Type 1 Polysaccharide Storage Myopathy is a glycogen storage disease that results in the accumulation of abnormal complex sugars in muscle cells, which can lead to muscle pain, weakness, and reluctance to move.
Congenital stationary night blindness (CSNB) is an inherited condition in which affected individuals are unable to see in low light or dark conditions. This test detects a causal variant specific to Tennessee Walking Horses, Standardbred and Missouri Fox Trotter.
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.
Champagne is a coat color dilution responsible for diluting both red and black pigment as well as causing pinkish/lavender skin and amber-colored eyes.
Multiple congenital ocular anomalies (MCOA) is an inherited eye disorder that is associated with the silver dilution and is characterized by ocular cysts, enlargement of the cornea, abnormally formed iris/retina, and additional abnormalities.
