OMOP Concept 4279923
X-linked agammaglobulinemia
StandardConditionSNOMED65880007Disorder
Maps from
6
Descendants
0
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
6 source codes normalize to X-linked agammaglobulinemia via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| CIEL | 122786 | X-linked agammaglobulinemia | Non-standard |
| MeSH | C537409 | Bruton type agammaglobulinemia | Non-standard |
| MeSH | C562478 | Hypogammaglobulinemia, X-Linked | Non-standard |
| Read | C390511 | Bruton's agammaglobulinaemia | Non-standard |
| Read | C390512 | Congenital X-linked agammaglobulinaemia | Non-standard |
| Read | C390513 | Congenital sex-linked agammaglobulinaemia | Non-standard |
Synonyms
Alternative names recorded for X-linked agammaglobulinemia across source vocabularies.
- agammaglobulinemia de Bruton
- agammaglobulinemia ligada a cromosoma X
- agammaglobulinemia ligada a cromosoma X (trastorno)
- Bruton's agammaglobulinaemia
- Bruton's agammaglobulinemia
- Bruton's hypogammaglobulinaemia
- Bruton's hypogammaglobulinemia
- Bruton's type agammaglobulinaemia
- Bruton's type agammaglobulinemia
- Bruton tyrosine kinase deficiency
- BTK-deficiency
- deficiencia de BTK
- XLA - X-linked agammaglobulinaemia
- XLA - X-linked agammaglobulinemia
- X linked agammaglobulinaemia
- X-linked agammaglobulinaemia
- X linked agammaglobulinemia
- X-linked agammaglobulinemia (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.
- 1Disorder of immune structure
- 1Hereditary disorder of immune system
- 1Isolated agammaglobulinemia
- 1X-linked hereditary disease
- 2Congenital agammaglobulinemia
- 2Disorder of body system
- 2Disorder of immune function
- 2Hereditary disease
- 2Hereditary disorder by system
- 2Primary immune deficiency disorder
- 2Sex-linked hereditary disorder
- 3Congenital immunodeficiency disease
- 3Disease
- 3Genetic disease
- 3Immunodeficiency disorder
- 4Clinical finding
- 4Congenital disease
- 5Fetal and/or neonatal disorder
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