Our health testing levels for the Tollerdoodle (Nova Scotia Duck Tolling Retriever x Poodle)
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
Elbow Dysplasia(ED)
Bewegungsapparat
Elbow dysplasia is a developmental disorder of the musculoskeletal system where the three bones forming the elbow joint do not fit together properly. This misalignment causes abnormal friction and wear on the joint cartilage, eventually leading to painful, chronic joint inflammation and arthritis. It is a complex genetic condition influenced by multiple genes.
Roentgen · Passing: 0 (Grade 0)
Patellar Luxation(PL)
Bewegungsapparat
Patellar luxation, also known as a luxating patella, is a physical condition affecting the knee joint where the kneecap slips out of its normal groove. This misalignment interferes with the mechanical movement of the hind leg and can cause the joint to lock. Over time, this abnormal friction can lead to painful joint wear and tear, known as osteoarthritis.
Physisch · Passing: Grade 0
Degenerative Myelopathy(DM)
Nervensystem
Degenerative Myelopathy is a progressive disease of the spinal cord where the protective sheath around the nerves slowly breaks down. This deterioration disrupts the vital communication signals between the brain and the muscles of the hind limbs. Over time, this lack of signal transmission leads to a complete loss of muscle control in the back legs.
DNA · Passing: Clear or Carrier
Von Willebrand disease type I(vWD1)
Von Willebrand Disease Type I is an inherited bleeding disorder that affects the blood's ability to clot properly. It is caused by a deficiency in von Willebrand factor, a specific protein that helps blood platelets stick together to plug damaged blood vessels. Because this is an autosomal-dominant condition, a dog only needs to inherit one copy of the mutated gene to potentially show symptoms.
Passing: Clear or Carrier
These levels are a comparison framework, not an official certification. They help compare breeding programs at a glance.