ORPHA:459345
Immunodeficiency due to a complement cascade component deficiency
- 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 component deficiency | |
| fr | Déficit immunitaire par déficit d'un composant de la cascade du complément | Immunodéficience due à un déficit d'un composant de la cascade du complément |
| de | Immundefekt durch Komponenten-Mangel der Komplement-Kaskase | |
| es | Inmunodeficiencia por deficiencia de un componente de la cascada del complemento | |
| it | Immunodeficienza da deficit di un componente della cascata del complemento | |
| nl | Immuundeficiëntie door deficiëntie van een component van complementcascade | |
| pt | Imunodeficiência por deficiência de um componente da cascata do complemento | |
| pl | Niedobór odporności spowodowany deficytem kaskady układu dopełniacza | |
| cs | Imunodeficit způsobený deficitem složky komplementové kaskády | |
| uk | Імунодефіцит, зумовлений дефіцитом компонентів каскаду комплементу | |
| zh | 补体级联成份缺乏引起的免疫缺陷病 | |
| tr | Kompleman kaskadı bileşen eksikliğine bağlı immün yetmezlik |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0003832 | E | validated | |
| MONDO | 3832 | E | validated | |
| UMLS | C5681110 | 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:101992Immunodeficiency due to a complement cascade protein anomaly
rare genetic diseases; rare immunological diseases
Children (5):
- ORPHA:280133Complement component 3 deficiency
- ORPHA:331187Immunodeficiency due to MASP-2 deficiency
- ORPHA:169147Immunodeficiency due to a classical component pathway complement deficiency
- ORPHA:169150Immunodeficiency due to a late component of complement deficiency
- ORPHA:331190Immunodeficiency due to ficolin3 deficiency
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/459345
- This record as JSON: /data/d/459345.json