mucopolysaccharidosis II
mucopolysaccharidosis characterized by a deficiency of the lysosomal enzyme iduronate sulfatase
Press Enter · cited answer in seconds
0 sources
mucopolysaccharidosis II
Summary
mucopolysaccharidosis II is a developmental defect during embryogenesis[1]. It ranks in the top 5% of developmental_defect_during_embryogenesis entities by monthly Wikipedia readership (762 views/month).[2]
Key Facts
- mucopolysaccharidosis II's instance of is recorded as developmental defect during embryogenesis[3].
- mucopolysaccharidosis II's instance of is recorded as rare disease[4].
- mucopolysaccharidosis II's instance of is recorded as class of disease[5].
- mucopolysaccharidosis II is a type of mucopolysaccharidosis[6].
- mucopolysaccharidosis II is a type of syndromic neurometabolic disease with X-linked intellectual disability[7].
- mucopolysaccharidosis II is a type of mucopolysaccharidosis with skin involvement[8].
- mucopolysaccharidosis II is a type of hypertrophic cardiomyopathy[9].
- mucopolysaccharidosis II is a type of lysosomal storage disease with skeletal involvement[10].
- mucopolysaccharidosis II is a type of ptosis[11].
- mucopolysaccharidosis II is a type of syndrome associated with hypertrophic cardiomyopathy[12].
- mucopolysaccharidosis II is a type of lysosomal disease with hypertrophic cardiomyopathy[13].
- mucopolysaccharidosis II is a type of disease[14].
- mucopolysaccharidosis II's Commons category is recorded as Hunter syndrome[15].
- mucopolysaccharidosis II's mode of inheritance is recorded as X-linked recessive[16].
- mucopolysaccharidosis II's NCI Thesaurus ID is recorded as C61260[17].
- mucopolysaccharidosis II's health specialty is recorded as endocrinology[18].
- mucopolysaccharidosis II's drug or therapy used for treatment is recorded as idursulfase[19].
- mucopolysaccharidosis II's genetic association is recorded as IDS[20].
- mucopolysaccharidosis II's exact match is recorded as http://purl.obolibrary.org/obo/DOID_12799[21].
- mucopolysaccharidosis II's exact match is recorded as http://identifiers.org/doid/DOID:12799[22].
- mucopolysaccharidosis II's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_580[23].
- mucopolysaccharidosis II's on focus list of Wikimedia project is recorded as WikiProject Medicine[24].
Why It Matters
mucopolysaccharidosis II ranks in the top 5% of developmental_defect_during_embryogenesis entities by monthly Wikipedia readership (762 views/month).[2] It has Wikipedia articles in 17 language editions, a strong signal of global cultural recognition.[25] It is known by 25 alternative names across languages and contexts.[26]