ORPHA:458775
Congenital hemangioma
Synonyms: Congenital haemangioma · Haemangioma congénitale
- 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 | Congenital hemangioma | Congenital haemangioma · Haemangioma congénitale |
| fr | Hémangiome congénitale | |
| de | Hämangiom, kongenitales | |
| es | Hemangioma congénito | |
| it | Emangioma congenito | |
| nl | Congenitaal hemangioom | |
| pt | Hemangioma congénito | |
| pl | Naczyniak wrodzony | = en |
| cs | Vrozený hemangiom | = en |
| uk | Вроджена гемангіома | |
| zh | 先天性血管瘤 | |
| tr | Doğumsal hemanjiyom |
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Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 0018715 | E | validated | |
| MONDO | 18715 | E | validated | |
| UMLS | C0235753 | E | validated | |
| MedDRA | 10018818 | 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
Codes that Orphanet moved or referred to this one:
- ORPHA:210592OBSOLETE: Giant infantile hemangioma referred to · inactive
- ORPHA:238691OBSOLETE: Congenital liver hemangioma referred to · inactive
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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/458775
- This record as JSON: /data/d/458775.json