Kingdom Kenelz Labradors

Parent health testing

• Hip Dysplasia , 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), 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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• Cardiac Evaluation (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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• Canine Good Citizen (CGC), Dentition, Ichthyosis, Golden Retriever Type

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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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• Nemaline Myopathy, American Bulldog Type, Narcolepsy, Doberman Pinscher Type, Narcolepsy, Dachshund Type, Myotonia Congenita, Australian Cattle Dog Type, Myotonia Congenita, Schnauzer Type, Musladin-Leuke Syndrome (MLS), Cavalier King Charles Spaniel Muscular Dystrophy (CKCS-MD), Mucopolysaccharidosis Type IIIB (MPS IIIB), Mucopolysaccharidosis IIIA (MPS IIIA), Dachshund Type, Methemoglobinemia, May-Hegglin Anomaly, Long QT Syndrome, Limb Girdle Muscular Dystrophy, Boston Terrier, Ligneous Membranitis, LM (PLG), Lethal Acrodermatitis (LAD), Bull Terrier Type, Polyneuropathy 1, Leonberger and Saint Bernard Type, Late Onset Ataxia, Spinocerebellar Ataxia (LOA, SCA), Laryngeal Paralysis (Bull Terrier Type) - Single Assay Test, Lagotto Storage Disease (LSD), Juvenile Laryngeal Paralysis & Polyneuropathy (JLPP), Juvenile Myoclonic Epilepsy (JME), Inherited Myopathy in Great Danes (IMGD), Inflammatory Myopathy (Myositis), Ichthyosis, Great Dane Type, Ichthyosis, German Shepherd Type, Ichthyosis, American Bulldog Type, Hypomyelination, Weimaraner Type, Hypocatalasia, Hereditary Footpad Hyperkeratosis (FAM83G), Hereditary Footpad Hyperkeratosis (DSG1), PRA, Golden Retriever 1, Gangliosidosis GM2, Japanese Chin Type, GM1 Gangliosidosis, Alaskan Husky Type, GM1 Gangliosidosis (GLB1), Shiba Inu Type, Glycogen Storage Disease Type VII, Phosphofructokinase Deficiency, PFK Deficiency (PFKM Wachtelhund Variant), Glycogen Storage Disease Type IIIA, GSD IIIA, Glycogen Storage Disease Type IA, GSD IA, Globoid Cell Leukodystrophy (GCL), Terrier Type, Glanzmann's Thrombasthenia, Otterhound Type, Glanzmann's Thrombasthenia, Great Pyrenees Type, Fanconi Syndrome, Familial Nephropathy, English Springer Spaniel Type, Familial Nephropathy, Cocker Spaniel Type, Factor XI Deficiency, Factor VII Deficiency, Episodic Falling Syndrome (EFS), Ehlers-Danlos Syndrome, Early Adult Onset Deafness (EAOD), Dystrophic Epidermolysis Bullosa, Dry Eye Curly Coat Syndrome (CKSID), Dilated Cardiomyopathy 2 (DCM2), Dilated Cardiomyopathy 1 (DCM1), Diffuse cystic renal dysplasia and hepatic fibrosis, Dental-skeletal-retinal anomaly (DSRA), Deafness and Vestibular Syndrome of Dobermans, DVDobs, DINGS, Cystinuria Type II-B, Miniature Pinscher Type, Cystinuria Type II-A, Australian Cattle Dog Type, Craniomandibular Osteopathy (CMO), Congenital Stationary Night Blindness (CSNB), Congenital Myasthenic Syndrome (CMS), Jack Russell Terrier Type, Congenital Myasthenic Syndrome (CMS), Old Danish Pointer Type, Congenital Macrothrombocytopenia, Congenital Hypothyroidism with Goiter (CHG), Compliment 3 Deficiency (C3), Collie Eye Anomaly (CEA), Intestinal Cobalamin Malabsorption (IGS CUBN Exon 53), Border Collie Type, Cleft Palate (DLX6), Cleft Palate (ADAMTS20), Chondrodystrophy, Norwegian Elkhound and Karelian Bear Dog Variant (ITGA10), Cardiomyopathy and Juvenile Mortality (YARS2), Canine Multiple System Degeneration (Chinese Crested Type), Canine Multifocal Retinopathy (cmr3; BEST1 Exon 10 SNP), Muscular Hypertrophy/Myostatin Deficiency, Bully Whippet Syndrome (Double Muscling), Bernard-Soulier Syndrome, Cocker Spaniel Type, Bald Thigh Syndrome (IGFBP5), Acral Mutilation Syndrome (AMS), X-Linked Myotubular Myopathy, Ullrich Congenital Muscular Dystrophy, Stargardt Disease, Skeletal Dysplasia (SD2), Pyruvate Kinase Deficiency (PKD), Labrador Retriever Type, PRA, Cone-Rod Dystrophy 1 (PRA-crd1), Narcolepsy, Labrador Retriever Type, Macular Corneal Dystrophy, MCD (CHST6), Hereditary Nasal Parakeratosis (HNPK), PRA, Rod-Cone Degeneration (PRA-prcd), Exercise Induced Collapse (EIC), Degenerative Myelopathy (DM; SOD1A), Day Blindness, Achromatopsia, Congenital Myasthenic Syndrome (CMS), Labrador Retriever Type, Centronuclear Myopathy (CNM), Alexander Disease, Full Embark Panel, D Locus (Dilute) DNA test

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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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