Dog Complete Disease & Trait Screen (300+ Tests)

Full Breed Profile includes:

Diseases:

Achromatopsia (Labrador Type)

Achromatopsia (Pointer Type)

Achromatopsia (Shepherd/Arctic Breed Type)

Acral Mutilation Syndrome (SPANIEL & POINTER TYPE)

Acute Respiratory Distress Syndrome (Dalmatian Type)

Adult Onset Deafness Border Collie (Linkage Association Test)

Adult Paroxysmal Dyskinesia

Afibrinogenemia, Variant 1

Airway Distress Syndrome (ADAMTS3) - Risk Marker

Alport Syndrome/ Hereditary Nephritis (Samoyed Type)

Amelogenesis Imperfecta (Akita Type)

Amelogenesis Imperfecta (Italian Greyhound Type)

Amelogenesis Imperfecta (Jack Russell Terrier Type), Variant 1

Ataxia (Norwegian Buhund Type)

Autosomal Hereditary Recessive Nephropathy

Bernard-Soulier Syndrome (Cocker Spaniel Type)

Beta Mannisidosis (German Shepherd Type)

Bilateral Deafness MYO7A Gene (Dobermann Type)

Brain Hypomyelination (Weimaraner Type)

Canine Leukocyte Adhesion Deficiency Type I (Irish Setter Type)

Canine Leukocyte Adhesion Deficiency Type III (German Shepherd Type)

Canine Multifocal Retinopathy 3

Canine Multifocal Retinopathy CMR1 (Coton de 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)

Charcot Marie Tooth Disease (Type 4B2)

Chondrodysplasia ITGA10 (Elkhound Type)

Chondrodystrophy (CDDY) & Intervertebral Disc Disease (IVDD) [RESEARCH ONLY]

Chronic Respiratory Tract Infection

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

Complement 3 Deficiency

Cone Degeneration (German Shepherd Dog Type)

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

Congenital Deafness (Cattle Dog Type) (LINKAGE CANDIDATE GENE)

Congenital Dyshormonogenic Hypothyroidism with Goiter (Shih Tzu)

Congenital Eye Malformation (Golden Retriever)

Congenital Hypothyroidism with Goiter (Tenterfield Terrier Type)

Congenital Hypothyroidism with Goiter (Toy Fox Terrier Type)

Congenital Macrothrombocytopenia

Congenital Methemoglobinemia (Poodle and Pomeranian Type)

Congenital Muscular Dystrophy (Italian Greyhound Type)

Congenital Myasthenic Syndrome (Jack Russell Terrier Type)

Congenital Myasthenic Syndrome (Labrador Retriever Type)

Congenital Myasthenic Syndrome (Old Danish Pointer Type)

Congenital Stationary Night Blindness

Congenital Stationary Night Blindness (Beagle Type)

Copper Toxicosis (Bedlington Terrier Type)

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

Cystinuria Type 3 [Bulldog Risk Factor Variant 1]

Cystinuria Type 3 [Bulldog Risk Factor Variant 2&3]

Dandy Walker Like Malformation (Eurasier Breed Type)

Darier Disease and Associated Infundibular Cyst Formation

Degenerative Myelopathy

Degenerative Myelopathy (Bernese Mountain Dog Type)

Dental Skeletal Retinal Anomaly [Cane Corso Type]

Diffuse Cystic Renal Dysplasia and Hepatic Fibrosis

Dihydroxyadenine Urolithiasis Type IA

Dilated Cardiomyopathy (Schnauzer Type)

Duchenne Muscular Dystrophy (Border Collie Type)

Duchenne Muscular Dystrophy (Pembroke Welsh Corgi Type)

Dystrophic Epidermolysis Bullosa (Asian Shepherd Type)

Dystrophic Epidermolysis Bullosa (Basset Hound Type)

Dystrophic Epidermolysis Bullosa (Golden Retriever Type)

Early Onset Adult Deafness (Rhodesian Ridgeback)

Early-Onset Progressive Retinal Atrophy

Early‑Onset Epilepsy, Mitochondrial Dysfunction and Neurodegeneration

Ectodermal Dysplasia (Chesapeake Bay Retriever Type)

Ectodermal Dysplasia, X-Linked (Dachshund Type)

Ectodermal Dysplasia, X-Linked (Shepherd Type)

Ehlers-Danlos Syndrome (Dobermann Type)

Ehlers-Danlos Syndrome (Labrador Retriever Type), Variant 2

Ehlers-Danlos Syndrome (Labrador Type)

Ehlers-Danlos Syndrome (Poodle Type), Variant 1

Ehlers-Danlos Syndrome (Poodle Type), Variant 2

Elliptocytosis B-spectrin (Labrador Retriever/Poodle Type)

Episodic Falling Syndrome (Cavalier Type)

Exercise Induced Collapse (Retriever Type)

Exercise Induced Metabolic Myopathy

Exfoliative Cutaneous Lupus Erythematosus (ECLE)

Factor IX Deficiency

Factor VII Deficiency

Factor XI Deficiency

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 Myoclonic Epilepsy (Rhodesian Ridgeback Type)

Generalised PRA 1 (Golden Retriever Type)

Generalised PRA 2 (Golden Retriever Type)

Glanzmann's Thrombasthenia (Great Pyrenees Type)

Globoid Cell Leukodystrophy (Irish Setter Type)

Globoid Cell Leukodystrophy/Krabbe’s Disease

Glomerulopathy (PLN) KIRREL2

Glomerulopathy (PLN) NPHS1

Glycogen Storage Disease IA (Maltese Type)

Glycogen Storage Disease IIIA (Curly Coat Retriever Type)

GM1 Gangliosidosis (Alaskan Husky Type)

Goniodysgenesis and Glaucoma (Border Collie)

Grey Collie Syndrome (Cyclic Hematopoiesis) AP3

Griscelli Syndrome Type 1

Haemophilia A (Rhodesian Ridgeback Type)

Haemophilia A / Factor VIII (German Shepherd Type)

Haemophilia A/Factor VIII Deficiency (Boxer Type)

Haemophilia B (Lhasa Apso Type)

Haemophilia B (Rhodesian Ridgeback Type)

Haemophilia B / Factor IX (Cairn Terrier Type)

Hemophilia A (German Shepherd Dog, Type 1)

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 Methemoglobinemia, Variant 1

Hereditary Methemoglobinemia, Variant 3

Hereditary Nasal Parakeratosis (Greyhound Type)

Hereditary Nasal Parakeratosis/Dry Nose (Labrador Retriever Type)

Hereditary Nephropathy (English Springer Spaniel)

Hyperuricosuria

Hypophosphatasia

Ichthyosis (American Bulldog)

Ichthyosis (Golden Retriever Type 2)

Ichthyosis (Great Dane)

Ichthyosis (Jack Russell Terrier Type)

Ichthyosis (Norfolk Terrier)

Ichthyosis A (Golden Retriever)

Inflammatory Myopathy

Intestinal Cobalamin Malabsorption (Giant Schnauzer Type)

Intestinal Cobalamin Malabsorption (Komondor Type)

Ivermectin Sensitivity MDR1 (Multi Drug Resistance)

Junctional Epidermolysis Bullosa

Juvenile Cataracts (Wirehaired Pointing Griffon Type)

Juvenile Dermatomyositis [MAP3K7CL RISK ALLELE]

Juvenile Dermatomyositis [PAN2 RISK ALLELE]

Juvenile Epilepsy (Benign Familial) - Lagotto Romagnolo Type

Juvenile Paroxysmal Dyskinesia

L2- Hydroxyglutaric Aciduria

L2-Hydroxyglutaric Aciduria (Staffordshire Bull Terrier Type) - Variant 2

L2-Hydroxyglutaric Aciduria (Yorkshire Terrier Type)

Laryngeal Paralysis (Bull Terrier Type)

Laryngeal Paralysis (St Bernard/Leonberger Type)

Leigh-Like Subacute Necrotising Encephalopathy

Lethal Acrodermatitis MKLN1 (Bull Terrier Type)

Leukoencephalomyelopathy (LEMP)

Ligneous Membranitis

Lundehund Syndrome

Macrothrombocytopenia (Cairn/Norfolk Terrier Type)

Macular Corneal Dystrophy (Labrador Type)

Malignant Hyperthermia

May-Hegglin Anomaly (Pug Type)

Microphthalmia, Anophthalmia & Coloboma (Wheaten Terrier Type)

Mucopolysaccharidosis (Huntaway Type)

Mucopolysaccharidosis I (Boston Terrier Type)

Mucopolysaccharidosis IIIB (Schipperke Type)

Mucopolysaccharidosis Type I (Plott Hound Type)

Mucopolysaccharidosis Type VII (Brazilian Terrier Type)

Mucopolysaccharidosis VI (Great Dane Type)

Mucopolysaccharidosis VI (Miniature Schnauzer 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)

Myostatin Deficiency

Myotonia Congenita (American Bulldog Type)

Myotonia Congenita (Labrador Retriever Type)

Myotonia Congenita (Miniature Schnauzer Type)

Myotonia Hereditaria (Cattle Dog Type)

Myotubular Myopathy 1 (Boykin Spaniel Type)

Myotubular Myopathy X-Linked (Labrador Retriever Type)

Myotubular Myopathy X-Linked (Rottweiler Type)

Myxomatous Mitral Valve Disease 1 [NEBL535 Risk Variant]

Myxomatous Mitral Valve Disease 2 [NEBL576 Risk Variant]

Myxomatous Mitral Valve Disease 3 [NEBL724 Candidate Variant]

Myxomatous Mitral Valve Disease 4 [NEBL890 Risk Variant]

Myxomatous Mitral Valve Disease 5 [NEBL498 Risk Variant]

Narcolepsy (Dachshund Type)

Narcolepsy (Dobermann Type)

Narcolepsy (Labrador)

Necrotising Meningoencephalitis (NME)

Neonatal Ataxia (Coton du Tulear Type)

Neonatal Cerebellar Cortical Degeneration (Beagle Type)

Neonatal Encephalopathy (Poodle Type)

Neuroaxonal Dystrophy (Giant Schnauzer Type)

Neuroaxonal Dystrophy (Papillon Type)

Neuroaxonal Dystrophy (Rottweiler Type)

Neuroaxonal Dystrophy (Spanish Water Dog Type)

Neurodegenerative Vacuolar Storage Disease (Lagotto RomagnoloType)

Neuronal Ceroid Lipofuscinosis 1 (Dachshund Type)

Neuronal Ceroid Lipofuscinosis 10 (American Bulldog Type)

Neuronal Ceroid Lipofuscinosis 5 (Border Collie Type)

Neuronal Ceroid Lipofuscinosis 6

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 (Cane Corso Type)

Neuronal Ceroid Lipofuscinosis NCL (Golden Retriever Type)

Neuronal Ceroid Lipofuscinosis NCL (Saluki Type)

Neuronal Ceroid Lipofuscinosis NCL 12 (Cattle Dog Type)

Nonsyndromic Hearing Loss

Oculo-Skeletal Dysplasia (Labrador Retriever Type)

Osteochondrodysplasia (Min Poodle Type)

Osteogenesis Imperfecta (Beagle Type)

Osteogenesis Imperfecta (Chow Chow)

Osteogenesis Imperfecta (Golden Retriever Type)

Osteogenesis Imperfecta SERPINH1 (Dachshund Type)

Paroxysmal Exercise-Induced Dyskinesia (PED) (Shetland Sheepdog Type)

Periodic Fever Syndrome (Shar Pei Fever)

Phosphofructokinase Deficiency (German Spaniel)

Phosphofructokinase Deficiency (Spaniel Type)

Pituitary Dwarfism

Polycystic Kidney Disease (Bull Terrier Type)

Polyneuropathy (NDRG1) (Alaskan Malamute)

Polyneuropathy (NDRG1) (Greyhound)

Polyneuropathy and Neuronal Vacuolation (JLPP)

Polyneuropathy ARHGEF10 (Leonberger/Saint Bernard Type)

Polyneuropathy GJA9 (Leonberger/St Bernard Type)

Polyneuropathy with Ocular Abnormalities and Neuronal Vacuolation

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 (Basset Fauve de Bretagne Type)

Primary Open Angle Glaucoma (Beagle Type)

Primary Open Angle Glaucoma and Primary Lens Luxation (Shar Pei Type)

Progressive Epidermal Nevi

Progressive Retinal Atrophy - crd1PRA

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 (Giant Schnauzer Type)

Progressive Retinal Atrophy (Puli Type)

Progressive Retinal Atrophy (Shetland Sheepdog)

Progressive Retinal Atrophy 3

Progressive Retinal Atrophy Dominant (Mastiff Type)

Progressive Retinal Atrophy PRA1 (Papillon Type)

Progressive Retinal Atrophy, crd SWD

Progressive Retinal Atrophy, Early Onset (Spanish Water Dog Type)

Progressive Rod Cone Degeneration (prcd) - PRA

Pyruvate Dehydrogenase Phosphatase Deficiency (Clumber Spaniel Type)

Pyruvate Kinase Deficiency (Basenji Type)

Pyruvate Kinase Deficiency (Beagle Type)

Pyruvate Kinase Deficiency (Labrador Type)

Pyruvate Kinase Deficiency (Pug)

Pyruvate Kinase Deficiency (Terrier Type)

Raine Syndrome Dental Hypomineralisation (Border Collie)

Recurrent Inflammatory Pulmonary (Collie Type)

Renal Cystadenocarcinoma and Nodular Dermatofibrosis (German Shepherd Type)

Retinal Degeneration

Retinal Degeneration (Norwegian Elkhound Type)

Retinal Degeneration RCD1a

Retinitis Pigmentosa (Lapponian Herder Type)

Retinopathy (Vallhund Type)

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)

Severe Combined Immunodeficiency Disease (Terrier Type)

Severe Combined Immunodeficiency Disease, X-Linked (Basset Hound Type)

Severe Combined Immunodeficiency Disease, X-Linked (Corgi Type)

Skeletal Dysplasia 2 (Mild Disproportionate Dwarfism)

Spinal Dysraphism (Weimaraner Type)

Spinocerebellar Ataxia

Spinocerebellar Ataxia (Alpine Dachsbracke Type)

Spinocerebellar Ataxia (CAPN1)

Spinocerebellar Ataxia (Jack Russell Type)

Spondylocostal Dysostosis (Miniature Schnauzer Type)

Spongy Degeneration with Cerebellar Ataxia (KCNJ10)

Spongy Degeneration with Cerebellar Ataxia (SDCA2) Belgian Shepherd

Stargardt Disease (Retinal Degeneration)

Startle Disease (Spanish Greyhound Type)

Succinic Semialdehyde Dehydrogenase Deficiency (SSADHD)

Thrombasthenic Thrombopathia (Otterhound Type)

Thrombopathia (Basset Hound Type)

Thrombopathia (Newfoundland Type)

Thrombopathia (Platelet Dysfunction)

Trapped Neutrophil Syndrome (Border Collie Type)

Type A PRA 1 (Miniature Schnauzer Type)

Ullrich-Like Musculary Dystrophy, Variant 1

Ullrich-Like Musculary Dystrophy, Variant 2

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

von Willebrand Disease III (Kooikerhondje Type)

von Willebrand Disease III (Shetland Sheepdog 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)

X-Linked PRA2 (Miniature Schnauzer Type)

Traits:

B Locus (Brown) - Siberian Husky Type

Behaviour Propensity (Belgian Shepherd Type), Variant 2

E Locus (Ancient Red) - eA (Spitz and Scent Hound Type)

Eh Locus (Sable, Cocker Spaniel Type)

Hairlessness (American Hairless Terrier Type)

Hairlessness (Scottish Deerhound Type)

Himalayan Colour Pattern

L Locus (Long Hair/Fluffy) - Lh2 (Akita, Eurasier, Samoyed, Siberian Husky Type)

L Locus (Long Hair/Fluffy) - Lh3 (Eurasier Breed Type)

Pheomelanin Intensity CFA18 (Poodle/Coonhound Type)

Pheomelanin Colour Intensity CFA2 (Various Breeds)

Pheomelanin Colour Intensity CFA21 (Various Breeds)

Pheomelanin Intensity CFA15 (Retriever and Poodle Type)

Polydactyl/Dewclaws

Polydactyly (Great Pyrenees Type)

Ticking & Roan (TR)

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 Pheomelanin Locus Colour Intensity

Brown Deletion = Bd

Brown Stop Codon = Bs

Brown Insertion = Bc

Brown TYRP1 [Australian Shepherd Type] = Ba

Cocoa/Brown HPS3 [French Bulldog Type] = Co

Brown TYRP1 [Lancashire Heeler Type] = Bl

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)

M Locus (Merle/Dapple)

Black and Tan/Saddle Coat Colour

Harlequin (H) Pattern (Great Dane Type)

Oculocutaneous Albinism (Small Breed Type)

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)

Improper Coat/Furnishings (RSPO2)

Body Size IGSF1 "Bulky Gene"

Natural Bob Tail (Short Tail Phenotype)

Screw Tail (DVL2)

Oculocutaneous Albinism (Bullmastiff)

DNA Profile:

Canine DNA Profile (ISAG SNP Panel 1 & 2)