OMOP Concept 37111662

Splenogonadal fusion, limb defect, micrognathia syndrome

StandardConditionSNOMED726724005Disorder
Maps from
1
Descendants
0
Valid from
31 Jul 2017
Valid to
31 Dec 2099
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Source codes that map to this concept

1 source code normalizes to Splenogonadal fusion, limb defect, micrognathia syndrome via the OMOP "Maps to" relationship.

VocabularyCodeNameType
MeSHC537318Splenogonadal fusion limb defects micrognatiaNon-standard

Synonyms

Alternative names recorded for Splenogonadal fusion, limb defect, micrognathia syndrome across source vocabularies.

  • SGFLD (splenogonadal fusion limb defect syndrome) syndrome
  • síndrome de fusión esplenogonadal, defecto de los miembros y micrognatia
  • síndrome de fusión esplenogonadal, defecto de los miembros y micrognatia (trastorno)
  • Splenogonadal fusion, limb defect, micrognathia syndrome (disorder)
  • Splenogonadal fusion limb defect syndrome

Where it sits in the hierarchy

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

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