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
Hyperuricosuria and Hyperuricemia (HUU)
Moderate Relevance
Centronuclear Myopathy
Some Relevance
Congenital Myasthenic Syndrome - COLQ related
Some Relevance
Copper Toxicosis, ATP7B Type
Some Relevance
Cystinuria Type I-A
Some Relevance
Exercise-Induced Collapse / EIC
Some Relevance
GM2 Gangliosidosis (Var 0)
Some Relevance
Macular Corneal Dystrophy
Some Relevance
Malignant Hyperthermia
Some Relevance
Menkes Disease
Some Relevance
Myotubular Myopathy 1 (XLMTM)
Some Relevance
Narcolepsy
Some Relevance
Nasal Parakeratosis
Some Relevance
Neonatal Encephalopathy with Seizures
Some Relevance
Oculoskeletal Dysplasia 1
Some Relevance
Osteochondrodysplasia
Some Relevance
Progressive Retinal Atrophy (PRA-prcd)
Some Relevance
Pyruvate Kinase Deficiency
Some Relevance
Skeletal Dysplasia 2 (SD2)
Some Relevance
Von Willebrand Disease I
Some Relevance
Coat Colour Dilution, dilution, MLPH-related
No Evidence
Congenital Myasthenic Syndrome - CHRNE related
No Evidence
Degenerative Myelopathy
No Evidence
Episodic Falling
No Evidence
Furnishings (moustache and eyebrows)
No Evidence
Glycogen Storage Disease VII (GSD VII)
No Evidence
Improper Coat/Furnishings
No Evidence
Familial Nephropathy
No Evidence
Progressive Retinal Atrophy crd4 (PRA crd4) / cord1
No Evidence
Progressive Retinal Atrophy rcd4 (PRA rcd4)
No Evidence
Progressive Retinal Atrophy, GR PRA2
No Evidence
Trapped Neutrophil Syndrome (TNS)
No Evidence
Hyperuricosuria and Hyperuricemia (HUU)
Moderate Relevance
Centronuclear Myopathy
Some Relevance
Congenital Myasthenic Syndrome - COLQ related
Some Relevance
Copper Toxicosis, ATP7B Type
Some Relevance
Cystinuria Type I-A
Some Relevance
Exercise-Induced Collapse / EIC
Some Relevance
The mutation associated with EIC has been identified in a number of breeds - particularly hunting/working breeds. As the EIC phenotype requires an environmental stimulus in most cases, it should be noted that dogs could be genetically affected for EIC without displaying the condition. It may be valuable to breeders of those breeds where the mutation has been detected to use a genetic test, where breed-specific research is ongoing.
GM2 Gangliosidosis (Var 0)
Some Relevance
Macular Corneal Dystrophy
Some Relevance
Malignant Hyperthermia
Some Relevance
Menkes Disease
Some Relevance
Myotubular Myopathy 1 (XLMTM)
Some Relevance
Narcolepsy
Some Relevance
Nasal Parakeratosis
Some Relevance
Neonatal Encephalopathy with Seizures
Some Relevance
BRR applies to standard poodle crosses origin
Oculoskeletal Dysplasia 1
Some Relevance
Osteochondrodysplasia
Some Relevance
Primary research was in the miniature poodle, but reports across all poodle types and crosses, over 40+ years, indicates it is likely widespread. Testing for any poodle-type or cross where relatives or the dog displays signs of disease may be prudent.
Progressive Retinal Atrophy (PRA-prcd)
Some Relevance
Multiple research sources indicate that this form of PRA-prcd could be present in many breeds, and testing could be relevant widely across a large number of different breeds of dog, many of which are terriers or breeds with terrier co?ancestry, but some of which have more diverse origins. Research indicates that the mutation is present at varying breed-specific frequency, but that testing and applying the test results can lead to signifigant reduction in the disease.
Pyruvate Kinase Deficiency
Some Relevance
Skeletal Dysplasia 2 (SD2)
Some Relevance
Von Willebrand Disease I
Some Relevance
Coat Colour Dilution, dilution, MLPH-related
No Evidence
Congenital Myasthenic Syndrome - CHRNE related
No Evidence
Incorrectly associated with Golden Retrievers; not the correct test
Degenerative Myelopathy
No Evidence
Both clinically rare and of complex inheritance. Test is considered poorly correlated with risk for development of DM, and recommendations are to not use the test for breed-wide breeding strategies. While the SOD 1 variant may be commonly found across many breeds, there are few clinical cases observed and confirmed, and in many cases DM has never been observed in the breeds.
Episodic Falling
No Evidence
Furnishings (moustache and eyebrows)
No Evidence
Furnishings have the potential relevance to any dog, but test usage is most often applied to those breeds with a heritage of these traits.
Glycogen Storage Disease VII (GSD VII)
No Evidence
May be relevant, as found in closely related breeds
Improper Coat/Furnishings
No Evidence
Familial Nephropathy
No Evidence
Progressive Retinal Atrophy crd4 (PRA crd4) / cord1
No Evidence
Reported only in miniature long-haired dachshunds (and their crosses).
Progressive Retinal Atrophy rcd4 (PRA rcd4)
No Evidence
Progressive Retinal Atrophy, GR PRA2
No Evidence
Trapped Neutrophil Syndrome (TNS)
No Evidence
Connections
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