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Scott Syndrome (MONDO:0009885)

Scott syndrome is an extremely rare congenital hemorrhagic disorder characterized by hemorrhagic episodes due to impaired platelet coagulant activity.

Overview

Category

hematologic disorder

Ontology ID

MONDO:0009885

Internal:11088

Synonyms

BDPLT7

SCTS

Scott syndrome

prothrombin consumption deficiency

Platelet factor X receptor deficiency

bleeding Abnormality due to deficiency of Platelet binding of Factor 10

bleeding disorder, Platelet-type, 7

prothrombin consumption inhibitor, familial

prothrombin conversion defect, familial

Mapped terms

DOID:0111052

GARD:0004777

MEDGEN:167107

MESH:C563120

NANDO:2200671

OMIM:262890

Orphanet:806

SCTID:128098009

UMLS:C0796149

icd11.foundation:186013982

Child terms

Unknown children.

Results

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