ORPHA:700746
OBSOLETE: Genetic common variable immunodeficiency phenotype and related disorders
inactive · referred to ORPHA:696851Common variable immunodeficiency and related disorders
Synonyms: OBSOLETE: Genetic CVID phenotype and related disorders
- 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 Common variable immunodeficiency and related disorders
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Names in Orphadata languages
9 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Genetic common variable immunodeficiency phenotype and related disorders | OBSOLETE: Genetic CVID phenotype and related disorders |
| fr | OBSOLETE : Phénotype de déficit immunitaire commun variable génétique et maladies associées | OBSOLETE : Phénotype d'immunodéficience commune variable génétique et maladies associées · OBSOLETE : Phénotype de CVID génétique et maladies associées · OBSOLETE : Phénotype de DICV génétique et maladies associées |
| de | OBSOLET: Genetisch bedingtes variables Immunfdefektsyndrom und verwandte Störungen | |
| es | OBSOLETO: Fenotipo genético de inmunodeficiencia común variable y trastornos relacionados | OBSOLETO: Fenotipo genético de IDCV y trastornos relacionados |
| it | OBSOLETO: Fenotipo dell'immunodeficienza comune variabile genetica e malattie correlate | OBSOLETO: Fenotipo della CVID genetica e malattie correlate |
| nl | OBSOLEET: Fenotype van genetische gewone variabele immuundeficiëntie en gerelateerde aandoeningen | OBSOLEET: CVID-fenotype en gerelateerde aandoeningen |
| pt | OBSOLETO: Genetic common variable immunodeficiency phenotype and related disorders | |
| pl | OBSOLETE: Genetic common variable immunodeficiency phenotype and related disorders | = en |
| cs | OBSOLETE: Genetic common variable immunodeficiency phenotype and related disorders | = en |
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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/700746
- This record as JSON: /data/d/700746.json