Australian Cobberdog
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
Copper Toxicosis, ATP7B Type
Some Relevance
Cystinuria Type I-A
Some Relevance
Menkes Disease
Some Relevance
Muscular Dystrophy (Duchenne-type, DMD) GRMD
Some Relevance
Narcolepsy
Some Relevance
Nasal Parakeratosis
Some Relevance
Von Willebrand Disease I
Some Relevance
Centronuclear Myopathy
No Evidence
Congenital Myasthenic Syndrome - CHRNE related
No Evidence
Congenital Myasthenic Syndrome - COLQ related
No Evidence
Curly Coat Dry Eye (CKCSID)
No Evidence
Degenerative Myelopathy
No Evidence
Episodic Falling
No Evidence
Exercise-Induced Collapse / EIC
No Evidence
Globoid Cell Leukodystrophy
No Evidence
Glycogen Storage Disease VII (GSD VII)
No Evidence
Malignant Hyperthermia
No Evidence
Neonatal Encephalopathy with Seizures
No Evidence
Familial Nephropathy
No Evidence
Progressive Retinal Atrophy (PRA-prcd)
No Evidence
Progressive Retinal Atrophy crd4 (PRA crd4) / cord1
No Evidence
Pyruvate Kinase Deficiency
No Evidence
Trapped Neutrophil Syndrome (TNS)
No Evidence
Hyperuricosuria and Hyperuricemia (HUU)
Moderate Relevance
Copper Toxicosis, ATP7B Type
Some Relevance
Cystinuria Type I-A
Some Relevance
Menkes Disease
Some Relevance
Muscular Dystrophy (Duchenne-type, DMD) GRMD
Some Relevance
Narcolepsy
Some Relevance
Nasal Parakeratosis
Some Relevance
Von Willebrand Disease I
Some Relevance
Centronuclear Myopathy
No Evidence
No paper
Congenital Myasthenic Syndrome - CHRNE related
No Evidence
Incorrectly associated with Golden Retrievers; not the correct test
Congenital Myasthenic Syndrome - COLQ related
No Evidence
Rare condition, with possible relevance due to it's presence in Labrador and Golden Retrievers.
Curly Coat Dry Eye (CKCSID)
No Evidence
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
Exercise-Induced Collapse / EIC
No Evidence
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.
Globoid Cell Leukodystrophy
No Evidence
May be relevant, as research indicates relevance in the Aust. Kelpie
Glycogen Storage Disease VII (GSD VII)
No Evidence
May be relevant, as found in closely related breeds
Malignant Hyperthermia
No Evidence
Neonatal Encephalopathy with Seizures
No Evidence
BRR applies to standard poodle crosses origin
Familial Nephropathy
No Evidence
Progressive Retinal Atrophy (PRA-prcd)
No Evidence
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.
Progressive Retinal Atrophy crd4 (PRA crd4) / cord1
No Evidence
Reported only in miniature long-haired dachshunds (and their crosses).
Pyruvate Kinase Deficiency
No Evidence
Trapped Neutrophil Syndrome (TNS)
No Evidence
Connections
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