OMOP Concept 4205583

Arthrochalasia Ehlers-Danlos syndrome

StandardConditionSNOMED55711009Disorder
Maps from
4
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept

4 source codes normalize to Arthrochalasia Ehlers-Danlos syndrome via the OMOP "Maps to" relationship.

Synonyms

Alternative names recorded for Arthrochalasia Ehlers-Danlos syndrome across source vocabularies.

  • Arthrochalasia Ehlers-Danlos syndrome (disorder)
  • Arthrochalasia multiplex congenita
  • Arthrochalasis multiplex congenita
  • artrocalasis múltiple congénita
  • deficiencia de procolágeno aminoproteasa
  • deficiencia de procolágeno peptidasa
  • deficiencia de procolágeno proteasa
  • Ehlers-Danlos syndrome type 7
  • síndrome de Ehlers-Danlos artrocalasia
  • síndrome de Ehlers-Danlos artrocalasia (trastorno)
  • síndrome de Ehlers - Danlos, autosómico recesivo tipo 7

Where it sits in the hierarchy

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

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