ORPHA:99865
Spermatocytic seminoma
- Type
- Disease
- Group
- Disorder
- Inheritance
- Unknown
- Age of onset
- Adolescent, Adult
- Status
- active
Spermatocytic seminoma (SS) is an extremely rare form of testicular cancer distinguished from testicular seminomatous germ cell tumors by a very low rate of metastasis and lack of an ovarian equivalent.
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Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Spermatocytic seminoma | |
| fr | Séminome spermatocytaire | |
| de | Seminom, spermatozytisches | |
| es | Seminoma espermatocítico | |
| it | Seminoma spermatocitico | |
| nl | Spermatocytisch seminoom | |
| pt | Seminoma espermatocítico | |
| pl | Nasieniak spermatocytowy | |
| cs | Spermatocytický seminom | |
| uk | Сперматоцитарна семінома | |
| zh | 精母细胞性精原细胞瘤 | |
| tr | Spermatositik seminom |
Definition in:
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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.Y | NTBT | index | validated |
| ICD-11 | XH80D1 | E | specific | validated |
| MONDO | 0020513 | E | validated | |
| UMLS | C0334517 | E | validated | |
| MedDRA | 10073118 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
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Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:363504Germ cell tumor of testis
rare urogenital diseases; rare neoplastic diseases; rare transplant-related disorders
No children.
Codes that Orphanet moved or referred to this one:
- ORPHA:99866OBSOLETE: Metastatic spermatocytic seminoma referred to · inactive
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Genes
0 directOrphanet records no gene directly on this code.
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Prevalence and incidence
2 records| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Annual incidence | <1 / 1 000 000 | 0.03 / 100 000 | Europe | Value and class | Validated | RARECARE surveillance of rare cancers in Europe[OTHER] |
| Point prevalence | Unknown | — | 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.
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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/99865
- This record as JSON: /data/d/99865.json