Mossy Creek Springers

Parent health testing

• Canine Good Citizen (CGC)

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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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• Progressive Retinal Atrophy (PRA), Generalized, Primary Lens Luxation (PLL), Primary Hyperoxaluria, Primary Ciliary Dyskenesia (Malamute Type) - Single Assay Test, Glycogen Storage Disease Type II or Pompe's Disease (GSD II), Persistent Müllerian Duct Syndrome, Adult Paroxysmal Dyskinesia, P2RY12 Receptor Platelet Disorder, Osteogenesis Imperfecta (OI), Beagle Type, Oculocutaneous Albinism, Myotonia Congenita, Australian Cattle Dog Type, Musladin-Leuke Syndrome (MLS), Cavalier King Charles Spaniel Muscular Dystrophy (CKCS-MD), Multiple Drug Sensitivity (MDR1), Mucopolysaccharidosis IIIA (MPS IIIA), Dachshund Type, Microphthalmia Syndrome (PES), Methemoglobinemia, May-Hegglin Anomaly, Macular Corneal Dystrophy, MCD (CHST6), Malignant Hyperthermia (MH), Lundehund Syndrome, Limb Girdle Muscular Dystrophy, Boston Terrier, Globoid Cell Leukodystrophy (GCL), Irish Setter Type, 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), L-2-Hydroxyglutaric Aciduria (L2HGA), Staffordshire Bull Terrier Type, Juvenile Laryngeal Paralysis & Polyneuropathy (JLPP), Juvenile Myoclonic Epilepsy (JME), Inflammatory Myopathy (Myositis), Ichthyosis, American Bulldog Type, Hypomyelination, Weimaraner Type, Hereditary Nasal Parakeratosis (HNPK), Hereditary Footpad Hyperkeratosis, Cerebellar Degeneration, Gondysgenesis and Glaucoma, Border Collie Type, Glaucoma (BCG), Border Collie Type, GM1 Gangliosidosis, Alaskan Husky Type, Glycogen Storage Disease Ia, Globoid Cell Leukodystrophy (GCL), Terrier Type, Glanzmann's Thrombasthenia, Great Pyrenees Type, Fetal-Onset Neonatal Neuroaxonal Dystrophy (MFN1), Factor XI Deficiency, Exercise Induced Collapse (EIC), Familial Enamel Hypoplasia (FEH), Parson Russell Terrier Type, Ehlers-Danlos Syndrome, Cerebellar Ataxia, Finnish Hound Type, Epidermolysis Bullosa (Eurasier), Dry Eye Curly Coat Syndrome (CKSID), Chondrodysplasia/Dwarfism, Dilated Cardiomyopathy 1 (DCM1), Cystic Renal Dysplasia and Hepatic Fibrosis, Dental-skeletal-retinal anomaly (DSRA), Deafness and Vestibular Dysfunction, Doberman Pinscher Type, Day Blindness, Achromatopsia, Cystinuria Type 1A, Labrador Retriever Type, Craniomandibular Osteopathy (CMO), Congenital Stationary Night Blindness (CSNB), Congenital Myasthenic Syndrome (CMS), Labrador Retriever Type, Congenital Macrothrombocytopenia, Congenital Hypothyroidism with Goiter, Terrier Type (CHG), Collie Eye Anomaly (CEA), Intestinal Cobalamin Malabsorption (IGS), Australian Shepherd Type, Chondrodystrophy and IVDD Risk (CDDY-IVDD), Cleft Palate (DLX6), Cleft Palate (ADAMTS20), Centronuclear Myopathy (CNM), Cardiomyopathy and Juvenile Mortality (YARS2), Canine Multiple System Degeneration, Kerry Blue Terrier Type, Multifocal Retinopathy 3 (CMR3), Multifocal Retinopathy 2 (CMR2), Canine Multifocal Retinopathy (cmr3; BEST1 Exon 10 SNP), Leukocyte Adhesion Deficiency, Type III, Elliptocytosis, Leukocyte Adhesion Deficiency, Type I, Muscular Hypertrophy/Myostatin Deficiency, Bully Whippet Syndrome (Double Muscling), Bernard-Soulier Syndrome, Cocker Spaniel Type, Bald Thigh Syndrome (IGFBP5), X-Linked Anhidrotic Ectodermal Dysplasia, Shepherd Type, Alexander Disease, Encephalopathy, Alaskan Husky Type, 2,8-Dihydroxyadenine (2,8-DHA) Urolithiasis, Full Embark Panel, PRA, Rod-Cone Degeneration (PRA-prcd), Phosphofructokinase Deficiency (PFK)

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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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