ORPHA:720301
T-B-NK+ severe combined immunodeficiency
Synonyms: T-B-NK+ SCID
- 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.
1
Names in Orphadata languages
9 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | T-B-NK+ severe combined immunodeficiency | T-B-NK+ SCID |
| fr | Déficit immunitaire combiné sévère T-B-NK+ | DICS T-B-NK+ · Immunodéficience combinée sévère T-B-NK+ · SCID T-B-NK+ |
| de | Immundefekt, kombinierter schwerer, T-B-NK+ | = en |
| es | Inmunodeficiencia combinada grave T-B-NK+ | IDCG T-B-NK+ · SCID T-B-NK+ |
| it | Immunodeficienza combinata grave T-B-NK+ | SCID T-B-NK+ |
| nl | T-B-NK+ ernstige gecombineerde immuundeficiëntie | T-B-NK+ SCID · T-cel negatieve B-cel negatieve NK-cel positieve ernstige gecombineerde immuundeficiëntie |
| pt | T-B-NK+ severe combined immunodeficiency | |
| pl | T-B-NK+ severe combined immunodeficiency | = en |
| cs | T-B-NK+ severe combined immunodeficiency | = en |
2
Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:317419T-B- severe combined immunodeficiency
rare genetic diseases; rare immunological diseases; rare transplant-related disorders
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
6
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/720301
- This record as JSON: /data/d/720301.json