MilkyWay Aussies with Tails

Parent health testing

• Hip Dysplasia

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  Hip testing reduces the chance of passing down hip dysplasia, which is primarily found in large breed dogs and can cause hip pain and the eventual loss of the function of the hip joint.

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• Elbow Dysplasia Finals (OFA, BVA, SV, FCI)

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  Elbow testing reduces the chance of passing down elbow dysplasia, which is primarily found in large breed dogs and can cause arthritis in the elbow joint and front leg lameness.

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• von Willebrand Disease II (vWD II), von Willebrand Disease I (vWD I), von Willebrand Disease III (vWD III), Kooikerhondje Type, von Willebrand Disease III (vWD III), Van Den Ende-Gupta Syndrome (VDEGS), Trapped Neutrophil Syndrome, Cohen Syndrome (TNS), Hyperekplexia, Startle Disease, Stargardt Disease, Spondylocostal Dysostosis, Spinocerebellar Ataxia (SCA), Spinal Dysraphism (SD), Skeletal Dysplasia (SD2), Severe Combined Immunodeficiency Disease, Terrier Type, Sensory Neuropathy, Border Collie Type (SN), Retinal Dysplasia/Oculoskeletal Dysplasia 2, Retinal Dysplasia/Oculoskeletal Dysplasia 1 (RD OSD), Recurrent Inflammatory Pulmonary (Collie Type) - Single Assay Test, Pyruvate Dehydrogenase Phosphatase 1 Deficiency (PDP1), Protein-Losing Nephropathy (PLN; NPHS1 Gene Variant), Progressive Retinal Atrophy (PRA), Generalized, Prekallikrein Deficiency, Fletcher Trait, Primary Open Angle Glaucoma and Primary Lens Luxation (POAG/PLL), Shar-Pei Type, Primary Lens Luxation (PLL), Primary Hyperoxaluria, Glycogen Storage Disease Type II or Pompe's Disease (GSD II), Persistent Müllerian Duct Syndrome, P2RY12 Receptor Platelet Disorder, Oculocutaneous Albinism, Neuronal Ceroid Lipofuscinosis 8 (NCL8), Setter Type, Neuronal Ceroid Lipofuscinosis 7 (NCL7), Neuronal Ceroid Lipofuscinosis 12 (NCL12), Australian Cattle Dog Type, Neuronal Ceroid Lipofuscinosis 5 (NCL5), Border Collie Type, Neuronal Ceroid Lipofuscinosis 4A (NCL4A), American Staffordshire Terrier Type, Neuronal Ceroid Lipofuscinosis 2 (NCL2), Neuronal Ceroid Lipofuscinosis 10 (NCL10), American Bulldog Type, Neuronal Ceroid Lipofuscinosis 1 (NCL1), Cane Corso Type, Neonatal Encephalopathy with Seizures (NEwS), Myotonia Congenita, Australian Cattle Dog Type, Multifocal Retinopathy 3 (CMR3), Multifocal Retinopathy 2 (CMR2), Multifocal Retinopathy 1 (CMR1), Mucopolysaccharidosis VII (MPS VII GUSB), Shepherd Type, Macular Corneal Dystrophy, MCD (CHST6), Lundehund Syndrome, Ligneous Membranitis, LM (PLG), Leukocyte Adhesion Deficiency, Type III, Leukocyte Adhesion Deficiency, Type I, Lethal Acrodermatitis (LAD), Bull Terrier Type, Late Onset Ataxia, Spinocerebellar Ataxia (LOA, SCA), Lagotto Storage Disease (LSD), Hereditary Nasal Parakeratosis (HNPK), Hereditary (Juvenile) Cataracts (HC; JC), Australian Shepherd Type, Glycogen Storage Disease Type VII, Phosphofructokinase Deficiency, PFK Deficiency (PFKM Wachtelhund Variant), Glycogen Storage Disease Ia, Glaucoma (BCG), Border Collie Type, Gall Bladder Mucocele Formation (Shetland Sheepdog Type), Fucosidosis, Factor IX Deficiency (G418E), Exercise Induced Collapse (EIC), Episodic Falling Syndrome (EFS), Epidermolytic Hyperkeratosis, Elliptocytosis, Ehlers-Danlos Syndrome, Ectodermal Dysplasia, X-Linked (Shepherd Type), Early Retinal Degeneration, Dystrophic Epidermolysis Bullosa, Dry Eye Curly Coat Syndrome (CKSID), Dilated Cardiomyopathy 2 (DCM2), Dilated Cardiomyopathy 1 (DCM1), Dental Hypomineralization (DH), Degenerative Myelopathy Early-Onset Risk Modifier, Pembroke Welsh Corgi Type, Dandy-Walker-like Malformation (DWLM), Eurasier Type, Cystinuria Type II-A, Australian Cattle Dog Type, Cyclic Neutropenia, Grey Collie Syndrome (CN), Congenital Stationary Night Blindness (CSNB), Cerebellar Degeneration, Cerebellar Cortical Degeneration (CCD), Centronuclear Myopathy (CNM), Catalase Deficiency, Canine Scott Syndrome (CSS), Acral Mutilation Syndrome (AMS), Neuronal Ceroid Lipofuscinosis 8 (NCL8), Australian Shepherd Type, Neuronal Ceroid Lipofuscinosis 6 (NCL 6), Hyperuricosuria (HUU), Canine Multifocal Retinopathy (cmr3; BEST1 Exon 10 SNP), Intestinal Cobalamin Malabsorption (IGS), Australian Shepherd Type, Degenerative Myelopathy (DM; SOD1A), Cone Degeneration, Collie Eye Anomaly (CEA), DNA Disease Panel, Multiple Drug Sensitivity (MDR1)

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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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