ORPHA:567558
Non-genetic systemic disease with glomerulopathy as a major feature
- 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 | Non-genetic systemic disease with glomerulopathy as a major feature | |
| fr | Maladie systémique non génétique avec une glomérulopathie comme manifestation majeure | |
| de | Nicht genetisch bedingte systemische Krankheit mit Glomerulopathie als Hauptmerkmal | |
| es | Enfermedad sistémica no genética con glomerulopatía como característica principal | |
| it | Malattia sistemica non genetica a prevalente espressione glomerulopatica | |
| nl | Niet-genetische systemische ziekte met glomerulopathie als hoofdkenmerk | |
| pt | Glomerulopatia como característica principal em doença sistémica não-genética | |
| pl | Niegenetyczna choroba układowa z glomerulopatią jako głównym objawem | |
| cs | Negenetické systémové onemocnění s glomerulopatií jako hlavním příznakem | |
| uk | Системне захворювання з гломерулопатією як основною ознакою без генетичного дефекту | |
| zh | 以肾小球病变为主要特征的非遗传性系统性疾病 | |
| tr | Esas klinik özelliği glomerülopati olan genetik olmayan sistemik hastalık |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5681296 | 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:567554Systemic disease with glomerulopathy as a major feature
rare renal diseases; rare transplant-related disorders
Children (17):
- ORPHA:85445AA amyloidosis
- ORPHA:439232AApoAIV amyloidosis
- ORPHA:442582AH amyloidosis
- ORPHA:85443AL amyloidosis
- ORPHA:829Adult-onset Still disease
- ORPHA:117Behçet disease
- ORPHA:221Dermatomyositis
- ORPHA:449395IgG4-related kidney disease
- ORPHA:93672Juvenile dermatomyositis
- ORPHA:93568Juvenile polymyositis
- ORPHA:809Mixed connective tissue disease
- ORPHA:86861Non-amyloid monoclonal immunoglobulin deposition disease
- ORPHA:732Polymyositis
- ORPHA:779Reynolds syndrome
- ORPHA:797Sarcoidosis
- ORPHA:90291Systemic sclerosis
- ORPHA:567560Systemic vasculitis associated with glomerulopathy
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/567558
- This record as JSON: /data/d/567558.json