inborn disorder of amino acid metabolism obsolete genetic skin disease albinism MEDGEN:182 MESH:D000417 ICD10CM:E70.3 MONDO:0043209 SCTID:15890002 NCIT:C84543 This groups multiple types, including those restricted to the eyes, the skin or both UMLS:C0001916 A congenital disorder characterized by partial or complete absence of melanin pigment in the eyes, hair, or skin. albinism