ORPHA:79450
Non-hereditary congenital primary lymphedema
inactive · moved to ORPHA:79452Milroy disease
- Type
- Disease
- Group
- Disorder
- Status
- inactive
- Flag
- Deprecated entity
This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Milroy disease
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Non-hereditary congenital primary lymphedema | |
| fr | Lymphoedème primaire congénital non héréditaire | |
| de | Lymphödem, kongenitales primäres, nicht-hereditäres | |
| es | Linfedema congénito primario no hereditario | |
| it | Linfedema primitivo congenito non ereditario | Malattia Milroy-simile |
| nl | Niet-erfelijk congenitaal primair lymfoedeem | |
| pt | Linfedema primário congénito não-hereditário | |
| pl | Niedziedziczny wrodzony pierwotny obrzęk limfatyczny | Choroba podobna do choroby Milroy'a |
| cs | Milroy-like disease | Nonhereditární vrozený primární lymfedém · Onemocnění podobné Milroyově nemoci |
| uk | Неспадкова вроджена первинна лімфедема | |
| zh | 非遗传性先天性原发性淋巴水肿 | |
| tr | Kalıtsal olmayan doğumsal primer lenfödem |
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Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
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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/79450
- This record as JSON: /data/d/79450.json