Evergreen Doodles

Parent health testing

• Elbow Dysplasia (Preliminary)

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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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• Ichthyosis, Golden Retriever Type, Brucellosis

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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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• Oculocutaneous Albinism, Oculocutaneous Albinism (Small Breed Type), Neuronal Ceroid Lipofuscinosis 8 (NCL8), Setter Type, Neuronal Ceroid Lipofuscinosis 8 (NCL8), Australian Shepherd Type, Neuronal Ceroid Lipofuscinosis 7 (NCL7), Neuronal Ceroid Lipofuscinosis 6 (NCL 6), 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 12 (NCL12), Australian Cattle Dog Type, Neuronal Ceroid Lipofuscinosis 10 (NCL10), American Bulldog Type, Neuroaxonal Dystrophy (NAD), Spanish Water Dog Type, Neuroaxonal Dystrophy (NAD), Rottweiler Type, Neonatal Cortical Cerebellar Degeneration (NCCD), Narcolepsy, Labrador Retriever Type, Narcolepsy, Doberman Pinscher Type, Narcolepsy, Dachshund Type, Myotubular Myopathy 1, Rottweiler Type, Myotubular Myopathy, Labrador Retriever Type, Myotonia Congenita, Schnauzer Type, Myotonia Congenita, Australian Cattle Dog Type, Muscular Hypertrophy/Myostatin Deficiency, Bully Whippet Syndrome (Double Muscling), Musladin-Leuke Syndrome (MLS), Multifocal Retinopathy 3 (CMR3), Multifocal Retinopathy 2 (CMR2), Multifocal Retinopathy 1 (CMR1), Mucopolysaccharidosis VII (MPS VII ARSB), German Shepherd Dog Type, Mucopolysaccharidosis IIIA (MPS IIIA), Dachshund Type, Mucopolysaccharidosis IIIA (MPS IIIA), New Zealand Huntaway Type, May-Hegglin Anomaly, 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), L-2-Hydroxyglutaric Aciduria (L2HGA), Staffordshire Bull Terrier Type, Juvenile Myoclonic Epilepsy (JME), Juvenile Laryngeal Paralysis & Polyneuropathy (JLPP), Intestinal Cobalamin Malabsorption (IGS CUBN Exon 53), Border Collie Type, Inherited Myopathy in Great Danes (IMGD), Ichthyosis, Great Dane Type, Ichthyosis, American Bulldog Type, Hypomyelination, Weimaraner Type, Hyperuricosuria (HUU), Hereditary Nephritis, Samoyed Type, Hereditary Nasal Parakeratosis (HNPK), Hereditary Footpad Hyperkeratosis, Hereditary (Juvenile) Cataracts (HC; JC), Australian Shepherd Type, Polyneuropathy, Greyhound Type (NDRG1), Gangliosidosis GM2, Japanese Chin Type, GM1 Gangliosidosis (GLB1), Shiba Inu Type, GM1 Gangliosidosis, Portuguese Water Dog Type, GM1 Gangliosidosis, Alaskan Husky Type, Glycogen Storage Disease Type VII, GSD VII, Glycogen Storage Disease Type IIIA, GSD IIIA, Glycogen Storage Disease Ia, Glaucoma (BCG), Border Collie Type, Glanzmann's Thrombasthenia, Otterhound Type, Glanzmann's Thrombasthenia, Great Pyrenees Type, Gall Bladder Mucocele Formation (Shetland Sheepdog Type), Fucosidosis, Familial Nephropathy, English Springer Spaniel Type, Familial Nephropathy, Cocker Spaniel Type, Factor XI Deficiency, Episodic Falling Syndrome (EFS), Elliptocytosis, Ehlers-Danlos Syndrome, Ectodermal Dysplasia, X-Linked (Shepherd Type), Ectodermal Dysplasia, X-Linked (Dachshund Type), Ectodermal Dysplasia, Chesapeake Bay Retriever Type, Early Retinal Degeneration, Epidermolysis Bullosa (Eurasier), Dry Eye Curly Coat Syndrome (CKSID), Dilated Cardiomyopathy (Schnauzer Type), Dilated Cardiomyopathy 2 (DCM2), Dilated Cardiomyopathy 1 (DCM1), Diffuse cystic renal dysplasia and hepatic fibrosis, Dental Hypomineralization (DH), Degenerative Myelopathy Early-Onset Risk Modifier, Pembroke Welsh Corgi Type, Degenerative Myelopathy (DM; SOD1A), Dandy-Walker-like Malformation (DWLM), Eurasier Type, Cystinuria Type 3 (Variant 1 & 2), Bulldog Type Risk Factor, Cystinuria Type 3 (Variant 3), Bulldog Type Risk Factor, Cystinuria Type 1A, Newfoundland Type, Cystinuria Type II-B, Miniature Pinscher Type, Cystinuria Type 1A, Labrador Retriever Type, Cystinuria Type II-A, Australian Cattle Dog Type, Cyclic Neutropenia, Grey Collie Syndrome (CN), Craniomandibular Osteopathy (CMO), Congenital Stationary Night Blindness (CSNB), Congenital Myasthenic Syndrome (CMS), Old Danish Pointer Type, Congenital Myasthenic Syndrome (CMS), Labrador Retriever Type, Congenital Myasthenic Syndrome (CMS), Jack Russell Terrier Type, Methemoglobinemia, Cone Degeneration, German Shepherd Dog Type, Cone Degeneration, German Shorthaired Pointer Type, Cone Degeneration, Labrador Retriever Type, Cone Degeneration, Collie Eye Anomaly (CEA), Cleft Palate (ADAMTS20), Chondrodystrophy, Norwegian Elkhound and Karelian Bear Dog Variant (ITGA10), Cerebellar Degeneration, Cerebellar Cortical Degeneration (CCD), Cerebellar Ataxia, Finnish Hound Type, Canine Scott Syndrome (CSS), Canine Multiple System Degeneration, Kerry Blue Terrier Type, Canine Multiple System Degeneration (Chinese Crested Type), Benign Familial Juvenile Epilepsy (BFJE), Amelogenesis Imperfecta (AI), Italian Greyhound Type, Polyneuropathy (NDRG1), Alaskan Malamute Type, Encephalopathy, Alaskan Husky Type, Adult Paroxysmal Dyskinesia, Acute Respiratory Distress Syndrome, Dalmatian Type, Acral Mutilation Syndrome (AMS), von Willebrand Disease I (vWD I), Osteogenesis Imperfecta (OI), Golden Retriever Type, Osteochondrodysplasia, Miniature Poodle Type, Neuronal Ceroid Lipofuscinosis 5 (NCL5), Golden Retriever Type, Neonatal Encephalopathy with Seizures (NEwS), Duchenne Muscular Dystrophy, Golden Retriever Type, Ichthyosis, Golden Retriever Type 1, Hereditary (Juvenile) Cataracts (HC; JC), GM2 Gangliosidosis, Poodle Type, Exercise Induced Collapse (EIC), Dystrophic Epidermolysis Bullosa, Degenerative Myelopathy (DM; SOD1B), Bernese Mountain Dog Type, Congenital Methemoglobinemia, Pomeranian 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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