ORPHA:93548
Glomerular disease
- 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 | Glomerular disease | |
| fr | Néphropathie glomérulaire | |
| de | Glomerulopathie | |
| es | Enfermedad glomerular | |
| it | Malattia glomerulare | |
| nl | Glomerulaire ziekte | |
| pt | Doença glomerular | |
| pl | Choroba kłębuszków nerkowych | |
| cs | Glomerulární onemocnění | |
| uk | Гломерулярна хвороба | |
| zh | 肾小球疾病 | |
| tr | Glomerüler hastalık |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0019722 | E | validated | |
| UMLS | C0268731 | 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 (2):
- ORPHA:506213Rare disorder potentially indicated for kidney transplant
rare transplant-related disorders - ORPHA:93626Rare renal disease
rare renal diseases
Children (12):
- ORPHA:84087Collagen type III glomerulopathy
- ORPHA:544590Collagen-related glomerular basement membrane disease
- ORPHA:567562Disorder with multisystemic involvement and glomerulopathy
- ORPHA:84090Fibronectin glomerulopathy
- ORPHA:567544Idiopathic non-lupus full-house nephropathy
- ORPHA:34145Immunoglobulin A nephropathy
- ORPHA:91137Immunotactoid or fibrillary glomerulopathy
- ORPHA:329481Lipoprotein glomerulopathy
- ORPHA:567564Nephrotic syndrome without extrarenal manifestations
- ORPHA:54370Primary membranoproliferative glomerulonephritis
- ORPHA:97560Primary membranous glomerulonephritis
- ORPHA:567554Systemic disease with glomerulopathy as a major feature
Codes that Orphanet moved or referred to this one:
- ORPHA:93551OBSOLETE: Secondary glomerular disease referred to · inactive
- ORPHA:97569OBSOLETE: Unclassified glomerulonephritis referred to · inactive
- ORPHA:102373OBSOLETE: Primary glomerular disease referred to · inactive
- ORPHA:280569OBSOLETE: Rapidly progressive glomerulonephritis referred to · inactive
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/93548
- This record as JSON: /data/d/93548.json