New England Cavapoos

Parent health testing

• May-Hegglin Anomaly, Phosphofructokinase Deficiency (PFK), von Willebrand Disease III (vWD III), Kooikerhondje Type, von Willebrand Disease II (vWD II), von Willebrand Disease I (vWD I), Factor VII Deficiency, Factor XI Deficiency, Macrothrombocytopenia, Pyruvate Kinase Deficiency (PKD), Pug Type, von Willebrand Disease III (vWD III), Shetland Sheepdog Type, von Willebrand Disease III (vWD III), Scottish Terrier Type, P2RY12 Receptor Platelet Disorder, Glanzmann's Thrombasthenia, Great Pyrenees Type, Leukocyte Adhesion Deficiency, Type I, Hyperuricosuria (HUU), Cystinuria Type II-A, Australian Cattle Dog Type, Fanconi Syndrome, Renal Cystadenocarcinoma and Nodular Dermatofibrosis (RCND), Ichthyosis, Great Dane Type, Chondrodysplasia/Dwarfism, Osteochondrodysplasia, Miniature Poodle Type, Craniomandibular Osteopathy (CMO), Skeletal Dysplasia (SD2), Musladin-Leuke Syndrome (MLS), Persistent Müllerian Duct Syndrome, Episodic Falling Syndrome (EFS), Globoid Cell Leukodystrophy (GCL), Terrier Type, Globoid Cell Leukodystrophy (GCL), Irish Setter Type, GM2 Gangliosidosis, Poodle Type, Adult Paroxysmal Dyskinesia, Neuronal Ceroid Lipofuscinosis 10 (NCL10), American Bulldog Type, Acral Mutilation Syndrome (AMS), Spinocerebellar Ataxia (SCA), Cerebellar Ataxia, Finnish Hound Type, Hypomyelination, Weimaraner Type, Hyperekplexia, Startle Disease, L-2-Hydroxyglutaric Aciduria (L2HGA), Staffordshire Bull Terrier Type, Centronuclear Myopathy (CNM), Nemaline Myopathy, American Bulldog Type, Mucopolysaccharidosis VII (MPS VII ARSB), German Shepherd Dog Type, Pyruvate Dehydrogenase Phosphatase 1 Deficiency (PDP1), Hypocatalasia, Glycogen Storage Disease Type IIIA, GSD IIIA, Acute Respiratory Distress Syndrome, Dalmatian Type, Congenital Hypothyroidism with Goiter, Terrier Type (CHG), Primary Open Angle Glaucoma, Basset Hound Type, Cone Degeneration, Cone-Rod Dystrophy (crd4), PRA (PRA1), Papillon Type, Cone Degeneration, German Shepherd Dog Type, Degenerative Myelopathy (DM; SOD1A), Dental Hypomineralization (DH), Amelogenesis Imperfecta (AI), Akita Type

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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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