Australian Terrier
Australianterrieri
Australian Terrier
FCI Group
Terriers
AKC Group
Terrier
TKC Group
Terrier
Country of Origin
AU
Australian Terrier
Health Testing Requirements by Country
Autoimmune and Allergies
FI
Endocrine and Pancreas
Ataxia, Locomotor, and Epilepsy
Eye Conditions and Blindness
SE
Skeletal and Muscular
Gastrointestinal, Digestive, and Metabolic
Genetic Material and Diversity
Temperament
Test Relevances
Ataxia, Spinocerebellar, CAPN1-related
Some Relevance
Pyruvate Kinase Deficiency
No Evidence
Von Willebrand Disease I
No Evidence
Von Willebrand Disease III
No Evidence
Coat Colour Dilution, dilution, MLPH-related
No Evidence
Degenerative Myelopathy
No Evidence
Primary Lens Luxation (PLL)
No Evidence
Ataxia, Spinocerebellar, CAPN1-related
Some Relevance
Pyruvate Kinase Deficiency
No Evidence
Von Willebrand Disease I
No Evidence
Mutation is widespred, so may be relevant
Von Willebrand Disease III
No Evidence
Coat Colour Dilution, dilution, MLPH-related
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.
Primary Lens Luxation (PLL)
No Evidence
Findings indicate the mutation segregates in 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 high frequency within most of the breeds in which it segregates. (Gould et. al, 2011)
- Updated