Orphanet: Scott syndrome
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Scott syndrome

Disease definition

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

ORPHA:806

Classification level: Disorder
  • Synonym(s): -
  • Prevalence: <1 / 1 000 000
  • Inheritance: Autosomal recessive 
  • Age of onset: All ages
  • ICD-10: D69.8
  • OMIM: 262890
  • UMLS: C0796149
  • MeSH: -
  • GARD: 4777
  • MedDRA: -

  A summary on this disease is available in Italiano (2005) Deutsch (2014) Español (2014) Français (2014) Nederlands (2014)

Additional information

Further information on this disease

Patient-centred resources for this disease

Research activities on this disease

Specialised Social Services

The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.