ORPHA:2416
Congenital primary lymphedema without systemic or visceral involvement
- Type
- Clinical group
- 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 | Congenital primary lymphedema without systemic or visceral involvement | |
| fr | Lymphoedème primaire congénital sans atteinte systémique ou viscérale | |
| de | Kongenitales primäres Lymphödem ohne systemische oder viszerale Beteiligung | |
| es | Linfedema congénito primario con afectación sistémica o visceral | |
| it | Linfedema primitivo congenito | |
| nl | Congenitaal primair lymfoedeem zonder systemische of viscerale betrokkenheid | |
| pt | Linfedema primário congénito sem envolvimento sistémico ou visceral | |
| pl | Wrodzony pierwotny obrzęk limfatyczny | |
| cs | Vrozený primární lymfedém bez systémového či orgánového postižení | |
| uk | Вроджена первинна лімфедема без системного або вісцерального ураження | |
| zh | 先天性原发性淋巴水肿不伴系统性或内脏受累 | |
| tr | Sistemik veya viseral tutulum olmayan doğumsal primer lenfödem |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| UMLS | C5680523 | 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:568041Primary lymphedema without systemic or visceral involvement
rare developmental anomalies during embryogenesis; rare genetic diseases; rare skin diseases; rare circulatory system diseases
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/2416
- This record as JSON: /data/d/2416.json