Our health testing levels for the Australian Kelpie
We group breeding programs into three levels based on testing depth. Ask your breeder directly which level they meet.
A breeder at the Great level performs all mandatory tests plus 5 additional clinically recommended screenings that reduce risk in this breed.
In addition to mandatory tests:
Collie eye anomaly (CEA)(CEA)
Augen
Collie Eye Anomaly is an inherited developmental defect affecting the eye, specifically the retina (the light-sensitive tissue at the back of the eye) and the choroid (the underlying layer of blood vessels). This genetic condition causes these structures to develop abnormally before birth. It is primarily seen in herding breeds and is inherited in an autosomal recessive manner.
Passing: Clear or Carrier
Cerebellar abiotrophy(CA)
Nervensystem
Cerebellar abiotrophy is an inherited neurological disorder affecting the brain, specifically the cerebellum, which regulates balance and movement coordination. In affected dogs, the nerve cells in this region prematurely degenerate and die off. This progressive cell loss disrupts the brain's ability to control smooth physical movements.
DNA · Passing: CLEAR
Globoid cell leukodystrophy (galactocerebrosidosis)(GCL)
Nervensystem
Globoid cell leukodystrophy is an inherited metabolic disorder affecting the nervous system, caused by a deficiency in an essential enzyme. This deficiency leads to the buildup of harmful substances that destroy myelin, which is the protective sheath surrounding nerve fibers in the brain and spinal cord. Without this protective covering, the nerves cannot transmit signals properly, resulting in progressive neurological decline.
DNA · Passing: CARRIER
Lipid malabsorption, ACSL5-related(ILM)
Stoffwechsel
This is an inherited metabolic disorder of the digestive system, primarily affecting the Australian Kelpie breed, where the intestines cannot properly absorb or process dietary fats. It is caused by a specific genetic deletion involving the ACSL5 gene, which is essential for fat metabolism. Without this functioning gene, the body cannot utilize fats from food, leading to severe nutritional deficiencies.
Passing: Clear or Carrier
Progressive Retinal Atrophy (prcd-PRA)(PRA)
Progressive rod-cone degeneration (prcd-PRA) is an inherited eye disease that causes the light-sensitive cells in the retina, which lines the back of the eye, to gradually break down and die. This degeneration affects both eyes and eventually leads to complete blindness. Because the retina cannot process light properly, the dog's brain stops receiving visual information.
Passing: Clear or Carrier
These levels are a comparison framework, not an official certification. They help compare breeding programs at a glance.