

(โรคตา)
Ophthalmologic
-
Achromatopsia (Labrador Type)
-
Achromatopsia (Pointer Type)
-
Canine Multifocal Retinopathy CMR1 (Coton de Tulear Type)
-
Canine Multifocal Retinopathy CMR2 (Coton du Tulear Type)
-
Canine Multifocal Retinopathy CMR3 (Lapphund 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 Stationary Night Blindness
-
Curly Coat Dry Eye Syndrome (Cavalier Type)
-
Generalised PRA 1 (Golden Retriever Type)
-
Generalised PRA 2 (Golden Retriever Type)
-
Goniodysgenesis and Glaucoma (Border Collie)
-
Hereditary Cataract
-
Hereditary Cataract (Dominant)
-
Macular Corneal Dystrophy (Labrador Type)
-
Microphthalmia, Anophthalmia & Coloboma (Wheaten Terrier Type)
-
Multifocal Retinopathy CMR1 (Mastiff/Bull Breeds Type)
-
Primary Glaucoma
-
Primary Lens Luxation
-
Primary Open Angle Glaucoma (Beagle Type)
-
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 Rod Cone Degeneration (prcd) - PRA
-
rcd4-PRA (Late Onset)
-
Retinal Degeneration (Norwegian Elkhound Type)
-
Retinal Degeneration RCD1a
-
Retinopathy (Vallhund Type)
-
Stargardt Disease (Retinal Degeneration)
-
Type A PRA 1 (Miniature Schnauzer Type)
-
Type B PRA 2 [HIVEP3] (Miniature Schnauzer Type)
-
X-Linked PRA (Samoyed/Husky Type)
-
X-Linked PRA2 (Miniature Schnauzer Type)

(โรคสมอง)
Nervous system
-
Grey Collie Syndrome
-
Adult Onset Deafness Border Collie (Linkage Association Test)
-
Bilateral Deafness MYO7A Gene (Dobermann Type)
-
Brain Hypomyelination (Weimaraner Type)
-
Canine Multiple System Degeneration (Kerry Blue Terrier Type)
-
Cerebellar Ataxia (American Staffordshire Terrier Type)
-
Cerebellar Ataxia (Finnish Hound Type)
-
Cerebellar Cortical Degeneration (Hungarian Vizsla Type)
-
Congenital Myasthenic Syndrome (Jack Russell Terrier Type)
-
Congenital Myasthenic Syndrome (Labrador Retriever Type)
-
Congenital Myasthenic Syndrome (Old Danish Pointer Type)
-
Congenital Myasthenic Syndrome (Spanish Water Dog Type)
-
Degenerative Myelopathy
-
Early Onset Adult Deafness (Rhodesian Ridgeback)
-
Encephalopathy (Alaskan Husky Type)
-
Episodic Falling Syndrome (Cavalier Type)
-
Exercise Induced Collapse (Retriever Type)
-
Generalised Myoclonic Epilepsy (Rhodesian Ridgeback Type)
-
Hereditary Ataxia (Autophagy)
-
Hereditary Deafness PTPRQ Gene (Dobermann Type)
-
Ivermectin Sensitivity MDR1 (Multi Drug Resistance)
-
Juvenile Epilepsy (Benign Familial) - Lagotto Romagnolo Type
-
L2- Hydroxyglutaric Aciduria
-
Laryngeal Paralysis (Bull Terrier Type)
-
Laryngeal Paralysis (St Bernard/Leonberger Type)
-
Leukoencephalomyelopathy (LEMP)
-
Leukoencephalomyelopathy (Leonberger 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 (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 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 (Cane Corso Type)
-
Neuronal Ceroid Lipofuscinosis NCL (Golden Retriever Type)
-
Neuronal Ceroid Lipofuscinosis NCL (Saluki Type)
-
Neuronal Ceroid Lipofuscinosis NCL 12 (Cattle Dog Type)
-
Polyneuropathy (NDRG1) (Alaskan Malamute)
-
Polyneuropathy (NDRG1) (Greyhound)
-
Polyneuropathy and Neuronal Vacuolation (JLPP)
-
Polyneuropathy GJA9 (Leonberger/St Bernard Type)
-
Sanfilippo Syndrome Type A / Mucopolysaccharidosis IIIA (Dachshund Type)
-
Sensory Neuropathy (Border Collie Type)
-
Spinal Dysraphism (Weimaraner Type)
-
Spinocerebellar Ataxia (CAPN1)
-
Spinocerebellar Ataxia (Jack Russell Type)
-
Spongy Degeneration with Cerebellar Ataxia (KCNJ10)
-
Spongy Degeneration with Cerebellar Ataxia (SDCA2) Belgian Shepherd
-
Startle Hyperekplexia (Wolfhound Type)
-
Van den Ende-Gupta Syndrome (Wire Fox Terrier Type)
-
ACRAL MUTILATION SYNDROME (SPANIEL & POINTER TYPE
-
Canine Multiple System Degeneration (Chinese Crested)
-
Leukoencephalomyelopathy (Leonberger Type)

(ระบบทางเดินหายใจ)
Respiratory
-
Acute Respiratory Distress Syndrome (Dalmatian Type)
-
Airway Distress Syndrome (ADAMTS3) - Risk Marker
-
Beta Manisidosis (German Shepherd Type)
-
Primary Ciliary Dyskenesia (Malamute Type)
-
Primary Ciliary Dyskinesia (Old English Sheepdog Type)

(โรคไตและระบบปัสสาวะ)
Urinary system
-
2,8-Dihydroxyadenine Urolithiasis Type IA
-
Alport Syndrome/ Hereditary Nephropathy (Samoyed Type)
-
Autosomal Hereditary Recessive Nephropathy
-
Copper Toxicosis (ATP7B & ATP7A) (Labrador Retriever Type)
-
Copper Toxicosis (Bedlington Terrier Type)
-
Cystinuria (Miniature Pinscher Type)
-
Cystinuria (Newfoundland Type)
-
Cystinuria (SLC3A1) (Australian Cattle Dog Type)
-
Cystinuria (SLC3A1) Labrador Retriever Type
-
Familial Nephropathy
-
Glomerulopathy (PLN) KIRREL2
-
Glomerulopathy (PLN) NPHS1
-
Hereditary Nephropathy
-
Hyperuricosuria
-
Polycystic Kidney Disease (Bull Terrier Type)
-
Primary Hyperoxaluria
-
Renal Cystadenocarcinoma and Nodular Dermatofibrosis (German Shepherd Type)
-
Cystinuria Type 3 [Bulldog Risk Factor Variant 2&3]
-
Polycystic Kidney Disease (Bull Terrier Type)

(โรคหัวใจ)
Cardiovascular
-
Arrhythmogenic Right Ventricular Cardiomyopathy (RESEARCH)
-
Cardiomyopathy and Juvenile Mortality (Belgian Shepherd)
-
Dilated Cardiomyopathy - 2nd VARIANT (Dobermann Type)
-
Dilated Cardiomyopathy (Dobermann Type)
-
Dilated Cardiomyopathy (Schnauzer Type)
-
Recurrent Inflammatory Pulmonary (Collie Type)
-
Myxomatous Mitral Valve Disease 1 [NEBL535 RiskVariant]
-
Myxomatous Mitral Valve Disease 2 [NEBL576 RiskVariant]
-
Myxomatous Mitral Valve Disease 3 [NEBL724CandidateVariant]
-
Myxomatous Mitral Valve Disease 4 [NEBL890 RiskVariant]
-
Myxomatous Mitral Valve Disease 5 [NEBL498 Risk Variant]

(กล้ามเนื้อและกระดูก)
Musculoskeletal
-
Centronuclear Myopathy (Labrador Retriever Type)
-
Centronuclear Myopathy /Inherited Myopathy (Great Dane Type)
-
Chondrodysplasia ITGA10 (Elkhound Type)
-
Chondrodystrophy (CDDY) & Intervertebral Disc Disease (IVDD) [RESEARCH ONLY]
-
Craniomandibular Osteopathy (Terrier Type)
-
Myotonia Congenita (Miniature Schnauzer Type)
-
Myotonia Hereditaria (Cattle Dog Type)
-
Myotubular Myopathy X-Linked (Labrador Retriever Type)
-
Myotubular Myopathy X-Linked (Rottweiler Type)
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Osteochondrodysplasia (Min Poodle Type)
-
Osteogenesis Imperfecta (Chow Chow)
-
Osteogenesis Imperfecta (Golden Retriever Type)
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Osteogenesis Imperfecta SERPINH1 (Dachshund Type)
-
Sarcoglycan Deficient Muscular Dystrophy (SDMD)
-
Skeletal Dysplasia 2 (Mild Disproportionate Dwarfism)
-
Spondylocostal Dysostosis (Miniature Schnauzer Type)
-
Spinal Dysraphism (Weimaraner Type)
-
Muscular Dystrophy (Landseer Type)
-
Myostatin Deficiency

(ระบบทางเดินอาหาร)
Digestive system
-
Gall Bladder Mucocele Formation (Shetland Sheepdog Type)

(ระบบเลือดและน้ำเหลือง)
Haemolymphatic
-
Bernard-Soulier Syndrome (Cocker Spaniel Type)
-
Congenital Macrothrombocytopenia
-
Elliptocytosis B-spectrin (Labrador Retriever/Poodle Type)
-
Factor VII Deficiency
-
Globoid Cell Leukodystrophy/Krabbe’s Disease
-
Grey Collie Syndrome (Cyclic Hematopoiesis) AP3
-
Haemophilia A / Factor VIII (German Shepherd Type)
-
Haemophilia A/Factor VIII Deficiency (Boxer Type)
-
Haemophilia B / Factor IX (Cairn Terrier Type)
-
Haemophilia B / Factor IX G418E
-
Macrothrombocytopenia (Cairn/Norfolk Terrier Type)
-
May-Hegglin Anomaly (Pug Type)
-
THROMBOPATHIA (PLATELET DYSFUNCTION)
-
Post Operative Haemorrhage / Platelet Disorder (Mountain Dog Type)
-
Prekallikrein Deficiency (Shih Tzu Type)
-
Scott Syndrome (German Shepherd Type)
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Thrombasthenic Thrombopathia (Otterhound Type)
-
Thrombopathia (Basset Hound Type)
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Thrombopathia (Finnish Spitz 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
-
Congenital Methemoglobinemia (Poodle and Pomeranian Type)
-
Haemophilia B (Lhasa Apso Type)

(โรคผิวหนัง)
Dermatologic
-
Dystrophic Epidermolysis Bullosa (Asian Shepherd Type)
-
Dystrophic Epidermolysis Bullosa (Golden Retriever Type)
-
Ectodermal Dysplasia (Chesapeake Bay Retriever Type)
-
Ehlers-Danlos Syndrome (Labrador Type)
-
Footpad Hyperkeratosis (Rottweiler)
-
Hereditary Footpad Hyperkeratosis
-
Hereditary Footpad Hyperkeratosis (Dogue de Bordeaux Type)
-
Hereditary Nasal Parakeratosis/Dry Nose (Labrador Retriever Type)
-
Ichthyosis (American Bulldog)
-
Ichthyosis (German Shepherd Type)
-
Ichthyosis (Great Dane)
-
Ichthyosis (Norfolk Terrier)
-
Ichthyosis A (Golden Retriever)
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Juvenile Dermatomyositis [MAP3K7CL RISK ALLELE]
-
Juvenile Dermatomyositis [PAN2 RISK ALLELE]
-
Lethal Acrodermatitis MKLN1 (Bull Terrier Type)
-
Coat Colour Dilution Alopecia
-
Musladin-Lueke Syndrome (Beagle Type)
-
Ichthyosis Golden Retriever Type 2

(ระบบสืบพันธุ์)
Reproductive
-
Cleft Lip Palate (Nova Scotia Duck Tolling Retriever Type)
-
Mullerian Duct Syndrome (Miniature Schnauzer Type)

(โรคฟัน)
Teeth and structures
-
Amelogenesis Imperfecta (Akita Type)
-
Amelogenesis Imperfecta (Italian Greyhound Type)
-
Raine Syndrome Dental Hypomineralisation (Border Collie)

(โ รคภูมิคุ้มกัน)
Immunologic
-
Canine Leukocyte Adhesion Deficiency Type I (Irish Setter Type)
-
Canine Leukocyte Adhesion Deficiency Type III (German Shepherd Type)
-
Severe Combined Immunodeficiency (Frisian Water Dog)
-
Trapped Neutrophil Syndrome (Border Collie Type)

(ต่อมไร้ท่อ)
Endocrine
-
Congenital Hypothyroidism with Goiter (Tenterfield Terrier Type)
-
Congenital Hypothyroidism with Goiter (Toy Fox Terrier Type)

(ระบบการทำงานของร่างกาย)
Metabolic
-
Cobalamin Malabsorption: Cubilin Deficiency (Border Collie Type)
-
Cobalamin Malabsorption (Beagle Type)
-
Fucosidosis (English Springer Spaniel 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)
-
Glycogen Storage Disease IA (Maltese Type)
-
Glycogen Storage Disease III
-
Glycogen Storage Disease IIIA (Curly Coat Retriever Type)
-
Malignant Hyperthermia
-
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)
-
Periodic Fever Syndrome (Shar Pei Fever)
-
Phosphofructokinase Deficiency (German Spaniel)
-
Phosphofructokinase Deficiency (Spaniel Type)
-
Pompes Disease (Lapphund Type)
-
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)
-
Catalase Deficiency (Beagle Type)
-
Dystrophic Epidermolysis Bullosa (Asian Shepherd Type)
-
Dystrophic Epidermolysis Bullosa (Golden Retriever Type)
-
Ectodermal Dysplasia (Chesapeake Bay Retriever Type)
-
Ehlers-Danlos Syndrome (Labrador Type)
-
Footpad Hyperkeratosis (Rottweiler)
-
Hereditary Footpad Hyperkeratosis
-
Hereditary Footpad Hyperkeratosis (Dogue de Bordeaux Type)
-
Hereditary Nasal Parakeratosis/Dry Nose (Labrador Retriever Type)
-
Ichthyosis (American Bulldog)
-
Ichthyosis (German Shepherd Type)
-
Ichthyosis (Great Dane)
-
Ichthyosis (Norfolk Terrier)
-
Ichthyosis A (Golden Retriever)
-
Juvenile Dermatomyositis [MAP3K7CL RISK ALLELE]
-
Juvenile Dermatomyositis [PAN2 RISK ALLELE]
-
Lethal Acrodermatitis MKLN1 (Bull Terrier Type)
-
Coat Colour Dilution Alopecia
-
Musladin-Lueke Syndrome (Beagle Type)
-
Ichthyosis Golden Retriever Type 2

(ยีนลักษณะ)
TRAITS
-
A Locus (Fawn/Sable;Tri/Tan Points)
-
B Locus [TYRP1] (Australian Shepherd Type)
-
Black and Tan/Saddle Coat Colour
-
Black Hair Follicular Dysplasia
-
Body Size IGSF1 "Bulky Gene"
-
Brown Coat Colour Profile
-
Coat Colour Dilution Alopecia
-
Coat Composition CFA28 Gene (Double/Single Coat)
-
Cocoa (Brown) Coat Colour
-
Curly Coat Phenotype (KRT71 - p.Ser422ArgfsTer)
-
Curly Coat/Hair Curl (KRT71 R151W)
-
D (Dilute) Locus
-
Dilute D2 Variant (Chow Chow Type)
-
E Locus - (Cream/Red/Yellow)
-
E Locus (Artic Breeds Pale/Yellow/White Variant) e3
-
E Locus (Cattle Dog Cream Variant) e2
-
EG Locus (Grizzle)
-
EM (MC1R) Locus - Melanistic Mask
-
Harlequin (H) Pattern (Great Dane Type)
-
I Locus Colour Intensity
-
Improper Coat (RSPO2)
-
K Locus (Dominant Black)
-
Liver [TYRP1] (Lancashire Heeler Type)
-
Long Hair Gene (Canine C95F)
-
Long Hair Gene (Canine DUP GG)
-
Merle
-
Natural Bob Tail (Short Tail Phenotype)
-
Oculocutaneous Albinism
-
Oculocutaneous Albinism (Bullmastiff)
-
Pied (BOTH SINE and REPEAT VARIANTS)
-
Polydactyl/Dewclaws
-
Screw Tail (DVL2)
-
Shedding (MC5R)
