Sugar Fig Kennel

Parent health testing

Goldendoodle

Labradoodle

Standard Poodle

• May-Hegglin Anomaly, Phosphofructokinase Deficiency (PFK), Pyruvate Kinase Deficiency (PKD), Labrador Retriever Type, P2RY12 Receptor Platelet Disorder, Trapped Neutrophil Syndrome, Cohen Syndrome (TNS), Pyruvate Kinase Deficiency (PKD), Terrier Type, Pyruvate Kinase Deficiency (PKD), Beagle Type, Glanzmann's Thrombasthenia, Great Pyrenees Type, von Willebrand Disease III (vWD III), Prekallikrein Deficiency, Fletcher Trait, Macrothrombocytopenia, Factor XI Deficiency, von Willebrand Disease I (vWD I), Factor VII Deficiency, Leukocyte Adhesion Deficiency, Type III, Dental Hypomineralization (DH), Multiple Drug Sensitivity (MDR1), Early Onset Progressive Retinal Atrophy (EOPRA), Primary Open Angle Glaucoma (ADAMST10 Exon 17), Cone-Rod Dystrophy 2 (crd2), American Pitbull Terrier Type, Cone Degeneration, PRA, Rod-Cone Dysplasia 2 (rcd2), PRA, Rod-Cone Dysplasia 3 (rcd3), Cone-Rod Dystrophy (crd4), Primary Lens Luxation (PLL), X-Linked Progressive Retinal Atrophy (XL-PRA), Dilated Cardiomyopathy 1 (DCM1), Long QT Syndrome, Congenital Hypothyroidism with Goiter (CHG), Congenital Hypothyroidism with Goiter, Terrier Type (CHG), Severe Combined Immunodeficiency Disease, X-Linked, Basset Hound Type (XSCID), Compliment 3 Deficiency (C3), Severe Combined Immunodeficiency Disease, Terrier Type, Cyclic Neutropenia, Grey Collie Syndrome (CN), Glycogen Storage Disease Type IIIA, GSD IIIA, Glycogen Storage Disease Type II or Pompe's Disease (GSD II), Pyruvate Dehydrogenase Phosphatase 1 Deficiency (PDP1), Hypocatalasia, Mucopolysaccharidosis IIIA (MPS IIIA), Dachshund Type, Duchenne Muscular Dystrophy, Golden Retriever Type, Myotubular Myopathy, Labrador Retriever Type, Centronuclear Myopathy (CNM), Myotonia Congenita, Australian Cattle Dog Type, X-Linked Tremors, Shaking Puppy Syndrome (SPS), Neonatal Ataxia, Bandera's Disease, Benign Familial Juvenile Epilepsy (BFJE), Neuronal Ceroid Lipofuscinosis 10 (NCL10), American Bulldog Type, Neuronal Ceroid Lipofuscinosis 8 (NCL8), Setter Type, Sensory Neuropathy, Border Collie Type (SN), Late Onset Ataxia, Spinocerebellar Ataxia (LOA, SCA), Neonatal Cortical Cerebellar Degeneration (NCCD), Cerebellar Cortical Degeneration (CCD), Spinocerebellar Ataxia (SCA), Narcolepsy, Doberman Pinscher Type, Narcolepsy, Dachshund Type, Juvenile Myoclonic Epilepsy (JME), Neonatal Encephalopathy with Seizures (NEwS), Hypomyelination, Weimaraner Type, Spinal Dysraphism (SD), Juvenile Laryngeal Paralysis & Polyneuropathy (JLPP), Cerebellar Degeneration, Lagotto Storage Disease (LSD), Neuroaxonal Dystrophy (NAD), Papillon Type, Hyperekplexia, Startle Disease, L-2-Hydroxyglutaric Aciduria (L2HGA), Staffordshire Bull Terrier Type, Hereditary Ataxia, Cerebellar Ataxia, Neuronal Ceroid Lipofuscinosis 1 (NCL1), Dachshund Type, Neuronal Ceroid Lipofuscinosis 7 (NCL7), GM2 Gangliosidosis, Poodle Type, Gangliosidosis GM2, Japanese Chin Type, Globoid Cell Leukodystrophy (GCL), Irish Setter Type, Exercise Induced Collapse (EIC), Episodic Falling Syndrome (EFS), Globoid Cell Leukodystrophy (GCL), Terrier Type, Polyneuropathy (NDRG1), Alaskan Malamute Type, Persistent Müllerian Duct Syndrome, Cleft Palate (ADAMTS20), Cleft Palate (DLX6), Craniomandibular Osteopathy (CMO), Osteogenesis Imperfecta (OI), Dachshund Type, Spongiform Leukoencephalomyelopathy (SLEM), Skeletal Dysplasia (SD2), Hereditary Vitamin D-Resistant Rickets (HVDRR), Musladin-Leuke Syndrome (MLS), Chondrodysplasia/Dwarfism, X-Linked Anhidrotic Ectodermal Dysplasia, Shepherd Type, Protein-Losing Nephropathy (PLN; NPHS1 Gene Variant), Hyperuricosuria (HUU), Fanconi Syndrome, Cystinuria Type II-A, Australian Cattle Dog Type, Cystinuria Type 1A, Labrador Retriever Type, Polycystic Kidney Disease (PKD), Renal Cystadenocarcinoma and Nodular Dermatofibrosis (RCND), von Willebrand Disease II (vWD II), Multifocal Retinopathy 2 (CMR2), Multifocal Retinopathy 1 (CMR1), Ichthyosis, Golden Retriever Type 1, PRA, Golden Retriever 1, PRA, Golden Retriever 2, Cone-Rod Dystrophy 1 (crd1), American Staffordshire Terrier Type, PRA, Cone-Rod Dystrophy (PRA-crd), Standard Wirehaired Dachshund Type, PRA, Rod-Cone Dysplasia 4 (rcd4), PRA, Rod-Cone Degeneration (PRA-prcd), Degenerative Myelopathy (DM; SOD1A)

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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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