Portia
F1 Australian Goldendoodle (Double Doodle)
(English Goldendoodle x Australian Labradoodle)
Size: Mini
Colour: Black Abstract
Coat: Curly
DNA: Cleared by Parentage
at/at, kb/kb, B/b, E/e, N/sp, F/F
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Sire: Roo - DNA Clear
Degenerative Myelopathy - Clear
Exercise-Induced Collapse - Clear
Hereditary Nasal Parakeratosis (Labrador Retriever Type) -Clear
Progressive Retinal Atrophy, Cone-Rod Dystrophy 4 - Clear
Progressive Retinal Atrophy, Progressive Rod-Cone Degeneration - Clear
Progressive Retinal Atrophy, Rod-Cone Dysplasia 4 - Clear
Von Willebrand Disease I - Clear
Ichthyosis (Golden Retriever Type 1) - Clear
Macular Corneal Dystrophy (Labrador Retriever Type) - -Clear
Multidrug Resistance 1 - Clear
Neonatal Encephalopathy with Seizures - Clear
Progressive Retinal Atrophy, Golden Retriever 2 - Clear
Stargardt Disease - Clear
Centronuclear Myopathy - Clear
Chondrodystrophy - Clear
Cone Degeneration (Labrador Retriever Type) - Clear
Congenital Myasthenic Syndrome (Labrador Retriever Type) - -Clear
Cystinuria (Labrador Retriever Type) - Clear
GM2 Gangliosidosis (Poodle Type) - Clear
Glycogen Storage Disease VII, PFK Deficiency - Clear
Hyperuricosuria - Clear
Myotubular Myopathy 1 - Clear
Narcolepsy (Labrador Retriever Type) - Clear
Osteochondrodysplasia
Pyruvate Kinase Deficiency (Labrador Retriever Type) - Clear
Skeletal Dysplasia 2 - Clear
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Dam:Jorja DNA Clear
Degenerative Myelopathy - Clear
Ichthyosis - Clear
Neonatal Encephalopathy with seizures - Clear
Progressive Retinal Atrophy (Golden Retriever) 1 - Clear
Progressive Retinal Atrophy, Progressive Rod cone Degeneration - Clear
Von Willebrand Disease 1 - Clear
Dystrophic Epidermolysis Bullosa - Clear
Gm2 Gangliosidosis (Poodle type) - Clear
Muscular Dystrophy (Golden Retriever type) - Clear
Osteochondrodysplasia - Clear
Osteogenesis Imperfecta (Golden Retriever type) - Clear
Sensory Ataxic Neuropathy - Clear
Neuronal Ceroid Lipofuscinosis - Clear
Exercise-Induced Collapse - Clear
Chondrodysplasia - Clear