ORPHA:231205
Common variable immunodeficiency without known genetic defect
Synonyms: CVID without known genetic defect
- Type
- Disease
- Group
- Disorder
- Status
- active
Orphadata ships no English definition for this code.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Common variable immunodeficiency without known genetic defect | CVID without known genetic defect |
| fr | Déficit immunitaire commun variable sans défaut génétique connu | CVID sans anomalie génétique connue · CVID sans défaut génétique connu · DICV sans défaut génétique connu · Immunodéficience commune variable sans défaut génétique connu |
| de | Immundefekt, allgemeiner variabler, ohne genetischen Defekt | CVID ohne bekannten genetischen Defekt |
| es | Inmunodeficiencia común variable sin anomalía genética conocida | IDCV sin anomalía genética conocida |
| it | Immunodeficienza variabile comune senza difetto genetico noto | |
| nl | Gewone variabele immuundeficiëntie zonder bekend genetisch defect | CVID zonder bekend genetisch defect |
| pt | Imunodeficiência variável comum sem anomalia genética conhecida | CVID sem anomalia genética conhecida |
| pl | Pospolity zmienny Niedobór odpornosci bez znanego bledu genetycznego | = en |
| cs | Běžná variabilní imunodeficience bez známé genetické vady | = en |
| uk | ЗАСТАРІЛО: Загальний варіабельний імунодефіцит без відомого генетичного дефекту | |
| zh | 弃用:普通可变性免疫缺陷不伴已知基因缺陷 | |
| tr | Eski adı: Bilinen genetik defekt olmayan yaygın değişken immün yetmezlik |
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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: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
0 recordsNo prevalence record in this release.
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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/231205
- This record as JSON: /data/d/231205.json