ORPHA:567560
Systemic vasculitis associated with glomerulopathy
- 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 | Systemic vasculitis associated with glomerulopathy | |
| fr | Vascularite systémique associée à une glomérulopathie | |
| de | Systemische Vaskulitis mit assoziierter Glomerulopathie | |
| es | Vasculitis sistémica asociada a glomerulopatía | |
| it | Vasculite sistemica associata a glomerulopatia | |
| nl | Systemische vasculitis geassocieerd met glomerulopathie | |
| pt | Vasculite sistémica associada a glomerulopatia | |
| pl | Układowe zapalenie naczyń z glomerulopatią | |
| cs | Systémová vaskulitida spojená s glomerulopatií | |
| uk | Системний васкуліт, асоційований з гломерулопатією | |
| zh | 与肾小球病变相关的系统性血管炎 | |
| tr | Glomerülopati ile seyreden sistemik vaskülit |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681300 | 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:567558Non-genetic systemic disease with glomerulopathy as a major feature
rare renal diseases; rare transplant-related disorders
Children (14):
- ORPHA:375Anti-glomerular basement membrane disease
- ORPHA:36258Buerger disease
- ORPHA:91138Cryoglobulinemic vasculitis
- ORPHA:183Eosinophilic granulomatosis with polyangiitis
- ORPHA:397Giant cell arteritis
- ORPHA:900Granulomatosis with polyangiitis
- ORPHA:761Immunoglobulin A vasculitis
- ORPHA:727Microscopic polyangiitis
- ORPHA:93126Pauci-immune glomerulonephritis
- ORPHA:93552Pediatric systemic lupus erythematosus
- ORPHA:767Polyarteritis nodosa
- ORPHA:728Relapsing polychondritis
- ORPHA:536Systemic lupus erythematosus
- ORPHA:3287Takayasu arteritis
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/567560
- This record as JSON: /data/d/567560.json