Low and Slow Bassets

Parent health testing

• Hip Dysplasia

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  Hip testing reduces the chance of passing down hip dysplasia, which is primarily found in large breed dogs and can cause hip pain and the eventual loss of the function of the hip joint.

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• Kidney Disease (UPCR), Ichthyosis, Golden Retriever Type

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  A breeder may perform additional tests on their dogs that do not fall into these general categories. These tests may be more uncommon or very specific to a particular breed.

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• Siberian Husky Shaking Puppy Syndrome, Type 1 (SPS1), Primary Hyperparathyroidism (PHPT), Primary Closed Angle Glaucoma (PCAG), Italian Greyhound Type, Multiple System Degeneration, Chinese Crested Type, Ichthyosis, Golden Retriever Type 2, Ichthyosis, Golden Retriever Type 1, Hereditary Footpad Hyperkeratosis, DNA Disease Panel, Congenital Myasthenic Syndrome (CMS), Spanish Water Dog Type, Chondrodystrophy (CDDY and IVDD Risk) with or without Chondrodysplasia (CDPA), Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC), Adult Onset Neuropathy (AON), 2,8-Dihydroxyadenine (2,8-DHA) Urolithiasis, Primary Open Angle Glaucoma, Petit Basset Griffon Vendeen Type, Primary Open Angle Glaucoma, Basset Hound Type, Animal Genetics Panel, Genetic Diversity Test, DNA Coat/Trait Panel, Full Embark Panel, Severe Combined Immunodeficiency Disease, X-Linked (XSCID), Corgi Type, X-Linked Myotubular Myopathy, von Willebrand Disease III (vWD III), Kooikerhondje Type, von Willebrand Disease III (vWD III), Shetland Sheepdog Type, von Willebrand Disease II (vWD II), von Willebrand Disease I (vWD I), von Willebrand Disease III (vWD III), von Willebrand Disease III (vWD III), Scottish Terrier Type, Deafness and Vestibular Dysfunction, Doberman Pinscher Type, Ullrich Congenital Muscular Dystrophy, Muscular Dystrophy, Ullrich-type; mutation originally found in Landseer, Trapped Neutrophil Syndrome, Cohen Syndrome (TNS), Thrombopathia (RASGRP2 Exon 8), Thrombopathia, American Eskimo Dog Type, Stargardt Disease, Spongy Degeneration with Cerebellar Ataxia (SDCA2) mutation originally found in Belgian Shepherd Dog, Spongy Degeneration with Cerebellar Ataxia (SDCA1) mutation originally found in Belgian Shepherd Dog and Malinois, Spinocerebellar Ataxia with Myokymia (KCNJ10), Spinocerebellar Ataxia (SCA), Skeletal Dysplasia (SD2), Shar-Pei Autoinflammatory Disease, X-Linked Tremors, Shaking Puppy Syndrome (SPS), Severe Combined Immunodeficiency Disease, Frisian Water Dog Type, Severe Combined Immunodeficiency Disease, Terrier Type, Sensory Neuropathy, Border Collie Type (SN), Retinal Dysplasia/Oculoskeletal Dysplasia 1 (RD OSD), Renal Cystadenocarcinoma and Nodular Dermatofibrosis (RCND), Recurrent Inflammatory Pulmonary (Collie Type) - Single Assay Test, Pyruvate Kinase Deficiency (PKD), Pug Type, Pyruvate Kinase Deficiency (PKD), Labrador Retriever Type, Pyruvate Kinase Deficiency (PKD), Basenji Type , Pyruvate Kinase Deficiency (PKD), Terrier Type, Pyruvate Kinase Deficiency (PKD), Beagle Type, Pyruvate Kinase Deficiency, Basenji Type (PKD), Pyruvate Dehydrogenase Phosphatase 1 Deficiency (PDP1), Protein-Losing Nephropathy (PLN; NPHS1 Gene Variant), X-Linked Progressive Retinal Atrophy 2, X-Linked Progressive Retinal Atrophy 1, X-Linked Progressive Retinal Atrophy (XL-PRA), Early Onset Progressive Retinal Atrophy (EOPRA), Progressive Retinal Atrophy, mutation originally found in Swedish Valhund, Primary Open Angle Glaucoma and Primary Lens Luxation (POAG/PLL), Shar-Pei Type, Primary Open Angle Glaucoma (ADAMST10 Exon 9), Primary Open Angle Glaucoma (ADAMST10 Exon 17), Primary Open Angle Glaucoma (ADAMST17 Exon 11), Primary Lens Luxation (PLL), Primary Hyperoxaluria, Primary Ciliary Dyskinesia, Kartagner Syndrome (PCD), Primary Ciliary Dyskenesia (Malamute Type) - Single Assay Test, Prekallikrein Deficiency, Fletcher Trait, Glycogen Storage Disease Type II or Pompe's Disease (GSD II), Polycystic Kidney Disease (PKD), Canine Scott Syndrome (CSS), Pituitary Dwarfism, Persistent Müllerian Duct Syndrome, Adult Paroxysmal Dyskinesia, Focal Non-Epidermolytic Palmoplantar Keratoderma, Pachyonychia Congenita (KRT16), P2RY12 Receptor Platelet Disorder, Osteogenesis Imperfecta (OI), Golden Retriever Type, Osteogenesis Imperfecta (OI), Dachshund Type, Osteogenesis Imperfecta (OI), Beagle Type, Osteochondrodysplasia, Miniature Poodle Type, Retinal Dysplasia/Oculoskeletal Dysplasia 2, Oculocutaneous Albinism (Small Breed Type), Oculocutaneous Albinism, Neuronal Ceroid Lipofuscinosis, Saluki Type, Neuronal Ceroid Lipofuscinosis 8 (NCL8), Setter Type, Neuronal Ceroid Lipofuscinosis 8 (NCL8), Australian Shepherd Type, Neuronal Ceroid Lipofuscinosis 7 (NCL7), Neuronal Ceroid Lipofuscinosis 6 (NCL 6), Neuronal Ceroid Lipofuscinosis 5 (NCL5), Golden Retriever Type, Neuronal Ceroid Lipofuscinosis 5 (NCL5), Border Collie Type, Neuronal Ceroid Lipofuscinosis 2 (NCL2), Neuronal Ceroid Lipofuscinosis 1 (NCL1), Dachshund Type, Neuronal Ceroid Lipofuscinosis 10 (NCL10), American Bulldog Type, Neuroaxonal Dystrophy (NAD), Spanish Water Dog Type, Neuroaxonal Dystrophy (NAD), Rottweiler Type, Neuroaxonal Dystrophy NAD, Neonatal Encephalopathy with Seizures (NEwS), Neonatal Cortical Cerebellar Degeneration (NCCD), Nemaline Myopathy, American Bulldog Type, Narcolepsy, Labrador Retriever Type, Narcolepsy, Doberman Pinscher Type, Narcolepsy, Dachshund Type, Myotonia Congenita, Schnauzer Type, Myotonia Congenita, Australian Cattle Dog Type, Musladin-Leuke Syndrome (MLS), Duchenne Muscular Dystrophy, Golden Retriever Type, Cavalier King Charles Spaniel Muscular Dystrophy (CKCS-MD), Multiple Drug Sensitivity (MDR1), Mucopolysaccharidosis VII (MPS VII), Brazilian Terrier Type, Mucopolysaccharidosis VII (MPS VII GUSB), Shepherd Type, Mucopolysaccharidosis VII (MPS VII ARSB), German Shepherd Dog Type, Mucopolysaccharidosis Type VI (MPS VI), Mucopolysaccharidosis IIIA (MPS IIIA), New Zealand Huntaway Type, Mucopolysaccharidosis Type IIIB (MPS IIIB), Mucopolysaccharidosis IIIA (MPS IIIA), Dachshund Type, Microphthalmia Syndrome (PES), Methemoglobinemia, Medium-Chain Acyl-CoA Dehydrogenase (MCAD) Deficiency, May-Hegglin Anomaly, Malignant Hyperthermia (MH), Macular Corneal Dystrophy, MCD (CHST6), Lundehund Syndrome, Long QT Syndrome, Limb Girdle Muscular Dystrophy, Boston Terrier, Ligneous Membranitis, LM (PLG), Globoid Cell Leukodystrophy (GCL), Irish Setter Type, Lethal Acrodermatitis (LAD), Bull Terrier Type, Polyneuropathy 2, Leonberger and Saint Bernard Type, Polyneuropathy 1, Leonberger and Saint Bernard Type, Neuronal Ceroid Lipofuscinosis 12 (NCL12), Australian Cattle Dog Type, Late Onset Ataxia, Spinocerebellar Ataxia (LOA, SCA), Laryngeal Paralysis (Bull Terrier Type) - Single Assay Test, Lagotto Storage Disease (LSD), L-2-Hydroxyglutaric Aciduria (L2HGA), Staffordshire Bull Terrier Type, Juvenile Myoclonic Epilepsy (JME), Juvenile Laryngeal Paralysis & Polyneuropathy (JLPP), Benign Familial Juvenile Epilepsy (BFJE), Epidermolysis Bullosa (Eurasier), Intestinal Cobalamin Malabsorption (IGS), Komondor Type, Inherited Myopathy in Great Danes (IMGD), Inflammatory Myopathy (Myositis), Epidermolytic Hyperkeratosis, Ichthyosis (KRY10), Ichthyosis, Great Dane Type, Ichthyosis, German Shepherd Type, Ichthyosis, American Bulldog Type, Hypomyelination, Weimaraner Type, Hypocatalasia, Hereditary Vitamin D-Resistant Rickets (HVDRR), Hereditary Nasal Parakeratosis (HNPK), Hereditary Footpad Hyperkeratosis (DSG1), Hereditary Footpad Hyperkeratosis (FAM83G), Hereditary (Juvenile) Cataracts (HC; JC), Australian Shepherd Type, Cerebellar Degeneration, Gondysgenesis and Glaucoma, Border Collie Type, Progressive Retinal Atrophy (PRA), Generalized, GM2 Gangliosidosis, Poodle Type, Gangliosidosis GM2, Japanese Chin Type, GM1 Gangliosidosis (GLB1), Shiba Inu Type, GM1 Gangliosidosis, Portuguese Water Dog Type, GM1 Gangliosidosis, Alaskan Husky Type, Glycogen Storage Disease Type VII, GSD VII, Glycogen Storage Disease Type VII, Phosphofructokinase Deficiency, PFK Deficiency (PFKM Wachtelhund Variant), Glycogen Storage Disease Type IIIA, GSD IIIA, Glycogen Storage Disease Type IA, GSD IA, Globoid Cell Leukodystrophy (GCL), Terrier Type, Glanzmann's Thrombasthenia, Otterhound Type, Glanzmann's Thrombasthenia, Great Pyrenees Type, Fetal-Onset Neonatal Neuroaxonal Dystrophy (MFN1), Fanconi Syndrome, Familial Nephropathy, English Springer Spaniel Type, Familial Nephropathy, Cocker Spaniel Type, Factor XI Deficiency, Factor VII Deficiency, Exercise Induced Collapse (EIC), Episodic Falling Syndrome (EFS), Familial Enamel Hypoplasia (FEH), Parson Russell Terrier Type, Familial Enamel Hypoplasia (FEH), Italian Greyhound Type, Ehlers-Danlos Syndrome, Hereditary Ataxia, Cerebellar Ataxia, Early Adult Onset Deafness (EAOD), Dystrophic Epidermolysis Bullosa, Dry Eye Curly Coat Syndrome (CKSID), Chondrodysplasia/Dwarfism, Dilated Cardiomyopathy 2 (DCM2), Dilated Cardiomyopathy (Schnauzer Type), Dilated Cardiomyopathy 1 (DCM1), Diffuse cystic renal dysplasia and hepatic fibrosis, Dental-skeletal-retinal anomaly (DSRA), Deafness and Vestibular Syndrome of Dobermans, DVDobs, DINGS, Day Blindness, Achromatopsia, Cystinuria Type II-B, Miniature Pinscher Type, Cystinuria Type II-A, Australian Cattle Dog Type, Cystinuria Type 1A, Newfoundland Type, Congenital Stationary Night Blindness (CSNB), Congenital Myasthenic Syndrome (CMS), Old Danish Pointer Type, Congenital Myasthenic Syndrome (CMS), Labrador Retriever Type, Congenital Myasthenic Syndrome (CMS), Jack Russell Terrier Type, Congenital Macrothrombocytopenia, Congenital Hypothyroidism with Goiter, Terrier Type (CHG), Congenital Hypothyroidism with Goiter (CHG), Compliment 3 Deficiency (C3), Collie Eye Anomaly (CEA), Intestinal Cobalamin Malabsorption (IGS), Australian Shepherd Type, Cleft Palate (DLX6), Cleft Palate (ADAMTS20), Chondrodystrophy, Norwegian Elkhound and Karelian Bear Dog Variant (ITGA10), Bernard-Soulier Syndrome, Cocker Spaniel Type, Polyneuropathy (NDRG1), Alaskan Malamute Type, Encephalopathy, Alaskan Husky Type, Centronuclear Myopathy (CNM), Cardiomyopathy and Juvenile Mortality (YARS2), Canine Multiple System Degeneration, Kerry Blue Terrier Type, Canine Multiple System Degeneration (Chinese Crested Type), Multifocal Retinopathy 3 (CMR3), Multifocal Retinopathy 2 (CMR2), Multifocal Retinopathy 1 (CMR1), Leukocyte Adhesion Deficiency, Type III, Leukocyte Adhesion Deficiency, Type I, Fucosidosis, Hereditary Elliptocytosis, Elliptocytosis, Muscular Hypertrophy/Myostatin Deficiency, Bully Whippet Syndrome (Double Muscling), Bald Thigh Syndrome (IGFBP5), Alanine Aminotransferase Activity, Alexander Disease, Acral Mutilation Syndrome (AMS), Severe Combined Immunodeficiency Disease, X-Linked, Basset Hound Type (XSCID), Craniomandibular Osteopathy (CMO), Chondrodystrophy and IVDD Risk (CDDY-IVDD), Thrombopathia, Basset Hound Type, Degenerative Myelopathy (DM; SOD1A)

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  Genetic testing reduces the chance of passing down a wide variety of hereditary diseases of differing prevalence and severity such as Progressive Retinal Atrophy (an eye disease) and Von Willebrand's Disease (a blood disease).

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