Royal Litter

Parent health testing

• 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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• DNA Disease Panel, von Willebrand Disease III (vWD III), Ullrich Congenital Muscular Dystrophy, Trapped Neutrophil Syndrome, Cohen Syndrome (TNS), Thrombopathia, American Eskimo Dog Type, Stargardt Disease, Spongy Degeneration with Cerebellar Ataxia (SDCA2) mutation originally found in Belgian Shepherd Dog, Spinocerebellar Ataxia with Myokymia (KCNJ10), Spinocerebellar Ataxia (SCA), Skeletal Dysplasia (SD2), Shar-Pei Autoinflammatory Disease, 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), Labrador Retriever Type, Protein-Losing Nephropathy (PLN; NPHS1 Gene Variant), Progressive Retinal Atrophy (PRA), Generalized, Primary Open Angle Glaucoma (ADAMST17 Exon 11), Primary Lens Luxation (PLL), Primary Hyperoxaluria, Primary Ciliary Dyskinesia, Kartagner Syndrome (PCD), Prekallikrein Deficiency, Fletcher Trait, Polycystic Kidney Disease (PKD), Pituitary Dwarfism, Persistent Müllerian Duct Syndrome, P2RY12 Receptor Platelet Disorder, Osteogenesis Imperfecta (OI), Golden Retriever Type, Osteochondrodysplasia, Miniature Poodle Type, Oculocutaneous Albinism, Neuronal Ceroid Lipofuscinosis, Tibetan Terrier Type, Neuronal Ceroid Lipofuscinosis 10 (NCL10), American Bulldog Type, Neuronal Ceroid Lipofuscinosis 6 (NCL 6), Neuronal Ceroid Lipofuscinosis 5 (NCL5), Golden Retriever Type, Neuronal Ceroid Lipofuscinosis 1 (NCL1), Dachshund Type, Neuroaxonal Dystrophy NAD, Nemaline Myopathy, American Bulldog Type, Narcolepsy, Dachshund Type, Narcolepsy, Labrador Retriever Type, Myotonia Congenita, Schnauzer Type, Myotonia Congenita, Australian Cattle Dog Type, Musladin-Leuke Syndrome (MLS), Muscular Dystrophy, Ullrich-type; mutation originally found in Landseer, Multiple Drug Sensitivity (MDR1), Mucopolysaccharidosis IIIA (MPS IIIA), New Zealand Huntaway 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), Lethal Acrodermatitis (LAD), Bull Terrier Type, 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), Inherited Myopathy in Great Danes (IMGD), Inflammatory Myopathy (Myositis), Ichthyosis, German Shepherd Type, Hypomyelination, Weimaraner Type, Hypocatalasia, Hereditary Vitamin D-Resistant Rickets (HVDRR), Hereditary Nasal Parakeratosis (HNPK), Hereditary Footpad Hyperkeratosis, 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, 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, Great Pyrenees Type, Fetal-Onset Neonatal Neuroaxonal Dystrophy (MFN1), Fanconi Syndrome, Familial Nephropathy, English Springer Spaniel Type, Factor XI Deficiency, Factor VII Deficiency, Exercise Induced Collapse (EIC), Episodic Falling Syndrome (EFS), Ehlers-Danlos Syndrome, Early Adult Onset Deafness (EAOD), Dystrophic Epidermolysis Bullosa, Dry Eye Curly Coat Syndrome (CKSID), Dilated Cardiomyopathy 2 (DCM2), Dilated Cardiomyopathy 1 (DCM1), Diffuse cystic renal dysplasia and hepatic fibrosis, Dental-skeletal-retinal anomaly (DSRA), Degenerative Myelopathy (DM; SOD1A), Deafness and Vestibular Dysfunction, Doberman Pinscher Type, Day Blindness, Achromatopsia, Cystinuria Type II-A, Australian Cattle Dog Type, Cystinuria Type II-B, Miniature Pinscher Type, Cystinuria Type 1, Newfoundland (PennGen), Craniomandibular Osteopathy (CMO), Copper Toxicosis, Labrador Retriever ATP7A, 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 (CHG), Compliment 3 Deficiency (C3), Collie Eye Anomaly (CEA), Cleft Palate (DLX6), Chondrodysplasia/Dwarfism, Centronuclear Myopathy (CNM), Canine Multifocal Retinopathy (cmr3; BEST1 Exon 10 SNP), Bernard-Soulier Syndrome, Cocker Spaniel Type, Bald Thigh Syndrome (IGFBP5), Alexander Disease, Acral Mutilation Syndrome (AMS), 2,8-Dihydroxyadenine (2,8-DHA) Urolithiasis

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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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