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Australian Labradoodle
poodle crosses
FCI Group Not Recognized
AKC Group Not Recognized
TKC Group Not Recognized
Country of Origin AU
Health Testing Requirements by Country
Test Relevances
4
Hyperuricosuria and Hyperuricemia (HUU)
Moderate Relevance
3
Centronuclear Myopathy
Some Relevance
3
Congenital Myasthenic Syndrome - COLQ related
Some Relevance
3
Copper Toxicosis, ATP7B Type
Some Relevance
3
Cystinuria Type I-A
Some Relevance
3
Exercise-Induced Collapse / EIC
Some Relevance
3
GM2 Gangliosidosis (Var 0)
Some Relevance
3
Macular Corneal Dystrophy
Some Relevance
3
Malignant Hyperthermia
Some Relevance
3
Menkes Disease
Some Relevance
3
Myotubular Myopathy 1 (XLMTM)
Some Relevance
3
Narcolepsy
Some Relevance
3
Nasal Parakeratosis
Some Relevance
3
Neonatal Encephalopathy with Seizures
Some Relevance
3
Oculoskeletal Dysplasia 1
Some Relevance
3
Osteochondrodysplasia
Some Relevance
3
Progressive Retinal Atrophy (PRA-prcd)
Some Relevance
3
Pyruvate Kinase Deficiency
Some Relevance
3
Skeletal Dysplasia 2 (SD2)
Some Relevance
3
Von Willebrand Disease I
Some Relevance
2
Coat Colour Dilution, dilution, MLPH-related
No Evidence
2
Congenital Myasthenic Syndrome - CHRNE related
No Evidence
2
Degenerative Myelopathy
No Evidence
2
Episodic Falling
No Evidence
2
Furnishings (moustache and eyebrows)
No Evidence
2
Glycogen Storage Disease VII (GSD VII)
No Evidence
2
Improper Coat/Furnishings
No Evidence
2
Familial Nephropathy
No Evidence
2
Progressive Retinal Atrophy crd4 (PRA crd4) / cord1
No Evidence
2
Progressive Retinal Atrophy rcd4 (PRA rcd4)
No Evidence
2
Progressive Retinal Atrophy, GR PRA2
No Evidence
2
Trapped Neutrophil Syndrome (TNS)
No Evidence
Connections
Oculoskeletal Dysplasia 1
Condition
Osteochondrodysplasia
Condition
Congenital Myasthenic Syndrome - COLQ related
Condition
Oculoskeletal Dysplasia 1
Condition
Osteochondrodysplasia
Condition
Progressive Retinal Atrophy (PRA-prcd)
Condition - Eye Conditions and Blindness
Centronuclear Myopathy
Condition
Pyruvate Kinase Deficiency
Condition
Skeletal Dysplasia 2 (SD2)
Condition
Congenital Myasthenic Syndrome - COLQ related
Condition
Copper Toxicosis, ATP7B Type
Condition
Von Willebrand Disease I
Condition
Cystinuria Type I-A
Condition - Renal and Urinary
Exercise-Induced Collapse / EIC
Condition - Neurological and Neuromuscular
GM2 Gangliosidosis (Var 0)
Condition
Hyperuricosuria and Hyperuricemia (HUU)
Condition
Myotubular Myopathy 1 (XLMTM)
Condition
Narcolepsy
Condition
Nasal Parakeratosis
Condition
Neonatal Encephalopathy with Seizures
Condition
Labradoodle Veterinary Care - Agria Breed Profiles
Reference - Data
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