Dog DNA Health Screen & Life Plan

Product includes:

Diseases:

2,8-Dihydroxyadenine Urolithiasis Type IA

Achromatopsia (Labrador Type)

Achromatopsia (Pointer Type)

Acral Mutilation Syndrome (SPANIEL & POINTER TYPE)

Acute Respiratory Distress Syndrome (Dalmatian Type)

Airway Distress Syndrome (ADAMTS3) - Risk Marker

Alport Syndrome/ Hereditary Nephropathy (Samoyed Type)

Amelogenesis Imperfecta (Akita Type)

Amelogenesis Imperfecta (Italian Greyhound Type)

Autosomal Hereditary Recessive Nephropathy

Bernard-Soulier Syndrome (Cocker Spaniel Type)

Brain Hypomyelination (Weimaraner Type)

Canine Chondrodysplasia (Norwegian Elkhound, Karelian Bear)*

Canine Leukocyte Adhesion Deficiency Type I (Irish Setter Type)

Canine Leukocyte Adhesion Deficiency Type III (German Shepherd Type)

Canine Multifocal Retinopathy CMR2 (Coton du Tulear Type)

Canine Multifocal Retinopathy CMR3 (Lapphund Type)

Canine Multiple System Degeneration (Chinese Crested)*

Canine Multiple System Degeneration (Kerry Blue Terrier Type)

Cardiomyopathy and Juvenile Mortality (Belgian Shepherd)

Catalase Deficiency (Beagle Type)

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 Degeneration (Shepherd/Arctic Breed Type)

Cone-Rod Dystrophy I - PRA (crd -4/cord I)

Congenital Eye Malformation (Golden Retriever)

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

Dilated Cardiomyopathy (Schnauzer Type)

Dystrophic Epidermolysis Bullosa (Asian Shepherd Type)

Dystrophic Epidermolysis Bullosa (Golden Retriever Type)

Early Onset Adult Deafness (Rhodesian Ridgeback)

Ectodermal Dysplasia (Chesapeake Bay Retriever Type)

Ehlers-Danlos Syndrome (Labrador 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*

Footpad Hyperkeratosis (Rottweiler)

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 (PLN) KIRREL2

Glomerulopathy (PLN) NPHS1

Glycogen Storage Disease IA (Maltese Type)

Glycogen Storage Disease III

Glycogen Storage Disease IIIA (Curly Coat Retriever Type)

Goniodysgenesis and Glaucoma (Border Collie)

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 Cataract (Dominant)

Hereditary Deafness PTPRQ Gene (Dobermann Type)

Hereditary Footpad Hyperkeratosis

Hereditary Footpad Hyperkeratosis (Dogue de Bordeaux Type)

Hereditary Nasal Parakeratosis/Dry Nose (Labrador Retriever Type)

Hereditary Nephropathy

Hyperuricosuria

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

Laryngeal Paralysis (Bull Terrier Type)

Lethal Acrodermatitis MKLN1 (Bull Terrier Type)

Leukoencephalomyelopathy (LEMP)

Leukoencephalomyelopathy (Leonberger Type)

Macrothrombocytopenia (Cairn/Norfolk Terrier Type)

Macular Corneal Dystrophy (Labrador Type)

Malignant Hyperthermia

May-Hegglin Anomaly (Pug Type)

Microphthalmia, Anophthalmia & 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)

Multifocal Retinopathy CMR1 (Mastiff/Bull Breeds 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*

Narcolepsy (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)

Neuronal Ceroid Lipofuscinosis MFSD8 (Chinese Crested Type)

Neuronal Ceroid Lipofuscinosis NCL (Saluki Type)

Neuronal Ceroid Lipofuscinosis NCL 12 (Cattle Dog Type)

Osteochondrodysplasia (Min Poodle Type)

Osteogenesis Imperfecta (Chow Chow)

Osteogenesis Imperfecta (Golden Retriever Type)

Osteogenesis Imperfecta SERPINH1 (Dachshund Type)

Periodic Fever Syndrome (Shar Pei Fever)

Phosphofructokinase Deficiency (German Spaniel)

Phosphofructokinase Deficiency (Spaniel Type)

Platelet Dysfunction

Polycystic Kidney Disease (Bull Terrier Type)

Polyneuropathy (NDRG1) (Alaskan Malamute)

Polyneuropathy (NDRG1) (Greyhound)

Polyneuropathy and Neuronal Vacuolation (JLPP)

Polyneuropathy GJA9 (Leonberger/St Bernard Type)

Pompes Disease (Lapphund Type)

Post Operative Haemorrhage / Platelet Disorder (Mountain Dog Type)

Prekallikrein Deficiency (Shih Tzu Type)

Primary Ciliary Dyskenesia (Malamute Type)

Primary Ciliary Dyskinesia (Old English Sheepdog Type)

Primary Glaucoma

Primary Hyperoxaluria

Primary Lens Luxation

Primary Open Angle Glaucoma (Beagle Type)

Progressive Retinal Atrophy - crd2PRA

Progressive Retinal Atrophy - Late Onset (Basenji Type)

Progressive Retinal Atrophy - rcd1 (Irish Setter)

Progressive Retinal Atrophy - rcd3 (Corgi/Crested Type)

Progressive Retinal Atrophy (Mastiff)

Progressive Retinal Atrophy (Puli 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)

rcd4-PRA (Late Onset)

Recurrent Inflammatory Pulmonary (Collie Type)

Renal Cystadenocarcinoma and Nodular Dermatofibrosis (German Shepherd Type)

Retinal Degeneration (Norwegian Elkhound Type)

Retinal Degeneration RCD1a

Sanfilippo Syndrome Type A / Mucopolysaccharidosis IIIA (Dachshund Type)

Sarcoglycan Deficient Muscular Dystrophy (SDMD)

Scott Syndrome (German Shepherd Type)

Sensory Neuropathy (Border Collie Type)

Severe Combined Immunodeficiency (Frisian Water Dog)

Skeletal Dysplasia 2 (Mild Disproportionate Dwarfism)

Spinal Dysraphism (Weimaraner Type)

Spinocerebellar Ataxia (CAPN1)

Spinocerebellar Ataxia (Jack Russell Type)

Spondylocostal Dysostosis (Miniature Schnauzer Type)

Spongy Degeneration SDCA2

Spongy Degeneration with Cerebellar Ataxia (KCNJ10)

Spongy Degeneration with Cerebellar Ataxia (SDCA2) Belgian Shepherd

Stargardt Disease (Retinal Degeneration)

Startle Hyperekplexia (Wolfhound Type)

Thrombasthenic Thrombopathia (Otterhound Type)

Thrombopathia (Basset Hound Type)

Thrombopathia (Finnish Spitz Type)

Trapped Neutrophil Syndrome (Border Collie Type)

Type A PRA 1 (Miniature Schnauzer Type)

Type A PRA 2 [HIVEP3] (Miniature Schnauzer Type)

Van den Ende-Gupta Syndrome (Wire Fox Terrier Type)

von Willebrand's Disease Type I

von Willebrand's Disease Type II

von Willebrand's Disease Type II (German Wirehaired Pointer)

von Willebrand's Disease Type III

X-Linked PRA (Samoyed/Husky Type)

Traits:

Polydactyl/Dewclaws

E Locus - (Cream/Red/Yellow)

E Locus (Cattle Dog Cream Variant) e2

E Locus (Artic Breeds Pale/Yellow/White Variant) e3

EM (MC1R) Locus - Melanistic Mask

EG Locus (Grizzle)

I Locus Colour Intensity

Brown (345DELPRO) Deletion

Brown (345DELPRO) Deletion

Brown (345DELPRO) Deletion

Brown (GLNT331STOP) Stop Codon

Brown (GLNT331STOP) Stop Codon

Brown (SER41CYS) Insertion Codon

Brown (SER41CYS) Insertion Codon

Brown (SER41CYS) Insertion Codon

B Locus [TYRP1] (Australian Shepherd Type)

Cocoa (Brown) Coat Colour

Liver [TYRP1] (Lancashire Heeler Type)

D (Dilute) Locus

Dilute D2 Variant (Chow Chow Type)

K Locus (Dominant Black)

A Locus (Fawn/Sable;Tri/Tan Points)

Pied (BOTH SINE and REPEAT VARIANTS)

Merle

Black and Tan/Saddle Coat Colour

Harlequin (H) Pattern (Great Dane Type)

Oculocutaneous Albinism

Long Hair Gene (Canine C95F)

Long Hair Gene (Canine DUP GG)

Shedding (MC5R)

Coat Composition CFA28 Gene (Double/Single Coat)

Curly Coat/Hair Curl (KRT71 R151W)

Curly Coat Phenotype (KRT71 - p.Ser422ArgfsTer)

Body Size IGSF1 "Bulky Gene"

Natural Bob Tail (Short Tail Phenotype)

Screw Tail (DVL2)

Oculocutaneous Albinism (Bullmastiff)

DNA Profile:

Canine DNA Profile (ISAG Canine 288 SNP Panel)