OMOP Concept 4231189
Hereditary factor IX deficiency disease without inhibitor
StandardConditionSNOMED438792009Disorder
Maps from
1
Descendants
3
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 Hereditary factor IX deficiency disease without inhibitor via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 438792009 | Hereditary factor IX deficiency disease without inhibitor | Non-standard |
Synonyms
Alternative names recorded for Hereditary factor IX deficiency disease without inhibitor across source vocabularies.
- enfermedad por deficiencia hereditaria de factor IX sin inhibidores
- enfermedad por deficiencia hereditaria de factor IX sin inhibidores (trastorno)
- Haemophilia B without inhibitor
- hemofilia B sin inhibidores
- Hemophilia B without inhibitor
- Hereditary factor IX deficiency disease without inhibitor (disorder)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(17)Roll up to these when you need a wider cohort.
- 1Hereditary factor IX deficiency disease
- 2Congenital disease
- 2Factor IX deficiency
- 2Hemophilia
- 2X-linked hereditary disease
- 3Coagulation factor deficiency syndrome
- 3Disorder of fetus and/or newborn
- 3Sex-linked hereditary disorder
- 4Blood coagulation disorder
- 4Disease
- 4Hereditary disease
- 5Clinical finding
- 5Disorder of hemostatic system
- 5Genetic disease
- 5OMOP Bleeding 1
- 5OMOP Bleeding 2
- 6Functional finding
Narrower concepts
(3)Included automatically when you query with descendants.
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