GENOPAWS — Pet Genetic Center and Services
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For dogs

Dog Disease Screening

Screen for inherited disease risks so you can plan ahead.

Tests genetic markers linked to heritable diseases in dogs, so you know the risks early and can plan annual check-ups and care accordingly.

Price

THB 6,999

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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