Albinism, Oculocutaneous D016115

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.   MeSH

Subtype Terms (1)

Hermanski-Pudlak Syndrome
12 approved drugs



Organization Involved with Other Experimental Indications (2)

Hierarchy Tree View

UMLS Data


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