<nowiki>Síndrome de Hunter; maladie de Hunter; Sindrom Hunter; Morbus Hunter; síndrome de Hunter; بیماری هانتر; 韓特氏症; Хантеров синдром; Hunter sendromu; ムコ多糖症II型; Болезнь Хантера; Sindromul Hunter; Hunters sjukdom; sindrome di Hunter; תסמונת האנטר; syndroom van Hunter; mucopolysaccharidosis II; Hunter syndrome; Hunterin oireyhtymä; 헌터 증후군; Гунтер синдромы; متلازمة هنتر; Хантеров синдром тип II; அண்டர் நோய்க்குறி; tipologia di mucopolisaccaridosi (la tipo II), una rara alterazione metabolica congenita dell'organismo, che fa parte dell'eterogeneo gruppo delle malattie da accumulo lisosomiale; Krankheit; 큰 설탕 분자가 신체 조직에 축적되는 희귀 유전 질환; mucopolysaccharidosis characterized by a deficiency of the lysosomal enzyme iduronate sulfatase; maladie génétique dégénérative lysosomale, mucopolysaccharidose de type II.; хвороба; Erfelijke genetische aandoening; Hunter's syndrome; MPS II - Hunter syndrome; Mucopolysaccharidosis, MPS-II (disorder); deficiency of iduronate-2-sulphatase; Hunter syndrome; MPS II; Mucopolysaccharidosis, MPS-II; Sids Deficiency; Iduronate 2-Sulfatase Deficiency; MPS2; MPSII; MUCOPOLYSACCHARIDOSIS, TYPE II; mucopolysaccharidosis type II; Mps 2; Ids Deficiency; Sulfoiduronate Sulfatase Deficiency; MUCOPOLYSACCHARIDOSIS, TYPE II; MPS2; mucopolysaccharidosis type 2; Hunter症候群; ハンター症候群; Sindrome de Hunter</nowiki>
mucopolysaccharidosis II
mucopolysaccharidosis characterized by a deficiency of the lysosomal enzyme iduronate sulfatase