mucopolysaccharidosis VI

Summary

mucopolysaccharidosis VI is a developmental defect during embryogenesis^[1]. It draws 79 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #74 of 308).^[2]

Key Facts

• mucopolysaccharidosis VI's instance of is recorded as developmental defect during embryogenesis^[3].
• mucopolysaccharidosis VI's instance of is recorded as rare disease^[4].
• mucopolysaccharidosis VI's instance of is recorded as class of disease^[5].
• Pierre Maroteaux is named after mucopolysaccharidosis VI^[6].
• mucopolysaccharidosis VI's subclass of is recorded as mucopolysaccharidosis^[7].
• mucopolysaccharidosis VI's subclass of is recorded as lysosomal storage disease with skeletal involvement^[8].
• mucopolysaccharidosis VI's subclass of is recorded as metabolic disease with corneal opacity^[9].
• mucopolysaccharidosis VI's subclass of is recorded as disease^[10].
• mucopolysaccharidosis VI's Commons category is recorded as Maroteaux–Lamy syndrome^[11].
• mucopolysaccharidosis VI's MeSH descriptor ID is recorded as D009087^[12].
• mucopolysaccharidosis VI's OMIM ID is recorded as 253200^[13].
• mucopolysaccharidosis VI's ICD-9 ID is recorded as 277.5^[14].
• mucopolysaccharidosis VI's ICD-10 ID is recorded as E76.2^[15].
• mucopolysaccharidosis VI's DiseasesDB is recorded as 29179^[16].
• mucopolysaccharidosis VI's Freebase ID is recorded as /m/0gj1sn^[17].
• mucopolysaccharidosis VI's KEGG ID is recorded as H00131^[18].
• mucopolysaccharidosis VI's MeSH tree code is recorded as C16.320.565.202.715.670^[19].
• mucopolysaccharidosis VI's MeSH tree code is recorded as C16.320.565.595.600.670^[20].
• mucopolysaccharidosis VI's MeSH tree code is recorded as C17.300.550.575.670^[21].
• mucopolysaccharidosis VI's MeSH tree code is recorded as C18.452.648.202.715.670^[22].
• mucopolysaccharidosis VI's MeSH tree code is recorded as C18.452.648.595.600.670^[23].
• mucopolysaccharidosis VI's eMedicine ID is recorded as 946474^[24].
• mucopolysaccharidosis VI's Disease Ontology ID is recorded as DOID:12800^[25].
• mucopolysaccharidosis VI's mode of inheritance is recorded as autosomal recessive^[26].
• mucopolysaccharidosis VI's Encyclopædia Britannica Online ID is recorded as science/Maroteaux-Lamy-syndrome^[27].

Why It Matters

mucopolysaccharidosis VI draws 79 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #74 of 308).^[2] It has Wikipedia articles in 11 language editions, a strong signal of global cultural recognition.^[28] It is known by 32 alternative names across languages and contexts.^[29]