ORPHA:101992
Immunodeficiency due to a complement cascade protein anomaly
- 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 | Immunodeficiency due to a complement cascade protein anomaly | |
| fr | Déficit immunitaire dû à une anomalie de la cascade du complément | Immunodéficience due à une anomalie de la cascade du complément |
| de | Immundefekt mit Störung des Komplement-Aktivierungsweg | |
| es | Inmunodeficiencia por anomalía en la cascada del complemento | |
| it | Immunodeficienza da anomalie delle proteine della cascata del complemento | |
| nl | Immuundeficiëntie door een complementcascade-eiwitanomalie | |
| pt | Imunodeficiência por anomalia da via alternativa do complemento | |
| pl | Niedobór odporności z powodu anomalii białek układu dopełniacza | |
| cs | Imunodeficience způsobená proteinovou anomálií v kaskádě komplementu | |
| uk | Імунодефіцит внаслідок аномалії білка каскаду комплементу | |
| zh | 补体级联蛋白异常所致免疫缺陷 | |
| tr | Kompleman kaskad protein anomalisine bağlı immün yetmezlik |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | D84.1 | E | specific | validated |
| ICD-11 | 4A00.1 | E | specific | validated |
| MONDO | 15136 | E | validated | |
| UMLS | C5681769 | E | validated | |
| GARD | 19811 | 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: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/101992
- This record as JSON: /data/d/101992.json