5C56.30Ангилал
Mucopolysaccharidosis type 1
Тодорхойлолт
Mucopolysaccharidosis type 1 (MPS 1) is a rare lysosomal storage disease belonging to the group of mucopolysaccharidoses. There are three variants, differing widely in their severity, with Hurler syndrome (57% of cases) being the most severe, Scheie syndrome (20% of cases) the mildest and Hurler-Scheie syndrome (23% of cases) giving an intermediate phenotype.
Индексийн нэр томьёо Index terms · 20
Mucopolysaccharidosis type 1Alpha-L-iduronidase deficiencyl-iduronidase deficiencyLipochondrodystrophydysostosis multiplexdysostosis multiplex syndromeGargoylismMPS1 - [Mucopolysaccharidosis type 1]Mucopolysaccharidosis type 1HHurler syndromeMucopolysaccharidosis type 1, severe formMPS1H - [Mucopolysaccharidosis type 1H]Mucopolysaccharidosis type 1H/SHurler-Scheie syndromeMucopolysaccharidosis type 1, intermediate formMPS1H/S - [Mucopolysaccharidosis type 1H/S]Mucopolysaccharidosis type 1SScheie syndromeMucopolysaccharidosis type 1, mild formMPS1S - [Mucopolysaccharidosis type 1S]
Монгол орчуулга хянагдаж байгаа тул англи эхийг харуулж байна. Эх сурвалж: WHO ICD-11 (MMS) · WHO сайтад харах ↗