ORPHA:696863
Common variable immunodeficiency phenotype due to somatic mutations
Synonyms: CVID phenotype due to somatic mutations
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- Adolescent, Adult, Childhood
- Status
- active
Orphadata ships no English definition for this code.
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Names in Orphadata languages
9 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Common variable immunodeficiency phenotype due to somatic mutations | CVID phenotype due to somatic mutations |
| fr | Phénotype de déficit immunitaire commun variable associé à des mutations somatiques | Phénotype d'immunodéficience commune variable associé à des mutations somatiques · Phénotype de CVID associé à des mutations somatiques · Phénotype de DICV associé à des mutations somatiques |
| de | Variables Immundefekt-Syndrom durch somatische Mutationen | CVID durch somatische Mutationen |
| es | Fenotipo de inmunodeficiencia común variable por mutaciones somáticas | Fenotipo de IDCV por mutaciones somáticas |
| it | Fenotipo dellimmunodeficienza comune variabile da mutazioni somatiche | Fenotipo della CVID da mutazioni somatiche |
| nl | Fenotype van gewone variabele immuundeficiëntie door somatische mutaties | CVID-fenotype door somatische mutaties |
| pt | Common variable immune deficiency phenotype due to somatic mutations | |
| pl | Common variable immunodeficiency phenotype due to somatic mutations | = en |
| cs | Common variable immunodeficiency phenotype due to somatic mutations | = en |
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Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:696851Common variable immunodeficiency and related disorders
rare genetic diseases; rare immunological diseases
No children.
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
1 record| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | Unknown | — | Worldwide | Class only | 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/696863
- This record as JSON: /data/d/696863.json