Reed's Radiant Dogs

Parent health testing

• Standard Veterinary Blood Panel

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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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• von Willebrand Disease III (vWD III), Shetland Sheepdog Type, von Willebrand Disease III (vWD III), Scottish Terrier Type, von Willebrand Disease III (vWD III), Kooikerhondje Type, von Willebrand Disease II (vWD II), von Willebrand Disease I (vWD I), X-Linked Tremors, Shaking Puppy Syndrome (SPS), Severe Combined Immunodeficiency Disease, X-Linked (XSCID), Corgi Type, Severe Combined Immunodeficiency Disease, X-Linked, Basset Hound Type (XSCID), X-Linked Progressive Retinal Atrophy 2, X-Linked Progressive Retinal Atrophy 1, X-Linked Myotubular Myopathy, Ectodermal Dysplasia, X-Linked (Dachshund Type), Van Den Ende-Gupta Syndrome (VDEGS), Trapped Neutrophil Syndrome, Cohen Syndrome (TNS), Stargardt Disease, Spongy Degeneration with Cerebellar Ataxia (SDCA2) mutation originally found in Belgian Shepherd Dog, Spongy Degeneration with Cerebellar Ataxia (SDCA1) mutation originally found in Belgian Shepherd Dog and Malinois, Spondylocostal Dysostosis, Spinocerebellar Ataxia with Myokymia (KCNJ10), Late Onset Ataxia, Spinocerebellar Ataxia (LOA, SCA), Skeletal Dysplasia (SD2), Severe Combined Immunodeficiency Disease, Terrier Type, Severe Combined Immunodeficiency Disease, Frisian Water Dog Type, Sensory Neuropathy, Border Collie Type (SN), PRA, Rod-Cone Dysplasia 3 (rcd3), Long QT Syndrome, Pyruvate Kinase Deficiency (PKD), Terrier Type, Pyruvate Kinase Deficiency (PKD), Pug Type, Pyruvate Kinase Deficiency (PKD), Beagle Type, Pyruvate Kinase Deficiency, Basenji Type (PKD), Pyruvate Dehydrogenase Phosphatase 1 Deficiency (PDP1), Protein-Losing Nephropathy (PLN; NPHS1 Gene Variant), Progressive Retinal Atrophy, mutation originally found in Swedish Valhund, Progressive Retinal Atrophy (PRA), Generalized, Primary Open Angle Glaucoma and Primary Lens Luxation (POAG/PLL), Shar-Pei Type, Primary Open Angle Glaucoma, Petit Basset Griffon Vendeen Type, Primary Open Angle Glaucoma, Basset Hound Type, Primary Lens Luxation (PLL), Primary Ciliary Dyskinesia, Kartagner Syndrome (PCD), Primary Ciliary Dyskenesia (Malamute Type) - Single Assay Test, Prekallikrein Deficiency, Fletcher Trait, Polycystic Kidney Disease (PKD), Phosphofructokinase Deficiency (PFK), Persistent Müllerian Duct Syndrome, Adult Paroxysmal Dyskinesia, P2RY12 Receptor Platelet Disorder, Osteogenesis Imperfecta (OI), Dachshund Type, Osteogenesis Imperfecta (OI), Beagle Type, Osteochondrodysplasia, Miniature Poodle Type, Obesity risk (POMC), Neuronal Ceroid Lipofuscinosis 8 (NCL8), Setter Type, Neuronal Ceroid Lipofuscinosis 8 (NCL8), Australian Shepherd Type, Neuronal Ceroid Lipofuscinosis 7 (NCL7), Neuronal Ceroid Lipofuscinosis 12 (NCL12), Australian Cattle Dog Type, Neuronal Ceroid Lipofuscinosis 1 (NCL1), Dachshund Type, Neuroaxonal Dystrophy (NAD), Rottweiler Type, Neuroaxonal Dystrophy (NAD), Papillon Type, Neuroaxonal Dystrophy (NAD), Spanish Water Dog Type, Neonatal Encephalopathy with Seizures (NEwS), Neonatal Cortical Cerebellar Degeneration (NCCD), Nemaline Myopathy, American Bulldog Type, Narcolepsy, Labrador Retriever Type, Narcolepsy, Dachshund Type, Myotubular Myopathy, Labrador Retriever Type, Myotonia Congenita, Schnauzer Type, Myotonia Congenita, Australian Cattle Dog Type, Myeloperoxidase Deficiency, mutation originally found in Italian Hound, Muscular Hypertrophy/Myostatin Deficiency, Bully Whippet Syndrome (Double Muscling), Duchenne Muscular Dystrophy, Norfolk Terrier Type, Muscular Dystrophy, Ullrich-type; mutation originally found in Landseer, Duchenne Muscular Dystrophy, Golden Retriever Type, Cavalier King Charles Spaniel Muscular Dystrophy (CKCS-MD), Mucopolysaccharidosis VII (MPS VII ARSB), German Shepherd Dog Type, Mucopolysaccharidosis IIIA (MPS IIIA), New Zealand Huntaway Type, Mucopolysaccharidosis IIIA (MPS IIIA), Dachshund Type, Microphthalmia Syndrome (PES), May-Hegglin Anomaly, Macrothrombocytopenia, Multiple Drug Sensitivity (MDR1), Ligneous Membranitis, LM (PLG), Lethal Acrodermatitis (LAD), Bull Terrier Type, Lamellar Ichthyosis, Lagotto Storage Disease (LSD), L-2-Hydroxyglutaric Aciduria (L2HGA), Staffordshire Bull Terrier Type, L-2-Hydroxyglutaric Aciduria (L2HGA), West Highland Terrier Type, Juvenile Myoclonic Epilepsy (JME), Juvenile Laryngeal Paralysis & Polyneuropathy (JLPP), Juvenile Encephalopathy, mutation orignally found in Parson Russell Terrier, Intestinal Cobalamin Malabsorption (IGS), Komondor Type, Intestinal Cobalamin Malabsorption (IGS CUBN Exon 8), Border Collie Type, Intestinal Cobalamin Malabsorption (IGS CUBN Exon 53), Border Collie Type, Ichthyosis, Great Dane Type, Ichthyosis, American Bulldog Type, Hypomyelination, Weimaraner Type, Hereditary Vitamin D-Resistant Rickets (HVDRR), Hereditary Nasal Parakeratosis (HNPK), Hereditary Footpad Hyperkeratosis, Hereditary Elliptocytosis, Ataxia, Norwegian Buhund Type, Glycogen Storage Disease Ia, Glycogen Storage Disease Type IIIA, GSD IIIA, Globoid Cell Leukodystrophy (GCL), Irish Setter Type, Globoid Cell Leukodystrophy (GCL), Terrier Type, Glanzmann's Thrombasthenia, Great Pyrenees Type, Early Onset Progressive Retinal Atrophy (EOPRA), GM2 Gangliosidosis, Poodle Type, Gangliosidosis GM2, Japanese Chin Type, GM1 Gangliosidosis (HEXB), Shiba Inu Type, GM1 Gangliosidosis (GLB1), Shiba Inu Type, GM1 Gangliosidosis, Portuguese Water Dog Type, Focal Non-Epidermolytic Palmoplantar Keratoderma, Pachyonychia Congenita (KRT16), Fetal-Onset Neonatal Neuroaxonal Dystrophy (MFN1), Fanconi Syndrome, Factor IX Deficiency (G418E), Factor VIII Deficiency, Old English Sheepdog Type, Factor VIII Deficiency, Havanese Type, Factor VIII Deficiency (Exon 1), German Shepherd Type, Factor VIII Deficiency (Exon 11), German Shepherd Type, Factor VIII Deficiency, Boxer Type, Factor VII Deficiency, Scottish Deerhound Type, Factor VII Deficiency, Alaskan Klee Kai Type, Exercise Induced Collapse (EIC), Episodic Falling Syndrome (EFS), Epidermolytic Hyperkeratosis, Epidermolysis Bullosa (Eurasier), Dystrophic Epidermolysis Bullosa, Dilated Cardiomyopathy (Schnauzer Type), Dental Hypomineralization (DH), Degenerative Myelopathy (DM; SOD1A), Deafness and Vestibular Dysfunction, Doberman Pinscher Type, Cystinuria Type 1A, Newfoundland Type, Cystinuria Type 1A, Labrador Retriever Type, Cystinuria Type II-A, Australian Cattle Dog Type, Cystic Renal Dysplasia and Hepatic Fibrosis, 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 Hypothyroidism with Goiter, Terrier Type (CHG), Congenital Hypothyroidism with Goiter (CHG), Congenital Dyshormonogenic Hypothyroidism with Goiter, Shih Tzu Type, Cone-Rod Dystrophy 2 (crd2), American Pitbull Terrier Type, Cone-Rod Dystrophy 1 (crd1), American Staffordshire Terrier Type, Cone Degeneration, German Shorthaired Pointer Type, Cone Degeneration, German Shepherd Dog Type, Cone Degeneration, Compliment 3 Deficiency (C3), Cleft Palate (DLX6), Cleft Palate (ADAMTS20), Chondrodysplasia/Dwarfism, Cerebral Dysfunction, Frisian Stabyhoun Type, Cerebellar Cortical Degeneration (CCD), Hereditary Ataxia, Cerebellar Ataxia, Cerebellar Ataxia, Spinone Italiano Type, Cerebellar Ataxia, Finnish Hound Type, Centronuclear Myopathy (CNM), Centronuclear Myopathy (CNM), Great Dane Type, Canine Scott Syndrome (CSS), Canine Multifocal Retinopathy (cmr3; BEST1 Exon 10 SNP), Leukocyte Adhesion Deficiency, Type III, Benign Familial Juvenile Epilepsy (BFJE), Neonatal Ataxia, Bandera's Disease, Amelogenesis Imperfecta (AI), Italian Greyhound Type, Amelogenesis Imperfecta (AI), Akita Type, Alexander Disease, Encephalopathy, Alaskan Husky Type, Acute Respiratory Distress Syndrome, Dalmatian Type, Acral Mutilation Syndrome (AMS), Musladin-Leuke Syndrome (MLS), Hypocatalasia, Factor VII Deficiency, Wisdom Panel, Animal Genetics Panel

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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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