ORPHA:719950
Complex lymphatic anomaly
- 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.
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Names in Orphadata languages
9 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Complex lymphatic anomaly | |
| fr | Anomalie lymphatique complexe | |
| de | Komplexe lymphatische Anomalie | |
| es | Anomalía linfática compleja | |
| it | Anomalia linfatica complessa | |
| nl | Complexe anomalie van lymfestelsel | Complexe lymfatische anomalie · Complexe lymfatische afwijking · Complexe afwijking van lymfestelsel |
| pt | Complex lymphatic anomaly | |
| pl | Complex lymphatic anomaly | |
| cs | Complex lymphatic anomaly |
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Cross-references
qualifier = Orphanet mapping relationNo cross-references in this release.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:2415Rare lymphatic malformation
rare developmental anomalies during embryogenesis; 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.
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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/719950
- This record as JSON: /data/d/719950.json