External Certifications
Certified BreederHealth Testing: Shar-Pei Autoinflammatory Disease, Polyneuropathy, Greyhound Type (NDRG1), Elbow Dysplasia Finals (OFA, BVA, SV, FCI), Elbow Dysplasia Prelims (registered with OFA), Hip Dysplasia Finals (OFA, PennHIP, BVA, SV, FCI), Hip Dysplasia Prelims (registered with OFA), Chondrodystrophy, Norwegian Elkhound and Karelian Bear Dog Variant (ITGA10), Craniomandibular Osteopathy (CMO), Osteochondrodysplasia, Miniature Poodle Type, Osteogenesis Imperfecta (OI), Golden Retriever Type, Osteogenesis Imperfecta (OI), Beagle Type, Osteogenesis Imperfecta (OI), Dachshund Type, Hereditary Vitamin D-Resistant Rickets (HVDRR), Cleft Palate (ADAMTS20), Bald Thigh Syndrome (IGFBP5), Oculocutaneous Albinism, Musladin-Leuke Syndrome (MLS), Hereditary Footpad Hyperkeratosis, Ichthyosis (KRY10), Ichthyosis, American Bulldog Type, Ichthyosis, Great Dane Type, Ichthyosis, Golden Retriever Type 1, Dystrophic Epidermolysis Bullosa, Adult Paroxysmal Dyskinesia, Congenital Myasthenic Syndrome (CMS), Old Danish Pointer Type, Intestinal Cobalamin Malabsorption (IGS CUBN Exon 8), Border Collie Type, Intestinal Cobalamin Malabsorption (IGS CUBN Exon 53), Border Collie Type, Malignant Hyperthermia (MH), Pyruvate Dehydrogenase Phosphatase 1 Deficiency (PDP1), Myotonia Congenita, Australian Cattle Dog Type, Myotonia Congenita, Schnauzer Type, Inherited Myopathy in Great Danes (IMGD), Duchenne Muscular Dystrophy, Golden Retriever Type, Cavalier King Charles Spaniel Muscular Dystrophy (CKCS-MD), Long QT Syndrome, Dilated Cardiomyopathy 2 (DCM2), Dilated Cardiomyopathy 1 (DCM1), Cerebellar Degeneration, Cerebellar Ataxia 2, Belgian Shepherd Type, Polyneuropathy 2, Leonberger and Saint Bernard Type, Juvenile Myoclonic Epilepsy (JME), Polyneuropathy 1, Leonberger and Saint Bernard Type, Acral Mutilation Syndrome (AMS), Multiple System Degeneration, Chinese Crested Type, Canine Multiple System Degeneration, Kerry Blue Terrier Type, Canine Multiple System Degeneration (Chinese Crested Type), Narcolepsy, Dachshund Type, Neonatal Encephalopathy with Seizures (NEwS), L-2-Hydroxyglutaric Aciduria (L2HGA), Staffordshire Bull Terrier Type, Neuroaxonal Dystrophy (NAD), Rottweiler Type, Neuroaxonal Dystrophy (NAD), Spanish Water Dog Type, Hypomyelination, Weimaraner Type, Spinocerebellar Ataxia (SCA), Cerebellar Ataxia, Finnish Hound Type, Cerebellar Cortical Degeneration (CCD), Neonatal Cortical Cerebellar Degeneration (NCCD), Deafness and Vestibular Dysfunction, Doberman Pinscher Type, Persistent Müllerian Duct Syndrome, Hypocatalasia, Globoid Cell Leukodystrophy (GCL), Terrier Type, Gangliosidosis GM2, Japanese Chin Type, Neuronal Ceroid Lipofuscinosis, Tibetan Terrier Type, Neuronal Ceroid Lipofuscinosis 12 (NCL12), Australian Cattle Dog Type, Neuronal Ceroid Lipofuscinosis 1 (NCL1), Cane Corso Type, Neuronal Ceroid Lipofuscinosis 8 (NCL8), Setter Type, Neuronal Ceroid Lipofuscinosis 10 (NCL10), American Bulldog 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 5 (NCL5), Golden Retriever Type, Neuronal Ceroid Lipofuscinosis 4A (NCL4A), American Staffordshire Terrier Type, Neuronal Ceroid Lipofuscinosis 2 (NCL2), Neuronal Ceroid Lipofuscinosis 1 (NCL1), Dachshund Type, Lagotto Storage Disease (LSD), Glycogen Storage Disease Type VII, GSD VII, Mucopolysaccharidosis VII (MPS VII GUSB), Shepherd Type, Mucopolysaccharidosis VII (MPS VII), Brazilian Terrier Type, Mucopolysaccharidosis VII (MPS VII GUSB), Shepherd Type, Mucopolysaccharidosis Type I (MPS I), Mucopolysaccharidosis IIIA (MPS IIIA), New Zealand Huntaway Type, Mucopolysaccharidosis IIIA (MPS IIIA), Dachshund Type, Fucosidosis, Renal Cystadenocarcinoma and Nodular Dermatofibrosis (RCND), Ectodermal Dysplasia, Chesapeake Bay Retriever Type, Dry Eye Curly Coat Syndrome (CKSID), Primary Ciliary Dyskinesia, Kartagner Syndrome (PCD), Familial Nephropathy, English Springer Spaniel Type, Protein-Losing Nephropathy (PLN; NPHS1 Gene Variant), Primary Hyperoxaluria, Polycystic Kidney Disease (PKD), Cystinuria Type II-B, Miniature Pinscher Type, Cystinuria Type II-A, Australian Cattle Dog Type, Cystinuria Type 1A, Labrador Retriever Type, Cystinuria Type 1, Newfoundland (PennGen), Primary Open Angle Glaucoma and Primary Lens Luxation (POAG/PLL), Shar-Pei Type, Primary Lens Luxation (PLL), Hereditary (Juvenile) Cataracts (HC; JC), Australian Shepherd Type, Gondysgenesis and Glaucoma, Border Collie Type, Primary Open Angle Glaucoma (ADAMST17 Exon 11), Primary Open Angle Glaucoma (ADAMST10 Exon 17), Multifocal Retinopathy 3 (CMR3), Multifocal Retinopathy 2 (CMR2), Multifocal Retinopathy 1 (CMR1), Coton de Tulear Type, Multifocal Retinopathy 1 (CMR1), PRA Dominant (DPRA), Mastiff Type, Collie Eye Anomaly (CEA), PRA, Golden Retriever 2, PRA3, Tibetan Terrier and Spaniel Type, PRA (PRA1), Italian Greyhound Type, PRA, Basenji Type, PRA, Cone-Rod Dystrophy 1 (PRA-crd1), PRA, Shetland Sheepdog Type, PRA, Golden Retriever 1, PRA (PRA1), Papillon Type, PRA, Rod-Cone Dysplasia 3 (rcd3), PRA, Irish Setter Type, Severe Combined Immunodeficiency Disease, X-Linked (XSCID), Corgi Type, Severe Combined Immunodeficiency Disease, X-Linked, Basset Hound Type (XSCID), Severe Combined Immunodeficiency Disease, Terrier Type, Severe Combined Immunodeficiency Disease, Frisian Water Dog Type, Compliment 3 Deficiency (C3), Pyruvate Kinase Deficiency (PKD), Cairn Terrier Type, Pyruvate Kinase Deficiency (PKD), Terrier Type, Pyruvate Kinase Deficiency (PKD), Beagle Type, Pyruvate Kinase Deficiency, Basenji Type (PKD), Pyruvate Kinase Deficiency (PKD), Pug Type, Pyruvate Kinase Deficiency (PKD), Basenji Type , Pyruvate Kinase Deficiency (PKD), Labrador Retriever Type, May-Hegglin Anomaly, Glanzmann's Thrombasthenia, Otterhound Type, Glanzmann's Thrombasthenia, Great Pyrenees Type, Macrothrombocytopenia, Leukocyte Adhesion Deficiency, Type III, Leukocyte Adhesion Deficiency, Type I, von Willebrand Disease II (vWD II), von Willebrand Disease III (vWD III), Shetland Sheepdog Type, von Willebrand Disease III (vWD III), Scottish Terrier Type, von Willebrand Disease III (vWD III), Thrombopathia, Finnish Spitz Type, Thrombopathia, Newfoundland Type, Factor VII Deficiency, Multiple Drug Sensitivity (MDR1), Congenital Myasthenic Syndrome (CMS), Jack Russell Terrier Type, Alexander Disease, Pyruvate Kinase Deficiency (PKD), Labrador Retriever Type, Elliptocytosis, Skeletal Dysplasia (SD2), Progressive Retinal Atrophy (PRA), Generalized, Patellar Luxation, OFA Auscultation and Echocardiogram, Narcolepsy, Labrador Retriever Type, Macular Corneal Dystrophy, MCD (CHST6), Hyperuricosuria (HUU), Day Blindness, Achromatopsia, Hereditary Nasal Parakeratosis (HNPK), Genetic Diversity Test, Full Embark Panel, Eye Certification (CAER, registered with OFA), DNA Profile, DNA Disease Panel, DNA Coat/Trait Panel, Dentition, Degenerative Myelopathy (DM; SOD1A), Cardiac Evaluation (registered with OFA), Brucellosis, Animal Genetics Panel, Exercise Induced Collapse (EIC), Centronuclear Myopathy (CNM), PRA, Rod-Cone Degeneration (PRA-prcd), D Locus (Dilute) DNA test, Elbow Dysplasia Finals (OFA, BVA, SV, FCI), Hip Dysplasia Finals (OFA, PennHIP, BVA, SV, FCI)CHIC CertifiedCanine Good Citizen EvaluatorProfessional GroomerAssociate Dog TrainerAmerican Kennel Club Canine CollegeAKC Canine Good Citizen EvaluatorAKC JudgeAKC Breeder with H.E.A.R.T.AKC Breeder of Merit
