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Results for: $119

The following are tests that we currently offer in this breed bundle. If you cannot find your test, please contact us for help or additional information on when tests might be available.
Breed Available Tests
Australian Cobberdog
  • Centronuclear Myopathy
  • Chondrodystrophy (CDDY and IVDD Risk) with or without Chondrodysplasia (CDPA)
  • Congenital Myasthenic Syndrome (Labrador Retriever Type)
  • Copper Toxicosis (Labrador Retriever Type)
  • Cystinuria (Labrador Retriever Type)
  • Degenerative Myelopathy (Common Variant)
  • Dry Eye Curly Coat Syndrome
  • Episodic Falling Syndrome
  • Exercise-Induced Collapse
  • Familial Nephropathy (Cocker Spaniel Type)
  • Globoid Cell Leukodystrophy (Terrier Type)
  • Glycogen Storage Disease VII, PFK Deficiency
  • Microphthalmia (Soft Coated Wheaten Terrier Type)
  • Muscular Dystrophy (Golden Retriever Type)
  • Narcolepsy (Labrador Retriever Type)
  • Neonatal Encephalopathy with Seizures
  • Progressive Retinal Atrophy, Cone-Rod Dystrophy 4
  • Progressive Retinal Atrophy, Progressive Rod-Cone Degeneration
  • Von Willebrand Disease I
Show all 19 Tests
Australian Shepherd
  • Chondrodystrophy (CDDY and IVDD Risk) with or without Chondrodysplasia (CDPA)
  • Coagulation Factor VII Deficiency
  • Collie Eye Anomaly
  • Cone Degeneration
  • Craniomandibular Osteopathy
  • Degenerative Myelopathy (Common Variant)
  • Exercise-Induced Collapse
  • Hereditary Ataxia (Australian Shepherd Type)
  • Hereditary Cataracts (Australian Shepherd Type)
  • Hyperuricosuria
  • Intestinal Cobalamin Malabsorption (Australian Shepherd Type)
  • Intestinal Cobalamin Malabsorption (Border Collie Type)
  • Junctional Epidermolysis Bullosa (Australian Shepherd Type)
  • Multidrug Resistance 1
  • Multifocal Retinopathy 1
  • Neuronal Ceroid Lipofuscinosis 5 (Herding Dog Type)
  • Neuronal Ceroid Lipofuscinosis 6
  • Neuronal Ceroid Lipofuscinosis 8 (Australian Shepherd Type)
  • Progressive Retinal Atrophy, Progressive Rod-Cone Degeneration
  • Von Willebrand Disease I
Show all 20 Tests
Cockapoo
  • Acral Mutilation Syndrome
  • Bernard-Soulier Syndrome
  • Chondrodystrophy (CDDY and IVDD Risk) with or without Chondrodysplasia (CDPA)
  • Congenital Methemoglobinemia
  • Degenerative Myelopathy (Common Variant)
  • Ehlers-Danlos Syndrome (Poodle Type, Variants 1 and 2)
  • Exercise-Induced Collapse
  • Familial Nephropathy (Cocker Spaniel Type)
  • GM2 Gangliosidosis (Poodle Type)
  • Gallbladder Mucoceles
  • Glycogen Storage Disease VII, PFK Deficiency
  • Hereditary Cataracts
  • Multidrug Resistance 1
  • Neonatal Encephalopathy with Seizures
  • Osteochondrodysplasia
  • Progressive Retinal Atrophy, Progressive Rod-Cone Degeneration
  • Progressive Retinal Atrophy, Rod-Cone Dysplasia 4
  • Von Willebrand Disease I
Show all 18 Tests
Miniature American Shepherd
  • Chondrodystrophy (CDDY and IVDD Risk) with or without Chondrodysplasia (CDPA)
  • Coagulation Factor VII Deficiency
  • Collie Eye Anomaly
  • Cone Degeneration
  • Craniomandibular Osteopathy
  • Degenerative Myelopathy (Common Variant)
  • Exercise-Induced Collapse
  • Hereditary Ataxia (Australian Shepherd Type)
  • Hereditary Cataracts (Australian Shepherd Type)
  • Hyperuricosuria
  • Intestinal Cobalamin Malabsorption (Australian Shepherd Type)
  • Intestinal Cobalamin Malabsorption (Border Collie Type)
  • Junctional Epidermolysis Bullosa (Australian Shepherd Type)
  • Multidrug Resistance 1
  • Multifocal Retinopathy 1
  • Neuronal Ceroid Lipofuscinosis 6
  • Neuronal Ceroid Lipofuscinosis 8 (Australian Shepherd Type)
  • Progressive Retinal Atrophy, Progressive Rod-Cone Degeneration
  • Von Willebrand Disease I
Show all 19 Tests
Miniature Australian Shepherd
  • Chondrodystrophy (CDDY and IVDD Risk) with or without Chondrodysplasia (CDPA)
  • Coagulation Factor VII Deficiency
  • Collie Eye Anomaly
  • Cone Degeneration
  • Craniomandibular Osteopathy
  • Degenerative Myelopathy (Common Variant)
  • Exercise-Induced Collapse
  • Hereditary Ataxia (Australian Shepherd Type)
  • Hereditary Cataracts (Australian Shepherd Type)
  • Hyperuricosuria
  • Intestinal Cobalamin Malabsorption (Australian Shepherd Type)
  • Intestinal Cobalamin Malabsorption (Border Collie Type)
  • Junctional Epidermolysis Bullosa (Australian Shepherd Type)
  • Multidrug Resistance 1
  • Multifocal Retinopathy 1
  • Neuronal Ceroid Lipofuscinosis 6
  • Neuronal Ceroid Lipofuscinosis 8 (Australian Shepherd Type)
  • Progressive Retinal Atrophy, Progressive Rod-Cone Degeneration
  • Von Willebrand Disease I
Show all 19 Tests
Schnoodle
  • Chondrodystrophy (CDDY and IVDD Risk) with or without Chondrodysplasia (CDPA)
  • Coagulation Factor VII Deficiency
  • Congenital Methemoglobinemia
  • Degenerative Myelopathy (Common Variant)
  • Ehlers-Danlos Syndrome (Poodle Type, Variants 1 and 2)
  • GM2 Gangliosidosis (Poodle Type)
  • Hereditary Cataracts
  • Multidrug Resistance 1
  • Myotonia Congenita (Schnauzer Type)
  • Neonatal Encephalopathy with Seizures
  • Osteochondrodysplasia
  • Persistent Müllerian Duct Syndrome
  • Progressive Retinal Atrophy, Progressive Rod-Cone Degeneration
  • Progressive Retinal Atrophy, Rod-Cone Dysplasia 4
  • Spondylocostal Dysostosis
  • Von Willebrand Disease I
Show all 16 Tests
Service/Assistance Lab/Golden Retriever cross
  • Centronuclear Myopathy
  • Congenital Myasthenic Syndrome (Golden Retriever Type)
  • Congenital Myasthenic Syndrome (Labrador Retriever Type)
  • Copper Toxicosis (Labrador Retriever Type)
  • Degenerative Myelopathy (Common Variant)
  • Exercise-Induced Collapse
  • Hereditary Nasal Parakeratosis (Labrador Retriever Type)
  • Ichthyosis (Golden Retriever Type 1)
  • Ichthyosis (Golden Retriever Type 2)
  • Macular Corneal Dystrophy (Labrador Retriever Type)
  • Neuronal Ceroid Lipofuscinosis 5 (Golden Retriever Type)
  • Progressive Retinal Atrophy, Cone-Rod Dystrophy 4
  • Progressive Retinal Atrophy, Golden Retriever 1
  • Progressive Retinal Atrophy, Golden Retriever 2
  • Progressive Retinal Atrophy, Progressive Rod-Cone Degeneration
  • Retinal Dysplasia/Oculoskeletal Dysplasia 1
  • Skeletal Dysplasia 2
  • Stargardt Disease
Show all 18 Tests
Toy Australian Shepherd
  • Chondrodystrophy (CDDY and IVDD Risk) with or without Chondrodysplasia (CDPA)
  • Coagulation Factor VII Deficiency
  • Collie Eye Anomaly
  • Cone Degeneration
  • Craniomandibular Osteopathy
  • Degenerative Myelopathy (Common Variant)
  • Exercise-Induced Collapse
  • Hereditary Ataxia (Australian Shepherd Type)
  • Hereditary Cataracts (Australian Shepherd Type)
  • Hyperuricosuria
  • Intestinal Cobalamin Malabsorption (Australian Shepherd Type)
  • Intestinal Cobalamin Malabsorption (Border Collie Type)
  • Junctional Epidermolysis Bullosa (Australian Shepherd Type)
  • Multidrug Resistance 1
  • Multifocal Retinopathy 1
  • Neuronal Ceroid Lipofuscinosis 6
  • Neuronal Ceroid Lipofuscinosis 8 (Australian Shepherd Type)
  • Progressive Retinal Atrophy, Progressive Rod-Cone Degeneration
  • Von Willebrand Disease I
Show all 19 Tests
UK Breed Council Labrador Retriever
  • Centronuclear Myopathy
  • Congenital Myasthenic Syndrome (Labrador Retriever Type)
  • Copper Toxicosis (Labrador Retriever Type)
  • Cystinuria (Labrador Retriever Type)
  • Degenerative Myelopathy (Common Variant)
  • Elliptocytosis
  • Exercise-Induced Collapse
  • Hemophilia A (Boxer Type)
  • Hereditary Nasal Parakeratosis (Labrador Retriever Type)
  • Hyperuricosuria
  • Macular Corneal Dystrophy (Labrador Retriever Type)
  • Narcolepsy (Labrador Retriever Type)
  • Progressive Retinal Atrophy, Cone-Rod Dystrophy 4
  • Progressive Retinal Atrophy, Golden Retriever 2
  • Progressive Retinal Atrophy, Progressive Rod-Cone Degeneration
  • Retinal Dysplasia/Oculoskeletal Dysplasia 1
  • Skeletal Dysplasia 2
  • Stargardt Disease
Show all 18 Tests
Yorkiepoo
  • Chondrodystrophy (CDDY and IVDD Risk) with or without Chondrodysplasia (CDPA)
  • Congenital Methemoglobinemia
  • Craniomandibular Osteopathy
  • Degenerative Myelopathy (Common Variant)
  • Ehlers-Danlos Syndrome (Poodle Type, Variants 1 and 2)
  • GM2 Gangliosidosis (Poodle Type)
  • Hereditary Cataracts
  • Hyperuricosuria
  • L-2-Hydroxyglutaric Aciduria (Yorkshire Terrier Type)
  • Multidrug Resistance 1
  • Neonatal Encephalopathy with Seizures
  • Osteochondrodysplasia
  • Primary Lens Luxation
  • Progressive Retinal Atrophy, Progressive Rod-Cone Degeneration
  • Progressive Retinal Atrophy, Rod-Cone Dysplasia 4
  • Subacute Necrotizing Encephalopathy (Yorkshire Terrier Type)
  • Von Willebrand Disease I
Show all 17 Tests