Jewells Poodles

Parent health testing

Miniature Poodle

Moyen Poodle

• Protein-Losing Nephropathy (PLN; NPHS1 Gene Variant), Progressive Retinal Atrophy (PRA), Generalized, Primary Lens Luxation (PLL), Primary Hyperoxaluria, Primary Ciliary Dyskinesia, Kartagner Syndrome (PCD), Polyneuropathy with Ocular Abnormalities and Neuronal Vacuolation, Polyneuropathy 2, Leonberger and Saint Bernard Type, Polyneuropathy 1, Leonberger and Saint Bernard Type, Duchenne Muscular Dystrophy, Pembroke Welsh Corgi Type, Persistent Müllerian Duct Syndrome, Pituitary Dwarfism, Neuroaxonal Dystrophy (NAD), Rottweiler Type, Neuroaxonal Dystrophy (NAD), Papillon Type, Neuroaxonal Dystrophy (NAD), Giant Schnauzer Type, Neonatal Cortical Cerebellar Degeneration (NCCD), Neonatal Ataxia, Bandera's Disease, Narcolepsy, Labrador Retriever Type, Narcolepsy, Doberman Pinscher Type, Narcolepsy, Dachshund Type, Myotonia Congenita, Schnauzer Type, Myotubular Myopathy 1, Rottweiler Type, Myotonia Congenita, Australian Cattle Dog Type, Muscular Hypertrophy/Myostatin Deficiency, Bully Whippet Syndrome (Double Muscling), Musladin-Leuke Syndrome (MLS), Multiple Drug Sensitivity (MDR1), Mucopolysaccharidosis VII (MPS VII ARSB), German Shepherd Dog Type, Mucopolysaccharidosis VII (MPS VII), Brazilian Terrier 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, Mucopolysaccharidosis Type I (MPS I), Microphthalmia Syndrome (PES), May-Hegglin Anomaly, Lundehund Syndrome, Limb Girdle Muscular Dystrophy, Boston Terrier, Ligneous Membranitis, LM (PLG), Leukocyte Adhesion Deficiency, Type III, Leukocyte Adhesion Deficiency, Type I, Lethal Acrodermatitis (LAD), Bull Terrier 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), Yorkshire Terrier Type, L-2-Hydroxyglutaric Aciduria (L2HGA), Staffordshire Bull Terrier Type, Juvenile Myoclonic Epilepsy (JME), Epidermolysis Bullosa (Eurasier), 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 1, Ichthyosis, American Bulldog Type, Hyperuricosuria (HUU), Primary Hyperparathyroidism (PHPT), 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, Polyneuropathy, Greyhound Type (NDRG1), Juvenile Laryngeal Paralysis & Polyneuropathy (JLPP), Gangliosidosis GM2, Japanese Chin Type, GM1 Gangliosidosis, Portuguese Water Dog Type, GM1 Gangliosidosis, Alaskan Husky Type, Glycogen Storage Disease Type IIIA, GSD IIIA, 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, Exercise Induced Collapse (EIC), Episodic Falling Syndrome (EFS), Epidermolytic Hyperkeratosis, Elliptocytosis, Ehlers-Danlos Syndrome, Ectodermal Dysplasia, X-Linked (Shepherd Type), Ectodermal Dysplasia, X-Linked (Dachshund Type), Ectodermal Dysplasia, Chesapeake Bay Retriever Type, Early Retinal Degeneration, Dystrophic Epidermolysis Bullosa, Dry Eye Curly Coat Syndrome (CKSID), Dilated Cardiomyopathy (Schnauzer Type), Diffuse cystic renal dysplasia and hepatic fibrosis, Deafness and Vestibular Dysfunction, Doberman Pinscher Type, Dandy-Walker-like Malformation (DWLM), Eurasier Type, Cystinuria Type 3, French Bulldog Type Risk Factor, Cystinuria Type 1, Newfoundland (PennGen), Cystinuria Type II-B, Miniature Pinscher Type, Cystinuria Type 1A, Labrador Retriever Type, Cystinuria Type II-A, Australian Cattle Dog Type, Cyclic Neutropenia, Grey Collie Syndrome (CN), 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, Methemoglobinemia, Macrothrombocytopenia, Cairn and Norfolk Terrier Type, 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), Chondrodystrophy, Norwegian Elkhound and Karelian Bear Dog Variant (ITGA10), Cerebellar Cortical Degeneration (CCD), Cerebellar Ataxia 2, Belgian Shepherd Type, Cerebellar Ataxia, Finnish Hound Type, Centronuclear Myopathy (CNM), Cardiomyopathy and Juvenile Mortality (YARS2), Canine Scott Syndrome (CSS), Canine Multiple System Degeneration, Kerry Blue Terrier Type, Bernard-Soulier Syndrome, Cocker Spaniel Type, Benign Familial Juvenile Epilepsy (BFJE), Ataxia, Norwegian Buhund Type, Amelogenesis Imperfecta (AI), Italian Greyhound Type, Polyneuropathy (NDRG1), Alaskan Malamute Type, Encephalopathy, Alaskan Husky Type, Adult Paroxysmal Dyskinesia, Acute Respiratory Distress Syndrome, Dalmatian Type, Acral Mutilation Syndrome (AMS), Chondrodystrophy (CDDY and IVDD Risk) with or without Chondrodysplasia (CDPA), Brachycephaly, Progressive Retinal Atrophy, mutation originally found in Swedish Valhund, Osteochondrodysplasia, Miniature Poodle Type, Neonatal Encephalopathy with Seizures (NEwS), GM2 Gangliosidosis, Poodle Type, Degenerative Myelopathy (DM; SOD1A), Agouti DNA Test

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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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