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
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