ORPHA:696851
Common variable immunodeficiency and related disorders
Synonyms: CVID and related disorders
- Type
- Category
- Group
- Group of disorders
- Age of onset
- Adolescent, Adult, Childhood
- Status
- active
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.
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Names in Orphadata languages
9 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Common variable immunodeficiency and related disorders | CVID and related disorders |
| fr | Déficit immunitaire commun variable et maladies associées | CVID et maladies associées · DICV et maladies associées · Immunodéficience commune variable et maladies associées |
| de | Variables Immundefektsyndrom und verwandte Störungen | CVID und verwandte Krankheiten |
| es | Inmunodeficiencia común variable y trastornos relacionados | IDCV y trastornos relacionados |
| it | Immunodeficienza comune variabile e malattie correlate | CVID e malattie correlate |
| nl | Gewone variabele immuundeficiëntie en gerelateerde aandoeningen | CVID en gerelateerde aandoeningen |
| pt | Common variable immunodeficiency and related disorders | |
| pl | Common variable immunodeficiency and related disorders | = en |
| cs | Common variable immunodeficiency and related disorders | = en |
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Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:101977Immunodeficiency due to predominantly antibodies defect
rare genetic diseases; rare immunological diseases
Children (4):
- ORPHA:696857Common variable immunodeficiency phenotype due to germinal digenic/polygenic mutations
- ORPHA:696870Common variable immunodeficiency phenotype due to germinal monogenic mutation
- ORPHA:696863Common variable immunodeficiency phenotype due to somatic mutations
- ORPHA:231205Common variable immunodeficiency without known genetic defect
Codes that Orphanet moved or referred to this one:
- ORPHA:1572OBSOLETE: Common variable immunodeficiency referred to · inactive
- ORPHA:77303OBSOLETE: Common variable immunodeficiency due to an intrinsic B cell defect referred to · inactive
- ORPHA:99831OBSOLETE: Common variable immunodeficiency due to an intrinsic T cell defect referred to · inactive
- ORPHA:183672OBSOLETE: Common variable immunodeficiency due to TNFR deficiency referred to · inactive
- ORPHA:700746OBSOLETE: Genetic common variable immunodeficiency phenotype and related disorders referred to · inactive
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
1 record| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | 1-9 / 100 000 | 2.5 / 100 000 | Worldwide | Value and class | Validated | ORPHANET |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
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HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/696851
- This record as JSON: /data/d/696851.json