De Blue Dachshunds

Parent health testing

• von Willebrand Disease III (vWD III), Van Den Ende-Gupta Syndrome (VDEGS), Trapped Neutrophil Syndrome, Cohen Syndrome (TNS), Stargardt Disease, Spondylocostal Dysostosis, Spinocerebellar Ataxia (SCA), Skeletal Dysplasia (SD2), Pyruvate Dehydrogenase Phosphatase 1 Deficiency (PDP1), Protein-Losing Nephropathy (PLN; NPHS1 Gene Variant), Cone-Rod Dystrophy 2 (crd2), American Pitbull Terrier Type, Cone-Rod Dystrophy 1 (crd1), American Staffordshire Terrier Type, PRA, Cone-Rod Dystrophy 4 (PRA-crd4), PRA, Rod-Cone Dysplasia 3 (rcd3), X-Linked Progressive Retinal Atrophy 2, X-Linked Progressive Retinal Atrophy 1, 2,8-Dihydroxyadenine (2,8-DHA) Urolithiasis, Early Onset Progressive Retinal Atrophy (EOPRA), PRA 2, Miniature Schnauzer - Type A, PRA, Cone-Rod Dystrophy 1 (PRA-crd1), Primary Open Angle Glaucoma and Primary Lens Luxation (POAG/PLL), Shar-Pei Type, Primary Open Angle Glaucoma, Basset Hound Type, Primary Open Angle Glaucoma (ADAMST10 Exon 17), Primary Lens Luxation (PLL), Primary Hyperoxaluria, Primary Ciliary Dyskenesia (Malamute Type) - Single Assay Test, Prekallikrein Deficiency, Fletcher Trait, Glycogen Storage Disease Type II or Pompe's Disease (GSD II), Polyneuropathy 2, Leonberger and Saint Bernard Type, Polyneuropathy 1, Leonberger and Saint Bernard Type, Mucopolysaccharidosis Type I (MPS I), Pituitary Dwarfism, Persistent Müllerian Duct Syndrome, Duchenne Muscular Dystrophy, Pembroke Welsh Corgi Type, P2RY12 Receptor Platelet Disorder, Osteogenesis Imperfecta (OI), Golden Retriever Type, Osteogenesis Imperfecta (OI), Dachshund Type, Osteogenesis Imperfecta (OI), Beagle Type, Oculocutaneous Albinism (Small Breed 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 4A (NCL4A), American Staffordshire Terrier Type, Neuronal Ceroid Lipofuscinosis 12 (NCL12), Australian Cattle Dog Type, Neuronal Ceroid Lipofuscinosis 1 (NCL1), Dachshund Type, Neuronal Ceroid Lipofuscinosis 2 (NCL2), Neuronal Ceroid Lipofuscinosis 1 (NCL1), Cane Corso Type, Neuronal Ceroid Lipofuscinosis 10 (NCL10), American Bulldog Type, Neuroaxonal Dystrophy (NAD), Spanish Water Dog Type, Neuroaxonal Dystrophy (NAD), Rottweiler Type, Neuroaxonal Dystrophy (NAD), Papillon Type, Neuroaxonal Dystrophy (NAD), Giant Schnauzer Type, Neuroaxonal Dystrophy NAD, Neonatal Encephalopathy with Seizures (NEwS), Neonatal Cortical Cerebellar Degeneration (NCCD), Neonatal Ataxia, Bandera's Disease, Narcolepsy, Labrador Retriever Type, Narcolepsy, Doberman Pinscher Type, Narcolepsy, Dachshund Type, Myotonia Congenita, Australian Cattle Dog Type, Myotubular Myopathy, Labrador Retriever Type, Myotonia Congenita, Schnauzer Type, Musladin-Leuke Syndrome (MLS), Duchenne Muscular Dystrophy, Golden Retriever Type, Multifocal Retinopathy 3 (CMR3), Multifocal Retinopathy 2 (CMR2), Multifocal Retinopathy 1 (CMR1), Mucopolysaccharidosis VII (MPS VII GUSB), Shepherd Type, Mucopolysaccharidosis VII (MPS VII), Brazilian Terrier Type, Mucopolysaccharidosis VII (MPS VII ARSB), German Shepherd Dog Type, Mucopolysaccharidosis Type VI (MPS VI), Mucopolysaccharidosis Type IIIB (MPS IIIB), Mucopolysaccharidosis IIIA (MPS IIIA), New Zealand Huntaway Type, Mucopolysaccharidosis IIIA (MPS IIIA), Dachshund Type, Microphthalmia Syndrome (PES), May-Hegglin Anomaly, Macular Corneal Dystrophy, MCD (CHST6), Lundehund Syndrome, Limb Girdle Muscular Dystrophy, Boston Terrier, Leukocyte Adhesion Deficiency, Type III, Leukocyte Adhesion Deficiency, Type I, Dental-skeletal-retinal anomaly (DSRA), Late Onset Ataxia, Spinocerebellar Ataxia (LOA, SCA), Laryngeal Paralysis (Bull Terrier Type) - Single Assay Test, Lagotto Storage Disease (LSD), Juvenile Myoclonic Epilepsy (JME), Juvenile Laryngeal Paralysis & Polyneuropathy (JLPP), Intestinal Cobalamin Malabsorption (IGS CUBN Exon 53), Border Collie Type, Inherited Myopathy in Great Danes (IMGD), Inflammatory Myopathy (Myositis), Ichthyosis, Great Dane Type, Ichthyosis, Golden Retriever Type 2, Ichthyosis, Golden Retriever Type 1, Ichthyosis, American Bulldog Type, Hypomyelination, Weimaraner Type, Hyperuricosuria (HUU), Hereditary Nephritis, Samoyed Type, Hereditary Nasal Parakeratosis (HNPK), Hereditary Footpad Hyperkeratosis, Hereditary (Juvenile) Cataracts (HC; JC), Australian Shepherd Type, Hereditary (Juvenile) Cataracts (HC; JC), Hereditary Ataxia, Cerebellar Ataxia, GM2 Gangliosidosis, Poodle Type, GM1 Gangliosidosis (GLB1), Shiba Inu Type, Gangliosidosis GM2, Japanese Chin Type, GM1 Gangliosidosis, Portuguese Water Dog Type, GM1 Gangliosidosis (HEXB), Shiba Inu Type, GM1 Gangliosidosis, Alaskan Husky Type, Glycogen Storage Disease Type VII, GSD VII, Glycogen Storage Disease Type IIIA, GSD IIIA, Glycogen Storage Disease Type IA, GSD IA, Glycogen Storage Disease Ia, Globoid Cell Leukodystrophy (GCL), Terrier Type, Globoid Cell Leukodystrophy (GCL), Irish Setter Type, Glaucoma (BCG), Border Collie Type, Glanzmann's Thrombasthenia, Otterhound Type, Glanzmann's Thrombasthenia, Great Pyrenees Type, Gall Bladder Mucocele Formation (Shetland Sheepdog Type), Fucosidosis, Familial Nephropathy, English Springer Spaniel Type, Familial Nephropathy, Cocker Spaniel Type, Factor IX Deficiency (G418E), Exercise Induced Collapse (EIC), Episodic Falling Syndrome (EFS), Epidermolytic Hyperkeratosis, Ehlers-Danlos Syndrome, Ectodermal Dysplasia, X-Linked (Shepherd Type), Ectodermal Dysplasia, X-Linked (Dachshund Type), Ectodermal Dysplasia, Chesapeake Bay Retriever Type, Early Retinal Degeneration, Early Adult Onset Deafness (EAOD), Dry Eye Curly Coat Syndrome (CKSID), Dilated Cardiomyopathy (Schnauzer Type), Dilated Cardiomyopathy 2 (DCM2), Dilated Cardiomyopathy 1 (DCM1), Dental Hypomineralization (DH), Degenerative Myelopathy Early-Onset Risk Modifier, Pembroke Welsh Corgi Type, Degenerative Myelopathy (DM; SOD1A), Degenerative Myelopathy (DM; SOD1B), Bernese Mountain Dog Type, Deafness and Vestibular Dysfunction, Doberman Pinscher Type, Dandy-Walker-like Malformation (DWLM), Eurasier Type, Cystinuria Type 3 (Variant 3), Bulldog Type Risk Factor, Cystinuria Type 3 (Variant 1 & 2), Bulldog Type Risk Factor, Cystinuria Type 3, French Bulldog Type Risk Factor, Cystinuria Type 1A, Newfoundland Type, Cystinuria Type 1, Newfoundland (PennGen), Cystinuria Type 1A, Labrador Retriever Type, Cyclic Neutropenia, Grey Collie Syndrome (CN), Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC), 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 Methemoglobinemia, Pomeranian Type, Congenital Macrothrombocytopenia, Alexander Disease, Congenital Hypothyroidism with Goiter, Terrier Type (CHG), Cone Degeneration, Labrador Retriever Type, Cone Degeneration, German Shorthaired Pointer Type, Cone Degeneration, German Shepherd Dog Type, Cone Degeneration, Collie Eye Anomaly (CEA), Cerebellar Degeneration, Cerebellar Cortical Degeneration (CCD), Cerebellar Ataxia 2, Belgian Shepherd Type, Cerebellar Ataxia, Finnish Hound Type, Centronuclear Myopathy (CNM), Catalase Deficiency, Cardiomyopathy and Juvenile Mortality (YARS2), Canine Scott Syndrome (CSS), Canine Multiple System Degeneration, Kerry Blue Terrier Type, Canine Multiple System Degeneration (Chinese Crested Type), Bernard-Soulier Syndrome, Cocker Spaniel Type, Benign Familial Juvenile Epilepsy (BFJE), Ataxia, Norwegian Buhund Type, Amelogenesis Imperfecta (AI), Akita Type, Adult Paroxysmal Dyskinesia, Acute Respiratory Distress Syndrome, Dalmatian Type, Acral Mutilation Syndrome (AMS)

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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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