ORPHA:156149
Immune complex mediated vasculitis
- 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 | Immune complex mediated vasculitis | |
| fr | Vascularite à complexes immuns | |
| de | Vaskulitis, Immunkomplex-vermittelte | |
| es | Vasculitis por depósito de complejos inmunes | |
| it | Vasculite mediata da immunocomplessi | |
| nl | Immuuncomplex-gemedieerde vasculitis | |
| pt | Vasculite mediada por complexos imunes | |
| pl | Zapalenie naczyń wywołane kompleksami immunologicznymi | |
| cs | Vaskulitida zprostředkovaná imunitním komplexem | |
| uk | Імунокомплексно опосередкований системний васкуліт | |
| zh | 免疫复合物介导的血管炎 | |
| tr | Bağışıklık kompleksi aracılı vaskülit |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0015491 | E | validated | |
| MONDO | 15491 | E | validated | |
| UMLS | C5680655 | 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:156146Predominantly small-vessel vasculitis
rare systemic and rheumatological diseases; rare circulatory system 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/156149
- This record as JSON: /data/d/156149.json