OMOP Concept 36714526

Chromosome Xp11.3 microdeletion syndrome

StandardConditionSNOMED719808002Disorder
Maps from
2
Descendants
0
Valid from
31 Jan 2017
Valid to
31 Dec 2099
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Source codes that map to this concept

2 source codes normalize to Chromosome Xp11.3 microdeletion syndrome via the OMOP "Maps to" relationship.

VocabularyCodeNameType
MeSHC537046Aldred syndromeNon-standard
Nebraska Lexicon719808002Chromosome Xp11.3 microdeletion syndromeNon-standard

Synonyms

Alternative names recorded for Chromosome Xp11.3 microdeletion syndrome across source vocabularies.

  • Aldred syndrome
  • Chromosome Xp11.3 microdeletion syndrome (disorder)
  • síndrome de Aldred
  • síndrome de microdeleción de cromosoma Xp11.3
  • síndrome de microdeleción de cromosoma Xp11.3 (trastorno)

Where it sits in the hierarchy

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

Broader concepts

(50)

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