OMOP Concept 4209366

Severe hereditary factor IX deficiency disease with inhibitor

StandardConditionSNOMED440866009Disorder
Maps from
1
Descendants
2
Valid from
31 Jan 2009
Valid to
31 Dec 2099
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Source codes that map to this concept

1 source code normalizes to Severe hereditary factor IX deficiency disease with inhibitor via the OMOP "Maps to" relationship.

VocabularyCodeNameType
Nebraska Lexicon440866009Severe hereditary factor IX deficiency disease with inhibitorNon-standard

Synonyms

Alternative names recorded for Severe hereditary factor IX deficiency disease with inhibitor across source vocabularies.

  • enfermedad grave por deficiencia hereditaria de factor IX con inhibidores
  • enfermedad grave por deficiencia hereditaria de factor IX con inhibidores (trastorno)
  • hemofilia B grave con inhibidores
  • Severe haemophilia B with inhibitor
  • Severe hemophilia B with inhibitor
  • Severe hereditary factor IX deficiency disease with inhibitor (disorder)

Where it sits in the hierarchy

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

Broader concepts

(18)

Roll up to these when you need a wider cohort.

Narrower concepts

(2)

Included automatically when you query with descendants.

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