Oculocutaneous Albinism (Albinism, Yellow Mutant)
261
relevant articles (1 outcomes,
9 trials/studies)
found for this Disease
Description:
Heterogeneous group of autosomal recessive disorders comprising at least four recognized types, all having in common varying degrees of hypopigmentation of the skin, hair, and eyes. The two most common are the tyrosinase-positive and tyrosinase-negative types.
Also Known As:
Albinism, Yellow Mutant; Albinism, Oculocutaneous; Albinism, Tyrosinase Negative; Albinism, Tyrosinase Positive; Tyrosinase-Negative Albinism; Tyrosinase-Positive Albinism; Yellow-Mutant Albinism; Albinism, Tyrosinase-Negative; Albinism, Tyrosinase-Positive; Albinism, Yellow-Mutant
Relationship Network
Disease Context: Research Results