ORPHA:494421
Sacrococcygeal teratoma
- Type
- Clinical subtype
- Group
- Subtype of disorder
- Inheritance
- Not applicable
- Age of onset
- All ages
- Status
- active
This disease is described under Extragonadal teratoma
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Sacrococcygeal teratoma | |
| fr | Tératome sacro-coccygien | |
| de | Sakrokokzygeales Teratom | |
| es | Teratoma sacrococcígeo | |
| it | Teratoma sacro-coccigeo | |
| nl | Sacrococcygeaal teratoom | |
| pt | Teratoma sacrococcígeo | |
| pl | Potworniak okolicy krzyżowo-guzicznej | |
| cs | Sakrokokcygeální teratom | |
| uk | Крижово-куприкова тератома | |
| zh | 骶尾部畸胎瘤 | |
| tr | Sakrokoksigeal teratom |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | C41.4 | BTNT | attributed | validated |
| MONDO | 0042727 | E | validated | |
| UMLS | C0559459 | E | validated | |
| GARD | 319 | 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:883Extragonadal teratoma
rare neoplastic diseases; rare transplant-related disorders
No children.
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
0 recordsNo prevalence record in this release.
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/494421
- This record as JSON: /data/d/494421.json