Partially involuting congenital hemangioma
Synonyms: Partially involuting congenital haemangioma
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- Antenatal
- Status
- active
A rare congenital hemangioma characterized by a superficial, red to violaceous lesion with overlying telangiectasia and a surrounding pale halo, which initially behaves like a rapidly involuting congenital hemangioma, beginning to involute shortly after birth. Involution is then aborted, and a residual tumor virtually indistinguishable from non-involuting congenital hemangioma remains. This lesion grows proportionally with the child and does not regress.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Partially involuting congenital hemangioma | Partially involuting congenital haemangioma |
| fr | Hémangiome congénital partiellement involutif | |
| de | Teilweise involutierendes kongenitales Hämangiom | PICH |
| es | Hemangioma congénito de involución parcial | |
| it | Emangioma congenito parzialmente involutivo | |
| nl | Partieel involuerend congenitaal hemangioom | |
| pt | Hemangioma congénito com involução parcial | |
| pl | Częściowo zanikający naczyniak wrodzony | = en |
| cs | Částečně involující vrozený hemangiom | = en |
| uk | Вроджена гемангіома з частковим залученням | |
| zh | 部分内卷的遗传性血管瘤 | |
| tr | Kısmi involüt doğumsal hemanjiyomu |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | D18.0 | NTBT | attributed | validated |
| ICD-11 | 2E81.2Y | NTBT | index | validated |
| MONDO | 0018716 | E | validated | |
| UMLS | C4733501 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:458775Congenital hemangioma
rare developmental anomalies during embryogenesis; rare circulatory system diseases; rare neoplastic diseases
No children.
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
0 recordsNo prevalence record in this release.
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/458785
- This record as JSON: /data/d/458785.json