ORPHA:329324
Inverse Klippel-Trénaunay syndrome
inactive · moved to ORPHA:90308Capillary-lymphatic-venous malformation with segmental distribution
Synonyms: Cutaneous hemangioma with muscle or bone atrophy
- Type
- Disease
- Group
- Disorder
- Status
- inactive
- Flag
- Deprecated entity
This entity has been excluded from the Orphanet nomenclature of rare diseases and moved to Capillary-lymphatic-venous malformation with segmental distribution
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Inverse Klippel-Trénaunay syndrome | Cutaneous hemangioma with muscle or bone atrophy |
| fr | Syndrome de Klippel-Trénaunay inverse | Hémangiome cutané avec atrophie osseuse ou musculaire |
| de | Inverses Klippel-Trenaunay-Syndrom | Kutanes Hämangiom mit Muskel- oder Knochenatrophie |
| es | Síndrome de Klippel-Trenaunay invertido | Hemangioma cutáneo con atrofia muscular u ósea |
| it | Sindrome inversa di Klippel-Trénaunay | Emangioma cutaneo con atrofia muscolare od ossea |
| nl | Invers syndroom van Klippel-Trenaunay | Cutaan hemangioom met spier- of botatrofie |
| pt | Síndrome Klippel-Trenaunay inverso | Hemangioma cutâneo com atrofia muscular ou óssea |
| pl | Odwrócony zespół Klippela i Trénaunay'a | Hemangioma skóry z atrofią mięśni lub kości |
| cs | Inverzní Klippelův-Trénaunayův syndrom | Kutánní hemangiom se svalovou nebo kostní atrofií · Inverzní Klippel-Trénaunayův syndrom |
| uk | Інвертований синдром Кліппеля-Треноне | Шкірна гемангіома з атрофією мязів або кісток |
| zh | 逆行性Klippel-TrÚnaunay综合征 | 皮肤血管瘤伴肌肉或骨骼萎缩 |
| tr | Ters Klippel-Trenaunay sendromu | Kas veya kemik atrofisi ile seyreden kutanöz hemanjiyom |
Definition in:
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0018001 | E | validated | |
| UMLS | C5679859 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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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/329324
- This record as JSON: /data/d/329324.json