External Certifications
Preferred BreederHealth Testing: 2,8-Dihydroxyadenine (2,8-DHA) Urolithiasis, Thrombopathia, Basset Hound Type, Elbow Dysplasia Finals (OFA, BVA, SV, FCI), Hip Dysplasia Finals (OFA, PennHIP, BVA, SV, FCI), P2RY12 Receptor Platelet Disorder, Trapped Neutrophil Syndrome, Cohen Syndrome (TNS), X-Linked Progressive Retinal Atrophy (XL-PRA), Hereditary (Juvenile) Cataracts (HC; JC), Protein-Losing Nephropathy (PLN; NPHS1 Gene Variant), Pyruvate Dehydrogenase Phosphatase 1 Deficiency (PDP1), Cerebellar Cortical Degeneration (CCD), Cerebellar Degeneration, Myotonia Congenita, Australian Cattle Dog Type, Osteogenesis Imperfecta (OI), Dachshund Type, Canine Good Citizen (CGC), Factor IX Deficiency, Cairn Terrier Type, von Willebrand Disease II (vWD II), Severe Combined Immunodeficiency Disease, X-Linked, Basset Hound Type (XSCID), Primary Open Angle Glaucoma, Basset Hound Type, Cystinuria Type II-A, Australian Cattle Dog Type, Fucosidosis, Neuronal Ceroid Lipofuscinosis 6 (NCL 6), X-Linked Tremors, Shaking Puppy Syndrome (SPS), Juvenile Dilated Cardiomyopathy, X-Linked Anhidrotic Ectodermal Dysplasia, Shepherd Type, von Willebrand Disease I (vWD I), Day Blindness, Achromatopsia, Centronuclear Myopathy (CNM), Pyruvate Kinase Deficiency (PKD), Labrador Retriever Type, Severe Combined Immunodeficiency Disease, X-Linked (XSCID), Corgi Type, Primary Lens Luxation (PLL), Primary Ciliary Dyskinesia, Kartagner Syndrome (PCD), Mucopolysaccharidosis VII (MPS VII GUSB), Shepherd Type, GM2 Gangliosidosis, Poodle Type, L-2-Hydroxyglutaric Aciduria (L2HGA), West Highland Terrier Type, Duchenne Muscular Dystrophy, Pembroke Welsh Corgi Type, Cleft Palate (ADAMTS20), Pyruvate Kinase Deficiency (PKD), Pug Type, Chondrodystrophy and IVDD Risk (CDDY-IVDD), Elbow Dysplasia Finals (OFA, BVA, SV, FCI), Primary Open Angle Glaucoma (ADAMST10 Exon 17), Mucopolysaccharidosis Type VI (MPS VI), Great Dane Type, GM1 Gangliosidosis, Portuguese Water Dog Type, L-2-Hydroxyglutaric Aciduria (L2HGA), Staffordshire Bull Terrier Type, Cavalier King Charles Spaniel Muscular Dystrophy (CKCS-MD), Duchenne Muscular Dystrophy, Golden Retriever Type, Chondrodysplasia/Dwarfism, Factor XI Deficiency, Agouti DNA Test, Glycogen Storage Disease Type IIIA, GSD IIIA, Neuronal Ceroid Lipofuscinosis 1 (NCL1), Dachshund Type, Hypomyelination, Weimaraner Type, Dilated Cardiomyopathy 1 (DCM1), Episodic Falling Syndrome (EFS), Skeletal Dysplasia (SD2), Factor VII Deficiency, Animal Genetics Panel, Multifocal Retinopathy 1 (CMR1), Cystinuria Type 1A, Labrador Retriever Type, X-Linked Anhidrotic Ectodermal Dysplasia, Dachshund type, Benign Familial Juvenile Epilepsy (BFJE), Neonatal Cortical Cerebellar Degeneration (NCCD), Hypocatalasia, Multiple Drug Sensitivity (MDR1), Factor VIII Deficiency, Boxer Type, Brucellosis, Collie Eye Anomaly (CEA), Renal Cystadenocarcinoma and Nodular Dermatofibrosis (RCND), Neuronal Ceroid Lipofuscinosis 10 (NCL10), American Bulldog Type, Spinocerebellar Ataxia (SCA), Hereditary Ataxia, Cerebellar Ataxia, Myotonia Congenita, Schnauzer Type, Craniomandibular Osteopathy (CMO), Retinal Dysplasia/Oculoskeletal Dysplasia 1 (RD OSD), Prekallikrein Deficiency, Fletcher Trait, Severe Combined Immunodeficiency Disease, Terrier Type, Multifocal Retinopathy 2 (CMR2), Cystinuria Type 1A, Newfoundland Type, Mucopolysaccharidosis IIIA (MPS IIIA), Dachshund Type, Neuronal Ceroid Lipofuscinosis 5 (NCL5), Golden Retriever Type, Dilated Cardiomyopathy (Schnauzer Type), Ichthyosis, Golden Retriever Type 1, von Willebrand Disease III (vWD III), Hereditary (Juvenile) Cataracts (HC; JC), Australian Shepherd Type, Primary Hyperoxaluria, Glycogen Storage Disease Type II or Pompe's Disease (GSD II), Neuronal Ceroid Lipofuscinosis 2 (NCL2), Neuroaxonal Dystrophy (NAD), Papillon Type, Long QT Syndrome, Hereditary Vitamin D-Resistant Rickets (HVDRR), Pyruvate Kinase Deficiency (PKD), Beagle Type, Early Onset Progressive Retinal Atrophy (EOPRA), Dry Eye Curly Coat Syndrome (CKSID), Phosphofructokinase Deficiency (PFK), Late Onset Ataxia, Spinocerebellar Ataxia (LOA, SCA), Juvenile Laryngeal Paralysis & Polyneuropathy (JLPP), Inherited Myopathy in Great Danes (IMGD), Musladin-Leuke Syndrome (MLS)Associate Dog TrainerPuppy Culture Breeder
