DOG DNA HEALTH SCREEN
Description
This test is designed for purebred dogs, or mixed breed dogs with known breed makeup. This is great value test will screen your pet for over 200 genetics diseases and traits. Breed specific diseases will be highlighted on the report. The additional health risk analysis will reveal the most relevant health risks for your pet based on their genetics, breed, age, weight, gender, location and lifestyle. 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.
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.
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)
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-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)
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 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)
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
Black Hair Follicular Dysplasia
Black and Tan/Saddle Coat Colour
Brown (345DELPRO) Deletion
Brown (GLNT331STOP) Stop Codon
Brown (SER41CYS) Insertion Codon
Brown Coat Colour Profile
Coat Colour Dilution Alopecia
D (Dilute) Locus
D2 (Dilute) Locus
E Locus - (Cream/Red/Yellow)
E Locus e2
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)
- Regular price
- $129.95
- Sale price
- $129.95 Sale
Description
This test is designed for purebred dogs, or mixed breed dogs with known breed makeup. This is great value test will screen your pet for over 200 genetics diseases and traits. Breed specific diseases will be highlighted on the report. The additional health risk analysis will reveal the most relevant health risks for your pet based on their genetics, breed, age, weight, gender, location and lifestyle. 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.
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.
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)
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-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)
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 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)
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
Black Hair Follicular Dysplasia
Black and Tan/Saddle Coat Colour
Brown (345DELPRO) Deletion
Brown (GLNT331STOP) Stop Codon
Brown (SER41CYS) Insertion Codon
Brown Coat Colour Profile
Coat Colour Dilution Alopecia
D (Dilute) Locus
D2 (Dilute) Locus
E Locus - (Cream/Red/Yellow)
E Locus e2
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)