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Start free with EleplanCommon variable immunodeficiency phenotype due to CD21 deficiency
ORPHA:696894Disease
Also called CVID phenotype due to CD21 deficiency · Common variable immunodeficiency phenotype due to cluster of differentiation 21 deficiency
What it is
Orphanet has not published a description for this disease yet. The identifiers, classification and cross-references below are still current.
Key facts
- Inheritance
- Autosomal recessive
- Classified as
- Disease
Gene
Cross-references
Orphadata Science: Free access data from Orphanet. © INSERM 1999. Data version 2026-06-23. Available under CC BY 4.0. This is a reference, not medical advice.
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