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Common variable immunodeficiency phenotype due to germinal monogenic mutation

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ORPHA:696870

Classification level: Group of disorders

Synonym(s):
  • Monogenic CVID phenotype
  • Monogenic common variable immunodeficiency phenotype
  • CVID phenotype due to germinal monogenic mutation

Source: PubMed ID 36198931 30776527 36796510

Prevalence: -

Inheritance: -

Age of onset:

Summary

This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.

Detailed information

Logo ERN: produced/endorsed by ERN(s) Logo FSMR: produced/endorsed by FSMR(s)

Guidelines
Emergency guidelines
Français (2020.pdf) - Orphanet Urgences
Additional information

Further information on this disease

Patient-centred resources for this disease

Research activities on this disease

Newborn screening

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