Our health testing levels for the Whippet
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:
Cataract(HC)
Augen und Sehvermögen
A cataract is a progressive clouding of the lens inside the dog's eye, which is the clear structure that focuses light onto the retina at the back of the eye. When the lens becomes cloudy or opaque, it blocks light from entering, gradually impairing the dog's vision. If left untreated, this condition can eventually lead to complete blindness in the affected eye.
Augen · Passing: CLEAR
Color Dilution Alopecia (CDA)(CDA)
Haut und Fell
Color Dilution Alopecia is a genetic skin disorder that affects dogs with diluted coat colors, such as blue, fawn, or lilac. It is caused by an abnormal distribution of pigment within the hair shafts, which makes the hair brittle and prone to breaking. This structural weakness leads to progressive hair loss and leaves the skin more vulnerable to irritation.
Haut · Passing: Clear/Normal
Ectodermal Dysplasia(ED-SFS)
Haut und Fell
Ectodermal dysplasia with skin fragility syndrome (ED-SFS) is a severe genetic disorder affecting the skin and its associated structures, such as hair, claws, and teeth. It is caused by a defect in the proteins that normally bind skin cells together, leading to extremely weak cell cohesion. This lack of structural integrity makes the skin highly vulnerable to tearing and peeling under normal wear and tear.
DNA · Passing: Clear or Carrier
Pattern baldness
Haut und Fell
Pattern baldness is a cosmetic, genetically influenced condition affecting the skin and coat. It occurs when hair follicles gradually shrink over time, leading to localized hair loss. Because there is no underlying inflammation or infection, the skin itself remains healthy and unaffected.
Haut
Phosphofructokinase (PFK) deficiency(PFK)
Hormonelles und Stoffwechsel
This inherited metabolic disorder is caused by a lack of a key enzyme needed to break down sugar for energy in red blood cells and muscles. Without this enzyme, these cells cannot function properly, leading to muscle damage and the premature destruction of red blood cells, which is called hemolysis. This deficiency primarily impacts the muscular and circulatory systems.
DNA · Passing: Clear or Carrier
These levels are a comparison framework, not an official certification. They help compare breeding programs at a glance.