis (Alaskan Husky type) Osteogenesis imperfecta (Beagle type) Pembroke Welsh Corgi Duchenne muscular dystrophy Adult-onset neuronal ceroid lipofuscinosis Chondrodysplasia (Karelian Bear Dog and Norwegian Elkhound type) Congenital myasthenic syndrome (Old Danish Pointer type) Glycogen storage disease IIIa GM1 Gangliosidosis (Shiba Inu type) Greyhound polyneuropathy Mucopolysaccharidosis I Myotonia congenita (Australian Cattle Dog type) Myotonia congenita (Schnauzer type) Pompe disease Vitamin D dependent rickets, type II (Pomeranian type) Alaskan Malamute polyneuropathy GM1 Gangliosidosis (Portuguese Water Dog type) Inherited myopathy of Great Danes Myostatin deficiency (Whippet and Longhaired Whippet type) Polyneuropathy (Leonberger and Saint Bernard type) Juvenile Laryngeal Paralysis and Polyneuropathy Neurologic Degenerative myelopathy Exercise-induced collapse GM2 Gangliosidosis (Poodle type) Sensory ataxic neuropathy Congenital myasthenic syndrome (Labrador Retriever type) Narcolepsy (Labrador Retriever type)
Neonatal encephalopathy with seizures Neuronal ceroid lipofuscinosis 4A Neuronal ceroid lipofuscinosis 5 Neuronal ceroid lipofuscinosis 6 Neuronal ceroid lipofuscinosis 8 (Australian Shepherd type) Alaskan Husky encephalopathy Benign familial juvenile epilepsy Canine multiple system degeneration (Chinese Crested type) Canine multiple system degeneration (Kerry Blue Terrier type) Cerebellar ataxia (Finnish Hound type) GM1 Gangliosidosis (Alaskan Husky type) Mucopolysaccharidosis IIIA (New Zealand Huntaway type) Neonatal cerebellar cortical degeneration Neuronal ceroid lipofuscinosis 1 Neuronal ceroid lipofuscinosis 2 Startle disease Adult-onset neuronal ceroid lipofuscinosis Congenital myasthenic syndrome (Old Danish Pointer type) Globoid cell leukodystrophy (Irish Setter type) Globoid cell leukodystrophy (Terrier type) GM1 Gangliosidosis (Shiba Inu type) Greyhound polyneuropathy Late onset ataxia Mucopolysaccharidosis I Myotonia congenita (Australian Cattle Dog type) Myotonia congenita (Schnauzer type) Narcolepsy (Doberman Pinscher type) Neuronal ceroid lipofuscinosis 10 Neuronal ceroid lipofuscinosis 8 (Setter type) Spinocerebellar ataxia Alaskan Malamute polyneuropathy
Episodic falling syndrome GM1 Gangliosidosis (Portuguese Water Dog type) GM2 Gangliosidosis (Japanese Chin type) L-2-hydroxyglutaric aciduria (Staffordshire Bull Terrier type) Mucopolysaccharidosis IIIA (Dachshund type) Narcolepsy (Dachshund type) Polyneuropathy (Leonberger and Saint Bernard type) Juvenile Laryngeal Paralysis and Polyneuropathy Neuromuscular Globoid cell leukodystrophy (Irish Setter type) Globoid cell leukodystrophy (Terrier type) Reproduction Primary ciliary dyskinesia Respiratory Primary ciliary dyskinesia Skin and Hair Anhidrotic ectodermal dysplasia Dystrophic epidermolysis bullosa Hereditary nasal parakeratosis Ichthyosis (Golden Retriever type) Ectodermal dysplasia
Renal cystadenocarcinoma and nodular dermatofibrosis Dry eye curly coat syndrome Epidermolytic hyperkeratosis Hereditary footpad hyperkeratosis (Irish Terrier and Kromfohrländer type) Urinary Tract Familial nephropathy (Cocker Spaniel type) Hyperuricosuria Renal cystadenocarcinoma and nodular dermatofibrosis Cystinuria (Australian Cattle Dog type) Cystinuria (Newfoundland type) Fanconi syndrome Hereditary nephritis (Samoyed type) Primary ciliary dyskinesia Cystinuria (Miniature Pinscher type) Familial nephropathy (English Springer Spaniel type) Persistent Müllerian duct syndrome Primary hyperoxaluria Carrier