Sly syndrome
mucopolysaccharidosis characterized by a deficiency of the lysosomal enzyme beta-glucuronidase resulting in the inability to degrade glucuronic acid-containing glycosaminoglycans
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Sly syndrome
Summary
Sly syndrome is a developmental defect during embryogenesis[1]. It has Wikipedia articles in 12 language editions, a strong signal of global cultural recognition.[2]
Key Facts
- Sly syndrome's instance of is recorded as developmental defect during embryogenesis[3].
- Sly syndrome's instance of is recorded as class of disease[4].
- Sly syndrome is a type of mucopolysaccharidosis[5].
- Sly syndrome is a type of lysosomal storage disease with skeletal involvement[6].
- Sly syndrome is a type of disease[7].
- Sly syndrome's mode of inheritance is recorded as autosomal recessive[8].
- Sly syndrome's ICD-9-CM is recorded as 277.6[9].
- Sly syndrome's NCI Thesaurus ID is recorded as C84903[10].
- Sly syndrome's health specialty is recorded as endocrinology[11].
- Sly syndrome's genetic association is recorded as GUSB[12].
- Sly syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_12803[13].
- Sly syndrome's exact match is recorded as http://identifiers.org/doid/DOID:12803[14].
- Sly syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_584[15].
- Sly syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[16].
Why It Matters
Sly syndrome has Wikipedia articles in 12 language editions, a strong signal of global cultural recognition.[2] It is known by 19 alternative names across languages and contexts.[17]