OMOP Concept 1449258
Autosomal dominant agammaglobulinemia due to E47 transcription factor deficiency
StandardConditionSNOMED1351668001Disorder
Maps from
0
Descendants
0
Valid from
1 Nov 2024
Valid to
31 Dec 2099
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Synonyms
Alternative names recorded for Autosomal dominant agammaglobulinemia due to E47 transcription factor deficiency across source vocabularies.
- agammaglobulinemia autosómica dominante debida a deficiencia de factor de transcripción E47
- agammaglobulinemia autosómica dominante debida a deficiencia de factor de transcripción E47 (trastorno)
- agammaglobulinemia autosómica dominante debida a mutación TCF3
- Autosomal dominant agammaglobulinaemia due to E47 transcription factor deficiency
- Autosomal dominant agammaglobulinaemia due to TCF3 mutation
- Autosomal dominant agammaglobulinemia due to E47 transcription factor deficiency (disorder)
- Autosomal dominant agammaglobulinemia due to TCF3 mutation
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(14)Roll up to these when you need a wider cohort.
- 1Autosomal dominant hereditary disorder
- 1Isolated agammaglobulinemia
- 2Autosomal hereditary disorder
- 2Congenital agammaglobulinemia
- 2Hereditary disease
- 2Primary immune deficiency disorder
- 3Congenital immunodeficiency disease
- 3Genetic disease
- 3Immunodeficiency disorder
- 4Congenital disease
- 4Disease
- 4Disorder of immune function
- 5Clinical finding
- 5Fetal and/or neonatal disorder
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