Happy Hill Poodle

Parent health testing

• Cardiac Evaluation (registered with OFA), Cardiac Evaluation (rDVM, not registered with OFA)

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  Heart testing reduces the chance of passing down congenital heart disease, which can cause a range of symptoms ranging from trouble exercising to heart failure.

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• Dermoid Sinus (DS), Congenital Deafness (BAER, registered with OFA), Brucellosis, Brachycephalic Obstructive Airway Syndrome (BOAS)

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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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• DNA Repository, Diffuse cystic renal dysplasia and hepatic fibrosis, Degenerative Myelopathy (DM; SOD1A), DNA Profile, Dermatomyositis, Deafness and Vestibular Dysfunction, Doberman Pinscher Type, Cystic Renal Dysplasia and Hepatic Fibrosis, Day Blindness, Achromatopsia, DNA Disease Panel, X-Linked Progressive Retinal Atrophy (XL-PRA), Craniomandibular Osteopathy (CMO), Copper Toxicosis, Labrador Retriever Type, Copper Toxicosis, Labrador Retriever ATP7A, Copper Toxicosis, Bedlington Terrier Type (COMMD1), Congenital Stationary Night Blindness (CSNB), Congenital Myasthenic Syndrome (CMS), Spanish Water Dog Type, Congenital Myasthenic Syndrome (CMS), Old Danish Pointer Type, Congenital Myasthenic Syndrome (CMS), Labrador Retriever Type, Congenital Myasthenic Syndrome (CMS), Jack Russell Terrier Type, Congenital Methemoglobinemia, Pomeranian Type, Congenital Macrothrombocytopenia, Congenital Hypothyroidism with Goiter, Terrier Type (CHG), Congenital Hypothyroidism with Goiter (CHG), Congenital Eye Disease; mutation originally found in Irish Soft Coated Wheaten Terrier, Congenital Dyshormonogenic Hypothyroidism with Goiter, Shih Tzu Type, Cone-Rod Dystrophy 2 (crd2), American Pitbull Terrier Type, Cone-Rod Dystrophy 1 (crd1), American Staffordshire Terrier Type, Cone Degeneration, Labrador Retriever Type, Cone-Rod Dystrophy (crd4), Cone Degeneration, Husky Type, Cone Degeneration, German Shorthaired Pointer Type, Cone Degeneration, German Shepherd Dog Type, Cone Degeneration, Compliment 3 Deficiency (C3), Collie Eye Anomaly (CEA), Cleft Palate (DLX6), Cleft Palate (ADAMTS20), Chondrodystrophy, Norwegian Elkhound and Karelian Bear Dog Variant (ITGA10), Chondrodystrophy (CDDY and IVDD Risk) with or without Chondrodysplasia (CDPA), Chondrodystrophy and IVDD Risk (CDDY-IVDD), Chondrodysplasia/Dwarfism, Cerebral Dysfunction, Frisian Stabyhoun Type, Cerebellar Degeneration, Cerebellar Cortical Degeneration (CCD), Cerebellar Ataxia, Spinone Italiano Type, Cerebellar Ataxia, Finnish Hound Type, Cerebellar Ataxia 2, Belgian Shepherd Type, Centronuclear Myopathy (CNM), Great Dane Type, Centronuclear Myopathy (CNM), Cavalier King Charles Spaniel Muscular Dystrophy (CKCS-MD), Catalase Deficiency, Cardiomyopathy and Juvenile Mortality (YARS2), Canine Scott Syndrome (CSS), Canine Multiple System Degeneration, Kerry Blue Terrier Type, Canine Multiple System Degeneration (Chinese Crested Type), Canine Multifocal Retinopathy (cmr3; BEST1 Exon 10 SNP), Brachycephaly, Bernard-Soulier Syndrome, Cocker Spaniel Type, Benign Familial Juvenile Epilepsy (BFJE), Behavior Propensity, Belgian Malinois, Bald Thigh Syndrome (IGFBP5), Ataxia, Norwegian Buhund Type, Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC), Animal Genetics Panel, Amelogenesis Imperfecta (AI), Italian Greyhound Type, Amelogenesis Imperfecta (AI), Akita Type, Alexander Disease, Alanine Aminotransferase Activity, Agouti DNA Test, Adult Paroxysmal Dyskinesia, Adult Onset Neuropathy (AON), Acute Respiratory Distress Syndrome, Dalmatian Type, 2,8-Dihydroxyadenine (2,8-DHA) Urolithiasis, Acral Mutilation Syndrome (AMS)

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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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