Rapidly involuting congenital hemangioma
Synonyms: RICH · Rapidly involuting congenital haemangioma
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- Antenatal
- Status
- active
A rare congenital hemangioma characterized by benign round or oval-shaped, solitary and raised or infiltrating vascular tumors that are fully formed in utero and differ from non-involuting congenital hemangiomas (NICH) mainly because they undergo rapid postnatal involution.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Rapidly involuting congenital hemangioma | RICH · Rapidly involuting congenital haemangioma |
| fr | Hémangiome congénital rapidement involutif | RICH |
| de | Rasch involutierendes kongenitales Hämangiom | RICH |
| es | Hemangioma congénito rápidamente involutivo | RICH |
| it | Emangioma congenito a rapida involuzione | RICH |
| nl | Snel involuerend congenitaal hemangioom | RICH |
| pt | Hemangioma rapidamente evolutivo, congénito | |
| pl | Naczyniak wrodzony szybko zanikający | RICH |
| cs | Rychle involující vrozený hemangiom | RICH |
| uk | Вроджена гемангіома, що швидко поширюється | RICH |
| zh | 快速消退性先天性血管瘤 | RICH |
| tr | Hızla gerileyen doğumsal hemanjiyom | RICH |
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 |
| ICD-11 | XH6RC4 | E | specific | validated |
| MONDO | 0015404 | E | validated | |
| UMLS | C1275421 | E | validated | |
| GARD | 19958 | 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
1 record| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | Unknown | — | Worldwide | Class only | Not yet 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.
HPO phenotypes
14 annotations · validated 2019-05-15| HPO | Term (as annotated by Orphanet) | Diagnostic |
|---|---|---|
| Obligate (100%) | ||
| HP:0001028 | Hemangioma | Diagnostic criterion |
| Frequent (79-30%) | ||
| HP:0007466 | Midfrontal capillary hemangioma | |
| HP:0031449 | Perineal hemangioma | |
| HP:0007618 | Subcutaneous calcification | |
| HP:0100585 | Telangiectasia of the skin | |
| Occasional (29-5%) | ||
| HP:0001635 | Congestive heart failure | |
| HP:0100784 | Peripheral arteriovenous fistula | |
| HP:0001015 | Prominent superficial veins | |
| HP:0001873 | Thrombocytopenia | |
| HP:0410266 | Visceral hemangioma | |
| Very rare (<4-1%) | ||
| HP:0010885 | Avascular necrosis | |
| HP:0031207 | Hepatic hemangioma | |
| HP:0100578 | Lipoatrophy | |
| Excluded (0%) | ||
| HP:0012329 | Tufted angioma | |
Run the differential on the 1 obligate / very frequent terms
Annotation source: 27058448[PMID]_18676554[PMID]_27540637[PMID]_7911127[PMID]
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/141184
- This record as JSON: /data/d/141184.json