The new version of OLS (OLS4) will be unavailable for the next few days while we resolve deployment issues.

You can continue to browse this version of OLS, but some ontologies may be out of date.


Scott syndrome is an extremely rare congenital hemorrhagic disorder characterized by hemorrhagic episodes due to impaired platelet coagulant activity. [ Orphanet : 806 ]

This is just here as a test because I lose it

Term information

database cross reference
  • Orphanet:806 (OMIM:262890)
  • UMLS:C0796149 (Orphanet:806/e)
  • SCTID:128098009 (MONDO:equivalentTo)
  • DOID:0111052 (MONDO:equivalentTo)
  • GARD:0004777 (MONDO:equivalentTo)
  • OMIM:262890 (Orphanet:806/e)
  • MESH:C563120 (MONDO:equivalentTo)
Subsets

gard_rare, ordo_disease

abbreviation
SCTS [ DOID : 0111052 MONDO : Lexical https://omim.org/entry/262890 ]
abbreviation
BDPLT7 [ DOID : 0111052 ]
definition
  • Scott syndrome is an extremely rare congenital hemorrhagic disorder characterized by hemorrhagic episodes due to impaired platelet coagulant activity.
exactMatch
  • https://omim.org/entry/262890
  • http://linkedlifedata.com/resource/umls/id/C0796149
  • http://www.orpha.net/ORDO/Orphanet_806
  • http://identifiers.org/mesh/C563120
  • http://identifiers.org/snomedct/128098009
  • http://purl.obolibrary.org/obo/DOID_0111052
has exact synonym
  • BDPLT7
  • SCTS
  • bleeding abnormality due to deficiency of platelet biding of factor X
  • familial prothrombin consumption inhibitor
  • prothrombin consumption deficiency
  • platelet-type bleeding disorder 7
  • familial prothrombin conversion defect
  • Scott syndrome
has related synonym
  • prothrombin conversion defect, familial
  • bleeding disorder, Platelet-type, 7
  • bleeding Abnormality due to deficiency of Platelet binding of Factor 10
  • prothrombin consumption inhibitor, familial
  • Platelet factor X receptor deficiency
id
  • MONDO:0009885
seeAlso
  • https://rarediseases.info.nih.gov/diseases/4777/scott-syndrome