ORPHA:719939
Central conducting lymphatic anomaly
Synonyms: CCLA
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- Adolescent, Adult, Childhood, Infancy
- Status
- active
Orphadata ships no English definition for this code.
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Names in Orphadata languages
9 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Central conducting lymphatic anomaly | CCLA |
| fr | Anomalie lymphatique à drainage central | |
| de | Zentrale Lymphabflussstörung durch lymphatische Malformation | = en |
| es | Anomalía linfática del conducto central | = en |
| it | Anomalia linfatica del condotto centrale | = en |
| nl | Central conducting lymphatic anomaly | CCLA · Anomalie van centrale verzamelende lymfevaten |
| pt | Central conducting lymphatic anomaly | |
| pl | Central conducting lymphatic anomaly | = en |
| cs | Central conducting lymphatic anomaly | = en |
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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:719950Complex lymphatic anomaly
rare developmental anomalies during embryogenesis; rare circulatory system diseases
No children.
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Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
1 record| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | Unknown | — | Worldwide | Class only | Validated | ORPHANET |
Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.
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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/719939
- This record as JSON: /data/d/719939.json