Testicular teratoma
Synonyms: Teratoma of the testis
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Age of onset
- Adolescent, Adult, Childhood, Infancy
- Status
- active
A rare neoplastic disease characterized by the presence of a testicular tumor composed of several, well-differentiated or immature, tissues derived from one or more of the 3 germinal layers. Patients typically present unilateral (occasionally bilateral) painless testicular swelling or a palpable testicular nodule/mass.
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Testicular teratoma | Teratoma of the testis |
| fr | Tératome testiculaire | Tératome des testicules |
| de | Teratom, testikuläres | Teratom des Hodens |
| es | Teratoma testicular | Teratoma de los testículos |
| it | Teratoma testicolare | Teratoma del testicolo |
| nl | Testiculair teratoom | Teratoom van de testis |
| pt | Teratoma testicular | |
| pl | Potworniak jądra | = en |
| cs | Testikulární teratom | Teratom varlat |
| uk | Тератома яєчка | Тератома яєчка |
| zh | 睾丸畸胎瘤 | 睾丸畸胎瘤 |
| tr | Testis teratomu | Testisin teratomu |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| OMIM | 273300 | NTBT | validated | |
| ICD-10 | C62.9 | NTBT | index | validated |
| ICD-11 | 2C80.2 | NTBT | index | validated |
| ICD-11 | 2F34 | NTBT | index | validated |
| MONDO | 0018193 | E | validated | |
| MeSH | C562472 | E | validated | |
| UMLS | C0238451 | E | validated | |
| MedDRA | 10073120 | 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:363472Tumor of testis and paratestis
rare urogenital diseases; rare neoplastic diseases
No children.
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
2 records| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Lifetime Prevalence | <1 / 1 000 000 | 0.04 / 100 000 | Europe | Value and class | Validated | 22033323[PMID]_RARECARE surveillance of rare cancers in Europe[OTHER] |
| Point prevalence | <1 / 1 000 000 | — | Europe | 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
Orphanet has no HPO annotation for this code in this release.
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/363483
- This record as JSON: /data/d/363483.json