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Albinism - Siamese Overview

Albinism - Siamese
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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

Test Overview: Albinism is a congenital disorder that is characterized by lack of pigment in hair, skin and eyes.

Research Citation(s): Anim Genet. 2006 Apr; 37(2): 175–178.

Associated Breed(s): Siamese,