Scheie syndrome
mucopolysaccharidosis characterized by corneal clouding, facial dysmorphism and normal lifespan
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Scheie syndrome
Summary
Scheie syndrome is a rare disease[1]. It draws 44 Wikipedia views per month (rare_disease category, ranking #198 of 627).[2]
Key Facts
- Scheie syndrome's instance of is recorded as rare disease[3].
- Scheie syndrome's instance of is recorded as class of disease[4].
- Scheie syndrome's subclass of is recorded as mucopolysaccharidosis I[5].
- Scheie syndrome's OMIM ID is recorded as 607016[6].
- Scheie syndrome's Disease Ontology ID is recorded as DOID:0060222[7].
- Scheie syndrome's Encyclopædia Britannica Online ID is recorded as science/Scheies-syndrome[8].
- Scheie syndrome's Orphanet ID is recorded as 93474[9].
- Scheie syndrome's NCI Thesaurus ID is recorded as C61265[10].
- Scheie syndrome's genetic association is recorded as IDUA[11].
- Scheie syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060222[12].
- Scheie syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0060222[13].
- Scheie syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_93474[14].
- Scheie syndrome's ICD-10-CM is recorded as E76.0[15].
- Scheie syndrome's GARD rare disease ID is recorded as 12561[16].
- Scheie syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[17].
- Scheie syndrome's Mondo ID is recorded as MONDO_0011760[18].
- Scheie syndrome's Microsoft Academic ID is recorded as 2777254179[19].
- Scheie syndrome's UniProt disease ID is recorded as DI-00772[20].
Why It Matters
Scheie syndrome draws 44 Wikipedia views per month (rare_disease category, ranking #198 of 627).[2] It has Wikipedia articles in 8 language editions, a strong signal of global cultural recognition.[21] It is known by 10 alternative names across languages and contexts.[22]