ORPHA:695164
Combined immunodeficiency with low B cells and hypogammaglobulinemia
Synonyms: CID with low B cells and hypogammaglobulinemia
- Type
- Category
- Group
- Group of disorders
- Status
- active
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.
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Names in Orphadata languages
9 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Combined immunodeficiency with low B cells and hypogammaglobulinemia | CID with low B cells and hypogammaglobulinemia |
| fr | Déficit immunitaire combiné avec faible nombre de cellules B et hypogammaglobulinémie | CID avec faible nombre de cellules B et hypogammaglobulinémie · DIC avec faible nombre de cellules B et hypogammaglobulinémie · Immunodéficience combinée avec faible nombre de cellules B et hypogammaglobulinémie |
| de | Kombinierter Immundefekt mit verminderter Anzahl an B-Zellen und Hypogammaglobulinämie | CID mit reduzierten B-Zell-Zahlen und Hypogammaglobulinämie |
| es | Inmunodeficiencia combinada con niveles bajos de linfocitos B e hipogammaglobulinemia | CID con niveles bajos de linfocitos B e hipogammaglobulinemia · IDC con niveles bajos de linfocitos B e hipogammaglobulinemia |
| it | Immunodeficienza combinata grave con livelli bassi di cellule B e ipogammaglobulinemia | CID con livelli bassi di cellule B e ipogammaglobulinemia · CID con numero ridotto di linfociti B |
| nl | Gecombineerde immuundeficiëntie met laag aantal B-cellen en hypogammaglobulinemie | CID met laag aantal B-cellen en hypogammaglobulinemie |
| pt | Combined immunodeficiency with low B cells | |
| pl | Combined immunodeficiency with low B cells and hypogammaglobulinemia | = en |
| cs | Combined immunodeficiency with low B cells and hypogammaglobulinemia | = en |
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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:480549Non-severe combined immunodeficiency
rare genetic diseases; rare immunological diseases; rare transplant-related disorders
Children (9):
- ORPHA:217390Combined immunodeficiency due to DOCK8 deficiency
- ORPHA:700205Combined immunodeficiency due to IKBKB gain-of-function mutation
- ORPHA:504530Combined immunodeficiency due to Moesin deficiency
- ORPHA:314689Combined immunodeficiency due to STK4 deficiency
- ORPHA:695172Combined immunodeficiency due to dimerization defective IKAROS mutation
- ORPHA:726442Combined immunodeficiency with hypo/agammaglobulinemia and opportunistic infections
- ORPHA:477661IL21-related infantile inflammatory bowel disease
- ORPHA:447731NIK deficiency
- ORPHA:39041Omenn syndrome
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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/695164
- This record as JSON: /data/d/695164.json