ORPHA:2415
Rare lymphatic malformation
Synonyms: LM · Lymphangioma
- Type
- Category
- Group
- Group of disorders
- Inheritance
- Not applicable
- Age of onset
- Infancy, Neonatal
- 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 | Rare lymphatic malformation | LM · Lymphangioma |
| fr | Malformation lymphatique rare | Lymphangiome · ML |
| de | Seltene lymphatische Fehlbildung | LM · Lymphangiom · Lymphatische Malformation |
| es | Malformación linfática rara | Linfangioma |
| it | Malformazione linfatica rara | Linfangioma · ML |
| nl | Zeldzame lymfatische malformatie | Zeldzame malformatie van lymfestelsel · LM · Lymfangioom |
| pt | Malformação linfática rara isolada | LM · Linfangioma |
| pl | Izolowana rzadka malformacja limfatyczna | Limfangioma · LM |
| cs | Vzácná lymfatická malformace | LM · Lymfangiom |
| uk | Рідкісна лімфатична мальформація | LM · Лімфангіома |
| zh | 罕见淋巴管畸形 | 淋巴管瘤 |
| tr | Nadir lenfatik malformasyon | LM · Lenfanjiyom |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | D18.1 | E | specific | validated |
| ICD-11 | LA90.1 | E | specific | validated |
| MONDO | 2013 | E | validated | |
| UMLS | C5575909 | E | validated | |
| GARD | 9789 | 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:211255Slow-flow malformation, lymphatic type
rare developmental anomalies during embryogenesis; rare circulatory system diseases
Codes that Orphanet moved or referred to this one:
- ORPHA:137923OBSOLETE: Cervicofacial lymphatic malformation referred to · inactive
4
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 | 1-5 / 10 000 | 12.5 / 100 000 | Europe | Value and class | 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.
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/2415
- This record as JSON: /data/d/2415.json