OMOP Concept 4122942
Congenital factor IX deficiency with inhibitor
StandardConditionSNOMED234445000Disorder
Maps from
1
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Congenital factor IX deficiency with inhibitor via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 234445000 | Congenital factor IX deficiency with inhibitor | Non-standard |
Synonyms
Alternative names recorded for Congenital factor IX deficiency with inhibitor across source vocabularies.
- Congenital factor IX deficiency with inhibitor (disorder)
- deficiencia congénita del factor IX con inhibidor
- deficiencia congénita del factor IX con inhibidor (trastorno)
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
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