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DNA Pet Lab Vitality

Original price was: $275.00.Current price is: $240.00.

Find out the breed of your dog by comparing your dog’s DNA to over 350 breeds using the most complete DNA breed test in the world. Also includes a personalized LifePlanTM based on the breeds determined, your pet’s age, weight, gender, geographic location, and lifestyle. If you are interested in testing your dog’s health in addition to their breed we suggest you buy our Breed Identification + Disease Screening product which tests the pet’s DNA for over 200 heritable diseases & traits.

  • Interactive online report you can update.
  • Share with your veterinarian, groomer, family & friends.
  • Nutritional suggestions & daily energy needs analysis.
  • Routine health care reminders & alerts.
  • Adult weight prediction (for puppies under 12 month old).
  • Proven & trusted by thousands of veterinarians worldwide.
  • Discover the genes that make your dog’s appearance so unique.

DISEASES:

  • 2,8-Dihydroxyadenine Urolithiasis Type IA
  • Achromatopsia (Pointer Type)
  • Acute Respiratory Distress Syndrome (Dalmatian Type)
  • Alport Syndrome/ Hereditary Nephropathy (Samoyed Type)
  • Amelogenesis Imperfecta (Italian Greyhound Type)
  • Arrhythmogenic Right Ventricular Cardiomyopathy (Boxer Type)
  • Autosomal Hereditary Recessive Nephropathy
  • Brain Hypomyelination (Weimaraner Type)
  • Canine Chondrodysplasia (Norwegian Elkhound, Karelian Bear)
  • Canine Hyperuricosuria
  • Canine Leucocyte Adhesion Deficiency Type I (Irish Setter Type)
  • Canine Leucocyte Adhesion Deficiency Type III (German Shepherd Type)
  • Canine Multifocal Retinopathy CMR1 (Coton de Tulear Type)
  • Canine Multifocal Retinopathy CMR1 (Mastiff/Bull Breeds Type)
  • Canine Multifocal Retinopathy CMR2 (Coton du Tulear Type)
  • Canine Multifocal Retinopathy CMR3 (Lapphund Type)
  • Canine Multiple System Degeneration (Chinese Crested)
  • Centronuclear Myopathy (Labrador Retriever Type)
  • Centronuclear Myopathy /Inherited Myopathy (Great Dane Type)
  • Cerebellar Ataxia (American Staffordshire Terrier Type)
  • Cerebellar Ataxia (Finnish Hound Type)
  • Cerebellar Cortical Degeneration (Hungarian Vizsla Type)
  • Chondrodysplasia ITGA10 (Elkhound Type)
  • Cleft Lip Palate (Nova Scotia Duck Tolling Retriever Type)
  • Cobalamin Malabsorption (Beagle Type)
  • Cobalamin Malabsorption: Cubilin Deficiency (Border Collie Type)
  • Collie Eye Anomaly/Choroidal Hypoplasia
  • Cone Degeneration
  • Cone-Rod Dystrophy I – PRA (cord I)
  • Congenital Hypothyroidism with Goiter (Tenterfield Terrier Type)
  • Congenital Hypothyroidism with Goiter (Toy Fox Terrier Type)
  • Congenital Macrothrombocytopenia
  • Congenital Myasthenic Syndrome (Jack Russell Terrier Type)
  • Congenital Myasthenic Syndrome (Labrador Retriever Type)
  • Congenital Myasthenic Syndrome (Old Danish Pointer Type)
  • Congenital Stationary Night Blindness
  • Craniomandibular Osteopathy (Terrier Type)
  • Curly Coat Dry Eye Syndrome (Cavalier Type)
  • Cystinuria (Miniature Pinscher Type)
  • Cystinuria (Newfoundland Type)
  • Cystinuria (SLC3A1) Australian Cattle Dog Type
  • Cystinuria (SLC3A1) Labrador Retriever Type
  • Degenerative Myelopathy
  • Dystrophic Epidermolysis Bullosa (Asian Shepherd Type)
  • Dystrophic Epidermolysis Bullosa (Golden Retriever Type)
  • Ectodermal Dysplasia (Chesapeake Bay Retriever Type)
  • Elliptocytosis B-spectrin (Labrador Retriever/Poodle Type)
  • Encephalopathy (Alaskan Husky Type)
  • Episodic Falling Syndrome (Cavalier Type)
  • Exercise Induced Collapse (Retriever Type)
  • Factor VII Deficiency
  • Familial Nephropathy
  • Focal Epilepsy
  • Fucosidosis (English Springer Spaniel Type)
  • Gall Bladder Mucocele Formation (Shetland Sheepdog Type)
  • Gangliosidosis (Portuguese Water Dog Type)
  • Gangliosidosis GM1 GLB1 (Shiba Inu Type)
  • Gangliosidosis GM2 (Japanese Chin Type)
  • Gangliosidosis GM2 (Poodle Type)
  • Gangliosidosis GM2 HEXB (Shiba Inu Type)
  • Generalised PRA (Schapendoes Type)
  • Generalised Myoclonic Epilepsy (Rhodesian Ridgeback Type)
  • Generalised PRA 1 (Golden Retriever Type)
  • Generalised PRA 2 (Golden Retriever Type)
  • Globoid Cell Leukodystrophy/Krabbe’s Disease
  • Glomerulopathy KIRREL2 (Wheaten Terrier)
  • Glomerulopathy NPHS1 (Wheaten Terrier)
  • Glycogen Storage Disease IA (Maltese Type)
  • Glycogen Storage Disease III
  • Glycogen Storage Disease IIIA (Curly Coat Retriever Type)
  • Cone DegeneGoniodysgenesis and Glaucoma (Border Collie)ration
  • Grey Collie Syndrome (Cyclic Hematopoiesis) AP3
  • Haemophilia A / Factor VIII (German Shepherd Type)
  • Haemophilia B / Factor IX (Cairn Terrier Type)
  • Haemophilia B / Factor IX G418E
  • Hereditary Ataxia (Autophagy)
  • Hereditary Cataract
  • Hereditary Footpad Hyperkeratosis
  • Hereditary Nasal Parakeratosis/Dry Nose (Labrador Retriever Type)
  • Hereditary Nephropathy
  • Ichthyosis (American Bulldog)
  • Ichthyosis (German Shepherd Type)
  • Ichthyosis (Great Dane)
  • Ichthyosis (Norfolk Terrier)
  • Ichthyosis A (Golden Retriever)
  • Ivermectin Sensitivity MDR1 (Multi Drug Resistance)
  • Juvenile Epilepsy (Benign Familial) – Lagotto Romagnolo Type
  • L2- Hydroxyglutaric Aciduria
  • Leukoencephalomyelopathy (Leonburger Type)
  • Macrothrombocytopenia (Cairn/Norfolk Terrier Type)
  • Macular Corneal Dystrophy (Labrador Type)
  • Malignant Hyperthermia
  • May-Hegglin Anomaly (Pug Type)
  • Microphthalmia, Anophthalmia, and Coloboma (Wheaten Terrier Type)
  • Mild Disproportionate Dwarfism (Labrador Type)
  • Mucopolysaccharidosis (Huntaway Type)
  • Mucopolysaccharidosis Type I (Plott Hound Type)
  • Mucopolysaccharidosis VI (Great Dane Type)
  • Mucopolysaccharidosis VI (Poodle Type)
  • Mucopolysaccharidosis VII – Type II (German Shepherd/Belgian Shepherd Type)
  • Mullerian Duct Syndrome (Miniature Schnauzer Type)
  • Muscular Dystrophy (Landseer Type)
  • Musladin-Lueke Syndrome (Beagle Type)
  • Myotonia Congenita (Miniature Schnauzer Type)
  • Myotonia Congenita CLCN1 (Cattle Dog Type)
  • Myotonia Hereditaria (Cattle Dog Type)
  • Myotubular Myopathy X-Linked (Labrador Retriever Type)
  • Myotubular Myopathy X-Linked (Rottweiler Type)
  • Myotubular Myopathy X-linked
  • Narcolepshy (Dachshund Type)
  • Narcolepsy (Dobermann Type)
  • Narcolepsy (Labrador)
  • Neonatal Ataxia (Coton du Tulear Type)
  • Neonatal Cerebellar Cortical Degeneration (Beagle Type)
  • Neonatal Encephalopathy (Poodle Type)
  • Neuroaxonal Dystrophy (Cane Corso Type)
  • Neuroaxonal Dystrophy (Papillon Type)
  • Neuroaxonal Dystrophy (Rottweiler Type)
  • Neurodegenerative Vacuolar Storage Disease (Lagotto RomagnoloType)
  • Neuronal Ceroid Lipofuscinosis 1 (Dachshund Type)
  • Neuronal Ceroid Lipofuscinosis 10 (American Bulldog Type)
  • Neuronal Ceroid Lipofuscinosis 2 (Dachshund Type)
  • Neuronal Ceroid Lipofuscinosis 5 (Border Collie Type)
  • Neuronal Ceroid Lipofuscinosis 6 (Australian Shepherd Type)
  • Neuronal Ceroid Lipofuscinosis 8 (English Setter Type)
  • Neuronal Ceroid Lipofuscinosis A (Tibetan Terrier Type)
  • Osteogenesis Imperfecta (Chow Chow)
  • Osteogenesis Imperfecta (Golden Retriever Type)
  • Osteogenesis Imperfecta SERPINH1 (Dachshund Type)
  • Phosphofructokinase Deficiency (German Spaniel)
  • Phosphofructokinase Deficiency (Spaniel Type)
  • Pituitary Dwarfism
  • Platelet Dysfunction
  • Polyneuropathy (NDRG1) (Alaskan Malamute)
  • Polyneuropathy (NDRG1) (Greyhound)
  • Polyneuropathy GJA9 (Leonberger/St Bernard Type)
  • Polyneuropathy and Neuronal Vacuolation (JLPP)
  • Pompes Disease (Lapphund Type)
  • Post Operative Haemorrhage / Platelet Disorder (Mountain Dog Type)
  • Prekallikrein Deficiency (Shih Tzu Type)
  • Primary Ciliary Dyskinesia (Old English Sheepdog Type)
  • Primary Glaucoma
  • Primary Hyperoxaluria
  • Primary Lens Luxation
  • Primary Open Angle Glaucoma
  • Progressive Retinal Atrophy (Puli Type)
  • Progressive Retinal Atrophy (Shetland Sheepdog)
  • Progressive Retinal Atrophy – Late Onset (Basenji Type)
  • Progressive Retinal Atrophy – Mastiff
  • Progressive Retinal Atrophy – Type A (Miniature Schnauzer Type)
  • Progressive Retinal Atrophy – rcd3 (Corgi/Crested Type)
  • Progressive Retinal Atrophy 3
  • Progressive Retinal Atrophy Dominant (Mastiff Type)
  • Progressive Retinal Atrophy PRA1 (Papillon Type)
  • Progressive Rod Cone Degeneration (prcd) – PRA
  • Pyruvate Dehydrogenase Phosphatase Deficiency (Clumber Spaniel Type)
  • Pyruvate Kinase Deficiency (Beagle Type)
  • Pyruvate Kinase Deficiency (Canine)
  • Pyruvate Kinase Deficiency (Labrador Type)
  • Pyruvate Kinase Deficiency (Pug)
  • Raine Syndrome Dental Hypomineralisation (Border Collie)
  • Renal Cystadenocarcinoma and Nodular Dermatofibrosis (German Shepherd Type)
  • Retinal Degeneration (Norwegian Elkhound Type)
  • Retinal Degeneration RCD1a
  • Sanfilippo Syndrome Type A / Mucopolysaccharidosis IIIA (Dachshund Type)
  • Scott Syndrome (German Shepherd Type)
  • Severe Combined Immunodeficiency (Frisian Water Dog)
  • Skeletal Dysplasia 2 (Mild Disproportionate Dwarfism)
  • Spinocerebellar Ataxia (CAPN1)
  • Spinocerebellar Ataxia (Jack Russell Type)
  • Spondylocostal Dysostosis (Miniature Schnauzer Type) – SINGLE ASSAY TEST
  • Spongy Degeneration SDCA2
  • Spongy Degeneration with Cerebellar Ataxia (KCNJ10)
  • Startle Hyperekplexia (Wolfhound Type)
  • Thrombasthenic Thrombopathia (Otterhound Type)
  • Trapped Neutrophil Syndrome (Border Collie Type)
  • X-Linked PRA (Samoyed/Husky Type)
  • von Willebrand’s Disease Type I
  • von Willebrand’s Disease Type II (German Wirehaired Pointer)
  • von Willebrand’s Disease Type II (RESEARCH ONLY)
  • von Willebrand’s Disease Type III

TRAITS:

  • A Locus (Fawn/Sable;Tri/Tan Points)
  • Black Hair Follicular Dysplasia
  • Black and Tan/Saddle Coat Colour
  • Brown (345DELPRO) Deletion
  • Black and Tan/Saddle Coat Colour
  • Brown (GLNT331STOP) Stop Codon
  • Brown Coat Colour Profile
  • Coat Colour Dilution Alopecia
  • D (Dilute) Locus
  • D2 (Dilute) Locus
  • E Locus – (Cream/Red/Yellow)
  • E Locus e2
  • E Locus e3
  • EG Locus (Grizzle)
  • EM (MC1R) Locus – Melanistic Mask
  • Harlequin (H) Pattern (Great Dane Type)
  • K Locus (Dominant Black)
  • Long Hair Gene (Canine)
  • Natural Bob Tail (Short Tail Phenotype)
  • Oculocutaneous Albinism (Bullmastiff)
  • Oculocutaneous Albinism (Lhasa Apso Type)
  • Skull Diversity (All Breeds)
  • Spotting (W) Locus (Mastiff Type)
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