ORPHA:101972
Combined T and B cell immunodeficiency
- 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
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Combined T and B cell immunodeficiency | |
| fr | Déficit immunitaire combiné T et B | Immunodéficience combinée T et B |
| de | T- und B-Zell-Immundefekt, kombinierter | |
| es | Inmunodeficiencia combinada de células B y T | |
| it | Immunodeficienza combinata da cellule T e B | |
| nl | Gecombineerde T- en B-cel-immuundeficiëntie | |
| pt | Imunodeficiência combinada de células B e T | |
| pl | Złożony Niedobór odporności komórek T i B | |
| cs | Kombinovaná T a B buněčná imunodeficience | |
| uk | Комбінований Т- і В-клітинний імунодефіцит | |
| zh | T细胞和B细胞联合免疫缺陷 | |
| tr | Kombine T ve B hücre immün yetmezliği |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | D81 | E | specific | validated |
| ICD-11 | 4A01.1 | E | specific | validated |
| MONDO | 15131 | E | validated | |
| UMLS | C5681793 | E | 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:179006Primary immunodeficiency due to a defect in adaptive immunity
rare genetic diseases; rare immunological diseases
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.
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Sources for this card
- Orphanet page: orpha.net/en/disease/detail/101972
- This record as JSON: /data/d/101972.json