our breeding program

Health Testing

This page documents the health examinations carried out on Włochata Pasja breeding dogs, from joint assessments to a broad panel of genetic diseases.

Hip and elbow examinationsA broad genetic disease panelInformed pairing of breeding dogs
Molly, an Australian Labradoodle
Molly, an Australian Labradoodle

Australian Labradoodles and Health Testing

Australian Labradoodles and health testing. These are the conditions for which we test our dogs:

Core Tests and Conditions

  • Hip and elbow dysplasia (FCI standards)

  • Improper Coat

  • Von Willebrand Disease Type I, Type I vWD (VWF)

  • Canine Elliptocytosis (SPTB Exon 30)

  • Pyruvate Kinase Deficiency (PKLR Exon 7, Labrador Retriever Variant)

  • Progressive Retinal Atrophy, prcd (PRCD Exon 1)

  • Golden Retriever Progressive Retinal Atrophy 2, GR-PRA2 (TTC8)

  • Progressive Retinal Atrophy, crd4/cord1 (RPGRIP1)

  • Achromatopsia (CNGA3 Exon 7, Labrador Retriever Variant)

  • Macular Corneal Dystrophy, MCD (CHST6)

  • Hyperuricosuria and Hyperuricemia or Urolithiasis, HUU (SLC2A9)

  • Congenital Keratoconjunctivitis Sicca and Ichthyosiform Dermatosis, Dry Eye Curly Coat Syndrome, CKCSID (FAM83H Exon 5)

  • GM2 Gangliosidosis (HEXB, Poodle Variant)

  • Alexander Disease (GFAP)

  • Degenerative Myelopathy, DM (SOD1A)

  • Neonatal Encephalopathy with Seizures, NEWS (ATF2)

  • Narcolepsy (HCRTR2 Intron 6, Labrador Retriever Variant)

  • Muscular Dystrophy (DMD, Cavalier King Charles Spaniel Variant 1)

  • Ullrich-like Congenital Muscular Dystrophy (COL6A3 Exon 10, Labrador Retriever Variant)

  • Centronuclear Myopathy, CNM (PTPLA)

  • Exercise-Induced Collapse, EIC (DNM1)

  • Myotubular Myopathy 1, X-linked Myotubular Myopathy, XL-MTM (MTM1, Labrador Retriever Variant)

Additional Tests

  • MDR1 Drug Sensitivity (ABCB1)

  • P2Y12 Receptor Platelet Disorder (P2Y12)

  • Factor IX Deficiency, Hemophilia B variants

  • Factor VII Deficiency (F7 Exon 5)

  • Factor VIII Deficiency, Hemophilia A variants

  • Thrombopathia variants

  • Von Willebrand Disease Type III and Type II variants

  • Canine Leukocyte Adhesion Deficiency Type I and III

  • Congenital Macrothrombocytopenia

  • Glanzmann's Thrombasthenia Type I variants

  • May-Hegglin Anomaly (MYH9)

  • Prekallikrein Deficiency (KLKB1 Exon 8)

  • Pyruvate Kinase Deficiency variants

  • Trapped Neutrophil Syndrome, TNS

  • Ligneous Membranitis, LM

  • Platelet Factor X Receptor Deficiency, Scott Syndrome

  • Methemoglobinemia (CYB5R3)

  • Congenital Hypothyroidism variants

  • Complement 3 Deficiency, C3 Deficiency

  • Severe Combined Immunodeficiency and X-linked Severe Combined Immunodeficiency variants

  • Progressive Retinal Atrophy variants including rcd1, rcd3, CNGA, PRA1, SAG, GR-PRA1, crd1, XL-PRA1 and PRA3

  • Collie Eye Anomaly, Choroidal Hypoplasia, CEA

  • Day Blindness, Cone Degeneration and Achromatopsia variants

  • Autosomal Dominant Progressive Retinal Atrophy (RHO)

  • Canine Multifocal Retinopathy variants

  • Primary Open Angle Glaucoma and Primary Lens Luxation variants

  • Goniodysgenesis and Glaucoma, Pectinate Ligament Dysplasia, PLD

  • Hereditary Cataracts, Early-Onset Cataracts, Juvenile Cataracts

  • Congenital Stationary Night Blindness variants

  • 2,8-Dihydroxyadenine Urolithiasis, 2,8-DHA Urolithiasis

  • Cystinuria Type I-A, II-A and II-B

  • Polycystic Kidney Disease, PKD

  • Primary Hyperoxaluria and Protein Losing Nephropathy, PLN

  • X-Linked Hereditary Nephropathy, XLHN

  • Autosomal Recessive Hereditary Nephropathy, Familial Nephropathy, ARHN

  • Primary Ciliary Dyskinesia variants

  • X-linked Ectodermal Dysplasia, Anhidrotic Ectodermal Dysplasia, XHED

  • Renal Cystadenocarcinoma and Nodular Dermatofibrosis, RCND

  • Canine Fucosidosis

  • Glycogen Storage Disease variants including GSD II, IA, IIIA and VII

  • Mucopolysaccharidosis variants including MPS IIIA and MPS VII

  • Lagotto Storage Disease (ATG4D)

  • Neuronal Ceroid Lipofuscinosis variants

  • GM1 and GM2 Gangliosidosis variants

  • Globoid Cell Leukodystrophy, Krabbe disease

  • Autosomal Recessive Amelogenesis Imperfecta, Familial Enamel Hypoplasia

  • Persistent Mullerian Duct Syndrome, PMDS

  • Deafness and Vestibular Syndrome of Dobermans, DVDob, DINGS

  • Shar-Pei Autoinflammatory Disease, SPAID, Shar-Pei Fever

  • Neonatal Interstitial Lung Disease

  • Alaskan Husky Encephalopathy

  • Cerebellar Abiotrophy, Cerebellar Ataxia and Cerebellar Hypoplasia variants

  • Spinocerebellar Ataxia variants

  • Hereditary Ataxia, Cerebellar Degeneration

  • Benign Familial Juvenile Epilepsy

  • Fetal-Onset Neonatal Neuroaxonal Dystrophy

  • Hypomyelination and Tremors

  • Shaking Puppy Syndrome, X-linked Generalized Tremor Syndrome

  • Neuroaxonal Dystrophy variants

  • L-2-Hydroxyglutaricaciduria, L2HGA

  • Alaskan Malamute Polyneuropathy, AMPN

  • Narcolepsy variants

  • Progressive Neuronal Abiotrophy, Canine Multiple System Degeneration

  • Juvenile Laryngeal Paralysis and Polyneuropathy

  • Hereditary Sensory Autonomic Neuropathy, Acral Mutilation Syndrome

  • Sensory Neuropathy

  • Juvenile-Onset Polyneuropathy and Leonberger Polyneuropathy variants

  • Juvenile Myoclonic Epilepsy

  • Spongy Degeneration with Cerebellar Ataxia variants

  • Dilated Cardiomyopathy variants

  • Long QT Syndrome and Cardiomyopathy and Juvenile Mortality

  • Muscular Dystrophy and Limb Girdle Muscular Dystrophy variants

  • Inherited Myopathy of Great Danes

  • Myostatin Deficiency, Bully Whippet Syndrome

  • Myotonia Congenita variants

  • Inflammatory Myopathy and Hypocatalasia, Acatalasemia

  • Pyruvate Dehydrogenase Deficiency

  • Malignant Hyperthermia

  • Imerslund-Grasbeck Syndrome variants

  • Inherited Selected Cobalamin Malabsorption with Proteinuria

  • Lundehund Syndrome

  • Congenital Myasthenic Syndrome variants

  • Myasthenia Gravis-Like Syndrome

  • Paroxysmal Dyskinesia, PxD

  • Demyelinating Polyneuropathy

  • Dystrophic Epidermolysis Bullosa variants

  • Ectodermal Dysplasia, Skin Fragility Syndrome

  • Ichthyosis variants

  • Hereditary Footpad Hyperkeratosis variants

  • Musladin-Lueke Syndrome, MLS

  • Oculocutaneous Albinism, OCA

  • Bald Thigh Syndrome

  • Lethal Acrodermatitis, LAD

  • Ehlers Danlos

  • Cleft Lip and/or Cleft Palate

  • Hereditary Vitamin D-Resistant Rickets

  • Osteogenesis Imperfecta variants

  • Craniomandibular Osteopathy, CMO

  • Raine Syndrome, Canine Dental Hypomineralization Syndrome

  • Chondrodystrophy

Continue exploring

Code of Ethics — The principles behind our breeding program and the way we prepare puppies.

Reservations — How the conversation, application and puppy-matching process works.

About Me — My story, the history of our breeding program and the expertise behind Włochata Pasja.