OMOP Concept 436678
Hereditary factor IX deficiency disease
StandardConditionSNOMED41788008Disorder
Maps from
16
Descendants
21
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
16 source codes normalize to Hereditary factor IX deficiency disease via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 138910 | Hereditary factor IX deficiency disease | Non-standard |
| CIM10 | D67 | Hereditary factor IX deficiency | Non-standard |
| ICD10 | D67 | Hereditary factor IX deficiency | Non-standard |
| ICD10CM | D67 | Hereditary factor IX deficiency | Non-standard |
| ICD10CN | D67 | Hereditary factor IX deficiency | Non-standard |
| ICD10CN | D67.x00 | Hereditary factor IX deficiency | Non-standard |
| ICD10CN | D67.x01 | Hemophilia B type (machine translation) | Non-standard |
| ICD10GM | D67 | Hereditary factor IX deficiency | Non-standard |
| ICD9CM | 286.1 | Congenital factor IX disorder | Non-standard |
| KCD7 | D67 | Hereditary factor Ⅸ deficiency | Non-standard |
| MeSH | D002836 | Hemophilia B | Non-standard |
| Nebraska Lexicon | 41788008 | Factor IX deficiency | Non-standard |
| OXMIS | 2861 | FACTOR IX DEFICIENCY | Non-standard |
| Read | D301.00 | Haemophilia-B (factor IX deficiency) | Non-standard |
| Read | D301.11 | Christmas disease | Non-standard |
| Read | D301.12 | Haemophilia B | Non-standard |
Synonyms
Alternative names recorded for Hereditary factor IX deficiency disease across source vocabularies.
- Christmas disease
- Congenital factor IX deficiency
- deficiencia congénita de factor IX
- enfermedad de Christmas
- enfermedad por deficiencia hereditaria de factor IX
- enfermedad por deficiencia hereditaria de factor IX ligada al sexo
- enfermedad por deficiencia hereditaria de factor IX (trastorno)
- Haemophilia B
- hemofilia B
- Hemophilia B
- Hereditary factor IX deficiency disease (disorder)
- PTC deficiency disease
- Sex-linked factor IX deficiency disease
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(16)Roll up to these when you need a wider cohort.
- 1Congenital disease
- 1Factor IX deficiency
- 1Hemophilia
- 1X-linked hereditary disease
- 2Coagulation factor deficiency syndrome
- 2Disorder of fetus and/or newborn
- 2Sex-linked hereditary disorder
- 3Blood coagulation disorder
- 3Disease
- 3Hereditary disease
- 4Clinical finding
- 4Disorder of hemostatic system
- 4Genetic disease
- 4OMOP Bleeding 1
- 4OMOP Bleeding 2
- 5Functional finding
Narrower concepts
(21)Included automatically when you query with descendants.
- 1Congenital factor IX deficiency variant
- 1Congenital factor IX deficiency with inhibitor
- 1Congenital factor IX deficiency without inhibitor
- 1Hemophilia B Leyden
- 1Hereditary factor IX deficiency disease with inhibitor
- 1Hereditary factor IX deficiency disease without inhibitor
- 1Mild hereditary factor IX deficiency disease
- 1Moderate hereditary factor IX deficiency disease
- 1Severe hereditary factor IX deficiency disease
- 2Mild hereditary factor IX deficiency disease with inhibitor
- 2Mild hereditary factor IX deficiency disease without inhibitor
- 2Moderate hereditary factor IX deficiency disease with inhibitor
- 2Moderate hereditary factor IX deficiency disease without inhibitor
- 2Severe hereditary factor IX deficiency disease with inhibitor
- 2Severe hereditary factor IX deficiency disease without inhibitor
- 3Mild hereditary factor IX deficiency disease with high response inhibitor
- 3Mild hereditary factor IX deficiency disease with low response inhibitor
- 3Moderate hereditary factor IX deficiency disease with high response inhibitor
- 3Moderate hereditary factor IX deficiency disease with low response inhibitor
- 3Severe hereditary factor IX deficiency disease with high response inhibitor
- 3Severe hereditary factor IX deficiency disease with low response inhibitor
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