External Certifications
Certified BreederHealth Testing: Canine Multiple System Degeneration, Kerry Blue Terrier Type, Polyneuropathy, Greyhound Type (NDRG1), Gangliosidosis GM2, Japanese Chin Type, GM1 Gangliosidosis (GLB1), Shiba Inu Type, GM1 Gangliosidosis, Alaskan Husky Type, GM1 Gangliosidosis, Portuguese Water Dog Type, Glanzmann's Thrombasthenia, Great Pyrenees Type, Glycogen Storage Disease Type IIIA, GSD IIIA, Globoid Cell Leukodystrophy (GCL), Terrier Type, Globoid Cell Leukodystrophy (GCL), Irish Setter Type, Glaucoma (BCG), Border Collie Type, Fucosidosis, Familial Nephropathy, English Springer Spaniel Type, Elliptocytosis, Familial Nephropathy, Cocker Spaniel Type, Episodic Falling Syndrome (EFS), Ehlers-Danlos Syndrome, Ectodermal Dysplasia, Chesapeake Bay Retriever Type, Early Onset Progressive Retinal Atrophy (EOPRA), Dry Eye Curly Coat Syndrome (CKSID), Dilated Cardiomyopathy 2 (DCM2), Dilated Cardiomyopathy (Schnauzer Type), Dilated Cardiomyopathy 1 (DCM1), Dental Hypomineralization (DH), Cystinuria Type 1, Newfoundland (PennGen), Cystinuria Type 1A, Newfoundland Type, Cystinuria Type 3, French Bulldog Type Risk Factor, Cystinuria Type 1A, Labrador Retriever Type, Cystinuria Type II-A, Australian Cattle Dog Type, Cyclic Neutropenia, Grey Collie Syndrome (CN), Congenital Methemoglobinemia, Pomeranian Type, Congenital Stationary Night Blindness (CSNB), Congenital Hypothyroidism with Goiter (CHG), Cone-Rod Dystrophy 2 (crd2), American Pitbull Terrier Type, Cone Degeneration, Labrador Retriever Type, Cone Degeneration, German Shorthaired Pointer Type, Cone Degeneration, German Shepherd Dog Type, Cone-Rod Dystrophy 1 (crd1), American Staffordshire Terrier Type, Cleft Palate (ADAMTS20), Chondrodysplasia/Dwarfism, Cerebellar Degeneration, Cerebellar Cortical Degeneration (CCD), Cerebellar Ataxia, Finnish Hound Type, Centronuclear Myopathy (CNM), Multiple System Degeneration, Chinese Crested Type, Canine Scott Syndrome (CSS), Catalase Deficiency, D Locus (Dilute) DNA test, Benign Familial Juvenile Epilepsy (BFJE), Agouti DNA Test, DNA Profile, DNA Coat/Trait Panel, Encephalopathy, Alaskan Husky Type, Amelogenesis Imperfecta (AI), Akita Type, Polyneuropathy (NDRG1), Alaskan Malamute Type, Acute Respiratory Distress Syndrome, Dalmatian Type, Adult Paroxysmal Dyskinesia, Acral Mutilation Syndrome (AMS), von Willebrand Disease II (vWD II), PRA, Rod-Cone Degeneration (PRA-prcd), Progressive Retinal Atrophy (PRA), Generalized, Neuronal Ceroid Lipofuscinosis 8 (NCL8), Australian Shepherd Type, Osteochondrodysplasia, Miniature Poodle Type, Multiple Drug Sensitivity (MDR1), Neonatal Encephalopathy with Seizures (NEwS), Neuronal Ceroid Lipofuscinosis 6 (NCL 6), Intestinal Cobalamin Malabsorption (IGS), Australian Shepherd Type, Chondrodystrophy and IVDD Risk (CDDY-IVDD), Hyperuricosuria (HUU), Multifocal Retinopathy 1 (CMR1), Hereditary (Juvenile) Cataracts (HC; JC), Australian Shepherd Type, Degenerative Myelopathy (DM; SOD1B), Bernese Mountain Dog Type, Hereditary (Juvenile) Cataracts (HC; JC), Craniomandibular Osteopathy (CMO), GM2 Gangliosidosis, Poodle Type, Exercise Induced Collapse (EIC), Degenerative Myelopathy (DM; SOD1A), Factor VII Deficiency, Cone Degeneration, Collie Eye Anomaly (CEA)
