Scott syndrome

Summary

Scott syndrome is a rare disease^[1]. It draws 2 Wikipedia views per month (rare_disease category, ranking #236 of 627).^[2]

Key Facts

• Scott syndrome's instance of is recorded as rare disease^[3].
• Scott syndrome's instance of is recorded as class of disease^[4].
• Scott syndrome's subclass of is recorded as blood coagulation disease^[5].
• Scott syndrome's subclass of is recorded as inherited blood coagulation disease^[6].
• Scott syndrome's subclass of is recorded as rare hemorrhagic disorder due to a qualitative platelet defect^[7].
• Scott syndrome's MeSH descriptor ID is recorded as C563120^[8].
• Scott syndrome's OMIM ID is recorded as 262890^[9].
• Scott syndrome's DiseasesDB is recorded as 32153^[10].
• Scott syndrome's KEGG ID is recorded as H01162^[11].
• Scott syndrome's Disease Ontology ID is recorded as DOID:0111052^[12].
• Scott syndrome's Orphanet ID is recorded as 806^[13].
• Scott syndrome's genetic association is recorded as ANO6^[14].
• Scott syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111052^[15].
• Scott syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0111052^[16].
• Scott syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_806^[17].
• Scott syndrome's UMLS CUI is recorded as C0796149^[18].
• Scott syndrome's ICD-10-CM is recorded as D69.8^[19].
• Scott syndrome's GARD rare disease ID is recorded as 4777^[20].
• Scott syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine^[21].
• Scott syndrome's Mondo ID is recorded as MONDO_0009885^[22].
• Scott syndrome's Microsoft Academic ID is recorded as 2779651361^[23].
• Scott syndrome's ICD-11 ID is recorded as 186013982^[24].
• Scott syndrome's UniProt disease ID is recorded as DI-03017^[25].

Why It Matters

Scott syndrome draws 2 Wikipedia views per month (rare_disease category, ranking #236 of 627).^[2]