OMOP Concept 4159966

Upshaw-Schulman syndrome

StandardConditionSNOMED373420004Disorder
Maps from
6
Descendants
0
Valid from
31 Jul 2002
Valid to
31 Dec 2099
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Source codes that map to this concept

6 source codes normalize to Upshaw-Schulman syndrome via the OMOP "Maps to" relationship.

Synonyms

Alternative names recorded for Upshaw-Schulman syndrome across source vocabularies.

  • Congenital ADAMTS-13 deficiency
  • deficiencia congénita de ADAMTS-13
  • Familial thrombotic thrombocytopenic purpura / haemolytic uraemic syndrome
  • Familial thrombotic thrombocytopenic purpura / hemolytic uremic syndrome
  • Familial TTP/HUS
  • púrpura trombocitopénica trombótica familiar/síndrome urémico hemolítico
  • síndrome de Upshaw-Schulman
  • síndrome de Upshaw-Schulman (trastorno)
  • TTP/HUS hereditaria
  • Upshaw-Schulman syndrome (disorder)

Where it sits in the hierarchy

Ordered by distance - 1 is a direct parent or child.

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