ORPHA:718079
Combined immunodeficiency with normal B cells and normal immunoglubulins
Synonyms: CID with normal B cells and normal Ig
- Type
- Clinical group
- 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 normal B cells and normal immunoglubulins | CID with normal B cells and normal Ig |
| fr | Déficit immunitaire combiné avec cellules B et immunoglobulines normales | CID avec cellules B normales et immunoglobulines normales · DIC avec cellules B normales et immunoglobulines normales · Immunodéficience combinée avec cellules B normales et immunoglobulines normales |
| de | Kombinierter Immundefekt mit normalen B-Zell-Zahlen und normalen Immunglobulin-Werten | CID mit normalen B-Zellen und normalen IG-Werten |
| es | Inmunodeficiencia combinada con niveles normales de células B e inmunoglobulinas | CID con niveles normales de células B e inmunoglobulinas · IDC con niveles normales de células B e inmunoglobulinas |
| it | Immunodeficienza combinata con livelli normali di cellule B e immunoglobuline | CID con livelli normali di cellule B e Ig |
| nl | Gecombineerde immuundeficiëntie met normale B-cellen en normale immunoglobulinen | CID met normale B-cellen en normale Ig |
| pt | Combined immunodeficiency with normal B cells and normal immunoglubulins | |
| pl | Combined immunodeficiency with normal B cells and normal immunoglubulins | = en |
| cs | Combined immunodeficiency with normal B cells and normal immunoglubulins | = en |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | D81.8 | NTBT | attributed | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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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 (5):
- ORPHA:169082Combined immunodeficiency due to CD3gamma deficiency
- ORPHA:647804Combined immunodeficiency due to FCHO1 deficiency
- ORPHA:431149Combined immunodeficiency due to OX40 deficiency
- ORPHA:324294T-cell immunodeficiency with epidermodysplasia verruciformis
- ORPHA:397959TCR-alpha-beta-positive T-cell deficiency
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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/718079
- This record as JSON: /data/d/718079.json