ORPHA:100090
Rare parathyroid 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 parathyroid tumor | |
| fr | Tumeur rare des parathyroïdes | |
| de | Seltener Tumor der Nebenschilddrüse | |
| es | Tumor de paratiroides | |
| it | Tumore delle paratiroidi | |
| nl | Zeldzame bijschildkliertumor | |
| pt | Tumor da paratiroide raro | |
| pl | Rzadki guz przytarczyc | |
| cs | Vzácný nádor příštítného tělíska | |
| uk | Рідкісна пухлина паращитовидної залози | |
| zh | 罕见性甲状旁腺肿瘤 | |
| tr | Nadir paratiroid tümörü |
2
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| MONDO | 15076 | E | validated | |
| UMLS | C5681807 | E | validated | |
| GARD | 19764 | 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:68415Rare parathyroid disease and phosphocalcic metabolism anomaly
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
0 recordsNo prevalence record in this release.
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/100090
- This record as JSON: /data/d/100090.json