ORPHA:331244
OBSOLETE: Other immunodeficiency syndrome with predominantly antibody defects
inactive · referred to ORPHA:101977Immunodeficiency due to predominantly antibodies defect
- Type
- Category
- Group
- Group of disorders
- Status
- inactive
- Flag
- Obsolete entity
This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>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.<br/><br/>Instead, consider using Immunodeficiency predominantly affecting antibody production
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Other immunodeficiency syndrome with predominantly antibody defects | |
| fr | OBSOLETE : Autre syndrome de déficit immunitaire par déficit de production d'anticorps | OBSOLETE : Autre syndrome d'immunodéficience par déficit de production d'anticorps |
| de | OBSOLET: Sonstiges Immundefekt-Syndrom mit vorwiegendem Antikörper-Defekt | |
| es | OBSOLETO: Otros síndromes de inmunodeficiencia con defectos predominantes de anticuerpos | |
| it | OBSOLETO: Altra sindrome da immunodeficienza con difetti predominanti degli anticorpi | |
| nl | OBSOLEET: Ander immuundeficiëntiesyndroom met predominante antilichaamdefecten | |
| pt | OBSOLETO: Outra síndrome de imunodeficiência com predominância defeitos de anticorpos | |
| pl | NIEAKTUALNE: Inny zespół z niedoborem odporności z dominującymi defektami przeciwciał | |
| cs | NEAKTUÁLNÍ: Jiný syndrom imunodeficience s převažující poruchou protilátek | |
| uk | Інші синдроми імунодефіциту з переважним дефіцитом антитіл | |
| zh | 以抗体缺陷为主的其他免疫缺陷综合征 | |
| tr | Ağırlıklı antikor defekti ile seyreden diğer immün yetmezlik sendromu |
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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/331244
- This record as JSON: /data/d/331244.json