mucopolysaccharidosis VI
lysosomal storage disease
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mucopolysaccharidosis VI
Summary
mucopolysaccharidosis VI is a developmental defect during embryogenesis[1]. It has Wikipedia articles in 11 language editions, a strong signal of global cultural recognition.[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 is a type of mucopolysaccharidosis[7].
- mucopolysaccharidosis VI is a type of lysosomal storage disease with skeletal involvement[8].
- mucopolysaccharidosis VI is a type of metabolic disease with corneal opacity[9].
- mucopolysaccharidosis VI is a type of disease[10].
- mucopolysaccharidosis VI's Commons category is recorded as Maroteaux–Lamy syndrome[11].
- mucopolysaccharidosis VI's mode of inheritance is recorded as autosomal recessive[12].
- mucopolysaccharidosis VI's NCI Thesaurus ID is recorded as C61264[13].
- mucopolysaccharidosis VI's health specialty is recorded as endocrinology[14].
- mucopolysaccharidosis VI's genetic association is recorded as ARSB[15].
- mucopolysaccharidosis VI's exact match is recorded as http://purl.obolibrary.org/obo/DOID_12800[16].
- mucopolysaccharidosis VI's exact match is recorded as http://identifiers.org/doid/DOID:12800[17].
- mucopolysaccharidosis VI's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_583[18].
- mucopolysaccharidosis VI's on focus list of Wikimedia project is recorded as WikiProject Medicine[19].
Why It Matters
mucopolysaccharidosis VI has Wikipedia articles in 11 language editions, a strong signal of global cultural recognition.[2] It is known by 32 alternative names across languages and contexts.[20]