OMOP Concept 4093515

Mild hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin

StandardConditionSNOMED24975009Disorder
Maps from
2
Descendants
0
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 Mild hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin via the OMOP "Maps to" relationship.

Synonyms

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

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

Where it sits in the hierarchy

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

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