OMOP Concept 24612

Multiple endocrine neoplasia, type 2

StandardConditionSNOMED61808009Disorder
Maps from
3
Descendants
3
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept

3 source codes normalize to Multiple endocrine neoplasia, type 2 via the OMOP "Maps to" relationship.

Synonyms

Alternative names recorded for Multiple endocrine neoplasia, type 2 across source vocabularies.

  • adenomatosis endocrina múltiple, tipo 2
  • cromafinomatosis familiar
  • Familial chromaffinomatosis
  • MEA, type 2
  • MEN, type 2
  • Multiple endocrine adenomatosis, type 2
  • Multiple endocrine neoplasia, type 2 (disorder)
  • NEM, tipo 2
  • neoplasia endocrina múltiple, tipo 2
  • neoplasia endocrina múltiple, tipo 2 (trastorno)
  • PTC syndrome
  • síndrome de PTC
  • síndrome de Sipple
  • Sipple's syndrome
  • Sipple syndrome

Where it sits in the hierarchy

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

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