OMOP Concept 1449373
Autosomal recessive combined variable immunodeficiency due to BAFF receptor deficiency
StandardConditionSNOMED1352023006Disorder
Maps from
0
Descendants
0
Valid from
1 Dec 2024
Valid to
31 Dec 2099
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Synonyms
Alternative names recorded for Autosomal recessive combined variable immunodeficiency due to BAFF receptor deficiency across source vocabularies.
- Autosomal recessive combined variable immunodeficiency due to BAFF-R deficiency
- Autosomal recessive combined variable immunodeficiency due to BAFF-R mutation
- Autosomal recessive combined variable immunodeficiency due to B cell-activating factor receptor mutation
- Autosomal recessive combined variable immunodeficiency due to B cell-activating factor receptor mutation (disorder)
- Autosomal recessive CVID (combined variable immunodeficiency) due to TNFRSF13C mutation
- inmunodeficiencia combinada variable autosómica recesiva debida a deficiencia del receptor de BAFF
- inmunodeficiencia combinada variable autosómica recesiva debida a mutación del receptor del factor activador de linfocitos B
- inmunodeficiencia combinada variable autosómica recesiva debida a mutación del receptor del factor activador de linfocitos B (trastorno)
- inmunodeficiencia combinada variable autosómica recesiva debida a mutación de TNFRSF13C
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 recessive hereditary disorder
- 1Common variable immunodeficiency
- 1Hereditary disorder of immune system
- 2Autosomal hereditary disorder
- 2Disorder of immune function
- 2Disorder of immune structure
- 2Hereditary disorder by system
- 2Primary immune deficiency disorder
- 3Disease
- 3Disorder of body system
- 3Hereditary disease
- 3Immunodeficiency disorder
- 4Clinical finding
- 4Genetic disease
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