ORPHA:675362
Hobnail hemangioma
Synonyms: HH · Hobnail haemangioma · THH · Targetoid hemosiderotic haemangioma · Targetoid hemosiderotic hemangioma
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- All ages
- Status
- active
Orphadata ships no English definition for this code.
1
Names in Orphadata languages
10 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Hobnail hemangioma | HH · Hobnail haemangioma · THH · Targetoid hemosiderotic haemangioma · Targetoid hemosiderotic hemangioma |
| fr | Hémangiome de Hobnail | Targetoid Hemosiderotic Hemangioma |
| de | Hobnail-Hämangiom | HH · THH · Targetoides hämosiderotisches Hämangiom |
| es | Hemangioma en clavo | Hemangioma hemosiderótico en diana |
| it | Emangioma a chiodo | Emangioma emosiderotico a bersaglio · HH · THH |
| nl | 'Hobnail'-hemangioom | HH · THH · Targetoïd hemosiderotisch hemangioom |
| pt | Hemangioma Hobnail | HH · Hemangioma hemosiderótico em alvo · THH |
| pl | Guzek naczyniowy występujący na kończynach | = en |
| cs | Cvočkovitý hemangiom | = en |
| uk | Гемангіома нігтя | HH · Таргетна гемосидеротична гемангіома · THH |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | D18.0 | NTBT | attributed | validated |
| ICD-11 | LA90.1Z | NTBT | index | validated |
| MONDO | 0003258 | E | validated | |
| MONDO | 3258 | E | validated | |
| UMLS | C0346076 | 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
1 record| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Point prevalence | <1 / 1 000 000 | — | Worldwide | Class only | 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.
6
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/675362
- This record as JSON: /data/d/675362.json