ORPHA:714692
Congenital disseminated pyogenic granuloma
Synonyms: CDPG
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- Antenatal, Neonatal
- Status
- active
Orphadata ships no English definition for this code.
1
Names in Orphadata languages
9 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Congenital disseminated pyogenic granuloma | CDPG |
| fr | Granulome pyogénique disséminé congénital | = en |
| de | Kongenitales disseminiertes pyogenes Granulom | = en |
| es | Granuloma piógeno diseminado congénito | = en |
| it | Granuloma piogenico disseminato congenito | = en |
| nl | Congenitaal gedissemineerd pyogeen granuloom | CDPG · Congenitaal gedissemineerd granuloma pyogenicum |
| pt | Congenital disseminated pyogenic granuloma | |
| pl | Wrodzony rozsiany ziarniniak ropny | = en |
| cs | Congenital disseminated pyogenic granuloma | = en |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | L98.0 | NTBT | attributed | 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 | 20 cases | Worldwide | Case(s) | Validated | ORPHANET | |
| 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/714692
- This record as JSON: /data/d/714692.json