Conditions / Syndrome
oculocutaneous albinism type III
info · Syndrome
An oculocutaneous albinism that has_material_basis_in an autosomal recessive mutation of the TYRP1 gene on chromosome 9p23.
Signs and symptoms
- Albinism
- Strabismus
- Nystagmus
- Red hair
- Partial albinism
Also known as: OCA3; Rufous Oculocutaneous Albinism