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Albinism, Oculocutaneous
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.
Subtype terms (1)
More specific conditions that are subtypes of Albinism, Oculocutaneous in the MeSH hierarchy.
- Hermanski-Pudlak Syndrome
12 drugs approved
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Organizations
Organization Involved with Phase 2 Indications (4)
Organization Involved with Other Experimental Indications (2)