OMOP Concept 4168441

Hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin

StandardConditionSNOMED47516005Disorder
Maps from
2
Descendants
2
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept

2 source codes normalize to Hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin via the OMOP "Maps to" relationship.

Synonyms

Alternative names recorded for Hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin across source vocabularies.

  • esferocitosis hereditaria por deficiencia combinada de espectrina Y anquirina
  • esferocitosis hereditaria por deficiencia combinada de espectrina Y anquirina (trastorno)
  • Hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin (disorder)

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

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