ORPHA:210589
Rare infantile hemangioma
Synonyms: Infantile haemangioma of rare localization · Infantile hemangioma of rare localization · Rare infantile haemangioma
- 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
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Rare infantile hemangioma | Infantile haemangioma of rare localization · Infantile hemangioma of rare localization · Rare infantile haemangioma |
| fr | Hémangiome infantile rare | |
| de | Seltenes infantiles Hämangiom | Seltenes Hämangiom im Kindesalter · Infantiles Hämangiom mit ungewöhnlicher Lokalisation |
| es | Hemangioma infantil raro | Hemangioma infantil de localización poco frecuente |
| it | Emangioma infantile raro | Emangioma infantile con localizzazione rara |
| nl | Zeldzaam infantiel hemangioom | Infantiel hemangioom met zeldzame lokalisatie |
| pt | Hemangioma da infância com localização rara | |
| pl | Naczyniak dziecięcy o rzadkiej lokalizacji | = en |
| cs | Infantilní hemangiom vzácné lokalizace | = en |
| uk | Рідкісна дитяча гемангіома | Інфантильна гемангіома рідкісної локалізації |
| zh | 罕见部位的婴儿血管瘤 | |
| tr | İnfantil hemanjiyomun nadir lokalizasyonu |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0016223 | E | validated | |
| MONDO | 16223 | E | validated | |
| UMLS | C3839613 | 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
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:673470Benign vascular tumor
rare developmental anomalies during embryogenesis; rare circulatory system diseases; rare neoplastic 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/210589
- This record as JSON: /data/d/210589.json