Duryea Cavapoos

Parent health testing

• Severe Combined Immunodeficiency Disease, X-Linked, Basset Hound Type (XSCID), Severe Combined Immunodeficiency Disease, X-Linked (XSCID), Corgi Type, von Willebrand Disease III (vWD III), Scottish Terrier Type, von Willebrand Disease III (vWD III), von Willebrand Disease III (vWD III), Shetland Sheepdog Type, von Willebrand Disease II (vWD II), von Willebrand Disease I (vWD I), Muscular Dystrophy, Ullrich-type; mutation originally found in Landseer, Ullrich Congenital Muscular Dystrophy, Trapped Neutrophil Syndrome, Cohen Syndrome (TNS), Thrombopathia, Basset Hound Type, Thrombopathia, Newfoundland Type, Thrombopathia, American Eskimo Dog Type, Succinic Semialdehyde Dehydrogenase (SSADH) Deficiency, Stargardt Disease, 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, Siberian Husky Shaking Puppy Syndrome, Type 1 (SPS1), Severe Combined Immunodeficiency Disease, Terrier Type, Sensory Neuropathy, Border Collie Type (SN), Renal Cystadenocarcinoma and Nodular Dermatofibrosis (RCND), Recurrent Inflammatory Pulmonary (Collie Type) - Single Assay Test, Pyruvate Kinase Deficiency (PKD), Basenji Type , Pyruvate Kinase Deficiency (PKD), Labrador Retriever Type, Pyruvate Kinase Deficiency (PKD), Pug Type, Pyruvate Kinase Deficiency (PKD), Beagle Type, Pyruvate Kinase Deficiency (PKD), Terrier Type, Pyruvate Dehydrogenase Phosphatase 1 Deficiency (PDP1), Protein-Losing Nephropathy (PLN; NPHS1 Gene Variant), Progressive Retinal Atrophy (PRA), Generalized, 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), Pituitary Dwarfism, Adult Paroxysmal Dyskinesia, Focal Non-Epidermolytic Palmoplantar Keratoderma, Pachyonychia Congenita (KRT16), P2RY12 Receptor Platelet Disorder, Osteogenesis Imperfecta (OI), Beagle Type, Osteogenesis Imperfecta (OI), Dachshund Type, Osteogenesis Imperfecta (OI), Golden Retriever Type, Osteochondrodysplasia, Miniature Poodle Type, Retinal Dysplasia/Oculoskeletal Dysplasia 2, Oculocutaneous Albinism (Small Breed Type), Neuronal Ceroid Lipofuscinosis 8 (NCL8), Setter Type, Neuronal Ceroid Lipofuscinosis 8 (NCL8), Australian Shepherd Type, Neuronal Ceroid Lipofuscinosis, Saluki Type, Neuronal Ceroid Lipofuscinosis 7 (NCL7), Neuronal Ceroid Lipofuscinosis 6 (NCL 6), Neuronal Ceroid Lipofuscinosis 5 (NCL5), Border Collie Type, Neuronal Ceroid Lipofuscinosis 5 (NCL5), Golden Retriever Type, Neuronal Ceroid Lipofuscinosis 2 (NCL2), Neuronal Ceroid Lipofuscinosis 10 (NCL10), American Bulldog Type, Neuronal Ceroid Lipofuscinosis 1 (NCL1), Dachshund Type, Neuroaxonal Dystrophy (NAD), Spanish Water Dog Type, Neuroaxonal Dystrophy (NAD), Rottweiler Type, Neonatal Encephalopathy with Seizures (NEwS), Neonatal Cortical Cerebellar Degeneration (NCCD), Nemaline Myopathy, American Bulldog Type, Narcolepsy, Doberman Pinscher Type, Narcolepsy, Labrador Retriever Type, Narcolepsy, Dachshund Type, Myotonia Congenita, Schnauzer Type, Myotonia Congenita, Australian Cattle Dog Type, Musladin-Leuke Syndrome (MLS), Cavalier King Charles Spaniel Muscular Dystrophy (CKCS-MD), Duchenne Muscular Dystrophy, Golden Retriever Type, Mucopolysaccharidosis VII (MPS VII), Brazilian Terrier Type, Mucopolysaccharidosis Type VI (MPS VI), Mucopolysaccharidosis IIIA (MPS IIIA), Dachshund Type, Mucopolysaccharidosis IIIA (MPS IIIA), New Zealand Huntaway Type, Mucopolysaccharidosis Type IIIB (MPS IIIB), Microphthalmia Syndrome (PES), Congenital Methemoglobinemia, Pomeranian Type, Multiple Drug Sensitivity (MDR1), 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), 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), Inherited Myopathy in Great Danes (IMGD), Inflammatory Myopathy (Myositis), Ichthyosis, Golden Retriever Type, Ichthyosis, Great Dane Type, Ichthyosis, American Bulldog Type, Hypomyelination, Weimaraner Type, Hypocatalasia, Hereditary Vitamin D-Resistant Rickets (HVDRR), Hereditary Nasal Parakeratosis (HNPK), Hereditary Footpad Hyperkeratosis (FAM83G), Hereditary Footpad Hyperkeratosis (DSG1), Hereditary Ataxia, Cerebellar Ataxia, GM2 Gangliosidosis, Poodle Type, GM1 Gangliosidosis (GLB1), Shiba Inu Type, GM1 Gangliosidosis, Alaskan Husky Type, GM1 Gangliosidosis, Portuguese Water Dog 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), Familial Enamel Hypoplasia (FEH), Italian Greyhound Type, Familial Enamel Hypoplasia (FEH), Parson Russell Terrier Type, Ehlers-Danlos Syndrome, Cerebellar Ataxia, Finnish Hound Type, Early Adult Onset Deafness (EAOD), Dystrophic Epidermolysis Bullosa, Dry Eye Curly Coat Syndrome (CKSID), Dilated Cardiomyopathy (Schnauzer Type), Dilated Cardiomyopathy 2 (DCM2), Dilated Cardiomyopathy 1 (DCM1), Diffuse cystic renal dysplasia and hepatic fibrosis, Deafness and Vestibular Dysfunction, Doberman Pinscher Type, Day Blindness, Achromatopsia, Cystinuria Type II-B, Miniature Pinscher Type, Cystinuria Type II-A, Australian Cattle Dog Type, Cystinuria Type 1A, Newfoundland Type, Craniomandibular Osteopathy (CMO), 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), Compliment 3 Deficiency (C3), Collie Eye Anomaly (CEA), Intestinal Cobalamin Malabsorption (IGS CUBN Exon 53), Border Collie Type, Intestinal Cobalamin Malabsorption (IGS CUBN Exon 8), Border Collie Type, Cleft Palate (DLX6), Cleft Palate (ADAMTS20), Chondrodystrophy, Norwegian Elkhound and Karelian Bear Dog Variant (ITGA10), Cardiomyopathy and Juvenile Mortality (YARS2), Canine Multiple System Degeneration, Kerry Blue Terrier Type, Canine Multiple System Degeneration (Chinese Crested Type), Multifocal Retinopathy 2 (CMR2), Multifocal Retinopathy 1 (CMR1), Canine Multifocal Retinopathy (cmr3; BEST1 Exon 10 SNP), Muscular Hypertrophy/Myostatin Deficiency, Bully Whippet Syndrome (Double Muscling), Bald Thigh Syndrome (IGFBP5), X-Linked Anhidrotic Ectodermal Dysplasia, Dachshund type, Alexander Disease, Polyneuropathy (NDRG1), Alaskan Malamute Type, Encephalopathy, Alaskan Husky 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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