ORPHA:169443
Specific antibody deficiency with normal immunoglobulin concentrations and normal numbers of B cells
- 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.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Specific antibody deficiency with normal immunoglobulin concentrations and normal numbers of B cells | |
| fr | Déficit en anticorps spécifiques avec une quantité normale d'immunoglobuline et de cellules B | |
| de | Antikörpermangel mit normalen Immunglobulinen und B-Zellen | |
| es | Deficiencia específica de anticuerpos con concentraciones normales de inmunoglobulina y valores normales de células B | |
| it | Deficit di anticorpi specifici associato a concentrazioni normali di immunoglobuline e normale numero di linfociti B | |
| nl | Specifieke antilichaamdeficiëntie met normale immunoglobulineconcentraties en normale aantallen van B-cellen | |
| pt | Deficiência de anticorpos específicos com concentrações normais de imunoglobina e contagem normal de células B | |
| pl | Niedobór specyficznych przeciwciał z prawidłowym stężeniem immunoglobulin i prawidłową liczbą komórek B | |
| cs | Specifický deficit protilátek s normálními koncentracemi imunoglobulinů a normálním počtem B lymfocytů | |
| uk | Специфічний дефіцит антитіл з нормальною концентрацією імуноглобулінів і нормальною кількістю В-клітин | |
| zh | 特异性抗体缺乏伴正常免疫球蛋白浓度及B细胞数量 | |
| tr | Normal immünoglobulin konsantrasyonları ve normal sayıda B hücresi ile seyreden spesifik antikor eksikliği |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-11 | 4A01.02 | E | specific | validated |
| MONDO | 15711 | E | validated | |
| UMLS | C5680449 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:101977Immunodeficiency due to predominantly antibodies defect
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/169443
- This record as JSON: /data/d/169443.json