Elysian Border Collies, LLC.

Parent health testing

• Ichthyosis, Golden Retriever Type

  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.

• Shar-Pei Autoinflammatory Disease, Hereditary Footpad Hyperkeratosis (FAM83G), Lethal Acrodermatitis (LAD), Bull Terrier Type, Ehlers-Danlos Syndrome, Hereditary Nasal Parakeratosis (HNPK), Focal Non-Epidermolytic Palmoplantar Keratoderma, Pachyonychia Congenita (KRT16), Bald Thigh Syndrome (IGFBP5), Musladin-Leuke Syndrome (MLS), Ectodermal Dysplasia, Chesapeake Bay Retriever Type, Epidermolysis Bullosa (Eurasier), Hereditary Footpad Hyperkeratosis (DSG1), Hereditary Footpad Hyperkeratosis, Oculocutaneous Albinism (Small Breed Type), Dystrophic Epidermolysis Bullosa, Ichthyosis (KRY10), Ichthyosis, American Bulldog Type, Ichthyosis, Golden Retriever Type 1, Gangliosidosis GM2, Japanese Chin Type, Glycogen Storage Disease Type II or Pompe's Disease (GSD II), Mucopolysaccharidosis VII (MPS VII ARSB), German Shepherd Dog Type, Neuronal Ceroid Lipofuscinosis 4A (NCL4A), American Staffordshire Terrier Type, Neuronal Ceroid Lipofuscinosis 1 (NCL1), Dachshund Type, Neuronal Ceroid Lipofuscinosis 1 (NCL1), Cane Corso Type, Neuronal Ceroid Lipofuscinosis 8 (NCL8), Setter Type, Neuronal Ceroid Lipofuscinosis 8 (NCL8), Australian Shepherd Type, GM2 Gangliosidosis, Poodle Type, Neuronal Ceroid Lipofuscinosis 7 (NCL7), Glycogen Storage Disease Type IIIA, GSD IIIA, Gall Bladder Mucocele Formation (Shetland Sheepdog Type), Late Onset Ataxia, Spinocerebellar Ataxia (LOA, SCA), Neuronal Ceroid Lipofuscinosis 12 (NCL12), Australian Cattle Dog Type, Renal Cystadenocarcinoma and Nodular Dermatofibrosis (RCND), Neuronal Ceroid Lipofuscinosis 10 (NCL10), American Bulldog Type, Neuronal Ceroid Lipofuscinosis 6 (NCL 6), Mucopolysaccharidosis IIIA (MPS IIIA), New Zealand Huntaway Type, Glycogen Storage Disease Type VII, Phosphofructokinase Deficiency, PFK Deficiency (PFKM Wachtelhund Variant), Neuronal Ceroid Lipofuscinosis 5 (NCL5), Golden Retriever Type, Glycogen Storage Disease Type IA, GSD IA, Glycogen Storage Disease Ia, Glycogen Storage Disease Type VII, GSD VII, von Willebrand Disease III (vWD III), Shetland Sheepdog Type, Phosphofructokinase Deficiency (PFK), Dry Eye Curly Coat Syndrome (CKSID), Lagotto Storage Disease (LSD), GM1 Gangliosidosis, Alaskan Husky Type, Fucosidosis, Mucopolysaccharidosis VII (MPS VII GUSB), Shepherd Type, Neuronal Ceroid Lipofuscinosis 2 (NCL2), GM1 Gangliosidosis (GLB1), Shiba Inu Type, Mucopolysaccharidosis IIIA (MPS IIIA), Dachshund Type, Mucopolysaccharidosis Type IIIB (MPS IIIB), GM1 Gangliosidosis, Portuguese Water Dog Type, Primary Ciliary Dyskinesia, Kartagner Syndrome (PCD), Primary Ciliary Dyskenesia (Malamute Type) - Single Assay Test, Cavalier King Charles Spaniel Muscular Dystrophy (CKCS-MD), Limb Girdle Muscular Dystrophy, Boston Terrier, Myotubular Myopathy, Labrador Retriever Type, Muscular Hypertrophy/Myostatin Deficiency, Bully Whippet Syndrome (Double Muscling), Duchenne Muscular Dystrophy, Golden Retriever Type, Exercise Induced Collapse (EIC), Inflammatory Myopathy (Myositis), Ullrich Congenital Muscular Dystrophy, Inherited Myopathy in Great Danes (IMGD), Nemaline Myopathy, American Bulldog Type, Myotonia Congenita, Schnauzer Type, Centronuclear Myopathy (CNM), Laryngeal Paralysis (Bull Terrier Type) - Single Assay Test, Congenital Myasthenic Syndrome (CMS), Old Danish Pointer Type, Congenital Myasthenic Syndrome (CMS), Jack Russell Terrier Type, Episodic Falling Syndrome (EFS), Adult Paroxysmal Dyskinesia, Congenital Myasthenic Syndrome (CMS), Labrador Retriever Type, Polyneuropathy with Ocular Abnormalities and Neuronal Vacuolation, Bernard-Soulier Syndrome, Cocker Spaniel Type, Factor VIII Deficiency (Exon 1), German Shepherd Type, Pyruvate Dehydrogenase Phosphatase 1 Deficiency (PDP1), Canine Scott Syndrome (CSS), Leukocyte Adhesion Deficiency, Type I, Factor VIII Deficiency (Exon 11), German Shepherd Type, Pyruvate Kinase Deficiency (PKD), Basenji Type , Thrombopathia, Basset Hound Type, Methemoglobinemia, Pyruvate Kinase Deficiency (PKD), Labrador Retriever Type, Trapped Neutrophil Syndrome, Cohen Syndrome (TNS), Factor VII Deficiency, von Willebrand Disease III (vWD III), Prekallikrein Deficiency, Fletcher Trait, Leukocyte Adhesion Deficiency, Type III, Elliptocytosis, von Willebrand Disease I (vWD I), Factor IX Deficiency, Rhodesian Ridgeback Type, Thrombopathia, American Eskimo Dog Type, May-Hegglin Anomaly, von Willebrand Disease II (vWD II), Congenital Macrothrombocytopenia, Glanzmann's Thrombasthenia, Otterhound Type, P2RY12 Receptor Platelet Disorder, Pyruvate Kinase Deficiency (PKD), Beagle Type, Factor IX Deficiency (G418E), Polycystic Kidney Disease (PKD), Glanzmann's Thrombasthenia, Great Pyrenees Type, Familial Enamel Hypoplasia (FEH), Parson Russell Terrier Type, Early Adult Onset Deafness (EAOD), Deafness and Vestibular Syndrome of Dobermans, DVDobs, DINGS, Persistent Müllerian Duct Syndrome, Recurrent Inflammatory Pulmonary (Collie Type) - Single Assay Test, Familial Enamel Hypoplasia (FEH), Italian Greyhound Type, Sensory Neuropathy, Border Collie Type (SN), Glaucoma (BCG), Border Collie Type, Gondysgenesis and Glaucoma, Border Collie Type, Optimal Selection Canine Genetic Breeding Analysis, Primary Lens Luxation (PLL), Neuronal Ceroid Lipofuscinosis 5 (NCL5), Border Collie Type, Myotonia Congenita, Australian Cattle Dog Type, Multiple Drug Sensitivity (MDR1), Intestinal Cobalamin Malabsorption (IGS CUBN Exon 8), Border Collie Type, Intestinal Cobalamin Malabsorption (IGS CUBN Exon 53), Border Collie Type, Degenerative Myelopathy (DM; SOD1A), Collie Eye Anomaly (CEA)

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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).