ORPHA:263310
Thymoma type A
- Type
- Histopathological subtype
- Group
- Subtype of disorder
- Inheritance
- Not applicable
- Age of onset
- Adult
- Status
- active
This disease is described under Thymoma
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Thymoma type A | |
| fr | Thymome type A | |
| de | Thymom Typ A | |
| es | Timoma tipo A | |
| it | Timoma, tipo A | Neoplasia epiteliale primitiva del timo, tipo A · Tumore epiteliale primitivo del timo, tipo A |
| nl | Thymoom type A | |
| pt | Timoma tipo A | |
| pl | Grasiczak typu A | Pierwotny guz nabłonkowy grasicy typu A · Pierwotny nowotwór nabłonkowy grasicy typu A |
| cs | Thymom, typ A | Primární epiteliální neoplázie thymu, typ A · Primární epiteliální nádor thymu, typ A |
| uk | Тимома, тип А | Первинне епітеліальне новоутворення тимуса, тип А · Первинна епітеліальна пухлина тимуса, тип А |
| zh | A型胸腺瘤 | A型原发性胸腺上皮性肿瘤 |
| tr | Timoma tip A | Primer timik epitelyal tümörü tipA · Primer timik epitelyal neoplazma tipA |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | C37 | NTBT | attributed | validated |
| ICD-10 | D15.0 | NTBT | attributed | validated |
| ICD-11 | 2C27.2 | NTBT | index | validated |
| ICD-11 | XH6WN9 | E | specific | validated |
| MONDO | 0002588 | E | validated | |
| UMLS | C1266091 | 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:99867Thymoma
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 |
|---|---|---|---|---|---|---|
| Annual incidence | <1 / 1 000 000 | — | Europe | Class only | Validated | RARECARE surveillance of rare cancers in Europe 2011[OTHER] |
| Point prevalence | Unknown | — | Worldwide | 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.
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/263310
- This record as JSON: /data/d/263310.json