ORPHA:431156
Primary immunodeficiency with predisposition to severe viral infection
- 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 | Primary immunodeficiency with predisposition to severe viral infection | |
| fr | Déficit immunitaire primaire avec prédisposition aux infections virales sévères | Immunodéficience primaire avec prédisposition aux infections virales sévères |
| de | Immundefekt, primärer, mit Prädisposition zur schweren Virusinfektion | |
| es | Inmunodeficiencia primaria con predisposición a infección viral grave | |
| it | Immunodeficienza primitiva con predispozione alle infezioni virali gravi | |
| nl | Primaire immuundeficiëntie met vatbaarheid voor ernstige virale infectie | |
| pt | Imunodeficiência primária com predisposição a infeção viral grave | |
| pl | Pierwotny Niedobór odporności z predyspozycją do ciężkich zakażeń wirusowych | |
| cs | Primární imunodeficit s predispozicí k těžkým virovým infekcím | |
| uk | Первинний імунодефіцит зі схильністю до тяжких вірусних інфекцій | |
| zh | 原发性免疫缺陷伴严重病毒易感 | |
| tr | Ağır viral enfeksiyona yatkınlık ile seyreden primer immün yetmezlik |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 18545 | E | validated | |
| UMLS | C5681211 | 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:101988Primary immunodeficiency due to a defect in innate 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/431156
- This record as JSON: /data/d/431156.json