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Common variable immunodeficiency phenotype due to germinal digenic/polygenic mutations
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ORPHA:696857
Summary
An Orphanet summary for this disease is currently under development. However, other data related to the disease are accessible from the Additional Information menu located at the bottom of this page.
Detailed information
: produced/endorsed by ERN(s)
: produced/endorsed by FSMR(s)
Guidelines
Emergency guidelines
Additional information
Further information on this disease
Patient-centred resources for this disease
Research activities on this disease
- Research project(s) (45)
- Clinical trial(s) (1)
- Biobank(s) (10)
- Registry(ies) (30)
- Network of experts (7)
Newborn screening
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