ORPHA:183672
OBSOLETE: Common variable immunodeficiency due to TNFR deficiency
inactive · referred to ORPHA:696851Common variable immunodeficiency and related disorders
Synonyms: OBSOLETE: CVID due to TNFR deficiency
- Type
- Etiological subtype
- Group
- Subtype of disorder
- Status
- inactive
- Flag
- Obsolete entity
This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Common variable immunodeficiency and related disorders
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Common variable immunodeficiency due to TNFR deficiency | OBSOLETE: CVID due to TNFR deficiency |
| fr | OBSOLETE : Déficit immunitaire commun variable dé au déficit en TNFR | OBSOLETE : CVID par déficit en TNFR |
| de | OBSOLET: Immundefekt, kombinierter schwerer, durch TNFR-Mangel | OBSOLET: CVID durch TNFR-Mangel |
| es | OBSOLETO: Inmunodeficiencia común variable por deficiencia de TNFR | OBSOLETO: IDCV por deficiencia de TNFR |
| it | OBSOLETO: Immunodeficienza variabile comune da deficit di TNFR | OBSOLETO: CVID da deficit di TNFR |
| nl | OBSOLEET: Algemene variabele immuundeficiëntie door TNFR-deficiëntie | OBSOLEET: CVID door TNFR-deficiëntie |
| pt | OBSOLETO: Hipogamaglobulinemia por deficiência de CD19 ou ICOS | |
| pl | NIEAKTUALNE: Pospolity zmienny Niedobór odpornosci z powodu deficytu TNFR | NIEAKTUALNE: CVID z powodu niedoboru TNFR |
| cs | NEAKTUÁLNÍ: Běžná variabilní imunodeficience způsobená deficitem TNFR | = en |
| uk | ЗАСТАРІЛО: Поширений варіабельний імунодефіцит внаслідок дефіциту TNFR | ЗАСТАРІЛО: CVID через дефіцит TNFR |
| zh | 弃用：常见的肿瘤坏死因子受体缺陷所致多种免疫缺陷 | TNFR基因缺陷所致CIND |
| tr | Eski adı: TNFR eksikliğine bağlı yaygın değişken immün yetmezlik | TNFR eksikliğine bağlı CVID |
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Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
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Classification
Not placed in any Orphanet classification in this release.
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/183672
- This record as JSON: /data/d/183672.json