Glanzmann thrombasthenia (GT) is a bleeding disorder characterized by platelet dysfunction. This test detects 2 variants associated with Glanzmann thrombasthenia in horses.
Atypical Equine Thrombasthenia is a bleeding disorder characterized by platelet dysfunction. This test detects a genetic variant associated with Atypical Equine Thrombasthenia in Thoroughbred horses.
Five mutations in the androgen receptor gene, located on the X chromosome, are known to result in androgen insensitivity. Androgen insensitivity syndrome causes male horses to be sterile and appear phenotypically female.
Equine familial isolated hypoparathyroidism (EFIH), previously called idiopathic hypocalcemia, is an invariably fatal condition that causes involuntary contraction of muscles and seizures due to low blood calcium concentrations in Thoroughbred foals.
The Full Color/Pattern Panel combines both the coat color panel and the White Pattern Panel 2. This is the most comprehensive of the horse coat color/patterning panels offered by the VGL.
Lethal white overo (LWO) is a genetic disorder that results from two copies of the version of the gene causing the frame overo coat color pattern. It is also known as Overo Lethal White Syndrome (OLWS).
