GENOPAWS — Pet Genetic Center and Services
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Dog Breed-Specific Disease Test

Screen only the diseases common to your pet’s breed — focused and better value.

Each breed carries its own common hereditary conditions. We select the disease panel relevant to your pet’s breed, so you learn the risks that actually matter — and can plan care ahead.

Disease testing has 3 levels: Single-gene (one marker) · Breed-Specific (the panel common to your pet’s breed) · Full screening (the whole panel) — this package is the middle tier: better value than single-gene, more focused than the full panel.

Price

THB 5,999

Message us on LINE @genopaws for pricing and details — our team is happy to help.

Book at-home visit Ask on LINE

What you get

  • Screening across multiple heritable disease markers
  • Status per condition: Clear / Carrier / At-risk
  • Care guidance based on results
  • At-home collection + expert result explanation

How it works

1

Book via LINE OA

Message GENOPAWS on LINE OA @genopaws to consult and choose the DNA package that suits your pet.

2

At-home sample collection

Within Bangkok metro, the GENOPAWS team visits your home to collect the sample — convenient, safe, and stress-free.

3

Expert result explanation

When results return from the lab, our specialist team explains every finding clearly and in detail.

Every package includes at-home sample collection (Bangkok area) and a result explanation by our specialist team.

What we screen for

We screen hundreds of genetic markers and report those relevant to your pet's breed — informational screening, not a diagnosis.

Genetic diseases screened (341)
  • Achromatopsia (German Shorthaired Pointer Type)
  • Achromatopsia (Labrador Type)
  • Achromatopsia (Shepherd/Arctic Breed Type)
  • Acral Mutilation Syndrome (SPANIEL & POINTER TYPE)
  • Acute Respiratory Distress Syndrome (Dalmatian Type)
  • 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 (Parson Russell Terrier Type), Variant 1
  • Ataxia (KCNIP4 - Norwegian Buhund Type)
  • Autosomal Hereditary Recessive Nephropathy (Familial Nephropathy)
  • Bernard-Soulier Syndrome (Cocker Spaniel Type)
  • Beta Mannisidosis (German Shepherd Type)
  • Bilateral Deafness MYO7A Gene (Doberman 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 (Finnish Hound Type) SEL1L gene
  • Cerebellar Cortical Degeneration (Hungarian Vizsla Type)
  • Cerebellar Degeneration (RAB24 gene)
  • Charcot Marie Tooth Disease (Type 4B2)
  • Chondrodysplasia ITGA10 (Elkhound Type)
  • Chondrodystrophy with Intervertebral Disc Disease Risk Factor (CDDY with IVDD)
  • 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-Rod Dystrophy I - PRA (crd -4/cord I)
  • Congenital Deafness (Australian Stumply Tail 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 (Golden Retriever 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 (ATP7B & ATP7A) (Labrador Retriever Type)
  • Copper Toxicosis (Bedlington 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)
  • Degenerative Myelopathy Early-Onset Risk Modifier (Pembroke Welsh Corgi Type)
  • Delayed Postoperative Haemorrhage (Scottish Deerhound Type)
  • Diffuse Cystic Renal Dysplasia and Hepatic Fibrosis
  • Dihydroxyadenine Urolithiasis Type IA
  • Dilated Cardiomyopathy - 2nd VARIANT (Dobermann Type)
  • Dilated Cardiomyopathy (Dobermann Type)
  • Dilated Cardiomyopathy (Schnauzer Type)
  • Dilated Cardiomyopathy and Sudden Death (Manchester Terrier, English Toy Terrier Type)
  • Disproportionate Dwarfism (Vizsla Type)
  • Duchenne Muscular Dystrophy (Border Collie Type)
  • Duchenne Muscular Dystrophy (Pembroke Welsh Corgi Type)
  • Dyserythropoietic Anemia and Myopathy Syndrome (DAMS) (English Springer Spaniel Type)
  • Dyserythropoietic Anemia and Polymyopathy (DAMS) (Labrador Retriever)
  • Dysphagia (French Bulldog)
  • Dystrophic Epidermolysis Bullosa (Asian Shepherd Type)
  • Dystrophic Epidermolysis Bullosa (Basset Hound Type)
  • Dystrophic Epidermolysis Bullosa (Golden Retriever Type)
  • Early Adult Onset Deafness Border Collie (Linkage Association Test)
  • Early Onset Adult Deafness (Rhodesian Ridgeback)
  • Early-Onset Progressive Retinal Atrophy
  • EarlyOnset 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)
  • Enamel Hypoplasia - Amelogenesis Imperfecta (Samoyed Type)
  • Encephalopathy (Alaskan Husky 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
  • Fanconi Syndrome
  • Fatal Neonatal Interstitial Lung Disease (LAMP)
  • 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)
  • Gastrointestinal Polyposis
  • 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 (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 (Australian Shepherd Type)
  • 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 Necrotising Myelopathy (Kooiker Type)
  • Hereditary Nephropathy (English Springer Spaniel)
  • Hyperuricosuria
  • Hypophosphatasia
  • Ichthyosis (American Bulldog)
  • Ichthyosis (German Shepherd Type)
  • Ichthyosis (Golden Retriever Type 2)
  • Ichthyosis (Great Dane)
  • Ichthyosis (Jack Russell Terrier Type)
  • Ichthyosis (Norfolk Terrier)
  • Ichthyosis A (Golden Retriever)
  • Increased Susceptibility to M. Avium Infection
  • Inflammatory Myopathy
  • Intestinal Cobalamin Malabsorption (Australian Shepherd Type)
  • 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 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)
  • Muscle Hypertrophy and Gait (French Bulldog Type)
  • Muscular Dystrophy (Golden Retriever Type)
  • Muscular Dystrophy (Landseer Type)
  • Musladin-Lueke Syndrome (Beagle Type)
  • Myelin and Lysosomal Storage Disease (Weimaraner 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)
  • 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 4A - Cerebellar Ataxia (American Staffordshire Terrier 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 (Karelian Bear Dog Type)
  • 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
  • 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 Hyperoxaluria
  • Primary Lens Luxation
  • Primary Open Angle Glaucoma (Basset Fauve de Bretagne Type)
  • Primary Open Angle Glaucoma (Beagle Type)
  • Primary Open Angle Glaucoma (Norwegian Elkhound 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 (BBS2)
  • Progressive Retinal Atrophy (CNGA)
  • Progressive Retinal Atrophy (Giant Schnauzer Type)
  • Progressive Retinal Atrophy (Lapponian Herder Type)
  • Progressive Retinal Atrophy (Puli Type)
  • Progressive Retinal Atrophy 3
  • Progressive Retinal Atrophy Dominant (Mastiff Type)
  • Progressive Retinal Atrophy PRA1 (Papillon Type)
  • Progressive Retinal Atrophy RCD4
  • Progressive Retinal Atrophy, Cone-rod Dystrophy (Dachshund Type)
  • Progressive Retinal Atrophy, Cone-Rod Dystrophy 3 (Glen of Imaal Terrier Type)
  • Progressive Retinal Atrophy, Early Onset (Spanish Water Dog Type)
  • Progressive Retinal Atrophy, PRA4 (Lhasa Apso 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 (Norwegian Elkhound Type)
  • Retinal Degeneration RCD1a
  • Retinal Dysplasia/Oculoskeletal Dysplasia 1
  • Retinal Dysplasia/Oculoskeletal Dysplasia 2
  • 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 (CAPN1) Parson Russell Terrier type
  • Spinocerebellar Ataxia (KCNJ10 Terrier type)
  • Spinocerebellar Ataxia (SCN8A - Alpine Dachsbracke Type)
  • Spinocerebellar Ataxia (SLC12A6) Belgian Shepherd type
  • Spondylocostal Dysostosis (Miniature Schnauzer Type)
  • Spongy Degeneration with Cerebellar Ataxia (KCNJ10) Belgian Shepherd type
  • Spongy Degeneration with Cerebellar Ataxia type 2 (SDCA2) (ATP1B2 gene)
  • Stargardt Disease (Retinal Degeneration)
  • Startle Disease (Spanish Greyhound Type)
  • Stickler Syndrome Type II (Old English Sheepdog 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)
  • Type B PRA 2 [HIVEP3] (Miniature Schnauzer Type)
  • Ullrich-Like Muscular Dystrophy, Variant 1
  • Ullrich-Like Muscular 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)
  • Xanthine Urolithiasis (Cavalier King Charles Spaniel Type)
  • Xanthine Urolithiasis (Dachshund Type)
  • Xanthine Urolithiasis (Manchester Terrier Type)
  • Xanthine Urolithiasis (Mixed Breed)

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