mucopolysaccharidosis I
lysosomal storage disease
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mucopolysaccharidosis I
Summary
mucopolysaccharidosis I is a rare disease[1]. It draws 63 Wikipedia views per month (rare_disease category, ranking #213 of 627).[2]
Key Facts
- mucopolysaccharidosis I's instance of is recorded as rare disease[3].
- mucopolysaccharidosis I's instance of is recorded as class of disease[4].
- mucopolysaccharidosis I is a type of mucopolysaccharidosis[5].
- mucopolysaccharidosis I is a type of disease[6].
- mucopolysaccharidosis I's Commons category is recorded as Hurler syndrome[7].
- mucopolysaccharidosis I's mode of inheritance is recorded as autosomal recessive[8].
- mucopolysaccharidosis I's NCI Thesaurus ID is recorded as C85053[9].
- mucopolysaccharidosis I's different from is recorded as Q124799819[10].
- mucopolysaccharidosis I's health specialty is recorded as endocrinology[11].
- mucopolysaccharidosis I's drug or therapy used for treatment is recorded as laronidase[12].
- mucopolysaccharidosis I's genetic association is recorded as IDUA[13].
- mucopolysaccharidosis I's exact match is recorded as http://purl.obolibrary.org/obo/DOID_12802[14].
- mucopolysaccharidosis I's exact match is recorded as http://identifiers.org/doid/DOID:12802[15].
- mucopolysaccharidosis I's exact match is recorded as http://purl.obolibrary.org/obo/HP_0000943[16].
- mucopolysaccharidosis I's on focus list of Wikimedia project is recorded as WikiProject Medicine[17].
Why It Matters
mucopolysaccharidosis I draws 63 Wikipedia views per month (rare_disease category, ranking #213 of 627).[2] It has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[18] It is known by 40 alternative names across languages and contexts.[19]