scott syndrome

Preferred Label : scott syndrome;

MeSH synonym : bleeding abnormality due to deficiency of platelet binding of factor X; prothrombin conversion defect, familial; prothrombin consumption deficiency; prothrombin consumption inhibitor, familial;

Details

Origin ID

C563120;

UMLS CUI

C0796149;

Currated CISMeF NLP mapping
- Scott syndrome [PASCAL descriptor]
- Scott syndrome [DO Concept]
- Scott syndrome [ICD-11 More detail]
- Scott syndrome [OMIM Phenotype]
- Scott syndrome [ORDO Disease]
- Scott syndrome (disorder) [SNOMED CT concept]
DO Cross reference
- Scott syndrome [DO Concept]
MeSH term(s) associated for indexing
- blood coagulation disorders [MeSH Descriptor]
Record concept(s)
- scott syndrome [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Scott syndrome [ORDO Disease]
- Scott syndrome [OMIM Phenotype]
- Scott syndrome [DO Concept]
- Scott syndrome [PASCAL descriptor]
- Scott syndrome (disorder) [SNOMED CT concept]

Keyword's position in hierarchy(ies) :

Main resources

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