ORPHA:675369
Microvenular hemangioma
Synonyms: MVH · Microvenular haemangioma
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- Adult
- Status
- active
Orphadata ships no English definition for this code.
1
Names in Orphadata languages
10 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Microvenular hemangioma | MVH · Microvenular haemangioma |
| fr | Hémangiome microveinulaire | HMV |
| de | Hämangiom, mikrovenöses | MVH |
| es | Hemangioma microvenular | |
| it | Emangioma microvenulare | MVH |
| nl | Microvenulair hemangioom | MVH |
| pt | Hemangioma microvenular | MVH |
| pl | Naczyniak dotyczący małych żył | = en |
| cs | Mikrovenulární hemangiom | = en |
| uk | Мікровенулярна гемангіома | MVH |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | D18.0 | NTBT | attributed | validated |
| ICD-11 | 2F2Y | NTBT | index | validated |
| MONDO | 0975758 | E | validated | |
| MONDO | 975758 | E | validated | |
| UMLS | C1304506 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
3
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
No children.
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
2 records| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Cases/families | 68 cases | Worldwide | Case(s) | Validated | 29445567[PMID] | |
| Point prevalence | <1 / 1 000 000 | — | Worldwide | Class only | Validated | 29445567[PMID]_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.
6
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
7
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/675369
- This record as JSON: /data/d/675369.json