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Childhood-onset common variable immunodeficiency due to ARHGEF1 deficiency
ORPHA:696942
Classification level: Disorder
- Childhood-onset CVID phenotype due to ARHGEF1 deficiency
- Childhood-onset common variable immunodeficiency phenotype due to Rho guanine nucleotide exchange factor 1 deficiency
Prevalence: -
Inheritance: Autosomal recessive
Age of onset:
OMIM: 618459
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.
: produced/endorsed by ERN(s)
: produced/endorsed by FSMR(s)
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- Research project(s) (45)
- Clinical trial(s) (1)
- Biobank(s) (10)
- Registry(ies) (30)
- Network of experts (7)
Newborn screening