Related MeSH Hierarchy (7)
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Genetic Diseases, Inborn » Skin Diseases, Genetic » Albinism » Albinism, Oculocutaneous
Diseases [C] » Skin and Connective Tissue Diseases [C17] » Skin Diseases » Pigmentation Disorders » Hypopigmentation » Albinism » Albinism, Oculocutaneous
Diseases [C] » Skin and Connective Tissue Diseases [C17] » Skin Diseases » Skin Diseases, Genetic » Albinism » Albinism, Oculocutaneous
Diseases [C] » Eye Diseases [C11] » Eye Diseases, Hereditary » Albinism » Albinism, Oculocutaneous
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Genetic Diseases, Inborn » Eye Diseases, Hereditary » Albinism » Albinism, Oculocutaneous
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Genetic Diseases, Inborn » Metabolism, Inborn Errors » Amino Acid Metabolism, Inborn Errors » Albinism » Albinism, Oculocutaneous
Diseases [C] » Nutritional and Metabolic Diseases [C18] » Metabolic Diseases » Metabolism, Inborn Errors » Amino Acid Metabolism, Inborn Errors » Albinism » Albinism, Oculocutaneous
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
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Subtype Terms (1)
Hermanski-Pudlak Syndrome
12 approved drugs
Phase 2 Indicated Drugs (3)
Organization Involved with Phase 2 Indications (4)
Organization Involved with Other Experimental Indications (2)
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UMLS Data
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