ORPHA:77241
OBSOLETE: Lymphedema praecox
inactive · referred to ORPHA:90186Meige disease
- Type
- Malformation syndrome
- Group
- Disorder
- Status
- inactive
- Flag
- Obsolete entity
This entity has been obsoleted from the Orphanet nomenclature of rare diseases.<br/><br/>Instead, consider using Meige disease
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | OBSOLETE: Lymphedema praecox | |
| fr | OBSOLETE : Lymphoedème précoce | |
| de | OBSOLET: Lymphoedema praecox | |
| es | OBSOLETO: Linfedema praecox | |
| it | OBSOLETO: Linfedema precoce | |
| nl | OBSOLEET: Lymphoedema praecox | |
| pt | OBSOLETO: Linfedema precoce | |
| pl | NIEAKTUALNE: Obrzek limfatyczny wczesny | |
| cs | NEAKTUÁLNÍ: Předčasný lymfedém | |
| uk | ЗАСТАРІЛО: Рання лімфедема | |
| zh | 弃用：早发型淋巴水肿 | |
| tr | Eski adı: Lenfödem prekoks |
2
Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
3
Classification
Not placed in any Orphanet classification in this release.
No children.
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/77241
- This record as JSON: /data/d/77241.json