Ohana Cavalier King Charles Spaniels

Parent health testing

• Hip Dysplasia (rDVM, not registered)

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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 (rDVM, not registered)

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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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• Eye Examination (rDVM, not registered with OFA)

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  Eye testing reduces the chance of passing down a wide range of hereditary eye illnesses including retinal dysplasia, lens luxation, and glaucoma, which can cause impared vision or blindness.

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• 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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• Patellar Luxation

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  Knee testing reduces the chance of passing down Patellar Luxation, which results in the kneecap becoming displaced or dislocated and can cause mild to severe joint pain.

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• Full Embark Panel, Fucosidosis, Focal Non-Epidermolytic Palmoplantar Keratoderma, Pachyonychia Congenita (KRT16), Fanconi Syndrome, Familial Enamel Hypoplasia (FEH), Parson Russell Terrier Type, Factor VIII Deficiency (Exon 1), German Shepherd Type, Factor VIII Deficiency, Boxer Type, Factor VII Deficiency, Factor XI Deficiency, Factor IX Deficiency, Rhodesian Ridgeback Type, Factor VIII Deficiency (Exon 11), German Shepherd Type, Exercise Induced Collapse (EIC), Episodic Falling Syndrome (EFS), Epidermolytic Hyperkeratosis, Encephalopathy, Alaskan Husky Type, Elliptocytosis, Ehlers-Danlos Syndrome, Early Onset Progressive Retinal Atrophy (EOPRA), Dystrophic Epidermolysis Bullosa, Dry Eye Curly Coat Syndrome (CKSID), D Locus (Dilute) DNA test, Dilated Cardiomyopathy 2 (DCM2), Dilated Cardiomyopathy 1 (DCM1), Dental Hypomineralization (DH), Degenerative Myelopathy (DM; SOD1A), Deafness and Vestibular Syndrome of Dobermans, DVDobs, DINGS, Day Blindness, Achromatopsia, Cystinuria Type II-B, Miniature Pinscher Type, Cystinuria Type II-A, Australian Cattle Dog Type, Cystinuria Type 1A, Newfoundland Type, Craniomandibular Osteopathy (CMO), Congenital Stationary Night Blindness (CSNB), Congenital Myasthenic Syndrome (CMS), Jack Russell Terrier Type, Congenital Dyshormonogenic Hypothyroidism with Goiter, Shih Tzu Type, Congenital Myasthenic Syndrome (CMS), Old Danish Pointer Type, Congenital Myasthenic Syndrome (CMS), Labrador Retriever Type, Congenital Hypothyroidism with Goiter (CHG), Congenital Macrothrombocytopenia, Cone Degeneration, German Shorthaired Pointer Type, Cone Degeneration, Compliment 3 Deficiency (C3), Collie Eye Anomaly (CEA), Cleft Palate (ADAMTS20), Cerebellar Degeneration, Cerebellar Cortical Degeneration (CCD), Chondrodystrophy (CDDY and IVDD Risk) with or without Chondrodysplasia (CDPA), Centronuclear Myopathy (CNM), Chondrodystrophy and IVDD Risk (CDDY-IVDD), Cardiomyopathy and Juvenile Mortality (YARS2), Chondrodysplasia/Dwarfism, Canine Scott Syndrome (CSS), Canine Multifocal Retinopathy (cmr3; BEST1 Exon 10 SNP), Bernard-Soulier Syndrome, Cocker Spaniel Type, Benign Familial Juvenile Epilepsy (BFJE), Bald Thigh Syndrome (IGFBP5), Acral Mutilation Syndrome (AMS), Alexander Disease, Alanine Aminotransferase Activity, Adult Paroxysmal Dyskinesia, 2,8-Dihydroxyadenine (2,8-DHA) Urolithiasis, Animal Genetics Panel, DNA Repository, DNA Disease Panel, DNA Coat/Trait Panel, DNA Profile

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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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