お買い物カゴを表示 “Dog DNA Health Screen + Breed Identification Test”をカートに追加しました。
$ 129.95
– INCLUDES PERSONALIZED LIFEPLAN™
説明
[vc_row][vc_column][vc_column_text]This is great value profile that includes over 180 diseases and traits in a single test. The Dog Health Screen also include a personalized LifePlan™ and a schedule you may follow with your veterinarian to implement a customized wellness plan for your pet. Note for a mixed breed pet you will need to know the breeds that make up your pet to get the most value of the LifePlan™.
What’s in the Kit?
- Sterile DNA Collection Swabs
- Information Brochure with DNA Collection Instructions
- Self Addressed Pre-Paid Envelope
How Do I Get My Results?
Results are presented in an interactive online account where you can constantly update your pet’s records such as weight, body condition nutrition, health records and medication. Your account will also give you access to special promotions and attractive offers via your very own personalized shop. You can easily share your pet’s profile with your veterinarian, health care providers, family and friends.
[/vc_column_text][vc_column_text]Includes the following
- 1. Dog Life Plan
- A Locus (Fawn/Sable;Tri/Tan Points)
- Achromatopsia
- Alport Syndrome/ Hereditary Nephropathy (Samoyed Type)
- Autosomal Hereditary Recessive Nephropathy
- Black Hair Follicular Dysplasia
- Black and Tan/Saddle Coat Colour
- Brown Coat Colour Profile
- Canine DNA Profile (Genetic Fingerprint)
- Canine Hyperuricosuria
- Canine Leucocyte Adhesion Deficiency
- Canine Multifocal Retinopathy CMR1
- Canine Multifocal Retinopathy CMR2
- Canine Multifocal Retinopathy CMR3
- Catalase Deficiency
- Centronuclear Myopathy (Inherited Myopathy)
- Centronuclear Myopathy (Labrador Retriever Type)
- Cerebellar Ataxia
- Cerebellar Cortical Degeneration
- Chondrodysplasia (ITGA10)
- Coat Colour Dilution Alopecia
- Cobalamin Malabsorption (Beagle Type)
- Cobalamin Malabsorption: Cubilin Deficiency
- 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 Myasthenic Syndrome
- Congenital Myasthenic Syndrome (Jack Russell Terrier Type)
- Congenital Myasthenic Syndrome (Labrador Retriever Type)
- Congenital Stationary Night Blindness
- Copper Toxicosis (ATP7B & ATP7A) Labrador Retriever Type
- Curly Coat Dry Eye Syndrome
- Cystinuria (Newfoundland Type)
- Cystinuria (SLC3A1) Australian Cattle Dog Type
- Cystinuria (SLC3A1) Labrador Retriever Type
- D (Dilute) Locus
- Degenerative Myelopathy
- Dilated Cardiomyopathy
- Dry Nose (Hereditary Nasal Parakeratosis)
- E Locus – (Cream/Red/Yellow)
- EG Locus (Grizzle)
- EM (MC1R) Locus – Melanistic Mask
- Elliptocytosis (B-spectrin)
- Episodic Falling Syndrome
- Exercise Induced Collapse
- Factor VII Deficiency
- Fucosidosis
- Gall Bladder Mucocele Formation
- Gangliosidosis GM1 (Shiba Inu Type)
- Gangliosidosis GM2 (HEX B)
- Generalised PRA 1
- Generalised PRA 2
- Globoid Cell Leukodystrophy/Krabbe’s Disease
- Glycogen Storage Disease III
- Grey Collie Syndrome (Cyclic Hematopoiesis) AP3
- Haemophilia A / Factor VIII
- Haemophilia B / Factor IX
- Harlequin Pattern (H Locus)
- Hereditary Ataxia (Autophagy)
- Hereditary Cataract
- Ichthyosis (American Bulldog)
- Ichthyosis (Norfolk Terrier)
- Ichthyosis A (Golden Retriever)
- Ivermectin Sensitivity MDR1 (Multi Drug Resistance)
- K Locus (Dominant Black)
- Krabbe’s Disease
- L2- Hydroxyglutaric Aciduria
- Long Hair Gene (Canine)
- Malignant Hyperthermia
- Mucopolysaccharidosis VI
- Mullerian Duct Syndrome
- Musladin-Lueke Syndrome
- Myotonia Congenita (Miniature Schnauzer Type)
- Myotonia Congenita CLCN1
- Myotubular Myopathy X-linked
- Narcolepsy (Dobermann)
- Narcolepsy (Labrador)
- Natural Bob Tail (Short Tail Phenotype)
- Neonatal Ataxia
- Neonatal Cerebellar Cortical Degeneration
- Neonatal Encephalopathy
- Neuroaxonal Dystrophy (NAD)
- Neurodegenerative Vacuolar Storage Disease
- Neuronal Ceroid Lipofuscinosis 1
- Neuronal Ceroid Lipofuscinosis 10
- Neuronal Ceroid Lipofuscinosis 5
- Neuronal Ceroid Lipofuscinosis 6
- Neuronal Ceroid Lipofuscinosis 8
- Neuronal Ceroid Lipofuscinosis A
- Neuronal Ceroid Lipofuscinosis MFSD8
- Oculo-Skeletal Dysplasia
- Osteogenesis Imperfecta (SERPINH1)
- Phosphofructokinase Deficiency
- Pituitary Dwarfism
- Platelet Dysfunction
- Polyneuropathy (NDRG1) (Alaskan Malamute)
- Polyneuropathy (NDRG1) (Greyhound)
- Polyneuropathy and Neuronal Vacuolation (JLPP)
- Pompes Disease
- Prekallikrein Deficiency
- Primary Ciliary Dyskinesia
- Primary Glaucoma
- Primary Lens Luxation
- Primary Open Angle Glaucoma
- Progressive Retinal Atrophy – Late (Adult) Onset
- Progressive Retinal Atrophy – Mastiff
- Progressive Retinal Atrophy – Type A
- Progressive Retinal Atrophy – rcd3
- Progressive Retinal Atrophy – rcd4
- Progressive Retinal Atrophy 3
- Progressive Retinal Atrophy Dominant (Mastiff Type)
- Progressive Retinal Atrophy PRA1
- Progressive Rod Cone Degeneration (prcd) – PRA
- Pyruvate Dehydrogenase Phosphatase Deficiency
- Pyruvate Kinase Deficiency (Canine)
- Renal Cystadenocarcinoma and Nodular Dermatofibrosis
- Retinal Degeneration
- Retinal Degeneration RCD1a
- Skeletal Dysplasia 2 (Dwarfism SD2)
- Spinocerebellar Ataxia (CAPN1)
- Spinocerebellar Ataxia (KCNJ10)
- Spongy Degeneration with Cerebellar Ataxia (KCNJ10)
- Spotting Locus (W Locus)
- Startle Hyperekplexia
- Trapped Neutrophil Syndrome
- X-Linked PRA
- von Willebrand’s Disease Type I
- von Willebrand’s Disease Type II
- von Willebrand’s Disease Type III
