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Test Overview:
Albinism is a congenital disorder that is characterized by lack of pigment in hair, skin and eyes.
Category:
Trait (Associated with Phenotype)
Gene:
TYR
Variant Detected:
Deletion
Severity:
Low. This disease generally causes mild signs of disease, or can be quite easily treated/managed.
Mode of Inheritance:
Autosomal Recessive
Research Citation(s):
Anim Genet. 2006 Apr; 37(2): 175–178.
Associated Breed(s):
Siamese,