ORPHA:2087
Glomerulonephritis-sparse hair-telangiectasis syndrome
inactive · moved to ORPHA:69735Hypotrichosis-lymphedema-telangiectasia-renal defect syndrome
- Type
- Malformation syndrome
- Group
- Disorder
- Status
- inactive
- Flag
- Deprecated entity
This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Hypotrichosis-lymphedema-telangiectasia-renal defect syndrome
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Glomerulonephritis-sparse hair-telangiectasis syndrome | |
| fr | Syndrome de glomérulopathie-hypotrichose-télangiectasies | |
| de | Glomerulonephritis-Spärliches Haar-Telangiektasien-Syndrom | |
| es | Síndrome de glomerulopatía-cabello escaso-telangiectasias | |
| it | Sindrome glomerulonefrite-capelli radi-telangectasia | |
| nl | Glomerulonefritis - dun haar - teleangiëctasieën-syndroom | |
| pt | Síndrome de glomerulonefrite-cabelo rarefeito-telangiectasia | |
| pl | Zapalenie kłębuszków nerkowych - rzadkie włosy - telangiektazja | |
| cs | Syndrom zahrnující glomerulonefritidu, řídké vlasy a teleangiektázii | |
| uk | Синдром гломерулонефриту-рідкого волосся-телеангіектазії | |
| zh | 肾小球性肾炎-头发稀疏-毛细血管扩张综合征 | |
| tr | Glomerülonefrit-seyrek saç-telenjiektazi sendromu |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MeSH | C536825 | E | validated | |
| UMLS | C1841989 | 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
Not placed in any Orphanet classification in this release.
No children.
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
0 recordsNo prevalence record in this release.
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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/2087
- This record as JSON: /data/d/2087.json