ORPHA:100087
Rare thyroid tumor
- Type
- Category
- Group
- Group of disorders
- Status
- active
This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.
1
Names in Orphadata languages
12 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Rare thyroid tumor | |
| fr | Tumeur rare de la thyroïde | |
| de | Seltener Schilddrüsentumor | |
| es | Tumor raro de tiroides | |
| it | Tumore tiroideo raro | |
| nl | Zeldzame schildkliertumor | Zeldzame tumor van thyroïd |
| pt | Tumor tiroideu raro | |
| pl | Guz tarczycy | Rzadki guz tarczycy |
| cs | Nádory štítné žlázy | |
| uk | Рідкісна пухлина щитовидної залози | |
| zh | 甲状腺肿瘤 | |
| tr | Tiroid tümörü |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15074 | E | validated | |
| UMLS | C5816813 | 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 (2):
- ORPHA:101955Rare thyroid disease
rare endocrine diseases - ORPHA:182130Tumor of endocrine glands
rare neoplastic diseases
4
Genes
0 directOrphanet records no gene directly on this code.
5
Prevalence and incidence
4 records| Type | Class | Value | Area | Qualification | Validation | Source |
|---|---|---|---|---|---|---|
| Annual incidence | 1-9 / 100 000 | 3.2 / 100 000 | Worldwide | Value and class | Not yet validated | 21513910[PMID]_ORPHANET |
| Annual incidence | 1-9 / 100 000 | 5 / 100 000 | Europe | Value and class | Not yet validated | 21513910[PMID] |
| Annual incidence | 1-9 / 100 000 | 5.7 / 100 000 | Italy | Value and class | Not yet validated | 23518150[PMID]_ORPHANET |
| Annual incidence | 1-9 / 100 000 | 5.35 / 100 000 | France | Value and class | Not yet validated | 21513910[PMID]_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/100087
- This record as JSON: /data/d/100087.json