Related MeSH Hierarchy (7)
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Genetic Diseases, Inborn » Metabolism, Inborn Errors » Amino Acid Metabolism, Inborn Errors » Albinism
Diseases [C] » Eye Diseases [C11] » Eye Diseases, Hereditary » Albinism
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Genetic Diseases, Inborn » Eye Diseases, Hereditary » Albinism
Diseases [C] » Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] » Genetic Diseases, Inborn » Skin Diseases, Genetic » Albinism
Diseases [C] » Skin and Connective Tissue Diseases [C17] » Skin Diseases » Pigmentation Disorders » Hypopigmentation » Albinism
Diseases [C] » Skin and Connective Tissue Diseases [C17] » Skin Diseases » Skin Diseases, Genetic » Albinism
Diseases [C] » Nutritional and Metabolic Diseases [C18] » Metabolic Diseases » Metabolism, Inborn Errors » Amino Acid Metabolism, Inborn Errors » Albinism
Description
General term for a number of inherited defects of amino acid metabolism in which there is a deficiency or absence of pigment in the eyes, skin, or hair. MeSH
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Subtype Terms (4)
Albinism, Oculocutaneous
8 approved drugs
Chediak-Higashi Syndrome
20 drugs (19 approved, 1 experimental)
Phase 2 Indicated Drugs (3)
Other Experimental Indicated Drugs (2)
Organization Involved with Phase 2 Indications (5)
Organization Involved with Other Experimental Indications (2)
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UMLS Data
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