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Common variable immunodeficiency phenotype due to CD19/CD81 deficiency
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ORPHA:696881
Classification level: Disorder
Synonym(s):
- CVID phenotype due to CD19/CD81 deficiency
- CD19 deficiency
- Common variable immunodeficiency phenotype due to cluster of differentiation 19/cluster or differentiation 81 deficiency
Prevalence: -
Inheritance: Autosomal recessive
Age of onset:
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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