Double T Mini Aussies

Parent health testing

• Brucellosis

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  A breeder may perform additional tests on their dogs that do not fall into these general categories. These tests may be more uncommon or very specific to a particular breed.

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• Late Onset Ataxia, Spinocerebellar Ataxia (LOA, SCA), Canine Multiple System Degeneration, Kerry Blue Terrier Type, Polyneuropathy, Greyhound Type (NDRG1), Thrombopathia, Basset Hound Type, Trapped Neutrophil Syndrome, Cohen Syndrome (TNS), Elliptocytosis, Glanzmann's Thrombasthenia, Great Pyrenees Type, Glanzmann's Thrombasthenia, Otterhound Type, Leukocyte Adhesion Deficiency, Type III, May-Hegglin Anomaly, P2RY12 Receptor Platelet Disorder, Prekallikrein Deficiency, Fletcher Trait, Pyruvate Kinase Deficiency, Basenji Type (PKD), Pyruvate Kinase Deficiency (PKD), Beagle Type, Pyruvate Kinase Deficiency (PKD), Labrador Retriever Type, Pyruvate Kinase Deficiency (PKD), Pug Type, Pyruvate Kinase Deficiency (PKD), Terrier Type, Thrombopathia, American Eskimo Dog Type, Thrombopathia, Newfoundland Type, von Willebrand Disease I (vWD I), von Willebrand Disease III (vWD III), Kooikerhondje Type, von Willebrand Disease III (vWD III), Scottish Terrier Type, Renal Cystadenocarcinoma and Nodular Dermatofibrosis (RCND), Amelogenesis Imperfecta (AI), Italian Greyhound Type, Multiple Drug Sensitivity (MDR1), Collie Eye Anomaly (CEA), Cone Degeneration, Cone Degeneration, German Shorthaired Pointer Type, Congenital Stationary Night Blindness (CSNB), Dry Eye Curly Coat Syndrome (CKSID), Early Onset Progressive Retinal Atrophy (EOPRA), GM1 Gangliosidosis, Alaskan Husky Type, GM1 Gangliosidosis, Portuguese Water Dog Type, GM1 Gangliosidosis (GLB1), Shiba Inu Type, GM2 Gangliosidosis, Poodle Type, Hereditary (Juvenile) Cataracts (HC; JC), Australian Shepherd Type, Hereditary (Juvenile) Cataracts (HC; JC), Juvenile Laryngeal Paralysis & Polyneuropathy (JLPP), Multifocal Retinopathy 1 (CMR1), Multifocal Retinopathy 2 (CMR2), Multifocal Retinopathy 3 (CMR3), Primary Lens Luxation (PLL), Primary Open Angle Glaucoma (ADAMST10 Exon 17), Progressive Retinal Atrophy (PRA), Generalized, Leukocyte Adhesion Deficiency, Type I, Primary Ciliary Dyskinesia, Kartagner Syndrome (PCD), Severe Combined Immunodeficiency Disease, Terrier Type, Severe Combined Immunodeficiency Disease, X-Linked, Basset Hound Type (XSCID), Glycogen Storage Disease Type IIIA, GSD IIIA, Intestinal Cobalamin Malabsorption (IGS), Australian Shepherd Type, Intestinal Cobalamin Malabsorption (IGS CUBN Exon 53), Border Collie Type, GM1 Gangliosidosis (HEXB), Shiba Inu Type, Globoid Cell Leukodystrophy (GCL), Irish Setter Type, Globoid Cell Leukodystrophy (GCL), Terrier Type, L-2-Hydroxyglutaric Aciduria (L2HGA), Staffordshire Bull Terrier Type, Mucopolysaccharidosis Type I (MPS I), Mucopolysaccharidosis IIIA (MPS IIIA), Dachshund Type, Mucopolysaccharidosis IIIA (MPS IIIA), New Zealand Huntaway Type, Mucopolysaccharidosis VII (MPS VII ARSB), German Shepherd Dog Type, Neuronal Ceroid Lipofuscinosis 1 (NCL1), Dachshund Type, Neuronal Ceroid Lipofuscinosis 10 (NCL10), American Bulldog Type, Neuronal Ceroid Lipofuscinosis 2 (NCL2), Neuronal Ceroid Lipofuscinosis 4A (NCL4A), American Staffordshire Terrier Type, Neuronal Ceroid Lipofuscinosis 5 (NCL5), Border Collie Type, Neuronal Ceroid Lipofuscinosis 6 (NCL 6), Neuronal Ceroid Lipofuscinosis 8 (NCL8), Australian Shepherd Type, Neuronal Ceroid Lipofuscinosis 8 (NCL8), Setter Type, Glycogen Storage Disease Type II or Pompe's Disease (GSD II), Spinal Dysraphism (SD), Polyneuropathy (NDRG1), Alaskan Malamute Type, Chondrodysplasia/Dwarfism, Degenerative Myelopathy (DM; SOD1A), Exercise Induced Collapse (EIC), Inherited Myopathy in Great Danes (IMGD), Duchenne Muscular Dystrophy, Golden Retriever Type, Myotonia Congenita, Australian Cattle Dog Type, Myotonia Congenita, Schnauzer Type, Myotubular Myopathy 1, Rottweiler Type, Osteogenesis Imperfecta (OI), Beagle Type, Osteogenesis Imperfecta (OI), Golden Retriever Type, Polyneuropathy 1, Leonberger and Saint Bernard Type, Skeletal Dysplasia (SD2), Hereditary Vitamin D-Resistant Rickets (HVDRR), Neuronal Ceroid Lipofuscinosis 12 (NCL12), Australian Cattle Dog Type, Encephalopathy, Alaskan Husky Type, Benign Familial Juvenile Epilepsy (BFJE), Multiple System Degeneration, Chinese Crested Type, Cerebellar Ataxia, Finnish Hound Type, Narcolepsy, Dachshund Type, Narcolepsy, Doberman Pinscher Type, Narcolepsy, Labrador Retriever Type, Neonatal Cortical Cerebellar Degeneration (NCCD), Neonatal Encephalopathy with Seizures (NEwS), Neuronal Ceroid Lipofuscinosis 1 (NCL1), Cane Corso Type, Neuronal Ceroid Lipofuscinosis 5 (NCL5), Golden Retriever Type, Polyneuropathy 2, Leonberger and Saint Bernard Type, Sensory Neuropathy, Border Collie Type (SN), Spinocerebellar Ataxia (SCA), Hyperekplexia, Startle Disease, X-Linked Anhidrotic Ectodermal Dysplasia, Shepherd Type, Ectodermal Dysplasia, Chesapeake Bay Retriever Type, Hereditary Nasal Parakeratosis (HNPK), Ichthyosis, Golden Retriever Type 1, Cystinuria Type II-A, Australian Cattle Dog Type, Cystinuria Type II-B, Miniature Pinscher Type, Familial Nephropathy, Cocker Spaniel Type, Familial Nephropathy, English Springer Spaniel Type, Hereditary Nephritis, Samoyed Type, Hyperuricosuria (HUU), Persistent Müllerian Duct Syndrome, Primary Hyperoxaluria

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  Genetic testing reduces the chance of passing down a wide variety of hereditary diseases of differing prevalence and severity such as Progressive Retinal Atrophy (an eye disease) and Von Willebrand's Disease (a blood disease).

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